BR112020013095A2 - safety systems for intelligent surgical stapling equipped with motor - Google Patents

Abstract

A surgical system is revealed which comprises a control circuit, a surgical instrument and a user interface. The end actuator assembly may comprise a sensor configured to detect a parameter associated with an end actuator function, and transmit the detected parameter to the control circuit. In addition, the control circuit can be configured to analyze the detected parameter based on a restriction defined by the system and avoid at least one function of the surgical instrument based on an analysis result. The user interface can be configured to provide a current status for at least one avoided function of the surgical instrument.

Description

Descriptive Report of the Invention Patent for "SAFETY SYSTEMS FOR INTELLIGENT SURGICAL STAPLING EQUIPPED WITH MOTOR".

REMISSIVE REFERENCE TO RELATED DEPOSIT REQUESTS

[0001] This application claims priority benefit under 35 USC 8,119 (e) to US provisional patent application serial number 62 / 691,227, entitled CONTROLLING A SURGICAL INSTRUMENT ACCORDING TO SENSED CLOSURE PARAMETERS, filed on June 28, 2018, the disclosure of each of which is incorporated herein by reference, in its entirety.

[0002] This application claims priority benefit under 35 USC8 $ 119 (e) to US provisional patent application No. 62 / 650,887, entitled SURGICAL SYSTEMS WITH OPTIMIZED SENSING CAPABILITIES, filed on March 30, 2018, to US provisional patent application serial number 62 / 650,877, entitled SURGICAL SMOKE EVACUATION SENSING AND CONTROLS, filed on March 30, 2018, to provisional patent application serial number 62 / 650,882, entitled SMOKE EVACUATION MODULE FOR INTERACTIVE SURGI - CAL PLATFORM, filed on March 30, 2018, and provisional patent application serial number 62 / 650.898, entitled CAPACITIVE COUPLED RETURN PATH PAD WITH SEPARABLE ARRAY E-MENTS, filed on March 30, 2018, with the disclosure of each of which is incorporated herein by reference, in its entirety.

[0003] This application also claims priority benefit under 35 US $ 119 (e) to US provisional patent application serial number 62 / 640,417, entitled TEMPERATURE CONTROL IN ULTRASONIC DEVICE AND CONTROL SYSTEM THEREFOR, filed on March 8, 2018 , and provisional patent application serial number 62 / 640,415, entitled ESTIMATING STATE OF ULTRASONIC END EFFECTOR

AND CONTROL SYSTEM THEREFOR filed on March 8, 2018, the disclosure of which is incorporated herein by reference, in its entirety.

[0004] This application claims priority under 35 USC8 $ 119 (e) to US provisional patent application serial number 62 / 611,341, entitled INTERACTIVE SURGICAL PLATFORM, filed on December 28, 2017, to the provisional patent application US serial number 62 / 611,340, entitled CLOUD-BASED MEDICAL ANALYTICS, filed on December 28, 2017, and provisional patent application US serial number 62 / 611,339, entitled ROBOT ASSISTED SURGICAL PLATFORM, filed on December 28 2017, the disclosure of each of which is incorporated herein by reference, in its entirety.

BACKGROUND

[0005] The present disclosure relates to several surgical systems.

SUMMARY

[0006] A surgical system comprises a control circuit and a surgical instrument. The surgical instrument comprises a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end of the drive shaft assembly. The end actuator assembly comprises a first jaw, a second jaw coupled pivotally to the first jaw, and a sensor. The sensor is configured to detect a parameter associated with an end actuator function and transmit the detected parameter to the control circuit. The control circuit is configured to analyze the detected parameter based on a restriction defined by the system and to avoid at least one function of the surgical instrument based on the analysis result. The surgical system additionally comprises a user interface configured to provide a current status for at least one avoided function of the surgical instrument.

[0007] A surgical system comprises a central surgical controller and a surgical instrument communicatively coupled to the central surgical controller. The surgical instrument comprises a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end of the drive shaft assembly. The end actuator assembly comprises a first jaw, a second jaw coupled pivotally to the first jaw, and a sensor. The sensor is configured to detect a parameter associated with an end actuator function and transmit the detected parameter to the central surgical controller. The central surgical controller comprises a processor and a memory attached to the processor. The memory stores instructions executable by the processor to analyze the detected parameter based on a constraint defined by the system and to avoid at least one function of the surgical instrument based on an analysis result. The surgical system additionally comprises a user interface configured to provide a current status for at least one avoided function of the surgical instrument.

[0008] A non-transitory, computer-readable medium stores computer-readable instructions that, when executed, cause a machine to analyze a detected parameter, associated with a function of an end actuator of a surgical system, based on a defined restriction by the system, and the surgical system includes a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end of the shaft assembly drive. The set of

The end handle comprises a first jaw, a second jaw pivotally coupled to the first jaw, and a sensor configured to detect the detected parameter and transmit the detected parameter to the machine. The instructions, when executed, additionally cause the machine to avoid at least one function of the surgical system based on an analysis result, and to generate a user interface. The user interface provides a current status for at least one avoided function of the surgical system.

FIGURES

[0009] The appeals of several aspects are presented with particularity in the attached claims. The various aspects, however, with regard to both the organization and the methods of operation, together with additional objects and advantages of the same, can be better understood in reference to the description presented below, considered together with the attached drawings as follows.

[0010] Figure 1 is a block diagram of an interactive surgical system implemented by computer, according to at least one aspect of the present disclosure.

[0011] Figure 2 is a surgical system being used to perform a surgical procedure in an operating room, according to at least one aspect of the present disclosure.

[0012] Figure 3 is a central surgical controller paired with a visualization system, a robotic system, and an intelligent instrument, according to at least one aspect of the present disclosure.

[0013] Figure 4 is a partial perspective view of a central surgical controller compartment, and of a generator module in combination that can be slidably received in a drawer of the central surgical controller compartment, according to least one aspect of the present disclosure.

[0014] Figure 5 is a perspective view of a generator module in combination with bipolar, ultrasonic and monopolar contacts and a smoke evacuation component, in accordance with at least one aspect of the present disclosure.

[0015] Figure 6 illustrates different power bus connectors for a plurality of side coupling ports of a side modular cabinet configured to receive a plurality of modules, in accordance with at least one aspect of the present disclosure.

[0016] Figure 7 illustrates a vertical modular cabinet configured to receive a plurality of modules, according to at least one aspect of the present disclosure.

[0017] Figure 8 illustrates a surgical data network that comprises a central modular communication controller configured to connect modular devices located in one or more operating rooms of a health care facility, or any environment in a hospital. installation of health services specially equipped for surgical operations, to the cloud, in accordance with at least one aspect of the present disclosure.

[0018] Figure 9 illustrates an interactive surgical system implemented by computer, according to at least one aspect of the present disclosure.

[0019] Figure 10 illustrates a central surgical controller that comprises a plurality of modules coupled to the modular control tower, according to at least one aspect of the present disclosure.

[0020] Figure 11 illustrates an aspect of a universal serial bus (USB) central controller device, in accordance with at least one aspect of the present disclosure.

[0021] Figure 12 illustrates a logical diagram of a control system for an instrument or surgical tool, according to at least one aspect of the present disclosure.

[0022] Figure 13 illustrates a control circuit configured to control aspects of the instrument or surgical tool, according to at least one aspect of the present disclosure.

[0023] Figure 14 illustrates a combinational logic circuit configured to control aspects of the instrument or surgical tool, according to at least one aspect of the present disclosure.

[0024] Figure 15 illustrates a sequential logic circuit configured to control aspects of the instrument or surgical tool, according to at least one aspect of the present disclosure.

[0025] Figure 16 illustrates an instrument or surgical tool that comprises a plurality of motors that can be activated to perform various functions, according to at least one aspect of the present disclosure.

[0026] Figure 17 is a schematic diagram of a robotic surgical instrument configured to operate a surgical tool described therein, in accordance with at least one aspect of the present disclosure.

[0027] Figure 18 illustrates a block diagram of a surgical instrument programmed to control the distal translation of the displacement member, according to an aspect of the present disclosure.

[0028] Figure 19 is a schematic diagram of a surgical instrument configured to control various functions, according to at least one aspect of the present disclosure.

[0029] Figure 20 is a stroke length graph that shows an example of a control system that modifies the stroke length of a gripping set based on the articulation angle.

[0030] Figure 21 is a positioning chart of the closing tube assembly that shows an example of a control system modifying a longitudinal position of the closing tube assembly based on the pivot angle;

[0031] Figure 22 is a comparison of a stapling method that uses controlled tissue compression versus a stapling method without controlled tissue compression.

[0032] Figure 23 is a force graph shown in section A and a related displacement graph shown in section B, where the force graph and the displacement graph have a geometry axis x that defines time, an axis geometric y of the displacement graph defines a displacement of a firing rod, and a geometric axis y of the force graph defines a torsional force detected in a motor configured to advance the firing rod.

[0033] Figure 24 is a schematic illustration of a fabric contact circuit that shows the completion of the circuit by contacting a pair of contact plates spaced with the fabric.

[0034] Figure 25 is a perspective view of a surgical instrument that has a set of interchangeable drive axles operationally coupled to it, according to at least one aspect of this disclosure.

[0035] Figure 26 is an exploded view of a portion of the surgical instrument of Figure 25, according to at least one aspect of this disclosure.

[0036] Figure 27 is a view of the exploded set of portions of the interchangeable drive shaft assembly, according to at least one aspect of this disclosure.

[0037] Figure 28 is an exploded view of an end actuator for the surgical instrument of Figure 25, according to at least one aspect of this disclosure.

[0038] Figure 29A is a block diagram of a control circuit for the surgical instrument of Figure 25, comprising two drawing sheets, according to at least one aspect of this disclosure.

[0039] Figure 29B is a block diagram of a control circuit for the surgical instrument of Figure 25, comprising two drawing sheets, according to at least one aspect of this disclosure.

[0040] Figure 30 is a block diagram of the control circuit of the surgical instrument of Figure 25 that illustrates interfaces between the handle assembly, the feeding assembly and the handle assembly and the interchangeable drive shaft assembly, according to at least one aspect of the present disclosure.

[0041] Figure 31 shows an example of a medical device that can include one or more aspects of the present invention.

[0042] Figure 32 represents an example of a medical device end actuator surrounding the tissue, according to one or more aspects of the present disclosure.

[0043] Figure 33 represents an example of a medical device end actuator compressing tissue, according to one or more aspects of the present disclosure.

[0044] Figure 34 represents exemplary forces exerted by an end actuator of a tissue compressing medical device, according to one or more aspects of the present disclosure.

[0045] Figure 35 also represents exemplary forces exerted by an end actuator of a medical tissue compressor device, according to one or more aspects of the present disclosure.

[0046] Figure 36 represents an example of a tissue compression sensor system, according to one or more aspects of the present disclosure.

[0047] Figure 37 also represents an example of a tissue compression sensor system, according to one or more aspects of the present disclosure.

[0048] Figure 38 also represents an example of a tissue compression sensor system, according to one or more aspects of the present disclosure.

[0049] Figure 39 is also an example of a circuit diagram, according to one or more aspects of the present disclosure.

[0050] Figure 40 is also an example of a circuit diagram, according to one or more aspects of the present disclosure.

[0051] Figure 41 is a graph that represents an example of frequency modulation according to one or more aspects of the present disclosure.

[0052] Figure 42 is a graph representing an RF compound according to one or more aspects of the present disclosure.

[0053] Figure 43 is a graph representing RF signals filtered according to one or more aspects of the present disclosure.

[0054] Figure 44 is a perspective view of a surgical instrument with an articulated interchangeable drive shaft.

[0055] Figure 45 is a side view of the tip of the surgical instrument.

[0056] Figures 46 to 50 are graphs plotting span size over time (Figure 46), trigger current over time (Figure 47), tissue compression over time (Figure 48), deformation anvil over time (Figure 49), and trigger strength over time (Figure 50).

[0057] Figure 51 is a graph plotting tissue displacement as a function of tissue compression for normal tissues.

[0058] Figure 52 is a graph plotting tissue displacement as a function of tissue compression to distinguish normal and diseased tissues.

[0059] Figure 53 illustrates a modality of an end actuator comprising a first sensor and a second sensor.

[0060] Figure 54 is a logic diagram illustrating a method for adjusting the measurement of the first sensor based on the input from the second sensor of the end actuator illustrated in Figure 53.

[0061] Figure 55 is a logic diagram illustrating a method for determining a query table for a first sensor based on input from a second sensor.

[0062] Figure 56 is a logic diagram illustrating a method for a process to calibrate a first sensor in response to an input from a second sensor.

[0063] Figure 57 is a logical diagram illustrating a method for determining and displaying the thickness of a section of tissue trapped between an anvil and an end actuator staple cartridge.

[0064] Figure 58 is a logical diagram illustrating a method for determining and displaying the thickness of a section of tissue stuck between the anvil and the end actuator staple cartridge.

[0065] Figure 59 is a graph illustrating an adjusted Hall thickness measurement, compared to an unmodified Hall thickness measurement.

[0066] Figure 60 illustrates a modality of an end actuator comprising a first sensor and a second sensor.

[0067] Figure 61 illustrates a modality of an end actuator comprising a first sensor and a plurality of second sensors.

[0068] Figure 62 is a logical diagram illustrating a modality

a process for adjusting a measurement of a first sensor in response to a plurality of secondary sensors.

[0069] Figure 63 illustrates a modality of a configured circuit for converting signals from a first sensor and a plurality of secondary sensors into digital signals receivable by a processor.

[0070] Figure 64 illustrates a modality of an end actuator comprising a plurality of sensors.

[0071] Figure 65 is a logic diagram illustrating a method of a process for determining one or more properties of tissues based on a plurality of sensors.

[0072] Figure 66 illustrates a modality of an end actuator comprising a plurality of sensors coupled to a second claw member.

[0073] Figure 67 illustrates an embodiment of a staple cartridge comprising a plurality of sensors formed integrally thereon.

[0074] Figure 68 is a logic diagram illustrating a method of a process for determining one or more parameters of a section of tissue trapped within an end actuator.

[0075] Figure 69 illustrates a modality of an end actuator comprising a plurality of redundant sensors.

[0076] Figure 70 is a logic diagram illustrating a method of a process for selecting the most reliable output from a plurality of redundant sensors.

[0077] Figure 71 illustrates a modality of an end actuator comprising a sensor that comprises a specific sampling rate to limit or eliminate false signals.

[0078] Figure 72 is a logic diagram illustrating a method for generating a thickness measurement for a section of tissue located between an anvil and a staple cartridge for an end actuator.

[0079] Figures 73 and 74 illustrate a modality of an end actuator comprising a sensor to identify clip cartridges of different types.

[0080] Figure 75 illustrates an aspect of a segmented flexible circuit configured to be fixedly attached to a claw member of an end actuator, in accordance with at least one aspect of the present disclosure.

[0081] Figure 76 illustrates an aspect of a segmented flexible circuit configured to be mounted on a clamp member of an end actuator, in accordance with at least one aspect of the present disclosure.

[0082] Figure 77 illustrates an aspect of an end actuator configured to measure a gap of GT fabric, according to at least one aspect of the present disclosure.

[0083] Figure 78 illustrates an aspect of an end actuator comprising a segmented flexible circuit, in accordance with at least one aspect of the present disclosure.

[0084] Figure 79 illustrates the end actuator shown in Figure 78 with the claw member holding the fabric between the claw member and the staple cartridge, in accordance with at least one aspect of the present disclosure.

[0085] Figure 80 is a diagram of an absolute positioning system for a surgical instrument, in which the absolute positioning system comprises an arrangement of the controlled motor drive circuit comprising a sensor arrangement, according to at least one aspect of the present disclosure.

[0086] Figure 81 is a diagram of a position sensor that comprises a magnetic rotating absolute positioning system.

according to at least one aspect of the present disclosure.

[0087] Figure 82 is a cross-sectional view of an end actuator of a surgical instrument, showing a course of the firing member in relation to the tissue trapped within the end actuator according to at least one aspect of the present revelation.

[0088] Figure 83 is a first graph of two closing force plots (FTC) that represents the force applied to a closing member to close on thick and thin tissue during a closing phase and a second graph of two plots of firing force (FTF) that represents the force applied to a firing member to fire through thick, thin tissue during a firing phase.

[0089] Figure 84 is a graph of a control system configured to provide progressive closure of a closing member during a firing stroke, when the displacement member advances distally and engages an arm clamping force to decrease the load of the closing force on the closing member at a desired speed and to decrease the load of the firing force on the firing member, according to at least one aspect of the present disclosure.

[0090] Figure 85 illustrates a feedback control system of the derivative integral proportional controller (PID), according to at least one aspect of the present disclosure.

[0091] Figure 86 is a logical flowchart that represents a process of a control program or a logical configuration to determine the speed of a closing member, according to at least one aspect of the present disclosure.

[0092] Figure 87 is a timeline showing the situational recognition of a central surgical controller, according to at least one aspect of the present disclosure.

[0093] Figure 88 illustrates a block diagram of a surgical system configured to control a surgical function, in accordance with at least one aspect of the present disclosure.

[0094] Figure 89 is a schematic diagram of a surgical instrument with situational recognition configured to control various functions, according to at least one aspect of the present report.

[0095] Figure 90 is a logical flowchart that represents an algorithm based on situational recognition to control a surgical function, according to at least one aspect of the present disclosure.

[0096] Figure 91 is a logical flowchart that represents an algorithm to control a surgical function, according to at least one aspect of the present disclosure.

[0097] Figure 92 illustrates a portion of the patient's tissue comprising a tumor as well as defined surgical margins with respect to the tumor, in accordance with at least one aspect of the present disclosure.

[0098] Figure 93 is a logical flowchart of a process that represents a control program or a logical configuration to solve device selection problems, according to at least one aspect of the present disclosure.

[0099] Figure 94 illustrates a block diagram of a surgical system configured to determine the suitability of a surgical instrument based on the parameters of the device and the detected parameters, according to at least one aspect of the present disclosure.

[0100] Figure 95 is a block diagram of a surgical instrument, according to at least one aspect of the present disclosure;

[0101] Figure 96 illustrates a logical flowchart of a process for controlling a surgical instrument according to the integrity of the attached tissue, according to at least one aspect of the present disclosure.

[0102] Figure 97 illustrates a first graph representing the force of the end actuator to close versus the time for illustrative shots of a surgical instrument, in accordance with at least one aspect of the present disclosure.

[0103] Figure 98 illustrates a second graph that represents the force of the end actuator to close versus the time for an illustrative shot of a surgical instrument, according to at least one aspect of the present disclosure.

[0104] Figure 99 illustrates a logical flow chart of a process for controlling a surgical instrument according to the physiological type of the tissue attached, in accordance with at least one aspect of the present disclosure.

[0105] Figure 100A illustrates a side elevation view of an end actuator pinching parenchyma, the end actuator being in the initial contact position with the parenchyma, in accordance with at least one aspect of the present disclosure.

[0106] Figure 100B illustrates a side elevation view of an end actuator clamping parenchyma, the end actuator being closed, in accordance with at least one aspect of the present disclosure.

[0107] Figure 101A illustrates a side elevation view of an end actuator clamping a vessel, the end actuator being in the initial contact position with the vessel, in accordance with at least one aspect of the present disclosure.

[0108] Figure 101B illustrates a side elevation view of an end actuator clamping a vessel, the end actuator being closed, in accordance with at least one aspect of the present disclosure.

[0109] Figure 102 illustrates a first graph and a second graph that represents the force of the end actuator to close and the speed of closure, respectively, versus the time for illustrative shots of a surgical instrument clamping the parenchyma, according to at least one aspect of the present disclosure.

[0110] Figure 103 illustrates a third graph and a fourth graph representing the force of the end actuator to close and the speed of closing, respectively, versus the time for illustrative shots of a surgical instrument clamping a vessel, according to at least one aspect of the present disclosure.

[0111] Figure 104 illustrates a fifth graph representing the force of the end actuator to close and the closing speed versus the time for an illustrative shot of a surgical instrument, according to at least one aspect of this revelation.

[0112] Figure 105 illustrates a fifth graph representing the force of the end actuator to close and the closing speed versus the time for an illustrative shot of a surgical instrument, according to at least one aspect of this revelation.

[0113] Figure 106 illustrates a fifth graph representing the force of the end actuator to close and the closing speed versus the time for an illustrative shot of a surgical instrument, in accordance with at least one aspect of this revelation.

[0114] Figure 107 illustrates a graph showing impedance versus time to determine when the claws of a surgical instrument come into contact with tissue and / or staples, in accordance with at least one aspect of the present disclosure.

[0115] Figure 108 illustrates a first graph representing various limits of tissue closure to control the closure of the end actuator, according to at least one aspect of the price.

feels revelation.

[0116] Figure 109 illustrates a second graph that represents various limits of tissue closure to control the closure of the end actuator, according to at least one aspect of the present disclosure.

[0117] Figure 110 is a logical flowchart of a process that represents a control program or a logical configuration for adjusting a closing rate algorithm, in accordance with at least one aspect of the present disclosure.

DESCRIPTION

[0118] The applicant for this application holds the following US patent applications, filed on June 29, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Patent application no. US series, entitled

CAPACITIVE COUPLED RETURN PATH PAD WITH SEPARABLE ARRAY ELEMENTS, Attorney Document No. END8542USNP / 170755; and US patent application serial number, entitled CONTROLLING A SURGICAL INSTRUMENT ACCORDING TO SENSED CLOSURE PARAMETERS, attorney document number END8543USNP / 170760; and US patent application serial number, entitled SYSTEMS FOR ADJUSTING END EFFECTOR PARAMETERS BA- SED ON PERIOPERATIVE INFORMATION, attorney document number END8543USNP1 / 170760-1; and US patent application serial number, entitled SAFETY SYSTEMS FOR SMART POWERED SURGICAL STAPLING, attorney document number END8543USNP2 / 170760-2; and US patent application serial number, entitled

SAFETY SYSTEMS FOR SMART POWERED SURGICAL STAPLING, document number of attorney END8543USNP3 / 170760-3; and US patent application serial number, entitled

SURGICAL SYSTEMS FOR DETECTING END EFFECTOR TISSUE DISTRIBUTION IRREGULARITIES, attorney's document no. END8543USNP4 / 170760-4; and US patent application serial number, entitled SYSTEMS FOR DETECTING PROXIMITY OF SURGICAL END EFFECTOR TO CANCEROUS TISSUE system, attorney document number END8543USNP5 / 170760-5; and US patent application serial number, entitled SURGICAL INSTRUMENT CARTRIDGE SENSOR ASSEMBLI- ES, attorney document number END8543USNP6 / 170760-6; and US patent application serial number, entitled VARIABLE OUTPUT CARTRIDGE SENSOR ASSEMBLY, attorney's document number END8543USNP7 / 170760-7; and US patent application serial number, entitled SURGICAL INSTRUMENT HAVING A FLEXIBLE ELECTRODE, attorney document number END8544USNP / 170761; and US patent application serial number, entitled SURGICAL INSTRUMENT HAVING A FLEXIBLE CIRCUIT, attorney document number END8544USNP1 / 170761-1; and US patent application serial number, entitled SURGICAL INSTRUMENT WITH A TISSUE MARKING AS-SEMBLY, attorney's document number END8544USNP2 / 170761-2; and US Patent Application Serial No., entitled SAFETY SURGICAL SYSTEMS WITH PRIORITIZED DATA TRANSMISSION CAPABILITIES, Attorney Document No. END8544 USNP3 / 170761-3; and US patent application serial number, intended

SURGICAL EVACUATION SENSING AND MOTOR CONTROL, document number of attorney END8545USNP / 170762; and US patent application serial number, entitled SURGICAL EVACUATION SENSOR ARRANGEMENTS, attorney document number END8545USNP1 / 170762-1; and US patent application serial number, entitled SURGICAL EVACUATION FLOW PATHS, attorney document number END8545USNP2 / 170762-2; and US patent application serial number, entitled SURGICAL EVACUATION SENSING AND GENERATOR CONTROL, attorney's document no. END8545USNP3 / 170762-3; and US patent application serial number, entitled SURGICAL EVACUATION SENSING AND DISPLAY, attorney's document number END8545USNP4 / 170762-4; and US patent application serial number, entitled COMMUNICATION OF SMOKE EVACUATION SYSTEM PARAME-

TERS TO HUB OR CLOUD IN SMOKE EVACUATION MODULE FOR INTERACTIVE SURGICAL PLATFORM, proxy document number END8546USNP / 170763; and US patent application serial number, entitled SMOKE EVACUATION SYSTEM INCLUDING A SEGMENTED CONTRROL CIRCUIT FOR INTERACTIVE SURGICAL PLATFORM, attorney document number END8546USNP1 / 170763-1; and US patent application serial number, entitled

SURGICAL EVACUATION SYSTEM WITH A COMMUNICATION

CIRCUIT FOR COMMUNICATION BETWEEN A FILTER AND A SMOKE EVACUATION DEVICE, Attorney's Document No. END8547USNP / 170764; e e US patent application serial number, entitled

DUAL IN-SERIES LARGE AND SMALL DROPLET FILTERS, Attorney Document No. END8548USNP / 170765.

[0119] The applicant for this application holds the following provisional US patent applications, filed on June 28, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US serial no. 62 / 691,228, entitled A METHOD OF USING REINFORCED FLEX CIRCUITS WITH MULTIPLE SENSORS WITH ELECTROSURGICAL DEVICES; and US Provisional Patent Application Serial No. 62 / 691,230, entitled SURGICAL INSTRUMENT HAVING A FLEXIBLE ELEC- TRODE; and US Provisional Patent Application Serial No. 62 / 691,219, entitled SURGICAL EVACUATION SENSING AND MOTOR CONTRROL; and US Provisional Patent Application Serial No. 62 / 691,257, entitled COMMUNICATION OF SMOKE EVACUATION SYSTEM PARAMETERS TO HUB OR CLOUD IN SMOKE EVACUATION MODULE FOR INTERACTIVE SURGICAL PLATFORM; and US Provisional Patent Application Serial No. 62 / 691,262, entitled SURGICAL EVACUATION SYSTEM WITH A COMMUNICA-

TION CIRCUIT FOR COMMUNICATION BETWEEN A FILTER AND A SMOKE EVACUATION DEVICE; and e US provisional patent application serial number 62 / 691,251, entitled DUAL IN-SERIES LARGE AND SMALL DROPLET FILTERS.

[0120] The applicant for this application holds the following US patent applications, filed on March 29, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e US patent application no. serial number 15 / 940,641, entitled

INTERACTIVE SURGICAL SYSTEMS WITH ENCRYPTED COMMUNICATION CAPABILITIES; and US Patent Application Serial No. 15 / 940,648, entitled

INTERACTIVE SURGICAL SYSTEMS WITH CONDITION HANDLING OF DEVICES AND DATA CAPABILITIES; and US Patent Application Serial No. 15 / 940,656, entitled SURGICAL HUB COORDINATION OF CONTROL AND COMMUNICATION OF OPERATING ROOM DEVICES; and US Patent Application Serial No. 15 / 940,666, entitled SPATIAL AWARENESS OF SURGICAL HUBS IN OPERATING RO-WHO; and US patent application serial no. 15 / 940,670, entitled COOPERATIVE UTILIZATION OF DATA DERIVED FROM SECONDARY SOURCES BY INTELLIGENT SURGICAL HUBS; and US patent application serial no. 15 / 940,677, entitled SURGICAL HUB CONTROL ARRANGEMENTS; and US patent application serial no. 15 / 940,632, entitled DATA STRIPPING METHOD TO INTERROGATE PATIENT REC- ORDS AND CREATE ANONYMIZED RECORD; and US Patent Application Serial No. 15 / 940,640, entitled

COMMUNICATION HUB AND STORAGE DEVICE FOR STORING

PARAMETERS AND STATUS OF A SURGICAL DEVICE TO BE SHARED WITH CLOUD BASED ANALYTICS SYSTEMS; and US Patent Application Serial No. 15 / 940,645, entitled

SELF DESCRIBING DATA PACKETS GENERATED AT AN ISSUING INSTRUMENT; and US Patent Application Serial No. 15 / 940,649, entitled DATA PAIRING TO INTERCONNECT A DEVICE MEASURED PA- RAMETER WITH AN OUTCOME; and US Patent Application Serial No. 15 / 940,654, entitled

SURGICAL HUB SITUATIONAL AWARENESS; and US patent application serial number 15 / 940,663, entitled SURGICAL SYSTEM DISTRIBUTED PROCESSING; and US patent application serial number 15 / 940,668, entitled AGGREGATION AND REPORTING OF SURGICAL HUB DATA; and US Patent Application Serial No. 15 / 940,671, entitled

SURGICAL HUB SPATIAL AWARENESS TO DETERMINE DEVICES IN OPERATING THEATER; and US Patent Application Serial No. 15 / 940,686, entitled DISPLAY OF ALIGNMENT OF STAPLE CARTRIDGE TO PRIOR LI-NEAR STAPLE LINE; and US patent application serial number 15 / 940,700, entitled STERILE FIELD INTERACTIVE CONTROL DISPLAYS; and US patent application serial no. 15 / 940,629, entitled COMPUTER IMPLEMENTED INTERACTIVE SURGICAL SYSTEMS; and US Patent Application Serial No. 15 / 940,704, entitled USE OF LASER LIGHT AND RED-GREEN-BLUE COLORATION TO DETERMINE PROPERTIES OF BACK SCATTERED LIGHT; and US Patent Application Serial No. 15 / 940,722, entitled

CHARACTERIZATION OF TISSUE IRREGULARITIES THROUGH THE USE OF MONO-CHROMATIC LIGHT REFRACTIVITY; and e US patent application serial number 15 / 940,742, entitled DUAL CMOS ARRAY IMAGING.

[0121] The applicant for this application holds the following US patent applications, filed on March 29, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e US patent application no. serial 15 / 940,636, entitled ADAPTIVE CONTROL PROGRAM UPDATES FOR SURGICAL DEVICES;

and US Patent Application Serial No. 15 / 940,653, entitled

ADAPTIVE CONTROL PROGRAM UPDATES FOR SURGICAL HUBS; and US Patent Application Serial No. 15 / 940,660, entitled CLOUD-BASED MEDICAL ANALYTICS FOR CUSTOMIZATION AND RECOMMENDATIONS TO A USER; and US Patent Application Serial No. 15 / 940,679, entitled CLOUD-BASED MEDICAL ANALYTICS FOR LINKING OF LOCAL USAGE TRENDS WITH THE RESOURCE ACQUISITION BEHAV- IORS OF LARGER DATA SET; and US Patent Application Serial No. 15 / 940,694, entitled CLOUD-BASED MEDICAL ANALYTICS FOR MEDICAL FACILITY SEGMENTED INDIVIDUALIZATION OF INSTRUMENT FUNCTION; and US Patent Application Serial No. 15 / 940,634, entitled CLOUD-BASED MEDICAL ANALYTICS FOR SECURITY AND AU-THENTICATION TRENDS AND REACTIVE MEASURES; and US Patent Application Serial No. 15 / 940,706, entitled

DATA HANDLING AND PRIORITIZATION IN A CLOUD ANALYTICS NETWORK; and e US patent application serial number 15 / 940,675, entitled CLOUD INTERFACE FOR COUPLED SURGICAL DEVICES.

[0122] The applicant for this application holds the following US patent applications, filed on March 29, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e US patent application no. serial 15 / 940,627, entitled DRIVE ARRANGEMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and US Patent Application Serial No. 15 / 940,637, entitled COMMUNICATION ARRANGEMENTS FOR ROBOT-ASSISTED

SURGICAL PLATFORMS; and US patent application serial number 15 / 940,642, entitled CONTROLS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and US Patent Application Serial No. 15 / 940,676, entitled AUTOMATIC TOOL ADJUSTMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and US patent application serial number 15 / 940,680, entitled CONTROLLERS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and US Patent Application Serial No. 15 / 940,683, entitled COOPERATIVE SURGICAL ACTIONS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and US Patent Application Serial No. 15 / 940,690, entitled DISPLAY ARRANGEMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and e US patent application serial number 15 / 940,711, entitled SENSING ARRANGEMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS.

[0123] The applicant for this application holds the following provisional US patent applications, filed on March 28, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US serial number 62 / 649,302, entitled INTERACTIVE SURGICAL SYSTEMS WITH ENCRYPTED COMMUNICATION CAPABILITIES; and US Provisional Patent Application Serial No. 62 / 649,294, entitled DATA STRIPPING METHOD TO INTERROGATE PATIENT RECORDS AND CREATE ANONYMIZED RECORD; and US Provisional Patent Application Serial No. 62 / 649,300, entitled SURGICAL HUB SITUATIONAL AWARENESS; and US Provisional Patent Application Serial No. 62 / 649,309,

titled SURGICAL HUB SPATIAL AWARENESS TO DETERMINE DEVICES IN OPERATING THEATER;

and US Provisional Patent Application Serial No. 62 / 649,310, entitled COMPUTER IMPLEMENTED INTERACTIVE SURGICAL SYSTEMS;

and US Provisional Patent Application Serial No. 62 / 649,291, entitled USE OF LASER LIGHT AND RED-GREEN-BLUE COLORED TO DETERMINE PROPERTIES OF BACK SCATTERED LIGHT;

and US Provisional Patent Application Serial No. 62 / 649,296, entitled ADAPTIVE CONTROL PROGRAM UPDATES FOR SURGI-CAL DEVICES;

and US Provisional Patent Application Serial No. 62 / 649,333, entitled CLOUD-BASED MEDICAL ANALYTICS FOR CUSTOMIZATION AND RECOMMENDATIONS TO A USER;

and US Provisional Patent Application Serial No. 62 / 649,327, entitled CLOUD-BASED MEDICAL ANALYTICS FOR SECURITY AND AUTHENTICATION TRENDS AND REACTIVE MEASURES;

and US Provisional Patent Application Serial No. 62 / 649,315, entitled DATA HANDLING AND PRIORITIZATION IN A CLOUD ANALYTICS NETWORK;

and US Provisional Patent Application Serial No. 62 / 649,313, entitled CLOUD INTERFACE FOR COUPLED SURGICAL DEVICES;

and US Provisional Patent Application Serial No. 62 / 649,320, entitled DRIVE ARRANGEMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS;

and US Provisional Patent Application Serial No. 62 / 649,307, entitled AUTOMATIC TOOL ADJUSTMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS; and e US provisional patent application serial number 62 / 649,323, entitled SENSING.

ARRANGEMENTS FOR ROBOT-ASSISTED SURGICAL PLATFORMS.

[0124] The applicant for the present application holds the following provisional US patent applications, filed on April 19, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US serial number 62 / 659,900, entitled METHOD OF HUB COMMUNICATION.

[0125] The applicant for this application holds the following provisional US patent applications, filed on March 30, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US serial number 62 / 650,887, entitled SURGICAL SYSTEMS WITH OPTIMIZED SENSING CAPA-BILITIES; and US Provisional Patent Application Serial No. 62 / 650,877, entitled SURGICAL SMOKE EVACUATION SENSING AND CONTRROLS; and US Provisional Patent Application Serial No. 62 / 650,882, entitled SMOKE EVACUATION MODULE FOR INTERACTIVE SURGICAL PLATFORM; and e US Provisional Patent Application Serial No. 62 / 650,898, entitled CAPACITIVE COUPLED RETURN PATH PAD WITH SEPA-RABLE ARRAY ELEMENTS.

[0126] The applicant for this application holds the following provisional US patent applications, filed on March 8, 2018, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US serial number 62 / 640,417, entitled TEMPERATURE CONTROL IN ULTRASONIC DEVICE AND CONTROL SYSTEM THEREFOR; and e US Provisional Patent Application Serial No. 62 / 640,415, entitled ESTIMATING STATE OF ULTRASONIC END EFFECTOR AND CONTROL SYSTEM THEREFOR.

[0127] The applicant for this application holds the following provisional US patent applications, filed on December 28, 2017, with the disclosure of each of which is incorporated herein by reference in its entirety: e Provisional patent application US Serial No. 62 / 611,341, entitled INTERACTIVE SURGICAL PLATFORM; and US Provisional Patent Application Serial No. 62 / 611,340, entitled CLOUD-BASED MEDICAL ANALYTICS; and e US Provisional Patent Application Serial No. 62 / 611,339, entitled ROBOT ASSISTED SURGICAL PLATFORM.

[0128] Before explaining in detail the various aspects of surgical instruments and generators, it should be noted that the illustrative examples are not limited, in terms of application or use, to the details of construction and arrangement of parts illustrated in the descriptions. in the attached description. Illustrative examples can be implemented or incorporated in other aspects, variations and modifications, and can be practiced or executed in several ways. In addition, except where otherwise indicated, the terms and expressions used in the present invention have been chosen for the purpose of describing illustrative examples for the convenience of the reader and not for the purpose of limiting it. In addition, it should be understood that one or more of the aspects, expressions of aspects, and / or examples described below can be combined with any one or more among the other aspects, expressions of aspects and / or examples described a follow.

[0129] Before explaining in detail the various aspects of surgical instruments and generators, it should be noted that the illustrative examples are not limited, in terms of application or use, to the details of construction and arrangement of parts illustrated in the descriptions in the attached description. Illustrative examples can be implemented or incorporated in other aspects, variations and modifications, and can be practiced or executed in several ways. In addition, except where otherwise indicated, the terms and expressions used in the present invention have been chosen for the purpose of describing illustrative examples for the convenience of the reader and not for the purpose of limiting it. In addition, it should be understood that one or more of the aspects, expressions of aspects, and / or examples described below can be combined with any one or more among the other aspects, expressions of aspects and / or examples described a follow.

[0130] Certain exemplary aspects will now be described to provide a general understanding of the principles of structure, function, manufacture and use of the devices and methods revealed in this document. One or more examples of these aspects are illustrated in the attached drawings. Those skilled in the art will understand that the devices and methods specifically described in this document and illustrated in the accompanying drawings are exemplary aspects without limitation, and that the scope of the various aspects is defined only by the claims. The characteristics illustrated or described in relation to an exemplifying aspect can be combined with the characteristics of other aspects. These modifications and variations are intended to be included in the scope of the appended claims.

[0131] Referring to Figure 1, a computer-implemented interactive surgical system 100 includes one or more surgical systems 102 and a cloud-based system (for example, cloud 104 which may include a remote server 113 attached to a device storage 105). Each surgical system 102 includes at least one central surgical controller 106 in communication with the cloud 104 which can include a remote server 113. In one example, as illustrated in Figure 1, surgical system 102 includes a display system 108, a robotic system 110, an intelligent hand-held surgical instrument 112, which are configured to communicate with each other and / or the central controller 106. In some respects, a surgical system 102 may include an M number of central controllers 106, an N number of visualization systems 108, an O number of robotic systems 110, and a P number of intelligent hand-held surgical instruments 112, where M, N, O, and P are integers greater than or equal to one.

[0132] Figure 3 represents an example of a surgical system 102 being used to perform a surgical procedure on a patient who is lying on an operating table 114 in a surgical operating room 116. A robotic system 110 is used in surgical procedure as a part of the surgical system 102. The robotic system 110 includes a surgeon console 118, a patient car 120 (surgical robot), and a surgical robotic central controller

122. The patient's carriage 120 can manipulate at least one removable-coupled surgical tool 117 through a minimally invasive incision in the patient's body while the surgeon views the surgical site through the surgeon's console 118. An image of the Surgical site can be obtained by a medical imaging device 124, which can be manipulated by patient car 120 to guide imaging device 124. Robotic central controller 122 can be used to process images from the surgical site to subsequent display to the surgeon via the surgeon console 118.

[0133] Other types of robotic systems can be readily adapted for use with the surgical system 102. Various examples of robotic systems and surgical instruments that are suitable for use with the present disclosure are described in provisional patent application no. 62 / 611,339, entitled ROBOT ASSISTED SURGI-CAL PLATFORM, filed on December 28, 2017, the disclosure of which is hereby incorporated by reference in its entirety.

[0134] Several examples of cloud-based analysis that are performed by the cloud 104, and are suitable for use with the present disclosure, are described in US provisional patent application serial number 62 / 611,340, entitled CLOUD-BASED MEDICAL ANALYTICS, filed on December 28, 2017, the disclosure of which is incorporated herein by reference, in its entirety.

[0135] In several aspects, the imaging device 124 includes at least one Image sensor and one or more optical components. Suitable image sensors include, but are not limited to, load-coupled device (CCD) sensors and complementary metal oxide semiconductor (CMOS) sensors.

[0136] The optical components of the imaging device 124 may include one or more light sources and / or one or more lenses. One or more light sources can be directed to illuminate portions of the surgical field. The one or more image sensors can receive reflected or refracted light from the surgical field, including reflected or refracted light from the tissue and / or surgical instruments.

[0137] One or more light sources can be configured to radiate electromagnetic energy in the visible spectrum, as well as in the invisible spectrum. The visible spectrum, sometimes called the optical spectrum or light spectrum, is that portion of the electromagnetic spectrum that is visible to (that is, can be detected by) the human eye and can be called visible light or simply light. A typical human eye will respond to wavelengths in the air that are from about 380 nm to about 750 nm.

[0138] The invisible spectrum (that is, the non-luminous spectrum) is that portion of the electromagnetic spectrum located below and above the visible spectrum (that is, wavelengths below about 380 nm and above about 750 nm). The invisible spectrum is not detectable by the human eye. Wavelengths greater than about 750 nm are longer than the visible red spectrum, and they become invisible infrared (IR), microwaves, radio and electromagnetic radiation. Wavelengths shorter than about 380 nm are shorter than the ultraviolet spectrum, and they become invisible ultraviolet, x-ray, and gamma-ray electromagnetic radiation.

[0139] In several respects, imaging device 124 is configured for use in a minimally invasive procedure. Examples of imaging devices suitable for use with the present disclosure include, but are not limited to, an arthroscope, angioscope, bronchoscope, choledocoscope, colonoscope, cytoscope, duodenoscope, enteroscope, esophagoscope-duodenoscope (gastroscope), endoscope, laryngoscope, nasopharyngoscope, sigmoidoscope, thoracoscope and ureteroscope.

[0140] In one aspect, the imaging device employs multiple spectrum monitoring to discriminate topography and underlying structures. A multi-spectral image is one that captures image data within wavelength bands across the electromagnetic spectrum. The wavelengths can be separated by filters or by using instruments that are sensitive to specific wavelengths, including light from frequencies beyond the visible light range, for example, IR and ultraviolet light. Spectral images can allow the extraction of additional information that the human eye cannot capture with its receivers for the colors red, green and blue. The use of multispectral imaging is described in more detail under the heading "Advanced Imaging Acquisition Module" in US provisional patent application serial number 62 / 611,341, entitled INTERACTIVE SURGICAL PLATFORM, deposited on December 28, 2017, whose revelation is hereby incorporated by reference in its entirety. Multispectral monitoring can be a useful tool for relocating a surgical field after a surgical task is completed to perform one or more of the tests previously described on the treated tissue.

[0141] It is axiomatic that strict sterilization of the operating room and surgical equipment is necessary during any surgery. The strict hygiene and sterilization conditions required in an "operating room", that is, an operating or treatment room, justify the highest possible sterilization of all medical devices and equipment. Part of this sterilization process is the need to sterilize anything that comes into contact with the patient or enters the sterile field, including the imaging device 124 and its connectors and components. It will be understood that the sterile field can be considered a specified area, such as inside a tray or on a sterile towel, which is considered free of microorganisms, or the sterile field can be considered an area, immediately around a patient, who was prepared to perform a surgical procedure. The sterile field may include members of the brushing team, who are properly dressed, and all furniture and accessories in the area.

[0142] In several aspects, the visualization system 108 includes one or more imaging sensors, one or more image processing units, one or more storage arrays and one or more screens that are strategically arranged in relation to the field sterile, as illustrated in Figure 2. In one aspect, the system

display theme 108 includes an interface for HL7, PACS and EMR. Various components of the 108 visualization system are described under the heading "Advanced Imaging Acquisition Module" in US provisional patent application serial number 62 / 611.341, entitled INTERACTIVE SURGICAL PLATFORM, filed on December 28, 2017, whose disclosure it is hereby incorporated by reference in its entirety.

[0143] As shown in Figure 2, a primary screen 119 is positioned in the sterile field to be visible to the operator on the operating table 114. In addition, a viewing tower 111 is positioned outside the sterile field. The display tower 111 includes a first non-sterile screen 107 and a second non-sterile screen 109, which are opposite each other. The visualization system 108, guided by the central controller 106, is configured to use screens 107, 109, and 119 to coordinate the flow of information to operators inside and outside the sterile field. For example, central controller 106 can have visualization system 108 display a snapshot of a surgical site, as recorded by an imaging device 124, on a non-sterile screen 107 or 109, while transmitting to the live from the surgical site on the main screen 119. The instant on the non-sterile screen 107 or 109 can allow a non-sterile operator to perform a diagnostic step relevant to the surgical procedure, for example.

[0144] In one aspect, the central controller 106 is also configured to route an entry or diagnostic feedback by a non-sterile operator in the display tower 111 to the primary screen 119 within the sterile field, where it can be seen by a sterile operator on the operating table. In one example, the entry may be in the form of a modification of the snapshot displayed on the non-sterile screen 107 or 109, which can be routed to main screen 119 by central controller 106.

[0145] With reference to Figure 2, a surgical instrument 112 is being used in the surgical procedure as part of the surgical system 102. The central controller 106 is also configured to coordinate the flow of information to a screen of the surgical instrument 112. For For example, in US provisional patent application serial number 62 / 611,341, entitled INTERACTIVE SURGICAL PLATFORM, deposited on December 28, 2017, the disclosure of which is hereby incorporated by reference in its entirety for reference. An entry or diagnostic feedback inserted by a non-sterile operator in the viewing tower 111 can be routed by the central controller 106 to the screen of the surgical instrument 115 in the sterile field, where it can be seen by the operator of the surgical instrument 112. Exemplary surgical instruments that are suitable for use with surgical system 102 are described under the title "Surgical Instrument Hardware" and in the provisional patent application serial number 62 / 611.341, entitled INTE-RACTIVE SURGICAL PLATFORM, filed on December 28, 2017, whose disclosure is hereby incorporated by reference in its entirety, for example.

[0146] Referring now to Figure 3, a central controller 106 is shown in communication with a visualization system 108, a robotic system 110 and a smart handheld surgical instrument 112. The central controller 106 includes a central controller screen 135, an imaging module 138, a generator module 140, a communication module 130, a processor module 132 and a storage matrix 134. In certain respects, as shown in Figure 3, central controller 106 additionally includes a module - smoke evacuation module 126 and / or a suction / irrigation module 128.

[0147] During a surgical procedure, the application of energy to the tissue, for sealing and / or cutting, is generally associated with

smoke, excess fluid suction and / or tissue irrigation. Fluid, power, and / or data lines from different sources are often intertwined during the surgical procedure. Valuable time can be wasted in addressing this issue during a surgical procedure. To untangle the lines, it may be necessary to disconnect the lines from their respective modules, which may require a restart of the modules. The modular compartment of the central controller 136 offers a unified environment to manage power, data and fluid lines, which reduces the frequency of interleaving between such lines.

[0148] Aspects of the present disclosure feature a central surgical controller for use in a surgical procedure that involves applying energy to tissue at a surgical site. The central surgical controller includes a central controller compartment and a combined generator module received slidingly at a central controller compartment docking station. The docking station includes data and power contacts. The combined generator module includes two or more of an ultrasonic energy generating component, a bipolar RF energy generating component, and a monopolar RF energy generating component which are housed in a single unit. In one aspect, the combined generator module also includes a smoke evacuation component, at least one power application cable to connect the combined generator module to a surgical instrument, at least one smoke evacuation component. configured to evacuate smoke, fluid, and / or particulates generated by the application of therapeutic energy to the tissue, and a fluid line that extends from the remote surgical site to the smoke evacuation component.

[0149] In one aspect, the fluid line is a first fluid line and a second fluid line extends from the surgical site

motorcycle to a suction and irrigation module received slidingly into the central controller compartment. In one aspect, the central controller compartment comprises a fluid interface.

[0150] Certain surgical procedures may require the application of more than one type of energy to the tissue. One type of energy may be more beneficial for cutting tissue, while a different type of energy may be more beneficial for sealing tissue. For example, a bipolar generator can be used to seal the tissue while an ultrasonic generator can be used to cut the sealed tissue. Aspects of the present disclosure present a solution in which a modular compartment of central controller 136 is configured to accommodate different generators and facilitate interactive communication between them. One of the advantages of the modular central controller compartment 136 is that it allows quick removal and / or replacement of several modules.

[0151] Aspects of the present disclosure feature a modular surgical compartment for use in a surgical procedure that involves applying energy to the tissue. The modular surgical compartment includes a first energy generator module, configured to generate a first energy for application to the tissue, and a first docking station that comprises a first docking port that includes first data contacts and energy contacts, being that the first power generator module is slidingly movable in an electric hitch with power and data contacts and the first power generator module is slidingly movable out of the electric hitch with the first - other power and data contacts.

[0152] In addition to the above, the modular surgical compartment also includes a second energy generator module configured to generate a second energy, different from the first energy, for application to the tissue, and a second docking station comprising a second docking port which includes second data and power contacts, the second power generating module is slidingly movable in an electrical coupling with the power and data contacts, and the second power generating module is slidingly mobile. out of the electrical coupling with the second power and data contacts.

[0153] In addition, the modular surgical cabinet also includes a communication bus between the first coupling port and the second coupling port, configured to facilitate communication between the first power generator module and the second power generator module .

[0154] With reference to Figures 3 to 7, aspects of the present disclosure are presented for a modular compartment of the central controller 136 that allows the modular integration of a generator module 140, a smoke evacuation module 126, and a suction / irrigation module 128. The modular central controller compartment 136 further facilitates interactive communication between modules 140, 126, 128. As illustrated in Figure 5, generator module 140 can be a generator module with monopoly components, integrated bipolar and ultrasonic devices, supported in a single cabinet unit 139 slidably insertable in the central controller modular compartment 136. As shown in Figure 5, generator module 140 can be configured to connect to a mobile device nopolar 146, a bipolar 147 device and an ultrasonic device

148. Alternatively, generator module 140 may comprise a series of monopolar, bipolar and / or ultrasonic generator modules that interact through the central controller modular compartment 136. The central controller modular compartment 136 can be configured to facilitate the insertion of multiple generators and interactive communication between generators embedded in the modular central controller compartment 136 so that the generators act as a single generator.

[0155] In one aspect, the modular central controller compartment 136 comprises a modular power and a back communication board 149 with external and wireless communication heads to allow removable fixing of modules 140, 126, 128 and interactive communication between them.

[0156] In one aspect, the modular central controller compartment 136 includes docking stations, or drawers, 151, here also called drawers, which are configured to receive modules 140, 126, 128 in a sliding manner. Figure 4 illustrates a partial perspective view of a central surgical controller compartment 136, and a combined generator module 145 received slidingly at a docking station 151 of the central surgical controller compartment 136. A docking port 152 with power and data contacts on a rear side of the combined generator module 145 is configured to engage a corresponding docking port 150 with the power and data contacts of a corresponding docking station 151 of the central controller 136 modular compartment according to the module combined generator 145 is slid into position in the corresponding docking station 151 of the central controller modular compartment

136. In one aspect, the combined generator module 145 includes a bipolar, ultrasonic and monopolar module and a smoke evacuation module integrated into a single cabinet unit 139, as shown in Figure 5.

[0157] In several respects, the smoke evacuation module 126 includes a fluid line 154 that carries trapped smoke.

from / collected fluid away from a surgical site and to, for example, the smoke evacuation module 126. The vacuum suction that originates from the smoke evacuation module 126 can pull the smoke into an opening in a utility conduit at the surgical site. The utility conduit, coupled to the fluid line, can be in the form of a flexible tube that ends in the smoke evacuation module 126. The utility conduit and the fluid line define a fluid path that extends towards the smoke evacuation module 126 which is received in the central controller compartment 136.

[0158] In several respects, the suction / irrigation module 128 is coupled to a surgical tool comprising a fluid suction line and a fluid suction line. In one example, the suction and suction fluid lines are in the form of flexible tubes that extend from the surgical site towards the suction / irrigation module 128. One or more drive systems can be configured to cause irrigation and aspiration of fluids to and from the surgical site.

[0159] In one aspect, the surgical tool includes a drive shaft that has an end actuator at a distal end of the same and at least an energy treatment associated with the end actuator, a suction tube, and a irrigation pipe. The suction tube can have an inlet port at a distal end of it and the suction tube extends through the drive shaft. Similarly, an irrigation pipe can extend through the drive shaft and may have an inlet port close to the power application implement. The energy application implement is configured to supply ultrasonic and / or RF energy to the surgical site and is coupled to the generator module 140 by a cable that initially extends through the drive shaft.

[0160] The irrigation tube can be in fluid communication with a fluid source, and the suction tube can be in fluid communication with a vacuum source. The fluid source and / or the vacuum source can be housed in the suction / irrigation module 128. In one example, the fluid source and / or the vacuum source can be housed in the central controller compartment 136 separately from the suction / irrigation module 128. In such an example, a fluid interface can be configured to connect the suction / irrigation module 128 to the fluid source and / or the vacuum source.

[0161] In one aspect, modules 140, 126, 128 and / or their corresponding docking stations in the central controller modular bay 136 may include alignment features that are configured to align the docking ports of the modules in engagement with their counterparts in the docking stations of the central controller modular compartment 136. For example, as shown in Figure 4, the combined generator module 145 includes side brackets 155 that are configured to slide the corresponding brackets in a sliding way 156 from the corresponding docking station 151 of the modular central controller compartment

136. The brackets cooperate to guide the coupling port contacts of the combined generator module 145 in an electrical engagement with the coupling port contacts of the 136 central controller modular compartment.

[0162] In some respects, the drawers 151 of the central controller modular compartment 136 are the same, or substantially the same size, and the modules are sized to be received in the drawers 151. For example, the side brackets 155 and / or 156 can be larger or smaller depending on the size of the module. In other respects, drawers 151 are different in size.

and are each designed to accommodate a specific module.

[0163] In addition, the contacts of a specific module can be switched to engage with the contacts of a specific drawer to avoid inserting a module in a drawer with unpaired contacts.

[0164] As shown in Figure 4, the coupling port 150 of a drawer 151 can be coupled to the coupling port 150 of another drawer 151 through a communication link 157 to facilitate interactive communication between the modules housed in the modular central controller compartment 136. The coupling ports 150 of the modular central controller compartment 136 can alternatively or additionally facilitate interactive wireless communication between modules housed in the modular central controller compartment 136. Any wireless communication is suitable - da can be used, such as Air Titan Bluetooth.

[0165] Figure 6 illustrates individual power bus connectors for a plurality of side docking ports of a side modular cabinet 160 configured to receive a plurality of modules from a central surgical controller 206. The side modular cabinet 160 it is configured to receive and interconnect the modules 161 laterally. The modules 161 are slidably inserted in the docking stations 162 of the side modular cabinet 160, which includes a back plate for interconnecting the modules 161. As illustrated in Figure 6, modules 161 are arranged laterally in the side modular cabinet 160. Alternatively, modules 161 can be arranged vertically in a side modular cabinet.

[0166] Figure 7 illustrates a vertical modular cabinet 164 configured to receive a plurality of modules 165 from the central surgical controller 106. Modules 165 are slidably inserted

in docking stations, or drawers, 167 of the vertical modular cabinet 164, which includes a rear panel for interconnecting the modules 165. Although the drawers 167 of the vertical modular cabinet 164 are arranged vertically, in certain cases, a modular cabinet vertical duct 164 may include drawers that are arranged laterally. In addition, modules 165 can interact with each other through the coupling ports of the vertical modular cabinet 164. In the example in Figure 7, a screen 177 is provided to show data relevant to the operation of modules 165. In addition, the vertical modular cabinet 164 includes a master module 178 that houses a plurality of submodules that are received slidingly in the master module 178.

[0167] In several respects, the imaging module 138 comprises an integrated video processor and a modular light source and is adapted for use with various imaging devices. In one aspect, the imaging device is comprised of a modular cabinet that can be mounted with a light source module and a camera module. The cabinet can be a disposable cabinet. In at least one example, the disposable case is removably coupled to a reusable controller, a light source module, and a camera module. The light source module and / or the camera module can be selected selectively depending on the type of surgical procedure. In one aspect, the camera module comprises a CCD sensor. In another aspect, the camera module comprises a CMOS sensor. In another aspect, the camera module is configured for imaging the scanned beam. Similarly, the light source module can be configured to provide a white light or a different light, depending on the surgical procedure.

[0168] During a surgical procedure, the removal of a device

positive surgical from the surgical field and its replacement by another surgical device that includes a different camera or other light source may be inefficient. Temporarily losing sight of the surgical field can lead to undesirable consequences. The imaging device module of the present disclosure is configured to allow the replacement of a light source module or a "midstream" camera module during a surgical procedure, without the need to remove the imaging device from the cyclic field. surgical.

[0169] In one aspect, the imaging device comprises a tubular housing that includes a plurality of channels. A first channel is configured to receive the Camera module in a sliding way, which can be configured for a snap-fit fit (pressure fit) with the first channel. A second channel is configured to receive the camera module in a sliding way, which can be configured for a snap-fit fit (pressure fit) with the first channel. In another example, the camera module and / or the light source module can be rotated to an end position within their respective channels. A threaded coupling can be used instead of the pressure fitting.

[0170] In several examples, multiple imaging devices are placed in different positions in the surgical field to provide multiple views. Imaging module 138 can be configured to switch between imaging devices to provide an ideal view. In several respects, imaging module 138 can be configured to integrate images from different imaging devices.

[0171] Various image processors and imaging devices suitable for use with the present disclosure are described in US patent No. 7,995,045 entitled COMBINED SBI AND CON-

VENTIONAL IMAGE PROCESSOR, granted on August 9, 2011, which is incorporated herein by reference in its entirety. In addition, US patent No. 7,982,776, entitled SBIl MOTION ARTIFACT REMOVAL APPARATUS AND METHOD, issued on July 19, 2011, which is incorporated herein by reference in its entirety, describes various systems for removing motion artifacts from the data of image. Such systems can be integrated with the imaging module 138. In addition to these, the publication of US patent application No. 2011/0306840, entitled CONTROLLA-BLE MAGNETIC SOURCE TO FIXTURE INTRACORPOREAL APPA- RATUS, published on December 15, 2011, and the publication of US patent application No. 2014/0243597, entitled SYSTEM FOR PERFORMING A MINIMALLY INVASIVE SURGICAL PROCEDURE, published on August 28, 2014, which are, the disclosure of each of which, incorporated herein by reference in its totality.

[0172] Figure 8 illustrates a surgical data network 201 comprising a central modular communication controller 203 configured to connect modular devices located in one or more operating rooms of a health care facility, or any environment in a hospital. installation of health services specially equipped for surgical operations, to a cloud-based system (for example, cloud 204 which may include a remote server 213 coupled to a storage device 205). In one aspect, the modular central communication controller 203 comprises a central network controller 207 and / or a network key 209 in communication with a network router. The modular central communication controller 203 can also be coupled to a local computer system 210 to provide local computer processing and data manipulation. The surgical data network 201 can be configured as a passive, intelligent, or switching network. A passive surgical data network serves as a conduit for the data, allowing the data to be transmitted from one device (or segment) to another and to cloud computing resources. An intelligent surgical data network includes additional features to allow traffic passing through the surgical data network to be monitored and to configure each port on the central network controller 207 or network key 209. A surgical data network Smart can be called a central controller or controllable key. A central switching controller reads the destination address of each packet and then forwards the packet to the correct port.

[0173] Modular devices 1a to 1n located in the operating room can be coupled to the central controller of modular communication 203. The central network controller 207 and / or the network switch 209 can be coupled to a network router 211 to connect devices 1a to 1h to the 204 cloud or the local computer system

210. Data associated with devices 1a to 1n can be transferred to cloud-based computers via the router for remote data processing and manipulation. The data associated with devices 1a to 1h can also be transferred to the local computer system 210 for processing and manipulation of the local data. Modular devices 2a to 2m located in the same operating room can also be coupled to a network switch 209. Network switch 209 can be attached to the central network controller 207 and / or to network router 211 to connect devices 2a 2m to cloud 204. Data associated with devices 2a to 2n can be transferred to cloud 204 via network router 211 for data processing and manipulation. The data associated with devices 2a to 2m can also be transmitted

injured to the local computer system 210 for processing and manipulating local data.

[0174] It will be understood that the surgical data network 201 can be expanded by interconnecting multiple central network controllers 207 and / or multiple network keys 209 with multiple network routers 211. The central communication controller 203 can be contained in a modular control roaster configured to receive multiple devices 1a to 1n / 2a to 2m. The local computer system 210 can also be contained in a modular control tower. The central modular communication controller 203 is connected to a screen 212 to display the images obtained by some of the devices 1a to 1n / 2a to 2m, for example, during surgical procedures. In several respects, devices 1a to 1n / 2a to 2m can include, for example, several modules such as an imaging module 138 coupled to an endoscope, a generator module 140 coupled to an energy-based surgical device, an evacuation module smoke 126, a suction / irrigation module 128, a communication module 130, a processor module 132, a storage matrix 134, a surgical device attached to a screen, and / or a non-contact sensor module, among others modular devices that can be connected to the modular communication central controller 203 of the surgical data network 201.

[0175] In one aspect, the surgical data network 201 may comprise a combination of central network controllers, network switches, and network routers that connect devices 1a to 1n / 2a to 2m to the cloud. Any or all of the devices 1a to 1n / 2a to 2m coupled to the central network controller or network key can collect data in real time and transfer the data to cloud computers for data processing and manipulation. It will be understood that cloud computing depends on sharing computing resources instead of having local servers or personal devices to handle software applications. The word "cloud" can be used as a metaphor for "the Internet", although the term is not limited as such. Consequently, the term "cloud computing" can be used here to refer to "a type of Internet-based computing", in which different services - such as servers, storage, and applications - are applied to the central controller of modular communication 203 and / or computer system 210 located in the operating room (for example, a fixed, mobile, temporary, or operating room or operating space) and devices connected to the central modular communication controller 203 and / or computer system 210 over the Internet. The cloud infrastructure can be maintained by a cloud service provider. In this context, the cloud service provider may be the entity that coordinates the use and control of devices 1a to 1n / 2a to 2m located in one or more operating rooms. Cloud computing services can perform a large number of calculations based on data collected by smart surgical instruments, robots, and other computerized devices located in the operating room. The central controller hardware allows multiple devices or connections to be connected to a computer that communicates with cloud computing and storage resources.

[0176] The application of cloud computer data processing techniques to the data collected by devices 1a to 1n / 2a to 2m, the surgical data network provides better surgical results, reduced costs, and better patient satisfaction. At least some of the devices 1a to 1n / 2a to 2m can be used to view tissue status to assess leakage or perfusion of sealed tissue after a tissue sealing and cutting procedure. At least some of the devices 1a to 1n / 2a to 2m can be used to identify pathology, such as the effects of disease, with the use of cloud-based computing to examine data including images of body tissue samples for diagnostic purposes. . This includes confirmation of the location and margin of the tissue and phenotypes. At least some of the devices 1a to 1n / 2a to 2m can be used to identify anatomical structures of the body using a variety of sensors integrated with imaging devices and techniques such as overlaying images captured by multiple imaging devices. Data collected by devices 1a to 1n / 2a to 2m, including image data, can be transferred to the cloud 204 or the local computer system 210 or both for data processing and manipulation including data processing and manipulation. Image. The data can be analyzed to improve the results of the surgical procedure by determining whether additional treatment, such as the application of endoscopic intervention, emerging technologies, targeted radiation, targeted intervention, precise robotics at specific sites and conditions of fabric, can be followed. This data analysis can additionally use analytical processing of the results, and with the use of standardized approaches they can provide beneficial standardized feedback both to confirm surgical treatments and the behavior of the surgeon or to suggest modifications to the surgical treatments and the behavior of the surgeon. surgeon.

[0177] In an implementation, operating room devices 1a to 1n can be connected to the modular central communication controller 203 via a wired channel or a wireless channel depending on the configuration of devices 1a to 1n in a central network controller. The central network controller 207 can be implemented, in one aspect, as a local network transmission device that acts on the physical layer of the OSI model ("open system interconnection"). The central network controller provides connectivity to devices 1a to 1n located on the same network as the operating room. The central network controller 207 collects data in the form of packets and sends them to the router in half-duplex mode. The central network controller 207 does not store any media access control / Internet protocol (MAC / IP) to transfer data from the device. Only one of devices 1a to 1n at a time can send data via the central network controller 207. The central network controller 207 has no routing tables or intelligence as to where to send information and broadcasts all data on the network via each connection and to a remote server 213 (Figure 9) through the cloud 204. The central network controller 207 can detect basic network errors, such as collisions, but have all the information broadcast to multiple input ports it can be a security risk and cause strangulation.

[0178] In another implementation, operating room devices 2a to 2m can be connected to a network switch 209 via a wired or wireless channel. The network key 209 works in the data connection layer of the OSI model. Network switch 209 is a multicast device for connecting devices 2a to 2m located in the same operation center to the network. The network key 209 sends data in frames to the network router 211 and works in full duplex mode. Multiple devices 2a to 2m can send data at the same time via network key 209. Network key 209 stores and uses MAC addresses of devices 2a to 2m to transfer data.

