CN117480562A - Selective and adjustable mixed reality overlay in surgical field of view - Google Patents

Abstract

The invention discloses a surgical visualization system, comprising: an imaging device; a display configured to display a live stream of a surgical field of view of a surgical procedure; a control module configured to detect surgical data competing for presentation on the display, generate visual content based on the surgical data, and selectively superimpose the visual content onto a live stream of the surgical field of view based on the surgical data. The live stream is captured by the imaging device.

Description

Selective and adjustable mixed reality overlay in surgical field of view

Cross Reference to Related Applications

The present application claims the benefit of U.S. 4, 14, 2021, U.S. provisional patent application No. 63/174,674 entitled "head UP DISPLAY" and U.S. provisional patent application No. 63/284,326 entitled "INTRAOPERATIVE DISPLAY FOR SURGICAL SYSTEMS", 2021, 11, 30, each of which is incorporated herein by reference in its entirety.

Background

The present disclosure relates to devices, systems, and methods for providing an augmented reality interactive experience during a surgical procedure. During a surgical procedure, it is desirable to provide an augmented reality interactive experience of a real-world environment in which objects residing in the real world are enhanced by superimposing computer-generated sensory information (sometimes across multiple sensory modalities, including visual, auditory, haptic, somatosensory, and olfactory). In the context of the present disclosure, the surgical field and the images of surgical instruments and other objects present in the surgical field are enhanced by superimposing computer-generated visual, auditory, tactile, somatosensory, olfactory, or other sensory information over the surgical field and the real world images of instruments or other objects present in the surgical field. The image may be streamed in real-time, or may be a still image.

Real world surgical instruments include a variety of surgical devices including energy, staplers, or a combination of energy and staplers. Energy-based medical devices include, but are not limited to, radio Frequency (RF) based monopolar and bipolar electrosurgical instruments, ultrasonic surgical instruments, combined RF electrosurgical and ultrasonic instruments, combined RF electrosurgical and mechanical staplers, and the like. Surgical stapler devices are surgical instruments used to cut and staple tissue in a variety of surgical procedures including weight loss, breast, colorectal, gynecological, urological, and general surgery.

Disclosure of Invention

In various cases, the present disclosure provides a surgical visualization system comprising: an imaging device; a display configured to display a live stream of a surgical field of view of a surgical procedure; a control module configured to detect surgical data competing for presentation on the display, generate visual content based on the surgical data, and selectively superimpose the visual content on a live stream of the surgical field based on the surgical data. The live stream is captured by the imaging device.

In various cases, the present disclosure provides a surgical visualization system comprising: a surgical device; an imaging device; a display configured to display a live stream of a surgical field of view of a surgical procedure; and a control module configured to detect surgical device data, generate visual content based on the surgical device data, and selectively adjust the visual content on the live stream of the surgical field of view. The live stream is captured by the imaging device.

Drawings

The various aspects (both as to the surgical organization and method) described herein, together with further objects and advantages thereof, may best be understood by reference to the following description taken in connection with the accompanying drawings.

Fig. 1 is a block diagram of a computer-implemented interactive surgical system according to one aspect of the present disclosure.

Fig. 2 is a surgical system for performing a surgical procedure in an operating room according to one aspect of the present disclosure.

Fig. 3 is a surgical hub paired with a visualization system, robotic system, and intelligent instrument, according to one aspect of the present disclosure.

Fig. 4 illustrates a surgical data network including a modular communication hub configured to enable connection of modular devices located in one or more operating rooms of a medical facility or any room specially equipped for surgical procedures in the medical facility to a cloud, according to one aspect of the present disclosure.

Fig. 5 illustrates a computer-implemented interactive surgical system in accordance with an aspect of the present disclosure.

Fig. 6 illustrates a surgical hub including a plurality of modules coupled to a modular control tower according to one aspect of the present disclosure.

Fig. 7 illustrates an Augmented Reality (AR) system including an intermediate signal combiner positioned in a communication path between an imaging module and a surgical hub display, according to one aspect of the present disclosure.

Fig. 8 illustrates an Augmented Reality (AR) system including an intermediate signal combiner positioned in a communication path between an imaging module and a surgical hub display, according to one aspect of the present disclosure.

Fig. 9 illustrates an Augmented Reality (AR) device worn by a surgeon to transmit data to a surgical hub, according to one aspect of the present disclosure.

Fig. 10 illustrates a system for augmenting surgical instrument information using an augmented reality display according to one aspect of the present disclosure.

Fig. 11 illustrates a timeline of a situational awareness surgical procedure in accordance with an aspect of the present disclosure.

Fig. 12 illustrates a surgical visualization system in accordance with at least one aspect of the present disclosure.

Fig. 13 is a flowchart illustrating operation of an exemplary method for determining a display arrangement competing for surgical data presented on a display in accordance with at least one aspect of the present disclosure.

Fig. 14 is a flowchart illustrating operation of an exemplary method 6020 for determining 6011 a display priority value of detected surgical data according to the method of fig. 13.

Fig. 15 is a flowchart illustrating operation of a method for determining a display priority value for tissue tension and/or pressure parameters within a surgical anastomosis, in accordance with at least one aspect of the present disclosure.

Fig. 16 is a flowchart illustrating operation of a method for determining a display priority value based on a trigger event in accordance with at least one aspect of the present disclosure.

Fig. 17 is a flow chart illustrating operation of a method in accordance with at least one aspect of the present disclosure.

Fig. 18 is a flowchart illustrating operation of a method for automatically switching between live streams of a surgical field in a surgical procedure in accordance with at least one aspect of the present disclosure.

FIG. 19 is a flowchart of the operation of a method for balancing system resources during a surgical procedure in accordance with at least one aspect of the present disclosure.

Fig. 19A is a flowchart illustrating operation of a method for transitioning between a static display mode and an active display mode based on surgical data in accordance with at least one aspect of the present disclosure.

Fig. 19B is a flowchart illustrating operation of a method for transitioning a visual representation of surgical data between a static display mode and an active display mode in accordance with at least one aspect of the present disclosure.

Fig. 20 is a flowchart illustrating operation of a method for resolving display conflicts in a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 21 is a flow chart illustrating operation of a method for addressing tissue changes in a surgical procedure employing a surgical instrument in accordance with at least one aspect of the present disclosure.

Fig. 22A-22C illustrate a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 23A-23B illustrate a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 24 illustrates a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 25 illustrates a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 26 shows a display arrangement according to the method of the present disclosure.

Fig. 27A to 27C illustrate display arrangements according to the methods of the present disclosure.

Fig. 28 shows a display arrangement according to the method of the present disclosure.

Fig. 29 shows a display arrangement according to the method of the present disclosure.

Fig. 30 shows a display arrangement according to the method of the present disclosure.

Fig. 31 is a flowchart illustrating operation of a method for manipulating a display arrangement based on risk during a surgical procedure in accordance with at least one aspect of the present disclosure.

Fig. 32 illustrates a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 33 illustrates a display arrangement in accordance with at least one aspect of the present disclosure.

Fig. 34 illustrates a display arrangement in accordance with at least one aspect of the present disclosure.

Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate various disclosed embodiments, in one form, and such exemplifications are not to be construed as limiting the scope of the invention in any manner.

Detailed Description

The applicant of the present application owns the following U.S. patent applications filed concurrently herewith, the disclosure of each of these patent applications being incorporated herein by reference in its entirety:

U.S. patent application entitled "METHOD FOR INTRAOPERATIVE DISPLAY FOR SURGICAL SYSTEMS", attorney docket END9352USNP 1/210120-1M;

U.S. patent application entitled "UTILIZATION OF SURGICAL DATA VALUES AND SITUATIONAL AWARENESS TO CONTROL THE OVERLAY IN SURGICAL FIELDVIEW", attorney docket END9352USNP 2/210120-2;

U.S. patent application entitled "RISK BASED PRIORITIZATION OF DISPLAY ASPECTS IN SURGICAL FIELDVIEW", attorney docket END9352USNP 4/210120-4;

U.S. patent application entitled "SYSTEMS AND METHODS FOR CONTROLLING SURGICAL DATA OVERLAY", attorney docket END9352USNP 5/210120-5;