[0179] The central network controller 207 and / or the network key 209 are coupled to the network router 211 for a connection to the network 204. The network router 211 works at the network layer of the mo-

OSI. Network router 211 creates a route to transmit data packets received from central network controller 207 and / or network key 211 to a computer with cloud-based resources for further processing and manipulation of data collected by any or all of the devices 1a to 1n / 2a to 2m. Network router 211 can be used to connect two or more different networks located in different locations, such as different operating rooms in the same healthcare facility or different networks located in different operating rooms of different facilities. - health services lists. Network router 211 sends data in packet form to cloud 204 and works in full duplex mode. Multiple devices can send data at the same time. The network router 211 uses IP addresses to transfer data.

[0180] In one example, the central network controller 207 can be implemented as a central USB controller, which allows multiple USB devices to be connected to a host computer. The USB central controller can expand a single USB port on several levels so that more ports are available to connect the devices to the host system computer. The central network controller 207 can include wired or wireless capabilities to receive information about a wired channel or a wireless channel. In one aspect, a wireless wireless, broadband and short-range wireless USB communication protocol can be used for communication between devices 1a to 1n and devices 2a to 2m located in the operating room.

[0181] In other examples, devices in the operating room 1a to 1n / 2a to 2m can communicate with the central modular communication controller 203 via standard Bluetooth wireless technology for exchanging data over short distances ( with the use of short-wavelength UHF radio waves in the ISM band of

2.4 to 2485 GHz) of fixed and mobile devices and build personal area networks (PANs). In other respects, operating room devices 1a to 1n / 2a to 2m can communicate with the central modular communication controller 203 via a number of wireless and wired communication standards or protocols, including, but not limited to, limited to, Wi-Fi (IEEE 802.11 family), WiMAX (IEEE 802.16 family), IEEE 802.20, long-term evolution (LTE, "long-term evolution"), and Ev-DO, HSPA +, HSDPA +, HSUPAr, EDGE , GSM, GPRS, CDMA, TDMA, DECT, and Ethernet derivatives thereof, as well as any other wireless and wired protocols that are designated as 3G, 4G, 5G, and beyond. The computing module can include a plurality of communication modules. For example, a first communication module can be dedicated to short-range wireless communications like Wi-Fi and Bluetooth, and a second communication module can be dedicated to longer-range wireless communications like GPS, EDGE, GPRS, CDMA , Wi-MAX, LTE, Ev-DO and others.

[0182] The modular communication central controller 203 can serve as a central connection for one or all operating room devices 1a to 1n / 2a to 2m and handles a data type known as frames. The tables carry the data generated by the devices 1a to 1n / 2a to 2m. When a frame is received by the central modular communication controller 203, it is amplified and transmitted to the network router 211, which transfers the data to the cloud computing resources using a series of standards or protocols wireless or wired communication, as described in the present invention.

[0183] The modular communication central controller 203 can be used as a standalone device or be connected to compatible central network controllers and network switches to form a larger network. The 203 modular communication central controller is, in general, easy to install, configure and maintain, making it a good option for the network of devices 1a to 1n / 2a to 2m from the operating room.

[0184] Figure 9 illustrates an interactive surgical system, implemented by computer 200. The interactive surgical system implemented by computer 200 is similar in many ways to the interactive surgical system, implemented by computer 100. For example, the surgical system, interactive , implemented by computer 200 includes one or more surgical systems 202, which are similar in many respects to surgical systems 102. Each surgical system 202 includes at least one central surgical controller 206 communicating with a cloud 204 which may include a remote server 213. In one aspect, the computer-implemented interactive surgical system 200 comprises a modular control tower 236 connected to multiple operating room devices, for example, smart surgical instruments, robots and other localized computerized devices - used in the operating room. As shown in Figure 10, the modular control tower 236 comprises a central modular communication controller 203 coupled to a computer system 210. As illustrated in the example in Figure 9, the modular control tower 236 is coupled to a imaging module 238 that is attached to an endoscope 239, a generator module 240 that is attached to a power device 241, a smoke evacuation module 226, a suction / irrigation module 228, a communication module 230, a module processor 232, a storage array 234, an intelligent device / instrument 235 optionally attached to a screen 237, and a non-contact sensor module 242. Operating room devices are coupled with cloud computing resources and the data storage via the modular control tower 236. The central robot controller 222 can also be connected to the modular control tower 236 and cloud computing resources. Devices / Instruments 235, display systems 208, among others, can be coupled to the modular control tower 236 by means of wired or wireless communication standards or protocols, as described in the present invention. The modular control tower 236 can be coupled to a central controller screen 215 (for example, monitor, screen) to display and overlay images received from the imaging module, device / instrument screen and / or other display systems 208 The central controller screen can also display the data received from the devices connected to the modular control tower in conjunction with overlapping images and images.

[0185] Figure 10 illustrates a central surgical controller 206 that comprises a plurality of modules coupled to the modular control tower 236. The modular control tower 236 comprises a central modular communication controller 203, for example, a device - network connectivity device, and a computer system 210 to provide local processing, visualization, and imaging, for example. As shown in Figure 10, the 203 modular central communication controller can be connected in a layered configuration to expand the number of modules (for example, devices) that can be connected to the 203 modular central communication controller and transfer data associated with modules to computer system 210, cloud computing resources, or both. As shown in Figure 10, each of the central controllers / network switches in the modular central communication controller 203 includes three downstream ports and one upstream port. The central controller / network switch upstream is connected to a processor to provide a communication connection with the com-

cloud computing and a local display 217. Communication with cloud 204 can be done via a wired or wireless communication channel.

[0186] The central surgical controller 206 employs a non-contact sensor module 242 to measure the dimensions of the operating room and generate a map of the operating room using non-contact measuring devices such as laser or ultrasonic. An ultrasound-based non-contact sensor module scans the operating room by transmitting an ultrasound explosion and receiving an echo when it bounces outside the perimeter of the operating room walls, as described under the heading “Surgical Hub Spatial Hardware Within an Operating Room "in US provisional patent application serial number 62 / 611,341, entitled INTERACTIVE SURGICAL PLAT-FORM, filed on December 28, 2017, which is hereby incorporated by reference in its entirety, in which the sensor module is configured to determine the size of the operating room and adjust the limits of the pairing distance with Bluetooth A laser-based non-contact sensor module scans the operating room by transmitting pulses of laser light, receiving pulses of laser light jumping from the perimeter walls of the operating room, and comparing the phase of the transmitted pulse to the received pulse to determine the size of the operating room and to adjust set the Bluetooth pairing distance limits, for example.

[0187] Computer system 210 comprises a processor 244 and a network interface 245. Processor 244 is coupled to a communication module 247, storage 248, memory 249, non-volatile memory 250, and an input / output interface 251 through of a system bus. The system bus can be any one of several types of bus structures, including the memory bus or memory controller, a peripheral bus

or external bus, and / or local bus using any variety of available bus architectures including, but not limited to, 9-bit bus, industry standard architecture (ISA), Micro-Charmel Architecture (MSA), Extended ISA (EISA), Smart Drive Electronics (IDE), VESA Local Bus (VLB), Peripheral Component Interconnection (PCI), USB, Accelerated Graphics Port (AGP), PCMCIA Bus (International Association of Memory Cards for Computers) personal computers, "Personal Computer Memory Card International Association"), small computer systems interface (SCSI), or any other proprietary bus.

[0188] Processor 244 can be any single-core or multi-core processor, such as those known under the ARM Cortex trade name available from Texas Instruments. In one respect, the processor may be a Core Cortex-M4F LM4F230H5QR ARM processor, available from Texas Instruments, for example, which comprises an integrated 256 KB single-cycle flash memory, or other non-volatile memory, up to 40 MHz , a seek-ahead buffer to optimize performance above 40 MHz, a 32 KB single cycle serial random access memory (SRAM), an internal read-only memory (ROM) loaded with the StellarisWareGO program, read-only memory programmable and electrically erasable (EEPROM) of 2 KB, one or more pulse width modulation (PWM) modules, one or more analogs of quadrature encoder (QEI) inputs, one or more analog to digital converters (ADC) ) 12 bits with 12 channels of analog input, details of which are available for the product data sheet.

[0189] In one aspect, processor 244 may comprise a safety controller comprising two controller-based families, such as TMS570 and RM4x, known under the tradename Hercules ARM Cortex R4, also by Texas Instruments. The safety controller can be configured specifically for IEC 61508 and ISO 26262 safety critical applications, among others, to provide advanced integrated safety features while providing scalable performance, connectivity and memory options.

[0190] System memory includes volatile and non-volatile memory. The basic input / output system (BIOS), containing the basic routines for transferring information between elements within the computer system, such as during startup, is stored in non-volatile memory. For example, non-volatile memory can include ROM, programmable ROM (PROM), electrically programmable ROM (EPROM), EE-PROM or flash memory. Volatile memory includes random access memory (RAM), which acts as an external cache memory. In addition, RAM is available in many forms such as SRAM, dynamic RAM (DRAM), synchronous DRAM (SDRAM), double data rate SDRAM (DDR SDRAM), enhanced SDRAM (ESDRAM), Synchlink DRAM (SLDRAM), and direct RAM Rambus RAM (DRRAM).

[0191] Computer system 210 also includes removable / non-removable, volatile / non-volatile computer storage media, such as disk storage. Disk storage includes, but is not limited to, devices such as a magnetic disk drive, floppy disk drive, tape drive, Jaz driver, Zip driver, LS-60 driver, flash memory card or memory stick ( pen drive). In addition, the storage disc may include storage media separately or in combination with other storage media including, but not limited to, an optical disc drive such as a compact disc ROM device ( CD-ROM) writable compact disc drive (CD-R

Drive), rewritable compact disk drive (CD-RW drive), or a versatile digital disk ROM drive (DVD-ROM). To facilitate the connection of disk storage devices to the system bus, a removable or non-removable interface can be used.

[0192] It is to be understood that computer system 210 includes software that acts as an intermediary between users and the basic resources of the computer described in an adequate operating environment. Such software includes an operating system. The operating system, which can be stored on disk storage, acts to control and allocate computer system resources. System applications benefit from management capabilities by the operating system through program modules and “program data stored in the system's memory or storage disk. It is to be understood that the various components described in the present invention can be implemented with various operating systems or combinations of operating systems.

[0193] A user enters commands or information into computer system 210 through the input device (s) coupled to the I / O interface 251. Input devices include, but are not limited to, a pointing device such as a mouse, trackball, stylus, touchpad, keyboard, microphone, joystick, game pad, satellite card, scanner, TV tuner card, digital camera, digital video camera, web camera, and the like. These and other input devices connect to the processor via the system bus via the interface port (s). The interface ports include, for example, a serial port, a parallel port, a game port and a USB. Output devices use some of the same types of ports as input devices. In this way, for example, a USB port can be used to provide input to the computer system and to provide computer system information to an output device. An output adapter is provided to illustrate that there are some output devices such as monitors, screens, speakers, and printers, among other output devices, that need special adapters. Output adapters include, by way of illustration and not limitation, video and sound cards that provide a means of connection between the output device and the system bus. It should be noted that other devices and / or device systems, such as remote computers, provide input and output capabilities.

[0194] Computer system 210 can operate in a networked environment using logical connections to one or more remote computers, such as cloud computers, or local computers. Remote cloud computers can be a personal computer, server, router, personal network computer, workstation, microprocessor-based device, peer device, or other common network node, and the like, and typically include - in many or all of the elements described in relation to the computer system. For the sake of brevity, only one memory storage device is illustrated with the remote computer. Remote computers are logically connected to the computer system via a network interface and then physically connected via a communication connection. The network interface covers communication networks such as local area networks (LANs) and wide area networks (WANs). LAN technologies include fiber-distributed data interface (FDDI), copper-distributed data interface (CDDI), Ethernet / IEEE 802.3, Token / IEEE 802.5 ring and the like. WAN technologies include, but are not limited to, point-to-point links, circuit switching networks such as digital integrated service networks (ISDN) and variations in them, packet switching networks and digital subscriber lines (DSL ).

[0195] In several respects, the computer system 210 of Figure 10, the imaging module 238 and / or display system 208, and / or the processor module 232 of Figures 9 to 10, may comprise an image processor. image, image processing engine, media processor, or any specialized digital signal processor (DSP) used for processing digital images. The image processor can employ parallel computing with single multi-data instruction (SIMD) or multi-data instruction (MIMD) technologies to increase speed and efficiency. The digital image processing engine can perform a number of tasks. The image processor can be an integrated circuit system with a multi-core processor architecture.

[0196] The communication connection (s) refers to the hardware / software used to connect the network interface to the bus. Although the communication connection is shown for illustrative clarity within the computer system, it can also be external to computer system 210. The hardware / software required for connection to the network interface includes, for illustrative purposes only, internal and external technologies such as modems, including regular telephone serial modems, cable modems and DSL modems, ISDN adapters and Ethernet cards.

[0197] Figure 11 illustrates a functional block diagram of an aspect of a USB 300 central network controller device, in accordance with at least one aspect of the present disclosure. In the illustrated aspect, the USB 300 network central controller device uses a TUSB2036 integrated circuit central controller available from Texas Instruments. The central network controller USB 300 is a CMOS device that provides a USB transceiver port 302 and up to three USB transceiver ports downstream 304, 306, 308 in accordance with the USB 2.0 specification. The upstream USB transceiver port 302 is a differential data root port comprising a "less" differential data input (DMO) paired with a "more" differential data input (DPO). The three ports of the downstream USB transceiver 304, 306, 308 are differential data ports, with each port including "more" differential data outputs (DP1-DP3) paired with different "less data outputs. "(DM1-DM3).

[0198] The USB 300 central network controller device is implemented with a digital state machine instead of a micro controller, and no firmware programming is required. Fully compatible USB transceivers are integrated into the circuit for the upstream USB transceiver port 302 and all downstream USB transceiver ports 304, 306, 308. The downstream USB transceiver ports 304, 306, 308 support both full speed as low speed automatically configuring the scan rate according to the speed of the device attached to the doors. The USB 300 network central controller device can be configured in bus powered or self powered mode and includes 312 central power logic to manage power.

[0199] The USB 300 network central controller device includes a 310 series interface engine (SIE). The SIE 310 is the front end of the USB 300 central network controller hardware and handles most of the protocol described in chapter 8 of the USB specification. SIE 310 typically comprises signaling down to the transaction level. The functions it handles could include: packet recognition, transaction sequencing, SOP, EOP, RESET, and RESUME signal detection / generation, clock / data separation, data encoding / decoding non-inverted zero ( NRZI), generation and verification of CRC (token and data), generation and verification

packet ID (PID) fication / decoding, and / or series-parallel / parallel-series conversion. The 310 receives a clock input 314 and is coupled to a suspend / resume logic circuit and frame timer 316 and a central controller repeater circuit 318 to control communication between the upstream USB transceiver port 302 and the downstream USB transceiver ports 304, 306, 308 via the logic circuits of ports 320, 322, 324. The SIE 310 is coupled to a 326 command decoder via the logic interface to control the commands of a serial EEPROM via 330 series EEPROM interface.

[0200] In several aspects, the USB 300 central network controller can connect 127 functions configured in up to six logical layers (levels) to a single computer. In addition, the USB 300 central network controller can connect all peripherals using a standardized four-wire cable that provides both communication and power distribution. Power settings are bus-powered and self-powered modes. The USB 300 central network controller can be configured to support four power management modes: a bus-powered central controller with individual port power management or grouped port power management, and the au central controller - powered, with individual door power management or grouped door power management. In one respect, using a USB cable, the USB 300 central network controller, the USB transceiver port 302 is plugged into a USB host controller, and the USB transceiver ports downstream 304, 306, 308 are exposed to connect compatible USB devices, and so on. Surgical instrument hardware

[0201] Figure 12 illustrates a logic diagram of a module of a 470 control system of an instrument or surgical tool, according to one or more aspects of the present disclosure. The 470 system comprises a control circuit. The control circuit includes a microcontroller 461 comprising a processor 462 and a memory 468. One or more of the sensors 472, 474, 476, for example, provide real-time feedback to the processor

462. A motor 482, driven by a motor drive 492, operationally couples a longitudinally movable displacement member to drive the beam's cutting element with an i-profile. A tracking system 480 is configured to determine the position of the longitudinally movable displacement member. Position information is provided to the 462 processor, which can be programmed or configured to determine the position of the longitudinally movable drive member, as well as the position of a firing member, firing bar and a cutting element of the beam with i-profile. Additional motors can be provided at the instrument driver interface to control the firing of the beam with an i-profile, the displacement of the closing tube, the rotation of the drive shaft and the articulation. A 473 screen displays a variety of instrument operating conditions and can include touchscreen functionality for data entry. The information displayed on screen 473 can be overlaid with images captured using endoscopic imaging modules.

[0202] In one aspect, the 461 microcontroller can be any single-core or multi-core processor, such as those known under the ARM Cortex trade name available from Texas Instruments. In one aspect, the 461 main microcontroller may be an LM4F230H5QR ARM Cortex-M4F processor, available from Texas Instruments, for example, which comprises a 256 KB single-cycle flash memory, or-

non-volatile memory, up to 40 MHz, a search-ahead buffer to optimize performance above 40 MHz, a 32 KB single cycle series random access memory (SRAM), an internal read-only memory (ROM) ) loaded with the StellisWareO program, 2 KB read-only programmable, electrically erasable memory (EEPROM), one or more pulse width modulation (PWM) modules, one or more analogous quadrature encoder inputs (QEI), and / or one or more 12-bit analog to digital converters (ADC) with 12 channels of analog input, details of which are available for the product data sheet.

[0203] In one aspect, the 461 microcontroller can comprise a safety controller that comprises two families based on controllers, such as TMS570 and RM4x known under the trade name of Hercules ARM Cortex R4, also available from Texas Instruments. The safety controller can be configured specifically for IEC 61508 and ISO 26262 safety critical applications, among others, to provide advanced integrated safety features while providing scalable performance, connectivity and memory options.

[0204] The 461 microcontroller can be programmed to perform various functions, such as precise control of the speed and position of the joint and knife systems. In one aspect, the 461 microcontroller includes a 462 processor and a 468 memory. Electric motor 482 can be a brushed direct current (DC) motor with a gearbox and mechanical connections with a linkage system. or scalpel. In one aspect, a motor drive 492 can be an A3941 available from Allegro Microsystems, Inc. Other motor drives can be readily replaced for use in tracking system 480 which comprises an absolute positioning system. A detailed description of a power system

absolute positioning is done in US patent application publication No. 2017/0296213, entitled SYSTEMS AND METHODS FOR CONSTROLLING A SURGICAL STAPLING AND CUTTING INSTRUMENT, published on October 19, 2017, which is hereby incorporated by reference in its entirety.

[0205] The 461 microcontroller can be programmed to provide precise control of the speed and position of the displacement members and articulation systems. The 461 microcontroller can be configured to compute a response in the 461 microcontroller software. The computed response is compared to a measured response from the real system to obtain an "observed" response, which is used for actual feedback-based decisions. The observed response is a favorable and adjusted value, which balances the uniform and continuous nature of the simulated response with the measured response, which can detect external influences in the system.

[0206] In one aspect, the 482 motor can be controlled by the 492 motor actuator and can be used by the instrument trigger system or surgical tool. In many ways, the 482 motor can be a brushed direct current (DC) drive motor, with a maximum speed of approximately 25,000 RPM, for example. In other arrangements, the 482 motor may include a brushless motor, a wireless motor, a synchronous motor, a stepper motor or any other suitable type of electric motor. The motor starter 492 can comprise an H bridge drive that comprises field effect transistors (FETs), for example. The 482 motor can be powered by a feed set mounted releasably in the handle assembly or tool compartment to provide control power for the instrument or surgical tool. The power pack may comprise a battery that may include several battery cells connected in series, which can be used as the power source to power the instrument or surgical tool. In certain circumstances, the battery cells in the power pack may be replaceable and / or rechargeable. In at least one example, the battery cells can be lithium ion batteries that can be coupled and separable from the power supply.

[0207] The 492 motor driver can be an A3941, available from Allegro Microsystems, Inc. The 492 A3941 driver is an entire bridge controller for use with semiconductor metal oxide field effect transistors (MOSFET). external power, N channel, specifically designed for inductive loads, such as brushed DC motors. The 492 actuator comprises a single charge pump regulator that provides full door drive (> 10 V) for batteries with voltage up to 7 V and allows the AS941 to operate with a reduced door drive, up to 5.5 V. A capacitor input control can be used to supply the voltage surpassing that supplied by the battery required for N channel MOSFETs. An internal charge pump for the drive on the upper side allows operation in direct current (100% duty cycle ). The entire bridge can be triggered in fast or slow drop modes using diodes or synchronized rectification. In the slow drop mode, the current can be recirculated by means of FET from the top or from the bottom. The energy FETs are protected from the shoot-through effect through programmable dead-time resistors. Integrated diagnostics provide indication of undervoltage, overtemperature and faults in the power bridge and can be configured to protect power MOSFETs in most short-circuit conditions. Other motor drives can be readily replaced for use in the 480 tracking system comprising an absolute positioning system.

[0208] Tracking system 480 comprises a controlled motor drive circuit arrangement comprising a position sensor 472 in accordance with at least one aspect of the present disclosure.

The 472 position sensor for an absolute positioning system provides a unique position signal that corresponds to the location of a displacement member.

In one aspect, the displacement member represents a longitudinally movable drive member comprising a rack of drive teeth for engagement with a corresponding drive gear of a gear reduction assembly.

In other respects, the displacement member represents the firing member, which can be adapted and configured to include a drive tooth rack.

In yet another aspect, the displacement member represents the firing bar or the beam with a profile in |, each of which can be adapted and configured to include a rack of drive teeth.

Consequently, as used in the present invention, the term displacement member is used generically to refer to any movable member of the surgical instrument or tool, such as the driving member, the firing member, the firing bar, the beam with profile in |, or any element that can be moved.

In one aspect, the longitudinally movable drive member is coupled to the firing member, the firing bar and the beam with an | profile. Consequently, the absolute positioning system can, in effect, track the linear displacement of the beam with | by tracking the linear displacement of the longitudinally movable drive member.

In many other respects, the displacement member can be coupled to any 472 position sensor suitable for measuring linear displacement.

In this way, the longitudinally movable drive member, the firing member, the

I-profile beam or beam, or combinations thereof, can be coupled to any suitable linear displacement sensor. Linear displacement sensors can include contact or non-contact displacement sensors. Linear displacement sensors can comprise Variable Differential Linear Transformers (LVDT), Variable Reluctance Differential Transducers (DVRT), a potentiometer, a magnetic detection system comprising a moving magnet and a series linearly arranged in Hall Effect Sensors, a magnetic detection comprising a fixed magnet and a series of furniture, linearly arranged in Hall Effect Sensors, a mobile optical detection system that comprises a mobile light source and a series of linearly arranged photodiodes or photodetectors, an optical detection system that comprises a fixed light source and a mobile series of linearly arranged photodiodes or photodetectors, or any combination thereof.

[0209] The 482 electric motor can include a rotary drive shaft, which interfaces operationally with a gear set, which is mounted in coupling hitch with a set or rack of driving teeth on the drive member. A sensor element can be operationally coupled to a gear assembly so that a single revolution of the position sensor element 472 corresponds to some linear longitudinal translation of the displacement member. An array of gears and sensors can be connected to the linear actuator by means of a rack and pinion arrangement, or by a rotary actuator, by means of a sprocket or other connection. A power source supplies power to the absolute positioning system and an output indicator can display the output from the absolute positioning system. The drive member represents the longitudinally movable drive member which comprises a drive tooth rack formed thereon for engagement with a corresponding drive gear of the gear reducer assembly. The displacement member represents the longitudinally movable firing member, the firing bar, the beam with a | profile, or combinations thereof.

[0210] A single revolution of the sensor element associated with the position sensor 472 is equivalent to a longitudinal linear displacement of di of the displacement member, where d1 represents the longitudinal linear distance by which the displacement member moves. from point "a" to point "b" after a single revolution of the sensor element coupled to the displacement member. The sensor arrangement can be connected by means of a gear reduction which results in the position sensor 472 completing one or more revolutions for the complete travel of the displacement member. The 472 position sensor can complete multiple revolutions for the full travel of the displacement member.

[0211] A series of keys, where n is an integer greater than one, can be used alone or in combination with a gear reduction to provide a single position signal for more than one revolution of the 472 position sensor. of keys is transmitted back to microcontroller 461 which applies logic to determine a single position signal corresponding to the longitudinal linear displacement of d1 + d2 + ... dn of the displacement member. The output of the position sensor 472 is supplied to the microcontroller 461. In several embodiments, the position sensor 472 of the sensor arrangement may comprise a magnetic sensor, an analog rotary sensor, such as a potentiometer, or a series of effect elements. Analog halls, which emit a unique combination of position of signals or values.

[0212] The position sensor 472 can comprise any number of magnetic detection elements, such as, for example, magnetic sensors classified according to whether they measure the total magnetic field or the vector components of the magnetic field. The techniques used to produce both types of magnetic sensors cover many aspects of physics and electronics. The technologies used for magnetic field detection include flow meter, saturated flow, optical pumping, nuclear precession, SQUID, Hall effect, anisotropic magnetoresistance, giant magnetoresistance, magnetic tunnel junctions, giant magnetoimpedance, magnetostrictive / piesoelectric compounds, magnetodiode, magnetic transistors, fiber optics, magneto-optics and magnetic sensors based on microelectromechanical systems, among others.

[0213] In one aspect, the position sensor 472 for the tracking system 480 comprising an absolute positioning system comprises a magnetic rotating absolute positioning system. The 472 position sensor can be implemented as a rotary, magnetic, single-circuit, ASSOSSEQFT position sensor, available from Austria Microsystems, AG. The position sensor 472 interfaces with the 461 microcontroller to provide an absolute positioning system. The 472 position sensor is a low voltage, low power component and includes four effect elements in an area of the 472 position sensor located above a magnet. A high-resolution ADC and an intelligent power management controller are also provided on the integrated circuit. A CORDIC processor (digital computer for coordinate rotation), also known as the digit by digit method and Volder algorithm, is provided to implement a simple and efficient algorithm for calculating hyperbolic and trigonometric functions that require only operations addition, subtraction, displacement

bits and lookup table. The angle position, alarm bits and magnetic field information are transmitted via a standard serial communication interface, such as a serial peripheral interface (SPI), to the 461 microcontroller. position 472 provides 12 or 14 bits of resolution. The position sensor 472 can be an ASS055 integrated circuit supplied in a small 16-pin QFN package whose measurement corresponds to 4x4x0.85 mm.

[0214] The tracking system 480 that comprises an absolute positioning system can comprise and / or be programmed to implement a feedback controller, such as a PID, status feedback, and adaptive controller. A power source converts the signal from the feedback controller to a physical input to the system, in this case the voltage. Other examples include a voltage, current and force PWM. Other sensors can be provided in order to measure the parameters of the physical system in addition to the position measured by the position sensor 472. In some respects, other sensors may include sensor arrangements as described in US patent No. 9,345 .481 entitled STAPLE CARTRIDGE TISSUE THICKNESS SENSOR SYSTEM, granted on May 24, 2016, which is incorporated by reference in its entirety into this document; US patent application serial number 2014/0263552, entitled STAPLE CARTRIDGE TISSUE THICKNESS SENSOR SYSTEM, published on September 18, 2014, is incorporated by reference in its entirety into this document; and US patent application serial number 15 / 628,175, entitled TECHNIQUES FOR ADAPTIVE CONTRROL OF MOTOR VELOCITY OF A SURGICAL STAPLING AND CU- TTING INSTRUMENT, submitted on June 20, 2017, is incorporated by reference in its entirety in this document. In a digital signal processing system, a positioning system

absolute is coupled to a digital data capture system where the output of the absolute positioning system will have a finite resolution and sampling frequency. The absolute positioning system can comprise a comparison and combination circuit to combine a computed response with a measured response through the use of algorithms, such as a weighted average and a theoretical control loop, that trigger the calculated response in the direction to the measured response. The computed response of the physical system considers the properties, such as mass, inertia, viscous friction, resistance to inductance, etc., to predict what the states and exits of the physical system will be, knowing the input.

[0215] The absolute positioning system provides an absolute positioning of the displaced member on the activation of the instrument without having to retract or advance the longitudinally movable drive member to the restart position (zero or initial), as may be required by conventional rotary encoders that merely count the number of progressive or regressive steps that the 482 motor has traversed to infer the position of a device actuator, actuation bar, scalpel, and the like.

[0216] A 474 sensor, such as a strain gauge or a micro strain gauge, is configured to measure one or more parameters of the end actuator, such as the amplitude of the strain exerted on the anvil during a gripping operation, which can be indicative of tissue compression. The measured effort is converted into a digital signal and fed to the 462 processor. Alternatively, or in addition to the 474 sensor, a 476 sensor, such as a load sensor, can measure the closing force applied by the drive system. anvil closure. The 476 sensor, such as a load sensor, can measure the firing force applied to a beam with an i-profile in a firing stroke of the surgical system or tool. The i-profile beam is configured to engage a hinge slider, which is configured to move the clamp actuators upward to force the clamps to deform in contact with an anvil. The i-profile beam includes a sharp cutting edge that can be used to separate fabric, as the i-profile beam is advanced distally by the firing bar. Alternatively, a current sensor 478 can be used to measure the current drained by the 482 motor. The force required to advance the trigger member can correspond to the current drained by the 482 motor, for example. The measured force is converted into a digital signal and supplied to the 462 processor.

[0217] In one form, a 474 strain gauge sensor can be used to measure the force applied to the tissue by the end actuator. A strain gauge can be attached to the end actuator to measure the force applied to the tissue being treated by the end actuator. A system for measuring forces applied to the tissue attached by the end actuator comprises a 474 strain gauge sensor, such as, for example, a microstrain meter, which is configured to measure one or more parameters of the end actuator, for example. In one aspect, the 474 strain gauge sensor can measure the amplitude or magnitude of the mechanical stress exerted on a clamp member of an end actuator during a gripping operation, which can be indicative of tissue compression. The measured effort is converted into a digital signal and fed to the 462 processor of a 461 microcontroller. A 476 load sensor can measure the force used to operate the knife element, for example, to cut the captured tissue between the anvil and staple cartridge. A magnetic field sensor can be used to measure the thickness of the captured tissue. The measurement of the magnetic field sensor can also be converted into a digital signal and supplied to the 462 processor.

[0218] Measurements of tissue compression, tissue thickness and / or force required to close the end actuator on the tissue, as measured by sensors 474, 476 respectively, can be used by microcontroller 461 to characterize the position trigger member and / or the corresponding trigger member speed value. In one case, a 468 memory can store a technique, an equation and / or a query table that can be used by the 461 microcontroller in the evaluation.

[0219] The control system 470 of the instrument or surgical tool can also comprise wired or wireless communication circuits for communication with the modular central communication controller shown in Figures 8 to 11.

[0220] Figure 13 illustrates a control circuit 500 configured to control aspects of the instrument or surgical tool, according to at least one aspect of this disclosure. The control circuit 500 can be configured to implement various processes described here. The control circuit 500 may comprise a microcontroller comprising one or more processors 502 (for example, microprocessor, microcontroller) coupled to at least one memory circuit 504. The memory circuit 504 stores instructions executable on the machine which, when executed by processor 502, cause processor 502 to execute machine instructions to implement several of the processes described here. Processor 502 can be any one of a number of single-core or multi-core processors known in the art. The memory circuit 504 may comprise volatile and non-volatile storage media. The processor 502 can include an instruction processing unit 506 and an arithmetic unit 508. The instruction processing unit can be configured to receive instructions from the memory circuit 504 of the present disclosure.

[0221] Figure 14 illustrates a combinational logic circuit 510 configured to control aspects of the instrument or surgical tool, according to at least one aspect of this disclosure. The combinational logic circuit 510 can be configured to implement various processes described here. The combinational logic circuit 510 may comprise a finite state machine comprising a combinational logic 512 configured to receive data associated with the instrument or surgical tool at an input 514, process the data using combinational logic 512 and provide an output 516.

[0222] Figure 15 illustrates a sequential logic circuit 520 configured to control aspects of the instrument or surgical tool, according to at least one aspect of this disclosure. Sequential logic circuit 520 or combinational logic 522 can be configured to implement the process described here. Sequential logic circuit 520 may comprise a finite state machine. Sequential logic circuit 520 may comprise combinational logic 522, at least one memory circuit 524, a clock 529 and, for example. The at least one memory circuit 524 can store a current state of the finite state machine. In certain cases, the sequential logic circuit 520 may be synchronous or asynchronous. Combinational logic 522 is configured to receive data associated with the surgical instrument or tool from an input 526, process the data using combinational logic 522, and provide an output 528. In other respects, the circuit may comprise a combination of a processor ( for example, processor 502, Figure 13) and a finite state machine to implement various processes of the present invention. In other respects, the finite state machine can

to understand a combination of a combinational logic circuit (for example, a combinational logic circuit 510, Figure 14) and the sequential logic circuit 520.

[0223] Figure 16 illustrates an instrument or surgical tool that comprises a plurality of motors that can be activated to perform various functions. In certain cases, a first engine may be activated to perform a first function, a second engine may be activated to perform a second function, a third engine may be activated to perform a third function, a fourth engine may be activated to perform a fourth function, and so on. In certain cases, the plurality of motors of the robotic surgical instrument 600 can be individually activated to cause triggering, closing, and / or articulation movements in the end actuator. The triggering, closing and / or articulation movements can be transmitted to the end actuator through a set of drive axes, for example.

[0224] In certain cases, the instrument or surgical tool system may include a 602 firing motor. The 602 firing motor can be operationally coupled to a 604 firing motor drive assembly, which can be configured to transmitting firing movements, generated by the motor 602 to the end actuator, particularly to move the beam element with profile in | In certain cases, the firing movements generated by the firing motor 602 can cause the staples to be positioned from the staple cartridge in the fabric captured by the end actuator and / or the cutting edge of the beam element with i-profile to be advanced in order to cut the captured tissue, for example. The beam element with an i-profile can be retracted by reversing the direction of the 602 motor.

[0225] In certain cases, the surgical instrument or tool may

to include a closing motor 603. The closing motor 603 can be operationally coupled to a drive assembly of the closing motor 605 that can be configured to transmit closing movements generated by the motor 603 to the end actuator, particularly to move a closing tube to close the anvil and compress the fabric between the anvil and the staple cartridge. Closing movements can cause the end actuator to transition from an open configuration to an approximate configuration to capture tissue, for example. The end actuator can be moved to an open position by reversing the direction of the 603 motor.

[0226] In certain cases, the surgical instrument or tool may include one or more articulation motors 606a, 606b, for example. The motors 606a, 606b can be operationally coupled to the drive assemblies of the articulation motor 608a, 608b, which can be configured to transmit articulation movements generated by the motors 606a, 606b to the end actuator. In some cases, articulation movements can cause the end actuator to be articulated in relation to the drive shaft assembly, for example.

[0227] As described above, the surgical instrument or tool can include a plurality of motors that can be configured to perform various independent functions. In certain cases, the plurality of motors of the instrument or surgical tool can be activated individually or separately to perform one or more functions, while other motors remain inactive. For example, the hinge motors 606a, 606b can be activated to cause the end actuator to be pivoted, while the firing motor 602 remains inactive. Alternatively, the firing motor 602 can be activated to fire the plurality of clamps, and / or advance the cutting edge, while the hinge motor 606 remains inactive. In addition, the closing motor 603 can be activated simultaneously with the firing motor 602 to cause the closing tube and the i-beam beam element to move distally, as described in more detail later in this document.

[0228] In certain cases, the surgical instrument or tool may include a common control module 610 that can be used with a plurality of the instrument's instruments or surgical tool. In certain cases, the common control module 610 can accommodate one of the plurality of motors at a time. For example, the common control module 610 can be coupled to and separable from the plurality of motors of the robotic surgical instrument individually. In certain cases, a plurality of instrument or surgical tool motors may share one or more common control modules, such as the common control module 610. In certain cases, a plurality of instrument or surgical tool motors may be individually and selectively engaged with the common control module 610. In certain cases, the common control module 610 can be selectively switched between interfacing with one of a plurality of instrument motors or surgical tool to interface with another among the plurality of motors of the instrument or surgical tool.

[0229] In at least one example, the common control module 610 can be selectively switched between the operating coupling with the 606a, 606B articulation motors, and the operating coupling with the 602 firing motor or the closing motor 603. In at least one example, as shown in Figure 16, a key 614 can be moved or transitioned between a plurality of positions and / or states. In the first position 616, the switch 614 can be electrically

the common control module 610 to trip motor 602; in a second position 617, the switch 614 can electrically couple the control module 610 to the closing motor 603; in a third position 618a, the switch 614 can electrically couple the common control module 610 to the first articulation motor 606a; and in a fourth position 618b, the switch 614 can electrically couple the common control module 610 to the second articulation motor 606b, for example. In certain cases, separate common control modules 610 can be electrically coupled to the firing motor 602, closing motor 603, and hinge motors 606a, 606b at the same time. In certain cases, key 614 can be a mechanical key, an electromechanical key, a solid state key, or any suitable switching mechanism.

[0230] Each of the 602, 603, 606a, 606b motors can comprise a torque sensor to measure the output torque on the motor drive shaft. The force on an end actuator can be detected in any conventional manner, such as by means of force sensors on the outer sides of the jaws or by a motor torque sensor that drives the jaws.

[0231] In several cases, as shown in Figure 16, the common control module 610 may comprise a motor starter 626 which may comprise one or more H-Bridge FETs. The motor driver 626 can modulate the energy transmitted from a power source 628 to a motor coupled to the common control module 610, based on an input from a microcontroller 620 (the "controller"), for example. In certain cases, microcontroller 620 can be used to determine the current drained by the motor, for example, while the motor is coupled to the common control module 610, as described above.

[0232] In certain cases, the microcontroller 620 may include a 622 microprocessor (the "processor") and one or more non-transitory computer-readable media or 624 memory units (the "memory"). In certain cases, memory 624 can store various program instructions that, when executed, can cause processor 622 to perform a plurality of functions and / or calculations described herein. In certain cases, one or more of the memory units 624 can be coupled to the processor 622, for example.

[0233] In certain cases, the power source 628 can be used to supply power to the microcontroller 620, for example. In certain cases, the 628 power source may comprise a battery (or "battery pack" or "power source"), such as a Li ion battery, for example. In certain cases, the battery pack can be configured to be releasably mounted to the handle to supply power to the surgical instrument 600. Several battery cells connected in series can be used as the power source

628. In certain cases, the power source 628 can be replaceable and / or rechargeable, for example.

[0234] In several cases, the 622 processor can control the motor drive 626 to control the position, direction of rotation and / or speed of a motor that is coupled to the common control module 610. In certain cases cases, the processor 622 can signal the motor driver 626 to stop and / or disable a motor that is coupled to the common control module 610. It should be understood that the term "processor", as used here, includes any microprocessor , microcontroller or other suitable basic computing device that incorporates the functions of a central computer processing unit (CPU) in an integrated circuit or, at most, some integrated circuits. The processor is a programmable multipurpose device that accepts digital data as input, processes it according to instructions stored in its memory,

and provides results as an output. This is an example of sequential digital logic, as it has internal memory. Processors operate on numbers and symbols represented in the binary numeral system.

[0235] In one case, the 622 processor can be any single-core or multi-core processor, such as those known by the Texas Instruments ARM Cortex trade name. In certain cases, the 620 microcontroller may be an LM 4F230H5QR, available from Texas Instruments, for example. In at least one example, the Texas Instruments LM4F230H5QR is an ARM Cortex-M4F processor core comprising an integrated 256 KB single cycle flash memory, or other non-volatile memory, up to 40 MHz, a search buffer anticipated to optimize performance above 40 MHz, a 32 KB single cycle SRAM, an internal ROM loaded with StellarisWare & software, 2 KB EEPROM, one or more PWM modules, one or more QEI analogs, one or more 12-bit ADCs with 12 analog input channels, among other features that are readily available for the product data sheet. Other microcontrollers can be readily replaced for use with the 4410 module. Consequently, the present disclosure should not be limited in this context.

[0236] In certain cases, memory 624 may include program instructions for controlling each of the motors of the surgical instrument 600 that are attachable to the common control module 610. For example, memory 624 may include program instructions for controlling the firing motor 602, the closing motor 603 and the hinge motors 606a, 606b. Such program instructions can cause the 622 processor to control the trigger, close, and link functions according to inputs from the instrument or surgical tool control algorithms or programs.

[0237] In certain cases, one or more mechanisms and / or sensors, such as 630 sensors, can be used to alert the 622 processor to program instructions that need to be used in a specific configuration. For example, sensors 630 can alert the 622 processor to use the program instructions associated with triggering, closing, and pivoting the end actuator. In certain cases, sensors 630 may comprise position sensors that can be used to detect the position of switch 614, for example. Consequently, the 622 processor can use the program instructions associated with firing the beam with the i-profile of the end actuator by detecting, through sensors 630, for example, that switch 614 is in the first position 616 ; the processor 622 can use the program instructions associated with closing the anvil upon detection through sensors 630, for example, that switch 614 is in second position 617; and processor 622 can use the program instructions associated with the articulation of the end actuator upon detection through sensors 630, for example, that switch 614 is in the third or fourth position 618a, 618b.

[0238] Figure 17 is a schematic diagram of a robotic surgical instrument 700 configured to operate a surgical tool described therein, in accordance with at least one aspect of this disclosure. The robotic surgical instrument 700 can be programmed or configured to control the distal / proximal translation of a displacement member, the distal / proximal displacement of a closing tube, the rotation of the drive shaft, and articulation, either with a single type or multiple articulation drive links. In one aspect, the surgical instrument 700 can be programmed or configured to individually control a firing member, a closing member, a driving shaft member and / or one or more hinge members. The surgical instrument 700 comprises a control circuit 710 configured to control motor-driven firing members, closing members, driving shaft members and / or one or more articulation members.

[0239] In one aspect, the robotic surgical instrument 700 comprises a control circuit 710 configured to control an anvil 716 and an i-profile beam portion 714 (including a sharp cutting edge) of an end actuator 702, a removable clamp cartridge 718, a drive shaft 740 and one or more hinge members 742a, 742b through a plurality of motors 704a to 704e. A position sensor 734 can be configured to provide feedback on the i-profile beam 714 to control circuit 710. Other sensors 738 can be configured to provide feedback to control circuit 710. A timer / counter 731 provides timing and counting information to control circuit 710. A power source 712 can be provided to operate motors 704a to 704e and a current sensor 736 provides motor current feedback to the control circuit

710. Motors 704a to 704e can be operated individually by control circuit 710 in an open loop or closed loop feedback control.

[0240] In one aspect, the control circuit 710 may comprise one or more microcontrollers, microprocessors or other processors suitable for executing instructions that cause the processor or processors to perform one or more tasks. In one aspect, a timer / counter 731 provides an output signal, such as elapsed time or a digital count, to control circuit 710 to correlate beam position with i 714 profile, as determined by position sensor 734, with the timer / counter output 731 so that the control circuit 710 can determine the position of the i-profile beam 714 at a specific time (t) in relation to an initial position or time (t) when the profile-beam i 714 is in a specific position in relation to an initial position. The timer / counter 731 can be configured to measure elapsed time, count external events, or measure eternal events.

[0241] In one aspect, control circuit 710 can be programmed to control functions of end actuator 702 based on one or more tissue conditions. The control circuit 710 can be programmed to directly or indirectly detect tissue conditions, such as thickness, as described here. Control circuit 710 can be programmed to select a trigger control program or closing control program based on tissue conditions. A trigger control program can describe the distal movement of the displacement member. Different trigger control programs can be selected to better treat different tissue conditions. For example, when a thicker tissue is present, control circuit 710 can be programmed to translate the displacement member at a lower speed and / or with a lower power. When a thinner tissue is present, control circuit 710 can be programmed to translate the displacement member at a higher speed and / or with greater power. A closure control program can control the closing force applied to the tissue by the anvil

716. Other control programs control the rotation of the drive shaft 740 and the hinge members 742a, 742b.

[0242] In one aspect, motor control circuit 710 can generate motor setpoint signals. Engine setpoint signals can be provided for various engine controllers

708a to 708e. Motor controllers 708a to 708e can comprise one or more circuits configured to provide motor start signals for motors 704a to 704e in order to drive motors 704a to 704e, as described here. In some instances, motors 704a to 704e may be brushed DC motors. For example, the speed of motors 704a to 704e can be proportional to the respective motor start signals. In some examples, motors 704a to 704e may be brushless DC electric motors, and the respective motor drive signals may comprise a PWM signal provided for one or more stator windings of motors 704a to 704e. In addition, in some instances, motor controllers 708a through 708e can be omitted and control circuit 710 can directly generate motor drive signals.

[0243] In one aspect, the control circuit 710 can initially operate each of the motors 704a to 704e in an open circuit configuration for a first open circuit portion of the travel of the travel member. Based on the response of the robotic surgical instrument 700 during the open circuit portion of the stroke, control circuit 710 can select a trigger control program in a closed circuit configuration. The instrument response may include a translation of the distance from the displacement member during the open circuit portion, a time elapsed during the open circuit portion, the energy supplied to one of the motors 704a to 704e during the open circuit portion, a sum of pulse widths of a motor start signal, etc. After the open circuit portion, control circuit 710 can implement the selected trigger control program for a second portion of the travel member travel. For example, during a portion of the closed loop course, control circuit 710 can modulate one of the motors 704a to 704e based on the translation of data describing a position of the closed displacement member to translate the displacement member to a constant speed.

[0244] In one aspect, motors 704a to 704e can receive power from a 712 power source. Power source 712 can be a DC power source powered by an alternating main power supply, a battery, a super capacitor, or any other suitable power source. Motors 704a to 704e can be mechanically coupled to individual moving mechanical elements such as the i-profile beam 714, the anvil 716, the drive shaft 740, the joint 742a and the joint 742b, through the respective transmissions 706a at 706e. Transmissions 706a through 706e may include one or more gears or other connecting components for coupling motors 704a to 704e to moving mechanical elements. A 734 position sensor can detect a beam position with a | 714. The position sensor 734 can be or can include any type of sensor that is capable of generating position data that indicate a beam position with profile in | 714. In some examples, the position sensor 734 may include an encoder configured to supply a series of pulses to the control circuit 710 according to the beam with profile | 714 transferred distally and proximally. The control circuit 710 can track the pulses to determine the position of the beam with profile in | 714. Other suitable position sensors can be used, including, for example, a proximity sensor. Other types of position sensors can provide other signals that indicate the movement of the beam with profile in | 714. In addition, in some examples, the position sensor 734 may be omitted. When any of the motors 704a to 704e is a stepper motor, the control circuit 710 can track the position of the beam with an i-profile 714 by adding the number and direction of the steps that the motor 704 was instructed to perform . Position sensor 734 can be located on end actuator 702 or any other portion of the instrument. The outputs of each of the motors 704a to 704e include a torque sensor 744a to 744e to detect force and have an encoder to detect the rotation of the drive shaft.

[0245] In one aspect, control circuit 710 is configured to drive a firing member as the i14 profile beam portion of end actuator 702. Control circuit 710 provides a motor setpoint for a motor control 708a, which provides a drive signal for motor 704a. The output shaft of the motor 704a is coupled to a torque sensor 744a. The torque sensor 744a is coupled to a transmission 706a which is coupled to the beam with profile in | 714. The 706a transmission comprises moving mechanical elements, such as rotating elements, and a firing member for distally and proximally controlling the movement of the i-profile beam 714 along a longitudinal geometric axis of the end actuator 702. In one In this respect, the 704a motor can be coupled to the knife gear assembly, which includes a knife gear reduction kit that includes a first knife drive gear and a second knife drive gear. A torque sensor 744a provides a feedback signal from the firing force to the control circuit 710. The firing force signal represents the force required to fire or move the beam with an i-profile 714. A 734 position sensor can be configured to provide the position of the beam with i 714 profile along the firing stroke or the firing member position as a feedback signal to the control circuit

710. End actuator 702 may include additional sensors 738 configured to provide feedback signals to the circuit.

control circuit 710. When ready for use, control circuit 710 can provide a trip signal to the 708a motor control. In response to the trigger signal, motor 704a can drive the trigger member distally along the longitudinal geometric axis of end actuator 702 from an initial proximal position of the stroke to a distal end position of the stroke in relation to the initial travel position. As the displacement member moves distally, a beam with a | 714 with a cutting element positioned at a distal end, advances distally to cut the tissue located between the staple cartridge 718 and the anvil 716.

[0246] In one aspect, control circuit 710 is configured to drive a closing member, such as anvil portion 716 of end actuator 702. Control circuit 710 provides a motor setpoint for motor control 708b, which provides a drive signal for motor 704b. The output shaft of the 704b motor is coupled to a 744b torque sensor. The torque sensor 744b is coupled to a transmission 706b which is coupled to the whisker 716. The transmission 706b comprises moving mechanical elements, such as rotating elements and a closing member, to control the movement of the anvil 716 between the open and closed positions. In one aspect, the 704b motor is coupled to a closing gear assembly, which includes a closing reduction gear assembly that is supported in gear engaged with the closing sprocket. The torque sensor 744b provides a closing force feedback signal to control circuit 710. The closing force feedback signal represents the closing force applied to the anvil 716. The position sensor 734 can be configured to provide the position of the closing member as a feedback signal for control circuit 710. Additional sensors 738 on end actuator 702 can provide the feedback signal for closing force to control circuit 710. A pivoting slide 716 it is positioned opposite the staple cartridge 718. When ready for use, the control circuit 710 can provide a closing signal to the motor control 708b. In response to the closing signal, motor 704b advances a closing member to secure the fabric between the anvil 716 and the staple cartridge 718.

[0247] In one aspect, control circuit 710 is configured to rotate a drive shaft member, such as drive shaft 740, to rotate end actuator 702. Control circuit 710 provides an adjustment point motor for a 708c motor control, which provides a drive signal for the 704c motor. The output shaft of the 704c motor is coupled to a 744c torque sensor. The torque sensor 744c is coupled to a transmission 706c which is coupled to the axis 740. The transmission 706c comprises moving mechanical elements, such as rotating elements, to control the rotation of the drive shaft 740 clockwise or anti-clockwise -time up to and over 360º. In one aspect, the 704c motor is coupled to the rotary drive assembly, which includes a pipe gear segment that is formed over (or attached to) the proximal end of the proximal closing tube for engagement operable by a gear assembly rotational that is operationally supported on the tool mounting plate. The torque sensor 744c provides a rotation force feedback signal for control circuit 710. The rotation force feedback signal represents the rotation force applied to the drive shaft 740. The position sensor 734 can be configured to provide the position of the closing member as a feedback signal to control loop 710. Additional sensors 738, such as a drive shaft encoder, can provide the rotational position of drive shaft 740 to the circuit control unit 710.

[0248] In one aspect, control circuit 710 is configured to pivot end actuator 702. Control circuit 710 provides a motor setpoint for a 708d motor control, which provides a drive signal for the motor 704d. The output shaft of the 704d motor is coupled to a 744d torque sensor. Torque sensor 744d is coupled to a transmission 706d which is coupled to a pivot member 742a. The 706d transmission comprises moving mechanical elements, such as articulation elements, to control the articulation of the 702 + 65º end actuator. In one aspect, the 704d motor is coupled to a pivot nut, which is rotatably seated on the proximal end portion of the distal column portion and is pivotally driven thereon by a pivot gear assembly. The torque sensor 744d provides a feedback signal from the articulation force to the control circuit 710. The feedback signal from the articulation force represents the articulation force applied to the end actuator 702. The sensors 738, as an articulation encoder, can supply the articulation position of end actuator 702 to control circuit 710.

[0249] In another aspect, the articulation function of the robotic surgical system 700 may comprise two articulation members, or connections, 742a, 742b. These articulation members 742a, 742b are driven by separate disks at the robot interface (the rack), which are driven by the two motors 708d, 708e. When the separate firing motor 704a is provided, each hinge link 742a, 742b can be antagonistically driven with respect to the other link to provide a resistive holding motion and a load to the head when it is not moving and to provide a articulation movement when the head is articulated. The hinge members 742a, 742b attach to the head in a fixed radius when the head is rotated. Consequently, the mechanical advantage of the push and pull link changes when the head is rotated. This change in mechanical advantage can be more pronounced with other drive systems for the articulation connection.

[0250] In one aspect, the one or more motors 704a to 704e may comprise a brushed DC motor with a gearbox and mechanical connections to a firing member, closing member or articulation member. Another example includes electric motors 704a to 704e that operate the moving mechanical elements such as the displacement member, the articulation connections, the closing tube and the drive shaft. An external influence is an excessive and unpredictable influence of things like tissue, surrounding bodies, and friction in the physical system. This external influence can be called drag, which acts in opposition to one of the electric motors 704a to 704e. External influence, such as drag, can cause the functioning of the physical system to deviate from a desired operation of the physical system.

[0251] In one aspect, the position sensor 734 can be implemented as an absolute positioning system. In one aspect, the 734 position sensor can comprise an absolute rotary magnetic positioning system implemented as a single integrated circuit rotary magnetic position sensor, ASSOSSEQFT, available from Austria Microsystems, AG. The position sensor 734 can interface with the control circuit 710 to provide an absolute positioning system. The position can include multiple Hall effect elements located above a magnet and coupled to a CORDIC processor, also known as the digit by digit method and Volder algorithm, which is provided to implement a simple and efficient algorithm for calculating functions.

hyperbolic and trigonometric definitions that require only addition, subtraction, bit shift and lookup table operations.

[0252] In one aspect, the control circuit 710 can be in communication with one or more sensors 738. The sensors 738 can be positioned on the end actuator 702 and adapted to work with the robotic surgical instrument 700 to measure various derived parameters such as span distance in relation to time, compression of the tissue in relation to time, and deformation of the anvil in relation to time. The 738 sensors can comprise a magnetic sensor, a magnetic field sensor, a strain gauge, a load cell, a pressure sensor, a force sensor, a torque sensor, an inductive sensor as a sensor eddy current, a resistive sensor, a capacitive sensor, an optical sensor and / or any other sensor suitable for measuring one or more parameters of the end actuator 702. The 738 sensors may include one or more sensors. The sensors 738 can be located on the platform of the staple cartridge 718 to determine the location of the tissue using segmented electrodes. The torque sensors 744a to 744e can be configured to detect force such as firing force, closing force, and / or articulation force, among others. Consequently, control circuit 710 can detect (1) the closing load experienced by the distal closing tube and its position, (2) the trigger member on the rack and its position, (3) which portion of the staple cartridge 718 has tissue in it, and (4) the load and position on both articulation rods.

[0253] In one aspect, the one or more sensors 738 may comprise a strain gauge such as, for example, a micro strain gauge, configured to measure the magnitude of the strain on the burner 716 during a stuck condition. The voltage meter provides an electrical signal whose amplitude varies with the magnitude of the voltage. The 738 sensors can comprise a pressure sensor configured to detect a pressure generated by the presence of compressed tissue between the anvil 716 and the staple cartridge 718. The sensors 738 can be configured to detect the impedance of a section of tissue located between the anvil 716 and the staple cartridge 718 which is indicative of the thickness and / or completeness of the fabric located between them.

[0254] In one aspect, the 738 sensors can be implemented as one or more limit switches, electromechanical devices, solid state switches, Hall effect devices, magneto-resistive devices (MR) giant magneto-resistive devices (GMR), magnetometers, among others. In other implementations, the 738 sensors can be implemented as solid state switches that operate under the influence of light, such as optical sensors, infrared sensors, ultraviolet sensors, among others. In addition, the switches can be solid state devices such as transistors (for example, FET, junction FET, MOSFET, bipolar and the like). In other implementations, the 738 sensors can include driverless electric switches, ultrasonic switches, accelerometers, inertia sensors and, among others.

[0255] In one aspect, sensors 738 can be configured to measure the forces exerted on the anvil 716 by the closing drive system. For example, one or more sensors 738 may be at a point of interaction between the closing tube and the anvil 716 to detect the closing forces applied by the closing tube on the anvil 716. The forces exerted on the anvil 716 can be representative of the tissue compression experienced by the tissue section captured between the anvil 716 and the staple cartridge 718. One or more sensors 738 can be positioned at various points of interaction throughout the drive system.

closing operation to detect the closing forces applied to the anvil 716 by the closing drive system. The one or more 738 sensors can be sampled in real time during a hold operation by the control circuit processor 710. The control circuit 710 receives sample measurements in real time to provide and analyze information based on time and evaluate, in real time, the closing forces applied to the anvil

716.

[0256] In one aspect, a current sensor 736 can be used to measure the current drawn by each of the 704a to 704e motors. The force required to advance any of the moving mechanical elements such as the beam with a profile | 714 corresponds to the current drawn by one of the motors 704a to 704e. The force is converted into a digital signal and supplied to the control circuit 710. The control circuit 710 can be configured to simulate the response of the instrument's actual system in the controller software. A displacement member can be used to move a beam with a profile in | 714 on end actuator 702 at or near a target speed. The robotic surgical instrument 700 may include a re-information controller, which may be one or any of the re-information controllers, including, but not limited to, a PID controller, state feedback, linear quadratic (LOR) and / or an adaptable controller, for example. The robotic surgical instrument 700 can include a power source to convert the signal from the feedback controller to a physical input such as case voltage, PWM voltage, frequency modulated voltage, current, torque and / or force, for example. Additional details are revealed in US patent application serial number 15 / 636,829, entitled CLOSED LOOP VELOCITY CONTROL TECHNIQUES FOR ROBOTIC SURGICAL INSTRUMENT, filed on June 29, 2017, which is hereby incorporated by reference in its entirety.

[0257] Figure 18 illustrates a block diagram of a surgical instrument 750 programmed to control the distal translation of the displacement limb, according to one aspect of this disclosure. In one aspect, the 750 surgical instrument is programmed to control the distal translation of a displacement member, such as the beam with a | 764. The surgical instrument 750 comprises an end actuator 752 which may comprise an anvil 766, a beam with a profile in | 764 (including a sharp cutting edge), and a removable staple cartridge 768.

[0258] The position, movement, displacement, and / or translation of a member of linear displacement, such as the beam with profile in | 764, can be measured by an absolute positioning system, sensor arrangement, and a position sensor 784. As the beam with | 764 is coupled to a longitudinally movable drive member, the beam position with | 764 can be determined by measuring the position of the longitudinally movable drive member using the 784 position sensor. Consequently, in the following description, the position, displacement and / or translation of the beam with profile in | 764 can be obtained by the position sensor 784, as described in the present invention. A control circuit 760 can be programmed to control the translation of the displacement member, such as the beam with | 764. The control circuit 760, in some examples, may comprise one or more microcontrollers, microprocessors or other suitable processors to execute the instructions that cause the processor or processors to control the displacement member, for example, the beam with profile on | 764, as described. In one aspect, a timer / counter 781 provides an output signal, such as elapsed time or a digital count, to control circuit 760 to correlate the position of the beam with | 764 as determined by the position sensor 784 with the timer / counter output 781 so that the control circuit 760 can determine the position of the beam with profile in | 764 at a specific time (t) in relation to an initial position. The 781 timer / counter can be configured to measure elapsed time, count external events, or measure timeless events.

[0259] Control circuit 760 can generate a 772 engine setpoint signal. The 772 engine setpoint signal can be supplied to a 758 motor controller. The 758 motor controller can comprise one or more circuits configured to provide a motor 774 drive signal to motor 754 to drive motor 754, as described in the present invention. In some instances, the 754 motor may be a DC motor with a brushed DC electric motor. For example, the speed of motor 754 can be proportional to the drive signal of motor 774. In some instances, motor 754 can be a brushless DC electric motor and the drive signal of motor 774 can comprise a supplied PWM signal for one or more motor stator windings 754. In addition, in some examples, motor controller 758 can be omitted, and control circuit 760 can generate motor drive signal 774 directly.

[0260] The 754 motor can receive power from a power source

762. The 762 power source can be or include a battery, a super capacitor, or any other suitable power source. The 754 motor can be mechanically coupled to the beam with a profile | 764 by means of a transmission 756. The transmission 756 may include one or more gears or other connecting components for coupling the motor 754 to the beam with profile | 764. A 784 position sensor can detect a beam position with | 764. The position sensor 784 can be or can include any type of sensor that is capable of generating position data that indicates a beam position with profile in | 764. In some examples, the position sensor 784 may include an encoder configured to supply a series of pulses to the control circuit 760 according to the beam with profile in | 764 moved distally and proximally. The control circuit 760 can track the pulses to determine the position of the beam with profile in | 764. Other suitable position sensors can be used, including, for example, a proximity sensor. Other types of position sensors can provide other signals that indicate the movement of the beam with profile in | 764. In addition, in some examples, the 784 position sensor may be omitted. When motor 754 is a stepper motor, control circuit 760 can track the beam position with | 764 by adding the number and orientation of the steps that the 754 engine was instructed to perform. The position sensor 784 can be located on end actuator 752 or any other portion of the instrument.

[0261] The control circuit 760 can be in communication with one or more sensors 788. The sensors 788 can be positioned on the end actuator 752 and adapted to work with the surgical instrument 750 to measure the various derived parameters, such as distance span in relation to time, compression of the tissue in relation to time and tension of the anvil in relation to time. The 788 sensors can comprise a magnetic sensor, a magnetic field sensor, a stress meter, a pressure sensor, a force sensor, an inductive sensor such as a eddy current sensor, a resistive sensor, a capacitive sensor, a sensor optical and / or any other sensors suitable for measuring one or more parameters of the 752 end actuator. The 788 sensors may include one or more sensors.

[0262] The one or more sensors 788 may comprise a strain gauge, such as a microstrain gauge, configured to measure the magnitude of strain on the anvil 766 during a grip condition. The voltage meter provides an electrical signal whose amplitude varies with the magnitude of the voltage. The 788 sensors can comprise a pressure sensor configured to detect a pressure generated by the presence of compressed tissue between the anvil 766 and the staple cartridge 768. The 788 sensors can be configured to detect the impedance of a section of tissue located between the anvil 766 and the staple cartridge 768 which is indicative of the thickness and / or completeness of the fabric located between them.

[0263] The sensors 788 can be configured to measure the forces exerted on the anvil 766 by a closing drive system. For example, one or more sensors 788 can be at a point of interaction between a closing tube and anvil 766 to detect the closing forces applied by a closing tube to anvil 766. The forces exerted on anvil 766 can be representative of the tissue compression experienced by the tissue section captured between the anvil 766 and the staple cartridge 768. The one or more sensors 788 can be positioned at various points of interaction throughout the closing drive system to detect the closing forces applied anvil 766 by the closing drive system. The one or more sensors 788 can be sampled in real time during a hold operation by a processor from the control circuit 760. The control circuit 760 receives sample measurements in real time to provide and analyze information based on time and evaluate, in real time, the closing forces applied to the anvil 766.

[0264] A current sensor 786 can be used to measure the current drained by the 754 motor. The force required to advance the beam with profile in | 764 corresponds to the current drained by the motor

754. The force is converted into a digital signal and supplied to the control circuit 760.

[0265] Control circuit 760 can be configured to simulate the response of the instrument's actual system in the controller software. A displacement member can be actuated to move a beam with a profile | 764 on end actuator 752 at or near a target speed. The surgical instrument 750 may include a feedback controller, which can be one or any of the feedback feedback controllers, including, but not limited to, a PID controller, status feedback, LOR, and / or an adaptive controller, for example. example. The surgical instrument 750 can include a power source to convert the signal from the feedback controller to a physical input such as case voltage, PWM voltage, voltage modulated by frequency, current, torque and / or force, for example plo.

[0266] The actual drive system of the surgical instrument 750 is configured to drive the displacement member, the cutting member or the beam with profile in | 764, by a brushed DC motor with gearbox and mechanical connections to an articulation system and / or a knife. Another example is the 754 electric motor which operates the displacement member and the articulation drive, for example, from an interchangeable drive shaft assembly. An external influence is an excessive and unpredictable influence on things like tissue, surrounding bodies, and friction in the physical system. This external influence can be called drag, which acts in opposition to the 754 electric motor. External influence, like drag, can cause the functioning of the physical system to deviate from a desired operation of the physical system.

[0267] Several exemplifying aspects are directed to a 750 surgical instrument that comprises a 752 end actuator with motor-driven surgical stapling and cutting implements. For example, a motor 754 can drive a displacement member distally and proximally along a longitudinal geometry axis of end actuator 752. End actuator 752 may comprise an articulating anvil 766 and, when configured for use, a ultrasonic blade 768 positioned on the opposite side of the anvil 766. A doctor can hold the tissue between the anvil 766 and the staple cartridge 768, as described in the present invention. When ready to use the 750 instrument, the physician can provide a trigger signal, for example, by pressing a trigger on the 750 instrument. In response to the trigger signal, the 754 motor can drive the displacement member distally along the axis longitudinal geometric pattern of end actuator 752 from a proximal start position to a distal end position from the start position. As the displacement member moves distally, the beam with a | 764 with a cutting element positioned at a distal end, you can cut the fabric between the staple cartridge 768 and the anvil 766.