U.S. patent application Ser. No. SYSTEMS AND METHODS FOR CHANGING DISPLAY OVERLAY OF SURGICAL FIELDVIEW BASED ON TRIGGERING EVENTS, attorney docket END9352USNP 6/210120-6;

U.S. patent application entitled "CUSTOMIZATION OF OVERLAID DATA AND CONFIGURATION", attorney docket END9352USNP 7/210120-7;

U.S. patent application entitled "INDICATION OF THE COUPLE PAIR OF REMOTE CONTROLS WITH REMOTE DEVICES FUNCTIONS", attorney docket END9352USNP 8/210120-8;

U.S. patent application Ser. No. COOPERATIVE OVERLAYS OF INTERACTING INSTRUMENTS WHICH RESULT IN BOTH OVERLAYS BEING EFFECTED, attorney docket END9352USNP 9/210120-9;

U.S. patent application entitled "ANTICIPATION OF INTERACTIVE UTILIZATION OF COMMON DATA OVERLAYS BY DIFFERENT USERS", attorney docket END9352USNP 10/210120-10;

U.S. patent application Ser. No. MIXING DIRECTLY VISUALIZED WITH RENDERED ELEMENTS TO DISPLAY BLENDED ELEMENTS AND ACTIONS HAPPENING ON-SCREEN AND OFF-SCREEN, attorney docket No. END9352USNP 11/210120-11;

U.S. patent application Ser. No. SYSTEM AND METHOD FOR TRACKING APORTION OF THE USER AS A PROXY FOR NON-MONITORED INSTRUMENT, attorney docket END9352USNP 12/210120-12;

U.S. patent application entitled "UTILIZING CONTEXTUAL PARAMETERS OF ONE OR MORE SURGICAL DEVICES TO PREDICT A FREQUENCY INTERVAL FOR DISPLAYING SURGICAL INFORMATION", attorney docket END9352USNP 13/210120-13;

U.S. patent application Ser. No. COOPERATION AMONG MULTIPLE DISPLAY SYSTEMS TO provider A HEALTHCARE USER CUSTOMIZED INFORMATION, attorney docket No. END9352USNP 14/210120-14;

U.S. patent application entitled "INTRAOPERATIVE DISPLAY FOR SURGICAL SYSTEMS", attorney docket END9352USNP 15/210120-15;

U.S. patent application entitled "ADAPTATION AND ADJUSTABILITY OR OVERLAID INSTRUMENT INFORMATION FOR SURGICAL SYSTEMS", attorney docket END9352USNP 16/210120-16; and

U.S. patent application Ser. No. MIXED REALITY FEEDBACK SYSTEMS THAT COOPERATE TO INCREASE EFFICIENT PERCEPTION OF COMPLEX DATA FEEDS, attorney docket END9352USNP 17/210120-17.

The applicant of the present application owns the following U.S. patent applications, the disclosure of each of which is incorporated herein by reference in its entirety:

U.S. patent application Ser. No. 16/209,423, entitled "METHOD OF COMPRESSING TISSUE WITHIN ASTAPLING DEVICE AND SIMULTANNEOUSLY DISPLAYING THE LOCATION OF THE TISSUE WITHIN THE JAWS", now U.S. patent application publication No. US-2019-0200981-A1;

U.S. patent application Ser. No. 16/209,453, entitled "METHOD FOR CONTROLLING SMART ENERGY DEVICES," now U.S. patent application publication No. US-2019-0201046-A1.

Before explaining aspects of the surgical device and generator in detail, it should be noted that the illustrative examples are not limited in their application or use to the details of construction and arrangement of parts illustrated in the accompanying drawings and description. The illustrative examples may be implemented alone or in combination with other aspects, variations and modifications and may be practiced or carried out in various ways. Furthermore, unless otherwise indicated, the terms and expressions employed herein have been chosen for the purpose of describing the illustrative examples for the convenience of the reader and are not for the purpose of limitation. Moreover, it is to be understood that the expression of one or more of the aspects, and/or examples described below may be combined with any one or more of the expression of other aspects, and/or examples described below.