[0268] In several examples, the surgical instrument 750 may comprise a control circuit 760 programmed to control the distal translation of the displacement member, such as the beam with profile in | 764, for example, based on one or more tissue conditions. The control circuit 760 can be programmed to directly or indirectly detect tissue conditions, such as thickness, as described here. Control circuit 760 can be programmed to select a control program based on tissue conditions. A trigger control program can describe the displacement member's distal movement. Different trigger control programs can be selected to better handle the different controls

conditions of the tissue. For example, when thicker tissue is present, control circuit 760 can be programmed to translate the displacement member at a lower speed and / or with a lower power. When a thinner fabric is present, the control circuit 760 can be programmed to transfer the displacement member at a higher speed and / or with greater power.

[0269] In some examples, control circuit 760 may initially operate motor 754 in an open circuit configuration for a first open circuit portion of a travel of the travel member. Based on an instrument response 750 during the open circuit portion of the stroke, control circuit 760 can select a trip control program. The response of the instrument may include a travel distance of the displacement member during the open circuit portion, a time elapsed during the open circuit portion, the power supplied to the motor 754 during the open circuit portion, a sum of pulse widths a motor start signal, etc. After the open circuit portion, control circuit 760 can implement the selected trigger control program for a second portion of the travel member travel. For example, during the closed loop portion of the stroke, control circuit 760 can modulate motor 754 based on translation data that describes a position of the displacement member in a closed circuit manner to translate the displacement member into a constant speed. Additional details are revealed in US patent application serial number 15 / 720,852, entitled SYSTEM AND METHODS FOR CONTROLLING A DISPLAY OF A SURGICAL INSTRUMENT, filed on September 29, 2017, which is hereby incorporated by reference in its entirety.

[0270] Figure 19 is a schematic diagram of a 790 surgical instrument configured to control various functions, according to at least one aspect of this disclosure. In one aspect, the 790 surgical instrument is programmed to control the distal translation of a displacement member, such as the beam with a | 764. Surgical instrument 790 comprises an end actuator 792 which may comprise an anvil 766, a beam with a profile in | 764 and a removable staple cartridge 768 that can be interchanged with an RF cartridge 796 (shown in dashed line).

[0271] In one aspect, 788 sensors can be implemented as a limit switch, electromechanical device, solid state switches, Hall effect devices, MRI devices, GMR devices, magnetometers, among others. In other implementations, 638 sensors can be solid state switches that operate under the influence of light, such as optical sensors, infrared sensors, ultraviolet sensors, among others. In addition, the switches can be solid state devices such as transistors (for example, FET, junction FET, MOSFET, bipolar and the like). In other implementations, 788 sensors can include driverless electric switches, ultrasonic switches, accelerometers, inertia sensors and, among others.

[0272] In one aspect, the 784 position sensor can be implemented as an absolute positioning system, which comprises a rotating magnetic absolute positioning system implemented as a rotating, magnetic position sensor. single integrated, ASSOSSEQFT, available from Austria Microsystems, AG. The position sensor 784 can interface with the control circuit 760 to provide an absolute positioning system. The position can include multiple Hall effect elements located above a magnet and coupled to a CORDIC processor, also

also known as the digit by digit method and Volder algorithm, which is provided to implement a simple and efficient algorithm for calculating hyperbolic and trigonometric functions that require only addition, subtraction, bit shift and lookup table operations.

[0273] In one aspect, the beam with | 764 can be implemented as a knife member comprising a knife body that operationally supports a tissue cutting blade in the same and can additionally include flaps or sling hitch features and channel hitch features or a base. In one aspect, the staple cartridge 768 can be implemented as a standard (mechanical) surgical clamp cartridge. In one aspect, the RF cartridge 796 can be implemented as an RF cartridge. These and other sensor arrangements are described in Commonly Owned U.S. Patent Application Serial No. 15 / 628,175, entitled

TECHNIQUES FOR ADAPTIVE CONTROL OF MOTOR VELOCITY OF A SURGICAL STAPLING AND CUTTING INSTRUMENT, deposited on June 20, 2017, which is hereby incorporated by reference in its entirety.

[0274] The position, movement, displacement and / or translation of a member of linear displacement, such as the beam with profile in | 764, can be measured by an absolute positioning system, sensor arrangement and position sensor represented as position sensor 784. As the beam with profile in | 764 is coupled to the longitudinally movable drive member, the beam position with | 764 can be determined by measuring the position of the longitudinally movable drive member that employs the position sensor 784. Consequently, in the description below, the position, displacement and / or translation of the beam with profile in | 764 can be obtained by the position sensor 784, as described in the present invention. A control circuit 760 can be programmed to control the translation of the displacement member, such as the beam with | 764, as described here. The control circuit 760, in some examples, may comprise one or more microcontrollers, microprocessors or other suitable processors to execute the instructions that cause the processor or processors to control the displacement member, for example, the beam with profile on | 764, as described. In one aspect, a timer / counter 781 provides an output signal, such as elapsed time or a digital count, to the control circuit 760 to correlate the beam position with | 764 as determined by position sensor 784 with timer / counter output 781 so that control circuit 760 can determine the position of the beam with profile in | 764 at a specific time (t) in relation to an initial position. The 781 timer / counter can be configured to measure elapsed time, count external events, or measure eternal events.

[0275] Control circuit 760 can generate a 772 motor setpoint signal. The 772 motor setpoint signal can be supplied to a 758 motor controller. The 758 motor controller can comprise one or more circuits configured to provide a motor 774 drive signal to motor 754 to drive motor 754, as described in the present invention. In some instances, the 754 motor may be a DC motor with a brushed DC electric motor. For example, the speed of motor 754 can be proportional to the drive signal of motor 774. In some instances, motor 754 can be a brushless DC electric motor and the drive signal of motor 774 can comprise a supplied PWM signal for one or more motor stator windings 754. In addition, in some examples, the motor controller 758 may be omitted, and the circuit

control loop 760 can generate the motor start signal 774 directly.

[0276] The 754 motor can receive power from a power source

762. The 762 power source can be or include a battery, a super capacitor, or any other suitable power source. The 754 motor can be mechanically coupled to the beam with a profile | 764 by means of a transmission 756. The transmission 756 may include one or more gears or other connecting components for coupling the motor 754 to the beam with profile | 764. A 784 position sensor can detect a beam position with | 764. The position sensor 784 can be or can include any type of sensor that is capable of generating position data that indicates a beam position with profile in | 764. In some examples, the position sensor 784 may include an encoder configured to supply a series of pulses to the control circuit 760 according to the beam with profile in | 764 moved distally and proximally. The control circuit 760 can track the pulses to determine the position of the beam with profile in | 764. Other suitable position sensors can be used, including, for example, a proximity sensor. Other types of position sensors can provide other signals that indicate the movement of the beam with profile in | 764. In addition, in some examples, the 784 position sensor may be omitted. When motor 754 is a stepper motor, control circuit 760 can track the beam position with | 764 by adding the number and orientation of the steps that the engine was instructed to perform. The position sensor 784 can be located on the end actuator 792 or any other portion of the instrument.

[0277] The control circuit 760 can be in communication with one or more sensors 788. The sensors 788 can be positioned on the end actuator 792 and adapted to work with the instrument.

surgical instrument 790 to measure the various derived parameters, such as span distance in relation to time, compression of the tissue in relation to time and anvil tension in relation to time. The 788 sensors can comprise a magnetic sensor, a magnetic field sensor, a stress meter, a pressure sensor, a force sensor, an inductive sensor such as a eddy current sensor, a resistive sensor, a capacitive sensor, a sensor optical and / or any other sensors suitable for measuring one or more parameters of the end actuator 792. The 788 sensors may include one or more sensors.

[0278] The one or more sensors 788 may comprise a strain gauge, such as a microstrain gauge, configured to measure the magnitude of strain on the anvil 766 during a grip condition. The voltage meter provides an electrical signal whose amplitude varies with the magnitude of the voltage. The 788 sensors can comprise a pressure sensor configured to detect a pressure generated by the presence of compressed tissue between the anvil 766 and the staple cartridge 768. The 788 sensors can be configured to detect the impedance of a section of tissue located between the anvil 766 and the staple cartridge 768 which is indicative of the thickness and / or completeness of the fabric located between them.

[0279] The 788 sensors can be configured to measure the forces exerted on the anvil 766 by the closing drive system. For example, one or more sensors 788 can be at a point of interaction between a closing tube and anvil 766 to detect the closing forces applied by a closing tube on anvil 766. The forces exerted on anvil 766 can be representative of the tissue compression experienced by the tissue section captured between the anvil 766 and the staple cartridge 768. The one or more sensors 788 can be positioned at various points of interaction throughout the closing drive system to detect the forces of closure applied to the anvil 766 by the closing drive system. The one or more sensors 788 can be sampled in real time during a gripping operation by a processor portion of the control circuit 760. The control circuit 760 receives sample measurements in real time to provide and analyze time-based information and assess, in real time, the closing forces applied to the anvil

766.

[0280] A current sensor 786 can be used to measure the current drained by the 754 motor. The force required to advance the beam with profile in | 764 corresponds to the current drained by the motor

754. The force is converted into a digital signal and supplied to the control circuit 760.

[0281] An RF power source 794 is coupled to the end actuator 792 and is applied to the RF 796 cartridge when the RF 796 cartridge is loaded on the end actuator 792 in place of the staple cartridge 768. The circuit Control Panel 760 controls the supply of RF energy to the 796 RF cartridge.

[0282] Additional details are revealed in US patent application serial number 15 / 636,096, entitled SURGICAL SYSTEM COUPLABLE WITH STAPLE CARTRIDGE AND RADIO FREQUENCY CARTRIDGE, AND METHOD OF USING SAME, filed on June 28, 2017, which is here incorporated as a reference in its entirety.

[0283] Figure 20 illustrates a 20740 stroke length graph that shows how a control system can change the stroke length of a closing tube assembly based on the hinge angle 9. Such a stroke length change includes shortening the stroke length to a compensated stroke length (for example, defined along the y-axis) as the pivot angle 8 increases (for example, defined along the x-axis). The compensated stroke length defines a stroke length of the closing tube assembly in the distal direction to close the claws of an end actuator, which depends on the pivot angle 8 and prevents excessive displacement of the closing tube assembly, causing damage to the surgical device.

[0284] For example, as shown in the stroke length chart 20740, the stroke length of the closing tube assembly for closing the jaws is approximately 0.250 inches when the end actuator is not pivoted and the - compensated stroke length is approximately 0.242 inches when the pivot angle 8 is approximately 60 degrees. Such measurements are provided as examples only and may include any of a variety of corresponding stroke angles and lengths and compensated stroke lengths without departing from the scope of this disclosure. In addition, the relationship between pivot angles 8 and compensated stroke lengths is non-linear and the rate at which the compensated stroke length decreases increases as the pivot angle increases. For example, the decrease in compensated stroke lengths between 45 and 60 degrees of articulation is greater than the decrease in compensated stroke lengths between zero and 15 degrees of articulation. Although with this approach the control system is adjusting the stroke length based on the angle of articulation 8 to prevent damage to the surgical device (for example, holding the distal end of the closing tube assembly in a distal position), the advancement of the distal closing tube is still allowed during the joint, potentially closing at least partially

claws.

[0285] Figure 21 illustrates a positioning graph for the 20750 closing tube assembly that shows an aspect in which a control system modifies a longitudinal position of a closing tube assembly based on the pivot angle; Such modification of the longitudinal position of the closing tube assembly includes retracting the closing tube assembly proximally by a compensation distance (for example, defined along the y-axis) as the end actuator articulates and based on the pivot angle 8 (for example, defined along the geometry axis x). The compensation distance that the closing tube assembly is proximally retracted prevents the distal advancement of the distal closing tube thus keeping the claws in the open position during the joint. Through the proximal retraction of the closing tube set by the compensation distance during the joint, the closing tube set can travel the length of the path from the proximally retracted position to close the claws after activating the closing set

[0286] For example, as shown in the 20750 closing tube assembly positioning chart, the compensation distance when the end actuator is not pivoted is zero and the compensation distance when the pivot angle 8 is approximately 60 degrees is approximately 0.008 inches. In this example, the closing tube assembly is retracted by a compensation distance of 0.008 inches during articulation. In this way, to close the claws, the closing tube assembly can advance the stroke length from this retracted position. Such measurements are provided for example purposes only and may include any of a variety of corresponding compensation angles and distances without departing from the scope of the disclosure.

As shown in Figure 21, the relationship between the pivot angle 8 and the compensation distance is non-linear and the speed at which the compensation distance increases increases as the pivot angle 8 increases. For example, the increase in the compensation distance between 45 degrees and 60 degrees is greater than the increase in the compensation distance between zero degrees and 15 degrees.

[0287] During the gripping of the patient's tissue, the forces exerted through the gripping device, for example, a linear stapler, and the tissue can reach an unacceptably high level. For example, when a constant closing rate is employed, the force can become high enough to cause excess trauma to the trapped tissue and can cause deformation of the gripping device so that an acceptable gap of tissue is not maintained throughout the clipping path. Figure 22 is a graph illustrating the power applied to the tissue during compression at a constant speed of the anvil closure rate (ie; no controlled tissue compression (CTC)) versus the power applied to the tissue during the compression with a variable anvil closure rate (ie, with CTC). The closure rate can be adjusted to control tissue compression so that the energy imparted to the tissue remains constant over a portion of the compression. The peak power transmitted to the tissue according to Figure 22 is much lower when a variable anvil closure rate is used. Based on the energy conferred, the force exerted by the surgical device (or a parameter related to or proportional to the force) can be calculated. In this sense, the power can be limited, so that the force exerted through the surgical device, for example, through the claws of a linear stapler, does not exceed a yield or pressure force that results in the opening of the claws, so that the fabric gap is not within an acceptable range along the entire length of the staple when in the fully closed position. For example, the jaws should be parallel or close enough that the fabric gap remains within the acceptable or target range for all staple positions along the entire length of the jaws. In addition, limiting the power exerted avoids, or at least reduces, trauma or tissue damage.

[0288] In Figure 22, the total energy exerted in the method without CTC is the same as the total energy exerted in the method with CTC, that is, the areas under the power curves in Figure 22 are the same or substantially the same. The difference in the power profiles used is, however, substantial, since the peak power is much less in the example with CTC compared to the example without CTC.

[0289] The power limitation is obtained in the example with CTC by reducing the closing rate, as illustrated by line 20760. Note that the compression time B 'is greater than the closing time B. As illustrated in Figure 22, a device and method that provides a constant closing rate (i.e., without CTC) achieves the same 50 pounds of compression force in the same 1 mm tissue gap as the device and the method that provides a closing rate variable (ie with CTC). While the device and method that provide a constant closure rate can achieve the compressive strength in the desired tissue span in a shorter period of time compared to a device and method that uses a variable closure rate, this results in the peak power applied to the fabric, as shown in Figure 22. In contrast, the example of an aspect illustrated with CTC begins to reduce the closure rate to limit the amount of power applied to the fabric below a certain level. By limiting the power applied to the tissue, trauma to the tissue can be minimized in relation to the system and method that does not use CTC.

[0290] Figure 22 and additional examples are further described in US Patent No. 8,499,992, filed on June 1, 2012, entitled DEVICE AND METHOD FOR CONTROLLING COMPRESSION OF TISSUE, which was issued on August 6, 2013, whose full disclosure is hereby incorporated by reference.

[0291] In some respects, a control system may include a plurality of predefined strength limits that assist the control system in determining a beam position with an E-profile and / or pivot angle of a firing drive shaft and properly controlling at least one engine based on such a determination. For example, the force limits can change depending on a stroke length of the firing bar configured to move the firing drive shaft, and such force limits can be compared to a measured torsional force of the one or more motors in communication with the control system. The comparison of the torsional forces measured against the force limits can provide a reliable way for the control system to determine a location of the E-profile beam and / or the end actuator joint. This can allow the control system to adequately control one or more motors (for example, reduce or stop torsional loads) to ensure the triggering of the end actuator trigger and joint assembly, as well as preventing damage to the system. theme, as will be described in more detail below.

[0292] Figure 23 illustrates a 20800 force and displacement graph including forces measured in section A that are related to the displacements measured in section B. Both sections A and B have a geometric axis x that defines time (for example, seconds ). The y-axis of section B defines a displacement (for example, in millimeters) of a firing rod and the y-axis of section A defines a force applied to the firing bar to advance

raise the trigger drive axis. As shown in section A, the displacement of the firing bar within a first articulation range 20902 (for example, a first path of approximately 12 mm) causes the end actuator to articulate. For example, in the 12 mm travel position, the end actuator is fully articulated to the right and is mechanically unable to articulate further. As a result of being in full articulation, the torsional force on the engine will increase and the control system can detect a 20802 pivot force peak that exceeds a predefined 20804 articulation limit, as shown in section A. The control system can include more than a predetermined articulation limit 20804 to detect more than one direction of maximum articulation (for example, articulation to the left and articulation to the right). After the control system detects a 20802 articulation force peak that exceeds the predetermined articulation limit 20804, the control system can reduce or prevent the engine from acting, thus at least protecting the engine from damage.

[0293] After the firing bar advances beyond the 20902 hinge band, a displacement mechanism within the surgical stapler can cause additional distal displacement of the firing bar to cause distal displacement of the firing drive shaft . For example, as shown in section B, the displacement between approximately 12 mm and 70 mm of travel can cause the beam with an E-profile to advance along a 20904 firing stroke and cut the captured tissue between the claws; however, other travel lengths are within the scope of this disclosure. In this example, a maximum firing stroke position 20906 of the E-profile beam occurs at 70 mm. At that point, the E-profile beam or the knife is contiguous to a distal end of the cutter or jaw, thus increasing the torsional forces on the motor and causing a peak in the 20806 knife displacement force, as shown in section A, be detected by the control system. As shown in section A, the control system can include a 20808 engine limit and a 20810 knife end path limit that extends from the 20808 engine limit and decreases (for example, non-linearly) as that the beam with an E-profile approaches the position of maximum firing stroke 20906.

[0294] The control system can be configured to monitor the detected torsional force of the motor during at least the last part of the distal path 20907 (for example, last 10 percent of the firing stroke 904) of the beam with E profile before reach the maximum firing stroke position 20906. While monitoring over the last part of the distal path 20907, the control system can cause the motor to reduce torsional forces in order to reduce the load on the beam with E-profile This can protect the surgical stapler from damage, including the E-profile beam, reducing the loads on the E-profile beam as the E-profile beam approaches the maximum firing stroke position 20906 , thus reducing the impact of the beam with an E-profile at the distal end of the cartridge or claw. As mentioned above, this impact can cause a peak travel force of knife 20806, which can exceed the travel limit of knife 20810 but not the motor limit 20808 so as not to damage the engine. In this way, the control system can stop the motor from acting after the peak 20806 knife travel force exceeds knife 20810 travel threshold and before the 20806 knife travel force peak exceeds the motor limit 20808, thus protecting the engine from damage. In addition, the increasing reduction in the 20810 knife travel limit prevents the control system from preliminarily thinking that the E-profile beam has reached the maximum firing stroke position 20906.

[0295] After the control system has detected a knife displacement force peak 20806 that exceeds the knife displacement limit 20810, the control system can confirm an E-beam beam position (for example, 70 mm displacement and / or at the end of the 20904 firing stroke) and can retract the firing bar based on that known displacement position to reset the E-profile beam to the most proximal position 20908 (for example, displacement of 0 mm ). In the most proximal position 20908, a peak knife retraction force 20812 that exceeds a predefined knife retraction limit 20814, as shown in section A, can be detected by the control system. At this point, the control system can recalibrate, if necessary, and associate the beam position with an E-profile as being in an initial position where subsequent advancement of the firing rod in the distal direction (for example, approximately 12 mm in length) will make with the shifter to disengage the E-profile beam from the firing bar. Once disengaged, displacement of the firing bar within the 20902 pivot range will again cause the end actuator to pivot.

[0296] In this way, the control system can detect torsional forces in the motor that control the displacement of the firing bar and compare these detected torsional forces with a plurality of limits to determine a beam position with an E-profile or articulation angle of the beam. end actuator and, thus, properly control the engine to avoid damage to the engine, as well as confirm the positioning of the shot bar and / or beam with E-profile.

[0297] As described above, contact with the tissue or pressure sensors determines when the claw members first come into contact with the "T" tissue. This allows a surgeon to determine the initial thickness of the "T" tissue and / or the thickness of the "T" tissue before gripping. In any of the aspects of the surgical instrument described above, as seen in Figure 24, the contact of the members of the claw with the "T" tissue closes a sensor circuit "SC" that is otherwise open, establishing contact with a pair opposite plates "P1, P2" provided on the claw members. Contact sensors can also include sensitive force transducers that determine the amount of force that is applied to the sensor, which can be assumed to be the same amount of force being applied to the "T" fabric. This force being applied to the tissue, can then be converted into a compressed amount of tissue. The force sensors measure the amount of compression a tissue is under and provide the surgeon with information about the force applied to the "T" tissue. Excessive tissue compression can have a negative impact on the "T" tissue being operated. For example, excessive compression of the "T" tissue can result in tissue necrosis and, in certain procedures, failure of the staple line. Information regarding the pressure being applied to the "T" tissue allows a surgeon to better determine if excessive pressure is not being applied to the "T" tissue.

[0298] Any of the contact sensors presented here may include, but is not limited to, electrical contacts placed on an internal surface of a claw that, when in contact with the tissue, close a detection circuit that is otherwise open . Contact sensors can also include sensitive force transducers that detect when the tissue being attached first resists compression. Force transducers may include, but are not limited to, piezoelectric elements, piezoresistive elements, metal film or semiconductor stress meters, inductive pressure sensors, caparcitive pressure sensors, and potentiometric pressure transducers that use bourbon tubes , capsules or bellows to activate a cleaning arm on a resistive element.

[0299] In one aspect, any of the aforementioned surgical instruments can include one or more piezoelectric elements to detect a change in pressure that occurs in the claw members. Piezoelectric elements are bidirectional transducers that convert voltage into an electrical potential. The elements may consist of metallized quartz or ceramic. In operation, when the stress is applied to the crystals there is a change in the load distribution of the material resulting in a generation of stress throughout the material. Piezoelectric elements can be used to indicate when either or both claw members come into contact with the "T" fabric and the amount of pressure exerted on the "T" fabric after a contact is established.

[0300] In one aspect, any of the aforementioned surgical instruments may include or be equipped with one or more metallic strain gauges placed inside or on a portion of the body thereof. Metallic stress meters operate according to the principle that the strength of the material depends on the length, width and thickness. Consequently, when the material of the metallic strain gauge undergoes deformation the resistance of the material changes. In this way, a resistor made of this material incorporated in a circuit will convert voltage to a change in an electrical signal. Desirably, the strain gauge can be placed over surgical instruments so that the pressure applied to the tissue affects the strain gauge.

[0301] Alternatively, in another aspect, one or more semiconductor stress meters can be used in a similar way as the metallic stress meter described above, although the transduction mode is different. In operation, when a crystal lattice structure of the semiconductor stress meter is deformed, as a result of an applied voltage, the resistance of the

material changes. This phenomenon is called the piezoresistive effect.

[0302] In yet another aspect, any of the aforementioned surgical instruments can include or be equipped with one or more inductive pressure sensors to transduce pressure or force in movement of inductive elements in relation to each other. This movement of the inductive elements in relation to each other alters the general inductance or inductive coupling. Capacitive pressure transducers also transduce pressure or force in movement of capacitive elements in relation to each other, changing the general capacitance.

[0303] In yet another aspect, any of the aforementioned surgical instruments can include or be equipped with one or more capacitive pressure transducers to transduce pressure or moving force of capacitive elements in relation to each other, changing a general capacitance .

[0304] In one aspect, any of the aforementioned surgical instruments can include or be equipped with one or more mechanical pressure transducers to transduce the pressure or force in motion. In use, a movement of a mechanical element is used to deflect a pointer or disc on a meter. This movement of the pointer or disc can be representative of the pressure or force applied to the "T" fabric. Examples of mechanical elements include, but are not limited to, bourbon tubes, capsules or bellows. As an example, mechanical elements can be coupled with other detecting and / or measuring elements, such as a pressure transducer for the potentiometer. In this example the mechanical element is coupled with a cleaner over the variable resistor. In use, the pressure or force can be converted into a mechanical movement that deflects said cleaner in the potentiometer thus changing the resistance to reflect the pressure or force applied.

[0305] The combination of the above aspects, in particular, the combination of the span and tissue contact sensors, provides the surgeon with feedback and / or real-time information regarding the condition of the operational site and / or "T" target tissue. For example, information about the initial thickness of the "T" tissue can guide the surgeon in selecting an appropriate staple size, information about the attached thickness of the "T" tissue can inform the surgeon if the selected staple will form correctly, information related to the initial thickness and stuck thickness of the "T" fabric can be used to determine the amount of compression or tension in the "T" fabric, and information related to the tension in the "T" fabric can be used. used in this tension to avoid compressing fabrics with excessive values of deformation and / or stapling fabrics that have suffered excessive tension.

[0306] Additionally, force sensors can be used to provide the surgeon with the amount of pressure applied to the tissue. The surgeon can use this information to avoid applying excessive pressure to the "T" tissue or stapling it to the "T" tissue that has suffered excessive tension.

[0307] Figure 24 and additional examples are further described in US Patent No. 8,181,839, filed on June 27, 2011, entitled SURGICAL INSTRUMENT EMPLOYING SENORS, granted on May 5, 2012, the description of which is incorporated by reference in the present invention.

[0308] Certain aspects are shown and described to provide an understanding of the structure, function, manufacture and use of the revealed devices and methods. The features shown or described in one example can be combined with the features in other examples and modifications and variations are within the scope of this disclosure.

[0309] The terms "proximal" and "distal" are with reference to a doctor who handles the handle of the surgical instrument, with the term "proximal" referring to the portion closest to the doctor and the term "distal" referring to the portion located farthest from the doctor. For convenience, the spatial terms "vertical", "horizontal", "up" and "down" used in relation to the drawings are not intended to be limiting and / or absolute, because surgical instruments can be used in many orientations and positions.

[0310] Exemplary devices and methods are provided for performing laparoscopic and minimally invasive surgical procedures. Such devices and methods, however, can be used in other surgical procedures and applications including open surgical procedures, for example. Surgical instruments can be inserted through a natural orifice or through an incision or perforation formed in the tissue. The functional portions or portions of the instrument's end actuator can be inserted directly into the body or via an access device that has a functional channel through which the end actuator and the elongated drive shaft can be advanced. surgical instrument.

[0311] Figures 25 to 28 illustrate a 150010 engine-driven surgical instrument for cutting and fixing that may or may not be reused. In the illustrated examples, the 150010 surgical instrument includes a 150012 cabinet comprising a 150014 handle assembly that is configured to be picked up, handled and operated by the physician. The 150012 cabinet is configured for operational fixation to an interchangeable drive shaft assembly 150200 that has an end actuator 150300 operationally coupled to it that is configured to perform one or more surgical tasks or procedures. According to the present description, various forms of interchangeable drive shaft assemblies can be effectively used in connection with robotically controlled surgical systems. The term "cabinet" may include a cabinet or similar portion of a robotic system that houses or otherwise operationally supports at least one drive system configured to generate and apply at least one control movement that can be used to drive the drive shaft assemblies. The term "structure" can refer to a portion of a hand held surgical instrument. The term "structure" can also represent a portion of a robotically controlled surgical instrument and / or a portion of the robotic system that can be used to operationally control the surgical instrument. The interchangeable drive shaft assemblies disclosed herein can be used with various robotic systems, instruments, components and methods disclosed in US Patent No. 9,072,535, entitled SURGICAL STAPLING INSTRUMENTS WITH ROTATABLE STAPLE DEPLOYMENT AR-RANGEMENTS, which is incorporated herein as a reference, in its entirety.

[0312] Figure 25 is a perspective view of a 150010 surgical instrument that has an exchangeable drive shaft assembly 150200 operationally coupled to it, in accordance with at least one aspect of this disclosure. The 150012 enclosure includes a 150300 end actuator comprising a surgical cutting and clamping device configured to operationally support a 150304 surgical clamp cartridge in it. The 150012 enclosure can be configured for use in connection with the interchangeable drive shaft assemblies that include end actuators that are adapted to hold different sizes and types of clamp cartridges, and that have different lengths, sizes and types of shaft drive. The 150012 enclosure can be used effectively with a variety of interchangeable drive shaft assemblies including assemblies configured to apply other movements and forms of energy such as radio frequency (RF) energy, ultrasonic energy and / or movement to actuator arrangements tips adapted for use in various applications and surgical procedures. End actuators, drive shaft assemblies, handles, surgical instruments and / or surgical instrument systems can use any suitable fastener, or fasteners, to attach tissue. For example, a fastener cartridge comprising a plurality of fasteners stored therein removably can be removably inserted into and / or attached to the end actuator of a drive shaft assembly.

[0313] The 150014 handle set can comprise a pair of interconnectable segments of the 150016 and 150018 handle compartments interconnected by screws, pressure inserts, adhesive, etc. The grip compartment segments 150016, 150018 cooperate to form a portion of the 150019 pistol grip that can be handled and manipulated by the clinician. The 150014 handle set operationally supports a plurality of drive systems configured to generate and apply control movements to the corresponding portions of the interchangeable drive shaft set that is operationally attached to it. A monitor can be provided below a 150045 cover.

[0314] Figure 26 is an exploded view of a portion of the surgical instrument 150010 in Figure 25, according to at least one aspect of this disclosure. The 150014 handle set can include a 150020 frame that operationally supports a plurality of drive systems. The structure

150020 can operationally support a "first" drive system or 150030 closing drive system, which can apply closing and opening movements to the 150200 interchangeable drive shaft assembly. The 150030 closing drive system can include a actuator as a 150032 closing trigger pivotally supported by the frame

150020. The 150032 lock trigger is pivotally coupled to the 150014 handle set by a 150033 pivot pin to allow the 150032 lock trigger to be handled by a physician. When the physician holds the 150019 pistol grip portion of the 150014 grip assembly, the 150032 closing trigger can pivot from an initial or "not acted" position to an "acted" position and, more particularly, to a completely compressed or fully actuated.

[0315] The 150014 handle set and the 150020 frame can operationally support a 150080 firing drive system configured to apply firing movements to the corresponding portions of the interchangeable drive shaft assembly attached to it. The 150080 firing drive system can employ an 150082 electric motor located in the 150019 pistol grip portion of the 150014 handle assembly. The 150082 electric motor can be a direct current (DC) motor with brushes having a maximum rotation of approximately 25,000 rpm, for example. In other arrangements, the motor may include a brushless motor, a wireless motor, a synchronous motor, a stepper motor or any other suitable electric motor. The 150082 electric motor can be powered by a 150090 power source which can comprise a 150092 removable power source. The 150092 removable power source can comprise a portion of the 150094 proximal compartment that is configured to attach to a portion of the distal compartment 150096. The proximal compartment portion 150094 and the distal compartment portion 150096 are configured to support operationally a plurality of 150098 batteries. Each of the 150098 batteries may comprise, for example, a lithium ion battery ("LI") or other suitable battery. The 150096 distal compartment portion is configured for removable operational fixation to a 150100 control circuit board that is operationally coupled to the 150082 electric motor. Several 150098 batteries connected in series can power the surgical instrument

150010. The 150090 power source can be replaceable and / or rechargeable. A 150043 monitor, which is located below the 150045 cover, is electrically coupled to the control circuit board

150100. The 150045 cover can be removed to expose the monitor

150043.

[0316] The 150082 electric motor can include a rotary drive shaft (not shown), which, operationally, interfaces with a 150084 gear reducer assembly mounted on a coupling gate with a set or rack , of drive teeth 150122 in a longitudinally movable drive member 150120. The longitudinally movable drive member 150120 has a rack of drive teeth 150122 formed thereon for coupling coupling with a corresponding drive gear 150086 from the assembly gear reducer 150084.

[0317] In use, a voltage polarity provided by the 150090 power source can operate the 150082 electric motor clockwise, and the voltage polarity applied to the electric motor by the battery can be reversed in order to operate the electric motor 150082 counterclockwise. When the 150082 electric motor is turned in one direction, the longitudinally movable drive member

150120 will be axially activated in the distal direction "DD". When electric motor 150082 is driven in the opposite rotating direction, the longitudinally movable driving member 150120 will be axially driven in the proximal direction "DP". The 150014 handle set can include a switch that can be configured to reverse the polarity applied to the 150082 electric motor by the power source

150090. The 150014 handle assembly can include a sensor configured to detect the position of the longitudinally movable drive member 150120 and / or the direction in which the longitudinally movable drive member 150120 is being moved.

[0318] The activation of the electric motor 150082 can be controlled by a trigger trigger 150130 that is pivotally supported on the handle set 150014. The trigger trigger 150130 can be pivoted between an unacted position and a acted position.

[0319] Returning to Figure 25, the interchangeable drive shaft assembly 150200 includes an end actuator 150300 comprising an elongated channel 150302 configured to operationally support a 150304 surgical clamp cartridge inside. The end actuator 150300 may include an anvil 150306 that is pivotally supported in relation to the elongated channel 150302. The interchangeable drive shaft assembly 150200 may include a hinge joint 150270. The construction and operation of the end actuator 150300 and the joint article 150270 are presented in US patent application publication No. 2014/0263541, entitled ARTICULATABLE SURGICAL INSTRUMENT COMPRISING AN ARTICULATION LOCK, which is hereby incorporated by reference in its entirety. The interchangeable drive shaft assembly 150200 may include a proximal housing or nozzle 150201 comprised of nozzle portions

150202, 150203. The interchangeable drive shaft assembly 150200 may include a closing tube 150260 that extends along a geometric axis of the drive shaft SA which can be used to close and / or open the anvil actuator 150306 - tremidity 150300.

[0320] Returning to Figure 25, the closing tube 150260 is translated distally (direction "DD") to close the anvil 150306, for example, in response to the action of the closing trigger 150032 in the manner described in the reference previously mentioned in the publication. cation of patent application No. 2014/0263541. The anvil 150306 is opened by proximal translation of the closing tube 150260. In the open position of the anvil, the closing tube 150260 of the drive shaft is moved to its proximal position.

[0321] Figure 27 is another view of the exploded set of portions of the 150200 interchangeable drive shaft assembly, according to at least one aspect of this disclosure. The interchangeable drive shaft assembly 150200 may include a firing member 150220 held to perform axial displacement within the center column 150210. The firing member 150220 includes one of the intermediate firing drive shaft 150222 configured to connect to a distal cutting portion or cutting bar 150280. The firing member 150220 can be called a "second drive shaft" or a "second drive shaft set". The intermediate firing drive axis 150222 can include a longitudinal slot 150223 at its end configured to receive a flap 150284 at the proximal end 150282 of the cutter bar 150280. The longitudinal slot 150223 and the proximal end 150282 can be configured to allow relative movement between them and may comprise a sliding joint 150286. Sliding joint 150286 may allow intermediate firing drive shaft 150222 of firing member 150220 to pivot end actuator 150300 around pivot joint 150270 without moving, or at least without substantially moving the cutter bar 150280. When the end actuator 150300 has been properly oriented, the intermediate firing drive shaft 150222 can be advanced distally to a proximal side wall of the longitudinal slot 150223 coming into contact with the flap 150284 to advance the cutting bar 150280 and fire a clip of staples positioned inside the channel 150302. The central column 150210 has an elongated opening or window 150213 inside it to facilitate the assembly and insertion of the intermediate trigger drive shaft 150222 inside the central column 150210. When the drive shaft intermediate firing mechanism 150222 has been inserted into it, an upper segment of the structure 150215 can be engaged with the driving shaft structure 150212 to enclose the intermediate firing drive axis 150222 and the cutting bar 150280 within itself. 150220 can be seen in US Patent Application Publication No. 2014/0263541. The central column 150210 can be configured to slide a firing member 150220 and the closing tube 150260 which extends around the central column

150210. The center column 150210 can slide a 150230 articulation actuator.

[0322] The 150200 interchangeable drive shaft assembly can include a 150400 clutch assembly configured to selectively and releasably link the 150230 hinge actuator to the 150220 firing member. The 150400 clutch assembly includes a ring or sleeve. locking device 150402 positioned around the trigger member 150220, the locking sleeve 150402 can be rotated between a engaged position, where the locking sleeve

150402 attaches hinge actuator 150230 to firing member 150220, and a disengaged position, where hinge actuator 150230 is not operably coupled to firing member 150220. When locking sleeve 150402 is in the engaged position , the distal movement of the firing member 150220 can move the hinge actuator 150230 distally, and correspondingly, the proximal movement of the firing member 150220 can move the hinge actuator 150230 proximally. When the locking sleeve 150402 is in the disengaged position, the movement of the trigger member 150220 is not transmitted to the hinge driver 150230 and, as a result, the trigger member 150220 can move independently of the hinge driver 150230. The 150201 nozzle can be used to operationally engage and disengage the articulation drive system with the trigger drive system in the various ways described in US patent application publication No. 2014/0263541.

[0323] The 150200 interchangeable drive shaft assembly may comprise a 150600 slip ring assembly that can be configured to conduct electrical energy to and from or on the end of the 150300 end actuator and / or communicate signals to the 150300 end actuator and / or from it, for example. The slip ring assembly 150600 may comprise a 150604 proximal connector flange and a 150601 distal connector flange positioned within a slot defined in the 150202, 1502083 nozzle portions. The 150604 proximal connector flange may comprise a first face and flange of the distal connector 150601 may comprise a second face positioned adjacent and movable with respect to the first face. The distal connector flange 150601 can rotate in relation to the proximal connector flange 150604 around the geometric axis of the SA-SA drive axis (Figure 25). The proximal connector flange 150604 can comprise a plurality of concentric or at least substantially concentric conductors 150602, defined on its first face. A 150607 connector can be mounted on the proximal side of the 150601 distal connector flange and can have a plurality of contacts, with each contact corresponding and in electrical contact with one of the 150602 conductors. This arrangement allows for relative rotation between the proximal connector flange 150604 and the distal connector flange 150601, while electrical contact is maintained between them. The 150604 proximal connector flange can include an electrical connector 150606 that can place the 150602 conductors in signal communication with a drive shaft circuit board, for example. In at least one case, an electrical harness comprising a plurality of conductors can extend between the electrical connector 150606 and the circuit board of the drive shaft. The electrical connector 150606 can extend proximally through a connector opening defined on the chassis mounting flange. US patent application publication No. 2014/0263551, entitled "STAPLE CARTRIDGE TISSUE THICKNESS SENSOR SYSTEM", is hereby incorporated by reference in its entirety. US patent application publication No. 2014/0263552, entitled "STAPLE CARTRIDGE TISSUE THICKNESS SENSOR SYS-TEM", is hereby incorporated by reference in its entirety. Additional details regarding the 150600 slip ring assembly can be found in US Patent Application Publication No. 2014/0263541.

[0324] The exchangeable drive shaft assembly 150200 may include a proximal portion mounted securely to the 150014 handle assembly, and a distal portion that is rotatable about a longitudinal geometric axis. The distal swivel portion of the drive shaft can be rotated relative to the proximal portion around the slip ring assembly 150600. The distal connector flange 150601 of the slip ring assembly 150600 can be positioned on the distal swivel portion of the shaft. drive.

[0325] Figure 28 is an exploded view of an aspect of an end actuator 150300 of the surgical instrument 150010 of Figure 25, in accordance with at least one aspect of this disclosure. The end actuator 150300 can include the anvil 150306 and the surgical clamp cartridge 150304. The anvil 150306 can be coupled to an elongated channel 150302. The openings 150199 can be defined in the elongated channel 150302 to receive pins 150152 that are extend from the anvil 150306 to allow the anvil 150306 to rotate from an open position to a closed position in relation to the elongated channel 150302 and surgical staple cartridge

150304. A 150172 firing bar is configured to move longitudinally into the end actuator

150300. The firing bar 150172 can be built in a solid section or can include a laminated material that comprises, for example, a stack of steel plates. The firing bar 150172 comprises a beam with an "Il" profile 150178 and a cutting edge 150182 at a distal end thereof. One end of the 150172 distally designed firing bar can be attached to the beam with a profile | 150178 to assist in spacing the anvil 150306 from a surgical staple cartridge 150304 positioned in the elongated channel 150302 when the anvil 150306 is in the closed position. The beam with profile in | 150178 can include a sharp cutting edge 150182, which can be used to separate the fabric, according to the beam with profile in | 150178 is advanced distally by the 150172 firing bar. In operation, the beam with profile | 150178 can, or fire, the 150304 surgical staple cartridge.

The surgical staple cartridge 150304 may include a molded cartridge body 150194 that holds a plurality of staples 150191 that rest on the staple actuators 150192 within the respective staple cavities opened upward

150195. A wedge slider 150190 is driven distally by the beam with a profile | 150178, sliding on a 150196 cartridge tray of the surgical staple cartridge 150304. The wedge slide 150190 moves the staple actuators 150192 upwards to expel the staples 150191 in deformation contact with the anvil 150306, while the cutting edge 150182 of the beam with profile | 150178 cuts the fabric tight.

[0326] The beam with profile in | 150178 can include upper pins 150180 that engage the anvil 150306 during firing. The beam with profile in | 150178 can include intermediate pins 150184 and a bottom foot 150186 to engage portions of the 150194 cartridge body, 150196 cartridge tray and elongated channel 150302. When a 150304 surgical staple cartridge is positioned inside the elongated channel 150302, a slot 150193 defined in the cartridge body 150194 can be aligned with a longitudinal slot 150197 defined in the cartridge tray 150196 and a slot 150189 defined in the elongated channel 150302. In use, the beam with profile | 150178 can slide through the aligned longitudinal cracks 150193, 150197 and 150189, and, as shown in Figure 28, the base 150186 of the beam with profile | 150178 can engage a groove positioned along the lower surface of the elongated channel 150302 along the length of the slot 150189, the middle pins 150184 can engage the upper surfaces of the cartridge tray 150196 along the length of the longitudinal slot 150197, and the upper pins 150180 can engage the 150306 anvil. The beam with | 150178 can space or limit the relative movement between the anvil 150306 and the surgical staple cartridge 150304, as the firing bar 150172 is advanced distally in order to fire the staples from the surgical staple cartridge 150304 and / or make an incision in the captured tissue between the anvil 150306 and the surgical staple cartridge 150304. The firing bar 150172 and the beam with profile | 150178 can be retracted proximally allowing the 150306 anvil to be opened to release the two stapled and cut tissue portions.

[0327] Figures 29A and 29B represent a block diagram of a control circuit 150700 of the surgical instrument 150010 of Figure 25 covering two drawing sheets, according to at least one aspect of this disclosure. Referring mainly to Figures 29A and 29B, a 150702 handle assembly can include a 150714 engine, which can be controlled by a 150715 engine driver and can be used by the 150010 surgical instrument trigger system. motor 150714 can be a direct current (DC) drive motor with brushes with a maximum speed of approximately 25,000 RPM. In other provisions, the 150714 motor may include a brushless motor, a wireless motor, a synchronous motor, a stepper motor or any other suitable type of electric motor. Motor driver 150715 may comprise an H bridge driver comprising field effect transistors (FETs) 150719, for example. The 150714 engine can be powered by the 150706 power pack releasably mounted to the 150200 handle set to provide control power to the 150010 surgical instrument. The 150706 power pack may comprise a battery that may include several battery cells connected in series, which can be used as the power source to power the 150010 surgical instrument. Under certain circumstances, the battery cells in the 150706 power pack can be replaceable and / or rechargeable. In at least one example, the battery cells can be lithium-ion batteries that can be separably coupled to the 150706 power pack.

[0328] The drive shaft assembly 150704 can include a controller of the drive shaft assembly 150722 that can communicate with a safety controller and a power management controller 150716 through an interface, while the shaft assembly drive 150704 and the power set 150706 are coupled to the handle set 150702. For example, the interface may comprise a first interface portion 150725, which may include one or more electrical connectors for coupling coupling with the corresponding electrical connectors of the drive shaft assembly, and a second portion of interface 150727, which may include one or more electrical connectors for coupling coupling with the corresponding electrical connectors of the power supply, to allow electrical communication between the controller of the power supply drive shaft 150722 and the power management controller 150716, while the shaft assembly drive unit 150704 and power set 150706 are coupled to the handle set 150702. One or more communication signals can be transmitted through the interface to communicate one or more of the power requirements of the fixed interchangeable drive shaft assembly 150704 to the power management controller 150716. In response, the power management controller can modulate the battery power output of the 150706 power pack, as described in more detail below, according to the power requirements of the fixed drive shaft assembly 150704. The connectors may comprise keys that can be activated after mechanically coupling the handle assembly 150702 to the drive shaft assembly 150704 and / or the assembly energy 150706 to allow electrical communication between the drive shaft assembly controller 150722 and the power management controller 150716.

[0329] The interface can facilitate the transmission of one or more communication signals between the energy management controller 150716 and the controller of the drive shaft assembly 150722 by routing these communication signals through a main controller 150717 located on the 150702 handle set, for example. In other circumstances, the interface can facilitate a direct communication line between the power management controller 150716 and the drive shaft controller 150722 via the handle assembly 150702, while the drive shaft 150704 and power set 150706 are coupled to the handle set

150702.

[0330] The main controller 150717 can be any single-core or multi-core processor, such as those known under the trade name ARM Cortex by Texas Instruments. In one respect, the main controller 150717 may be a Core Cortex-M4F LM4F230H5QR ARM processor, available from Texas Instruments, for example, which comprises an integrated 256 KB single cycle flash memory, or other non-volatile memory , up to 40 MHz, a prefetch buffer to optimize performance above 40 MHz, a 32 KB single cycle serial random access memory (SRAM), an internal read-only memory (ROM) loaded with the program StellarisWareG &, 2 KB electronically erasable, programmable read-only memory (EEPROM), one or more pulse width modulation (PWM) modules, one or more analogs of quadrature encoder (QEI) inputs, one or more 12-bit analog to digital converters (ADC) with 12 channels of analog input, details of which are available for the product data sheet.

[0331] The safety controller can be a safety controller platform that comprises two families based on controllers, such as TMS570 and RM4x, known under the trade name of Hercules ARM Cortex R4, also by Texas Instruments. The safety controller can be configured specifically for IEC 61508 and ISO 26262 safety critical applications, among others, to provide advanced integrated safety features while providing scalable performance, connectivity and memory options.

[0332] The power supply 150706 may include a power management circuit which may comprise the power management controller 150716, a power modulator 150738 and a current sensing circuit 150736. The power management circuit can be configured to modulate the battery power output based on the power needs of the 150704 drive shaft assembly, while the 150704 drive shaft assembly and the 150706 power assembly are coupled to the 150702 handle assembly. power 150716 can be programmed to control power modulator 150738 from the power output of the power supply 150706 and the current sensor circuit 150736 can be employed to monitor the power output of the power supply 150706 for - provide feedback to the power management controller 150716 on the battery power output so that the power management controller 150716 power supply can adjust the power output of the 150706 power pack to maintain a desired output. The power management controller 150716 and / or the controller for the drive shaft assembly 150722 can comprise, in each case, one or more processors and / or memory units that can store multiple software modules.

[0333] The 150010 surgical instrument (Figures 25 to 28) can comprise an output device 150742 that can include devices to provide sensory feedback to a user. Such devices may comprise, for example, visual feedback devices (for example, an LCD monitor, LED indicators), hearing feedback devices (for example, a speaker, a bell) or devices tactile feedback (eg haptic actuators). In certain circumstances, the output device 150742 may comprise a display 150743 which may be included in the handle assembly 150702. The drive shaft assembly controller 150722 and / or the power management controller 150716 can provide feedback - training a user of the surgical instrument 150010 through the output device 150742. The interface can be configured to connect the drive shaft assembly controller 150722 and / or the power management controller 150716 to the output device 150742. The output device 150742 can instead be integrated with the power supply 150706. In these circumstances, communication between the output device 150742 and the drive shaft assembly controller 150722 can be done via the interface, while the drive shaft assembly 150704 is coupled to the handle assembly 150702.

[0334] The control circuit 150700 comprises circuit segments configured to control the operations of the energized surgical instrument 150010. A safety controller segment (segment 1) comprises a safety controller and the main controller segment 150717 (segment 2 ). The safety controller

and / or the main controller 150717 are configured to interact with one or more additional circuit segments such as an acceleration segment, a display segment, a drive axis segment, an encoder segment, a engine, and a power segment. Each of the circuit segments can be coupled to the safety controller and / or the main controller 150717. The main controller 150717 is also coupled to a flash memory. The main controller 150717 also includes a serial communication interface. The main controller 150717 comprises a plurality of inputs coupled, for example, to one or more circuit segments, a battery, and / or a plurality of switches. The segmented circuit can be implemented by any suitable circuit, such as, for example, a printed circuit board (PCBA) assembly within the energized surgical instrument 150010. It should be understood that the term processor, as used here, includes any microprocessor, processor, controller, controllers or other basic computing device that incorporates the functions of a central computer processing unit (CPU) in an integrated circuit or at most some integrated circuits. The main controller 150717 is a programmable multipurpose device that accepts digital data as input, processes it according to the instructions stored in its memory, and provides results as output. This is an example of sequential digital logic, as it has internal memory. The control circuit 150700 can be configured to implement one or more of the processes described here.

[0335] The acceleration segment (segment 3) comprises an accelerometer. The accelerometer is configured to detect the movement or acceleration of the energized surgical instrument 150010. The entry from the accelerometer can be used to make the transition to and from a suspend mode, identify the orientation of the surgical instrument energized, and / or identify when the surgical instrument is dropped. In some examples, the acceleration segment is coupled to the safety controller and / or the main controller 150717.

[0336] The screen or display segment (segment 4) comprises a screen connector coupled to the main controller 150717. The screen connector couples the primary controller 150717 to a screen through one or more drivers of the integrated circuits of the screen. The drivers of the integrated circuits of the display may be integrated with the display and / or may be located separately from the display. The display may comprise any suitable display, such as an organic light-emitting diode (OLED) display, a liquid crystal display (LCD), and / or any other suitable display. In some examples, the screen segment is coupled to the safety controller.

[0337] The drive shaft segment (segment 5) comprises controls for an interchangeable drive shaft assembly 150200 (Figures 25 and 27) coupled to the 150010 surgical instrument (Figures 25 to 28) and / or one or more controls for an end actuator 150300 coupled to the exchangeable drive shaft assembly 150200. The drive shaft segment comprises a drive shaft connector configured to couple the main controller 150717 to a drive shaft PCBA. The drive shaft PCBA comprises a low power microprocessor with a ferroelectric random access memory (FRAM), a toggle switch, a drive shaft release Hall effect switch, and a shaft PCBA EEPROM memory. drive. The drive shaft PCBA EEPROM comprises one or more parameters, routines, and / or programs specific to the 150200 interchangeable drive shaft assembly and / or the drive shaft PCBA. The drive shaft PCBA can be coupled to the exchangeable drive shaft assembly 150200 and / or integral with the surgical instrument 150010. In some instances, the drive shaft segment comprises a second drive shaft EEPROM drive. The second EE-PROM of the drive shaft comprises a plurality of algorithms, routines, parameters and / or other data that correspond to one or more sets of drive shafts 150200 and / or end actuators 150300 that can interface with the 150010 energized surgical instrument.

[0338] The position encoder segment (segment 6) comprises one or more magnetic encoders of the rotation angle position. One or more magnetic encoders for the rotation angle position are configured to identify the rotational position of the motor 150714, an interchangeable drive shaft assembly 150200 (Figures 25 and 27) and / or an end actuator 150300 of the 150010 surgical instrument (Figures 25 to 28). In some examples, magnetic encoders for the rotation angle position can be coupled to the safety controller and / or the main controller 150717.

[0339] The motor circuit segment (segment 7) comprises a motor 150714 configured to control the movements of the energized surgical instrument 150010 (Figures 25 to 28). The 150714 motor is coupled to the main microcontroller processor 150717 by an H bridge driver comprising one or more H bridge field effect transistors (FETs) and a motor controller. The H bridge actuator is also coupled to the safety controller. A motor current sensor is coupled in series with the motor to measure the current drain from the motor. The motor current sensor is in signal communication with the main controller 150717 and / or with the safety processor. In some examples, the 150714 motor is coupled to an electromagnetic interference (EMI) filter on the motor.

[0340] The motor controller controls a first motor signal and a second motor signal to indicate the status and position of the motor 150714 to the main controller 150717. The main controller 150717 provides a high pulse width modulation signal (PWM), a low PWM signal, a direction signal, a synchronization signal, and a motor restart signal to the motor controller via a buffer. The supply segment is configured to supply a segment voltage to each of the circuit segments.

[0341] The power segment (segment 8) comprises a battery coupled to the safety controller, the main controller 150717, and additional circuit segments. The battery is coupled to the circuit segmented by a battery connector and a current sensor. The current sensor is configured to measure the total current drain from the segmented circuit. In some examples, one or more voltage converters are configured to provide predetermined voltage values to one or more circuit segments. For example, in some instances, the segmented circuit may comprise 3.3 V voltage converters and / or V voltage converters. A voltage amplification converter is configured to provide a voltage rise to an amount predetermined, such as up to 13 V. The voltage amplification converter is configured to supply additional voltage and / or current during operations that require a lot of energy and to avoid blackouts or low power conditions.

[0342] A plurality of keys are coupled to the safety controller and / or the main controller 150717. The keys can be configured to control the operations of the 150010 surgical instrument (Figures 25 to 28), the segmented circuit, and / or indicate a surgical instrument status 150010. An ejection port switch and an ejection Hall switch are configured to indicate the status of an ejection port. A plurality of hinge keys, such as a left hinge key for the left side, a right hinge key for the left side, a central hinge key for the left side, a key from the left pivot side to the right side, a key from the right pivot side to the right side, and a central pivot key to the right side are configured to control the articulation of an interchangeable drive shaft assembly 150200 (Figures 25 and 27) and / or the end actuator 150300 (Figures 25 and 28). A reverse key on the left side and a reverse key on the right side are coupled to the main controller 150717. The keys on the left side comprise the key on the left side of the hinge, the key on the right side of the hinge for the the left side, the central articulation key for the left side and the reverse key for the left side are coupled to the primary controller 150717 by a flex connector on the left. The keys on the right side comprising the key on the left pivot side for the right side, the key on the right pivot side for the right side, the central pivot key for the right side, and the reverse key on the right side are coupled to the main controller 150717 via a flex connector on the right. A trip key, a clamping release key, and a key attached to the drive shaft are coupled to main controller 150717.

[0343] Any suitable mechanical, electromechanical, or solid state keys can be used to implement the plurality of keys, in any combination. For example, keys can limit keys operated by the movement of components associated with the 150010 surgical instrument (Figures 25 to 28) or the presence of an object. These switches can be used to control various functions associated with the 150010 surgical instrument. A limit switch is an electromechanical device consisting of an actuator mechanically connected to a set of contacts. When an object comes into contact with the actuator, the device operates the contacts to make or break an electrical connection. Limit switches are used in a variety of applications and environments because of their robustness, ease of installation and reliable operation. They can determine the presence or absence, passage, positioning and end of an object's displacement. In other implementations, the switches can be solid state switches that work under the influence of a magnetic field such as Hall effect devices, magnetoresistive devices (MR), giant magnetic resistive devices (GMR), magnetometers, among others . In other implementations, the switches can be solid state switches that operate under the influence of light, such as optical sensors, infrared sensors, ultraviolet sensors, among others. In addition, the switches can be solid state devices such as transistors (for example, FET, junction FET, metal oxide semiconductor FET (MOSFET), bipolar, and the like). Other keys may include wireless keys, ultrasonic keys, accelerometers, inertia sensors, among others.

[0344] Figure 30 is another block diagram of the control circuit 150700 of the surgical instrument of Figure 25 that illustrates the interfaces between the handle set 150702 and the power set 150706 and between the handle set 150702 and the set of interchangeable drive shaft 150704, in accordance with at least one aspect of the present disclosure. The set of companies

The 150702 handle may comprise a main controller 150717, a drive shaft assembly connector 150726 and a power assembly connector 150730. The power assembly 150706 may include a power assembly connector 150732, a management circuit 150734 power supply that can comprise the 150716 power management controller, a 150738 power modulator, and a current sensing circuit

150736. The drive shaft assembly connectors 150730, 150732 form an interface 150727. The power management circuit 150734 can be configured to modulate the output power of the 150707 battery based on the power needs of the interchangeable drive shaft assembly 150704 while the interchangeable drive shaft assembly 150704 and the feed assembly 150706 are coupled to the handle assembly

150702. The 150716 power management controller can be programmed to control the 150738 power modulator of the 150706 power pack power output and the current sensor circuit 150736 can be used to monitor the power output of the power pack 150706 to provide feedback to the 150716 power management controller about the 150707 battery power output so that the 150716 power management controller can adjust the power output of the 150706 power pack to maintain a desired output. The drive shaft assembly 150704 comprises a drive shaft processor 150720 coupled to a non-volatile memory 150721 and a drive shaft assembly connector 150728 to electrically couple the drive shaft assembly 150704 to the handle assembly 150702. The connectors of the drive shaft assembly 150726, 150728 form an interface 150725. The main controller 150717, the drive shaft processor 150720 and / or the power management controller 150716 can be configured to implement one or more of the processes described here.

[0345] The surgical instrument 150010 (Figures 25 to 28) can comprise an output device 150742 for sensory feedback to a user. Such devices may comprise visual feedback devices (for example, a monitor with an LCD screen, LED indicators), hearing feedback devices (for example, a speaker, a bell) or tactile feedback devices (for example , haptic actuators). In certain circumstances, the output device 150742 may comprise a screen 150743 which may be included in the handle assembly 150702. The drive shaft assembly controller 150722 and / or the power management controller 150716 po - provide feedback to a user of the surgical instrument 150010 via output device 150742. Interface 150727 can be configured to connect the drive shaft assembly controller 150722 and / or the power management controller 150716 to the output 150742. Output device 150742 can be integrated with power supply 150706. Communication between output device 150742 and drive shaft assembly controller 150722 can be done via interface 150725 while the shaft set interchangeable drive unit 150704 is coupled to the handle assembly 150702. Having described a control circuit 150700 (Figures 29A, 29B and 6) to control the operation of the 150010 surgical instrument (Figures 25 to 28), the disclosure now turns to various configurations of the 150010 surgical instrument (Figures 25 to 28) and the control circuit

150700.

[0346] Referring to Figure 31, a surgical stapler

151000 can include a handle component 151002, a drive shaft component 151004, and an end actuator component 151006. Surgical stapler 151000 is constructed and equipped in a similar manner to the surgical instrument for motor-driven cutting and fixing 150010 described in connection with Figure 25. Consequently, for the sake of brevity and clarity, the details of operation and construction will not be repeated here. The end actuator 151006 can be used to compress, cut, or staple the fabric. Referring now to Figure 32, the end actuator 151030 can be positioned by a physician to surround the 151032 tissue prior to compression, cutting or stapling. As shown in Figure 32, compression may not be applied to the fabric when preparing the end actuator for use. Referring now to Figure 33, by engaging the handle (for example, handle 151002) of the surgical stapler, the doctor can use the end actuator 151030 to compress the 151032 tissue. In one aspect, the 151032 tissue can be compressed to its maximum limit, as shown in Figure 33.

[0347] With reference to Figure 34, various forces can be applied to the fabric 151032 by the end actuator 151030. For example, vertical forces F1 and F2 can be applied by the anvil 151034 and the channel structure 151036 of the end actuator 151030 as the fabric 151032 is compressed between the two. Referring now to Figure 35, diagonal forces and / or lateral forces can also be applied to fabric 151032 when compressed by end actuator 151030. For example, force F3 can be applied. For the purpose of operating a medical device, such as a 151000 surgical stapler, it may be desirable to detect or calculate the various forms of compression being applied to the tissues by the end actuator. For example, knowledge

lateral or vertical compression can allow the end actuator to perform a stapling operation more precisely and accurately, or it can inform the operator of the surgical stapler so that the surgical stapler can be used more safely and conveniently.

[0348] Compression through tissue 151032 can be determined from an impedance of tissue 151032. At various levels of compression, impedance Z of tissue 151032 may increase or decrease. By applying a voltage V and a current | to fabric 151032, the Z impedance of fabric 151032 can be determined at various levels of compression. For example, impedance Z can be calculated by dividing the voltage V applied by the current |.

[0349] Referring now to Figure 36, in one aspect, an RF electrode 151038 can be positioned on the end actuator 151030 (for example, on a staple cartridge, knife or channel structure of the end actuator 151030) . In addition, an electrical contact 151040 can be positioned on the anvil 151034 of the end actuator 151030. In one aspect, the electrical contact can be placed on the channel structure of the end actuator. As the fabric 151032 is compressed between the anvil 151034 and, for example, the channel structure 151036 of the end actuator 151030, an Z impedance of changes in the fabric 151032. The vertical compression of the fabric 151042 caused by the end actuator 151030 can be measured depending on the Z impedance of the fabric

151032.

[0350] Referring now to Figure 37, in one aspect, an electrical contact 151044 can be positioned at an opposite end of anvil 151034 from end actuator 151030 as RF electrode 151038 is positioned. As the fabric 151032 is compressed between the anvil 151034 and, for example, the channel structure

End actuator 151036, a Z impedance of tissue changes 151032. The lateral tissue compression 151046 caused by end actuator 151030 can be measured as a function of the Z impedance of tissue 151032.

[0351] Referring now to Figure 38, in one aspect, the electrical contact 151050 can be positioned on the anvil 151034 and the electrical contact 151052 can be positioned on the opposite end of the end actuator 151030 in the channel structure

151036. The RF electrode 151048 can be positioned laterally in the center to the end actuator 151030. As the fabric 151032 is compressed between the anvil 151034 and, for example, the channel structure 151036 of the end actuator 151030, an impediment Z density of tissue changes 151032. Side compression or angular compressions 151054 and 151056 on each side of RF electrode 151048 can be caused by end actuator 151030 and can be measured as a function of different Z impedances of tissue 151032, based on relative positioning of RF electrode 151048 and electrical contacts 151050 and 151052.

[0352] Referring now to Figure 39, the frequency generator 151222 can receive energy or current from a 151221 power source, and can provide one or more RF signals to one or more RF electrodes 151224. As discussed above, the one or more RF electrodes can be positioned in various locations or components on the end actuator or surgical stapler, such as a staple cartridge or a channel structure. One or more electrical contacts, such as electrical contacts 151226 or 151228, can be positioned on a channel structure or on an anvil of an end actuator. In addition, one or more filters, such as filters 151230 or 151232, can be communicatively connected to electrical contacts 151226 or 151228. Filters 151230 and 151232 can

filter one or more RF signals provided by the frequency generator 151222, before joining a single return path

151234. A voltage V and a current | associated with one or more RF signals can be used to calculate an impedance Z associated with a tissue that can be compressed and / or communicatively coupled between the one or more RF electrodes 151224 and electrical contacts 151226 or 151228.

[0353] With reference also to Figure 39, several components of the tissue compression sensor system described here can be located on a 151236 handle of a surgical stapler. For example, as shown in circuit diagram 151220a, frequency generator 151222 can be located on handle 151236, and receive energy from power source 151221. Also, current | 1 and current 12 can be measured on a return path. corresponding to electrical contacts 151228 and 151226. With the use of a voltage V applied between the supply and the return paths, impedances Z1 and Z2 can be calculated. Z1 can correspond to a compressed tissue impedance and / or be communicatively coupled between one or more RF electrodes 151224 and electrical contact 151228. Furthermore, Z2 can correspond to a compressed tissue impedance and / or be communicatively coupled between one or more RF 151224 electrodes and electrical contact

151226. Using the formulas and Z1 = V / I1 and Z2 = V / I2, the impedances Z1 and Z2 corresponding to the different levels of compression of a tissue compressed by an end actuator can be calculated.

[0354] Referring now to Figure 40, one or more aspects of the present disclosure are described in circuit diagram 151250. In one implementation, a power source in a 151252 handle of a surgical stapler can supply power to a generator.

frequency pain 151254. The frequency generator 151254 can generate one or more RF signals. The one or more RF signals can be multiplexed or overlaid on a 151256 multiplexer, which can be on a 151258 drive shaft of the surgical stapler. In this way, two or more RF signals can be superimposed (or, for example, grouped or modulated together) and transmitted to the end actuator. The one or more RF signals can energize one or more RF electrodes 151260 on a 151262 end actuator (for example, positioned on a staple cartridge) of the surgical stapler. A tissue (not shown) can be compressed and / or coupled communicatively between one or more RF electrodes, and one or more electrical contacts 151260. For example, the tissue can be compressed and / or coupled communicatively between the one or more RF electrodes 151260 and electrical contact 151264 positioned in a channel structure of the end actuator 151262 or electrical contact 151266 positioned on an anvil of the end actuator 151262. A filter 151268 can be coupled in a communicative way to the electrical contact 151264, and a filter 151270 can be connected communicatively to electrical contact 151266.

[0355] A voltage V and a current | associated with one or more RF signals can be used to calculate an impedance Z associated with a tissue that can be compressed between the staple cartridge (and communicatively coupled to one or more RF electrodes 151260) and the channel or anvil structure (and communicatively coupled to one or more electrical contacts 151264 or 151266).