Various aspects relate to a screen display for a surgical system for various energy and surgical stapler-based medical devices. Energy-based medical devices include, but are not limited to, radio Frequency (RF) based monopolar and bipolar electrosurgical instruments, ultrasonic surgical instruments, combined RF electrosurgical and ultrasonic instruments, combined RF electrosurgical and mechanical staplers, and the like. The surgical stapler device includes a combination surgical stapler having an electrosurgical device and/or an ultrasonic device. Aspects of the ultrasonic surgical device may be configured to transect and/or coagulate tissue, for example, during a surgical procedure. Aspects of the electrosurgical device may be configured for transecting, coagulating, sealing, welding, and/or desiccating tissue, for example, during a surgical procedure. Aspects of the surgical stapler device can be configured to transect and staple tissue during a surgical procedure, and in some aspects, the surgical stapler device can be configured to deliver RF energy to tissue during a surgical procedure. The electrosurgical device is configured to deliver therapeutic and/or non-therapeutic RF energy to tissue. The elements of the surgical stapler device, electrosurgical device, and ultrasonic device may be used in combination in a single surgical instrument.

In various aspects, the present disclosure provides an on-screen display of real-time information to an OR team during a surgical procedure. In accordance with various aspects of the present disclosure, a number of new and unique screen displays are provided to display various visual information feedback to an OR team on a screen. In accordance with the present disclosure, visual information may include one or more various visual media, whether audible or silent. Generally, visual information includes still photography, movie photography, video or audio recordings, graphic arts, visual aids, models, displays, visual presentation services, and supporting processes. Visual information may be conveyed on any number of display options, such as, for example, a main OR screen, the energy OR surgical stapler device itself, a tablet computer, augmented reality glasses, and the like.

In various aspects, the present disclosure provides a large number of possible lists of options to communicate visual information to an OR team in real-time without providing excessive visual information to the OR team. For example, in various aspects, the present disclosure provides a screen display of visual information to enable a surgeon OR other member of an OR team to selectively activate the screen display, such as an icon surrounding a screen option, to manage a large amount of visual information. The active display may be determined using one or a combination of various factors, which may include an energy-based (e.g., electrosurgical, ultrasound) or mechanical-based (e.g., stapler) surgical device in use, estimating the risk associated with a given display, the experience level of the surgeon, the surgeon's choice, and so forth. In other aspects, the visual information may include a large amount of data superimposed or overlaid into the surgical field to manage the visual information. In various aspects described below, overlapping images that require video analysis and tracking are included in order to properly overlay data. In contrast to static icons, visual information data transmitted in this manner may provide additional useful visual information to the OR team in a more concise and easily understood manner.

In various aspects, the present disclosure provides techniques for selectively activating a screen display, such as an icon surrounding the screen, to manage visual information during a surgical procedure. In other aspects, the present disclosure provides techniques for determining an active display using one or a combination of various factors. In various aspects, techniques according to the present disclosure may include selecting an energy-based OR mechanical-based surgical device for use as an active display, estimating risk associated with a given display, utilizing an experience level of a surgeon OR OR team making the selection, and so forth.

In other aspects, techniques according to the present disclosure may include overlaying or overlaying a large amount of data onto a surgical field of view to manage visual information. The various display arrangements described in this disclosure relate to superimposing various visual representations of surgical data on a live stream of a surgical field of view. As used herein, the term overlay includes semi-transparent overlays, partial overlays, and/or moving overlays. The graphic overlay may be in the form of a transparent graphic, a translucent graphic, or an opaque graphic, or a combination of transparent, translucent, and opaque elements or effects. Further, the superimposed layers may be positioned on or at least partially on or near objects in the surgical field such as, for example, end effectors and/or critical surgical structures. Some display arrangements may include changes in one or more display elements of the superimposed layers, including changes in color, size, shape, display time, display location, display frequency, highlighting, or combinations thereof, based on changes in display priority values. The graphic overlay is rendered on top of the active display monitor to quickly and efficiently communicate important information to the OR team.

In other aspects, techniques according to the present disclosure may include overlapping images that require analysis of video and tracking in order to properly overlay visual information data. In other aspects, techniques according to the present disclosure may include transmitting rich visual information instead of simple static icons, thereby providing additional visual information to the OR team in a more concise and easily understood manner. In other aspects, the visual overlay may be used in combination with an audible and/or somatosensory overlay (such as thermal, chemical and mechanical devices, and combinations thereof).