[0356] In one aspect, several components of the tissue compression sensor system described in the present invention can be located on a drive shaft 151258 of the surgical stapler. For example, as shown in circuit diagram 151250 (and in addition to frequency generator 151254), an

pedometer 151272, a controller 151274, a non-volatile memory 151276, and a communication channel 151278 can be located on drive axis 151258. In one example, frequency generator 151254, impedance calculator 151272, controller 151274 , the non-volatile memory 151276, and the communication channel 151278 can be positioned on a circuit board on the drive shaft 151258.

[0357] The two or more RF signals can be returned over a common path through the electrical contacts. In addition, the two or more RF signals can be filtered before joining the RF signals in the common path to differentiate separate tissue impedances represented by the two or more RF signals. Current 11 and current 12 can be measured on a return path corresponding to electrical contacts 151264 and 151266. Using a voltage V applied between the supply and the return paths, impedances Z1 and Z2 can be calculated. Z1 can correspond to an impedance of the compressed tissue and / or be coupled in a communicative way between one or more RF electrodes 151260 and electrical contact 151264. Also, Z2 can correspond to an impedance of the compressed tissue and / or be coupled to communicative mode between one or more RF electrodes 151260 and electrical contact 151266. Applying formulas Z1 = V / 1 and Z2 = V / I2, impedances Z1 and Z2 corresponding to different compressions of a tissue compressed by an actuator endpoint 151262 can be calculated. In the example, impedances Z1 and Z2 can be calculated using the impedance calculator 151272. Impedances Z1 and Z2 can be used to calculate various levels of tissue compression.

[0358] With reference now to Figure 41, a frequency graph 151290 is shown. The frequency graph 151290 shows a frequency modulation to group two RF signals. The two RF signals can be grouped together before reaching the RF electrodes on an end actuator as described above. For example, an RF signal with frequency 1 and an RF signal with frequency 2 can be grouped together. Referring now to Figure 42, the resulting grouped RF signal is shown on a 151300 frequency graph. The composite signal shown on the 151300 frequency graph includes the two RF signals from the combined 151290 frequency graph. Referring now to Figure 43, a 151400 frequency graph is shown. The frequency graph 151400 shows the RF signals with Frequencies 1 and 2, after they have been filtered (through, for example, filters 151268 and 151270). The resulting RF signals can be used to make the impedance calculations or measurements separately or on a return path, as described above.

[0359] In one aspect, filters 151268 and 151270 can be High Q filters, so that the filter range is narrow (for example, Q = 10). Q can be defined using the center frequency (Wo) / Bandwidth (BW) where Q = Wo / BW. In one example, Frequency 1 can be 150 kHz and Frequency 2 can be 300 kHz. A viable impedance measurement range can be 100 kHz - 20 MHz. In many instances, other sophisticated techniques, such as correlation, quadrature detection, etc., can be used to separate RF signals.

[0360] With the use of one or more of the techniques and characteristics described in the present invention, a single electrode energized in a staple cartridge or in a knife isolated from an end actuator can be used to make multiple measurements of tissue pressure simultaneously. If two or more RF signals are superimposed or multiplexed (or nested or modulated), they can be transmitted along a single supply side of the end actuator and can return either over the cable structure.

end anvil or anvil. If a filter is built into the channel and anvil contacts before they join the common return path, the fabric impedance represented by both paths could be differentiated. This can provide a measure of vertical tissue vs. lateral tissue compression. In addition, this approach can provide compression of proximal and distal tissues depending on the placement of filters and the location of the metallic return trajectories. A frequency generator and the signal processor can be located on one or more chips on a circuit board or a subplate (which may already exist in a surgical stapler).

[0361] In one aspect, the present disclosure provides an instrument 150010 (described in relation to Figures 25 to 30) configured with various detection systems. Consequently, for the sake of brevity and clarity, the details of operation and construction will not be repeated here. In one aspect, the detection system includes a viscoelasticity / rate of change sensor system to monitor knife acceleration, impedance change rate, and tissue contact change rate. In one example, the rate of change of acceleration of the knife can be used as a measure of the type of fabric. In another example, the rate of change in impedance can be measured with a pulse sensor and can be used as a measure for compressibility. Finally, the rate of change in contact with the tissue can be measured with a sensor based on the knife firing rate to measure tissue flow.

[0362] The rate of change of a detected or otherwise established parameter, the amount of time required for a tissue parameter to reach an asymptotic steady state value, is a separate measurement in itself, and can be more valuable than the detected parameter from which it was derived. To improve the measurement of tissue parameters, such as waiting for a predetermined amount

Once time has elapsed before taking a measurement, the present disclosure provides a new technique for employing the measurement derivative as the rate of change of the tissue parameter.

[0363] The derived technique or measurement change rate becomes more useful with the understanding that there is no single measurement that can be used alone to dramatically improve the formation of the clamp. This is the combination of multiple measures that make the measures valid. In the case of the fabric span, it is useful to know how much of the claw is covered with fabric to make the span measurement relevant. The rate of impedance change measurements can be combined with the strain measurements on the anvil to relate the force and compression applied to the tissue trapped between the claw members of the end actuator such as the anvil and the staple cartridge. The measured rate of change can be used by the endosurgical device to determine the type of tissue and not just the compression of the tissue. Although stomach and lung tissue are sometimes similar in thickness, and even with similar compression properties, when lung tissue is calcified, an instrument may be able to distinguish these types of tissue using a combination of measurements as will, compression, applied force, the tissue contact area, and the rate of change of compression or rate of change of span. If any of these measures were used alone, it may be difficult for the endosurgical device to distinguish one type of tissue from another. The rate of change in compression can also be useful in allowing the device to determine if the tissue is "normal" or if there is any abnormality. Measuring not only how much time has passed, but the variation of the sensor signals and determining the signal derivative would provide another measure to allow the endosurgical device to measure the signal. Information on the rate of change can also be used to determine

determination of when a stable state was reached to signal the next step in a process. For example, after tightening the tissue between the end actuator claw members such as the anvil and the staple cartridge, when the tissue compression reaches a stable state (for example, about 15 seconds), an indicator or the trigger to start shooting the device can be enabled.

[0364] Methods, devices, and systems are also provided here for the time-dependent evaluation of sensor data to determine the stability, creep, and viscoelastic characteristics of the tissue during the operation of the surgical instrument. A surgical instrument, such as the stapler illustrated in Figure 25, can include a variety of sensors to measure operational parameters, such as the size or distance of the jaw span, trigger current, tissue compression, the amount of jaw that is covered by the fabric, deformation of the anvil and force of the trigger, to name a few. These detected measures are important for the automatic control of the surgical instrument and for providing feedback to the clinician.

[0365] The examples shown in relation to Figures 30 to 49 can be used to measure the various derived parameters, such as span distance as a function of time, compression of the fabric as a function of time, and the anvil deformation as a function of time. The motor current can be monitored using a current sensor in series with the 2308 battery.

[0366] Turning now to Figure 44, it is shown that a surgical instrument for cutting and fixing powered by a 151310 motor may or may not be reused. The 151310 motor-driven surgical cutting and fixation instrument is similarly constructed and equipped as the 150010 motor-driven surgical cutting and fixation instrument described with reference to Figures 25 to 30. In the example shown in Figure 44, the instrument 151310 includes one compartment

151312 which comprises a handle set 151314 which is configured to be picked up, handled and operated by the physician. Enclosure 151312 is configured for operational attachment to a 151500 interchangeable drive shaft assembly that has a 151600 surgical end actuator operably attached to it that is configured to perform one or more surgical tasks or procedures. Since the 151310 motor-driven surgical cutting and fixation instrument is similarly constructed and equipped as a 150010 motor-driven surgical cutting and fixation instrument described with reference to Figures 25 to 30, for the sake of clarity and conciseness the details of the operation and construction will not be repeated in this document.

[0367] The compartment 151312 shown in Figure 44 is shown in relation to an interchangeable drive shaft assembly 151500 that includes an end actuator 151600 that comprises a surgical cutting and clamping device that is configured to operationally support a 151304 surgical staple cartridge in it. Enclosure 151312 can be configured for use in connection with interchangeable drive shaft assemblies that include end actuators that are adapted to support different sizes and types of clamp cartridges, have different lengths, sizes, and types drive shaft, etc. In addition, compartment 151312 can also be used effectively with a variety of other interchangeable drive shaft assemblies including those that are configured to apply other motions and forms of energy such as radio frequency energy (RF), ultrasonic energy and / or movement to extremity actuator arrangements adapted for use in various surgical applications and procedures. In addition, end actuators, driveshaft assemblies

However, grips, surgical instruments and / or surgical instrument systems can use any one or more suitable fasteners to hold tissue. For example, a fastener cartridge comprising a plurality of fasteners stored therein removably can be removably inserted into and / or attached to the end actuator of a drive shaft assembly.

[0368] Figure 44 illustrates the surgical instrument 151310 with an interchangeable drive shaft assembly 151500 operably coupled to it. In the illustrated arrangement, the grip compartment forms a portion of the 151319 pistol grip that can be handled and manipulated by the physician. The handle set 151314 operationally supports, inside, a plurality of drive systems, which are configured to generate and apply various control movements to the corresponding portions of the interchangeable drive shaft set that is operationally fixed to it. Trigger 151332 is operatively associated with the pistol grip to control several of these control movements.

[0369] Still referring to Figure 44, the interchangeable drive shaft assembly 151500 includes a surgical end actuator 151600 that comprises an elongated channel 151302 that is configured to operationally support a 151304 clamp cartridge inside. The actuator end cap 151600 can additionally include an anvil 151306 which is pivotally supported in relation to the elongated channel 151302.

[0370] The inventors found that the derived parameters can be even more useful for the control of a surgical instrument, such as the instrument illustrated in Figure 44, than the detected parameter (s) of which the derived parameter is based. Some non-limiting examples of derived parameters include the rate of change of a detected parameter (for example, distance from the claw span) and how long it takes before a tissue parameter reaches a steady-state asymptotic value (for example, 15 seconds). Derived parameters, such as rate of change, are particularly useful because they dramatically improve measurement accuracy and also provide information that is not otherwise evident directly from the detected parameters. For example, the rate of change in impedance (ie, tissue compression) can be combined with anvil deformation to relate to compression and strength, which allows the microcontroller to determine the type of tissue and not just the amount of tissue compression. This example is illustrative only, and any derived parameters can be combined with one or more detected parameters to provide more accurate information about tissue types (eg, stomach versus lung), tissue health (calcified versus normal), and condition surgical device (for example, full grip). The different tissues have viscoelastic properties and unique rates of change, making these and other parameters discussed here useful indications for automatically monitoring and adjusting a surgical procedure.

[0371] Figure 46 is an illustrative graph that shows the distance of the gap over time, where the gap is the space between the claws being occupied by the trapped tissue. The vertical drive axis (y) is distance and the horizontal drive axis (x) is time. Specifically, with reference to Figures 44 and 45, the span distance 151340 is the distance between the anvil 151306 and the elongated channel 151302 of the end actuator. In the open position of the claw, at time zero, the gap 151340 between the anvil 151306 and the elongated member is at its maximum distance. The width of the gap 151340 decreases as the anvil 151306 closes, as during the gripping of the fabric. The rate of change in the gap may vary, as the fabric has non-uniform resilience. For example, certain types of tissue may initially show rapid compression, resulting in a faster rate of change. However, as the fabric is compressed continuously, the viscoelastic properties of the fabric can cause the rate of change to decrease until the fabric cannot be compressed further, at which point the gap distance remains substantially constant. The span decreases over time, as the fabric is squeezed between the sleeve 151306 and the staple cartridge 151304 of the end actuator 151340. The one or more sensors described with respect to Figures 31 a 43 such as, for example, a magnetic field sensor, an effort meter, a pressure sensor, a force sensor, an inductive sensor, such as, for example, a parasitic current sensor, a resistive sensor, a sensor capacitive, an optical sensor, and / or any other suitable sensor, can be adapted and configured to measure the distance of the gap "d" between the anvil 151306 and the staple cartridge 151304 over time "t" as shown in the graph - Figure 46. The rate of change in the distance of span "d" over time "t" is the slope of the curve shown in Figure 46, where the slope = Ad / At.

[0372] Figure 47 is an illustrative graph showing the trigger current of the end actuator claws. The vertical geometric axis (y) is the current and the horizontal geometric axis (x) is time. As discussed in this document, the surgical instrument and / or the microcontroller, as shown and described in connection with Figure 25, can include a current sensor that detects the current used during various operations, such as gripping, cutting, and / or stapling of the fabric. For example, when the resistance of the fabric increases, the instrument's electric motor may need more current to clamp, cut and / or staple the fabric.

Similarly, if the resistance is less, the electric motor may need less current to clamp, cut and / or staple the fabric.

As a result, the trigger current can be used as an approximation of the tissue resistance.

The detected current can be used alone or, more preferably, in conjunction with other measurements to provide feedback on the target tissue.

Still referring to Figure 47, during some operations, such as stapling, the tripping current is high at time zero, but decreases over time.

During other operations of the device, the current may increase over time if the motor draws more current to overcome the increase in mechanical load.

In addition, the rate of change of the trigger current can be used as an indicator that the tissue is changing from one state to another.

Consequently, the trigger current, and in particular the rate of change of the trigger current, can be used to monitor the operation of the device.

The firing current decreases over time as the knife cuts through the fabric.

The rate of change of the firing current can vary if the fabric being cut offers more or less resistance due to the properties of the fabric or the knife edge 151305 (Figure 45). As cutting conditions vary, the work being done by the motor varies and therefore the tripping current will vary over time.

A current sensor can be used to measure the trigger current over time while knife 151305 is triggered as shown graphically in Figure 47. For example, the motor current can be monitored using a current sensor. chain.

Current sensors can be adapted and configured to measure the tripping current "i" of the motor over time "t", as shown graphically in Figure 47. The rate of change in tripping current "i" over time of time "t" is the slope of the curve shown in Figure 47, where the slope = Ai / At.

[0373] Figure 48 is an illustrative graph of impedance over time. The vertical geometric axis (y) is impedance and the horizontal geometric axis (x) is time. At zero time, the impedance is low, but increases over time as the pressure for manipulating the tissue increases (for example, gripping and stapling). The rate of change varies over time, as the fabric between the anvil 151306 and the staple cartridge 151304 of the end actuator 151340 is cut by the knife or is sealed using RF energy between the electrodes located between the anvil 151306 and the end actuator clamp cartridge 151304

151340. For example, when the fabric is cut, the electrical impedance increases and reaches infinity when the fabric is completely cut by the knife. Also, if the 151340 end actuator includes electrodes coupled to an RF energy source, the electrical impedance of the tissue increases as energy is distributed through the tissue between the 151306 anvil and the 151304 staple cartridge of the actuator. end 151340. The electrical impedance increases as the energy through the tissue dries the tissue by vaporizing moisture in the tissue. Eventually, when an adequate amount of energy is applied to the fabric, the impedance increases to a very high or infinite value when the fabric is cut. In addition, as shown in Figure 48, different tissues can have unique compression properties, such as the compression rate, which distinguishes the tissues. The impedance of the tissue can be measured by directing a sub-therapeutic RF current through the tissue trapped between the first and second claw members 9014, 9016. One or more electrodes can be positioned on one or the other or both the anvil 151306 and the staple cartridge 151304. The impedance of tissue compression between the anvil 151306 and the staple cartridge 151304 can be measured over time, as represented graphically in Figure 48. The sensors described with respect to - Refer to Figures 31 to 43 such as, for example, a magnetic field sensor, an effort meter, a pressure sensor, a force sensor, an inductive sensor, such as, for example, a parasitic current sensor, a resistive sensor, a capacitive sensor, an optical sensor, and / or any other suitable sensor, can be adapted and configured to measure tissue impedance / compression. The sensors can be adapted and configured to measure the impedance of the tissue "Z" over time "t", as represented graphically in Figure 48.

[0374] Figure 49 is a graph illustrating the deformation of the 151306 bib (Figures 44, 45) over time. The vertical geometric axis (y) is the strain and the horizontal geometric axis (x) is the time. During stapling, for example, the deformation of the 151306 anvil is initially high, but decreases as the tissue reaches a stable state and exerts less pressure on the anvil

151306. The rate of change in strain of the anvil 151306 can be measured by a pressure sensor or strain gauge positioned on one or both of the anvil 151306 and the staple cartridge 151304 (Figures 44, 45) to measure pressure or stresses applied to the tissue trapped between the anvil 151306 and the staple cartridge 151304. The deformation of the anvil 151306 can be measured over time as plotted in Figure 49. The rate of change in deformation "S" over time "t "is the slope of the curve shown in Figure 49, where the slope = AS / At.

[0375] Figure 50 is a graphic illustrating the trigger force over time. The vertical geometric axis (y) is the trigger force and the horizontal geometric axis (x) is time. In certain instances, the trigger force is progressive, to provide the physician with tactile feedback. Therefore, in a zero time, the pressure on the 151320 trigger (Figure 44) may be at its lowest value and the trigger pressure may increase until the completion of the operation (for example, gripping, cutting or stapling). The rate of change of the trigger force can be measured by a pressure sensor or strain gauge positioned on the trigger 151302 of the handle 151319 of the instrument 151310 (Figure 44) to measure the force required to drive the knife 151305 (Figure 45) through the tissue stuck between the anvil 151306 and the staple cartridge 151304. The force of the trigger 151332 can be measured over time as shown graphically in Figure 50. The rate of change in the tension force on the trigger "F" over time " t "is the slope of the curve shown in Figure 50, where the slope = AF / At.

[0376] For example, the stomach and lung tissue may be differentiated, although these tissues are similar in thickness, and may have similar compression properties if the lung tissue is calcified. Lung and stomach tissues can be distinguished by analyzing claw gap distance, tissue compression, force applied, tissue contact area, compression rate, and claw gap change rate. For example, Figure 51 shows a graph of pressure "P" versus tissue displacement for various tissues. The vertical geometric axis (y) is the tissue pressure and the horizontal geometric axis (x) is the tissue displacement. When tissue pressure reaches a predetermined limit, such as 50 to 100 pounds per square inch (psi), the amount of tissue displacement as well as the rate of tissue displacement before reaching the tissue limit can be used to differentiate fabrics. For example, blood vessel tissue reaches the predetermined pressure threshold with less tissue displacement and with a faster rate of change than colon, lung, or stomach tissue. In addition, the rate of change (pressure on tissue over displacement) for blood vessel tissue is almost asymptotic at a limit of 50 to 100 psi, while the rate of change for the colon, lung and stomach is not asymptotic. at a limit of 50 to 100 psi. As will be understood, any pressure limit can be used, for example, between 1 and 1,000 psi, more preferably between 10 and 500 psi, and most preferably between 50 and 100 psi. In addition, multiple thresholds or progressive thresholds can be used to provide more resolution as to the types of tissue that have similar viscoelastic properties.

[0377] The rate of change in compression may also allow the microcontroller to determine whether the tissue is "normal" or whether there is any abnormality, such as calcification. For example, with reference to Figure 52, compression of calcified tissue follows a different lung curve than compression of normal lung tissue. Tissue displacement and tissue displacement change rate, therefore, can be used to diagnose and / or differentiate calcified lung tissue from normal lung tissue.

[0378] In addition, certain measurements detected may benefit from additional sensory inputs. For example, in the case of the claw span, knowing how much of the claw is covered with the fabric can make span measurement more useful and accurate. If a small portion of the claw is covered with tissue, the compression of the tissue may appear to be less than if the entire claw was covered with tissue. Thus, the amount of claw coverage can be taken into account by the microcontroller when analyzing tissue compression and other detected parameters.

[0379] In certain circumstances, elapsed time can also be an important parameter. Measuring the amount of time that has elapsed, along with detected parameters, and the parameters derived (for example, rate of change) provides additional useful information. For example, if the rate of change of the grapple gap remains constant after a specified period of time (for example, 5 seconds), then the parameter may have reached its asymptotic value.

[0380] Information about the rate of change is also useful in determining when a steady state has been achieved, thereby signaling the next step in a process. For example, during grip, when tissue compression reaches a steady state - for example, negligible rate of change after a specified period of time - the microcontroller can send a signal to the monitor to alert the doctor to start the next step in the operation, such as triggering the clamp. Alternatively, the microcontroller can be programmed to automatically initiate the next stage of operation (for example, triggering the clamp), once a stable state is reached.

[0381] Similarly, the rate of change in impedance can be combined with deformation in the anvil to relate force and compression. The measured rate of change would allow the device to determine the type of fabric and not just the measurement of the compression value. For example, the stomach and lung sometimes have similar thicknesses, and even more similar compressive properties, if the lung is calcified.

[0382] The combination of one or more detected parameters with derived parameters provides a more reliable and accurate assessment of tissue types and tissue health, and allows for better monitoring, device control and feedback to the clinician.

[0383] Figure 53 illustrates a modality of an actuator for

tremor 152000 comprising a first sensor 152008a and a second sensor 152008b. The end actuator 152000 is similar to the end actuator 150300 described above. The end actuator 152000 comprises a first claw member, or a beak, 152002 pivotally coupled to a second claw member 152004. Claw member 152004 is configured to receive a 152006 staple cartridge inside. The staple cartridge 152006 comprises a plurality of staples (not shown). The plurality of staples is implantable from the staple cartridge 152006 during a surgical operation. The 152000 end actuator comprises a first sensor 152008a. The first sensor 152008a is configured to measure one or more parameters of the end actuator 152000. In one embodiment, for example, the first sensor 152008a is configured to measure the span 152010 between the anvil 152002 and the second claw member 152004. The first sensor 152008a may comprise, for example, a Hall effect sensor configured to detect a magnetic field generated by a magnet 152012 incorporated in the second claw member 152004 and / or the staple cartridge 152006. As another example - in one embodiment, the first sensor 152008a is configured to measure one or more forces exerted on the anvil 152002 by the second claw member 152004 and / or the tissues trapped between the anvil 152002 and the second claw member 152004.

[0384] The end actuator 152000 comprises a second sensor 152008b. The second sensor 152008b is configured to measure one or more parameters of the end actuator 152000. For example, in several modalities, the second sensor 152008b can comprise an effort meter configured to measure the magnitude of the stress on the anvil 152002 during a condition prey. The voltage meter provides an electrical signal whose amplitude varies with the magnitude of the voltage. In various embodiments, the first sensor 152008a and / or the second sensor 152008b may comprise, for example, a magnetic sensor such as a Hall effect sensor, an effort meter, a pressure sensor, a pressure sensor, force, an inductive sensor such as an eddy current sensor, a resistive sensor, a capacitive sensor, an optical sensor, and / or any other sensors suitable for measuring one or more parameters of the 152000 end actuator. The first sensor 152008a and the second sensor 152008b can be arranged in a series configuration and / or a parallel configuration. In a series configuration, the second sensor 152008b can be configured to directly affect the output of the first sensor 152008a. In a parallel configuration, the second sensor 152008b can be configured to indirectly affect the output of the first sensor 152008a.

[0385] In one embodiment, one or more parameters measured by the first sensor 152008a are related to one or more parameters measured by the second sensor 152008b. In one embodiment, for example, the first sensor 152008a is configured to measure the span 152010 between the anvil 152002 and the second claw member 152004. The span 152010 is representative of the thickness and / or compressibility of a section of attached tissue between the anvil 152002 and the staple cartridge 152006. The first sensor 152008a may comprise, for example, a Hall effect sensor configured to detect a magnetic field generated by the magnet 152012 coupled to the second claw member 152004 and / or the staple cartridge 152006. Measurement in a single location accurately describes the thickness of compressed tissue for a full calibrated tissue bite, but can provide inaccurate results when a partial tissue bite is placed between the anvil 152002 and the second claw member 152004 A partial bite of tissue, whether a

partial proximal tear or partial distal bite, alters the grip geometry of the anvil 152002.

[0386] In some embodiments, the second sensor 152008b is configured to detect one or more parameters indicative of a type of tissue bite, for example, a total bite, a proximal partial bite and / or a distal partial bite. The measurement of the second sensor 152008b can be used to adjust the measurement of the first sensor 152008a to accurately represent the true thickness of compressed tissue from a partial bite in a proximal or distal position. In one embodiment, for example, the second sensor 152008b comprises a strain gauge such as, for example, a micro strain gauge, configured to monitor the amplitude of the strain on the anvil during a stuck condition. The stress range of the anvil 152002 is used to modify the output of the first sensor 152008a, for example, a Hall effect sensor, to accurately represent the true thickness of the compressed tissues of a partial bite in a proximal position. or distal. The first sensor 152008a and the second sensor 152008b can be measured in real time during a gripping operation. Real-time measurement allows time-based information to be analyzed, for example, by a primary processor (462 processor (Figure 12), for example), and used to select one or more algorithms and / or look-up tables to recognize tissue characteristics and pressure positioning to dynamically adjust tissue thickness measurements.

[0387] In some modalities, the thickness measurement of the first sensor 152008a can be supplied to an output device of a 150010 surgical instrument coupled to the end actuator

152000. In one embodiment, for example, the end actuator

152000 is coupled to the surgical instrument 150010 which comprises a screen (for example, screen 473 (Figure 12)). The measurement of the first sensor 152008a is provided to a processor, for example, the primary processor. The primary processor adjusts the measurement of the first sensor 152008a based on the measurement of the second sensor 152008b to reflect the true thickness of the fabrics of a tissue section stuck between the anvil 152002 and the staple cartridge 152006. The primary processor issues the fabric thickness measurement is adjusted for the fabric and an indication of total or partial bite. An operator can determine whether or not to staple the staples to the 152006 staple cartridge, based on the displayed values.

[0388] In some embodiments, the first sensor 152008a and the second sensor 152008b can be located in different environments, for example, the first sensor 152008a being located inside a patient, in a treatment site, and the second sensor 152008b being located externally to the patient. The second sensor 152008b can be configured to calibrate and / or modify the output of the first sensor 152008a. The first sensor 152008a and / or the second sensor 152008b can comprise, for example, an environmental sensor. Environmental sensors can comprise, for example, temperature sensors, humidity sensors, pressure sensors and / or any other suitable environmental sensor.

[0389] Figure 54 is a logical diagram illustrating a method for a 152020 process to adjust the measurement of a first sensor 152008a based on the input from a second sensor 152008b. A first signal 152022a is captured by the first sensor 152008a. The first signal 152022a can be conditioned based on one or more predetermined parameters such as, for example, a smoothing function, a look-up table and / or any other suitable conditioning parameters. A second signal

152022b is captured by the second sensor 152008b. The second signal 152022b can be conditioned based on one or more predetermined conditioning parameters. The first signal 152022a and the second signal 152022b are supplied to a processor, such as the primary processor. The processor adjusts the measurement of the first sensor 152008a, as represented by the first signal 152022a, based on the second signal 152022b coming from the second sensor. In one embodiment, for example, the first sensor 152008a comprises a Hall effect sensor and the second sensor 152008b comprises an effort meter. The distance measurement of the first sensor 152008a is adjusted by the amplitude of the effort measured by the second sensor 152008b to determine the completeness of the tissue bite on the end actuator 152000. The adjusted measurement 152026 is displayed to an operator by means of, for example , a screen incorporated into the surgical instrument 150010.

[0390] Figure 55 is a logic diagram illustrating a method for a 152030 process to determine a lookup table for a first sensor 152008a based on input from a second sensor 152008b. The first sensor 152008a captures an indicative signal 152022a of one or more parameters of the end actuator 152000. The first signal 152022a can be conditioned based on one or more predetermined parameters such as a smoothing function, a consultation and / or any other suitable conditioning parameters. A second signal 152022b is captured by the second sensor 152008b. The second signal 152022b can be conditioned based on one or more predetermined conditioning parameters. The first signal 152022a and the second signal 152022b are supplied to a processor, such as the primary processor. The processor selects a lookup table from one or more available lookup tables 152034a, 152034b, based on the value of the second signal. The selected look-up table is used to convert the first signal into a measurement of tissue thickness between the anvil 152002 and the staple cartridge 152006. The adjusted measurement 152026 is displayed to an operator by means of, for example, a screen incorporated into the surgical instrument 150010.

[0391] Figure 56 is a logic diagram illustrating a method for a 152040 process to calibrate a first sensor 152008a in response to an input from a second sensor 152008b. The first sensor 152008a is configured to capture a signal 152022a indicative of one or more parameters of the end actuator 152000. The first signal 152022a can be conditioned based on one or more predetermined parameters such as a smoothing function, a table consultation and / or any other suitable conditioning parameters. A second signal 152022b is captured by the second sensor 152008b. The second signal 152022b can be conditioned based on one or more predetermined conditioning parameters. The first signal 152022a and the second signal 152022b are supplied to a processor, such as the primary processor. The primary processor calibrates 152042 the first signal 152022a in response to the second signal 152022b. The first signal 152022a is calibrated 152042 to reflect the completeness of the tissue capture pressure on the end actuator 152000. The calibrated signal 152026 is displayed to an operator by means of, for example, a screen incorporated into the 150010 surgical instrument.

[0392] Figure 57 is a logic diagram illustrating a method for a 152050 process for determining and displaying the thickness of a section of tissue stuck between the anvil 152002 and the staple cartridge 152006 of the end actuator 152000. The process

152050 comprises obtaining a Hall effect voltage 152052, for example, by means of a Hall effect sensor located at the distal end of the anvil 152002. The Hall effect voltage 152052 is supplied to an analog-digital converter 152054 and converted into a digital signal . The digital signal is supplied to a processor, such as the primary processor. The primary processor calibrates 152056 the input curve of the Hall effect voltage signal 152052. A strain gauge 152058, such as a micro strain gauge, is configured to measure one or more parameters of the end actuator 152000, such as, for example, the magnitude of the effort exerted on the anvil 152002 during a gripping operation. The measured effort is converted 152060 into a digital signal and supplied to the processor, such as the primary processor. The primary processor uses one or more algorithms and / or look-up tables to adjust the Hall effect voltage 152052 in response to the effort measured by the 152058 effort meter to reflect the true thickness and completeness of the bite of the tissues trapped by the anvil 152002 and the staple cartridge 152006. The adjusted thickness 152026 is displayed to an operator using, for example, a screen incorporated into the 150010 surgical instrument.

[0393] In some embodiments, the surgical instrument may additionally comprise a load cell or sensor 152082. The load sensor 152082 can be located, for example, on the drive shaft assembly 150200, described above, or in the 150012, also described above. Figure 58 is a logic diagram illustrating a modality of a 152070 process for determining and displaying the thickness of a section of fabric stuck between the anvil 152002 and the staple cartridge 152006 of the end actuator 152000. The process comprises obtaining a Hall effect voltage 152072, for example, by means of a Hall effect sensor located

at the distal end of the anvil 152002. The Hall effect voltage 152072 is supplied to an analog-to-digital converter 152074 and converted into a digital signal. The digital signal is supplied to a processor, such as the primary processor. The primary processor calibrates 152076 the curve input of the Hall effect voltage signal 152072. A 152078 effort meter, such as a microstrain meter, is configured to measure one or more parameters of the 152000 end actuator, such as, for example, the magnitude of the effort exerted on the anvil 152002 during a gripping operation. The measured effort is converted 152080 to a digital signal and supplied to the processor, such as the primary processor. The load sensor 152082 measures the grip force of the anvil 152002 against the staple cartridge 152006. The measured grip force is converted 152084 into a digital signal and supplied to the processor, such as the primary processor. The primary processor uses one or more algorithms and / or look-up tables to adjust the Hall effect voltage 152072 in response to the stress measured by the 152078 stress meter and the grip force measured by the 152082 load sensor to reflect the true thickness and the completeness of the bite of the tissues trapped by the anvil 152002 and the staple cartridge 152006. The adjusted thickness 152026 is displayed to an operator by means of, for example, a screen incorporated into the surgical instrument 150010.

[0394] Figure 59 is a graph 152090 illustrating an adjusted thickness measurement for Hall effect 152092, compared to an unmodified thickness measurement for Hall effect 152094. As shown in Figure 59, the thickness measurement for Hall effect unmodified 152094 indicates a measurement of thicker tissues, as the single sensor is not able to compensate for partial distal / proximal bites that result in incorrect thickness measurements.

The adjusted thickness measurement 152092 is generated, for example, by the process 152050 illustrated in Figure 57. The adjusted thickness measurement by Hall effect 152092 is calibrated based on the input from one or more additional sensors, such as a effort meter. The adjusted Hall effect thickness 152092 reflects the true thickness of the fabrics located between an anvil 152002 and a staple cartridge 152006.

[0395] Figure 60 illustrates a modality of an end actuator 152100 comprising a first sensor 152108a and a second sensor 152108b. End actuator 152100 is similar to end actuator 152000 illustrated in Figure 53. End actuator 152100 comprises a first claw member, or anvil, 152102 pivotally coupled to a second claw member 152104. The claw member 152104 it is configured to receive a staple cartridge 152106 inside. The end actuator 152100 comprises a first sensor 152108a coupled to the anvil 152102. The first sensor 152108a is configured to measure one or more parameters of the end actuator 152100 such as the gap 152110 between the anvil 152102 and the staple cartridge 152106. The span 152110 can correspond, for example, to a thickness of tissue stuck between the anvil 152102 and the staple cartridge 152106. The first sensor 152108a it can comprise any sensor suitable for measuring one or more parameters of the end actuator. In various embodiments, for example, the first sensor 152108a may comprise a magnetic sensor, such as a Hall effect sensor, a stress meter, a pressure sensor, an inductive sensor, such as a eddy current sensor, a resistive sensor, a capacitive sensor, an optical sensor and / or any other suitable sensor.

[0396] In some embodiments, the end actuator

152100 comprises a second sensor 152108b. The second sensor 152108b is coupled to the second claw member 152104 and / or the staple cartridge 152106. The second sensor 152108b is configured to detect one or more parameters of the end actuator

152100. In some embodiments, for example, the second sensor 152108b is configured to detect one or more conditions of the instrument, such as a color of the staple cartridge 152106 coupled to the second claw member 152104, a length of the staple cartridge. staples 152106, a hold condition of end actuator 152100, the number of uses / number of remaining uses of end actuator 152100 and / or staple cartridge 152106, and / or any other suitable instrument condition. The second sensor 152108b can comprise any sensor suitable for detecting one or more conditions of the instrument, such as a magnetic sensor, such as a Hall effect sensor, an effort meter, a pressure sensor, an inductive sensor such as a eddy current sensor, resistive sensor, capacitive sensor, optical sensor and / or any other suitable sensor.

[0397] The end actuator 152100 can be used in conjunction with any of the processes shown in Figures 54 to

57. In one embodiment, for example, the input from the second sensor 152108b can be used to calibrate the input from the first sensor 152108a. The second sensor 152108b can be configured to detect one or more parameters of the staple cartridge 152106, for example, the color and / or the length of the staple cartridge 152106. The detected parameters, such as the color and / or the - staple cartridge length 152106, can correspond to one or more properties of the cartridge, for example, the height of the cartridge holder, the thickness of fabrics useful / optimal for the staple cartridge and / or the staple pattern staple cartridge 152106.

The known parameters of the staple cartridge 152106 can be used to adjust the thickness measurement provided by the first sensor 152108a. For example, if the staple cartridge 152106 has a higher support height, the thickness measurement provided by the first sensor 152108a can be reduced to compensate for the additional support height. The adjusted thickness can be displayed to an operator, for example, through a screen attached to the surgical instrument 150010.

[0398] Figure 61 illustrates an embodiment of an end actuator 152150 comprising a first sensor 152158 and a plurality of second sensors 152160a, 152160b. The end actuator 152150 comprises a first claw member, or anvil, 152152 and a second claw member 152154. Claw member 152154 is configured to receive a staple cartridge

152156. Anvil 152152 is pivotally movable relative to the second claw member 152154, for clamping fabrics between the anvil 152152 and the staple cartridge 152156. The anvil comprises a first sensor 152158. The first sensor 152158 is configured to detect a or more parameters of the end actuator 152150, such as the gap 152110 between the anvil 152152 and the staple cartridge 152156. The span 152110 can correspond, for example, to a thickness of fabric stuck between the anvil 152152 and the clamps 152156. The first sensor 152158 can comprise any sensor suitable for measuring one or more parameters of the end actuator. In various embodiments, for example, the first 152158 sensor may comprise a magnetic sensor, such as a Hall effect sensor, a stress meter, a pressure sensor, an inductive sensor, such as a eddy current sensor, a resistive sensor, a capacitive sensor, an optical sensor and / or any other suitable sensor.

[0399] In some embodiments, the end actuator 152150 comprises a plurality of secondary sensors 152160a, 152160b. The secondary sensors 152160a, 152160b are configured to detect one or more parameters of the end actuator 152150. In some modalities, for example, the secondary sensors 152160a, 152160b are configured to measure the amplitude of the effort exerted on the anvil 152152 during a gripping procedure. In various modalities, the secondary sensors 152160a, 152160b can comprise a magnetic sensor, such as a Hall effect sensor, a stress meter, a pressure sensor, an inductive sensor, such as a current sensor. rasita, a resistive sensor, a capacitive sensor, an optical sensor and / or any other suitable sensor. Secondary sensors 152160a, 152160b can be configured to measure one or more identical parameters at different locations on anvil 152152, different parameters at identical locations on anvil 152152, and / or different parameters at different locations on anvil 152152.

[0400] Figure 62 is a logic diagram illustrating a method for a 152170 process for adjusting a measurement of a first sensor 152158 in response to a plurality of secondary sensors 152160a, 152160b. In one embodiment, the Hall effect voltage is obtained 152172, for example, by a Hall effect sensor. The Hall effect voltage is converted to 152174 by an analog-to-digital converter. The converted Hall effect voltage signal is calibrated 152176. The calibrated curve represents the thickness of a section of tissue located between the anvil 152152 and the staple cartridge 152156. A plurality of secondary measurements are obtained 152178a, 152178b by a plethora of secondary sensors, such as a plurality of effort meters. The input of the effort meters is converted 152180a, 152180b into one or more digital signals, for example,

by a plurality of electronic uStrain conversion circuits. The calibrated Hall effect voltage and the plurality of secondary measurements are supplied to a processor, such as the primary processor. The primary processor uses secondary measurements to adjust 152182 the Hall effect voltage, for example, by applying an algorithm and / or using one or more consultation tables. The adjusted Hall effect tension represents the true thickness and completeness of the capture pressure of the tissue trapped by the beaker 152152 and the staple cartridge 152156. The adjusted thickness 152026 is displayed to an operator by, for example, example, a screen built into the 150010 surgical instrument.

[0401] Figure 63 illustrates a modality of a circuit 152190 configured to convert signals from the first sensor 152158 and the plurality of secondary sensors 152160a, 152160b into digital signals receivable by a processor, such as the primary processor. Circuit 152190 comprises an analog-to-digital converter 152194. In some embodiments, the analog-to-digital converter 152194 comprises an 18-bit, 4-channel analog-to-digital converter. Those skilled in the art will recognize that the 152194 analog-digital converter can comprise any suitable number of channels and / or bits to convert one or more analog to digital inputs. Circuit 152190 comprises one or more level displacement resistors 152196 configured to receive an input from the first sensor 152158 such as, for example, a Hall effect sensor. Level displacement resistors 152196 adjust the input of the first sensor, shifting the value to a higher or lower voltage, depending on the input. The level displacement resistors 152196 provide the level displacement input of the first sensor 152158 to the analog-to-digital converter.

[0402] In some embodiments, a plurality of secondary sensors 152160a, 152160b is coupled to a plurality of points 152192a, 152192b within circuit 152190. The plurality of points 152192a, 152192b can provide filtering of the input provided the plurality of secondary sensors 152160a, 152160b. After filtering the input signals, the plurality of bridges 152192a, 152192b supplies the inputs from the plurality of secondary sensors 152160a, 152160b to the analog-to-digital converter 152194. In some embodiments, a switch 152198 coupled to one or more resistors of The level shift can be coupled to the analog-to-digital converter 152194. Switch 152198 is configured to calibrate one or more of the input signals, such as an input from a Hall effect sensor. Switch 152198 can be engaged to provide one or more level shift signals to adjust the input of one or more of the sensors, such as, for example, to calibrate the input of a Hall effect sensor. In some embodiments, adjustment is not necessary, and key 152198 is left in the open position to decouple the level displacement resistors. Switch 152198 is coupled to the analog-to-digital converter

152194. The 152194 analog-to-digital converter provides output to one or more processors, such as the primary processor. The primary processor calculates one or more parameters of the end actuator 152150 based on the input from the 152194 analog-to-digital converter. In one embodiment, for example, the primary processor calculates a thickness of the tissues between the 152152 anvil and the staple cartridge 152156, based on the input from one or more sensors 152158, 152160a, 152160b.

[0403] Figure 64 illustrates a modality of an end actuator 152200 comprising a plurality of sensors 152208a to 152208d. The end actuator 152200 comprises an anvil 152202 pivotally coupled to a second claw member 152204. The claw member 152204 is configured to receive inside a staple cartridge 152206. The anvil 152202 comprises a plurality of sensors 152208a 152208d on it. The plurality of sensors 152208a to 152208d is configured to detect one or more parameters of the end actuator 152200 such as the anvil 152202. The plurality of sensors 152208a to 152208d can comprise one or more identical sensors and / or different sensors . The plurality of sensors 152208a to 152208d can comprise, for example, magnetic sensors, such as a Hall effect sensor, effort meters, pressure sensors, inductive sensors, such as a parasitic current sensor, resistive sensors, capacitive sensors , optical sensors and / or any other suitable sensors or combinations thereof. In one embodiment, for example, the plurality of sensors 152208a through 152208d may comprise a plurality of effort meters.

[0404] In one embodiment, the plurality of sensors 152208a to 152208d allows a robust process to detect tissue thickness to be implemented. By detecting various parameters along the length of the anvil 152202, the plurality of sensors 152208a to 152208d allows a surgical instrument, such as the 150010 surgical instrument, to calculate the thickness of the tissues in the claws, regardless of the bite, for example, a partial or total bite. In some embodiments, the plurality of sensors 152208a through 152208d comprises a plurality of effort meters. The plurality of strain gauges are configured to measure mechanical stress at various points on anvil 152202. The amplitude and / or slope of mechanical stress at each of the various points on anvil 152202 can be used to determine the thickness of the fabric arranged between the anvil 152202 and the staple cartridge 152206. The plurality of strain gauges can be configured to optimize the maximum breadth and / or the angular coefficient differences based on the grip dynamics. to determine the thickness, the positioning of the fabric and / or the material properties of the fabric. Time-based monitoring of the plurality of sensors 152208a to 152208d during gripping enables a processor, such as the primary processor, to use algorithms and query tables to recognize tissue characteristics and gripping positions and dynamically adjust the end actuator 152200 and / or the tissue trapped between the anvil 152202 and the staple cartridge

152206.

[0405] Figure 65 is a logic diagram illustrating a method for a 152220 process for determining one or more tissue properties based on a plurality of sensors 152208a through 152208d. In one embodiment, a plurality of sensors from 152208a to 152208d generate, from 152222a to 152222d, a plurality of signals indicative of one or more parameters of the end actuator

152200. The plurality of generated signals is converted, from 152224a to 152224d, into digital signals and supplied to a processor. In one embodiment, for example, comprising the plurality of effort meters, the plurality of electronic uStrain conversion circuits (microstrain) converts, from 152224a to 152224d, the signals of the effort meter into digital signals. The digital signals are supplied to a processor, such as the primary processor. The primary processor determines 152226 one or more characteristics of the tissue based on the plurality of signals. The processor can determine one or more characteristics of the tissue by applying an algorithm and / or a look-up table. One or more characteristics of the

152026 are displayed to an operator, for example, by a screen incorporated into the surgical instrument 150010.

[0406] Figure 66 illustrates an embodiment of an end actuator 152250 comprising a plurality of sensors 152260a to 152260d coupled to a second claw member 3254. End actuator 152250 comprises an anvil 152252 coupled pivotally to a second claw member 152254. Anvil 152252 is movable relative to the second claw member 152254 to clamp one or more materials together, such as a section of fabric 152264. The second claw member 152254 is configured to receive a cartridge clamps 152256. A first sensor 152258 is coupled to the anvil 152252. The first sensor is configured to detect one or more parameters of the end actuator 152150, such as the gap 152110 between the anvil 152252 and the staple cartridge 152256. The span 152110 can correspond, for example, to a thickness of tissue stuck between the anvil 152252 and the staple cartridge 152256. The first sensor 152258 can comprise any sensor suitable for measuring one or more parameters of the end actuator. In various embodiments, for example, the first sensor 152258 may comprise a magnetic sensor, such as a Hall effect sensor, a stress meter, a pressure sensor, an inductive sensor, such as a eddy current sensor, a resistive sensor, a capacitive sensor, an optical sensor and / or any other suitable sensor.

[0407] A plurality of secondary sensors 152260a to 152260d is coupled to the second claw member 152254. The plurality of secondary sensors 152260a to 152260d can be formed integrally with the second claw member 152254 and / or the staple cartridge 152256. In one embodiment, for example, the plurality of secondary sensors 152260a to 152260d is arranged on an outer row of the staple cartridge 152256 (see Figure 67). The plurality of secondary sensors 152260a to 152260d is configured to detect one or more parameters of the end actuator 152250 and / or a section of fabric 152264 stuck between the beaker 152252 and the staple cartridge 152256. The plurality of senses Secondary sensors 152260a to 152260d can comprise any sensors suitable for detecting one or more parameters of the end actuator 152250 and / or the tissue section 152264, such as magnetic sensors, such as a Hall effect sensor, stress meters, pressure sensors, inductive sensors, such as eddy current sensor, resistive sensors, capacitive sensors, optical sensors and / or any other suitable sensors or combinations thereof. The plurality of secondary sensors 152260a to 152260d can comprise identical sensors and / or different sensors.

[0408] In some modalities, the plurality of secondary sensors 152260a to 152260d comprises elements with dual purpose of sensors and tissue stabilizers. The plurality of secondary sensors 152260a to 152260d comprise electrodes and / or sensing geometries configured to create a stabilized tissue condition when the plurality of secondary sensors 152260a to 152260d are engaged with a tissue section 152264, such as, for example , during a gripping operation. In some embodiments, one or more of the plurality of secondary sensors 152260a to 152260d can be replaced by non-detecting tissue stabilizing elements. Secondary sensors 152260a to 152260d create a condition of stabilized tissue by controlling the flow of tissue, the formation of staples, and / or other tissue conditions during a hold, stapling, and / or other treatment process.

[0409] Figure 67 illustrates an embodiment of a staple cartridge 152270 comprising a plurality of sensors 152272a to 152272h integrally formed therein. The staple cartridge 152270 comprises a plurality of rows containing a plurality of holes for storing staples therein. One or more of the holes in the outer row 152278 are replaced by a sensor out of the plurality of sensors 152272a through 152272h. A cut-out section is shown to illustrate a sensor 152272f coupled to a metallic wire from sensor 152276b. The metallic sensor wires 152276a, 152276b can comprise a plurality of metallic wires to couple the plurality of sensors 152272a to 152272h to one or more circuits of a surgical instrument such as the 150010 surgical instrument. some modalities, one or more among the plurality of sensors 152272a to 152272h comprise elements with dual purpose of sensors and tissue stabilizers, having electrodes and / or detection geometries configured to provide tissue stabilization. In some embodiments, the plurality of sensors 152272a to 152272h can be replaced by and / or copopulated with a plurality of tissue stabilizing elements. Tissue stabilization can be provided, for example, by controlling the flow of tissue and / or forming staples during a gripping and / or stapling process. The plurality of sensors 152272a to 152272h provide signals to one or more circuits of the 150010 surgical instrument to improve feedback on stapling performance and / or tissue thickness detection.

[0410] Figure 68 is a logic diagram illustrating a method for a 152280 process to determine one or more parameters of a section of tissue 152264 trapped within an end actuator, such as the end actuator 152250 illustr-

in Figure 66. In one embodiment, a first sensor 152258 is configured to detect one or more parameters of the end actuator 152250 and / or the tissue section 152264 located between the beaker 152252 and the staple cartridge 152256. A first signal is generated 152282 by the first sensors 152258. The first signal is indicative of one or more parameters detected by the first sensor

152258. One or more secondary sensors 152260 are configured to detect one or more parameters of end actuator 152250 and / or tissue section 152264. Secondary sensors 152260 can be configured to detect the same parameters, additional parameters or parameters other than those detected by the first sensor 152258. Secondary signals 152284 are generated by secondary sensors 152260. Secondary signals 152284 are indicative of one or more parameters detected by secondary sensors 152260. The first signal and secondary signals are supplied to a processor such as, for example , the primary processor. The processor adjusts 152286 the first signal generated by the first sensor 152258 based on the input generated by the secondary sensors 152260. The adjusted signal can be indicative, for example, of the true thickness of a section of tissue 152264 and the completeness of the bite . The adjusted signal is displayed to an operator 152026 by means of, for example, a screen incorporated into the surgical instrument

150010.

[0411] Figure 69 illustrates a modality of a 152300 end actuator comprising a plurality of redundant sensors 152308a, 152308b. The end actuator 152300 comprises a first claw member, or anvil, 152302 pivotally coupled to a second claw member 152304. The second claw member 152304 is configured to receive a 152306 staple cartridge inside. anvil 152302 is movable relative to the staple cartridge 152306 to hold a material, such as a section of fabric, between the anvil 152302 and the staple cartridge 152306. A plurality of sensors 152308a, 152308b is coupled to the anvil. The plurality of sensors 152308a, 152308b is configured to detect one or more parameters of the end actuator 152300 and / or a section of fabric located between the anvil 152302 and the staple cartridge 152306. In some modes, the plurality of sensors 152308a, 152308b is configured to detect a gap 152310 between the anvil 152302 and the staple cartridge 152306. The span 152310 can correspond, for example, to the thickness of the fabric located between the anvil 152302 and the staple cartridge 152306. The plurality sensor 152308a, 152308b can detect the gap 152310 by, for example, detecting a magnetic field generated by a magnet 152312 coupled to the second claw member 152304.

[0412] In some embodiments, the plurality of sensors 152308a, 152308b comprises redundant sensors. The redundant sensors are configured to detect the same properties as the end actuator 152300 and / or a section of tissue located between the anvil 152302 and the staple cartridge 152306. The redundant sensors can comprise, for example, Hall effect configured to detect the gap 152310 between the anvil 152302 and the staple cartridge 152306. The redundant sensors provide signals representative of one or more parameters that allow a processor, such as the primary processor, to evaluate the multiple inputs and determine the most reliable entry. In some modalities, redundant sensors are used to reduce noise, false signals and / or deviations. Each of the redundant sensors can be measured in real time during the gripping, allowing time-based information to be analyzed and algorithms and / or look-up tables to recognize the characteristics of the tissue and the position of the grasp dynamically. The entry of one or more of the redundant sensors can be adjusted and / or selected to identify the true thickness of the tissue and the bite of a section of tissue located between the anvil 152302 and the staple cartridge 152306.

[0413] Figure 70 is a logic diagram illustrating a method for a 152320 process for selecting the most reliable output from a plurality of redundant sensors, such as the plurality of sensors 152308a, 152308b illustrated in Figure 69. In one mode, a first signal is generated by a first sensor 152308a. The first signal is converted 152322a by an analog-to-digital converter. One or more additional signals are generated by one or more redundant 152308b sensors. The one or more additional signals are converted 152322b by an analog-to-digital converter. The converted signals are supplied to a processor, such as the primary processor. The primary processor evaluates 152324 redundant inputs to determine the most reliable output. The most reliable output can be selected based on one or more parameters such as, for example, algorithms, look-up tables, inputs from additional sensors and / or instrument conditions. After selecting the most reliable output, the processor can adjust the output based on one or more additional sensors to reflect, for example, the true thickness and capture pressure of a section of tissue between the anvil 152302 and the staple cartridge

152306. The most reliable adjusted output is displayed 152026 to an operator via, for example, a screen built into the 150010 surgical instrument.

[0414] Figure 71 illustrates a modality of a 152350 end actuator comprising a 152358 sensor that comprises

specific sampling rate to limit or eliminate false signals. The end actuator 152350 comprises a first claw member, or anvil, 152352 pivotally coupled to a second claw member 152354. Claw member 152354 is configured to receive a staple cartridge inside

152356. The staple cartridge 152356 contains a plurality of staples that can be applied to a section of tissue located between the anvil 152352 and the staple cartridge 152356. A 152358 sensor is coupled to the anvil 152352. The 152358 sensor is configured to detect a or more parameters of the end actuator 152350, such as the gap 152364 between the anvil 152352 and the staple cartridge 152356. The gap 152364 can correspond to the thickness of a material such as a section of fabric and / or complete with a material bite between the anvil 152352 and the staple cartridge 152356. The sensor 152358 can comprise any sensor suitable for detecting one or more parameters of the end actuator 152350, such as a magnetic sensor, such as a Hall effect sensor, an effort meter, a pressure sensor, an inductive sensor such as an eddy current sensor, a resistive sensor, a capacitive sensor, an optical sensor and / or any other the proper sensor.

[0415] In one embodiment, sensor 152358 comprises a magnetic sensor configured to detect a magnetic field generated by an electromagnetic source 152360 coupled to the second claw member 152354 and / or the staple cartridge 152356. The electromagnetic source 152360 generates a magnetic field detected by the sensor 152358. The strength of the detected magnetic field can correspond, for example, to the thickness and / or the completeness of a tissue bite located between the 152352 anvil and the staple cartridge

152356. In some embodiments, the electromagnetic source 152360 generates a signal at a frequency known as, for example, 1 MHz. In other embodiments, the signal generated by the electromagnetic source 152360 can be adjustable based, for example, on the type of cartridge clamps 152356 installed on the second claw member 152354, on one or more additional sensors, an algorithm and / or one or more parameters.

[0416] In one embodiment, a 152362 signal processor is coupled to the 152350 end actuator, such as anvil 152352. The 152362 signal processor is configured to process the signal generated by sensor 152358 to eliminate false signals and to reinforce the input from sensor 152358. In some embodiments, the signal processor 152362 may be located separately from the end actuator 152350, for example, on the handle 150014 of the surgical instrument 150010. In some embodiments, the 152362 signal processor is formed entirely with and / or comprises an algorithm executed by a general processor, such as the primary processor. The 152362 signal processor is configured to process the signal from sensor 152358 at a frequency substantially equal to the frequency of the signal generated by the 152360 electromagnetic source. In one embodiment, for example, the 152360 electromagnetic source generates a signal at a frequency of 1 MHz. The signal is detected by the sensor

152358. The 152358 sensor generates a signal indicating the detected magnetic field, which is supplied to the 152362 signal processor. The signal is processed by the 152362 signal processor at a frequency of 1 MHz to eliminate false signals. The processed signal is supplied to a processor, such as the primary processor. The primary processor correlates the received signal to one or more parameters of the end actuator 152350, such as the gap 152364 between the anvil 152352 and the staple cartridge 152356.

[0417] Figure 72 is a logical diagram illustrating a method for a 152370 process to generate a thickness measurement for a section of tissue located between an anvil and a staple cartridge for an end actuator, such as the end actuator 152350 illustrated in Figure 71. In a process modality 152370, a signal is generated 152372 by a modulated electromagnetic source 152360. The generated signal can comprise, for example, a 1 MHz signal. A 152358 magnetic sensor is configured to detect 152374 the signal generated by the electromagnetic source

152360. Magnetic sensor 152358 generates a signal indicative of the detected magnetic field and supplies the signal to a signal processor

152362. The 152362 signal processor processes 152376 the signal to remove noise, false signals and / or to reinforce the signal. The processed signal is supplied to an analog-to-digital converter for converting 152378 to a digital signal. The digital signal can be calibrated 152380, for example, by applying an algorithm and / or an input table of the calibration curve input. Signal processing 152376, conversion 152378 and calibration 152380 can be performed by one or more circuits. The calibrated signal is displayed to a user 152026 by means of, for example, a screen formed entirely with the 150010 surgical instrument.

[0418] Figures 73 and 74 illustrate an embodiment of an end actuator 152400 comprising a sensor 152408 to identify 152406 clip cartridges of different types. The end actuator 152400 comprises a first claw member, or anvil, 152402 pivotally coupled to a second claw member or elongated channel 152404. The elongated channel 152404 is configured to operationally hold a cartridge 152406 surgical clamps. The 152400 end actuator additionally comprises the 152408 sensor located in the proximal area. The 152408 sensor can be any of an optical sensor, a magnetic sensor, an electrical sensor or any other suitable sensor.

[0419] The 152408 sensor can be operable to detect a property of the 152406 staple cartridge and thus identify the type of the 152406 staple cartridge. Figure 74 illustrates an example where the 152408 sensor is an optical emitter and detector 152410 . The staple cartridge body 152406 can be of different colors, so that the color identifies the type of staple cartridge 152406. An emitter and optical detector 152410 can be operable to interrogate the color of the body of staple cartridge 152406. No illustrated example, the emitter and optical detector 152410 can detect white 152412 by receiving the light reflected in the red, green and blue spectra in equal intensity. The emitter and optical detector 152410 can detect red 152414 by receiving very little light reflected in the green and blue spectrum, while receiving light in the red spectrum in greater intensity.

[0420] Alternatively or additionally, the emitter and optical detector 152410, or another suitable 152408 sensor, can interrogate and identify some other symbol or mark on the staple cartridge

152406. The symbol or mark can be any one of a bar code, a shape or character, a color-coded emblem or any other suitable mark. The information read by the sensor 152408 can be communicated to a microcontroller in the surgical device 150010, such as, for example, a microcontroller (the 461 microcontroller (Figure 12), for example). The microcontroller can be configured to communicate information about the staple cartridge 152406 to the instrument operator. For example, the identified staple cartridge 152406 may not be suitable for a given application; in this case, the instrument operator may be informed, and / or an instrument function is inadequate. In that instance,

The microcontroller can optionally be configured to disable a function of the surgical instrument that can be disabled. Alternatively or additionally, the microcontroller can be configured to inform the operator of the 150010 surgical instrument about the parameters of the staple cartridge type 152406 identified, for example, the staple cartridge length 152406, or information about staples , such as height and length.

[0421] Figure 75 illustrates an aspect of a segmented flexible circuit 153430 configured to be fixedly attached to a claw member 153434 of an end actuator. The segmented flexible circuit 153430 comprises a distal segment 153432a and side segments 153432b, 153432c that include individually addressable sensors to enable the detection of the presence of local tissue. Segments 153432a, 153432b, 153432c are individually addressable to detect tissue and to measure tissue parameters based on individual sensors located within each of segments 153432a, 153432b, 153432c. Segments 153432a, 153432b, 153432c of segmented flexible circuit 153430 are mounted on claw member 153434 and are electrically coupled to a power source, such as an electrical circuit through conductive electrical members 153436. A Hall effect sensor 153438, or any suitable magnetic sensor is located at a distal end of the claw member 153434. The Hall effect sensor 153438 operates in conjunction with a magnet to provide a measurement of an aperture defined by the claw member 153434 that would otherwise it can be called a tissue gap, as shown in particular in Figure 77. The flexible circuit segmented 153430 can be used to measure tissue thickness, strength, displacement, compression, tissue impedance and lo -

calization of the tissue inside an end actuator.

[0422] Figure 76 illustrates an aspect of a segmented flexible circuit 153440 configured to be mounted on a claw member 153444 of an end actuator. The segmented flexible circuit 153440 comprises a distal segment 153442a and side segments 153442b, 153442c that include individually addressable sensors for tissue control. The segments 153442a, 153442b, 153442c are individually addressable to treat the fabric and to read individual sensors located within each of the segments 153442a, 153442b, 153442c. The segments 153442a, 153442b, 153442c of the segmented flexible circuit 153440 are mounted on the claw member 153444 and are electrically coupled to a power source, through conductive electrical members 153446. A Hall effect sensor 153448, or other suitable magnetic sensor - do, is provided at a distal end of the claw member

153444. The Hall effect sensor 153448 operates in conjunction with a magnet to provide a measurement of an aperture defined by the claw member 153444 of the fabric end or span actuator, as shown in particular in Figure 77. In addition, a plurality of lateral asymmetric temperature sensors 153450a, 153450b are mounted on or formally integrated into the segmented flexible circuit 153440 to provide feedback on the fabric temperature to the control circuit. The 153440 segmented flexible circuit can be used to measure tissue thickness, force, displacement, compression, tissue impedance and tissue location within an end actuator.

[0423] Figure 77 illustrates an aspect of an end actuator 153460 configured to measure a gap of tissue Gr. The end actuator 153460 comprises a claw member 153462 and a claw member 153444. The flexible circuit 153440, as described in Figure 76, it is mounted on the claw member 153444. The flexible circuit 153440 comprises a Hall effect sensor 153448 that operates with a magnet 153464 mounted on the claw member 153462 to measure the gap of tissue Gr. This technique can be used to measure the defined gap between claw member 153444 and claw member 153462. Claw member 153462 can be a staple cartridge.

[0424] Figure 78 illustrates an aspect of a 153470 end actuator comprising a segmented flexible circuit

153468. The end actuator 153470 comprises a claw member 153472 and a clip cartridge 153474. The segmented flexible circuit 153468 is mounted on the claw member 153472. Each of the sensors arranged within segments 1 to 5 is configured to detect the presence of tissue positioned between claw member 153472 and staple cartridge 153474 and represents tissue zones 1 through 5. In the configuration shown in Figure 78, end actuator 153470 is shown in an open position ready to receive or secure the fabric between the clamp member 153472 and the staple cartridge 153474. The segmented flexible circuit 153468 can be used to measure the thickness of the fabric, the force, displacement, compression, impedance of the fabric and the location of the tissue inside the 153470 end actuator.

[0425] Figure 79 illustrates end actuator 153470, shown in Figure 78, with claw member 153472 securing the fabric 153476 between claw member 153472, for example, the anvil and the staple cartridge. As shown in Figure 79, tissue 153476 is positioned between segments 1 to 3 and represents tissue zones 1 to 3. Consequently, tissue 153476 is detected by sensors in segments 1 to 3 and the absence of tissue (void) ) is detected in section 153469 by segments 4 and 5. Information regarding the presence and absence of 153476 tissue positioned within certain segments 1 to 3 and 4 and 5, respectively, is communicated to a control circuit, as described here, through , for example, of interface circuits. The control circuit is configured to detect the tissue located in segments 1 to 3. It will be recognized that segments 1 to 5 may contain any suitable magnetic sensors for temperature, force / pressure and / or Hall effect to measure the parameters of tissue located in certain segments 1 to 5 and electrodes to supply energy to the tissue located in certain segments 1 to 5

5. The 153468 segmented flexible circuit can be used to measure tissue thickness, force, displacement, compression, tissue impedance and tissue location within the 153470 end actuator.

[0426] Figure 80 is a diagram of a 153100 absolute positioning system that can be used with a surgical instrument or a system according to the present disclosure. The absolute positioning system 153100 comprises a controlled motor drive circuit arrangement comprising a sensor arrangement 153102 in accordance with at least one aspect of the present disclosure. The sensor layout 153102 of an absolute positioning system 153100 provides a unique position signal that corresponds to the location of a displacement member

153111. In one aspect, the displacement member 153111 represents the longitudinally movable drive member coupled to the cutting instrument or knife (for example, a cutting instrument, a beam with a | profile and / or a beam with a | profile) 153514 (Figure 82)). In other respects, the displacement member 153111 represents the firing member coupled to the cutting instrument or knife, which can be adapted and configured to include a rack of driving teeth. In yet another aspect, the displacement member

153111 represents the firing bar or a beam with a | profile, each of which can be adapted and configured to include a rack of drive teeth.

[0427] Consequently, as used in the present invention, the term "displacement member" is used generically to refer to any movable member of a surgical instrument or system as described here, such as a driving member, a firing member , a firing bar, a cutting instrument, a knife and / or a beam with a profile | or any element that can be moved. Consequently, the 153100 absolute positioning system can, in effect, track the displacement of the beam with | 153514 of the cutting instrument (Figure 82) by tracking the displacement of a longitudinally movable drive member. In several other aspects, the displacement member 153111 can be coupled to any suitable sensor for measuring displacement. In this way, the longitudinally movable drive member, the firing member, the firing bar or the beam with an i-profile, or combinations thereof, can be coupled to any suitable displacement sensor. Displacement sensors can include contact or non-contact displacement sensors. The displacement sensors can comprise linear variable differential transformers ("LVDT" - linear variable differential transformers), "differential variable reluctance transducers" (DVRT), a slide potentiometer, a detection system magnet comprising a movable magnet and a series of linearly movable Hall effect sensors, a magnetic detection system comprising a fixed magnet and a series of linearly arranged Hall sensors mobile, an optical detection system comprising a mobile light source and a series of photodiodes

anodes or photodetectors arranged in a linearly mobile manner, or an optical detection system comprising a fixed light source and a series of photodiodes or photodetectors arranged in a linearly mobile manner, or any combination thereof.

[0428] An electric motor 153120 can include a rotary drive shaft 153116, which, operationally, interfaces with a gear set 153114, which is mounted on a coupling hitch with a set, or rack, of gear teeth. displacement member 153111. A sensor element 153126 can be operationally coupled to gear set 153114, so that a single revolution of sensor element 153126 corresponds to some linear longitudinal translation of displacement member 153111. One Gear and sensor arrangement 153118 can be connected to the linear actuator by means of a rack and pinion arrangement, or by a rotary actuator, by means of a sprocket or other connection. A 153129 power source supplies power to the 153100 absolute positioning system and an 153128 output indicator can show the output from the 153100 absolute positioning system.