The following description relates generally to devices, systems, and methods that provide an Augmented Reality (AR) interactive experience during a surgical procedure. In this context, the surgical field and the images of surgical instruments and other objects present in the surgical field are enhanced by superimposing computer-generated visual, auditory, tactile, somatosensory, olfactory, or other sensory information on the surgical field, the real world images of instruments and other objects present in the surgical field. The image may be streamed in real-time, or may be a still image. Augmented reality is a technology for rendering and displaying virtual or "augmented" virtual objects, data, or visual effects superimposed on a real environment. The real environment may include a surgical field of view. A virtual object superimposed on a real environment may be represented as anchored or in a set position relative to one or more aspects of the real environment. In a non-limiting example, if a real world object leaves the real environment field of view, then a virtual object anchored to the real world object will also leave the augmented reality field of view.

The various display arrangements described in this disclosure relate to superimposing various visual representations of surgical data on a live stream of a surgical field of view. As used herein, the term overlay includes semi-transparent overlays, partial overlays, and/or moving overlays. Further, the superimposed layers may be positioned on or at least partially on or near objects in the surgical field such as, for example, end effectors and/or critical surgical structures. Some display arrangements may include changes in one or more display elements of the superimposed layers, including changes in color, size, shape, display time, display location, display frequency, highlighting, or combinations thereof, based on changes in display priority values.

As described herein, AR is an enhanced version of the real physical world, achieved through the use of digital visual elements, sounds, or other sensory stimuli delivered via technology. Virtual Reality (VR) is a computer-generated environment with scenes and objects that appear to be real, so that users feel themselves immersed in their surroundings. The environment is perceived by a device called a virtual reality headset or helmet. Both Mixed Reality (MR) and AR are considered immersive techniques, but they are not identical. MR is an extension of mixed reality, allowing real and virtual elements to interact in an environment. While AR often adds digital elements to a real-time view through the use of cameras, MR experiences combine elements of both AR and VR, in which real world and digital objects interact.

In an AR environment, one or more computer-generated virtual objects may be displayed with one or more real (i.e., so-called "real world") elements. For example, real-time images or videos of the surrounding environment may be displayed on a computer screen display along with one or more overlaid virtual objects. Such virtual objects may provide supplemental information about the environment or generally enhance the user's perception and participation in the environment. Instead, real-time images or videos of the surrounding environment may additionally or alternatively enhance user engagement with virtual objects shown on the display.

Apparatus, systems, and methods in the context of the present disclosure enhance images received from one or more imaging devices during a surgical procedure. The imaging device may include various endoscopes, AR devices, and/or cameras used during non-invasive and minimally invasive surgical procedures to provide images during open surgical procedures. The image may be streamed in real-time, or may be a still image. The devices, systems, and methods enhance images of a real-world surgical environment by overlaying virtual objects or representations of data and/or real objects on the real-world surgical environment, thereby providing an augmented reality interactive experience. The augmented reality experience may be viewed on a display and/or AR device that allows a user to view the overlaid virtual object on the real world surgical environment. The display may be located in the operating room or remote from the operating room. AR devices are worn on the head of a surgeon or other operating room personnel and typically include two stereoscopic display lenses or screens, one for each eye of the user. Natural light can pass through two transparent or translucent display lenses so that aspects of the real environment are visible, while also projecting light so that the virtual object is visible to the user of the AR device.

Two or more displays and AR devices may be used in a coordinated manner, such as a first display or AR device controlling one or more additional displays or AR devices in a defined character control system. For example, when the display or AR device is activated, the user may select a role (e.g., surgeon, surgical assistant, nurse, etc. during a surgical procedure) and the display or AR device may display information related to the role. For example, the surgical assistant may have a virtual representation of the displayed instrument that the surgeon needs when performing the next step of the surgical procedure. The surgeon's attention to the current step may see different display information than the surgical assistant.