[0429] A single revolution of the sensor element 153126 associated with the position sensor 153112 is equivalent to a longitudinal displacement di of the displacement member 153111, where di is the longitudinal distance by which the displacement member 153111 moves from the point " a "to point" b "after a single revolution of the sensor element 153126 coupled to the displacement member 153111. The arrangement of the sensor 153102 can be connected by means of a gear reduction which results in the completion of one or more revolutions - tions by the position sensor 153112 of the full travel of the travel member 153111. The position sensor 153112 can complete multiple revolutions of the full travel of the travel member

153111.

[0430] A series of keys 153122a to 153122n, where n is an integer greater than one, can be used alone or in combination with gear reduction to provide a single position signal for more than one sensor revolution position 153112. The status of keys 153122a to 153122n is retrieved to a controller 153110 that applies logic to determine a single position signal corresponding to the longitudinal displacement d: + da + ... dh of displacement member 153111. A output 153124 of position sensor 153112 is supplied to controller 153110. position sensor 153112 of the sensor arrangement 153102 can comprise a magnetic sensor, an analog rotary sensor, such as a potentiometer, an array of analog Hall effect elements , which emit a unique combination of signals or position values. Controller 153110 may be contained within a master controller or may be contained within a compartment of the tool mounting portion of a surgical instrument or a system in accordance with the present disclosure.

[0431] The absolute positioning system 153100 provides absolute positioning of the displacement member 153111 with the energization of the surgical instrument or system without having to retract or advance the driving member 153111 to the reset position (zero or initial), as it may be the case with conventional rotary encoders that merely count the number of progressive or regressive steps that the 153120 motor has traveled to infer the position of a device actuator, actuation bar, scalpel, and the like.

[0432] The 153110 controller can be programmed to perform various functions, such as precise control of the speed and position of the joint and knife systems. In one respect, the controller

153110 includes a 153108 processor and a 153106 memory. The 153120 electric motor can be a brushed DC motor with a gearbox and mechanical connections with a hinge or knife system. In one aspect, a 153110 motor driver can be an A3941 available from Allegro Microsystems, Inc. Other motor drivers can be readily replaced for use in the 153100 absolute positioning system.

[0433] Controller 153110 can be programmed to provide precise control of the speed and position of travel member 153111 and articulation systems. The 153110 controller can be configured to compute a response in the 153110 controller software. The computed response is compared to a measured response from the real system to obtain an "observed" response, which is used for actual feedback-based decisions. The observed response is a favorable and adjusted value, which balances the uniform and continuous nature of the simulated response with the measured response, which can detect external influences in the system.

[0434] The 153100 absolute positioning system can comprise and / or be programmed to implement a feedback controller, such as a PID, status feedback and adaptive controller. A 153129 power source converts the signal from the feedback controller to a physical input to the system, in this case, the voltage. Other examples include pulse width modulation (PWM) of voltage, current and force. Other 153118 sensors can be provided to measure the physical parameters of the physical system, in addition to the position measured by the position sensor 153112. In a digital signal processing system, an absolute positioning system 153100 is coupled to a digital data capture where the output of the 153100 absolute positioning system will have a finite resolution and sampling frequency. The system

absolute positioning system 153100 can comprise a comparison and combination circuit to combine a computed response with a measured response through the use of algorithms, such as a weighted average and a theoretical control closed loop, which triggers a computed response in towards the measured response. The computed response of the physical system considers the properties, such as mass, inertia, viscous friction, resistance to inductance, etc., to predict what will be the states and outputs of the physical system, knowing the input.

[0435] The 153110 motor driver can be an A3941, available from Allegro Microsystems, Inc. The 153910 A3941 driver is an entire bridge controller for use with metal oxide semiconductor field effect transistors (MOSFETs - metal oxide semiconductor field effect transistors) of external N-channel power, specifically designed for inductive loads, such as brushed DC motors. The 153110 actuator comprises a single charge pump regulator, which provides complete door drive (> 10 V) for batteries with voltage up to 7 V and allows the A3941 to operate with a reduced door drive, up to 5.5 V. input command capacitor can be used to supply the voltage supplied by the above battery needed for N channel MOSFETs. An internal charge pump for the upper side drive allows direct current operation (100% duty cycle ). The entire bridge can be operated in fast or slow drop modes using diodes or synchronized rectification. In the slow drop mode, the current can be recirculated by means of FET from the top or from the bottom. The power FETs are protected from the shoot-through effect by means of resistors with programmable dead time. The integrated diagnosis provides indication of undervoltage, overtemperature and faults in the power bridge, and can be configured to protect

Power MOSFETs in most short-circuit conditions. Other motor starters can be replaced immediately for use in the 153100 absolute positioning system.

[0436] Figure 81 is a diagram of a position sensor 153200 of an absolute positioning system 153100, which comprises a rotating magnetic absolute positioning system, according to at least one aspect of this disclosure. The absolute positioning system 153100 'is similar in many ways to the absolute positioning system 153100. The position sensor 153200 can be implemented as a rotary, magnetic, single-circuit, ASSOSSEQFT position sensor, available from Austria Microsystems , AG. The 153200 position sensor interfaces with the 153110 controller to provide the 153100 absolute positioning system. The 153200 position sensor is a low voltage and low power component and includes four Hall effect elements 153228A, 153228B, 153228C, 153228D in an area 153230 of the position sensor 153200 which is located above a magnet located on a rotating element associated with a displacement member, such as the cutting drive gear, and / or the driving gear of closing, so that the displacement of a firing member and / or a closing member can be accurately tracked. A 153232 high-resolution ADC converter and a 153238 intelligent power management controller are also featured on the integrated circuit. A CORDIC 153236 processor (Coordinate Rotation Digital Computer, digital coordinate rotation computer), also known as digit-by-digit method and Volder algorithm, is provided to implement a simple and efficient algorithm for calculating hyperbolic functions. and trigonometry that require only addition, subtraction, bit shift and lookup table operations. The position

angular function, alarm bits and magnetic field information are transmitted via a standard serial communication interface, such as a SPI 153234 interface, to the 153110 controller. The 153200 position sensor provides 12 or 14 bits of resolution. The position sensor 153200 can be an ASS055 integrated circuit supplied in a small 16-pin QFN package whose measurement corresponds to 4x4x0.85 mm.

[0437] Hall effect elements 153228A, 153228B, 153228C, 153228D are located directly above the rotating magnet. The Hall effect is a well-known effect and for convenience it will not be described here in detail, however, in general, the Hall effect produces a voltage difference (the Hall voltage) through an electrical conductor transverse to a current conductor and a magnetic field perpendicular to the current. The Hall coefficient is defined as the ratio between the induced electric field and the product of the current density by the applied magnetic field. It is a characteristic of the material from which the conductor is made, since its value depends on the type, number and properties of the load carriers that make up the chain. In the ASS055 153200 position sensor, Hall effect elements 153228A, 153228B, 153228C, 153228D are capable of producing a voltage signal indicative of the absolute positioning of the magnet in terms of the angle relative to a single revolution of the magnet. This angle value, which is a single position signal, is calculated by the CORDIC 153236 processor and stored integrated in the ASS055 153200 position sensor in a register or memory. The angle value that is indicative of the magnet's position during a revolution is provided to the 153110 controller in a variety of techniques, for example, by energizing or upon demand by the 153110 controller.

[0438] The AS5055 153200 position sensor requires only a few external components to operate when connected to the controller

153110. Six wires are required for a simple application using a single power supply: two wires for power and four wires 153240 for the SPI 153234 interface with the 153110 controller. A seventh connection can be added to send an interrupt signal to the controller 153110 informing that a new valid angle can be read. Upon energization, the ASS055 153200 position sensor performs a complete energization sequence, including an angle measurement. The completion of this cycle is indicated as an INT 153242 output, and the angle value is stored in an internal register. Once this output is configured, the ASS5055 153200 position sensor goes into suspended mode. The 153110 controller can respond to the INT request on the INT 153242 output by reading the angle value from the position sensor ASS055 153200 via the SPI 153234 interface. After the angle value is read by the 153110 controller, the INT output 153242 is released again. The sending of a "read angle" command via the SPI 153234 interface via controller 153110 to the position sensor 153200 also automatically energizes the integrated circuit and starts another angle measurement. As soon as the 153110 controller has finished reading the angle value, the INT 153242 output is released and a new result is stored in the angle register. The completion of this angle measurement is again indicated by the definition of the INT 153242 output and the corresponding identification in the status register.

[0439] Due to the measurement principle of the AS5055 153200 position sensor, only a single angle measurement is performed in a very short time (-600 us) after each energization sequence. As soon as an angle measurement is completed, the ASS055 153200 position sensor enters the de-energized state. There is no filter of the angle value by digital average implemented in the integrated circuit,

as this would require more than one angle measurement and, consequently, a longer energization time, which is not desired in low power applications. Angle variation can be reduced by averaging multiple angle samples in the controller

153110. For example, an average of four samples reduces the variation by 6 dB (50%).

[0440] Figure 82 is a sectional view of a 153502 end actuator showing a beam with a profile | 153514 firing a stroke in relation to the 153526 fabric trapped inside the end actuator 153502, in accordance with at least one aspect of the present disclosure. The 153502 end actuator is configured to operate with any of the surgical instruments or systems in accordance with the present disclosure. The end actuator 153502 comprises an anvil 153516, an elongated channel 153503 with a staple cartridge 153518 positioned in the elongated channel

153503. A firing bar 153520 is translatable distally and proximally along a longitudinal geometric axis 153515 of the end actuator 153502. When the end actuator 153502 is not pivoted, the end actuator 153502 is in line with the drive shaft instrument. A beam with profile in | 153514 comprising a cutting edge 153509 is shown in a distal portion of the firing bar 153520. A wedge slide 153513 is positioned on the staple cartridge 153518. As the beam with profile | 153514 moved distally, the cutting edge 153509 comes into contact and can cut the fabric 153526 positioned between the anvil 153516 and the staple cartridge 153518. In addition, the beam with profile | 153514 contacts the 153513 wedge slide and pushes it distally, causing the 153513 wedge slide to contact the 153511 clamp drivers. The 153511 clamp drivers can be con-

into the clips 153505, causing the clips 153505 to advance through the fabric and into pockets 153507 defined in the anvil 153516, which forms the clips 153505.

[0441] A beam firing course with profile in | Example 153514 is illustrated by a graphic 153529 aligned with the end actuator 153502. The example 153526 fabric is also shown aligned with the end actuator 153502. The stroke of the trigger member may comprise a starting position of the 153527 stroke and a final stroke position 153528. During a firing stroke of the beam with profile in | 153514, the beam with profile in | 153514 can be advanced distally from the initial position of the stroke 153527 to the final position of the stroke 153528. The beam with | 153514 is shown in an example location of an initial position of the 153527 course. The 153529 course graphic of the beam shooting member with profile in | 153514 illustrates five travel regions of the firing member 153517, 153519, 153521, 153523, 153525. In a first firing region 153517, the beam with profile | 153514 can begin to advance distally. In the first firing stroke region 153517, the beam with a profile | 153514 can contact the wedge slider 153513 and start moving it distally. While in the first region, however, cutting edge 153509 may not come into contact with the fabric and the wedge slider 153513 may not come into contact with a staple driver

153511. After the static friction is overcome, the force required to drive the beam with profile in | 153514 in the first region 153517 can be substantially constant.

[0442] In the second stroke region of the firing member 153519, the cutting edge 153509 can start to come into contact and cut the fabric 153526. In addition, the wedge slider 153513 can start to come into contact with the clamp 153511 for

to activate the clamps 153505. The force required to drive the beam with profile in | 153514 may start to increase gradually.

As shown, the tissue initially found can be compressed and / or thinner due to the way the anvil 153516 rotates in relation to the staple cartridge 153518. In the third stroke region of the firing member 153521, the cutting edge 153509 can enter continuously in contact and cut the fabric 153526 and the wedge slider 153513 can repeatedly come into contact with the clamp drivers 153511. The force required to drive the beam with profile in | 153514 can reach the plateau in the third region 153521. In the fourth region of the 153523 firing stroke, the force required to drive the beam with a profile in | 153514 may start to decrease.

For example, the fabric in the end actuator portion 153502 corresponding to the fourth firing region 153523 may be less compressed than the fabric closest to the pivot point of the anvil 153516, requiring less force to cut.

In addition, the cutting edge 153509 and the wedge slider 153513 can reach the end of the fabric 153526 while in the fourth region 153523. When the beam with | 153514 reaches the fifth region 153525, the fabric 153526 can be completely separated.

The wedge slider 153513 can come into contact with one or more staple drivers 153511 at or near the end of the fabric.

The force to advance the beam with profile in | 153514 through the fifth region 153525 can be reduced and, in some examples, it can be similar to the force to drive the beam with profile in 1 153514 in the first region 153517. At the conclusion of the course of the firing member, the beam with profile in | 153514 can reach the final stroke position 153528. The positioning of the stroke regions of the firing member 153517, 153519, 153521, 153523, 153525 in Figure 82 is just an example.

In some examples, different regions can start at different positions along the geographic axis.

longitudinal ometric of the end actuator 153515, for example, based on the positioning of the fabric between the anvil 153516 and the staple cartridge 153518.

[0443] As discussed above and with reference now to Figures 80 to 82, the electric motor 153120 positioned inside the master controller of the surgical instrument can be used to advance and / or retract the trigger system of the shaft assembly drive, including the i-profile beam 153514, in relation to the end actuator 153502 of the drive shaft assembly in order to staple and / or cut the tissue captured inside the end actuator 153502. The beam with profile in | 153514 can be advanced or retracted at a desired speed, or within a desired speed range. The 153110 controller can be configured to control the speed of the beam with | 153514. The 153110 controller can be configured to predict the speed of the beam with | 153514 based on various parameters of the energy supplied to the 153120 electric motor, such as voltage and / or current, for example, and / or other operational parameters of the 153120 electric motor or external influences. The 153110 controller can be configured to predict the current speed of the beam with | 153514 based on the previous values of current and / or voltage supplied to the electric motor 153120 and / or the previous states of the system, such as speed, acceleration and / or position. The 153110 controller can be configured to detect the speed of the beam with profile in | 153514 using the absolute positioning sensor system described here. The controller can be configured to compare the predicted speed of the beam with | 153514 and the detected speed of the beam with profile in | 153514 to determine if the energy for the 153120 electric motor should be increased, in order to increase the speed of the beam with profile in | 153514 and / or decreased,

in order to decrease the speed of the beam with profile in | 153514.

[0444] The force acting on the beam with profile in | 153514 can be determined using several techniques. The force on the beam with profile in | 153514 can be determined by measuring the motor current 153120, in which the motor current 153120 is based on the load on the beam with profile | 153514 as it advances distally. The strength of the 153514 i-beam beam can be determined by placing a strain gauge on the drive member, on the firing member, on the 153514 i-profile beam, on the firing bar and / or at a proximal end of the cutting edge 153509. The strength of the beam with profile in | 153514 can be determined by monitoring the actual position of the beam with profile in | 153514 moving at an expected speed based on the current set speed of the engine 153120 after a predetermined period of time T, elapsed and by comparing the actual beam position with | 153514 in relation to the expected position of the beam with profile in | 153514 based on the current set speed of the 153120 engine at the end of the T1 period. Thus, if the real position of the beam with a profile in | 153514 is less than the expected position of the beam with profile in | 153514, the strength in the beam with profile in | 153514 is greater than a nominal force. On the other hand, if the actual position of the beam with | 153514 is greater than the expected position of the beam with profile in | 153514, the strength in the beam with profile in | 153514 is less than the nominal force. The difference between the actual and expected positions of the beam with profile in | 153514 is proportional to the deviation of the force in the beam with profile | 153514 from the nominal force.

[0445] Before starting a description of closed loop control techniques for the closing tube and firing member, the description briefly returns to Figure 83. Figure 83 is a 153600 graph representing two plots of closing force ( FTC)

153606, 153608 representing the force applied to a closing member to close on thick and thin tissue during a closing phase, and a 153601 plot of two plots of firing force (FTF) 153622, 153624 representing the applied force to a firing member to fire through thick, thin tissue during a firing phase.

With reference to Figure 83, the graph 153600 shows an example of the force applied to the thick and thin tissue during a closing stroke to close the end actuator 153502 in relation to the tissue trapped between the anvil 153516 and the staple cartridge 153518, in which the closing force is plotted as a function of time.

The closing force plots 153606, 153608 are plotted on two geometric axes.

A vertical geometric axis 153602 indicates the closing force (FTC) of the end actuator 153502 in Newtons (N). A 153604 horizontal geometric axis indicates time in seconds and is marked from to to t13 for clarity of the description.

The first closing force plot 153606 is an example of the force applied to the thick tissue during a closing stroke to close the end actuator 153502 in relation to the tissue stuck between the anvil 153516 and the staple cartridge 153518 and a second plot 153608 is an example of the force applied to the thin tissue during a closing stroke to close the end actuator 153502 in relation to the tissue trapped between the anvil 153516 and the staple cartridge 153518. The first and the second closing force plot 153606, 153608 are divided into three phases, a closing stroke (CLOSING), a waiting period (WAITING) and a triggering stroke (SHOOTING). During the closing stroke, a closing tube is moved distally (direction "DD") to move the anvil 153516, for example, in relation to the staple cartridge 153518 in response to the closing stroke acting by a closing motor. In other cases, the closing stroke involves the movement of the staple cartridge 153518 in relation to an anvil 153516 in response to the activation of the closing motor, and in other cases, the closing stroke involves the movement of the staple cartridge 153518 and the anvil 153516 in response to the activation of the closing motor. With reference to the first closing force plot 153606, during the closing stroke, the closing force 153610 increases from O to a maximum force F; from time to you. With reference to the second closing force graph 153608, during the closing stroke, the closing force 153616 increases from 0 to a maximum force F3 from time to ti. The relative difference between the maximum forces F1 and F3 is due to the difference in the closing force required for the thick tissue in relation to the thin tissue, where a greater force is required to close the anvil over the thick tissue in relation to the thin tissue.

[0446] The first and second plots of closing force 153606, 153608 indicate that the closing force on end actuator 153502 increases during an initial hold period ending in time (t1). The closing force reaches a maximum force (F1, F3) in time (t1). The initial hold period can be about one second, for example. A waiting period can be applied before starting a trip course. The waiting period allows fluid to escape from the compressed tissue through the end actuator 153502, which reduces the thickness of the compressed tissue by producing a smaller gap between the anvil 153516 and the staple cartridge 153518 and a reduction in strength closing period at the end of the waiting period. With reference to the first closing force plot 153606, there is a nominal drop in closing force 153612 from F1 to F2 during the waiting period between t; and ok. Similarly, with reference to the second closing force plot

ment 153608, the closing force 153618 nominally falls from F; 3 to Fa during the waiting period between t; and ok. In some examples, a waiting period (t1 to t1) selected from a range of about 10 seconds to about 20 seconds is typically used. In the example of the first and second closing force plot 153606, 153608, a period of about 15 seconds is used. The waiting period is followed by the triggering stroke, which typically lasts for a period selected from a range of about 3 seconds, for example, to about 5 seconds, for example. The closing force decreases as the beam with i-profile 153514 is advanced in relation to the end actuator through the firing stroke. As indicated by the closing force 153614, 153620 of the first and the second closing force plot 153606, 153608, respectively, the closing force 153614, 153620 exerted on the closing tube drops precipitously from the time of about ta to the time of about of ts. The time ta represents the moment when the beam with i-profile 153514 is coupled to the anvil 153516 and begins to assume the closing load. Consequently, the closing force decreases as the firing force increases as shown by the first and second firing force plots 153622, 153624.

[0447] Figure 83 also represents a graph 153601 of the first and second plot of the firing force 153622, 153624 that plots the applied force to advance the beam with profile in | 153514 during the course of firing a surgical instrument or system according to the present disclosure. The plots of the firing force 153622, 153624 are plotted on two geometric axes. A vertical geometric axis 153626 indicates the firing force, in Newtons (N), applied to advance the beam with an i-profile 153514 during the firing stroke. The beam with i-profile 153514 is configured to advance a knife or cutting element and motivate the drivers to implant the clamps during the firing stroke. A horizontal geometric axis 153605 indicates the time in seconds on the same time scale as the horizontal geometric axis 153604 of the top graph

153600.

[0448] As previously described, the strength of the closing tube drops precipitously from time t 'to the time of about ts, which represents the moment when the beam with i-profile 153514 is coupled to the anvil 153516 and it begins to receive the load and the closing force decreases as the firing force increases, as shown by the first and second plots of the firing force 153622, 153624. The beam with profile in | 153514 is advanced from the start position of the stroke at time t, to the end positions of the stroke between tg and ta for plotting the firing force 153624 for thin tissue and at t13 for plotting the firing force 153622 for the thick tissue. As the i-profile beam 153514 is advanced distally during the firing stroke, the closing assembly delivers control of the staple cartridge 153518 and the anvil 153516 to the firing assembly, which causes the firing force to increase and the closing force decreases.

[0449] In the firing force plot of the thick tissue 153622, during the firing period (SHOOTING), plot 153622 is divided into three distinct segments. A first segment 153628 indicates the firing force, as it increases from O a ta to a peak of force F ', just before ts. The first segment 153628 is the firing force during the initial phase of the firing stroke when the i-beam beam 153514 advances distally from the top of the closing ramp until the i-beam beam 153514 comes into contact with the fabric. A second segment 153630 indicates the firing force during a second phase of the firing stroke in which the i-profile beam 153514 is advancing distally by implanting staples and cutting the fabric. During the second phase of the firing stroke, the firing force drops from F '; to F'2 at about t12. A third segment 153632 indicates the firing force during the third and last phase of the firing stroke when the beam with i-profile 153514 leaves the fabric and advances to the end of the course in a non-woven zone. During the third phase of the firing stroke, the firing force drops from F'2 to zero (0) at about t13 where the beam with i-shaped profile 153514 reaches the end of the stroke. In summary, during the firing stroke, the firing force increases dramatically as the i-profile beam 153514 enters a fabric zone, steadily decreases in the fabric zone during the stapling and cutting operation and it falls dramatically as the i-profile beam 153514 leaves the fabric zone and enters a non-fabric zone at the end of the course.

[0450] The thin tissue firing force plot 153624 follows a similar pattern to the thick tissue firing force plot 153622. Thus, during the first phase of the firing stroke, the firing force 153634 increases dramatically from O to F '; in about ts. During the second phase of the firing stroke, firing force 153636 drops steadily from F'3 to F's at about ts. During the final phase of the firing stroke, firing force 153638 drops dramatically from F's to O between tg and to.

[0451] To overcome the drastic drop in the closing force from time ta to around time ts, which represents the moment when the beam with profile in | 153514 engages the anvil 153516 and begins to receive the load and the closing force decreases as the firing force increases, as shown by the first and second firing force plots 153622, 153624, the closing tube can be advanced distally as the firing member, such as the beam with profile in | 153514, advances distally. The closing tube is represented as the transmission element that applies a closing force to the 153516 anvil. As described here, a control circuit applies motor set points to the motor control that applies a motor control signal. motor to motor to drive the transmission element and advance the closing tube distally to apply a closing force to the 153516 anvil. A torque sensor coupled to a motor output drive shaft can be used to measure the force applied to the pipe closing. In other respects, the closing force can be measured with an effort meter, a load cell or other suitable force sensors.

[0452] Figure 84 is a diagram of a 153950 control system configured to provide progressive closure of a closing member (for example, a closing tube) when the firing member (for example, the profile beam) in i 153514) advances distally and is coupled to a clamping arm (for example, anvil 153516) to decrease the load of the closing force on the closing member at a desired speed and to decrease the load of the firing force on the member according to at least one aspect of the present disclosure. In one aspect, the 153950 control system can be implemented as a nested PID feedback controller. A PID controller is a feedback loop mechanism for the control circuit (controller) to continuously calculate an error value such as the difference between a desired setpoint and a measured process variable and apply a correction based on proportional, integral terms. and derivatives (sometimes indicated P, |, and D respectively). The 153950 nested PID controller feedback control system includes a primary controller 153952, on a primary (external) feedback circuit 153954 and a secondary controller 153955 on a secondary (internal) feedback circuit 153956. The primary controller 153952 can be a PID controller 153972, as shown in Figure 84, and the secondary controller 153955 can also be a PID controller 153972 as shown in Figure 85. The primary controller 153952 controls a primary process 153958 and the secondary controller 153955 controls a secondary process 153960. Output 153966 of primary processor 153958 (OUTPUT) is subtracted from a primary setpoint SP; by a first adder 153962. The first adder 153962 produces a single output sum signal that is applied to the primary controller 153952. The output of the primary controller 153952 is the secondary setpoint SP2. Output 153968 of secondary processor 153960 is subtracted from a primary setpoint SP2 by a first adder 153964.

[0453] In the context of controlling the displacement of the closing tube, the 153950 control system can be configured so that the primary setpoint SP is a desired closing force value and the primary controller 153952 is configured to receive the closing force from the torque sensor coupled to the output of the closing motor and to determine a motor speed from setpoint SP2 to the closing motor. In other respects, the closing force can be measured with strain gauges, load cells, or other suitable force sensors. The SP2 closing motor speed setpoint is compared to the actual closing tube speed, which is determined by the secondary controller 153955. The actual closing tube speed can be measured by comparing the displacement of the closing tube. closing with the position sensor and measuring the elapsed time with a timer / counter. Other techniques, such as linear or rotary encoders, can be used to measure the displacement of the closing tube. Output 153968 of the secondary process

Daily 153960 is the actual speed of the closing tube. This output of the closing tube speed 153968 is provided to the primary processor 153958 which determines the force acting on the closing tube and is fed back to the adder 153962, which subtracts the measured closing force from the primary setpoint SP1 . The main setpoint SP, can be an upper threshold or a lower threshold. Based on the output of the 153962 adder, the primary controller 153952 controls the speed and direction of the closing tube motor as described here. The secondary controller 153955 controls the speed of the closing motor based on the actual speed of the closing tube measured by the secondary process 153960 and the secondary setpoint SP2, which is based on a comparison of the upper and lower limits of the firing force and the actual firing force.

[0454] Figure 85 illustrates a PID 153970 feedback control system, in accordance with at least one aspect of this disclosure. Primary controller 153952 or secondary controller 153955, or both, can be implemented as a PID controller 153972. In one aspect, PID controller 153972 can comprise a proportional element 153974 (P), an integral element 153976 (|), and a derivative element 153978 (D). The outputs of elements P, | and D 153974, 153976, 153978 are added by an adder 153986, which provides the control variable u (t) to the process

153980. Process output 153980 is the process variable y (t). A 153984 adder calculates the difference between a desired setpoint r (t) and a measured process variable y (t). The PID controller 153972 continuously calculates an error value e (t) (for example, the difference between the limit of the closing force and the measured closing force) as the difference between a desired setpoint r (t) ( for example, the closing force limit) and the process variable

are measured y (t) (for example, the speed and direction of the closing tube) and apply a correction based on the proportional, integral and derivative terms calculated by the proportional element 153974 (P), the integral element 153976 ( |), and the derivative element 153978 (D), respectively. The PID controller 153972 tries to minimize the error e (t) over time by adjusting the control variable u (t) (for example, the speed and direction of the closing tube).

[0455] According to the PID algorithm, the "P" element 153974 represents the present error values. For example, if the error is large and positive, the control output will also be large and positive. According to the present disclosure, the error term e (t) is the difference between the desired closing force and measured closing force of the closing tube. The "I" element 153976 represents the past error values. For example, if the current output is not strong enough, the integral of the error will accumulate over time, and the controller will respond by applying a stronger action. The "D" element 153978 represents possible future trends of the error, based on its actual rate of change. For example, continuing example P above, when the large positive control output succeeds in bringing the error closer to zero, it also puts the process in a major negative error mode in the near future. In this case, the derivative becomes negative and module D reduces the force of the action to avoid this excess.

[0456] It will be understood that other variables and set points can be monitored and controlled according to the feedback control systems 153950, 153970. For example, the adaptive closing member speed control algorithm described here can mediate the least two of the following parameters: the location of the firing member, the firing of the firing member, the displacement of the cutting element, the speed of the cutting element

the location of the closing tube, the loading of the closing tube, among others.

[0457] Figure 86 is a logical flowchart that represents a control program 153990 process or a logical configuration to determine the speed of a closing member, according to at least one aspect of the present disclosure. A control circuit of a surgical instrument or system according to the present disclosure is configured to determine 153992 the actual closing force of a closing member. The control circuit compares 153994 the actual closing force to a limit closing force and determines 153996 a setpoint speed for displacing the closing member based on the comparison. The control circuit controls 153998 the actual speed of the closing member based on the setpoint speed.

[0458] Now with reference also to Figures 84 and 85, in one aspect, the control circuit comprises a proportional, integral and derivative feedback system (PID) 153950,

153970. The PID 153950 feedback control system, 153970 comprises a primary PID feedback loop 153954 and a secondary PID feedback loop 153956. Primary feedback loop 153954 determines a first error between the actual closing force of the closing member and a limit closing force SP, and defines the speed setting point of the closing member SP2 based on the first error . Secondary feedback loop 153956 determines a second error between the actual speed of the closing member and the setpoint speed of the closing member and defines the speed of the closing member based on the second error.

[0459] In one aspect, the closing force limit SP comprises an upper limit and a lower limit. The SP setpoint speed? is configured to advance the closing member distally when the actual closing force is less than the lower limit and the setpoint speed is configured to retract the closing member proximally when the actual closing force is greater than the lower limit. In one respect, the setpoint speed is set to keep the closing member in place when the actual closing force is between the upper and lower limits.

[0460] In one aspect, the control system additionally comprises a force sensor (for example, any of the sensors 472, 474, 476 (Figure 12), for example) coupled to the control circuit. A force sensor is configured to measure the closing force. In one aspect, the force sensor comprises a torque sensor coupled to an output drive shaft of a motor coupled to the closing member. In one aspect, the force sensor comprises an effort meter coupled to the closing member. In one aspect, the force sensor comprises a load cell coupled to the closing member. In one aspect, the control system comprises a position sensor coupled to the closing member, the position sensor being configured to measure the position of the closing member.

[0461] In one aspect, the control system comprises a first motor configured to couple the closing member and the control circuit is configured to advance the closing member during at least a portion of a firing stroke.

[0462] The functions or processes 153990 described in the present invention can be performed by any of the processing circuits described here. Aspects of the motorized surgical instrument can be practiced without the specific details revealed here. Some aspects were shown as block diagrams instead of details.

[0463] Parts of this disclosure can be presented in terms of instructions that operate on data stored in a computer's memory. An algorithm refers to a self-consistent sequence of steps that lead to the desired result, in which a "step" refers to the manipulation of physical quantities that can take the form of electrical or magnetic signals that can be stored, transferred, combined, compared and manipulated in any other way. These signs can be called bits, values, elements, symbols, characters, terms, numbers. These terms and similar terms can be associated with the appropriate physical quantities and are merely convenient identifications applied to these quantities.

[0464] In general, the aspects described here, which can be implemented, individually and / or collectively, by a wide range of hardware, software, firmware, or any combination of them, can be seen as being composed of various types of "electrical circuits". Consequently, the term "electrical circuit" includes electrical circuits that have at least one electrical circuit isolated, electrical circuits that have at least one integrated circuit, electrical circuits that have at least one integrated circuit for specific application. , electrical circuits that form a general-purpose computing device configured by a computer program (for example, a general-purpose computer or processor configured by a computer program that at least partially executes processes and / or devices described herein, electrical circuits that form a memory device (for example, forms of random access memory) and / or electrical circuits that form a communications device (for example, a modem, routers or optical-electrical equipment). positive aspects

be implemented in analogue or digital form, or combinations thereof.

[0465] The previously mentioned description presented aspects of the devices and / or processes through the use of block diagrams, flowcharts, and / or examples, which may contain one or more functions and / or operation. Each function and / or operation within such block diagrams, flowcharts or examples can be implemented, individually and / or collectively, by a wide range of hardware, software, firmware or virtually any combination of them. In one aspect, several portions of the subject described here can be implemented by means of specific application integrated circuits (ASICs), field programmable port arrangements (FPGAs), digital signal processors (DSPs), programmable logic devices (PLDs), circuits, registers and / or software components, for example, programs, subroutines, logic and / or combinations of hardware and software components. Logic gates or other integrated formats. Some aspects revealed here, in whole or in part, can be implemented in an equivalent way in integrated circuits, such as one or more computer programs running on one or more computers (for example, as one or more programs operating on one or more computers). computer systems), as one or more programs operating on one or more processors (for example, as one or more programs operating on one or more microprocessors), as firmware, or virtually as any combination thereof, and to design the circuitry and / or writing the code for the software and firmware would be within the scope of practice of a person skilled in the art in the light of this disclosure.

[0466] The mechanisms of the revealed subject can be distributed as a program product in a variety of ways, and an illustrative aspect of the subject described here is applicable regardless

regardless of the specific type of signal transmission media used to effectively perform the distribution. Examples of a signal transmission medium include, but are not limited to, the following: recordable type media such as a floppy disk, a hard disk drive, a compact disc (CD), a digital video disc (DVD), a tape digital, computer memory, etc .; and transmission-type media, such as digital and / or analog communication media (for example, a fiber optic cable, a waveguide, a wired communication link, a wireless communication link (for example example, transmitter, receiver, transmission logic, reception logic, etc.).

[0467] The previously mentioned description of one or more aspects was presented for purposes of illustration and description. This description is not intended to be exhaustive or to limit the invention to the precise form disclosed. Modifications or variations are possible in light of the above teachings. These aspects were chosen and described with the purpose of illustrating the principles and practical application, thus allowing the person skilled in the art to use the various aspects and with several modifications, as they are convenient to the specific use contemplated. It is intended that the claims presented in the annex define the global scope. Situational recognition

[0468] Situational recognition is the ability of some aspects of a surgical system to determine or infer information related to a surgical procedure from data received from databases and / or instruments. The information may include the type of procedure being performed, the type of tissue being operated on, or the body cavity that is the object of the procedure. With contextual information related to the surgical procedure, the surgical system can, for example, improve the way in which it controls the modular devices (for example a robotic arm and / or robotic surgical instrument) that are connected to it and provide contextualized information or suggestions to the surgeon during the course of the surgical procedure.

[0469] With reference now to FIG. 87, a timeline 5200 is shown that represents the situational recognition of a central controller, such as central surgical controller 106 or 206, for example. Timeline 5200 is an illustrative surgical procedure and the contextual information that the central surgical controller 106, 206 can derive from data received from data sources at each stage in the surgical procedure. Timeline 5200 represents typical steps that would be taken by nurses, surgeons, and other medical personnel during the course of a pulmonary segmentectomy procedure, starting with the setup of the operating room and ending with the transfer of the patient to a post-op recovery room.

[0470] Situational recognition of a central surgical controller 106, 206 receives data from data sources throughout the course of the surgical procedure, including data generated each time medical personnel use a modular device that is paired with the central surgical controller 106, 206. Central surgical controller 106, 206 can receive this data from paired modular devices and other data sources and continuously derives inferences (ie contextual information) about the ongoing procedure as new data is received, as which step of the procedure is being performed at any given time. The situational recognition system of the central surgical controller 106, 206 is, for example, able to record data referring to the procedure to generate reports, verify the steps being taken by medical personnel, provide data or warnings (for example , via a display screen) that may be relevant for the specific step of the procedure, adjust the modular devices based on the context (for example, activate monitors, adjust the field of view (FOV) of the medical imaging device, or change the energy level of an ultrasonic surgical instrument or RF electrosurgical instrument), and take any other action described above.

[0471] In the first step 5202, in this illustrative procedure, members of the hospital team retrieve the electronic patient record (PEP) from the hospital's PEP database. Based on patient selection data in the PEP, the central surgical controller 106, 206 determines that the procedure to be performed is a thoracic procedure.

[0472] In the second step 5204, the team members scan the incoming medical supplies for the procedure. Central surgical controller 106, 206 cross-references the scanned supplies with a list of supplies that are used in various types of procedures and confirms that the supply mix corresponds to a thoracic procedure. In addition, the central surgical controller 106, 206 is also able to determine that the procedure is not a wedge procedure (because the inlet supplies have an absence of certain supplies that are necessary for a thoracic wedge procedure or, otherwise, that inlet supplies do not correspond to a thoracic wedge procedure).

[0473] In the third step 5206, the medical staff scans the patient's band with a CT scanner that is communicably connected to the central surgical controller 106, 206. The central surgical controller 106, 206 can then confirm the patient's identity with based on the scanned data.

[0474] In the fourth step 5208, the medical staff connects the equipment

auxiliary. The auxiliary equipment being used may vary according to the type of surgical procedure and the techniques to be used by the surgeon, but in this illustrative case they include a smoke evacuator, an insufflator and a medical imaging device. When activated, auxiliary equipment that is modular devices can automatically pair with the central surgical controller 106, 206 which is located within a specific vicinity of the modular devices as part of its initialization process. The central surgical controller 106, 206 can then derive contextual information about the surgical procedure by detecting the types of modular devices that correspond with it during this preoperative or initialization phase. In this particular example, the central surgical controller 106, 206 determines that the surgical procedure is a VATS (video-assisted thoracic surgery) procedure based on this specific combination of paired modular devices. Based on the combination of data from the electronic patient record (PEP), the list of medical supplies to be used in the procedure, and the type of modular devices that connect to the central controller, the central surgical controller 106, 206 can, in general , infer the specific procedure that the surgical team will perform. After the central surgical controller 106, 206 recognizes which specific procedure is being performed, the central surgical controller 106, 206 can then retrieve the steps of that process from a memory or from the cloud and then cross over the data that subsequently receives from connected data sources (for example, modular devices and patient monitoring devices) to infer which stage of the surgical procedure the surgical team is performing.

[0475] In the fifth step 5210, the team members fix the elements

electrocardiogram (ECG) trodes and other patient monitoring devices on the patient. ECG electrodes and other patient monitoring devices are able to pair with the central surgical controller 106, 206. As central surgical controller 106, 206 begins to receive data from the patient's monitoring devices, the central surgical controller 106, 206 thus confirms that the patient is in the operating room.

[0476] In the sixth step 5212, medical personnel induced anesthesia in the patient. Central surgical controller 106, 206 can infer that the patient is under anesthesia based on data from modular devices and / or patient monitoring devices, including ECG data, blood pressure data, ventilator data, or combinations of them, for example. After the completion of the sixth step 5212, the preoperative portion of the lung segmentectomy procedure is completed and the operative portion begins.

[0477] In the seventh step 5214, the lung of the patient who is being operated on is retracted (while ventilation is switched to the contralateral lung). The central surgical controller 106, 206 can infer from the ventilator data that the patient's lung has been retracted, for example. The central surgical controller 106, 206 can infer that the operative portion of the procedure started when it can compare the detection of the patient's lung collapse in the expected stages of the procedure (which can be accessed or retrieved earlier) and thus determine that lung retraction is the first operative step in this specific procedure.

[0478] In the eighth step 5216, the medical imaging device (for example, a visualization device) is inserted and the video from the medical imaging device is started. Central surgical controller 106, 206 receives data from the medical imaging device (i.e., video or image data) through its connection to the medical imaging device.

After receiving data from the medical imaging device, central surgical controller 106, 206 can determine that the portion of the laparoscopic surgical procedure has started.

In addition, the central surgical controller 106, 206 can determine that the specific procedure being performed is a segmentectomy, rather than a lobectomy (note that a wedge procedure has already been discarded by the central surgical controller 106, 206 with based on the data received in the second step 5204 of the procedure). The medical imaging device data 124 (Figure 2) can be used to determine contextual information about the type of procedure being performed in a number of different ways, including by determining the angle at which the medical imaging device is. oriented towards visualizing the patient's anatomy, monitor the number or medical imaging devices being used (ie, that are activated and paired with the central surgical controller 106, 206), and monitor the types of display used.

For example, a technique to perform a VATS lobectomy places the camera in the lower anterior corner of the patient's chest cavity above the diaphragm, while a technique to perform a VATS segmentectomy places the camera in an anterior inter-costal position in relation to the segment fissure. .

With the use of standard recognition or machine learning techniques, for example, the situational recognition system can be trained to recognize the positioning of the medical imaging device according to the visualization of the patient's anatomy.

As another example, a technique for performing a VATS lobectomy uses a single medical imaging device, while another technique for performing a VATS segmentectomy uses multiple cameras.

As yet another example, a technique for performing a VATS segmentectomy uses an infrared light source (which can be connected in a communicable way to the central surgical controller as part of the visualization system) to visualize the segment crack, which it is not used in a VATS lobectomy. By tracking any or all of these data from the medical imaging device, the central surgical controller 106, 206 can thus determine the specific type of surgical procedure being performed and / or the technique being used for a specific type of procedure surgical.

[0479] In the ninth step 5218 of the procedure, the surgical team starts the dissection step. Central surgical controller 106, 206 can infer that the surgeon is in the process of dissecting to mobilize the patient's lung because he receives data from the RF or ultrasonic generator that indicate that an energy instrument is being triggered. The central surgical controller 106, 206 can cross-check the received data with the steps retrieved from the surgical procedure to determine that an energy instrument is being fired at that point in the process (that is, after completion of the steps previously discussed in the procedure) corresponds to the dissection step. In certain cases, the energy instrument can be a power tool mounted on a robotic arm of a robotic surgical system.

[0480] In the tenth step 5220 of the procedure, the surgical team proceeds to the connection step. The central surgical controller 106, 206 can infer that the surgeon is ligating the arteries and veins because he receives data from the stapling and surgical cutting instrument indicating that the instrument is being fired. Similar to the previous step, the central surgical controller 106, 206 can derive this inference by crossing the reception data of the stapling and surgical cutting instrument with the steps recovered in the procedure.

cess. In certain cases, the surgical instrument can be a surgical tool mounted on a robotic arm of a robotic surgical system.

[0481] In the eleventh step 5222, the segmentectomy portion of the procedure is performed. Central surgical controller 106, 206 can infer that the surgeon is transecting the parenchyma based on data from the surgical stapling and cutting instrument, including data from its cartridge. The cartridge data can correspond to the size or type of clamp being triggered by the instrument, for example. As different types of staples are used for different types of fabrics, the cartridge data can thus indicate the type of fabric being stapled and / or transected. In this case, the type of clamp that is fired is used for the parenchyma (or other similar types of tissue), which allows the central surgical controller 106, 206 to infer which segment of the procedure is being performed.

[0482] In the twelfth step 5224, the node dissection step is then performed. The central surgical controller 106, 206 can infer that the surgical team is dissecting the node and performing a leak test based on the data received from the generator that indicates which ultrasonic or RF instrument is being fired. For this specific procedure, an RF or ultrasonic instrument being used after the parenchyma has been transected corresponds to the node dissection step, which allows the central surgical controller 106, 206 to make this inference. It should be noted that surgeons regularly alternate between surgical stapling / cutting instruments and surgical energy instruments (that is, RF or ultrasonic) depending on the specific step in the procedure because different instruments are better adapted for such specific changes. Therefore, the specific sequence in which the instru-

cutting / stapling instruments and surgical energy instruments are used can indicate which step of the procedure the surgeon is performed on. In addition, in certain cases, robotic tools can be used for one or more steps in a surgical procedure and / or Hand held surgical instruments can be used for one or more steps in the surgical procedure. The surgeon can switch between robotic tools and hand-held surgical instruments and / or can use the devices simultaneously, for example. After the completion of the twelfth stage 5224, the incisions are closed and the post-operative portion of the process begins.

[0483] In the thirteenth stage 5226, the patient's anesthesia is reversed. The central surgical controller 106, 206 can infer that the patient is emerging from anesthesia based on ventilator data (that is, the patient's respiratory rate begins to increase), for example.

[0484] Finally, in the fourteenth step 5228 is that medical personnel remove the various patient monitoring devices from the patient. Central surgical controller 106, 206 can therefore infer that the patient is being transferred to a recovery room when the central controller loses ECG, blood pressure and other data from patient monitoring devices. As can be seen from the description of this illustrative procedure, the central surgical controller 106, 206 can determine or infer when each step of a given surgical procedure is taking place according to the data received from the various data sources that are communicably coupled to the central surgical controller 106, 206.

[0485] Situational recognition is further described in US provisional patent application serial number 62 / 611,341, entitled INTERACTIVE SURGICAL PLATFORM, filed on December 28, 2017, which is hereby incorporated by reference in its entirety . In certain cases, the operation of a robotic surgical system, including the various robotic surgical systems disclosed herein, for example, can be controlled by the central controller 106, 206 based on its situational recognition and / or feedback from the components of the same and / or based on information from the cloud

104.

Safety systems for intelligent surgical stapling equipped with motor

[0486] Several aspects of the present disclosure are directed to improved security systems capable of adapting, controlling, and / or adjusting internal actuation operations of a surgical instrument in response to tissue parameters detected through one or more of the sensor. surgical instrument. According to at least one aspect, a force detected, by means of one or more of a sensor, in the claws of an end actuator may be of a magnitude that prohibits one or more of a subsequent / additional functionality of the end actuator be carried out. According to another aspect, a metallic object can be detected, by means of one or more of a sensor, as inside the claws of the end actuator which prohibits one or more of a subsequent / additional functionality of the end actuator to be realized. Figure 88 illustrates a surgical system 23000 comprising a surgical instrument 23002, a central surgical controller 23004, and a user interface 23006. In such an aspect, surgical instrument 23002 can comprise one or more of a 23008 sensor and the parameters detected by one or more of a sensor 23008 of the surgical instrument 23002 can be transmitted / communicated (for example, wirelessly) to a control circuit 23010 of the central surgical controller 23004. In addition, in this respect, the central surgical controller 23004 can be configured to determine whether a surgical function (eg, dissecting, clamping, coagulating, stapling, cutting, rotating, articulating, etc.) associated with a component (eg, end actuator, drive shaft, etc.) of the surgical instrument 23002 can be safely performed based on the parameters detected by one or more of a sensor 23008 of the surgical instrument 23002. Notably, in this aspect, the controller Central surgical or 23004 can be configured to transmit / communicate one or more results (that is, a warning associated with the surgical function, a reason why the surgical function is prevented, etc.) associated with this determination of the interface of the user 23006. Additionally, in accordance with various aspects, various user interfaces disclosed herein may comprise a selectable user interface feature (eg, cancellation element 23012) to proceed with the surgical function, despite any warnings and / or reasons that support prevention. Notably, in such aspects, such a user interface feature (for example, cancellation element 23012) may not be displayed (for example, performing the surgical function may endanger the patient).

[0487] With reference to Figure 89, according to various aspects of the present disclosure, a 23100 surgical system may comprise a control circuit (23112, 23122, 23132 and / or 23142, for example, in dashed line to show locations optional), a user interface (23118, 23128, 23138, 23148 and / or 23158, for example, dashed line to show optional locations) and a 23102 surgical instrument including, for example, a 23110 handle set, a drive shaft assembly 23120 and an end actuator assembly 23130. In such aspects, the control circuit can be integrated into one or more of a component (for example, the handle assembly 23110, the drive shaft assembly drive 23120 and / or the end actuator set 23130, etc.) of surgical instrument 23102 (for example, 23112, 23122 23142, and / or 23132) and / or integrated with a central surgical controller 23140 (for example, 23142) paired (for example, wireless ) with the surgical instrument 23102. Notably, according to several aspects, the surgical instrument 23102 and / or the central surgical controller 23140 can be a surgical instrument with situational recognition and / or a central surgical controller with recognition situational. Situational recognition refers to the ability of a surgical system, for example, 23100, to determine or infer information related to a surgical procedure from data received from databases (for example, historical data associated with a surgical procedure, for example, 23149 and / or 23150) and / or surgical instruments (for example, sensor data during a surgical procedure). For example, determined or inferred information may include the type of procedure being performed, the type of tissue being operated on, the body cavity that is the subject of the procedure, etc. Based on this contextual information related to the surgical procedure, the surgical system can, for example, control a paired surgical instrument 23102 or a component thereof (for example, 23110, 23120 and / or 23130) and / or provide information or su - contextualized management to a surgeon during the entire course of the surgical procedure (for example, through user interface 23118, 23128, 23138, 23148 and / or 23158). Additional details regarding situational awareness can be found, for example, above under the heading "Situational Awareness".

[0488] Also in Figure 89, according to one aspect, a central surgical controller with situational recognition 23140 is paired (for example, wireless) with a surgical instrument 23102 being used to perform a surgical procedure. In such an aspect, the surgical instrument 23102 may comprise a set of end actuator 23130, including a first jaw, a second jaw pivotally coupled to the first jaw, and a sensor 23134 configured to detect a parameter associated with a function (for example, dissecting, holding, coagulating, cutting, stapling, etc.) from the end actuator set 23130 and to transmit the detected parameters to a control circuit 23142 of the central surgical controller 23140.

[0489] In addition, in this respect, the surgical instrument 23102 can additionally comprise a set of drive shaft 23120 that includes a sensor 23124 configured to detect a parameter associated with a function (for example, rotation, articulation , etc.) of the drive shaft assembly 23120 and to transmit the detected parameter to the control circuit 23142 of the central surgical controller 23140. Notably, it should be understood that a sensor, as mentioned here and in other aspects revealed, it can comprise a plurality of sensors configured to detect a plurality of parameters associated with a plurality of end actuator set and / or drive shaft set functions. Thus, in addition, in such an aspect, the control circuit of central surgical controller 23142 can be configured to receive detected parameters (for example, sensor data) from such sensors 23134 and / or 23124 throughout the course of the surgical procedure.

[0490] A detected parameter can be received each time an associated 23130 end actuator set function (eg dissection, gripping, coagulation, cutting, stapling, etc.) and / or a drive shaft set function associated 23120 (for example, rotation, articulation, etc.) is performed. The control circuit of the central surgical controller 23142 can be additionally configured to receive data from an internal database (for example, a database of the central surgical controller 23149) and / or an external database (for example, from a database in the cloud 23150) during the entire course of the surgical procedure. According to various aspects, the data received from internal and / or external databases may comprise procedural data (for example, steps to perform the surgical procedure) and / or historical data (for example, data indicating pa- expected parameters based on historical data associated with the surgical procedure).

[0491] In several respects, procedural data may comprise current / recognized standard care procedures for the surgical procedure and historical data may comprise preferred / ideal parameters and / or ranges of preferred / ideal parameters based on in historical data associated with the surgical procedure (for example, system-defined restrictions). Based on the data received (eg sensor data, internal and / or external data, etc.), the control circuit of the central surgical controller 23142 can be configured to continuously derive inferences (for example, contextual information) about the surgical procedure in progress. That is, the central surgical controller with situational recognition of the situation can be configured, for example, to record data related to the surgical procedure to generate reports, check the steps that are being taken by the surgeon to perform the surgical procedure, provide data or warnings (for example, through a user interface associated with the central surgical controller with situational recognition and / or the surgical instrument, for example, 23148, 23158, 23118, 23128, and / or 23138) that may be relevant to a certain procedural stage

control a function of a surgical instrument, etc. According to several aspects, the central surgical controller with situational recognition 23140 can (for example, after an initial surgical function of the end actuator set 23130 or drive shaft set 23120 is performed) to infer a next surgical function to be carried out on the basis of procedural data received from an internal database 23149 and / or an external database 23150.

[0492] Additionally, in such an aspect, the central surgical controller with situational recognition 23140 can evaluate detected parameters (for example, received from sensors 23134 and / or 23124 in response to the initial surgical function) based on historical data cos received from internal database 23149 and / or external database 23150 (for example, preferred / ideal parameters). Here, if the detected parameters do not exceed the preferred / ideal parameters and / or are within the respective ranges of preferred / ideal parameters, the central surgical controller with situational recognition 23140 can allow the next surgical function performed and / or does not prevent / control that the next surgical function is performed. Alternatively, if the detected parameters exceed the preferred / ideal parameters and / or are not within the respective preferred / ideal parameter ranges, the central surgical controller with situational recognition 23140 can proactively prevent the execution of the next surgical function.

[0493] According to another aspect of the present disclosure, the central surgical controller with situational recognition 23140 can receive a communication (for example, from a component, for example, 23130 and / or 23120, from the surgical instrument 23102) that a function specific surgical procedure is being attempted / requested / performed. In this respect, the 23140 situational recognition central surgical controller can compare that specific surgical function with an upcoming inferred surgical function to ensure that current / recognized standard treatment procedures are being adhered to. If so, the central surgical controller with situational recognition 23140 can then evaluate detected parameters (for example, as described) before allowing the specific surgical function to proceed (as described). Otherwise, the central surgical controller with situational recognition 23140 can prevent this specific surgical function from being performed or prevent this specific surgical function from being performed until a cancellation is received (for example, through a user interface 23, 158 , 23148, 23138, 23128 and / or 23118, see, for example, Figure 88, selectable user interface element 23012). In such an aspect, if cancellation is received, the 23140 situational recognition central surgical controller can then evaluate detected parameters before allowing the specific surgical function to proceed (as described).

[0494] Again with reference to Figure 89, according to another aspect, a surgical instrument with situational recognition 23102 can be used to perform a surgical procedure. In such an aspect, surgical instrument 23102 also includes a handle set 23110, a drive shaft set 23120 and an end actuator 23130. The end actuator set 23130 may include a first claw, a second claw attached pivotally attached to the first claw, and a 23134 sensor configured to detect a parameter associated with a function (for example, dissecting, holding, coagulating, cutting, stapling, etc.) of the 23130 end actuator assembly and to transmit the detected parameters to a control circuit (23112, 23122, 23132 and / or 23142, for example, in dashed line to show optional locations.

[0495] For example, in this respect, the detected parameter can be transmitted to a control circuit 23132 of the end actuator set 23130. Here, the end actuator set of the control circuit 23132 can be configured to receive detected parameters (eg sensor data) from sensor 23134 during the entire course of the surgical procedure. A detected parameter can be received each time an associated function of the 23130 end actuator set (for example, dissection, fixation, coagulation, cutting, stapling, etc.) is performed.

[0496] The end actuator set 23130 can be additionally configured to receive data from an internal database (for example, an end actuator memory 23136) and / or an external database (for example, a cloud database 23150 via a central surgical controller 23140, a central surgical controller database 23149, etc.) over the course of the surgical procedure. According to several aspects, the data received from the internal and / or external databases may comprise staple cartridge data (for example, staple sizes and / or types associated with a staple cartridge positioned in the actuator assembly). end) and / or historical data (for example, data indicating expected fabrics and / or types of staples to be stapled with historical data). In many respects, the data received may comprise preferred / ideal parameters and / or preferred / ideal parameter ranges associated with those sizes and / or types of staples or those woven and / or expected types of fabric, based on historical data (for example, system-defined restrictions). Based on the received data (for example, sensor data, internal and / or external data, etc.), the control circuit of the end actuator 23132 can

to be configured to continually derive inferences (for example, contextual information) about the current surgical procedure.

Notably, according to an alternative aspect, sensor 23134 of end actuator set 23130 can transmit the detected parameter to a control circuit (for example, 23112 and / or 23122) associated with another component of the 23102 surgical instrument, for example, the handle assembly 23110 and / or the drive shaft assembly 23120. In this respect, this other surgical instrument component control circuit (for example, 23112 and / or 23122) can be configured to perform the various aspects of the 23132 end actuator control circuit, as described above.

In addition, according to various aspects, the drive shaft assembly 23120 of the surgical instrument 23102 may include a sensor 23124 configured to detect a parameter associated with a function (for example, rotation, articulation, etc.) of the assembly drive axis 23120 and transmit the detected parameter to a control circuit (for example, 23112) similarly configured to perform the various aspects of the control circuit of the end actuator 23132 as described above.

In the end, the surgical instrument with situational recognition 23102 can be configured to, for example, alert its user to a discrepancy (for example, via a 23138 user interface of the 23130 end actuator set, via a user interface (for example 23128 and / or 23118) of another surgical instrument component 23102, for example, the drive shaft assembly 23120 and / or the handle assembly 23110 and / or via a user interface 23148 and / or 23158 associated with a central surgical controller 23140 coupled to surgical instrument 23102). For example, the discrepancy may include a detected parameter that exceeds an ideal parameter

l / preferential and / or a range of preferential / ideal parameters associated with these sizes and / or types of staples or with the fabrics and / or types of fabrics expected. As another example, the 23102 situational recognition surgical instrument can be configured to control a 23102 surgical instrument function based on the discrepancy. According to at least one aspect, the surgical instrument with situational recognition 23102 can avoid a surgical function based on a discrepancy. Functionality control with situational recognition

[0497] As highlighted in this document, several aspects of this disclosure belong to a surgical instrument that performs a function (for example, grasping), detecting a parameter associated with that function, using aspects of situational recognition to assess, for example, a control circuit, if that detected parameter is below or exceeds a predefined parameter (for example, considered ideal / preferred) or is below or exceeds a predefined interval (for example, considered normal) for that parameter and performs a action (eg interrupting a function or more functions, alerting the user, informing the user of possible causes, etc.) in response to the detected parameter being outside the predefined parameter and / or predefined parameter / interval. For example, Figure 90 illustrates an algorithm 23200 to implement these aspects in which a control circuit receives one or more detected parameters associated with a surgical function performed by a 23202 surgical instrument and retrieves situational recognition data from a base internal and / or external data bank 23204. The control circuit then evaluates the detected parameter (s) in view of the 23206 situational recognition data and performs an action based on the evaluation

23208.

[0498] According to various aspects of the present disclosure, a force detected (for example, through one or more of a sensor) in the jaws of an end actuator assembly may be of a magnitude that prohibits one or more of an subsequent / additional functionality of the end actuator assembly is performed. For example, with reference again to Figure 12, the force can be detected by means of the sensors 474, 476 and / or 478. In such an aspect, the sensor 474 can be a strain gauge coupled to the end actuator the stress meter is configured to measure the magnitude / amplitude of stress on one or more claws of the end actuator, which is indicative of closing forces being applied to the claws. In addition, in such an aspect, the sensor 476 can be a load sensor configured to measure a closing force applied to the grips by a closing drive system. In addition, in such an aspect, the 478 sensor can be a current sensor configured to measure a current drained by the motor, which correlates with a closing force applied to the jaws. In addition to or as another example, with reference again to Figure 17, the force can be detected by means of sensors 744a and / or 744b. In such an aspect, sensor 744a and / or 744b can be a torque sensor configured to provide a trigger force feedback signal that represents the closing force being applied to the grips by the closing drive system.

[0499] In one aspect, with reference again to Figure 58, a load sensor 152082 (for example, positioned on the drive shaft assembly or the handle assembly) can be configured to detect a load after the fixing the drive shaft assembly to the handle assembly. In this respect, the detected load can exceed a predefined load and / or a predefined load range. In such an aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, Integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can assess that it has detected load and determine, using situational recognition (for example, based on historical data), that the drive shaft assembly and / or the end actuator assembly is / should be damaged. In this respect, the control circuit can be configured to record a unique identifier associated with the drive shaft assembly 23120 and / or the end actuator assembly 23130 and designate this unique identifier as prohibited from further use and / or attachment for the 23110 handle set.

[0500] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can be configured to evaluate a force detected in the grips (for example, through one or more of a sensor as described) and determine the impedance of a function / trip cycle of the end actuator assembly. In particular, the control circuit can determine, with the use of situational recognition (for example, based on historical data), that the force detected in the claws (for example, detected before a function / cycle start) exceeds a predefined force and / or a predefined force range. In this respect, the control circuit can be configured to prevent the trigger function / cycle from starting. In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to alert the user (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) that the function / firing cycle cannot be performed and / or inform the user of possible causes (for example, so that the user can try to reduce the force detected in the claws). According to several aspects, the control circuit can be configured to allow the function / firing cycle to start if the force detected in the claws is reduced to the predefined force and / or within the predefined force range.

[0501] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the grips (for example, through one or more of a sensor, for example load sensor, torque sensor, etc. as described) and initially determine the permission of a trigger function / cycle of the end actuator assembly. However, after the triggering function / cycle starts, the control circuit can determine, using situational recognition (for example, based on historical data), that a triggering force (for example, detected during the function / trip cycle) exceeds a predefined force for firing and / or a predefined force range for firing. In this respect, the control circuit can be configured to interrupt the triggering function / cycle (for example, preventing the triggering function / cycle from continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the trigger force or trigger force range

assigned. According to various aspects, the control circuit can be additionally configured to receive a cancel command (for example, via user interface (s), see, for example, Figure 88, selectable user interface element 23012 ) to allow the trigger function / cycle to continue. In this regard, the control circuit can determine, with the use of situational recognition (for example, based on historical data), that a second trigger force (for example, detected during the continuous trigger function / cycle) exceeds a second pre-defined force for firing and / or a second pre-defined force range for firing (for example, higher limits). In such an aspect, the control circuit can be configured to prevent the firing function / cycle again, alert the surgeon, and / or receive a cancellation command as described.

[0502] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the claws (for example, through one or more of a sensor as described). In addition, the control circuit can additionally evaluate a force detected within the drive shaft assembly (that is, through one or more of a sensor as described). Here, according to various aspects, the control circuit can cross-reference the force detected in the claws and / or the force detected within the drive shaft assembly with the surgical procedure being performed. According to this aspect, the control circuit can determine, using situational recognition (for example, based on procedural and / or historical data), that the force detected within the drive shaft assembly exceeds a force of the drive shaft. triggered

predefined drive and / or a predefined drive shaft force range.

In one example, the drive shaft assembly may comprise a specialized drive shaft assembly configured for use with a specific tissue type in a specific surgical procedure.

In this respect, the control circuit can determine, using situational recognition (for example, based on procedural and / or historical data), that the force detected in the specialized drive shaft assembly is very high (for example, exceeds the force predefined drive shaft and / or the predefined drive shaft force range associated with the specialized drive shaft assembly) and / or that the force detected in the grips is not a predefined force and / or within a predefined range (for example, an expected force historically associated with the surgical procedure being performed). In this respect, the control circuit can be configured to interrupt a function / trip cycle (for example, preventing the function / trip cycle from starting and / or continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the drive shaft force and / or the drive shaft range exceeded.

In several respects, the alert can inform the surgeon to consider removing the specialized drive shaft assembly, for example 23120, from the 23110 handle assembly and attaching another drive shaft assembly (for example, a regular refill set for the detected forces and the tissue being found) to the 23110 handle assembly. In this respect, the control circuit can be configured to allow the trigger function / cycle to start and / or continue when a suitable drive shaft assembly is fi - fixed.

[0503] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated in a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the jaws (for example, through one or more of a sensor as described) during a surgical procedure. According to this aspect, the control circuit can determine, with the use of situational recognition (for example, based on procedural and / or historical data), that a tissue creep waiting time is below a time predefined creep waiting time and / or predefined creep time interval associated with a specific thickness and a specific tissue being attached during the surgical procedure. In other words, in the light of Figures 83 and 84 in the present invention, an initial closing force may have declined and achieved creep stability at a lower closing force faster than expected. In this respect, the control circuit can be configured to interrupt a function / trip cycle (for example, to prevent the function / trip cycle from starting and / or continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the shortened creep timeout. In several respects, the alert can inform the surgeon to consider removing the end actuator set, for example, 23130 of the handle set and fixing another end actuator set (for example, a set of end actuators). end actuator configured to treat tissues that have detected creep timeout) to handle set 23110. In this respect, the control circuit can be configured to allow the trigger function / cycle to start and / or continue when a suitable end actuator set is attached.

[0504] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the claws (for example, through one or more of a sensor as described). In addition, the control circuit can additionally evaluate a position detected by a hinge member (that is, through one or more of a sensor). For example, with reference again to Figure 12, the position can be detected by the sensor 472 coupled to the articulation member. In one aspect, sensor 472 can be a position sensor configured to measure linear displacement, with a single rotation of a sensor element corresponding to a specific linear displacement of the articulation member. In another example, with reference again to Figure 17, the position can be detected by the position sensor 734 located on the end actuator. Here, position sensor 734 can be a proximity sensor or a sensor configured to provide a series of pulses traceable by the control circuit to determine a position of the hinge member. Here, according to several aspects, the control circuit can cross-reference the force detected in the claws and / or the position detected within the joint member with the surgical procedure being performed. According to this aspect, the control circuit can determine, with the use of situational recognition

(for example, based on procedural and / or historical data), that the position detected for the articulation member indicates that the articulation member has advanced (for example, within the drive shaft assembly) in addition to a forward position predetermined position and / or a predetermined forward position range. In several aspects, the predetermined forward position and / or the predetermined forward position range can be correlated to the closing force detected in the claws. In such an aspect, with the designated predetermined forward position exceeded, the control circuit can be configured to interrupt a trip function / cycle (for example, preventing the trip function / cycle from starting and / or continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, via a user interface of a 23138 surgical instrument component) , 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the predetermined forward position and / or the predetermined forward position range exceeded. In several aspects, the alert can inform the surgeon to consider retracting the joint member to the predetermined forward position and / or the predetermined forward position range. Here, in an example, the predetermined forward position and / or the predetermined forward position range can have historically performed and / or desired trip cycles / functions suitable for the corresponding closing force. In this regard, the control circuit can be configured to allow the trigger function / cycle to start and / or continue when a suitable forward position is reached.