While there are many known screen displays and warnings, the present disclosure provides many new and unique augmented reality interactive experiences during a surgical procedure. Such augmented reality interactive experiences include visual, auditory, tactile, somatosensory, olfactory, or other sensory feedback information to a surgical team inside or outside the operating room. Virtual feedback information superimposed on the real world surgical procedure environment may be provided to an Operating Room (OR) team, including personnel internal to the OR, including, but not limited to, for example, a knife surgeon, a surgeon assistant, a swabbing personnel, an anesthesiologist, and a round nurse, among others. The virtual feedback information may be transmitted over any number of display options, such as a master OR screen display, AR device, energy OR surgical stapler instrument, tablet computer, augmented reality glasses, device, and the like.

Fig. 1 shows a computer-implemented interactive surgical system 1 comprising one or more surgical systems 2 and a cloud-based system 4. The cloud-based system 4 may include a remote server 13 coupled to the storage 5. Each surgical system 2 includes at least one surgical hub 6 in communication with the cloud 4. For example, the surgical system 2 may include a visualization system 8, a robotic system 10, and a hand-held intelligent surgical instrument 12, each configured to communicate with each other and/or with the hub 6. In some aspects, the surgical system 2 may include M hubs 6, N visualization systems 8, O robotic systems 10, and P smart handheld surgical instruments 12, where M, N, O and P are integers greater than or equal to 1. The computer-implemented interactive surgical system 1 may be configured to provide an augmented reality interactive experience during a surgical procedure as described herein.

Fig. 2 shows an example of a surgical system 2 for performing a surgical procedure on a patient lying on an operating table 14 in a surgical operating room 16. The robotic system 10 is used as part of the surgical system 2 in a surgical procedure. The robotic system 10 includes a surgeon's console 18, a patient side cart 20 (surgical robot), and a surgical robotic hub 22. When the surgeon views the surgical site through the surgeon's console 18 or an Augmented Reality (AR) device 66 worn by the surgeon, the patient-side cart 20 may manipulate at least one removably coupled surgical tool 17 through a minimally invasive incision in the patient. Images of the surgical site during the minimally invasive procedure (e.g., still images or live images streamed in real time) may be obtained by the medical imaging device 24. The patient side cart 20 may maneuver the imaging device 24 to orient the imaging device 24. An image of the open surgical procedure may be obtained by the medical imaging device 96. The robotic hub 22 processes the image of the surgical site for subsequent display on the surgeon's console 18 or on an AR device 66 worn by the surgeon or to other personnel in the surgical room 16.

The optical components of imaging device 24, 96 or AR device 66 may include one or more illumination sources and/or one or more lenses. One or more illumination sources may be directed to illuminate portions of the surgical field. The one or more image sensors may receive light reflected or refracted from tissue and instruments in the surgical field.

In various aspects, the imaging device 24 is configured for use in minimally invasive surgical procedures. Examples of imaging devices suitable for use in the present disclosure include, but are not limited to, arthroscopes, angioscopes, bronchoscopes, choledochoscopes, colonoscopes, cytoscopes, duodenoscopes, enteroscopes, esophageal-duodenal scopes (gastroscopes), endoscopes, laryngoscopes, nasopharyngeal-renal endoscopes, sigmoidoscopes, thoracoscopes, and hysteroscopes. In various aspects, the imaging device 96 is configured for open (invasive) surgical procedures.

In various aspects, the visualization system 8 includes one or more imaging sensors, one or more image processing units, one or more storage arrays, and one or more displays strategically placed relative to the sterile field. In one aspect, the visualization system 8 includes interfaces for HL7, PACS, and EMR. In one aspect, the imaging device 24 may employ multispectral monitoring to distinguish between topography and underlying structures. Multispectral images capture image data over a specific range of wavelengths across the electromagnetic spectrum. Wavelengths, including light from frequencies outside the visible range, such as IR and ultraviolet, are separated by filters or devices sensitive to the particular wavelengths. Spectral imaging can extract information that is not visible to the human eye. Multispectral monitoring can reposition the surgical field after completion of the surgical task to perform a test on the treated tissue.