[0505] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated in a component of the surgical instrument

23132, 23122, and / or 23112 or a 23142 central surgical controller attached) can evaluate a force detected in the jaws (for example, through one or more of a sensor as described) during a surgical procedure.

According to this aspect, the control circuit can determine, using situational recognition (for example, based on procedural and / or historical data), that a closing force is above a closing force range. preset and / or a preset closing force associated with a specific tissue being trapped during the surgical procedure.

Put another way, in the light of Figures 83 and 84 in the present invention, the force detected for closing is greater than expected to allow a firing function / cycle to proceed.

In this respect, the control circuit can be configured to interrupt a function / trip cycle (for example, preventing the function / trip cycle from starting and / or continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the high closing force.

In several respects, the alert can inform the surgeon to consider adjusting a trigger motor speed.

In one example, if the specific tissue is rigid tissue, the alert may suggest that the surgeon adjust the speed of the firing engine downwards to avoid tearing the rigid tissue.

In such an aspect, the downward adjustment can be based on historical data associated with the surgical procedure being performed.

In another example, if the specific tissue is woven with a weak shear force, the alert may suggest that the surgeon adjust the speed of the firing engine to ensure that the tissue is properly secured.

In such an aspect

However, the upward adjustment can be based on historical data associated with the surgical procedure being performed. In such respects, the control circuit can be configured to allow the trip function / cycle to start and / or continue when an appropriate trip motor speed is set.

[0506] In another aspect, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the jaws (for example, through one or more of a sensor as described) during a surgical procedure. According to this aspect, the control circuit can determine, with the use of situational recognition (for example, based on procedural and / or historical data), that a cyclic force on the firing system is above a force predefined cyclic cycle and / or a predefined cyclic force range during the surgical procedure. In other words, the cyclical force detected is greater than expected and may be indicative of impending engine failure based on historical data. In this respect, the control circuit can be configured to interrupt a function / trip cycle (for example, to prevent the function / trip cycle from starting and / or continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the high cyclic force and possible engine failure. According to several aspects, the control circuit can be additionally configured to receive a cancellation command (for example, via the user interface, see, for example, Figure 88, selectable user interface element 23012) to allow trigger function / cycle to continue. In this regard, the control circuit can continue to monitor whether the Cyclic force on the trigger system is above a predefined cyclic force and / or a predefined cyclic force range during the surgical procedure. In such an aspect, the control circuit can be configured to prevent the trigger function / cycle again, alert the surgeon, and / or receive a cancel command as described.

[0507] According to another aspect of the present disclosure, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated in a component of the surgical instrument 23132, 23122, and / or 23112 or a 23142 central surgical controller attached) can assess a force detected in the claws (for example, through one or more of a sensor as described). In addition, the control circuit can additionally evaluate a force / torque to articulate the 23130 end actuator assembly. In such an aspect, the articulation force / torque can be detected by means of one or more of a sensor (for example, example, a force sensor associated with a pivot member, a torque sensor associated with a pivot member, a Current sensor associated with a motor configured to drive the pivot member, etc.). For example, with reference again to Figure 17, the articulation force / torque can be detected by torque sensors 744d and / or 744e coupled to a articulation drive system. In addition to and / or alternatively, again with reference to Figure 17, the articulation force / torque can be correlated to a current drained by 704d and / or 704e motors as measured by sensor 736. Here, according to various aspects, the circuit of control can cross-reference the force detected in the claws and / or the strength / torque of the joint detected within the joint member with the surgical procedure being performed.

According to this aspect, the control circuit can determine, using situational recognition (for example, based on procedural and / or historical data), that the joint force / torque detected for the joint member exceeds a force / predefined articulation torque and / or a predefined articulation force / torque range.

In several respects, the predefined articulation force / torque and / or the predefined articulation force / torque range can be correlated to the force detected in the jaws.

In such an aspect, with a designated joint torque force exceeded, the control circuit can be configured to stop the joints of the end actuator assembly (for example, to prevent the joints from continuing). In addition, in such an aspect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, via a user interface of a 23138 surgical instrument component) , 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the joint strength / torque exceeded and / or the joint strength / torque range exceeded.

According to several aspects, the control circuit can be additionally configured to receive a cancel command (for example, via the user interface, see, for example, Figure 88, selectable user interface element 23012) to allow that the joint continues.

In this regard, the control circuit can continue to monitor whether the articulation force / torque is above the predefined articulation force / torque and / or the predefined articulation force / torque range during the surgical procedure.

In this respect, the control circuit can be configured to prevent the joint again, alert the surgeon, and / or receive a cancellation command

as described.

[0508] According to yet another aspect of the present disclosure, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can evaluate a force detected in the jaws (for example, through one or more of a sensor as described). In addition, the control circuit can additionally evaluate a force / torque to rotate the drive shaft assembly 23120 (for example, drive shaft member). In such an aspect, the rotation force / torque can be detected by means of one or more of a sensor (for example, a force sensor associated with a drive / rotation shaft member, a torque sensor associated with the drive / rotation shaft member, a current sensor associated with a motor configured to rotate the drive / rotation shaft member, etc.). For example, with reference again to Figure 17, the rotation force / torque can be detected by the torque sensor 744c coupled to a drive / rotation shaft member drive system. In addition to and / or alternatively, again with reference to Figure 17, the rotating force / torque can be correlated to a current drained by a 704c motor as measured by sensor 736. Here, according to various aspects, the control circuit it can cross reference the force detected in the claws and / or the rotation force / torque detected within the drive / rotation shaft member with the surgical procedure being performed. According to this aspect, the control circuit can determine, using situational recognition (for example, based on procedural and / or historical data), that the rotation force / torque detected for the drive / rotation shaft member exceed a preset rotation force / torque and / or a preset rotation force / torque range. In several aspects, the predefined rotation force / torque and / or the preset rotation force / torque range can be correlated to the force detected in the grips. In other respects, the predefined rotation force / torque and / or the predefined rotation force / torque range may correspond to a force / torque that the drive / rotation shaft member itself is capable of withstanding. In such an aspect, with a designated torque force exceeded, the control circuit can be configured to stop the rotation of the end actuator assembly (for example, to prevent the rotations of the drive / rotation shaft member from continuing) . In addition, in such a respect, again with reference to Figure 89, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a surgical instrument component 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the exceeded rotation force / torque and / or the exceeded rotation force / torque range. According to several aspects, the control circuit can be additionally configured to receive a cancellation command (for example, through the user interface, see, for example, Figure 88, selectable user interface element 23012) to allow the rotation to continue. In this respect, the control circuit can continue to monitor whether the rotating force / torque is above the predefined rotation force / torque and / or the predefined rotation force / torque range during the surgical procedure. In such an aspect, the control circuit can be configured to prevent rotation again, alert the surgeon, and / or receive a cancel command as described.

[0509] According to yet another aspect of the present disclosure, with reference to Figure 89, for example, a control circuit associated with the surgical instrument (for example, integrated into a component of the surgical instrument 23132, 23122, and / or 23112 or a central surgical controller 23142 coupled) can be configured to evaluate an opening force detected in the jaws (for example, through one or more of a sensor as described) and determine prevention of jaw opening. In particular, the control circuit can determine, with the use of situational recognition (for example, based on Historical data), that the Opening force detected in the claws exceeds a predefined opening force and / or a range of predefined opening force. In such an aspect, the control circuit can be configured to keep the claws in a clamped or partially clamped position. In addition, in this respect, again with reference to Figure 89, the control circuit can be configured to alert the user (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) that the jaws cannot be opened and / or inform the user of possible causes (for example, so that the user can try to reduce the opening force detected in the claws). According to several aspects, the control circuit can be configured to allow the jaws to open if the opening force detected in the jaws is reduced to the predefined opening force and / or within the predefined opening force range. . Short detection and functionality control

[0510] According to several other aspects of the present disclosure, the functionality of a surgical instrument can be controlled based on one or more of a sensor configured to detect a short. That is, if a metallic object is detected inside the claws, at least one function / performance of the surgical instrument (for example, cutting, coagulation, etc.) can be prevented / prohibited. For example,

Figure 91 illustrates a 23300 algorithm to implement such aspects in which a control circuit receives one or more detected parameters indicative of a 23302 short circuit. The control circuit can also retrieve data from the internal database and / or external

23304. The control circuit then evaluates the detected parameter or parameters and / or data from the 23306 database and performs an action based on the 23308 evaluation.

[0511] Referring again to Figure 89, according to various aspects of the present disclosure, a 23100 surgical system may comprise a control circuit (23112, 23122, 23132 and / or 23142, for example, in dashed line to show optional locations), a user interface (23118, 23128, 23138, 23148 and / or 23158, for example, dashed line to show optional locations) and a 23100 surgical instrument including, for example, a handle set 23110, a drive shaft assembly 23120 and an end actuator assembly 23130. In such aspects, the control circuit can be integrated into one or more of a component (for example, the handle assembly 23110, the con - near drive shaft 23120 and / or end actuator set 23130, etc.) of surgical instrument 23102 (eg 23112, 23122 23142, and / or 23132) and / or integrated with a cyclic controller central surgery 23140 (for example, 23142) paired (for example example, wireless) with the 23102 surgical instrument. In these respects, the 23130 end actuator assembly may include a first jaw, a second jaw pivotally coupled to the first jaw, and a 23134 sensor configured to detect a parameter associated with a function (for example, dissecting, holding, coagulating, cutting, stapling, etc.) of the end actuator set 23130 and for transmitting the detected parameter to a control circuit (eg 23112, 23122, 23132, and / or 23142). In several aspects, the first jaw may comprise a fixed jaw and the second jaw may comprise an elongated channel configured to receive a staple cartridge.

In addition, in this regard, the surgical instrument 23102 can additionally comprise a set of drive shaft 23120 that includes a sensor 23124 configured to detect a parameter associated with a function (for example, rotation, articulation, etc.). ) of the drive shaft assembly 23120 and to transmit the detected parameter to the control circuit (for example, 23112, 23122, 23132, and / or 23142). In such aspects, the control circuit can be configured to receive detected parameters (for example, sensor data) from such sensors, for example, 23134 and / or 23124, throughout the course of a surgical procedure. .

A detected parameter can be received each time an associated end actuator set function 23130 (for example, dissection, gripping, coagulation, cutting, stapling, etc.) and / or a function of the associated drive shaft set 23120 ( for example, rotation, articulation, etc.) is performed.

The control circuit can be additionally configured to receive data from an internal database (for example, in the memory of a component of the surgical instrument 23136, 23126 and / or 23116 or a database of the central surgical controller 23149) and / or an external database (for example, a database of the central surgical controller 23149, a cloud database 23150, etc.) throughout the surgical procedure.

According to several aspects, the data received from the internal and / or external databases can comprise procedural data (for example, steps to perform the surgical procedure) and / or historical data (for example, data indicating expected parameters based on historical data associated with the surgical procedure). In many respects, procedural data may comprise current / recognized standard care procedures for the surgical procedure and historical data may comprise preferred / ideal parameters and / or ranges of preferred / ideal parameters based on historical data associated with the surgical procedure. (for example, system-defined restrictions). Based on the received data (for example, sensor data, internal and / or external data, etc.), the control circuit (for example, 23112, 23122, 23132, and / or 23142) can be configured to continuously derive inferences (for example, contextual information) about the ongoing procedure. That is, the surgical instrument can be configured to, for example, record data regarding the surgical procedure to generate reports, check the steps that are being taken by the surgeon to perform the surgical procedure, provide data or warnings (for example, through a user interface associated with the central surgical controller 23148 and / or 23158 and / or the surgical instrument 23138, 23128, and / or 23118) that may be relevant for a given procedural step, control an instrument function surgical 23102, etc.

[0512] Again with reference to Figure 89, in one aspect, during and / or after the target tissue is held between the claws of the end actuator assembly, the control circuit (23112, 23122, 23132 and / or 23142 ) can be configured to, before allowing a subsequent function (for example, firing, coagulation, etc.), check the continuity between the claws. Here, according to various aspects, the surgical instrument may comprise an electrosurgical instrument that comprises an electrode in at least one of the claws (for example, integrated with the anvil and / or the staple cartridge). In such aspects, if a short exists between the electrodes, it can be difficult to treat the tissue trapped between the claws with electrosurgical energy (for example, RF energy). In one example, a conductive object (for example, a clamp, clamp, metal element, etc.) between the electrodes can result in continuity between the claws. In another example, if sufficient space does not exist between the claws (for example, after attaching the target tissue) the electrodes can touch each other resulting in continuity between the claws. Again with reference to Figure 53, for example, in one aspect of the present description the sensor 152008a is configured to measure a gap between the claws of the end actuator. In such an aspect, the sensor 152008a of the first claw may comprise a Hall effect sensor configured to detect a magnetic field generated by the magnet 152012 of the second claw to measure the gap between the first claw and the second claw. Notably, the gap may be representative of the thickness of the fabric stuck between the first jaw and the second jaw. Here, if there is continuity between the jaws, an unwanted surgical result can result (for example, treatment of incomplete tissue, excessive heating of the conductive object, etc.).

[0513] According to one aspect (for example, bipolar mode), the first jaw can comprise a fixed jaw and the second jaw can comprise an elongated channel configured to receive a staple cartridge, as shown in Figure 25. In one for example, the staple cartridge may comprise an active electrode to deliver electrosurgical energy (eg, RF energy) to the trapped tissue and at least a portion of the anvil can act as a return electrode. In another example, the anvil may comprise an active electrode to deliver electrosurgical energy (for example, RF energy) to the trapped tissue and at least a portion of the elongated channel can act as a return electrode. According to another aspect (for example, monopolar mode), the first jaw may comprise a fixed jaw and the second jaw may comprise an elongated channel configured to receive a staple cartridge. In one example, the staple cartridge may comprise an active electrode to deliver electrosurgical energy (eg, RF energy) to the trapped tissue and a return electrode (eg, grounding plate) can be separately located on the body of the patient. In another example, the anvil may comprise an active electrode to deliver electrosurgical energy (eg, RF energy) to the trapped tissue and a return electrode (eg, grounding plate) can be separately located on the patient's body. Various configurations for detecting short-circuits are described in US patent no.

9,554,854, entitled DETECTING SHORT CIRCUITS IN ELECTRO-SURGICAL MEDICAL DEVICES, the description of which is incorporated here for reference.

[0514] Again with reference to Figure 89, according to several aspects, the control circuit (23112, 23122, 23132 and / or 23142) can be configured to check continuity in several ways. In one aspect, a generator that produces electrosurgical energy and / or a sensor, for example, 23134, integrated in the surgical instrument can be configured to detect when the impedance between the electrodes falls below a threshold value for a period of time limit (ie impedance drops which indicates a short). Here, again with reference to Figure 48, the sensor, for example, 23134, can be configured to measure impedance over time. In one example, when the electrodes encounter a line of conductive clamps, the current can rise, while the impedance and voltage drop sharply. In another example, continuity can be presented as a current collector with minimal voltage changes. Various alternative methods for checking continuity / detecting a short, such as those described in US patent No. 9,554,854, entitled DETECTING SHORT CIRCUITS IN ELECTROSURGICAL MEDICAL DEVICES, are expressly incorporated herein by reference (for example, comparing values impedance at different positions within a pulse in a series of pulses).

[0515] In such aspects, if continuity is detected, a conductive object (for example, a clamp, a clamp, a line of clamps, a metal element, etc.) may be present / exposed in the tissue trapped between the claws. Notably, such a conductive object may be from the current surgical procedure and / or from a previous surgical procedure. In such an aspect, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or an associated user interface to a central surgical controller 23148 and / or 23158) in relation to the detection of the conductive object. For example, the alert may suggest that the surgeon reposition the 23130 end actuator assembly so that the electrodes are not in contact with any conductive object and / or remove the conductive object causing the short circuit. According to several aspects, the control circuit can be further configured to receive a cancel command (for example, via the user interface, see, for example, Figure 88, selectable user interface element 23012) to allow subsequent function (eg cutting, coagulation, etc.) despite the detection of the conductive object (eg clamp, clamp, line of clamps, metal element, etc.).

[0516] According to one aspect, the control circuit (23112, 23122, 23132 and / or 23142) can be configured to check continuity to avoid the transection of clips. In such an aspect, after a short is detected, the control circuit can be configured to provide an alert to the surgeon (for example, through a user interface of a component of the surgical instrument 23138, 23128 and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the detection of a conductive object between the jaws. In one aspect, the surgeon can adjust the sensitivity of the control circuit via a user interface (for example, an interactive user interface element on the surgical instrument, the central surgical controller, a generator, etc.) . In such an aspect, based on the adjustment, the control circuit can be configured to prevent firing if a conductive object is detected between the claws.

[0517] Again with reference to Figure 89, according to another aspect, the control circuit 23142 can be integrated into a central surgical controller 23140 paired (for example, wireless) with the electrosurgical instrument 23102. In such an aspect, the surgical hub 23140 can be preloaded with surgeon / user settings for detecting a conductive object between the jaws. In one example, a surgeon / user configuration comprises avoiding firing if a conductive object is detected between the claws. In another example, a surgeon / user configuration comprises alerting before allowing firing if a conductive object is detected between the claws. In yet another aspect, a surgeon / user configuration comprises allowing the surgeon / user to cancel an alert. In yet another aspect, a surgeon / user configuration comprises a temporary reset that allows the surgeon / user to remedy the situation (for example, move the claws, remove the conductive object) before checking again. continuity.

[0518] Again with reference to Figure 89, according to yet another aspect, the control circuit (23112, 23122, 23132 and / or 23142) can be configured to check the continuity to deliberately cross a line of clamps. Here, in some surgical procedures, it may be beneficial to have cross clamp lines to ensure a contiguous transection (for example, lung resections, especially wedges from various angles, glove procedures, etc.). In such an aspect, after continuity is detected, the control circuit can be configured to provide an alert (for example, audible and / or visual) to the surgeon (for example, through a component user interface) surgical instrument 23138, 23128, and / or 23118 and / or a user interface associated with a central surgical controller 23148 and / or 23158) in relation to the detection of a conductive object (for example, existing staple line) between the claws.

[0519] Again with reference to Figure 89, according to other aspects, the control circuit (23112, 23122, 23132 and / or 23142) can be configured to receive data from an internal database (for example, in memory of a component of the surgical instrument 23136, 23126 and / or 23116 or a database of the central surgical controller 23149) and / or an external database (for example, of a database of the central surgical controller 23149, a 23150 cloud database, etc.) throughout the surgical procedure. According to various aspects, the data received from internal and / or external databases may comprise data from the surgical history (for example, data on previous surgical procedures performed on the patient, data on the current surgical procedure, etc.). ). In one example, surgical history data may indicate that staples were used in a previous surgery and / or where staples were used and current surgical procedure data may indicate whether a clip applicator was used to apply clips. Based on the data received (eg, surgical history data, etc.), the control circuit (23112, 23122, 23132 and / or 23142) can be configured to continuously derive inferences (for example, contextual information) about the procedure ongoing. That is, the 23120 surgical instrument can be aware of the situation and can be configured to, for example, infer / determine that a detected continuity can be a staple line from a previous surgical procedure or a clip from the current surgical procedure. . As another example, if the patient has never performed a surgical procedure, a clip applicator was not used in the current surgical procedure and a staple cartridge was triggered in the current surgical procedure, the control circuit can be configured to infer / determine that the conductive object detected between the claws is an anterior clamp line. As another example, if the patient has never had a surgical procedure, a clip applicator was used in the current procedure and no staple cartridges have yet been triggered in the current surgical procedure, the control circuit can be configured to infer / determine that the conductive object detected between the claws is a clip. Examples

[0520] Various aspects of the subject described here under the heading "SAFETY SYSTEMS FOR SMART POWERED SURGICAL STAPLING" are defined in the Examples below:

[0521] Example 1 - A surgical system comprises a control circuit and a surgical instrument. The surgical instrument comprises a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end of the drive shaft assembly. The end actuator assembly comprises a first jaw, a second jaw pivotally coupled to the first jaw, and a sensor. The sensor is configured to detect a parameter associated with an end actuator function and transmit the detected parameter to the control circuit. The control circuit is configured to analyze the detected parameter based on a restriction defined by the system and prevent at least one function of the surgical instrument based on the analysis result. The surgical system additionally comprises a user interface configured to provide a current status for at least one impaired function of the surgical instrument.

[0522] Example 2 - The surgical system of Example 1, with the restriction defined by the system comprising at least one of a predefined parameter or a range of predefined parameters based on historical data associated with a surgical procedure being performed by the surgical system.

[0523] Example 3 - The surgical system of Example 1 or 2, the current state of which comprises a first message that at least one function of the surgical instrument is prevented and a second message indicating a reason why at least a function of the surgical instrument is prevented.

[0524] Example 4 - The surgical system of Examples 1, 2 or 3, in which the user interface comprises a user interface element selectable to cancel the control circuit to allow at least one function of the surgical instrument.

[0525] Example 5 - The surgical system of Examples 1, 2, 3 or 4, the sensor comprising a force sensor coupled to the end actuator, the detected parameter comprising a force applied to at least one among the first claw or second claw of the end actuator, and the at least one function prevented by the control circuit comprises one or more to prevent the use of a connected drive shaft, preventing the start of a firing cycle, preventing the articulation of the end actuator, preventing the rotation of the drive shaft or preventing one or more of the first jaw or second jaw from opening.

[0526] Example 6 - The surgical system of Examples 1, 2, 3, 4 or

5, where the function of the end actuator associated with the detected parameter comprises a clamping function and the at least one function of the surgical instrument prevented by the control circuit comprises one or more of a dissection function, a clotting function, a clamp function or a cutting function.

[0527] Example 7 - The surgical system of Examples 1, 2, 3,4, 5 or 6, additionally comprising a central surgical controller connected communicatively to the surgical instrument, the central surgical controller comprising the control circuit.

[0528] Example 8 - The surgical system of Example 7, with one of the handle set or the central surgical controller comprising the user interface.

[0529] Example 9 - The surgical system of Examples 1, 2, 3, 4,5, 6, 7 or 8, one of the handle sets, drive shaft set or instrument end actuator set surgical comprises the control circuit.

[0530] Example 10 - The surgical system of Example 1, 2, 3, 4,5, 6, 7,8 or 9, with the drive shaft assembly comprising a sensor configured to detect an axis parameter activation associated with an axis function and transmit the detected drive axis parameter to the control circuit. The control circuit is additionally configured to prevent at least one function of the surgical instrument additionally based on the detected drive axis parameter.

[0531] Example 11 - A surgical system comprises a central surgical controller and a surgical instrument communicatively coupled to the central surgical controller. The surgical instrument comprises a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end of the drive shaft assembly. The end actuator assembly comprises a first jaw, a second jaw pivotally coupled to the first jaw, and a sensor. The sensor is configured to detect a parameter associated with an end actuator function and transmit the detected parameter to the central surgical controller. The central surgical controller comprises a processor and a memory attached to the processor. The memory stores instructions executable by the processor to analyze the detected parameter based on a constraint defined by the system and to avoid at least one function of the surgical instrument based on an analysis result. The surgical system additionally comprises a user interface configured to provide a current status for at least one impaired function of the surgical instrument.

[0532] Example 12 - The surgical system of Example 11, the constraint defined by the system comprising at least one within a predefined parameter or a range of predefined parameters based on historical data associated with a surgical procedure being performed by the surgical system.

[0533] Example 13 - The surgical system of Example 11 or 12, the current state of which comprises a first message that at least one function of the surgical instrument is prevented and a second message indicating a reason why at least one function of the surgical instrument is prevented.

[0534] Example 14 - The surgical system of Examples 11, 12 or 13, in which the user interface comprises a user interface element selectable to cancel the central surgical controller to allow at least one function of the surgical instrument .

[0535] Example 15 - The surgical system of Examples 11, 12, 13 or 14, the sensor comprising a force sensor coupled to the end actuator, the detected parameter comprising a force applied to at least one among the first jaw or second jaw of the end actuator, and the least at least one function prevented by the central surgical controller comprises one or more to prevent the use of a connected drive shaft, preventing the start of a cycle trigger, preventing the articulation of the end actuator, preventing the rotation of the drive shaft or preventing one or more of the first jaw or second jaw from opening.

[0536] Example 16 - The surgical system of Examples 11, 12, 13, 14 or 15, with the function of the end actuator associated with the detected parameter comprising a clamping function and the at least one function of the surgical instrument being prevented through the central surgical controller it comprises one or more of a dissection function, a coagulation function, a clamp function or a cutting function.

[0537] Example 17 - The surgical system of Example 11, 12, 13, 14, 15, or 16, with at least one of the handle set or the central surgical controller comprising the user interface.

[0538] Example 18 - The surgical system of Example 11.12, 13, 14, 15, 16 or 17, with the drive shaft set comprising a sensor configured to detect a drive shaft parameter associated with a axis function and transmit the detected drive axis parameter to the central surgical controller. The Memory additionally stores instructions executable by the processor to avoid at least one function of the surgical instrument additionally based on the detected drive axis parameter.

[0539] Example 19 - Non-transitory computer-readable media stores computer-readable instructions that, when executed, cause a machine to analyze a detected parameter, associated with a function of an end actuator of a surgical system, based on a constraint defined by the system, the surgical system including a handle assembly, a drive shaft assembly that extends distally from the handle assembly and an end actuator assembly coupled to a distal end drive shaft assembly. The end actuator assembly comprises a first jaw, a second jaw pivotally coupled to the first jaw, and a sensor configured to detect the detected parameter and transmit the detected parameter to the machine. The instructions, when executed, additionally cause the machine to avoid at least one function of the surgical system based on an analysis result, and to generate a user interface. The user interface provides a current status for at least one function that is prevented from the surgical system.

[0540] Example 20 - the non-transitory, computer-readable media of Example 19 additionally comprises instructions that, when executed, still cause the machine to generate a cancellation element in the user interface. The cancellation element is selectable to allow at least one function of the surgical system. Safety systems for intelligent surgical stapling equipped with motor Safety systems for evaluating operational parameters

[0541] Several aspects of the present disclosure are directed to improved security systems capable of adapting, controlling, and / or adjusting internal actuation operations of a surgical instrument in response to tissue parameters detected through one or more of the sensor. surgical instrument. More specifically,

various aspects are directed towards the detection and indication of an adequacy of the current parameters of the device to detected tissue parameters.

[0542] For example, detected tissue parameters may include a tissue type, tissue thickness, tissue stiffness, tissue position on a patient's anatomy, tissue vascularization, etc., and current device parameters can include cartridge color, cartridge type, auxiliary compounds, clamp load, span, firing rate, etc. Thus, according to aspects of the present disclosure, physiological detection can indicate an inappropriate use of a device or a component of it and / or an improper positioning of the device.

[0543] In one example, an inappropriate use of a surgical instrument or a component of it and / or an inappropriate position of the surgical instrument can be determined, through an associated control circuit, based on the physiological detection detected by by means of one or more of a sensor in the claws of the end actuator. In such an example, after improper use has been determined and / or improper positioning has been determined, the associated control loop may prevent one or more of a feature (for example, stapling) from the end actuator from being performed. In addition, in this example, the associated control circuit may allow one or more of an end actuator functionality if the associated control circuit determines that the surgical instrument or its component and / or the position of the instrument have been rectified (for example, inadequate staple cartridge replaced, repositioned surgical instrument, etc.) or a cancellation has been received (for example, through a user interface on the surgical instrument, on a central surgical controller attached to the surgical instrument, in the operating room

ca, etc.)

[0544] With reference to Figure 94, according to various aspects of the present disclosure, a 24200 surgical system may comprise a control circuit (24212, 24222, 24232 and / or 24242, for example, in dashed line to show locations optional), a user interface (24214, 24224, 22234, 24244 and / or 24254, for example, dashed line to show optional locations) and a 24202 surgical instrument. The 24202 surgical instrument includes a plurality of components, such as Component-A 24216 to Component-N 24218 of end actuator set 24210 and likewise, in abbreviated form for purposes of illustration, Component-A (CA) to Component-N (CN) of the set of drive shaft 24220 and handle set 24230, respectively. In several respects, each component of the 24202 surgical instrument can comprise at least one device parameter. For example, Component-A 24216 of end actuator set 24210 may include parameters PAa to PAn 24217, Component-N 24218 of end actuator set 24210 may include parameters PNa to PNn 24219, and so on. against. As another example, each from C-A to C-N of the drive shaft assembly 24220 and each from C-A to C-N of the handle assembly 24230 may similarly include at least one device parameter. Each component can be configured to transmit its respective device parameters to the control circuit. The surgical instrument 24202 additionally includes a sensor (24213, 24223, and / or 24233) configured to detect a tissue parameter associated with a function of the surgical instrument and transmit the detected tissue parameters to the control circuit. The control circuit can be configured to analyze the tissue parameter detected in cooperation with each respective device parameter based on constraints.

predefined system settings.

[0545] Again with reference to Figure 94, the control circuit 24212, 24222 and / or 24232 (for example, shown as an element of the end actuator assembly 24210, the drive shaft assembly 24220, and the handle set 24230, respectively) can, in several respects, be integrated into one or more of one of the plurality of components (for example, a handle of the handle set 24230, a drive shaft of the set of drive shaft 24220, and an end actuator for the end actuator set 24210, a clamp cartridge for the end actuator set, etc.) of the 24202 surgical instrument or integrated into a central surgical controller 24240 (eg 24242) paired (for example, wirelessly) to the surgical instrument 24202. Similarly, the sensor or sensors 24213, 24223 and / or 24233; the user interface 24214, 24224 and / or 24234; and memory 24215, 24225 and / or 24235 (for example, shown as elements of the end actuator assembly 24210, the drive shaft assembly 24220 and the handle assembly 24230, respectively) can be, in several respects, integrated into one or more of one of the plurality of components. Notably, according to several aspects, the surgical instrument 24202 and / or the central surgical controller 24240 can be a surgical instrument with situational recognition and / or a central surgical controller with situational recognition. Situational recognition refers to the ability of a surgical system, for example, 24200, to determine or infer information related to a surgical procedure from data received from databases (for example, associated history data to a surgical procedure) and / or surgical instruments (for example, sensor data during a surgical procedure). For example, information

Determined or inferred tions may include the type of procedure being performed, the type of tissue being operated on, the body cavity that is the subject of the procedure, etc. Based on this contextual information related to the surgical procedure, the surgical system can, for example, control a paired surgical instrument or a component of it and / or provide contextualized information or suggestions to a surgeon during the entire course of the surgical procedure. .

[0546] According to one aspect, a central surgical controller with situational recognition (for example, 24240) is paired (for example, wireless) with a 24202 surgical instrument being used to perform a surgical procedure. In such an aspect, the surgical instrument 24202 can comprise a plurality of components, including an end actuator (for example, Component-A 24216). End actuator 24216 can comprise a first claw, a second claw pivotally attached to the first claw, a cutting blade, and an integrated sensor 24213 configured to detect a tissue parameter associated with a function (for example, dissecting , fasten, clot, cut, staple, etc.) from end actuator 24216, and transmit the detected tissue parameters to a control circuit 24242 of central surgical controller 24240. Each of the plurality of components of surgical instrument 24202 (for example, Component-N 24218, for example, a staple cartridge, etc.), including end actuator 24216, is also configured to transmit its respective parameter or device parameters (for example, example, 24219 and 24217, respectively) for the central surgical controller 24240. Notably, it should be understood that a sensor (for example, 24213), as mentioned here and in other aspects disclosed, can be understand a plurality of sensors configured

designed to detect a plurality of tissue parameters associated with a plurality of end actuator assembly functions

24216. Thus, in addition, in this respect, the control circuit of the central surgical controller 24242 can be configured to receive this parameter data (for example, detected tissue parameter (s), device parameter each component including the end actuator, etc.) throughout the course of the surgical procedure. A detected tissue parameter can be received each time an associated end actuator function (for example, dissection, grasping, coagulation, cutting, stapling, etc.) must be performed. The control circuit of the central surgical controller 24242 can be additionally configured to receive data from an internal database (for example, a database of the central surgical controller 24249) and / or an external database (for example, from a 24269 cloud database) during the entire course of the surgical procedure. According to various aspects, the data received from the internal 24249 and / or external 24269 databases may comprise procedural data (for example, steps to perform the surgical procedure, data indicating the respective device parameters associated with the surgical procedure. - logical) and / or historical data (for example, data indicating expected tissue parameters based on historical data associated with the surgical procedure, data on the patient's surgical history, etc.). In many respects, procedural data may comprise current / recognized standard care procedures for the surgical procedure and historical data may comprise preferred / ideal tissue parameters and / or preferred / ideal tissue parameter ranges for each tissue parameter received based on historical data associated with the surgical procedure (for example, system-defined restrictions). Based on the data received (for example, parameter data, internal and / or external data, etc.), the control circuit of the central surgical controller 24242 can be configured to continuously derive inferences (for example, contextual information) about the surgical procedure in progress. That is, the central surgical controller with situational recognition can be configured to, for example, record data related to the surgical procedure to generate reports, verify the steps that are being taken by the surgeon to perform the surgical procedure, provide data or warnings (for example, via a user interface associated with the central surgical controller 24244 and / or 24254 and / or the surgical instrument 24214, 24224, and / or 24234) that may be relevant for a given procedural step , control a function of the surgical instrument, etc.

[0547] According to another aspect, a surgical instrument with situational recognition (for example, 24202) can be used to perform a surgical procedure. In such an aspect, as described herein, the surgical instrument 24202 can comprise a plurality of components, including a 24216 end actuator. The end actuator can comprise a first jaw, a second jaw pivotally coupled to the first jaw - ra, a cutting blade, and an integrated sensor 24213 configured to detect a tissue parameter associated with a function (eg, dissect, clamp, coagulate, cut, staple, etc.) of end actuator 24216 , and transmit the detected tissue parameters to a control circuit. Notably, in such an aspect, the detected tissue parameter can be transmitted to an integrated control circuit 24212 of end actuator 24216. Each of the plurality of components of the surgical instrument (for example, the component controller 24218, for example , the staple cartridge, etc.), including end actuator 24216, is configured to transmit its respective device parameter (s) to the control circuit of integrated end actuator 24212. In this respect, the integrated control circuit the end actuator 24212 can be configured to receive this parameter data (for example, detected tissue parameter (s), device parameter (s) of each component including the end actuator, etc.) over the course of the surgical procedure.

A detected tissue parameter can be received each time an associated end actuator function (for example, dissection, grasping, coagulation, cutting, stapling, etc.) is performed.

The control circuit integrated with end actuator 24212 can be additionally configured to receive data from an internal database (for example, the memory end actuator 24215) and / or an external database (for example, the from a 24269 cloud database via a central surgical controller 24240, from a central surgical controller database 24249, etc.) during the course of the surgical procedure.

According to various aspects, the data received from and / or internal and / or external databases may comprise staple cartridge data (for example, sizes and / or types of staples associated with a staple cartridge (for example, 24218) so that a parameter or device parameters were received by the control circuit of the end actuator 24212) and / or in historical data (for example, data indicating expected fabrics and / or types of staples to be stapled based on historical data). In many respects, internal and / or external data may comprise preferred / ideal tissue parameters and / or preferred / ideal tissue parameter ranges for each device parameter received based on historical data associated with the surgical procedure ( for example, system-defined restrictions). In one example, internal and / or external data may comprise preferred / ideal tissue parameters and / or preferred / ideal tissue parameter ranges for expected tissues and / or tissue types or for sizes and sizes. / or staple types associated with the staple cartridge device parameter (for example, 24218) based on historical data (for example, system-defined restrictions). Based on the received data (for example, parameter data, internal and / or external data, etc.), the control circuit of the end actuator 24212 can be configured to continuously infer inferences (for example, contextual information) about the ongoing procedure.

Notably, according to an alternative aspect, the integrated sensor 24213 of the end actuator 24216 can transmit the detected tissue parameter (s) to a control circuit (for example, 24222 and / or 24232) associated to another component of the surgical instrument, for example, a handle of the handle assembly 24230. In that respect, this other surgical instrument component control circuit (for example, 24222 and 24232) can be similarly configured to perform the various aspects of the 24212 end actuator control circuit, as described above.

In the end, the surgical instrument with situational recognition (for example, 24202) can be configured to, for example, alert its user (for example, through a user interface of the end actuator 24214, through an interface of user of another component of surgical instrument 24224 and / or 24234, for example, the handle of the handle assembly 24230, or via a user interface 24244 associated with a central surgical controller 24240 coupled to the surgical instrument 24202) a discrepancy.

For example, the discrepancy may include a detected tissue parameter that exceeds an ideal / preferred tissue parameter and / or a range of preferred / ideal tissue parameters associated with these sizes and / or types of staples or with the fabrics and / or types of fabrics expected. As another example, the surgical instrument with situational recognition (for example, 24202) can be configured to control a surgical instrument function based on the discrepancy. According to at least one aspect, the surgical instrument with situational recognition (for example, 24202) can avoid a surgical function based on a discrepancy. Inappropriate device placement

[0548] According to various aspects of the present disclosure, physiological detection (for example, detected by one or more of a sensor) may indicate problems with the positioning of the device. More specifically, according to these aspects, a physiological incompatibility may be present within / between a first claw and a second claw of an end actuator (eg, after gripping) and additional functionality (eg, coagulation, cutting, stapling, etc.) of the end actuator can be prohibited / prevented.

[0549] According to several aspects, the surgical procedure may comprise the resection of target tissue (for example, a tumor). Referring to Figure 92, for example, a portion of tissue from patient 24000 can comprise a tumor 24002. In such an aspect, a surgical margin 24004 can be defined around the tumor

24002. Notably, during a surgical procedure, it is ideal for preventing and / or minimizing the resection of healthy tissue that surrounds a tumor. However, to ensure complete removal of the tumor, the current standard / recognized care procedures associated with that surgical procedure may endorse the resection of a predetermined surgical margin defined by a distance around the tumor and / or a defined predetermined surgical margin range. for a distance band around the tumor. In one aspect, the endorsed surgical margin may be tumor-dependent (for example, based on the type of tumor, tumor size, etc.). In another aspect, the endorsed surgical margin may depend on an extension of the tumor's micro-invasion in the surrounding tissue. In other respects, the endorsed surgical margin can be correlated with improved long-term survival based on historical data associated with this tumor and / or this surgical procedure. In still other aspects, an associated control circuit (for example, in the view of Figure 94, on the surgical instrument, on a component of the surgical instrument 24212, 24222, 24232, on a central surgical controller coupled to the surgical instrument 24242 , etc.) can proactively adjust an endorsed surgical margin based on data received from an internal database 24215, 24225 and / or 24235 and / or external database 24249 and / or 24269 (for example , patient's surgical history data, patient's medical history data, standard of care procedures for recurrent tumors etc. from the cloud, from a central surgical controller, etc.). In this respect, returning to Figure 92, a normally endorsed surgical margin (for example, 24004) can be changed by a determined amount / distance (for example, 24010) to an adjusted surgical margin (for example, 24012) based on data received (for example, surgical data and / or medical history data for that patient may suggest that the tumor may have further invaded the surrounding tissue, that the patient may already have a case of recurrent tumor, etc.)

[0550] In addition, in several respects, after a target surgical margin (eg 24004 and / or 24012) is established for a surgical procedure, it can be difficult to identify and resect the tumor efficiently and / or precisely and / or your target surgical margin during a surgical procedure. Referring again to Figure 94, according to various aspects of the present disclosure, an end actuator (for example, 24216) of a 24202 surgical instrument may comprise a first sensor (for example, 24213) configured to measure a first signal and transmit the first signal to an associated control circuit (for example, on the surgical instrument, on a component of the surgical instrument 24212, 24222 and / or 24232, on a central surgical controller coupled to the surgical instrument 24242, etc.). In such an aspect, a second sensor configured to measure a second signal and transmit the second signal to the associated control circuit can be positioned over / inside the tumor (see Figure 92, for example, 24006, from a central position in relation to the tumor) before using the surgical instrument to resect the tumor. Here, according to several aspects, the second sensor can be separated from the surgical instrument. In addition, and / or alternatively, in such an aspect, the second sensor may comprise a sensor positioned on a periphery of the tumor (see Figure 92, for example, 24008) before using the surgical instrument to resect the tumor . According to another aspect, a plurality of second sensors can be positioned around the periphery of the tumor. Here, in these aspects, the control circuit can be configured to dynamically calculate a distance between the first sensor and the second sensor based on the first signal and the second signal. According to several aspects, the first sensor can be positioned at / close to the cutting blade of the end actuator. Additional sample methods for detecting a target surgical margin are described in US patent application publication No. 2016/0192960, entitled SYSTEM AND METHOD FOR A TISSUE RESECTION MARGIN MEASUREMENT DEVICE, the description of which is incorporated here - taken as a reference.

[0551] In one example, if the second sensor is positioned over

bre / inside the tumor (for example, in a central position, 24006), the control circuit can be additionally configured to determine a margin of distance between the second sensor and the target surgical margin established for the surgical procedure. In such an example, the control circuit can compare the dynamically calculated distance (for example, between the first sensor and the second sensor) to that determined margin distance to efficiently and precisely locate the end actuator ( eg cutting blade) at the target surgical margin (for example, when the dynamically calculated distance is equal or substantially equal to the determined margin distance, the end actuator is positioned correctly). The control circuit can be configured to use this technique to efficiently and accurately locate the end actuator (for example, the cutting blade) around the target surgical margin (for example, during resection).

[0552] In another example, if the second sensor is positioned on the periphery of the tumor or a plurality of second sensors are positioned around a periphery of the tumor, for example, 24008, the control circuit can be additionally configured to determine - specify a distance between the second sensor or sensors and the target surgical margin established for the surgical procedure. In such an example, the control circuit can compare the dynamically calculated distance (for example, between the first sensor and the second sensor) to that determined margin distance to efficiently and accurately locate the end actuator (for example, cutting blade ) at the target surgical margin (for example, when the dynamically calculated distance is equal or substantially equal to the determined margin distance, the end actuator is correctly positioned). The control circuit can be configured to use this technique to efficiently and accurately locate the end actuator (for example, the cutting blade) around the target surgical margin (for example, during resection). Such an aspect can be beneficial when the tumor is abnormally shaped.

[0553] Again with reference to Figure 94, according to several aspects, the control circuit can be configured to inform the surgeon (for example, in real time through a user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a central surgical controller coupled to the surgical instrument 24244 and / or a user interface in the operating room 24254, etc.) when the end actuator (for example, or the cutting blade) is located / positioned properly in relation to the target surgical margin (for example, 24004 and / or 24012). For example, the user interface may comprise at least one of i) a video image of the surgical site with a digital overlay indicating the target surgical margin for the surgeon to visually confirm that the end actuator (eg 24216) is positioned on the target surgical margin and / or navigate on the end actuator (for example, or the cutting blade) in relation to the target surgical margin, ii) haptic feedback on the surgical instrument itself 24202 to indicate that the actuator cutting blade endpoint is positioned at the target surgical margin and / or iii) auditory feedback to indicate that the cutting blade of the end actuator is positioned at the target surgical margin.

[0554] Again with reference to Figure 94, according to additional aspects, the control circuit can be configured to prevent the surgical instrument 24202 from firing if the end actuator (for example, cutting blade) is very close to and / or within a cancerous margin (for example, within the target surgical margin, to close the surrounding micro tissue invaded by the tumor,

etc.). According to such aspects, the control circuit can be further configured to receive a cancel command (for example, via the user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a surgical controller central unit attached to the surgical instrument 24244 and / or a user interface in the operating room 24254, etc.) to allow firing to continue. In one example, this user interface may comprise a selectable user interface element to allow firing to continue, for example, 24251. In this respect, the control circuit may continue to accompany the end actuator (for example, or the cutting blade thereof) with respect to the cancerous margin. Additionally, in such an aspect, the control circuit can be configured to prevent triggering again, alert the surgeon, and / or receive a cancel command as described. According to other aspects, the control circuit can be configured to prevent triggering until a reset event occurs (for example, opening the end actuator claws and repositioning the end actuator claws in relation to the cancerous margin. ).

[0555] Again with reference to Figure 94, according to other aspects of the present description, one or more of a sensor in a 24200 surgical system can detect blood flow through the tissue trapped between / within a first claw and a second claw of an end actuator (for example, 24216). For example, a doppler image detector (for example, integrated in end actuator 24213, coupled to a central surgical controller, for example, a parameter detection component 24253 comprising a doppler image detector, etc.) configured to locate and identify blood vessels that would not otherwise be visible at a surgical site (for example, by means of a red, green and / or blue laser) and a stain contrast analysis can be performed to determine the amount and / or speed of blood flow through such blood vessels.

Notably, in one example, it may be desired to seal some blood vessels (for example, associated with a tumor) but not to seal others (for example, associated with healthy tissues / organs). In this way, an associated control circuit (for example, on the surgical instrument, on a component of the surgical instrument 24212, 24, 222 and / or 24232, on a central surgical controller coupled to the surgical instrument 24242 etc.) to prevent the 24202 surgical instrument from firing if the blood flow exceeds a predetermined amount and / or rate of blood flow.

According to these aspects, the control circuit can be additionally configured to receive a cancel command (for example, via the user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a surgical controller central coupled to the surgical instrument 24244 and / or a user interface in the operating room 24254, etc.) to allow firing to continue (for example, if blood flow is associated with the tumor). In one example, this user interface may comprise a selectable user interface element to allow firing to continue, for example, 24251. In this respect, the control circuit can continue to monitor the blood flow of trapped tissue.

Additionally, in such an aspect, the control circuit can be configured to prevent triggering again, alert the surgeon, and / or receive a cancel command as described.

According to other aspects, the control circuit can be configured to prevent firing until a reset event occurs (for example, opening the claws and repositioning the claws of the end actuator in relation to the blood vessel comprising a blood flow exceeding the predefined amount and / or blood flow rate).

[0556] Again with reference to Figure 94, according to other aspects of the present disclosure, one or more of a sensor in a 24200 surgical system can detect an increase in blood pressure concomitant with and / or immediately after the tissue is seized. between / within a first jaw and a second jaw of an end actuator (for example, 24216). For example, a blood pressure monitor (for example, coupled to the central surgical controller, for example, component detection parameter 24253 including a blood pressure monitor, etc.) can detect the increase in blood pressure contemporary to the grasp. According to several aspects, the surgical system 24200 is endowed with situational recognition and can infer that the detected increase in blood pressure was caused by the trapping of the tissue between / within the claws of the end actuator. For example, a blood vessel that comprises critical blood flow may have been captured between / within the claws, resulting in restricted blood flow. Thus, according to several aspects, an associated control circuit (for example, in the surgical instrument, in a component of the surgical instrument 24212, 24, 222 and / or 24232, in a central surgical controller coupled to the surgical instrument 24242 etc.) can be configured to prevent a 24202 surgical instrument from firing if the increase in blood pressure exceeds a predetermined amount and / or a predetermined range. According to these aspects, the control circuit can be additionally configured to receive a cancel command (for example, through the user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a central surgical controller coupled to surgical instrument 24244 and / or a user interface in the operating room

24254, etc.) to allow firing to continue (for example, the surgeon observes that blood pressure has decreased while the tissue is still trapped, the situational recognition surgical system attributes the increase in blood pressure to another cause, etc.). ). In one example, this user interface may comprise a selectable user interface element to allow the trigger to continue, for example, 24251. In such an aspect, the control circuit may continue to monitor the patient's blood pressure. In addition, in this regard, the control circuit can be configured to prevent triggering again, alert the surgeon, and / or receive a cancellation command as described. According to other aspects, the control circuit can be configured to prevent firing until a reset event occurs (for example, opening of the jaws and repositioning of the jaws of the end actuator in relation to the trapped tissue).

[0557] Again with reference to Figure 94, according to other aspects of the present disclosure, one or more of a sensor in a surgical system can detect a substantial nerve bundle within the tissue trapped between a first claw and a second claw. an end actuator (for example, 24216). For example, a heart rate monitor (for example, integrated in the end actuator 24213, coupled to the central surgical controller, for example, detection parameter component 24253 comprising a heart rate monitor, etc.) detect an increase in heart rate concomitant with and / or immediately after the tissue is trapped between / within the first jaw and the second jaw. According to several aspects, the surgical system 24200 is endowed with situational recognition and can infer that the detected increase in heart rate, in the context of data received from an internal database 24215, 24225, 24235, 24249 and / or database outside

na 24249 and / or 24269 (for example, anatomical information associated with the surgical site of the surgical procedure being performed) were caused by the tightening of the tissue between / within the jaws of the end actuator. According to these aspects, an associated control circuit (for example, in the surgical instrument, in a component of the surgical instrument 24212, 24, 222 and / or 24232, in a central surgical controller coupled to the surgical instrument 24242 etc.) can be configured to prevent a 24202 surgical instrument from firing based on inference. In addition, according to such aspects, the control circuit can be configured to receive a cancellation command (for example, via the user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface in a central surgical controller attached to the 24244 surgical instrument and / or a user interface in the operating room 24254, etc.) to allow firing to continue (for example, the surgeon observes that the patient's heart rate has decreased while the tissue is still is stuck, the surgical system with situational recognition attributes the increase in heart rate to another cause, etc.). In one example, this user interface may comprise a selectable user interface element to allow triggering to continue, for example, 24251. In such an aspect, the control circuit can continue to monitor the patient's heart rate. Additionally, in such an aspect, the control circuit can be configured to prevent triggering again, alert the surgeon, and / or receive a cancellation command as described. According to other aspects, the control circuit can be configured to prevent firing until a reset event occurs (for example, opening the claws and repositioning the claws of the end actuator in relation to the trapped tissue ).

[0558] Again with reference to Figure 94, according to other

In other aspects of the present disclosure, one or more of a sensor in a 24200 surgical system can detect that a 24202 surgical instrument is in contact with an energized device (for example, an RF instrument / device). In one example, the surgical instrument and the energized device can be communicated to a central surgical controller 24240 in the surgical system 24200. For example, with reference again to Figure 9, a device / instrument 235 as well as an energy device 241 can be coupled to a modular control tower 236 of a central surgical controller 206. In such an example, both a generator 240 producing electrosurgical energy for the energized device 241 and / or a sensor integrated in the energized device can be configured to detect when the impedance associated with the energized device, falls below a limit value for a period of time | limit (for example, impedance drops which indicates a short). Similar to Figure 48, an integrated sensor of the energized device can be configured to measure impedance over time.

Several alternative methods for detecting a short, such as those described in US patent No. 9,554,854, entitled DETECTING SHORT CIRCUITS IN ELECTROSURGICAL MEDICAL DEVICES, are expressly incorporated by reference (for example, to compare impedance values at different positions within a pulse in a series of pulses). According to various aspects, the surgical system 24200 is endowed with situational recognition and can infer that a short detected, in the context of data received from an internal database 24215, 24225, 24235, 24249 and / or external 24249 and / or 24269 (for example, procedure data indicating that a step and / or the current stage of the surgical procedure involves the use of a separate surgical instrument, for example, an electrosurgical instrument / device), was caused by the surgical instrument separate

(for example, a conductive surface of the surgical instrument may be in contact with the energized device causing the short). According to such aspects, an associated control circuit (for example, in the surgical instrument, in a component of the surgical instrument 24212, 24, 222 and / or 24232, in the central surgical controller coupled to the surgical instrument and the energized device 24242 etc. ) can be configured to prevent a 24202 surgical instrument from firing based on inference.

If a short exists, it can be difficult to treat (for example, clotting) tissue with electrosurgical energy (for example, RF energy) and an unwanted surgical result can result (for example, incomplete tissue treatment, overheating conductive object, etc.). In such a context, the control circuit can be configured to inform the surgeon (for example, in real time via a user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a surgical controller central coupled to the surgical instrument 24244, and / or a user interface in the operating room 24254, etc.) that the short exists and that the triggering of the surgical instrument 24202 has been suspended.

In addition, according to such aspects, the control circuit can be configured to receive a cancel command (for example, via the user interface on the surgical instrument 24214, 24224 and / or 24234, a user interface on a central surgical controller coupled to surgical instrument 24244 and / or a user interface in operating room 24254, etc.) to allow firing to continue (for example, the surgeon checks that there is no short, the target tissue comprises a low impedance , etc.). In one example, this user interface may comprise a selectable user interface element to allow the shooting to continue, for example, 24251. In this respect, the control circuit may continue to monitor for a short time.

Additionally, in such an aspect, the control circuit can be configured to prevent triggering again, alert the surgeon, and / or receive a cancel command as described. According to other aspects, the control circuit can be configured to prevent triggering until a reset event occurs (for example, surgical instrument repositioned in relation to the energized device in such a way that they are no longer in contact). Inadequate device selection / proposed use

[0559] According to various aspects of the present disclosure, physiological detection (for example, detected by one or more of a sensor) may indicate problems with the selection of the device / surgical instrument. More specifically, according to these aspects, an incompatibility between surgical device and tissue may be present and additional functionality (eg coagulation, cutting, stapling, etc.) of the end actuator may be prohibited / prevented.

[0560] Referring again to Figure 94, in accordance with one aspect of the present disclosure, a control circuit (for example, on a component of the surgical instrument 24212, 24, 222 and / or 24232, on a controller central surgical device attached to surgical instrument 24242, etc.) can be configured to provide a warning if a specific tissue stapler (for example, a vascular stapler) and any combination of detected information (for example, detected through one or more of one sensor) suggests that the target tissue may be unsuitable (for example, contraindicated) for that specific tissue stapler.

[0561] Figure 93 illustrates an example of a 24100 security process for addressing problems with device selection according to various aspects of the present disclosure. According to at least one aspect, the 24100 security process can be performed

o / implemented (for example, during a surgical procedure) by a control circuit associated with a central surgical controller with situational recognition (for example, 24242 in Figure 94) of a surgical system (for example, 24200 in Figure 94) . According to other aspects, the 24100 safety process can be executed / implemented (for example, during a surgical procedure) by a control circuit associated with a surgical instrument with situational recognition (for example, 24212, 24222 and / or 24232 of Figure 94) of a surgical system (for example, 24200 of Figure 94).

[0562] Referring to Figure 93, a tissue identification process 24108 can receive inputs comprising a device selection 24102 (for example, a stapler choice, for example, a stapler suitable for parenchyma firing, a stapler suitable for firing vascular, a stapler suitable for bronchial firing, etc.), various measures of device 24104 detected by one or more of a sensor (for example, closing angle of the end actuator, length of tissue in contact with the actuator edge, force to close / compression curve, etc.) and information with situational recognition 24106 (for example, procedure information, surgeon trends, etc.).

[0563] In the view of Figure 93, in device selection 24102, the control circuit that executes / implements the 24100 security process can be configured to receive a device parameter from a selected stapler / device and / or device parameters. associated with each component (eg staple cartridge) of the selected stapler / device to indicate device selection. For example, device parameters associated with a staple cartridge can include a type of cartridge,

a color of the cartridge, adjuncts to the cartridge, a clip load limit for the cartridge, a span of the cartridge, a firing rate for the cartridge, etc. According to one aspect, the device parameter (s) can be transmitted by the stapler / device to the control circuit after coupling to the surgical system. According to alternative aspects, the device selection can be entered through a user interface (for example, associated with a central surgical controller and / or in the operating room, for example, 24244 and / or 24254 in Figure 94) and / or received from an internal and / or external database (for example, data referring to the surgical procedure being performed and / or surgical instruments available 24249 and / or 24269 of Figure 94).

[0564] In addition to the view in Figure 93, the measurements from device 24104 can be detected through one or more of a sensor (for example, as described in Figures 17, 18, 53, 78, etc.) associated to an end actuator (for example, Component-A, 24216 of Figure 94) and / or other components of the surgical instrument (for example, Component-N, 24218 of Figure 94, for example, a staple cartridge). For example, one or more of a tissue sensor can be positioned and configured to check continuity and / or measure tissue impedance along the length of the end actuator to assess a length of tissue in contact with the actuator. end (for example, sensor or sensors 738 in Figure 17 to determine tissue location using segmented electrodes and / or measure tissue impedance, sensors 153468 in Figure 78 to determine the presence of tissue over the length of the end actuator, etc.). As an additional example, one or more of a sensor can be positioned and configured to detect / estimate the closing angle of the end / claw actuator (eg a displacement sensor, eg a position sensor 734 from the Figure 17, to detect the displacement of a gripping actuator / driving member, span sensor, for example, the sensor 152008a of Figure 53, to detect a gap between a first claw and a second claw of the end actuator, etc.). As an additional example, one or more of a sensor can be positioned and configured to detect a force to compress / close the tissue between the first jaw and the second jaw (eg, force sensor, eg, sensor 738 of Figure 17 comprising a force sensor, on the fabric surface of the first claw and / or second claw to detect forces when the fabric is attached, sensor, for example, current sensor 736 of Figure 17, to detect the consumption of current of the drive member correlated to the forces applied to the fabric, torque sensor, for example, 744b of Figure 17, to measure a closing force, etc.). Several additional aspects to detect an angle of closure of the end actuator, a length of tissue in contact with the end actuator, and a force curve for closing / compressing have been discussed elsewhere in this document.

[0565] Then, in the view of Figure 93, surgical recognition information 24106 can, in the light of Figure 94, be received through internal databases 24249 and / or external databases 24269 associated with a central surgical controller 24242 and / or via internal databases 24215, 24225, 24235 and / or external databases 24249, 24269 associated with a surgical instrument 24202, etc.

[0566] Returning to Figure 93, the tissue identification process 24108 is configured to determine a type of tissue found by the surgical instrument (for example, parenchyma, vessel, bronchi, etc.). In one example, the tissue identification process 24108 can determine that the tissue type is parenchyma based on multiple inputs (eg, tissue contact detected along the length of the jaws when the jaws are fully open, closing curve versus opening suggests a consistent tissue with parenchyma, etc.). In another example, the tissue identification process 24108 may determine that the tissue type is a vase (for example, PA / PV) based on multiple inputs (for example, the tissue contact detected almost immediately during the closure, tissue contact detected as just over a small area of the stapler and is detected as bounded on the distal side, initially detected closing forces suggest a tissue structure consistent with a vessel, etc.). In another example, the tissue identification process 24108 may determine that the tissue type is bronchial based on multiple inputs (for example, the contact of the tissue detected almost immediately during closure, the contact of the tissue detected on a small area of the stapler and is detected as delimited on both the distal and proximal sides, initially detected closing forces suggest a tissue structure consistent with bronchi, etc.). According to various aspects, these tissue type determinations can further be based on tissue parameters comprising a thickness of the tissue, a stiffness of the tissue, a location of the tissue (for example, with respect to the patient) and vascularization in the tissue. detected by and / or derived from measurements taken using one or more of the sensors described here.

Notably, the tissue identification process 24108 can additionally assess such initial tissue determinations in the context of additional inputs (eg, stapler choice, surgical procedure information, surgeon trends, etc.) before reaching a output / result of tissue identification.

This situational recognition ends up resulting in the output / result of tissue identification.

Here, go-

several aspects for the identification of a tissue found were discussed elsewhere in this document (for example, an example of thoracic surgery, etc.).

[0567] Again with reference to Figure 93, the tissue identification output / result can be used to determine whether the selected stapler / device and / or each component of the selected stapler / device (eg staple cartridge, and i - activation rate, etc.) is ideal 24110 for the surgical procedure. In this respect, the control circuit can receive additional information 24112 from internal and / or external databases (for example, referring to Figure 94, internal databases 24249 and / or external 24269 associated with a central surgical controller 24242, internal databases 24215, 24225, 24235 and / or external databases 24249, 24269 associated with a surgical instrument 24202, etc.). More specifically, additional information 24112 may comprise other available staplers, other available energy devices, other stapler components (for example, staple cartridges, drive shafts, etc.) available for use with the stapler / device selected, etc. according to at least one aspect, availability may be subject to the current inventory at the surgical site. Notably, the additional information 24112 may also comprise device parameters associated with each other available stapler, each other available energy device, each other staple component available for use with the selected stapler / device, etc.

[0568] According to several aspects, when assessing whether the stapler / device selected is ideal 24110, the control circuit that executes / implements the 24100 security process can be configured to analyze each tissue parameter detected (for example, example, detected by one or more of the sensor described here) in cooperation

operation with each received device parameter associated with the stapler / device 24102 selected based on restrictions defined by the system. In addition, according to such aspects, the control circuit can be configured to analyze each tissue parameter detected (for example, detected through one or more of a sensor described here) with the parameters of the received device associated with each other stapler. available, another available power device, another stapler component available for use with the selected stapler / device, etc., based on system-defined restrictions. According to such aspects, the control circuit can be configured to determine whether one or more of one among the other available staplers, the other available power devices, and / or the other stapler components available for use with the stapler / selected device are more ideal than the selected stapler / device 24102 and / or stapler / device components 24102 selected based on detected tissue parameters.

[0569] In several respects, one or more tissue parameters detected may comprise, for example, a type of tissue, a thickness of the tissue, a stiffness of the tissue, a location of the tissue, a vascularization in the tissue, etc. and a received device parameter may comprise, for example, a type of staple cartridge, a color of the staple cartridge, adjacent to the staple cartridge, a hold load limit for the staple cartridge, a span range for the staple cartridge and a firing rate for the staple cartridge, etc. According to several aspects, a constraint defined by the system (for example, based on historical data and / or procedural data accessed in the surgical system with situational recognition) may comprise preferential / ideal tissue parameters and / or Preferred / ideal tissue parameter ranges for each device parameter received. For example, a preferred / ideal tissue thickness and / or preferred / ideal tissue thickness range can be associated with each staple cartridge color. In this example, each color of the staple cartridge can indicate the types and / or sizes of staples in the staple cartridge. Here, a staple cartridge that comprises short staples may not be ideal for thick fabric. According to additional aspects, a restriction defined by the system (for example, based on historical data and / or procedural data accessed in the surgical system with situational recognition) may comprise a preferred / ideal grip load limit and / or range preferential / ideal grip load limit for each type of tissue detected. For example, each staple cartridge associated with its respective staple load limit can indicate the types of fabric that can be stapled optimally. Here, various combinations of device parameters received (eg staple cartridge type, staple cartridge color, staple cartridge adjunct, staple cartridge gripping load limit, span span staple cartridge, staple cartridge firing rate, etc.) and detected tissue parameters (eg tissue type, tissue thickness, tissue stiffness, tissue location, tissue vascularity, etc.) and restrictions defined by the established system (for example, associated with received device parameters and / or tissue parameters detected based on historical data and / or procedural data accessed in the surgical system with situational recognition) are covered by the present disclosure.

[0570] Again with reference to Figure 93, if it is determined that the selected device 24102 is ideal, the control circuit that executes / implements the 24100 security process can be configured to initially do nothing (for example, recommend more later) and / or document that the analysis was performed 24114. Instead, if it is determined that the selected device 24102 is not ideal, the control circuit can be configured to determine if there is a security problem 24116. According to several aspects, when assessing whether a safety problem exists with the stapler / device selected 24102, the control circuit can be configured to analyze each tissue parameter detected in cooperation with each parameter of received device associated with the stapler / device 24102 selected based on restrictions defined by the system.

[0571] Similar to that described above, a detected tissue parameter can comprise, for example, a type of tissue, a thickness of the tissue, a stiffness of the tissue, a location of the tissue, a vascularization in the tissue etc. and a received device parameter may comprise, for example, a type of staple cartridge, a color of the staple cartridge, adjacent to the staple cartridge, a staple charge limit of the staple cartridge, a span of span for the cartridge of staples and a firing rate for the staple cartridge, etc. According to several aspects, a system-defined constraint (for example, based on historical and / or procedural data accessed in the surgical system with situational recognition) may comprise preferential / ideal tissue parameters and / or preferred / ideal tissue parameters for each device parameter received. For example, a preferred / ideal tissue thickness and / or preferred / ideal tissue thickness range can be associated with each staple cartridge color. In this example, each color of the staple cartridge can indicate the types and / or sizes of staples in the staple cartridge. Here, continuing the example, if a device parameter received from the selected stapler / device 24102 comprises a staple cartridge color (for example, indicating short staples) and the detected tissue parameter indicates a tissue thickness exceeding that - preferred / ideal fabric thickness and / or the preferred / ideal fabric thickness range associated with the staple cartridge color of the selected stapler / device 24102, there is a security problem with the selected stapler / device 24102. The use of an inappropriate staple cartridge can lead to less than satisfactory results and / or undesired results (eg, failed stapling, draining, bleeding, etc.). In such a case, the control circuit can be configured to alert the surgeon 24118 (for example, with reference to Figure 94, via a user interface on the selected stapler / device 24214, 24224 and / or 24234, via a user interface associated with the central surgical controller 24244, through a user interface in operating room 24254, etc.) for security reasons. In this regard, the control circuit can be additionally configured to receive a cancellation command 24120 (for example, via the user interface on the selected stapler / device 24214, 24224 and / or 24234, via the associated user interface. with the central surgical controller 24244, through a user interface in operating room 24254, etc.) to allow the surgical process to proceed. In an example, with reference to Figure 94, this user interface may comprise a selectable user interface element to allow the procedure to continue, for example,

24251. In an alternative aspect, in response to the warning, the surgeon can correct the observed security problem (for example, by replacing the inappropriate staple cartridge with another staple cartridge) at the point where the device selection process security 24100 can be run / implemented again.

[0572] Similar to the one described above, according to additional aspects

a constraint defined by the system (for example, based on historical data and / or procedural data accessed in the surgical system with situational recognition) may comprise a preferred / ideal gripping load limit and / or load limit range preferential / ideal grip for each type of tissue detected.

For example, each staple cartridge associated with its respective staple load limit can indicate the types of fabric that can be stapled optimally.

Here, continuing the example, if a device parameter received from the selected stapler / device 24102 comprises its cartridge staple load limit and the fabric identified by the tissue identification process 24108 indicates a type of fabric that requires a print cartridge. staple with a higher grip load limit, there is a safety problem with the selected stapler / device 24102. Using an inappropriate staple cartridge can lead to less than satisfactory results and / or unwanted results (for example, example, failed stapling, oozing, bleeding, etc.). In such a case, the control circuit can be configured to alert the surgeon 24118 (for example, with reference to Figure 94, via a user interface on the selected stapler / device 24214, 24224 and / or 24234, via a user interface associated with the central surgical controller 24244, through a user interface in operating room 24254, etc.) for security reasons.

In this regard, the control circuit can be additionally configured to receive a cancellation command 24120 (for example, via the user interface on the selected stapler / device 24214, 24224 and / or 24234, via the associated user interface. with the central surgical controller 24244, through a user interface in operating room 24254, etc.) to allow the surgical process to proceed.

In an example, with reference to Figure 94, this user interface may comprise a selectable user interface element to allow the procedure to continue, for example,

24251. In an alternative aspect, in response to the warning, the surgeon can correct the observed security problem (for example, by replacing the inappropriate staple cartridge with another staple cartridge) at the point where the device selection process security 24100 can be run / implemented again. Again, various combinations of device parameters received (eg staple cartridge type, staple cartridge color, staple cartridge adjunct, staple cartridge staple load limit, span span staple cartridge, staple cartridge firing rate, etc.) and detected tissue parameters (eg, tissue type, tissue thickness, tissue stiffness, tissue location, tissue vascularity, etc.) and constraints defined by the established system (for example, associated with received device parameters and / or tissue parameters detected based on historical data and / or procedural data accessed in the surgical system with situational recognition) are contemplated by this revelation.

[0573] Referring again to Figure 93, if it is determined that a security issue does not exist with the selected stapler / device 24116, the control circuit that executes / implements the security process 24100 can be configured to offer - receive a recommendation to the surgeon 24122. According to at least one aspect of the present disclosure, if another stapler is available, another available energy device and / or another component of the stapler (for example, staples, drive shaft, etc. available for use with the selected stapler / device) 24112 is more ideal or optional, the control circuit can be configured to alert the surgeon (for example, referring to the

Figure 94, through a user interface on the stapler / device selected 24214, 24224 and / or 24234, through a user interface associated with the surgical cube 24244, through a user interface in the operating room 24254, etc. .) of its availability and recommend its use in the current surgical procedure. In this regard, the control circuit can be further configured to receive an acceptance (for example, via the user interface on the selected stapler / device 24214, 24224 and / or 24234, via the user interface associated with the central surgical controller. 24244, via a user interface in operating room 24254, etc.) of the recommendation. After acceptance, the control circuit can be configured to display an infomercial 24124 in relation to the other available stapler, the other available energy device and / or the other stapler component (for example, referring to Figure 94, Components A to N, eg staple cartridge, drive shaft etc. available for use with the selected stapler / device) 24112 which is more ideal. After rejection, the control circuit can be configured to terminate 24126 of the device selection security algorithm and / or perform a subsequent process.

[0574] According to several other aspects, although discussed specifically with respect to a stapler / device of the present invention, the present disclosure should not be so limited. More specifically, the revealed aspects equally applicable to other surgical instruments including energy devices (for example RF energy and / or ultrasonic surgical instruments) and / or their respective components and / or endoscopic devices and / or their respective components. Examples

[0575] Various aspects of the subject described here under the title "SA-

FETY SYSTEMS FOR SMART POWERED SURGICAL STAPLING "are defined in the Examples below:

[0576] Example 1 - A surgical system comprises a control circuit and a surgical instrument. The surgical instrument comprises a plurality of components and a sensor. Each one of the plurality of components of the surgical instrument comprises a parameter of the device. Each component is configured to transmit its respective parameter from the device to the control circuit. The sensor is configured to detect a tissue parameter associated with a proposed function of the surgical instrument and transmit the detected tissue parameter to the control circuit. The control circuit is configured to analyze the tissue parameter detected in cooperation with each respective device parameter based on a constraint defined by the system. The surgical system additionally comprises a user interface configured to indicate whether the surgical instrument comprising the plurality of components is suitable to perform the proposed function.

[0577] Example 2 - The surgical system of Example 1, with the detected tissue parameter comprising at least one of a type of tissue, a thickness of the tissue, a tissue stiffness, a tissue location, or vascularization of the fabric.

[0578] Example 3 - The surgical system of Example 1 or 2, where a component of the surgical instrument includes a staple cartridge, and the device parameter includes at least one among a type of staple cartridge, a color of the staple staple cartridge, compounds auxiliary to the staple cartridge, a hold load limit for the staple cartridge, a span for the staple cartridge, and a firing rate for the staple cartridge.

[0579] Example 4 - The surgical system of Example 1, 2 or 3, feeling

than a component of the surgical instrument includes an end actuator, and the detected tissue parameter comprises at least one of the closing angle of the end actuator in the tissue, a length of the tissue in contact with a surface contact with the fabric of the end actuator, and a force to compress the fabric in the end actuator.

[0580] Example 5 - The surgical system of Example 4, the control circuit being additionally configured to identify the tissue as a parenchyma, vessel or bronchi based on at least one detected tissue parameter.

[0581] Example 6 - The surgical system of Example 1, 2, 3,4 or 5, the control circuit being additionally configured to recommend at least one alternative component for use with the surgical instrument to perform the proposed function .

[0582] Example 7 - The surgical system of Example 1, 2, 3, 4, 5 or 6, the constraint defined by the system comprising at least one of a predetermined tissue parameter or a predetermined tissue parameter range associated with each device parameter transmitted.

[0583] Example 8 - The surgical system of Example 1, 2, 3,4, 5,6 or 7, the control circuit being additionally configured to avoid the proposed function when the restriction defined by the system is exceeded.

[0584] Example 9 - The surgical system of Example 8, the user interface comprising an element of the user interface selectable to cancel the control circuit to allow the proposed function of the surgical instrument.

[0585] Example 10 - The surgical system of Example 1, 2, 3, 4,5, 6, 7, 8, or 9, with the proposed function of the surgical instrument comprising one or more of the tissue grips, coagulates -

fabric cutting, fabric cutting, and fabric stapling.

[0586] Example 11 - The surgical system of Examples 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10, additionally comprising a central surgical controller coupled communicatively to the surgical instrument, the surgical controller being control comprises the control circuit.

[0587] Example 12 - The surgical system of Example 11, with one of the surgical instruments or the central surgical controller comprising the user interface.

[0588] Example 13 - A surgical system comprises a central surgical controller and a surgical instrument communicatively coupled to the central surgical controller. The surgical instrument comprises a plurality of components and a sensor. Each of the plurality of components of the surgical instrument comprises a parameter of the device. Each component is configured to transmit its respective parameter from the device to the central surgical controller. The sensor is configured to detect a tissue parameter associated with a proposed function of the surgical instrument and transmit the detected tissue parameter to the central surgical controller. The central surgical controller comprises a processor and a memory attached to the processor. The memory stores instructions executable by the processor to analyze the tissue parameter detected in cooperation with each respective device parameter based on a constraint defined by the system. The surgical system additionally comprises a user interface configured to indicate whether the surgical instrument that comprises the plurality of components is suitable to perform the proposed function.

[0589] Example 14 - The surgical system of Example 13, with the detected tissue parameter comprising at least one

between a type of tissue, tissue thickness, tissue stiffness, tissue site, or tissue vascularization.

[0590] Example 15 - The surgical system of Example 13 or 14, where a component of the surgical instrument includes a staple cartridge, and the device parameter includes at least one among a type of staple cartridge, a color of the staple staple cartridge, compounds auxiliary to the staple cartridge, a hold load limit for the staple cartridge, a span for the staple cartridge, and a firing rate for the staple cartridge.

[0591] Example 16 - The surgical system of Example 13, 14 or 15, where a component of the surgical instrument includes an end actuator, and the detected tissue parameter comprises at least one of an angle of closure of the end actuator on the tissue, a length of the tissue in contact with a tissue contact surface of the end actuator, and a force to compress the tissue in the end actuator.

[0592] Example 17 - The surgical system of Example 13, 14, 15, or 16, the instructions being additionally executable by the central surgical controller processor to recommend at least one alternative component for use with the surgical instrument to perform the proposed function.

[0593] Example 18 - The surgical system of Example 13, 14, 15, 16 or 17, the instructions being additionally executable by the processor of the central surgical controller to prevent the proposed function when the restriction defined by the system is exceeded.

[0594] Example 19 - Non-transitory, computer-readable media stores computer-readable instructions that, when executed, cause a machine to analyze a tissue parameter detected in cooperation with a device parameter from each of them. plurality of components of a surgical instrument in a surgical system, based on a constraint defined by the system, with the detected tissue parameter being associated with a proposed function of the surgical instrument. The surgical system includes the surgical instrument that includes a plurality of components. Each component is configured to transmit its respective parameter from the device to the machine. The surgical system additionally includes a sensor configured to detect the detected tissue parameter and transmit the detected tissue parameters to the machine. The instructions, when executed, additionally cause the machine to generate a user interface, and the user interface provides an indication of whether the surgical instrument including the plurality of components is suitable to perform the proposed function of the system surgical.

[0595] Example 20 - The computer-readable non-transitory media of Example 19, the instructions, when executed, additionally cause the machine to generate a cancellation element in the user interface, the cancellation element being selectable to allow the proposed function of the surgical instrument. Control a surgical instrument according to the detected closure parameters Compression rate to determine tissue integrity

[0596] In several respects, a surgical instrument can detect a variety of different variables or parameters associated with closing the claws of the surgical instrument, which in turn can be used to adjust or affect various operating parameters that dictate how the instrument surgical works. The rate at which the claws of a surgical instrument are transitioned from the open position to the closed position to secure the tissue between them can be defined as the grip rate or closing rate.

In many respects, the closing rate can be variable or constant during the course of an instance of claw closure. A limit against which a specific parameter associated with closing the jaws is compared can be defined as a closing limit.

[0597] Tightening the fabric to an inappropriate closing rate or with inappropriate closing limits can result in damage to the fabric (for example, the fabric can be torn due to the claws applying too much force to the fabric) and / or operational failures by the surgical instrument (for example, staples may be malformed due to the tissue not being fixed by the claws as the staples are released). Consequently, in some respects, the surgical instrument is configured to detect the characteristics of the tissue being trapped by the surgical instrument and adjust the closing rate (s), the limit (s) of closing, and other operating parameters accordingly. In addition, each surgical procedure can involve multiple different types of tissue and / or tissues with different characteristics. Consequently, in some respects, the surgical instrument is configured to dynamically detect the characteristics of the tissue each time a tissue is attached and adjust the closing rate (s), the closing limit (s) , and other operating parameters accordingly.

[0598] The present disclosure provides at least one solution, since a surgical instrument is configured to detect parameters associated with the compression of the tissue being trapped by the end actuator. The surgical instrument can additionally be configured to differentiate between tissues that have different integrity according to the detected tissue compression characteristics. The motor can then be controlled to affect the clamping rate and / or provide feedback to the user according to the integrity of the fabric. For example, the surgical instrument can be configured to decrease the rate of closure of the jaws if the compression characteristics of the detected tissue indicate that the tissue is rigid and / or provide a suggestion to the user to use adjunct reinforcement if the compression characteristics of the fabric indicate that the fabric has low shear resistance.

[0599] Figure 95 is a block diagram of a 21000 surgical instrument, according to at least one aspect of the present disclosure. In one aspect, a 21000 surgical instrument includes a 21002 control circuit coupled to a 21006 motor, a 21010 user interface and a 21004 sensor or sensors. The 21006 motor is coupled to a 21008 end actuator so that the 21006 motor makes with the claws (for example, the anvil 150306 and / or channel 150302 of the surgical instrument 150010 shown in Figure 25) of the end actuator 21008 to transition between a first configuration or an open configuration and a second configuration or a closed configuration, as discussed in relation to Figure 26, for example. The sensor or sensors 21004 can be connected in a communicable way to the control circuit 21002 so that the control circuit 21002 receives data and / or signals from them. The control circuit 21002 can be connected in a communicable way to the motor 21006 so that the control circuit 21002 controls the operation of the motor 21006 according to, for example, data and / or signals received from the sensor or sensors 21004. A 21010 user interface includes a device configured to provide feedback to a user of the surgical instrument, such as a screen or a speaker.

[0600] In several respects, the 21004 sensor or sensors can be configured to detect the compression parameters of a tissue trapped in the end actuator.

In one aspect, the sensor or sensors 21004 can be configured to detect the force to close (FTC) the claws of the end actuator 21008, that is, the force exerted to transition the claws from the open configuration to the closed configuration .

For example, the 21004 sensor or sensors may include a motor current sensor configured to detect the current drained by the motor, as discussed in Figures 12, 18 or 19. For direct current motors, the current drained by the motor corresponds to the motor torque (for example, the torque of the motor output drive shaft 21006), which is the FTC representative the end actuator 21008. The FTC of the end actuator 21008 corresponds to the tissue compression of the tissue stuck because it represents the force transmitted from the 21008 end actuator to the attached tissue as the 21008 end actuator closes on the tissue.

The more force is being applied to the tissue, the more the tissue is being compressed.

In another aspect, the sensor or sensors 21004 includes a first electrode disposed on the end actuator 21008 which is configured to receive an RF signal from a corresponding second electrode, as is discussed in relation to Figures 36 to 38. The electrical impedance of a fabric can correspond to the thickness of the fabric, which in turn can correspond to the tissue compression of the attached fabric.

In yet another aspect, the 21004 sensor or sensors includes a force sensitive transducer that is configured to determine the amount of force being applied to the 21004 sensor or sensors, as discussed in Figure 24. Similar to the discussion above with respect to FTC, the force detected by the transducer represents the force transmitted from the end actuator 21008 to the trapped tissue as the end actuator 21008 closes over the tissue.

The more force is being applied to the

the more the tissue is being compressed. User interface 21010 includes a device configured to provide feedback to a user of the surgical instrument, such as a screen or a speaker. In still other aspects, the 21004 sensor or sensors may include various combinations of the aforementioned sensors and other such sensors capable of detecting compression parameters associated with a safe tissue in the end actuator. For example, an end actuator, such as end actuator 15200 shown in Figure 53, can include a first sensor 152008a which comprises a force sensitive transducer and a second sensor 152008b which comprises an impedance sensor.

[0601] The 21002 control circuit can be configured to adjust the closing rate of the end actuator claws 21008 to accommodate different types of fabric. The control circuit 21002 can be configured to monitor the compression force exerted on the tissue (eg, FTC) or another parameter associated with tissue compression (eg, tissue impedance) during an initial compression period and, Based on the rate of change of the tissue compression parameter, adjust the claw closure rate or time accordingly. For example, it may be beneficial to reduce the closing rate or increase the closing time for more viscoelastic tissues, instead of applying full compression force over a short period of time, as discussed above with respect to Figure 22.

[0602] Figure 96 illustrates a logical flowchart of a 21050 process for controlling a surgical instrument according to the integrity of the attached tissue, according to at least one aspect of the present disclosure. In the following description of process 21050, reference is also made to Figure 95. The illustrated process can be performed, for example, by the control circuit 21002 of the surgical instrument

21000. Consequently, the control circuit 21002 that executes the process receives 21052 data and / or signals (for example, digital or analog) from the sensor or sensors 21004 belonging to a tissue compression parameter detected in this way. In several respects, the tissue compression parameter can include a parameter associated with a characteristic, type, property and / or condition of a tissue being operated; a parameter associated with an internal operation and / or a property of the 21000 surgical instrument; or a component thereof. In one aspect, the tissue compression parameter may include, for example, the FTC of the end actuator 21008. In another aspect, the tissue compression parameter may include, for example, the thickness of the trapped tissue. The control circuit 21002 can receive 21052 data related to a tissue compression parameter as one or more distinct values transmitted by the 21004 sensor or sensors, a signal transmitted by the 21004 sensor or sensors that can then be correlated to the value (s) (s) associated (ies), and so on.

[0603] Consequently, the control circuit 21002 determines how the value of the tissue compression parameter detected with- to one or more limits and then generates a response accordingly. In one aspect, the control circuit 21002 determines 21054 the value of the tissue compression parameter detected in relation to a first limit. For example, control circuit 21002 can determine 21054 if the tissue compression parameter detected exceeds or is greater than a first upper limit. In one aspect, if the tissue compression parameter detected exceeds the first limit, then the process proceeds along the SIM 21050 branch and control circuit 21002 controls 21056 motor 21006 to increase the time taken to close the end actuator claws 21008. The control circuit 21002 can control

21056 the 21006 engine to increase the claw closing time, for example, decreasing the rate at which the claws are closed, increasing the time when the movement of the claws is paused after the initial tightening of the fabric (that is, the waiting time for tissue fluency) or reducing the stabilization limit to end the gripping phase. If the detected tissue compression parameter does not exceed the first limit, the 21050 process will proceed along the NO branch and, in several respects, the 21050 process can terminate or the 21050 process can continue and the 21002 control circuit you can compare the value of the tissue compression detected to one or more additional limits or continue to receive 21052 data and / or signals from the tissue parameter.

[0604] In another aspect, the control circuit 21002 additionally determines 21058 the value of the tissue compression parameter detected in relation to a second limit. For example, the control circuit 21002 can determine 21058 if the tissue compression parameter detected is below or is less than a second or less limit. In one aspect, if the detected tissue parameter is below the second limit, then the process proceeds along the SIM 21050 branch and the control circuit 21002 provides corresponding information 21060 via, for example, the user interface 21010. The feedback provided 21060 may include, for example, visual feedback provided through a screen or audio feedback provided by a speaker. In one respect, feedback can suggest that the user takes one or more corrective actions to improve the situation resulting in the detected tissue compression parameter being unexpectedly low. Such corrective action may include, for example, the use of auxiliary reinforcement (ie, a tissue thickness compensator), as revealed in US patent application No. 8,657,176, entitled TISSUE THICKNESS COMPEN-

SATOR FOR A SURGICAL STAPLER, which is incorporated by reference. The adjunct reinforcement can, in several aspects, comprise a layer or series of layers of compressible material configured to adapt and / or apply additional compressive force to the tissue captured between the anvil 150306 (Figure 25) and the staple cartridge 150304 ( Figure 25).

[0605] The limits discussed above may include, for example, values for the parameter (s) detected by the sensor or sensors 21004 and / or derived from the parameter (s) detected by the sensor or sensors 21004 (for example, changing the time rate of a detected parameter). In aspects where the tissue compression parameter includes FTC, the end actuator 21008, the first limit can indicate the de-linearization above which the trapped tissue is considered rigid. Rigid tissue may be relatively prone to tearing, due to the mechanical actions of the claws on the tissue or, for the lung tissue, during reinflation. In addition, the second limit can indicate the downward linearization in which the trapped tissue is considered to have a weak shear force (ie, being soft). The fabric that has a low shear strength may be relatively difficult for the end actuator 21008 to hold firmly or otherwise hold in place during stapling and / or firing of the cutting member (ie beam with profile in | 150178 with cutting edge 150182).

[0606] It should be noted that although the steps in the specific 21050 process example in Figure 96 are shown to have occurred in a particular order or sequence, this representation is for illustrative purposes only and not a specific 21050 process sequence it is intended, unless a specific sequence of specific steps is explicitly required from the above description. For example, in other aspects of the 21050 process, the control circuit 21002 can determine 21058 if the detected tissue compression parameter is below a second or lower limit, before determining 21054 if the detected tissue compression parameter exceeds a first or higher limit.

[0607] Figure 97 illustrates a first graph 21100 representing the end actuator FTC 21104 versus time 21102 for illustrative shots of a 21000 surgical instrument, in accordance with at least one aspect of the present disclosure. In the following description of the first graph 21100, reference is also made to Figures 95 and

96. The first graph 21100 represents a first shot 21110 and a second shot 21114, which are illustrative shots by a surgical instrument 21000 controlled by a control circuit 21002 that performs the 21050 process described above in relation to Figure 96. In this example illustrative, the first limit 21106 includes a specific FTC time change rate (ie, AFTC) and the second limit 21108 includes a specific FTC. In many respects, limits 21106, 21108 can be fixed or predetermined values, defined in relation to one or more other variables, or programmed or configured by a user of the 21000 surgical instrument.

[0608] For the first shot 21110, the control circuit 21002 that performs the process illustrated in Figure 96 receives 21052 the data and / or signals from the tissue compression parameter and determines 21058 that the FTC falls below the second limit 21108 in time you. Consequently, the 21002 control circuit provides 21060 feedback to the user, including a suggestion for the user to take certain measures and / or indicate that the 21008 end actuator is holding onto a fabric that has a low shear resistance. . In one aspect, the feedback provided 21060 may include a suggestion that the user release and redisplay the 21000 surgical instrument with a tissue compensator (for example, a tissue compensator described in US patent application No. 8,657,176) applied to the actuator. end 21008 to reinforce and / or compensate for the low shear resistance of the fabric. In one aspect, the control circuit 21002 can still be configured to cause the motor 21006 to stop closing the claws of the end actuator 21008 if the FTC is below the second limit. In another aspect, the control circuit 21002 can be configured to provide a suggestion that the user stop closing the claws of the end actuator 21008 if the FTC is below the second limit. The feedback provided 21060 can take a variety of forms, including, for example, an instruction displayed on the operating room screen 107, 109, 119 (Figure 2) and / or on the surgical instrument screen, an audible message emitted by a loudspeaker located in the operating room and / or on the surgical instrument, tactile feedback through the surgical instrument or combinations thereof.

[0609] For the second shot 21114 (which can be a shot using a tissue compensator subsequent to the first shot 21110), the control circuit 21002 executing the 21050 process illustrated in Figure 96 receives 21052 the data and / or signals of the parameter tissue compression parameter and does not cause the FTC to fall below the second limit or exceed the first limit at any point during the closing stroke of end actuator 21008. Consequently, control circuit 21002 does not affect the rate to close the grapple, provide feedback to the user, or take any other action of this type.

[0610] Figure 98 illustrates a second graph 21116 representing the end actuator FTC 21102 versus time 21104 for an illustrative shot of a 21000 surgical instrument, in accordance with at least one aspect of the present disclosure. In the following description of the second graph 21116, reference is also made to the Figures

95 and 96. The second graph 21116 represents a third shot 21118 which is an illustrative shot by a surgical instrument 21000 controlled by a control circuit 21002 that performs the 21050 process described above in relation to Figure 96. In this illustrative example, the first limit 21106 includes a specific FTC time change rate (ie, AFTC).

[0611] For the third trigger 21116, the control circuit 21002 that performs the process illustrated in Figure 96 receives 21052 the data and / or signals from the tissue compression parameter and determines 21058 that the FTC falls below the first limit 21106 in time t2. As a result, control circuit 21002 controls 21056 motor 21006 to increase the claw closing time, such as decreasing the clamping closing rate, which correspondingly reduces the rate at which FTC 21102 increases. Increasing the claw closing time can be beneficial, for example, to prevent it from causing damage to the rigid tissue by preventing a greater amount of force from being exerted on the tissue for a short period of time. In one aspect, the first limit 21106 may include a standard FTC rate of change (AFTCp), that is, the standard or baseline FTC rate for a 21000 surgical instrument absent any modifications to the FTC by a control algorithm in accordance with with the type of fabric and other parameters. In this respect, if the FTC experienced by the surgical instrument 21000 during a surgical procedure exceeds the FTCp, then the control circuit 21002 by executing the 21050 process can control the 21056 engine 21006 to increase the clamping time.

[0612] The time in which the control circuit 21002 that executes the algorithm or process mentioned above compares the parameter detected by the sensor or sensors 21004 with one or more limits can include a discrete instance during the triggering stroke of the instrument surgical 21000, a series of discrete instances during the firing stroke and / or a continuous time interval during the firing stroke. The tissue compression parameter monitored by the control circuit 21002 and compared to a limit can include, for example, an FTC value (for example, the second limit 21108 shown in Figure 97) or an AFTC value (for example example, the first limit 21106 represented in Figures 97 and 98).

[0613] In one aspect, the control circuit 21002 can be further configured to store data related to the shots of the surgical instrument 21000 and then optionally use the data from the previous shots to adjust an algorithm to determine tissue integrity of a stuck tissue. For example, data from previous shots can be used to adjust the first and / or second process limits 21050 shown in Figure

96. In one aspect, the 21000 surgical instrument can be configured to pair with a central surgical controller 106 (Figures 1 to 3) that runs a system with situational recognition, as described above under the heading "Situational Awareness" and described in US patent application No. 15 / 940,654, entitled SURGICAL HUB SIUTICAL AWARENESS filed on March 29, 2018, which is hereby incorporated by reference in the present invention in its entirety. In this regard, the situational recognition system can determine the type of tissue being operated on during the surgical procedure and adjust the algorithm to determine the tissue integrity of a trapped tissue, accordingly. In another aspect, the 21000 surgical instrument can be configured to receive data input by the user indicating the type of tissue being operated and adjust the algorithm to determine the tissue integrity accordingly. For example, the 21000 surgical instrument can be configured to adjust the first and / or second limit

process 21050 represented in Figure 96 of standard values according to the type of fabric inserted by the user.

[0614] The techniques described above allow the 21000 surgical instrument to avoid damaging the trapped tissue and to avoid operational failures (for example, malformed staples) resulting from claw closure rates that are inappropriate or not ideal for specific characteristics. of the tissue being operated. Additionally, the techniques described above optimize the ability of the surgical instrument to respond adequately to the characteristics of the tissues found during the course of a surgical procedure. Initial fabric contact to determine the type of fabric

[0615] Tightening the fabric to an inappropriate closing rate or with inappropriate closing limits can result in damage to the fabric (for example, the fabric can be torn due to the claws applying too much force to the fabric) and / or operational failures by the surgical instrument (for example, staples may be malformed due to the tissue not being fixed by the claws as the staples are released). Consequently, in some respects, the surgical instrument is configured to detect the characteristics of the tissue being trapped by the surgical instrument and adjust the closing rate (s), the closing limit (s), and other operating parameters. - corresponding accordingly. In addition, each surgical procedure may involve multiple different types of tissue and / or tissues with different characteristics. Consequently, in some aspects, the surgical instrument is configured to dynamically detect the characteristics of the tissue each time a tissue is attached and adjust the closing rate (s), the limit (s) closing, and other operating parameters accordingly.

[0616] The present disclosure provides at least one solution, as a surgical instrument is configured to characterize the type of tissue in the tissue being attached according to the degree of contact of the tissue against the surfaces of the claws and the relative positions of the claws at the initial point in contact with the fabric. The rate of closure of the jaws and the limit for adjusting the rate of closure of the jaw can then be adjusted to levels appropriate for the type of tissue characterized by the detected degree of contact with the tissue and the detected position of the jaws. For example, the surgical instrument can be configured to differentiate between parenchyma and vessels because the parenchyma comes into contact to a greater degree with the surfaces of the claws and the claws at a greater angle at the initial contact point compared to the pots. The surgical instrument can then control the motor to affect the rate of closure of the jaw and adjust the limit according to the type of tissue detected.

[0617] Referring again to Figure 95, in one aspect, a 21000 surgical instrument includes a 21002 control circuit coupled to a 21006 motor, a 21010 user interface and a 21004 sensor (or sensors). The 21006 motor is coupled to an end actuator 21008 so that the engine 21006 causes the claws (for example, the anvil 150306 and / or channel 150302 of the surgical instrument 150010 shown in Figure 25) to end the actuator 21008 to transition between a first configuration or open configuration and a second configuration or closed configuration, as discussed in relation to Figure 26. The sensor or sensors 21004 can be connected in a communicable way to the control circuit 21002 so that the control circuit 21002 receives data and / or signals. The control circuit 21002 can be connected in a communicable way to the motor 21006 so that the control circuit 21002 controls the operation of the motor 21006 according to, for example, data and / or signals received from the sensor or sensors 21004 .

[0618] In several respects, the 21004 sensor or sensors can be configured to detect the physical contact of a tissue against the surface of the 21008 end actuator claws. In one aspect, the 21004 sensor or sensors can include one or more sensors of contact with the fabric arranged along the surfaces of contact with the fabric of the end actuator 21008, such as the anvil and the cartridge or channel.

The sensors of contact with the fabric can include, for example, a plurality of sensors or segments of a segmented circuit arranged sequentially along the surfaces of the claws that are configured to determine whether the fabric is positioned against them, as is discussed above with respect to Figures 75 to 79. In one aspect, the sensor or sensors 21004 include a plurality of electrodes that are each configured to receive an RF signal from a corresponding electrode disposed on the opposite claw, such as is discussed in relation to Figures 36 to 38. Consequently, the control circuit 21002 can perform continuity tests along the length of the end actuator 21008 to determine that the tissue is present in the locations corresponding to each electrode that is able to receive the signal from its corresponding electrode (because a signal transmission medium, that is, a fabric, must be located between them for an electrode to receive the corresponding electrode signal). In another aspect, the 21004 sensor or sensors include a plurality of force-sensitive transducers that are each configured to determine the amount of force being applied to the 21004 sensor or sensors, as discussed in relation to to Figure 24. Consequently, the control circuit 21002 can determine that the tissue is present in the locations corresponding to each force sensitive transducer that is detecting a non-zero force against it.

In other respects, the 21004 sensor or sensors include a plurality of load cells, pressure sensors and / or other sensors configured to detect physical contact against them. Like the discussion above regarding the force sensitive transducer, the 21002 control circuit can determine that the tissue is present in the locations corresponding to each load cell, pressure sensor and / or other sensor that is detecting a non-zero force. In yet another aspect, the 21004 sensor or sensors includes a current sensor that is configured to detect the amount of electrical current being drained by the 21006 motor, as is discussed in relation to Figures 12, 18 or 19. Consequently , the control circuit 21002 can determine the point at which the claws of the end actuator 21008 initially come into contact with the fabric according to the moment when the current drained by the 21006 motor increases to compensate for the increased clamp load experienced by the motor 21006 when the claws come into contact with fabric and begin to exert a gripping force against it, as discussed in Figure 83 (ie, the FTC increases 153610, 153616 when the claws hold the fabric and the FTC corresponds to the motor current). The various aspects described earlier in this document can be used, individually or in combination with other aspects, to determine the initial point of contact between the end actuator 21008 and the fabric being stapled and / or the degree of contact between the fabric and the 21008 end actuator.

[0619] Figure 99 illustrates a logical flow chart of a 21200 process for controlling a surgical instrument according to the physiological type of the tissue trapped, in accordance with at least one aspect of the present disclosure. In the following description of process 21200, reference is also made to Figure 95. The illustrated process can be performed, for example, by the control circuit 21002 of the surgical instrument 21000. Consequently, the control circuit 21002 that performs the illustrated process 21200 receives 21202 fabric contact data and / or signals from the sensor or sensors 21004, such as the fabric contact sensors discussed above and represented in Figures 100A to 101B. The received fabric contact data and / or signals 21202 indicate whether the fabric is in contact with at least one of the sensors

21004. Consequently, control circuit 21002 can determine 21204 the initial contact point between end actuator 21008 and the fabric being trapped. In one aspect, the control circuit 21002 determines 21204 when the initial contact of the fabric occurs by means of detection when at least one of the 21004 sensors arranged in each of the claws detects the contact of the fabric against it.

[0620] Consequently, the control circuit 21002 determines 21206 the position of the claws at the initial contact point of the fabric. In one aspect, the control circuit 21002 is coupled in a communicable way to a Hall Effect sensor disposed on one of the claws of the end actuator 21008 which is configured to detect the relative position of a corresponding magnetic element disposed on the opposite claw. , as discussed in relation to Figure 77. The control circuit 21002 can then determine the position of the claws 21206 according to the detected distance or span between them. In another aspect, the control circuit 21002 is coupled in a communicable way to a position sensor that is configured to detect the absolute or relative position of a closing tube that is configured to close the claws according to the tube. closing is triggered from a first position or position proximal to a second or distal position, as discussed in Figures 20 to 21 and 25. Control circuit 21002 can then determine 21206 the position of the claws according to the position detected from the

chamento. In yet another aspect, the 21002 control circuit is communicably coupled to an angle sensor, such as an Infineon Technologies TLESO12B 360º angle sensor, configured to detect the angle at which at least one of the claws is oriented . The control circuit 21002 can then determine 21206 the position of the jaws according to the detected angle at which the jaw or jaws are oriented.

[0621] Consequently, control circuit 21002 determines 21208 the degree of contact between the insured tissue and the surface or surfaces of contact with the tissue of the claws. The degree of contact with the tissue may correspond to the number or ratio of the 21004 sensors that have detected the presence (or absence) of the tissue, as discussed in Figure 79. In one aspect, the 21002 control circuit can determine the degree of tissue contact according to the reason of the sensor or sensors 21004 that detected the presence of tissue and the sensor or sensors 21004 that did not detect the presence of tissue.

[0622] Consequently, the control circuit 21002 applies 21210 control parameters to the motor 21006 according to the determined position 21206 of the claws and the determined degree 21208 of contact with the fabric. The motor control parameters can include, for example, the time to close the claws and / or the closing limit (s). In one aspect, the 21002 control circuit can be configured to perform a run time calculation and / or access a memory (for example, a look-up table) to retrieve the motor control parameters (for example, the claw closing rate and closing limit) associated with the specific position of the claws and the particular degree of contact with the tissue detected through the various sensors. In several respects, the 21002 control circuit can control the 21006 engine to adjust the claw closing time, for example, adjust the rate at which the claws are transitioned from the open to the closed position, adjust the interval time when the claws are paused after the initial engagement of the fabric (that is, the waiting time for the fabric to creep) and / or the adjustment of the stabilization limit that ends the fixation phase. In several respects, the closing limit (s) may include, for example, the maximum allowable FTC, end actuator 21008 or FTC change rate (i.e. AFTC) at which the circuit control number 21002 for the 21006 motor that activates the jaw closure or performs other actions, as discussed above, under the heading "Compression Rate to Determine Tissue Integrity". Control circuit 21002 can then control motor 21206 according to the set of motor control parameters 21210 by means of process 21200.

[0623] The position of the claws and the degree of contact with the tissue at the initial point of contact with the tissue corresponds to the thickness or geometry of the tissue being held, which in turn corresponds to the physiological type of the tissue. In this way, the control circuit 21002 can be configured to distinguish between types of fabric and then adjusted 21210 to control the parameters for the 21006 engine accordingly. For example, control circuit 21002 can be configured to determine whether parenchyma or vascular tissue has been trapped by end actuator 21008 and then adjust 21210 the motor control parameters that are appropriate for the type of tissue detected.

[0624] In some respects, the claw closure rate can be selected for each type of fabric to maintain the maximum FTC and / or AFTC under a certain closure limit, which can likewise be selected for each type of fabric. In one aspect, the 21002 control circuit can be configured to institute a minimum grip rate, so that the closing movement of the jaws is never interrupted permanently. In one aspect,

Therefore, the 21002 control circuit can be configured to control the maximum pause times to ensure that the closing of the jaw progresses at least at a standard rate. In one aspect, the 21002 control circuit can be configured to stop the 21006 engine and / or provide feedback to the user when the closing limit or limits are exceeded or otherwise stranded while using the 21000 surgical instrument.

[0625] It should be noted that although the steps in the specific example of process 21200 in Figure 99 are shown to have occurred in a particular order or sequence, this representation is for illustrative purposes only and not a specific sequence of process 21200 it is intended, unless a specific sequence of specific steps is explicitly required from the above description. For example, in other aspects of the 21200 process, the 21002 control circuit can determine the 21208 degree of contact with the 21206 fabric before determining the claw position at the initial contact point.

[0626] Figures 100A and 101B illustrate several side elevation views of an end actuator 21008 holding the parenchyma 21030 and a vessel 21032, in the positions of initial contact with the tissue and in the closed positions, according to at least one aspect of the present revelation. In the aspect shown, end actuator 21008 includes a plurality of fabric contact sensors 21016 arranged along the fabric contact surfaces of the claws, which include anvil 21012 and channel 21014. In other aspects, the tissue contact sensors 21016 can be arranged over a 150304 cartridge (Figure 25), in addition to or instead of being arranged along channel 21014 of the surgical instrument

21000. For the sake of brevity, the 21016 tissue contact sensors will be discussed as being arranged along the channel

21014 in the following description; however, it should be noted that the concepts discussed in the present invention also apply to the aspects where the 21016 fabric contact sensors are arranged along the 150304 cartridge. The 21016 fabric contact sensors can include, for example, impedance sensors, load cells, force sensitive transducers and combinations thereof, as discussed above. The tissue contact sensors 21016 can be outlined in activated sensors 21018 (ie sensors that detect the presence of tissue) and non-activated sensors 21020 (ie sensors that do not detect the presence of tissue) while using the instrument surgical 21000 in a surgical procedure.

[0627] Figures 100A and 101A illustrate the initial contact point of end actuator 21008 with parenchyma 21030 and vessel 21032, respectively. In one aspect, the initial point of contact between end actuator 21008 and a tissue can be defined as the point at which there is at least one sensor activated 21018 on both anvil 21012 and channel 21014. As described above, the types of tissue they can be differentiated according to the position of the claws (ie, the anvil 21012 and / or the channel 21014) and the degree of contact between the fabric and the claws at the initial point of contact with the fabric. For example, Figures 100A and 101A illustrate how parenchyma 21030 and a vessel 21032 can be differentiated based on the proportion of activated sensors 21018 at the initial contact point of the tissue. In other words, holding a 21032 vessel results in fewer activated sensors 21018 compared to holding parenchyma 21030. It should also be noted that the number of activated tissue sensors 21018 on anvil 21012 and channel 21014 does not have to be the same at the initial contact point of the tissue. As another example, Figures 100A and 101A illustrate how parenchyma 21030 and a vessel 21032 can be differentiated based on the angle at which anvil 21012 is oriented in relation to channel 21014 at the initial point of contact of the tissue. That is, the canister 21012 is oriented at a first angle 81 at the initial contact point with the parenchyma 21030 and at a second angle 82 at the initial contact point with the vessel 21032. The differences between the proportion of activated sensors 21018 and the angle at which the anvil 21012 is oriented can be used individually or in combination (for example, by the process 21200 shown in Figure 99) to characterize the physiological type of tissue being tightened and then define the appropriate jaw closure rate, closing limits and other motor control parameters for the type of fabric.

[0628] Figures 100B and 101B illustrate the point where the end actuator 21008 has the parenchyma and a fully attached 21032 vessel 21030, respectively. As can be seen, the change in the number or proportion of activated sensors 21018 and non-activated sensors 21020 when end actuator 21008 secures the fabric in the same way can be used to determine the type of fabric and / or physical characteristics of the fabric , the degree to which the tissue is compressed and / or the distance between anvil 21012 and channel 21014 and various other parameters. For example, a 21032 vessel deforms much more than parenchyma 21030 when fully attached, which results in a relatively greater change in the number of sensors activated 21018 when end actuator 21008 holds the vessel

21032. In some respects, a control circuit may perform a process to determine the type of tissue (ie, physiological type of tissue or tissue with certain physical characteristics) according to the change or rate of change in the number of sensors activated 21018 when end actuator 21008 is attached. In some aspects, a control circuit may perform a process to determine the degree to which the tissue is compressed and / or deformed according to the change or rate of change in the number of activated sensors 21018 when the end actuator 21008 is attached.

[0629] In some aspects where the surgical instrument 21000 includes a control circuit 21002 executing the process 21200 described above in Figure 99, when the control circuit 21002 determines that the claws 21013 initially came into contact with the tissue, the control circuit 21002 can be configured to detect or measure the separation between claws 6 and the length or degree of fabric contact between the fabric and claws L. The closing limits (for example, the FTC or AFTC limit) , the initial closing speed and the adjusted closing speed (s) (i.e., the closing speed (s) at which claws 21013 are closed after a closing limit is exceeded) can each be a function of 8 and L. As shown in Figures 100A and B, the claw separation can be set to 81 and the degree of contact with the fabric can be set to Li: at the initial contact with a first tissue (for example, parenchyma 21030). As shown in Figures 101A and B, the claw separation can be defined as 82 and the degree of contact with the fabric can be defined as L2 at the point of initial contact with a second fabric (for example, a 21032 vessel). Consequently, in some aspects where 8:> 8 and L1> L2, the FTC limit, of the FTC parenchyma> the FTC limit, of the FTC vessel; the AFTC limit, of the AFTC parenchyma> the AFTC limit, of the angular coefficient of the vessel; and the initial closing speed of the vessel Vv1> the initial closing speed of the parenchyma Vp1. Operational differences between these limits are discussed in more detail below with respect to Figures 102 and 103.

[0630] Figure 102 illustrates a first graph 21300 and a second graph 21302 representing end actuator FTC 21304 and closing speed 21306, respectively, versus time 21308 for shots illustrating a surgical instrument 21000 grasping the parenchyma 21030 , according to at least one aspect of the present disclosure. In the following description of the first graph 21300 and the second graph 21302, reference should also be made to Figures 95 and 99 to 100B. The illustrative shots described here are intended to demonstrate the concepts discussed above in relation to Figures 95 and 99 to 100B and should not be construed as limiting in any way.

[0631] A first shot of a 21000 surgical instrument can be represented by a first FTC curve 21310 and a corresponding first velocity curve 21310 ', which illustrate the change in FTC and closing speed over time during the course of the first shot, respectively. The first trigger can represent, for example, a standard trigger of the surgical instrument 21000 or a trigger of the surgical instrument 21000 that does not include a control circuit 21002 executing the process 21200 shown in Figure 99. When the trigger of the surgical instrument 21000 is initiated control circuit 21002 controls motor 21006 to start driving anvil 21014 from its open position, causing the closing speed of anvil 21012 to drastically increase 21318 until it reaches a first or standard speed of closing goes. As the anvil 21012 is activated from the open position, it comes into contact with the trapped tissue which, for this specific shot, is the parenchyma 21030. As the anvil 21012 comes into contact with the tissue that is being stuck at time to, the FTC increases 21312 from an initial FTC (e.g., zero) to a peak 21314 at time t1. At time t1, the control circuit 21002 of the surgical instrument 21000 determines that the FTC has reached or exceeded an FTC limit (which can, for example, be a standard limit regardless of the type of tissue) and controls the 21006 inter- breaking the movement of the anvil 21012, causing the velocity

closing capacity drops 21320 to zero. The movement of the anvil 21012 can be paused for a period p1, during which the closing speed is kept 21322 at zero. During the pause, the FTC gradually decreases 21316 as the trapped tissue relaxes.

[0632] A second shot from a 21000 surgical instrument can be represented by a second FTC curve 21324 and a corresponding first speed curve 21324 ', which illustrate the change in FTC and closing speed over time during second shot, respectively. In contrast to the first shot, the second shot may represent, for example, a shot from the surgical instrument 21000 that includes a control circuit 21002 that performs the process shown in Figure 99. When the shot from the surgical instrument 21000 is started, the circuit control 21002 controls motor 21006 to start driving anvil 21014 from its open position, which causes the closing speed of anvil 21014 to increase dramatically

21336. Due to the relative thickness and / or geometry of the parenchyma 21030, the initial point of contact between the tissue (ie parenchyma 21030) and the claws 21013 occurs shortly after the anvil 21012 starts to be driven by the 21006 engine; therefore, the control circuit 21002 that executes the process 21200 represented in Figure 99 is able to determine almost immediately that the parenchyma 21030 is being attached and, correspondingly, to define the time to close the claws, the limit (s) ) closing and other closing parameters at a relatively early point in the closing process. Therefore, control circuit 21002 controls motor 21006 to cause the closing speed of anvil 21014 to increase markedly 21336 to an initial closing speed vp1 specific to the tissue of parenchyma 21320.

[0633] As the anvil 21012 is activated from the position

open contact, it comes into contact with the trapped tissue which, for this specific shot, is parenchyma 21030. As anvil 21012 comes into contact with the tissue being trapped in time, the FTC increases 21326 from an FTC (for example, zero) for a first peak 21328 at time t2. It should be noted that the FTC increases 21326 more slowly during the second trip, compared to the first trip, because the control circuit 21002 that performs the 21200 process selected an initial closing speed or first vp: in the second shot, appropriate for the type of tissue being fixed, which reduces the amount of force exerted on the tissue compared to an unmodified shot of the surgical instrument 21000. At time t2, the control circuit 21002 of the instrument surgical procedure 21000 determines that the FTC has reached or exceeded an FTC limit, FTC, (which had been defined by the control circuit 21002 on or after when the control circuit 21002 determined that the tissue of the parenchyma 21030 was being tightened). The FTC parenchyma limit FTC, can represent, for example, the maximum force that can be safely or desirably exerted on the parenchyma tissue 21030. Consequently, the control circuit 21002 controls the motor 21006 to stop the movement beaker 21012, causing the closing speed to drop 21338 to zero. The movement of anvil 21012 can be paused for a period p> 2, during which the closing speed is kept 21340 at zero. During the pause, the FTC gradually decreases 21330 as the trapped tissue relaxes. The pause duration p2 can be equal to a standard pause duration (for example, p1) or a closing parameter selected by the control circuit 21002 for the tissue of the parenchyma 21030.

[0634] After the pause duration, having elapsed at time t3, control circuit 21002 re-engages motor 21006 and resumes closing anvil 21012. Consequently, the closing speed increases 21342 for a second closing speed vp2. In some respects, after the parenchyma FTC limit is exceeded for the first time, control circuit 21002 reduces the closing speed at which the anvil 21012 is closed to a second tissue-specific vp2 closing speed of the parenchyma 21030 , where vp2 <vp1. Control circuit 21002 can be configured to close anvil 21012 at a lower speed subsequent to the FTC limit, of the parenchyma FTC being exceeded because this may indicate that the tissue is thicker, more rigid or more resistant to the closing forces of the anvil 21012 than expected for the type of tissue detected. Thus, it may be desirable to reduce the closing speed to try to reduce the amount of closing forces subsequently exerted on the tissue being trapped.

[0635] As anvil 21012 resumes closing at time ts, the FTC starts increasing again until it reaches peak 21332 at time ta and once again reaches or exceeds the strength limit of the FTC parenchyma. At time ta, control circuit 21002 of surgical instrument 21000 determines that the FTC has reached or exceeded the limit of FTC, FTC ,. Consequently, control circuit 21002 controls motor 21006 to stop movement of anvil 21012, causing the closing speed to drop 21346 to zero. The movement of anvil 21012 can be paused for a period p3, during which the closing speed is maintained 21348 at zero. During the pause, the FTC gradually decreases by 21334 as the trapped tissue relaxes.

[0636] Figure 103 illustrates a third graph 21350 and a fourth graph 21352 representing end actuator FTC 21354 and closing speed 21356, respectively, versus time

21358 for illustrative shots of a 21000 surgical instrument grasping vessel 21032, in accordance with at least one aspect of the present disclosure. In the following description of the third graph 21350 and the second graph 21352, reference should also be made to Figures 95, 99, 101A to B. The illustrative shots described here are intended to demonstrate the concepts discussed above in relation to Figures 95, 99, 101A and B and should not be construed as limiting in any way.

[0637] A third shot from a 21000 surgical instrument can be represented by a third FTC curve 21360 and a corresponding first speed curve 21360 ", which illustrate the change in FTC and closing speed over time during the course of the third trigger, respectively The third trigger can represent, for example, a standard trigger of the surgical instrument 21000 or a trigger of the surgical instrument 21000 that does not include a control circuit 21002 executing the process represented in Figure 99. When the trigger of the surgical instrument 21000 is started, the control circuit 21002 controls the motor 21006 to start turning the anvil 21014 from its open position, which causes the closing speed of the anvil 21012 to increase dramatically 21370 until it reaches a first or standard closing speed va2. The initial closing speed va2 may or may not be equal to the initial closing speed va in Figure 102. As the anvil 21012 is moved from the open position, it travels for a period of time before making contact with the trapped tissue which, for this particular shot, is a 21032 vessel. It should be noted that this con - fret with shots where the surgical instrument 21000 is gripping the parenchyma 21030, as shown in Figure 102. Since a 21032 vessel is relatively thin, the anvil 21012 must generally travel a distance before making initial contact with the vessel

21032, while parenchyma 21032 is generally thicker than a 21032 vessel, and therefore the anvil 21012 generally almost immediately makes initial contact with the vessel 21032. Therefore, the FTC is initially void 21362 because the anvil 21012 travels for a period of time without contacting the fabric. After anvil 21012 comes into contact with tissue at time to, the FTC increases 21364 from an initial or flat FTC 21376 (e.g., zero) to a peak 21366 at time t2. At time t2, the control circuit 21002 of the surgical instrument 21000 determines that the FTC has reached or exceeded an FTC limit (which can be, for example, a standard limit regardless of the type of tissue) and controls the 21006 motor interrupted stopping the movement of the anvil 21012, causing the closing speed to drop 21372 to zero. The movement of the anvil 21012 can be paused for a period pa, during which the closing speed is maintained 21374 at zero. During the pause, the FTC gradually decreases by 21368 as the trapped tissue relaxes.

[0638] A fourth shot of a 21000 surgical instrument can be represented by a second FTC curve 21375 and a corresponding first speed curve 21375 ", which illustrate the change in FTC and closing speed over time during the course of the second shot In contrast to the first shot, the fourth shot can represent, for example, a shot from the surgical instrument 21000 that includes a control circuit 21002 that executes the process 21200 shown in Figure 99. When the surgical instrument 21000 is started, the control circuit 21002 controls the motor 21006 to start driving the anvil 21014 from its open position, which causes the closing speed of the anvil 21014 to increase dramatically

21386. Due to the relative fineness and / or geometry of vessel 21032 (compared to, for example, parenchyma 21030), the con-

initial touch between the fabric (ie, the vase 21032) and the claws 21013 does not occur until after the anvil 21012 is driven by the engine 21006 for a period of time; therefore, the control circuit 21002 that executes the process 21200 represented in Figure 99 is not able to determine that a vessel 21032 is being attached and, correspondingly, defines the time to close the claws, the limit (s) closing and other appropriate closing parameters until the closing process has been carried out for a period of time. Since the anvil 21012 does not come into contact with the thinner tissue of vessel 21032 for a period of time, therefore, the control circuit 21002 cannot detect which type of tissue is being pressed, the control circuit 21002 controls the motor 21006 to cause the closing speed of the anvil 21014 to increase sharply 21386 to the standard speed va.

[0639] As the anvil 21012 is activated from the open position, the FTC is initially flat 21376 because the anvil 21012 moves for a period of time without coming in contact with the fabric. After the anvil 21012 comes into contact with the tissue in time to, the FTC increases 21378 from an initial FTC (for example, zero). After coming in contact with container 21032, the control circuit 21002 executing process 21200 illustrated in Figure 99 is able to determine that a 21032 vessel is being attached and, correspondingly, sets the time to close the claws , the closing limit (s) and other closing parameters at that point in the closing process. At time ti, control circuit 21002 determines that the AFTC has reached or exceeded an AFTC limit, AFTC, (which had been defined by control circuit 21002 on or after to when control circuit 21002 determined that a vessel 21032 was feeling - of the prisoner). The AFTC vessel limit, AFTC ,, can represent, for example, the maximum rate of force change that can be safely or desirably exerted on a 21032 vessel fabric. Consequently, control circuit 21002 controls motor 21006 to drop 21388 the closing speed for a vessel closing speed vv: which is specific for the tissue of vessel 2032, where vv <Va.

[0640] As the anvil 21012 advances at the lowest closing speed of vessel vv1, the FTC increases 21380 more slowly than previously until it reaches a peak 21382 at time t3. At time t3, control circuit 21002 determines that the FTC has reached or exceeded an NDG limit, NDG, (which had been defined by control circuit 21002 on or after all when control circuit 21002 determines that a 21032 vessel was being arrested). The vessel limit FTC, FTC ,, can represent, for example, the maximum force that can be exerted safely or desirably on a fabric of vessel 21032. Consequently, control circuit 21002 controls motor 21006 to stop movement of the mustache 21012, causing the closing speed to drop 21932 to zero. The movement of the anvil 21012 can be paused for a period ps, during which the closing speed is maintained 21394 at zero. During the pause, the FTC gradually decreases 21384 as the trapped tissue relaxes. The duration of the ps pause can be equal to a standard pause duration (for example, p1) or a closing parameter selected by the control circuit 21002 for the fabric of the 21032 vessel.

[0641] In short, Figures 102 and 103 highlight the different ways in which a 21000 surgical instrument works with and without a 21002 control circuit that performs the 21200 process illustrated in Figure 99.

[0642] Figure 104 illustrates a fifth graph 21400 that represents the FTC 21402 end actuator and the closing speed

21404 versus time 21406 for an illustrative shot of a surgical instrument, in accordance with at least one aspect of the present disclosure. In the following description of the fifth graph 21400, reference should also be made to Figures 95 and 99 to 101B. The illustrative shots described here are intended to demonstrate the concepts discussed above in relation to Figures 95 and 99 to 101B and should not be construed as limiting in any way.

[0643] A fifth shot from a 21000 surgical instrument can be represented by a fifth FTC curve 21408 and a corresponding fifth speed curve 21408 ', which illustrate the change in FTC and closing speed over time during the course of the fifth shot , respectively. The fifth trigger can represent, for example, a trigger of the surgical instrument 21000 that includes a control circuit 21002 that executes the process shown in Figure 99. When the trigger of the surgical instrument 21000 is initiated, the control circuit 21002 controls the motor 21006 to start driving anvil 21014 from its open position, which causes the closing speed of anvil 21014 to dramatically increase 21416 up to a specific plateau 21418 of a specific closing speed. As the anvil 21012 closes, the FTC increases 21412 until it reaches its peak 21410 at a specific time. From peak 21412, the FTC decreases 21414 until the tissue is fully trapped, at which point the control circuit 21002 controls the motor 21006 to interrupt the closing of the anvil 21012 and the closing speed drops 21420 to zero .

[0644] The fifth shot thus represents a shot from the surgical instrument 21000, with no part of the FTC limit, the AFTC limit, or any other closing limit being reached or exceeded during clamping 21013. In other words , the fifth trigger remains within all control parameters during the course of closing the claws 21013. In this way, the control loop 21002 does not pause anvil 21012, adjusts the closing speed of anvil 21012, or take any other corrective action during the closing stroke of the 21013 jaws.

[0645] Figure 105 illustrates a sixth graph 21422 representing the end actuator FTC 21402 and the closing speed 21404 versus time 21406 for an illustrative shot of a surgical instrument, in accordance with at least one aspect of the present disclosure. In the following description of the sixth graph 21422, reference should also be made to Figures 95 and 99 to 101B. The illustrative shots described here are intended to demonstrate the concepts discussed above in relation to Figures 95 and 99 to 101B and should not be construed as limiting in any way.

[0646] A sixth shot from a 21000 surgical instrument can be represented by a sixth FTC curve 21424 and a corresponding sixth speed curve 21424 ', which illustrate the change in FTC and closing speed over time during the course of the sixth shot , respectively. The sixth trigger can represent, for example, a trigger of the surgical instrument 21000 that includes a control circuit 21002 that executes the process 21200 represented in Figure 99. When the trigger of the surgical instrument 21000 is initiated, the control circuit 21002 controls motor 21006 to start driving anvil 21014 from its open position, which causes the closing speed of anvil 21014 to increase drastically 21432 until reaching a specific closing speed. As the anvil 21012 closes, the FTC increases 21428 until it reaches its peak 21426 at a specific time. In this specific case, the operator of the surgical instrument 21000 chooses to open the claws 21013 of the surgical instrument 21000 in order to readjust the tissue in it. In this way, the closing speed drops 21434 until it reaches a negative closing speed, indicating that claws 21013 are being opened to, for example, easily allow the fabric to be readjusted within claws 21013. Closing speed then returns 21436 back to zero, claws 21013 stopped. Correspondingly, the FTC decreases 21430 to zero as claws 21013 are released from the fabric.

[0647] Figure 106 illustrates a seventh graph 21438 representing the end actuator FTC 21402 and the closing speed 21404 versus time 21406 for an illustrative shot of a surgical instrument, in accordance with at least one aspect of the present revelation. In the following description of the seventh graph 21438, reference should also be made to Figures 95 and 99 to 101B. The illustrative shots described here are intended to demonstrate the concepts discussed above in relation to Figures 95 and 99 to 101B and should not be construed as limiting in any way.

[0648] A seventh shot from a 21000 surgical instrument can be represented by a seventh FTC curve 21440 and a corresponding seventh speed curve 21440 ', which illustrate the change in FTC and closing speed over time during the course of the seventh shot, respectively. The seventh shot can represent, for example, a shot of the surgical instrument 21000 that includes a control circuit 21002 that executes the process 21200 represented in Figure 99. When the trigger of the surgical instrument 21000 is initiated, the control circuit 21002 controls motor 21006 to start driving anvil 21014 from its open position, which causes the closing speed of anvil 21014 to dramatically increase 21450 until reaching a first closing speed vi. As the anvil 21012 closes, the FTC increases 21442 until time ti. At time t1, control circuit 21002 determines that the AFTC has reached or exceeded the AFTC limit,

AFTCr, which can be a standard AFTC limit or an AFTC limit for a particular type of physiological tissue detected by control circuit 21002 according to process 21200 represented in Figure 99. As another example, AFTC71 can be defined by another process performed by the control circuit 21002 and / or another control circuit of the surgical instrument 2100 in response to other parameters detected or according to another algorithm. For example, if the claw closure is taking place within the operational parameters of the 21200 process illustrated in Figure 99, but another sensor and / or process of the 21000 surgical instrument determines that the tissue to be attached, however, deviates from the parameters expected in some way (for example, the fabric is thicker or thinner than expected for the type of fabric provided) and then sets the time to close the claws 21013, the limit (s) closing and other control parameters, consequently. In one example, a second sensor detects at time t that the tissue is thinner than expected. Consequently, control circuit 21002 defines a new AFTCr (which, in this example, is less than the previous AFTCr), which control circuit 21002 determines is being reached or exceeded at time t :.

[0649] Consequently, control circuit 21002 controls motor 21006 to decrease 21452 the closing speed of beaker 21012 to a second closing speed v2, where v1> v2. From t1 onwards, the drop in closing speed results in the FTC increasing 21444 at a slower rate. The FTC increases 21444 until it reaches a peak 21446 below the FTC limit, FTC7 and then decreases thereafter. As the seventh trip remains within all closing parameters after t1, the closing speed is maintained 21454 at the second closing speed v2 until the fabric is fully attached, at which point the control circuit 21002 controls the motor 21006 to stop closing anvil 21012 and the closing speed drops 21456 to zero.

[0650] Figure 107 illustrates a graph 21500 showing impedance 21502 versus time 21504 to determine when the claws of a surgical instrument come into contact with tissue and / or staples, in accordance with at least one aspect of the present disclosure. In the description below of the seventh graph 21438, reference should also be made to Figure 95. As discussed above, the 21004 sensor or sensors that are configured to detect the degree of compression of a tissue trapped by the end actuator 21008 and / or are configured to detect initial contact with a tissue may include, for example, impedance sensors. The impedance and / or rate of change of the tissue impedance, as detected by the impedance sensor or sensors, can be used to determine the state of the fabric being attached. For example, if the detected impedance has a 21506 plateau at a Zoc impedance that indicates an open circuit condition, then a 21002 control circuit coupled to impedance sensors can determine whether the jaws are open and / or are in contact with a tissue. As another example, when the impedance detected initially decreases 21508 from the open circuit impedance Zoc, then a control circuit 21002 coupled to the impedance sensors can determine that the initial contact with a tissue has been made. As another example, as the detected impedance decreases 21510 from the Zoc open circuit impedance, the shape of the impedance curve versus time and / or the rate of change of the detected impedance can be used by a control circuit 21002 coupled to impedance sensors to determine the tissue compression rate and / or the degree to which the tissue is being compressed. As yet another example, if the detected impedance drops 21512 to zero, then a control circuit 21002 coupled to impedance sensors can determine whether the claws of the end actuator 21008 have come into contact with a clamp, which shortens the detection system impedance. Examples

[0651] Several aspects of the subject described here under the title "Controlling a surgical instrument according to sensed closure parameters" are presented in the following examples:

[0652] Example 1 - A surgical instrument comprises an end actuator that comprises jaws that can be transposed between an open and a closed configuration. The surgical instrument additionally comprises a motor operationally coupled to the jaws. The motor is configured to transition the jaws between the open configuration and the closed configuration. The surgical instrument additionally comprises a sensor configured to transmit at least one signal indicating a tissue compression parameter associated with a tissue between the jaws. The surgical instrument additionally comprises a control circuit coupled to the sensor and the motor. The Control Circuit is configured to receive at least one signal, determine a value of the tissue compression parameter based on at least one signal as the claws transition from the open configuration to the closed configuration, make with the motor to increase the time for the transition of the jaws to the closed configuration according to whether the value of the tissue compression parameter is above a first limit, and to provide feedback according to whether the value of the compression parameter of tissue is below a second limit.

[0653] Example 2 - The surgical instrument of Example 1, with the tissue compression parameter comprising a force exerted by the engine to make the transition from the claws to the closed configuration.

[0654] Example 3 - The surgical instrument of Example 1, with the tissue compression parameter comprising a rate of time change of a force exerted by the engine to make the transition from the claws to the closed configuration.

[0655] Example 4 - The surgical instrument, according to Examples 1, 2, or 3, and the feedback includes a suggestion for adjunct reinforcement.

[0656] Example 5 - The surgical instrument of Example 1, 2, 3 or 4, in which the control circuit is configured to increase the time of transition from the jaws to the closed configuration by decreasing a rate at which the motor makes the transition from the claws to the closed configuration.

[0657] Example 6 - The surgical instrument of Example 1, 2, 3 or 4, in which the control circuit is configured to increase the time of transition from the jaws to the closed configuration by increasing the time interval in which the motor stops while making the transition from the claws to the closed configuration.

[0658] Example 7 - The surgical instrument of Example 1, 2, 3 or 4, in which the control circuit is configured to increase the transition time of the jaws to the closed configuration by reducing a stabilization limit to stop the engine when making the transition from the claws to the closed configuration.

[0659] Example 8 - A surgical instrument comprising an end actuator. The end actuator comprises transitional claws between an open and closed configuration and one or more sensors arranged along a fabric contact surface of each of the claws. The one or more sensors are configured to detect contact with a tissue. The surgical instrument additionally comprises a motor operationally coupled to the jaws. The motor is configured to transition the jaws between the open configuration and the closed configuration. The surgical instrument additionally comprises a control circuit coupled to one or more sensors and the motor. The control circuit is configured to determine an initial contact point at which the fabric comes into contact with the surfaces in contact with the claw fabric, determines a separation between the claws at the initial contact point, determines a degree of contact between the surfaces in contact with the fabric and the fabric, causes the motor to transition from the jaws to the closed configuration at a rate corresponding to the separation between the jaws and the degree of contact between the surfaces in contact with the fabric and the fabric at the initial contact point and causes the motor to adjust the rate at which the jaws are transferred to the closed configuration according to whether a force exerted by the motor to transition the jaws to the closed configuration exceeds a limit. The limit corresponds to the separation between the claws and the degree of contact between the contact surfaces of the fabric and the fabric at the initial point of contact.

[0660] Example 9 - The surgical instrument of Example 8, the one or more sensors comprising pressure sensors.

[0661] Example 10 - The surgical instrument of Example 8, the one or more sensors comprising impedance sensors.

[0662] Example 11 - The surgical instrument of Example 8, 9, or 10, the separation between the claws comprising an angle between the claws.

[0663] Example 12 - The surgical instrument of Example 8, 9 or 10, the separation between the claws comprising a gap between the claws.

[0664] Example 13 - A surgical instrument comprising an end actuator. The end actuator comprises grips configured to transition between an open configuration and a closed configuration to hold a tissue and a contact sensor assembly configured to detect the tissue against it. The surgical instrument additionally comprises a position sensor configured to detect a jaw configuration and a motor coupled to the jaws. The motor is configured to transition the jaws between the open configuration and the closed configuration. The surgical instrument additionally comprises a control circuit coupled to the contact sensor assembly, the position sensor and the motor. The control circuit is configured to determine an initial contact point at which the fabric comes into contact with the jaws, determine the configuration of the jaws via the position sensor at the initial contact point, determine a contact amount of the jaws. fabric between the fabric and the jaws through the contact of the sensor assembly at the initial contact point, set a closing rate at which the motor transits the jaws to the closed configuration according to the jaws configuration and the amount of fabric contact at the initial contact point, define a closing limit according to the jaws configuration and the amount of fabric contact at the initial contact point and control the motor according to a force exerted by the motor to make the transition from the jaws to the closed configuration in relation to a limit.

[0665] Example 14 - The surgical instrument of Example 13, since the sensor set comprises a pressure sensor.

[0666] Example 15 - The surgical instrument of Example 13, since the sensor set comprises an impedance sensor.

[0667] Example 16 - The surgical instrument of example 13, 14, or 15, with the configuration of the jaws corresponding to an angle between the jaws.

[0668] Example 17 - The surgical instrument of example 13, 14, or 15, with the configuration of the jaws corresponding to a gap between the jaws. Systems for adjusting end actuator parameters based on preoperative information

[0669] Aspects of the present disclosure are presented to adjust the closing limit and closing rate implemented by a closing control program executed by a control circuit of a surgical instrument, in which the adjustment is made based on pre- operative. The adjustment of the closing limits can be an example of performance of the situational recognition by the interactive surgical system implemented by computer (including one or more surgical systems 102 and cloud-based medical analysis system, such as the cloud 104, 204, which is referred to as cloud 104 for the sake of clarity). For example, closure limits can be adjusted to a patient-specific closure limit based on perioperative information received from cloud 104 or determined by operating rooms or surgical instruments. As used here, perioperative information comprises preoperative, intraoperative and postoperative information.

[0670] Preoperative information refers to information received prior to performing a surgical operation with a surgical instrument, while intraoperative information refers to information received during a surgical operation (for example, as a stage of the operation surgery is being performed). In particular, the computer-implemented interactive surgical system can determine or infer closing parameters of the end actuator, such as an appropriate end actuator closing limit and a closing rate algorithm, for specific portable intelligent surgical instruments. Such inferences can be based on contextual information related to a surgical procedure to be performed and related to the corresponding patient. Contextual information can include or be determined based on perioperative information. Surgical instruments can be any suitable type of surgical instrument described in the present disclosure, such as surgical instrument 112, 600, 700, 750, 790, 150010. For the sake of clarity, surgical instrument 112 is mentioned.

[0671] Perioperative information, such as diseases and treatments diagnosed in the perioperative period, can affect the properties or characteristics of the tissue being treated by the surgical instrument 112. For example, a patient may have been previously diagnosed with cancer and received radiation treatments to treat the cancer. Consequently, this preoperative information would indicate that the patient's tissue may have an increased stiffness characteristic. However, the closure control program currently in place may not consider this increased rigidity. Consequently, using the closure control program to perform a surgical procedure according to a general closing rate algorithm could result in unnecessary trauma or tissue damage due to excessive compression of the patient's tissue. In addition, during a surgical operation, intraoperative information can be analyzed, such as identifying which type of tissue among multiple types of potential tissues is being treated. Different types of fabric may also have different characteristics of the fabric such as fabric stiffness. Consequently, changes in intraoperative information can be used to perform intraoperative adjustments alternatively or in addition to perioperative adjustments. In short, closure control programs may not consider that different closure rate limits should be applied, depending on perioperative information, such as type of tissue, surgical procedure being performed and surgical steps already performed.

[0672] It may be desirable for a surgical instrument to consider different types of tissues and the various characteristics of these different types of tissues when a surgical operation is performed with the surgical instrument 112. In particular, it may be desirable for the surgical instrument 112 effectively determine the type of tissue and the characteristics of that type of tissue before the clinician performs a surgical operation with the surgical instrument, as well as during the execution of a surgical operation.

[0673] Therefore, in some respects, a cloud-based medical analysis system (eg, interactive surgical system implemented by computer 100) is provided, in which perioperative information can be considered to determine the type of tissue to be treated and the characteristics of the treated tissue before treatment. For example, the surgical procedure to be performed and other patient information may be instances of preoperative information retrieved prior to the execution of the surgical procedure. Previous stages of a surgical operation, another surgical history and a change in the type of tissue are examples of intraoperative information that can be considered. In general, this perioperative information can be used in conjunction with sensor signals indicative of a closing parameter to determine, infer or adjust parameters of an end actuator (for example, rate of change and closing limit) of the surgical instrument 112. The end actuator can be any end actuator described in the present disclosure, such as end actuator 702, 151600, 150300, 151340, 152000, 152100, 152150, 152200, 152300, 152350, 152400, 153460 , 153470,

153502. For clarity, end actuator 702 is mentioned.

[0674] The analysis of perioperative information regarding situational recognition related to the closing rate can be obtained in several ways. Based on perioperative information, a control circuit, such as control circuit 500, 710, 760, 150700 (discussed above in relation to Figures 12, Figure 15, Figure 17 and Figures 29A and B) of a surgical instrument could adjust the rate of change of entries and closing limits used in the selected closing control program. For the sake of clarity, the control circuit 500 is referenced. The control circuit 500 can also select a different control program based on perioperative information. Additionally or alternatively, a central surgical controller such as central surgical controller 106, 206 (called central surgical controller 106 for the sake of clarity) can receive perioperative information from cloud 104 or surgical instrument 112. For example, the surgical controller central physician 106 can receive an electronic medical record (EMR) from a patient from cloud 104 or initial measurements of tissue thickness, which are determined based on contact with the tissue or pressure sensors (as shown in Figure 24, for example) of surgical instrument 112.

[0675] The central surgical controller 106 can then analyze the perioperative information received. Based on this analysis, the central surgical controller 106 can then transmit a signal to the surgical instrument 112 to adjust the input change rate and the closing limits used in the selected closing control program. Central surgical controller 106 can also instruct surgical instrument 112 to select a different closing control program, such as through the control circuit by selecting a different control program. The selection of a different control program can be based on a signal received from the central controller 106 or by the surgical instrument 112 receiving an updated control program from the central controller 106. The cloud 104 can also perform the analysis to adjust the closing rate and maximum limit used. In particular, cloud 104 processors can analyze perioperative information to determine the type and characteristics of the tissue to change the inputs of a closure control program or select a different appropriate closure control program to be run by the instructor. surgical instrument, for example.

[0676] In this way, the surgical instrument 112 can be instructed by the cloud 104 (through the central controller 106, for example) to apply an algorithm of adequate closing rate and maximum closing limit. The type and characteristics of the fabric can be further determined based on a sensor signal indicative of a closing parameter. The sensors can be fabric contact or pressure sensors, force sensors, motor current sensors, position sensors, load sensors or other suitable sensors such as sensors 472, 474, 476, 630, 734, 736, 738, 744a — 744e, 784, 788, 152408, 153102, 153112, 153118, 153126, 153200, 153438, 153448, 153450a, 153450b, 153474, described above. For the sake of clarity, the 474 sensor is mentioned. Sensor 474 is configured to transmit a sensor signal indicative of a parameter of the surgical instrument 112. Some types of perioperative information can be stored in cloud 104 before determining the type and characteristics of the tissue. For example, patient EMRs can be stored in cloud memory 104 (for example, cloud databases). In general, surgical instruments 112, centers 106 or cloud 104 can analyze perioperative information to determine tissue type and

features of situational recognition.

[0677] Therefore, the type of tissue and the characteristics determined based on perioperative information can be used to proactively adjust the closure rate and maximum limit used. That is, perioperative information can be used to predict more effective closing parameters (for example, 702 end actuator parameters), so that the closing control program applied by the surgical instrument 112 uses a rate and a closure limit that take into account the specific characteristics of the patient and the type of tissue. Consequently, the use of the closure rate and situational recognition of the limit, as described in this document, can advantageously allow the surgical instrument 112 to apply an adjusted rate and closure limit without over-compressing the tissue to be treated. Super compression can be based on the first and second claw members of the end actuator 702. A first and a second claw member can be the first claw member 152002, 152152, 152154 and the second claw member 152204, 152254, 152304, respectively, for example. The first and second claw members can also refer to anvil 716, 766 and staple cartridge 718, 768. For the sake of clarity, the first claw member is called 152002 while the second member claw is called 152204. The first and second claw members 152002, 152004 can define an aperture of end actuator 702, which is defined as the distance between claw member 152002 and second claw member

152004.

[0678] Unnecessary tissue damage or trauma from excessive compression can occur when the opening of the end actuator 702 is unnecessarily small, for example. The reduction or prevention of such excessive compression can be achieved by adjustment using perioperative information and / or signals from the sensor of the 474 sensors. In addition, the compression applied during measurements of the initial closing parameters, such as based on the sensor of load 474 (clamping force measurement) and at the 474 sensor positioned (measurement of the position of the first claw member 152002 and second claw member 152004) can be minimized. In general, sensors 474 can be configured to measure the closing force exerted by the end actuator 702 of the surgical instrument 112. In addition to proactively inferring characteristics and tissue type from perioperative information, one or more of the surgical instruments 112 , central controller 106 and cloud 104 can use measurements detected by sensors 474 (as shown in Figure 12) to check or make other adjustments to the applied closing force, closing rate and closing limit, if necessary. Specifically, contact sensors can be used to determine the thickness of the undeformed tissue. In addition, the load sensor 474 in combination with the position sensor 474 can be used to determine the thickness of the fabric based on the closing force applied in relation to the position of the first claw member 152002 and the second claw member 152004, respectively. These additional checks or adjustments can be performed pre- or intraoperatively.

[0679] The closing parameter with situational recognition can be performed continuously. In this way, the doctor or surgeon can use this perioperative information to continuously adjust the closing parameters of the 702 end actuator (for example, from a closing control program) as appropriate (for example, when the steps of a surgical procedure are performed). For example, perioperative information can be used to adjust the end parameters of the end actuator 702 when it is determined, based on clinical history (for example, a surgeon's routine practice), that the next step of the surgical procedure being performed involves vascular tissue. In this situation, the surgical instrument with situational recognition 112 can apply closing force with a constant closing change rate. Such perioperative information can be used together with a sensor signal indicating a closing parameter of the surgical instrument 112 to adjust the closing parameters of the end actuator 702 (for example, closing change rate and closing limit - control program). Perioperative information, such as intraoperative information, may indicate that the patient was previously treated by radiotherapy.

[0680] Based on this information, the control circuit 500 can infer increased tissue stiffness, which is a characteristic of the tissue that can be considered throughout the stages of the surgical procedure. In one example, this increased tissue stiffness can be perioperative information used to supplement a sensor signal indicative of tissue thickness, so that adjustment to a more appropriate value of the end parameter of the end actuator 702 can be achieved. Perioperative information may also indicate that the surgical procedure being applied is a lobectomy procedure, which could be determined from data stored in the cloud 104. Based on knowledge of the lobectomy procedure, it can be determined that the possible Various types of tissues to be treated (for example, stapled) include blood vessels, bronchial tissue and parenchyma tissue.

[0681] Consequently, based on perioperative information, the specific tissue type and characteristics of the tissue currently being treated by the surgical instrument 112 can be predicted or inferred prior to the initiation of therapeutic tissue treatment. For example, considering the initial thickness of the tissue (measured when the tissue currently being treated comes into contact with the 702 end actuator) in conjunction with treatment, diagnosis, and patient information may allow an inference that the tissue of the previously irradiated parenchyma is being treated. As the type and characteristics of the tissue being treated can be determined contextually before the start of the surgical procedure, the closure control program implemented by the control circuit 500 of the surgical instrument 112 can be advantageously adjusted (for example , changing the input parameters according to the inference of the type or characteristics of the tissue) or changed (for example, selecting a different control program) before the beginning of the therapeutic treatment. Specifically, the maximum tissue closure limit can be lowered to address the rigidity and fragility of the irradiated parenchyma being treated. The maximum limit can refer to a maximum closing force that can be applied or a maximum closing change rate. In addition, the closing control program's closing algorithm could also be adjusted to apply a slower and more conservative closing rate based on the identification of the irradiated parenchyma.

[0682] In addition, it can be determined whether the surgical instrument 112 is a suitable stapling surgical instrument 112 for the irradiated parenchyma, for example. If the perioperative information indicates that the selected surgical instrument 112 is not suitable for its intended use, an alert can be generated. For example, if it is possible to infer, based on perioperative information, that the tissue currently being treated is bronchial tissue.

a surgical instrument of inadequate vascular stapling 112 is selected, a warning will be generated to the doctor. In general, the surgical instrument 112 can generate an alert based on a determined, predicted or inferred inconsistency between the type of surgical instrument, the perioperative information and the sensor signal. In addition, as discussed above, intraoperative information can also be used for adjustments during the general surgical procedure. For example, the current step in a general procedure operation may be the treatment of rigid bronchial tissue, which would normally result in a slower closing rate. Additional adjustments can also be made after an initial adjustment. Specifically, additional adjustments can be made during the operation, such as adjusting the slower closing rate to a faster closing rate when additional intraoperative information (for example, detected information) is analyzed and the force to close is inferred applied in the currently applied closing algorithm must be modified or adjusted. Such adjustments can also be made post-op in certain circumstances.

[0683] Therefore, the closure rate and limits can be benefited based on the type of tissue, tissue characteristics and perioperative information determined before the start or during the therapeutic treatment. Consequently, this adjustment can advantageously prevent or minimize tissue damage resulting from excessive strain and facilitate the proper formation of staples from a 112 stapling instrument.

[0684] Figures 108 and 109 are graphs 22000, 22100 illustrating various end actuator closing limit functions that can be used based on perioperative information and illustrating an adjusted end actuator closing control algorithm, according to various aspects of this disclosure

dog. Graph 22100 is an enlarged view of Graph 22000. In Figures 108 and 109, the clamping or closing force (FTC), which can be understood as the clamping force applied to end actuator 702, is indicated on the geometric axis y 22002, 22102 of graphs 22000, 22100. The time elapsed or covering a surgical cycle is indicated on the geometric axis x 22004, 22104. The geometric axis x 22004 in Figure 108 Indicates that the cycle covers 13 seconds, for example. In contrast, the geometric axis x 22104 in Figure 109 spans just under 2 seconds. As shown in Figure 108, a standard universal tissue closure limit function (denoted as FTCJa 22006) can generally be applied to the control of end actuator 702 that closes surgical instruments 112 used in generic surgical procedures.

[0685] Limits that are more conservative than the FTCq 22006 standard are also shown in charts 22000, 22100. However, less conservative limits could also be used. As represented by FTC: 22008 and FTC12 22010, the more conservative closing limits are employed to reduce the closing force of the surgical instrument in relation to the standard closing force function. FTC, 1 22008 and FTC.2 22010 can be limits that are stored in a memory of surgical instrument 112, central controller 106 or cloud 104. Additionally or alternatively, FTCJ 22006 could be dynamically adjusted in one point - so adequate during the surgical cycle. The dynamic adjustment could be performed by the control circuit 500, the corresponding central controller 106 or the cloud 104. In addition, the graphs 22000, 22100 indicate the corresponding angular coefficients of the different closing limit functions FTCa, FTC11 and FTC12 22006, 22008, 22010. Because the closing limits can vary as a function of time in the corresponding surgical cycle, the slope of a closing limit can be constant throughout or change as appropriate during the surgical cycle.

[0686] In other words, the instantaneous rate of change defined by the specific function of the closing limit may be different between different time intervals in the surgical cycle. For example, the particular closing limit function can define a relatively slower rate of increase around the beginning of the surgical cycle and a relatively faster rate of increase around the middle of the surgical cycle. The closing limit functions AFTCa, AFTC1 and AFTC.2 22106, 22108, 22110 are extended in the views of the functions FTCa, FTCu and FTC12 22006, 22008, 22010 and illustrate the corresponding inclinations of the closing limit functions. As shown in Figure 109, it can be seen that the slope is constant, although the slope can change as appropriate. The closing change rate can be adjusted according to a selected closing limit function. An example of adjustment is illustrated by the "x" in Figures 108 and 109 and is shown in larger size in the enlarged view of graph 22100. In this example, the rate of change of closure as represented by lines 22012, 22112 is adjusted so that they do not exceed AFTCi2

22110.

[0687] In one aspect, an engine such as engine 482, 704a to 704e, 754, 150082, 150714 of surgical instrument 112 can move the first claw member 152002 relative to the second claw member 152004 of the end actuator 702 For the sake of clarity, the 482 engine is mentioned. The 482 motor can move or close the end actuator 702 according to the closing change rate, represented by lines 22012, 22112 and the selected closing limit. For this purpose, the control circuit 500 can adjust a current drawn by the motor 482 to change the speed or torque of the motor 482 based on the selected limit. For example, graphs 22000, 22100 illustrate how control circuit 500 can adjust motor 482 at the point "x" (as shown in the graphs), so that the parameter of the rate of change of the surgical instrument 112 is changed to remain within the selected limit FTC, 2 22010. FTC.2 22010, which can be a specific limit for the patient, can be selected and determined based on perioperative information.

[0688] The limits of FTC 22006, 22008, 22010 shown in graphs 22000, 22100 can be parameters of different or equal closing control programs, executed by the control circuit 500. These closing control programs can be stored locally in the memory of the surgical instrument 112 or remotely stored on the central controller 106 or cloud

104. In general, the closing limit functions define how the closing limits are changed as a function of time in a cycle, so that the instantly applicable closing limit is indicated for any point of time during the cycle. The closing limits can define a maximum closing force that can be applied to close the claws of the end actuator or a maximum rate of change of the closing force used, for example. Figure 108 illustrates the use of limits as maximum rates of change in the closing force used. At a point selected in time on graphs 22000, 22100, lines 22012, 22112 plotted against time on the x axis 22004, 22104 and FTC on the geometric axis y 22002, 22102 indicate the instantaneous force applied to close the claws 152002, 152004 at that time .

[0689] As illustrated by line 22012, the applied force increases over time from time zero to time ti, after which the rate of increase decreases to zero and then to a rate of decreasing force. Just before time t2, the rate of decrease is much steeper. After time t2, the force applied to close the jaws starts to transition to a zero rate before decreasing again at a non-zero rate. As illustrated by line 22112 of graph 22100, the closing force applied to close claws 152002, 152004 is increasing between time zero and time | just before 0.5 seconds (shown on the x-axis 22104). At the moment corresponding to "x" in graph 22100, the control circuit 500 can adjust the motor 482 to adjust the selected closing algorithm, so that the rate of increase of the closing is reduced. In this way, the motor 482 can be controlled by the control circuit 500 to stay within the specific AFTCi2 limit 22110 selected from the patient. In addition, as shown in graph 22100, after the time corresponding to "x", the slowest rate of increase in the applied closing force becomes a constant rate.

[0690] In one aspect, the same total amount of applied FTC can be applied during a surgical cycle. However, the force applied to close the end actuator can be applied more gradually or immediately as appropriate. This is illustrated by the rate of change represented by the lines of the rates of closing change such as lines 22012, 22112. Although Figure 109 shows each of the three limits represented AFTCa, AFTCU 'and AFTC.2 22106, 22108, 22110 as expanded in the views of FTCa, FTC and FTC1I2 22006, 22008, 22010, in some respects, AFTC «a, AFTC, 1 and AFTC, 2 22106, 22108, 22110, represent different closing limit functions. In other words, the control circuit 500 can adjust from any of the FTC, FTC limits. and FTC12 22006, 22008, 22010 to the limits AFTCa, AFTC, 1 and AFTC, 2 22106, 22108, 22110, which would be completely different limits in this situation.

[0691] As discussed above, it is possible that the slope of a closure limit function changes during a surgical cycle. In such circumstances, the dynamic slope can be adjusted consistently or individually over the entire surgical cycle. In general, a closing limit parameter setting can be achieved by changing the parameter of the current closing control program (for example, through the control circuit 500 by directly changing a closing limit function being implemented by the control circuit 500) or switching to a new closing control program completely. Switching or adjustment can be carried out using control circuit 500, central controller 106 or cloud 104 based on perioperative information. For example, control circuit 500 can switch from the current control program to a second closing control program received from cloud 104. The second closing control program can also be transmitted from cloud 104 to the central controller

106.

[0692] As discussed above, one or more of the surgical instrument 112 used to treat tissue, the corresponding central controller 106 and cloud 104 can be used to receive, infer or determine perioperative information to determine, infer or predict the type and characteristics of the tissue currently being treated therapeutically. These inferences and predictions of closing situational recognition are useful for adjusting the rate of closure of change limits. Therefore, in addition to FTCa, AFTCa 22006, 22106, graphs 22000, 21000 show, for example, a second rate of tissue closure change of the FTC limit function, AFTCuU 22008, 22108, that the closure algorithm used by surgical instrument 112 can incorporate automatically. That is, the surgical instrument 112 can adjust the inputs for the current closing control program or adjust for a different control program to be executed by the control circuit 500. For example, the central surgical controller with situational recognition 106 can determine that the surgical procedure currently applied is a surgical procedure of the lung based on the target area that is in the thoracic cavity. In turn, the chest cavity can be inferred as the target area based on the ventilation outlet of another device used in the operating room, for example. Thus, it is determined that the type of tissue treated is lung tissue. Consequently, the surgical instrument 112 can adjust to the use of the standard closing limit function FTC; 22008, 22108 for lung tissue from the FTCa limit 22006, 22106, which was previously used. Such adjustments can be made during the surgical cycle that covers the geometric axis y 22004, 22104.

[0693] For example, the central surgical controller with situational recognition 106 can predict that the patient's lung will comprise relatively brittle tissue. Consequently, a closing limit function could be adjusted to a lower FTC limit function, as shown in Figures 108 and 109. The closing limit could be a maximum allowed FTC value applied by the end actuator or an FTC change rate maximum allowed, for example. The inference of relatively high stiffness in the lung tissue can be confirmed by other perioperative information. For example, a patient's EMR stored in cloud 104 can be analyzed to determine that the patient has previously been diagnosed with cancer and has undergone radiation treatments. This type of preoperative information can be used to infer that the characteristics of the lung tissue include relatively high stiffness and significant liquid content (for example, percentage of water in the tissue).

[0694] In addition to confirming the initial forecast, perioperative information could also be used to adapt from an inaccurate initial forecast. For example, surgical instrument 112 could be applying a subideal closure algorithm based on an erroneous assumption that the tissue has more elasticity than it actually has. In this situation, preoperative information from the patient's history can be used as part of a correction for the erroneous assumption. In general, perioperative information can be used in conjunction with sensor signals indicative of a closing parameter. Advantageously, the perioperative information could confirm an initial closing algorithm determined based on the sensor signals or could be used to adjust the initial closing algorithm to a different, more appropriate closing algorithm. For example, the sensor signal can be indicative of the relationship between the detected closing force applied and the Opening position of the end actuator 702 (for example, the position of the first jaw 152002 in relation to the second jaw 152004). This signal can be used to determine tissue stiffness and can be used in conjunction with other perioperative information to adjust the closure algorithm before or during the surgical procedure.

[0695] Consequently, the graphs 22000, 22100 of Figures 108 and 109 show that the standard lung tissue limit function FTC: can be further adjusted based on the specific characteristics of the patient. As illustrated in Figures 108 and 109, the surgical instrument can further adjust the FTC limit function, 22008 to FTC, 2 22010 or FTCJ 22006, for example, based on patient-specific perioperative information. Thus, the adjustment could occur before the surgical procedure begins or during the surgical procedure. In addition, could the adjustment be made from FTCJg 22006 to FTC12 22010, or the FTC limit function? 22010 could simply be implemented directly. Adjustment between any of the available closing limit functions is possible based on perioperative information.

[0696] Although Figures 108 and 109 illustrate adjustment for lower limits, adjustment for higher limits is also possible. The limit functions shown in Figures 108 and 109 can correspond to specific control processes, which can be implemented by a specific closing control program. Alternatively, the control processes could correspond to different closure control programs. The control circuit 500 can directly modify the selected closing control algorithm itself or switch to a different closing control algorithm, for example. That is, the closing limit function for a specific closing control algorithm or a specific applied closing change rate, represented by lines 22012, 22112, for example, can be modified. The modification of the function of the closing limit can be performed during a surgical procedure based on perioperative information. In addition, the limit functions can also be a function of some other parameter in addition to or in addition to time, such as the size of the clamp used, for example.

[0697] Additionally or alternatively, the closing adjustment may comprise simply adjusting the inputs for a closing limit function. For example, if a tissue characteristic, such as tissue thickness, is an input to a closure limit function, perioperative information can be used to predictively or inferentially modify the entries, so that the closure limits output are modified according to the predicted or inferred tissue thickness input. This way

Also, the applied limit limit function can be modified based on perioperative information. As discussed above, the applied closing limit function is defined by the applied closing control algorithm. In addition, the closing force lines or applied FTC 22012, 22112 can be adjusted based on perioperative information.

[0698] In one aspect, the closing force lines or FTC 22012, 22112 represent a closing rate change parameter of the corresponding closing control program executed by control circuit 500. The FTC 22012, 22112 line it is also defined by the applied closing control algorithm. In one aspect, the applied closing force can be dynamically adjusted during the cycle of a surgical procedure being performed, as indicated by the "x" in Figures 108 and 109. This dynamic adjustment could also be an application of situational recognition . In other words, perioperative information can be incorporated to infer or predict adjustments to the limit or limit function during the surgical procedure. Thus, as shown in Figures 108 and 109, at the moment or moments corresponding to the "x" indicated in Figures 108 and 109, the applied FTC is adjusted or modified to remain within the corresponding instantaneous closing limit. In short, the applied closing control algorithm can comprise a closing limit function and a closing change rate, both of which can be adjusted based on perioperative information.

[0699] In general, the adjustment for different closing limits or different closing limit functions can be performed based on a determined, inferred or predicted characteristic or type, or type of tissue to be treated. As discussed above, the characteristics or types of tissue can be determined, inferred, or predicted

based on perioperative information. The adjustment for another closing limit can be understood as the adjustment of a maximum limit in relation to a maximum torque generated by the motor 482 of the surgical instrument 112 or a rate of change of the motor speed. Several examples of perioperative information can be used to determine, infer or predict the type or characteristics of the tissue. For example, the amount of water, muscle properties and tissue vasculature can influence the closing rate algorithm (including the closing limit) that would be applied. In one aspect, these properties, as well as other fabric type and characteristic properties, are used to determine the standard closure limit FTCp 22006 or any other initial parameter of the closure control program.

[0700] Thus, the high vasculature may be a characteristic of the tissue used to infer a standard function of closure limit with relatively low slope. In addition, to determine the initial parameters of the control program, if preoperative information, such as the surgical procedure being applied and the surgical history (for example, the typical routine of the clinician who performs the procedure in relation to the steps surgical procedures), can be used to infer that a vascular tissue with a high hemoglobin content is being targeted, so the rate of shear change applied by the surgical instrument can be adjusted to be slower. Thus, these properties can be used to determine the parameters of the control program in the pre and intraoperative. In addition, perioperative information could be used to confirm that a suitable vascular stapler is being used for the procedure on vascular tissue.

[0701] Figure 110 is a flowchart 22200 of an aspect of the adjustment of a closure rate algorithm by the computer-implemented interactive surgical system 100, in accordance with an aspect of the present disclosure. In step 22202, the current closing algorithm is determined. This can refer to the determination of the closing control program currently run by the control circuit 500 of a surgical instrument 112. As described above in connection with Figures 108 and 109, the current closing algorithm or control program it can include a closing limit function (for example, closing limit parameter) and applied closing force (FTC) function (for example, closing change rate parameter). Flowchart 22200 continues next to step 22204, where preoperative information is received and analyzed. As discussed above, preoperative information may include initial tissue thickness based on the 474 tissue contact sensors, patient history, including previous diagnoses and treatments (for example, listed in an EMR record of information of the patient stored in the central controller or in the cloud), clinical history, such as the surgeon's typical surgical routine, identified surgical instrument and associated materials and current surgical procedure identified. This preoperative information can be used to determine, infer or predict the type or characteristics of the tissue in step 22206.

[0702] For example, the initial non-deformed thickness of the fabric, measured by the tissue contact sensors 474, can be used to determine an initial closure algorithm. Preoperative information, such as a history of lung problems in the patient, can be used to determine that the current surgical procedure being performed is a thoracic procedure and the type of tissue is a pulmonary tissue. This preoperative information can also be used to determine an adjustment to the initial closing algorithm. Additionally or alternatively, an initial tissue stiffness measured through

By comparing a non-therapeutic (or almost non-therapeutic) initial tissue compression measurement and a closing limb position measurement (for example, the position of the first and second claws of the end actuator) could also be used. together with preoperative information. Preoperative ventilation information received from a ventilation device in the operating room could also be used to infer that the current procedure is thoracic. Other preoperative information can also be used to further predict the specific chest procedure being performed. For example, based on the patient's EMR record in the cloud indicating that the patient has cancer, it can be inferred in step 22206 that the thoracic procedure is a pulmonary lobectomy to excise cancerous tissue in a pulmonary lobe.

[0703] In addition, the patient's EMR record may also indicate that the patient's history indicates that the patient has previously undergone radiation treatments for cancer. In this situation, it can be inferred or predicted that the irradiated lung tissue would be rigid, but also susceptible to the application of monopolar RF energy by the surgical instrument 112, for example. This would be an example of an inferred tissue characteristic. In addition, the inference that a pulmonary lobectomy is being performed can also be used to determine which possible tissues for stapling by the surgical instrument 112 include blood vessels (PA / PV), bronchi and parenchyma. In step 22208, the settings in the current closing algorithm are determined based on preoperative information and applied. As discussed above, the closure limit and the applied FTC can be adjusted based on the type and characteristics of the fabric. For example, high tissue stiffness may require a more conservative and slower rate of change in the applied FTC.

da (for example, as represented by lines FTC 22012, 22112), as well as a closing limit that generally generates a lower upper limit (for example, represented by FTC.2 22010 and AFTC, 2 22110).

[0704] The upper limit may indicate the limit at which the first and second claw members 152002, 152004 are in a position sufficient for the surgical instrument 112 to trigger clamps. A relatively thicker fabric can correspond to a rate of change in the slower closing force and also a higher maximum closing limit, for example. In addition, the type or structure of the tissue can be inferred based on the determined surgical procedure and clinical history to identify other adjustments to the closure algorithm in step 22208. For example, the clinical history of the surgeon responsible for treatment may indicate a practice of treating blood vessels first. It can be inferred that the type and structure of the tissue are vascular pulmonary tissues with a high blood content (that is, high vasculature). Based on this type of inferred tissue and characteristic information, it could be determined that adjusting for a slower applied FTC rate of change would be beneficial. In short, the adjustments in the current closing algorithm are determined based on the information inferred and applied in step 22208. Consequently, the current surgical operation can be performed with the surgical instrument 112 using the adjusted flow closing algorithm.

[0705] Flowchart 22200 then proceeds to decision operation 22210, in which it is determined whether any stages of the identified surgical procedure are missing. If there are no remaining steps (that is, the answer to decision operation 22210 is no), flowchart 22200, in some respects, ends. However, if the answer to decision 22210 is affirmative, there are other

remaining parts of the surgical procedure. Therefore, the current state of flowchart 22200 is intraoperative. In this case, the flowchart continues to step 22212, where intraoperative information can be received and analyzed. For example, intraoperative information may indicate that the type of tissue treated during this stage of the surgical procedure is parenchyma. In particular, it can be confirmed that the tissue is parenchyma based on clinical history, for example. This inference can be made in conjunction with measurements from the tissue contact sensor 474 and the load sensor 474 versus measurements of the position of the closing member. In addition, the medical history may indicate that the surgeon undergoing treatment routinely completes a pulmonary fissure (a double fold of the visceral pleura that folds into the pulmonary parenchyma compartment) after dissection with a monopolar energy surgical instrument. RF. In this situation, it can be inferred, based on the previously completed mono-polar RF dissection, that the current stage of the surgical procedure is the lung parenchyma tissue.

[0706] Additionally, the central surgical controller 106 can determine whether the surgical instrument 112 being used is an appropriate stapler for parenchyma shots, for example. Initial measurements from the fabric contact sensor 474 may indicate that the fabric is relatively thick, as based on the fabric that comes in contact with the length of the first and second claw members 152002, 152004 when the end actuator 702 is completely open (at the maximum opening of the claw), which can be consistent with the parenchyma. In addition, load sensor measurements 474 versus closure member position, as represented by a closure compared to the jaw opening curve, may indicate relatively high tissue stiffness. This stiffness characteristic can be consistent with the irradiated parenchyma, a

view that can be confirmed by reference to the patient's EMR data in the cloud. In this way, for example in Step 22212, the sensor signals and perioperative information could be used together.

[0707] Based on this intraoperative information received and analyzed, it can be determined in decision operation 22214, that an additional adjustment is necessary. On the other hand, if the answer is no in decision operation 22214, the flowchart will return to decision operation 22210. When the answer in decision operation 22214 is affirmative, the type of fabric and fabric characteristics are inferred as to determine the structure of the parenchyma tissue and stiffness characteristics, similar to those described above in step 22206. Subsequently, adjustments to the currently applied closure algorithm can be determined and applied in step 22208. In particular, the inference that the tissue of the rigid and fragile parenchyma being treated can cause adjustment to a slower and more conservative rate of change in the applied closing force.

[0708] Consequently, the current closing algorithm can be adjusted to an algorithm that minimizes the closing limit and rate of change. In other words, the adjusted limit may have a reduced maximum limit of the closing force, a more gradual rate of change in the closing force, a reduced rate of change in the limit of the closing force or some combination or subcombination of the items above. In situations in which the doctor inadvertently exceeds the closing limit, a waiting time can be instituted, for example. Exceeding the closing limit may indicate that the fabric or material being compressed is too thick to trigger staples, for example, so that this waiting time may be necessary. In this way, the waiting time may allow some tissue material or fluid in the end actuator 702 to evacuate or exit. After an adequate waiting time, it is determined that the tissue can be compressed properly to achieve an appropriate end actuator configuration 702, so that the stapling surgical instrument 112 can trigger staples. Due to the fact that the adjusted closing algorithm is more conservative, a long waiting time can be used. However, the physician can cancel this long waiting time or the conservative adjusted closing algorithm by manually selecting a faster use of the clamping protocol on the 112 surgical instrument.

[0709] After applying this modified closing algorithm to the parenchyma tissue in step 22208, the flow diagram again proceeds to decision operation 22210. Here, the answer can be yes again because there are remaining steps of the surgical procedure. For example, the lobectomy procedure can then proceed to a vessel stapling step. Again, in step 22212, intraoperative information is received and analyzed. For example, the central surgical controller may determine that the clinician has selected a surgical instrument for vascular stapler. In addition, an initial measurement from the 474 tissue contact sensors may indicate that the tissue contact occurs almost immediately during closing. In addition, contact with the tissue can be determined to cover a small area of the vascular stapler 112 and is bounded on the distal side of the stapler 112. Measurements from the load sensor 474 can also indicate a compatible tissue structure. In addition, it can be inferred that the tissue may have relatively low stiffness that may be consistent with a pulmonary vessel. In addition, clinical history may indicate that the surgeon under treatment generally uses a vascular stapler 112 for blood vessels as the step subsequent to the completion of the pulmonary fissure. Thus, intraoperative information, in

together with the signals from the closing parameter sensor, for example, they can be used to infer the type and characteristics of the fabric. In particular, it can be predicted that the tissue in the vessel is being treated based on the specific characteristics of the selected vascular stapler 112. The initial contact of the tissue and the measurements from the load sensor 474 can confirm this initial prediction, for example.

[0710] Consequently, in decision operation 22214 it can be determined that additional adjustment is necessary, which makes flowchart 22200 proceed to step 22206. In step 22206, it can be inferred that the fabric is a blood vessel with relatively low thickness and stiffness. Consequently, flowchart 22200 proceeds to step 22208, where the conservative closing algorithm previously applied is adjusted to a normal closing algorithm. A normal closing algorithm can comprise a constant closing change rate. In addition, the closure limit may be greater than the limit used in the control algorithm for parenchyma tissue. In other words, the normal closing algorithm can achieve a higher maximum closing force applied and the rate of change of closure can be faster than in the tissue of the parenchyma. The surgical instrument can also inform the doctor about the adjustment to the normal closing algorithm through an appropriate indicator, such as a light-emitting diode (LED) indicator displaying a specific color. In another example, it can be determined at step 22206 that the patient has a complete lung cleft. Consequently, there would still have been no firing of staples in tissue from the parenchyma in the surgical procedure. In response to this determination, the surgical instrument can ask the doctor to confirm that this inference is correct, as through a display of the surgical instrument. The physician can then manually select an appropriate closure control algorithm for this stage or stage of the surgical procedure. In addition or alternatively, surgical instrument 112 may use a conservative closure algorithm as a standard because the inferences made in step 22206 may not be definitive. In any case, the adjusted closing algorithm is applied in step 22208.

[0711] Continuing the description of the example of the pulmonary lobectomy procedure, the flowchart proceeds to decision operation 22210. In decision operation 22210, it can be determined that there are remaining stages of the surgical procedure. Consequently, in step 22212, intraoperative information is received and analyzed. Based on intraoperative information, it can be inferred that the type of tissue to be treated is bronchial tissue. In addition, the initial tissue contact sensor 474 measurements could indicate that the tissue trapped between end actuator 702 comes into contact with the first and second claw members 152002, 152004 almost immediately during the initial closure of the end actuator 702 and that such contact corresponds to a small area of the surgical stapling instrument 112. In addition, such contact is delimited on both sides of the claw members 152002 and 152004.

[0712] Consequently, it can be predicted that this tissue contact scenario corresponds to the bronchial tissue. As discussed above, these initial 474 tissue contact sensor measurements can be non-therapeutic or almost non-therapeutic. In addition, the measurements of the closing load sensor 474, represented by a closure compared to the opening curve of the claw, may indicate a rigid tissue structure that is consistent with the bronchial tissue. The indication from the history of the surgical procedure that a vascular stapler 112 has already been used in the cyclic procedure

surgery may also mean that it is likely that parenchyma staple shots have already been made and that significant use of monopolar RF energy has occurred. This history of surgical procedure considered in conjunction with the physician's history, for example, can be used to predict that the surgeon is treating bronchial tissue. This prediction would be consistent with the surgeon's routine practice of stapling the bronchus as the last stage of a lobectomy procedure. Based on the analysis of this type and other appropriate intraoperative information in step 22212, it can be determined in decision operation 22214 that an additional adjustment is necessary. As the answer to decision operation 22214 is yes, the flowchart proceeds to step 22206, where it is inferred that the treated tissue is bronchial tissue with normal tissue thickness and stiffness.

[0713] In one aspect, it may be easy to conclude that the treated tissue is bronchial tissue because the surgical instrument 112 is configured only for a specific type of tissue. For example, the surgical instrument 112 may only be adaptable for firing staples that are used for bronchi. On the other hand, the surgical instrument 112 can only be adaptable to fire clips that are used for parenchyma tissue. In this scenario, an alert can be generated by the surgical instrument 112 because the surgeon is trying to treat bronchial tissue with staples used exclusively for parenchyma tissue. This notice may be an auditory, visual, or other appropriate notice. In another example, a warning may be provided by a vascular stapler 112 if vascular stapler 112 is selected for use with bronchial tissue. As discussed above, it can be determined based on perioperative information that the tissue to be treated is bronchial tissue against which the vascular stapler is contraindicated. Similarly, other information

Operative operations, such as closing loads and stapler cartridge selection, can be used to provide warnings when surgical instruments 112 are used for types or characteristics of tissue with which they are not compatible. As discussed above, inferences made using perioperative information can be made in conjunction with the sensor signals from the closing parameters. In all situations, safety checks can be implemented to ensure that the surgical instrument 112 being used is safe for the tissue being treated.

[0714] According to the type of tissue inferred and the characteristics, in step 22208, an adjustment is made to the current closing algorithm. Although it can be determined that a constant closing rate is adequate, the closing rate can be adjusted to be faster or slower, depending on the inferred characteristics of the bronchial tissue, for example. The closing limit can be modified in the same or similar way. In addition, the current closing algorithm can also be adjusted so that if and when the surgical instrument 112 exceeds the instantly applicable closing limit, a longer waiting time is automatically activated or suggested. For example, this waiting time for bronchial tissue may be longer than the waiting time used for parenchyma tissue. As discussed above, the surgeon is informed of the selected setting for algorithmic closure through the LED indicators, for example. A doctor's cancellation command for the longest waiting time is also possible, so that the surgeon can fire the surgical instrument from the stapler 112 under appropriate circumstances. Flowchart 22200 then proceeds to step 22212, where it can be determined that no other stage of the surgical procedure remains.

[0715] In one aspect, flow chart 22200 can be implemented

through the control circuit. However, in other respects, flow chart 22200 can be implemented by central surgical controller 106 or cloud 104. Additionally, although steps 22204 and 22212 are described in terms of preoperative information and intraoperative information, respectively, they are not limited in that way. Specifically, perioperative information in general can be received and analyzed, rather than specific preoperative or intraoperative information. As discussed above, perioperative information includes pre-, intra- and post-operative information. In addition, the sensor signals can be used in conjunction with perioperative information for contextual and inferential adjustments of the closing algorithm. Examples

[0716] Various aspects of the subject described here under the title "SYS-

TEMS FOR ADJUSTING END EFFECTOR PARAMETERS BASED ON PREOPERATIVE INFORMATION "are defined in the Examples below:

[0717] Example 1 - A surgical system comprises a surgical instrument. The surgical instrument comprises an end actuator comprising a first jaw and a second jaw. The first claw is configured to move in relation to the second claw. The surgical instrument additionally comprises an engine configured to move the first jaw in relation to the second jaw according to a closing change rate parameter and a closing limit parameter. The surgical instrument additionally comprises a sensor configured to transmit a sensor signal indicating a closing parameter of the end actuator. The surgical system additionally comprises a control circuit coupled communicatively to the sensor. The control circuit is configured to receive perioperative information.

perioperative information comprises one or more of a perioperative disease, perioperative treatment and a type of surgical procedure. The control circuit is additionally configured to receive the sensor signal from the sensor and determine an adjustment for the closing rate change parameter and the closing limit parameter based on perioperative information and the signal of the sensor.

[0718] Example 2 - The surgical system of Example 1, the control circuit being additionally configured to determine a characteristic of a tissue to be treated by the surgical instrument based on one or more of the perioperative information and the sensor signal.

[0719] Example 3 - The surgical system of Example 2, with the tissue characteristic comprising one or more of the tissue type characteristic, muscle characteristic, vasculature characteristic, water content characteristic, characteristic of stiffness and thickness feature.

[0720] Example 4 - The surgical system of Example 1, 2, or 3, the control circuit being additionally configured to change a motor speed based on the setting determined for the parameter of the rate of closing change and the parameter of | closing limit.

[0721] Example 5 - The surgical system of Example 1, 2, 3 or 4, the control circuit being additionally configured to generate an alert based on an inconsistency between a type of surgical instrument and one or more of the perioperative information and the sensor signal.

[0722] Example 6 - The surgical system of Example 1, 2, 3,4 or 5, the perioperative information additionally comprising one or more of a type of tissue to be treated by the surgical instrument, a characteristic of the tissue, a clinical history and a type of staple cartridge for use with the surgical instrument.

[0723] Example 7 - The surgical system of Example 1, 2, 3, 4, 5, or 6, the closing limit parameter being a maximum limit of the closing force and the control circuit is still configured to disable the motor for a predetermined period of time, based on reaching the maximum closing force limit.

[0724] Example 8 - A surgical system comprises a central surgical controller configured to receive perioperative information transmitted from a remote database of a cloud computing system. The central surgical controller is communicatively coupled to the cloud computing system. The surgical system additionally comprises a surgical instrument coupled communicatively to the central surgical controller. The surgical instrument comprises an end actuator that comprises a first jaw and a second jaw. The first claw is configured to move in relation to the second claw. The end actuator further comprises a motor configured to move the first jaw relative to the second jaw according to a change parameter closing rate and a closing limit parameter of a closing control program received from the surgical controller. central. The end actuator additionally comprises a sensor configured to transmit a sensor signal indicative of a closing parameter of the end actuator. The central surgical controller is additionally configured to receive the sensor signal from the sensor and determine an adjustment for the closing change rate parameter and for the closing limit parameter based on perioperative information and the signal of the sensor.

[0725] Example 9 - The surgical system of Example 8, with the closing control program being a first closing control program, the central surgical controller is additionally configured to transmit a second closing control program to the surgical instrument, and the second closure control program defines the adjustment for the parameter of the rate of change of closure and the adjustment for the parameter of closure limit.

[0726] Example 10 - The surgical system of Example 9, with the cloud computing system being configured to transmit the second closure control program to the central surgical controller, and the setting for the closing change rate parameter. to and the closing limit parameter of the second control program is adjusted based on perioperative information.

[0727] Example 11 - The surgical system of Example 8, 9 or 10, the surgical instrument being configured to generate an alert based on an inconsistency between a type of surgical instrument and one or more of the perioperative information and the sensor signal.

[0728] Example 12 - The surgical system of Example, 8, 9, 10, or 11, with the closing limit parameter being a maximum limit of the closing force and the central surgical controller is additionally configured for deactivate the motor for a predetermined period of time, based on reaching the maximum closing force limit.

[0729] Example 13 - The surgical system of example 8, 9, 10, 11, or 12, with perioperative information comprising one or more of a perioperative disease, perioperative treatment, a type of surgical procedure, a history clinical, a type of surgical instrument, a type of tissue being treated by the surgical instrument and a characteristic of the tissue.

[0730] Example 14 - The surgical system of example 9, the central surgical controller being additionally configured to

a motor speed based on the setting determined for the closing rate change parameter and the closing limit parameter.

[0731] Example 15 - A surgical instrument comprising an end actuator comprising a first jaw and a second jaw. The first claw is configured to move in relation to the second claw. The surgical instrument additionally comprises a motor configured to move the first jaw in relation to the second jaw according to a closing change rate parameter and a closing limit parameter of a first closing control program. received from a central surgical controller. The surgical instrument further comprises a sensor configured to transmit a sensor signal indicative of a closing parameter of the end actuator and a control circuit communicatively coupled to the sensor and the motor. The control circuit is configured to receive the sensor signal from the sensor and determine an adjustment for the closing change rate parameter and for the closing limit parameter based on perioperative information and the sensor signal.

[0732] Example 16 - The surgical system of Example 15, the surgical instrument being configured to generate an alert based on an inconsistency between a type of surgical instrument and one or more of the perioperative information and the sensor signal.

[0733] Example 17 - The surgical system of Example 15 or 16, the control circuit being additionally configured to switch from the first closure control program to a second closure control program received from a closure system cloud computing and changing an engine speed based on the second closing control program.

[0734] Example 18 - The surgical instrument of example 15, 16 or 17, the control circuit being additionally configured to determine a characteristic and type of tissue to be treated by the surgical instrument based on one or more perioperative information and the sensor signal.

[0735] Example 19 - The surgical system of Example 15, 16, 17, or 18, the parameter of the closing limit being a maximum limit of the closing force.

[0736] Example 20 - The surgical system of Example 19, the parameter of the closing limit being a maximum limit of the closing force.

[0737] In several respects, the sensors of a sensor array, according to the present disclosure, can be placed in a staple cartridge. An adhesive mask can be incorporated with the sensors at predetermined locations. In many respects, the sensors are attached to the projections on the staple cartridge so that the sensors are positioned higher than a staple cartridge cartridge platform to ensure contact with the fabric. The adhesive mask can be created in bulk using screen printing technology on a polyester substrate, for example. Conductive blocks can be printed in a common location.

[0738] In several examples, in addition to detecting proximity to cancerous tissue, an end actuator of the present disclosure can also be configured to target specific types of cancer in specific tissues. As indicated in the publication of the magazine Altenberg B and Greulich KO, Genomics 84 (2004) pp. 1014-1020, which is incorporated by reference in its entirety, certain types of cancer are characterized by an overexpression of glycolysis genes, while other types of cancer are not characterized by an overexpression of glycolysis genes. Consequently

an end actuator of the present disclosure may be equipped with a set of sensors with high specificity for cancerous tissues characterized by an overexpression of glycolysis genes, such as lung cancer or liver cancer.

[0739] In several respects, the sensor readings from a set of sensors, in accordance with the present disclosure, are communicated by the surgical instrument to a central surgical controller (for example, central surgical controller 106, 206) for further analysis and / or for situational recognition.

[0740] The previous detailed description presented various forms of devices and / or processes through the use of block diagrams, flowcharts and / or examples. Although these block diagrams, flowcharts and / or examples contain one or more functions and / or operations, it will be understood by those skilled in the art that each function and / or operation within these block diagrams, flowcharts and / or examples can be implemented , individually and / or collectively, through a wide range of hardware, software, firmware or almost any combination thereof. Those skilled in the art will recognize, however, that some aspects of the aspects disclosed here, in whole or in part, can be implemented in an equivalent way in integrated circuits, such as one or more computer programs running on one or more computers (for example , such as one or more programs running on one or more computer systems), as one or more programs running on one or more processors (for example, as one or more programs running on one or more microprocessors), as firmware, or virtually like any combination thereof, and that designing the set of circuits and / or writing the code for the software and firmware would be within the scope of practice of those skilled in the art, in light of this disclosure. In addition, those skilled in the art will understand that the mechanisms of the subject described here can be distributed as one or more program products in a variety of ways and that an illustrative form of the subject described here is applicable regardless of the specific type of program. means of signal transmission used to effectively carry out the distribution.

[0741] The instructions used to program the logic to execute various revealed aspects can be stored in a memory in the system, such as dynamic random access memory (DRAM), cache, flash memory or other storage. In addition, instructions can be distributed over a network or through other computer-readable media. In this way, machine-readable media can include any mechanism to store or transmit information in a machine-readable form (for example, a computer), but is not limited to, floppy disks, optical discs, memory-only compact discs. (CD-ROMs), and optical-dynamic disks, read-only memory (ROM), random access memory (RAM), erasable programmable read-only memory (EPROM), electrically erasable programmable read-only memory ( EEPROM), magnetic or optical cards, flash memory, or a machine-readable tangible storage medium used to transmit information over the Internet via an electrical, optical, acoustic cable or other forms of propagated signals ( for example, carrier waves, infrared signal, digital signals, etc.). Consequently, computer-readable non-transitory media includes any type of machine-readable media suitable for storing or transmitting instructions or electronic information in a machine-readable form (for example, a computer).

[0742] As used in any aspect of the present invention, the term "control circuit" can refer to, for example, a set of wired circuits, programmable circuits (for example, a process

computer processor comprising one or more individual instruction processing cores, processing unit, processor, microcontroller, microcontroller unit, controller, digital signal processor (DSP), programmable logic device (PLD), logic matrix programmable (PLA), or field programmable port arrangement (FPGA)), state machine circuits, firmware that stores instructions executed by the programmable circuit, and any combination thereof.

The control circuit can, collectively or individually, be incorporated as an electrical circuit that is part of a larger system, for example, an integrated circuit (IC), an application-specific integrated circuit (ASIC), an on-chip system (SoC), desktop computers, laptop computers, tablet computers, servers, smart headsets, etc.

Consequently, as used in the present invention, "control circuit" includes, but is not limited to, electrical circuits that have at least one discrete electrical circuit, electrical circuits that have at least one integrated circuit, electrical circuits that have at least one integrated circuit for a specific application, electrical circuits that form a general-purpose computing device configured by a computer program (for example, a general-purpose computer configured by a computer program that at least partially runs processes and / or devices described here, or a microprocessor configured by a computer program that at least partially performs the processes and / or devices described here), electrical circuits that form a memory device (for example, memory forms of random access), and / or electrical circuits that form a communications device (for example, a modem, communication key cation, or optical-electrical equipment). Those skilled in the art will recognize that the subject described here can be implemented in an analog or digital way, or in some combination.

these.

[0743] As used in any aspect of the present invention, the term "logic" can refer to an application, software, firmware and / or circuit configured to perform any of the aforementioned operations. The software can be incorporated as a software package, code, instructions, instruction sets and / or data recorded on the computer-readable non-transitory storage media. The firmware can be incorporated as code, instructions or instruction sets and / or data that are hard-coded (for example, non-volatile) in memory devices.

[0744] As used in any aspect of the present invention, the terms "component", "system", "module" and the like may refer to a computer-related entity, be it hardware, a combination of hardware and software, software or software running.

[0745] As used here in one aspect of the present invention, an "algorithm" refers to the self-consistent sequence of steps leading to the desired result, where a "step" refers to the manipulation of physical quantities and / or logical states that they may, although not necessarily need, take the form of electrical or magnetic signals that can be stored, transferred, combined, compared and manipulated in any other way. It is common use to call these signs bits, values, elements, symbols, characters, terms, numbers or the like. These terms and similar terms may be associated with the appropriate physical quantities and are merely convenient identifications applied to these quantities and / or states.

[0746] A network can include a packet-switched network. Communication devices may be able to communicate with each other using a selected packet switched network communications protocol. An exemplary communications protocol may include an Ethernet communications protocol that may be able to allow communication using a transmission control protocol / Internet protocol (TCP / IP). The Ethernet protocol can conform to or be compatible with the Ethernet standard published by the Institute of Electrical and Electronics Engineers (IEEE) entitled "IEEE 802.3 Standard", published in December 2008 and / or later versions of this standard. Alternatively or in addition, communication devices may be able to communicate with each other using an X.25 communications protocol. The X.25 communications protocol can conform or be compatible with a standard promulgated by the International Telecommunication Union-Telecommunication Standardization Sector (ITU-T). Alternatively or in addition, communication devices may be able to communicate with each other using a frame-relay communications protocol. The frame-relay communications protocol can conform to or be compatible with a standard promulgated by the Consultative Committee for International Telegraph and Telephone (CCITT) and / or the American National Standards Institute (ANSI). Alternatively or additionally, transceivers may be able to communicate with each other using an ATM communication protocol ("asynchronous transfer mode"). The ATM communication protocol can conform or be compatible with an ATM standard published by the ATM forum entitled "ATM-MPLS Network Interworking 2.0" published in August 2001, and / or later versions of this standard. Obviously, different and / or post-developed connection-oriented network communication protocols are also contemplated in the present invention.

[0747] Unless stated otherwise, as is evident

from the preceding disclosure, it is understood that, throughout the preceding disclosure, discussions using terms such as "processing", or "computation", or "calculation", or "determination", or "display" , or similar, refer to the action and processes of a computer, or similar electronic computing device, that manipulates and transforms the data represented in the form of physical (electronic) quantities in the computer's records and memories into other data similarly represented in the form of physical quantities in memories or computer registers, or in other similar storage, transmission or display devices.

[0748] One or more components in the present invention may be called "configured for", "configurable for", "operable / operational for", "adapted / adaptable for", "capable of", "conformable / conformed to ", etc. Those skilled in the art will recognize that "configured for" can, in general, encompass components in an active state and / or components in an inactive state and / or components in a standby state, except when the context determines otherwise.

[0749] The terms "proximal" and "distal" are used in the present invention with reference to a physician who handles the handle portion of the surgical instrument. The term "proximal" refers to the portion closest to the doctor, and the term "distal" refers to the portion located in the opposite direction to the doctor. It will also be understood that, for the sake of convenience and clarity, spatial terms such as "vertical", "horizontal", "up" and "down" can be used in the present invention with respect to drawings. However, surgical instruments can be used in many orientations and positions, and these terms are not intended to be limiting and / or absolute.

[0750] People skilled in the art will recognize that in general

In general, the terms used here, and especially in the appended claims (for example, bodies of the appended claims) are generally intended as "open" terms (for example, the term "including" should be interpreted as "including, but not limited to ", the term" having "must be interpreted as" having, at least ", the term" includes "must be interpreted as" includes, but is not limited to ", etc.). It will also be understood by those skilled in the art that, when a specific number of a claim statement entered is intended, that intention will be expressly mentioned in the claim and, in the absence of such mention, no intention will be present. For example, as an aid to understanding, the following appended claims may contain the use of the introductory phrases "at least one" and "one or more" to introduce claim statements. However, the use of such phrases should not be interpreted as implying that the introduction of a claim statement by the indefinite articles "one, ones" or "one, ones" limits any specific claim containing the claim mention. claims that contain only such a mention are introduced, even when the same claim includes the introductory phrases "one or more" or "at least one" and indefinite articles, such as "one, ones" or "one, ones" (for example, example, "one, ones" and / or "one, ones" should typically be interpreted as meaning "at least one" or "one or more"); the same goes for the use of defined articles used to introduce claims.

[0751] The terms "understands" (and any form of understanding, such as "understands" and "that understands"), "has" (and any form of has, such as "has" and "that has"), " includes "(and any form of includes, such as" includes "and" which includes ") and" contains "(and any form of contains, such as" contains "and" which contains ") are unrestricted linking verbs. As a result, a system, device or surgical device that "compares

includes "," has "," includes "or" contains "one or more elements has those one or more elements, but is not limited to having only those one or more elements. Likewise, an element of a system, device or surgical apparatus that "comprises", "has", "includes" or "contains" one or more resources has those one or more resources, but is not limited to having only those one or more resources.

[0752] Furthermore, even if a specific number of an introduced claim statement is explicitly mentioned, those skilled in the art will recognize that that statement must typically be interpreted as meaning at least the number mentioned (for example, the mere mention of "two mentions", without other modifiers, typically means at least two mentions, or two or more mentions). In addition, in cases where a convention analogous to "at least one of A, B and C, etc." is used, in general this construction is intended to have the meaning in which the convention would be understood by (for example, For example, "a system that has at least one of A, B and C" would include, but not be limited to, systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and / or A, B and C together, etc.). In cases where a convention analogous to "at least one of A, B or C, etc." is used, this construct is generally intended to have the meaning in which the convention would be understood by (for example, "a system that has at least one of A, B and C" would include, but not be limited to, systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and / or A, B and C together, etc.). It will be further understood by those skilled in the art that typically a disjunctive word and / or phrase presenting two or more alternative terms, whether in the description, in the claims or in the drawings, should be understood as contemplating the possibility of including one of the terms , either term, or both terms, except where the context dictates to indicate something different. For example, the phrase "A or B" will typically be understood to include the possibilities of "A" or "B" or "AeB".

[0753] With respect to the attached claims, those skilled in the art will understand that the operations mentioned in the same can, in general, be performed in any order. In addition, although several operational flow diagrams are presented in one or more sequences, it must be understood that the various operations can be performed in other orders than those shown, or can be performed simultaneously. Examples of such alternative orderings may include overlapping, interleaved, interrupted, reordered, incremental, preparatory, supplementary, simultaneous, inverse or other variant orders, unless the context determines otherwise. Furthermore, terms such as "responsive to", "related to" or other adjectival principles are not generally intended to exclude these variants, except when the context determines otherwise.

[0754] It is worth noting that any reference to "one (1) aspect", "one aspect", "an exemplification" or "one (1) exemplification" ", and the like means that a particular feature, structure or characteristic described in connection with the aspect it is included in at least one aspect. Thus, the use of expressions such as "in one (1) aspect", "in one aspect", "in an exemplification", "in one (1) exemplification", in several places throughout this specification it does not necessarily refer to the same aspect. In addition, specific resources, structures or characteristics can be combined in any appropriate way in one or more aspects.

[0755] Any patent application, patent, non-patent publication or other description material mentioned in this specification and / or mentioned in any specific order data sheet

it is incorporated here by way of reference, to the extent that the materials incorporated are not inconsistent with this. In this way, and to the extent necessary, the disclosure as explicitly presented herein replaces any conflicting material incorporated by reference in this invention. Any material, or portion thereof, which is incorporated herein by reference, but which conflicts with the definitions, statements, or other disclosure materials contained herein, will be incorporated here only to the extent that there is no conflict. between the embedded material and the existing developer material.

[0756] In short, numerous benefits have been described that result from the use of the concepts described in this document. The previously mentioned description of one or more modalities has been presented for purposes of illustration and description. This description is not intended to be exhaustive or to limit the invention to the precise form disclosed. Modifications or variations are possible in light of the above teachings. One or more modalities were chosen and described in order to illustrate the principles and practical application to, thus, allow those skilled in the art to use the various modalities and with various modifications, as they are convenient to the specific use contemplated. It is intended that the claims presented in the annex define the global scope.

Claims (20)

UT CLAIMS 1. Surgical system characterized by comprising: a control circuit; a surgical instrument, comprising: a handle set; a drive shaft assembly that extends distally from the handle assembly; and an end actuator assembly coupled to a distal end of the drive shaft assembly, the end actuator assembly comprising: a first jaw; a second claw pivotally attached to the first claw; and a sensor configured to: detect a parameter associated with an end actuator function; and transmit the detected parameter to the control circuit; the control circuit is configured to: analyze the detected parameter based on a restriction defined by the system; and avoid at least one function of the surgical instrument based on an analysis result; and a user interface configured to provide a current status for at least one avoided function of the surgical instrument. 2. Surgical system, according to claim 1, characterized in that the restriction defined in the system comprises at least one among a predefined parameter or a predefined parameter range based on historical data associated with a surgical procedure being performed by the surgical system. 3. Surgical system, according to claim 1, characterized in that the current state comprises a first message that at least one function of the surgical instrument is avoided and a second message indicating a reason why at least one function of the surgical instrument is avoided. surgical instrument is avoided. 4. Surgical system, according to claim 1, characterized in that the user interface comprises a selectable user interface element to overcome the control circuit to allow at least one function of the surgical instrument. 5. Surgical system, according to claim 1, characterized by the sensor comprising a force sensor coupled to the end actuator, the detected parameter comprising a force applied to at least one of the first claw or the second claw of the end actuator, and the at least one function avoided through the control circuit comprises one or more of one among avoiding the use of a connected drive shaft, preventing a firing cycle from starting, preventing the articulation of the end actuator, prevent rotation of the drive shaft or avoid opening one or more of one between the first jaw or the second jaw. 6. Surgical system, according to claim 1, characterized by the function of the end actuator associated with the detected parameter comprising a gripping function, and the at least one function of the surgical instrument being avoided through the control circuit comprises one or more of a dissecting function, a clotting function, a stapling function or a cutting function. 7. Surgical system, according to claim 1, characterized by additionally comprising a central surgical controller coupled communicatively to the surgical instrument, the central surgical controller comprising the control circuit. 8. Surgical system according to claim 7, characterized by one of the handle set or the central surgical controller comprising the user interface. 9. Surgical system, according to claim 1, characterized by one of the handle set, the drive shaft set, or the end actuator set of the surgical instrument comprising the control circuit. 10. Surgical system, according to claim 1, characterized in that the drive shaft assembly comprises a sensor configured to: detect a drive shaft parameter associated with a drive shaft function; and transmit the detected parameter of the drive shaft to the control circuit; and since the control circuit is configured to: avoid at least one function of the surgical instrument additionally based on the detected drive axis parameter. 11. Surgical system characterized by comprising: a central surgical controller; a surgical instrument communicatively coupled to the central surgical controller, the surgical instrument comprising: a handle set; a drive shaft assembly that extends distally from the handle assembly; and an end actuator assembly coupled to a distal end of the drive shaft assembly, the end actuator assembly comprising: a first jaw; a second claw pivotally attached to the first claw; and a sensor configured to: detect a parameter associated with an end actuator function; and transmit the detected parameter to the central surgical controller; the central surgical controller comprising: a processor; and a memory attached to the processor, and the memory stores instructions executable by the processor to: analyze the detected parameter based on a restriction defined by the system; and avoid at least one function of the surgical instrument based on an analysis result; and a user interface configured to provide a current status for at least one avoided function of the surgical instrument. 12. Surgical system, according to claim 11, characterized in that the restriction defined by the system comprises at least one among a predefined parameter or a predefined parameter range based on historical data associated with a surgical procedure being performed by surgical system. 13. Surgical system, according to claim 11, characterized in that the current state comprises a first message that at least one function of the surgical instrument is avoided and a second message indicating a reason why at least one function of the surgical instrument is avoided. surgical instrument is avoided. 14. Surgical system according to claim 11, characterized in that the user interface comprises a selectable user interface element to overcome a central surgical controller to allow at least one function of the surgical instrument. 15. Surgical system, according to claim 11, characterized in that the sensor comprises a force sensor coupled to the end actuator, with the detected parameter comprising a force applied to at least one of the first claw or the second claw of the end actuator, and since at least one function avoided via the central surgical controller comprises one or more of one to avoid the use of a connected drive shaft, prevent a firing cycle from starting, avoid the articulation of the end actuator, avoid the rotation of the drive shaft or avoid opening one or more of the first claw or the second claw. 16. Surgical system according to claim 11, characterized in that the function of the end actuator associated with the detected parameter comprises a gripping function, and the at least one function of the surgical instrument avoided through the central surgical controller comprises one or more among a dissecting function, a clotting function, a stapling function or a cutting function. 17. Surgical system according to claim 11, characterized in that at least one of the handle set or the central surgical controller comprises the user interface. 18. Surgical system according to claim 11, characterized in that the drive shaft assembly comprises a sensor configured to: detect a drive shaft parameter associated with a drive shaft function; and transmit the detected parameter from the drive shaft to the central surgical controller; and the memory additionally stores instructions executable by the processor to: avoid at least one function of the surgical instrument additionally based on the detected drive axis parameter. 19. Non-transient computer-readable media characterized by storing computer-readable instructions that, when executed, cause a machine to: analyze a detected parameter, associated with a function of an end actuator of a surgical system, with based on a constraint defined by the system, and the surgical system includes a handle assembly, a drive shaft assembly that extends distally from the handle assembly, and an end actuator assembly coupled to a distal end of the drive shaft assembly, the end actuator assembly comprising a first claw, a second claw pivotably coupled to the first claw, and a sensor configured to detect the detected parameter and transmit the parameter detected by the machine; avoid at least one function of the surgical system based on an analysis result; and manages a user interface, with the user interface providing a current status for at least one function avoided from the surgical system. 20. Computer readable non-transitory media, according to claim 19, characterized by instructions, when executed, to make the machine: 7I7 manages an overlapping element at the user interface, with the overlapping element being selectable to allow at least one function of the surgical system.