Fig. 2 shows the main display 19 positioned in the sterile field to be visible to an operator at the operating table 14. The visualization tower 11 is positioned outside the sterile zone and comprises a first non-sterile display 7 and a second non-sterile display 9 facing away from each other. The visualization system 8 guided by the hub 6 is configured to be able to coordinate the information flow to operators inside and outside the sterile field using the displays 7, 9, 19. For example, hub 6 may cause visualization system 8 to display AR images of the surgical site recorded by imaging devices 24, 96 on non-sterile displays 7, 9 or by AR device 66, while maintaining a real-time feed of the surgical site on primary display 19 or AR device 66. For example, the non-sterile displays 7, 9 may allow a non-sterile operator to perform diagnostic steps related to a surgical procedure.

Fig. 3 shows the surgical hub 6 in communication with the visualization system 8, the robotic system 10, and the hand-held intelligent surgical instrument 12. Hub 6 includes a hub display 35, an imaging module 38, a generator module 40, a communication module 30, a processor module 32, a memory array 34, and an operating room mapping module 33. The hub 6 further comprises a smoke evacuation module 26 and/or a suction/flushing module 28. In various aspects, the imaging module 38 includes an AR device 66 and the processor module 32 includes an integrated video processor and augmented reality modeler (e.g., as shown in fig. 10). The modular light source may be adapted for use with a variety of imaging devices. In various examples, multiple imaging devices may be placed at different locations in the surgical field to provide multiple views (e.g., non-invasive, minimally invasive, or open surgical procedures). The imaging module 38 may be configured to be switchable between imaging devices to provide an optimal view. In various aspects, the imaging module 38 may be configured to integrate images from different imaging devices and provide an augmented reality interactive experience during a surgical procedure as described herein.

Fig. 4 shows a surgical data network 51 including a modular communication hub 53 configured to enable connection of modular devices located in one or more operating rooms/rooms of a medical facility to a cloud-based system. Cloud 54 may include a remote server 63 (fig. 5) coupled to storage 55. Modular communication hub 53 includes a network hub 57 and/or a network switch 59 in communication with a network router 61. Modular communication hub 53 is coupled to local computer system 60 to process data. The modular devices 1a-1n located in the operating room may be coupled to a modular communication hub 53. The network hub 57 and/or the network switch 59 may be coupled to a network router 61 to connect the devices 1a-1n to the cloud 54 or the local computer system 60. The data associated with the devices 1a-1n may be transmitted via routers to cloud-based computers for remote data processing and manipulation. The operating room devices 1a-1n may be connected to the modular communication hub 53 by a wired channel or a wireless channel. The surgical data network 51 environment can be used to provide an augmented reality interactive experience during a surgical procedure as described herein, and in particular to provide an augmented image in a surgical field of view to one or more remote displays 58.

Fig. 5 illustrates a computer-implemented interactive surgical system 50. The computer-implemented interactive surgical system 50 is similar in many respects to the computer-implemented interactive surgical system 1. The computer-implemented interactive surgical system 50 includes one or more surgical systems 52 that are similar in many respects to the surgical system 2. Each surgical system 52 includes at least one surgical hub 56 in communication with a cloud 54, which may include a remote server 63. In one aspect, the computer-implemented interactive surgical system 50 includes a modular control tower 23 that is connected to a plurality of operating room devices, such as, for example, intelligent surgical instruments, robots, and other computerized devices located in an operating room. As shown in fig. 6, modular control tower 23 includes a modular communication hub 53 coupled to a computer system 60.

Returning to fig. 5, modular control tower 23 is coupled to imaging module 38 (which is coupled to endoscope 98), generator module 27 (which is coupled to energy device 99), smoke extractor module 76, suction/irrigation module 78, communication module 13, processor module 15, storage array 16, smart device/appliance 21 (which is optionally coupled to display 39), and sensor module 29. The operating room devices are coupled to cloud computing resources, such as servers 63, data storage 55, and display 58, via modular control tower 23. The robotic hub 72 may also be connected to the modular control tower 23 and to the server 63, the data storage 55, and the display 58. The device/instrument 21, visualization system 58, etc. may be coupled to the modular control tower 23 via a wired or wireless communication standard or protocol, as described herein. The modular control tower 23 may be coupled to a hub display 65 (e.g., monitor, screen) to display the received enhanced images, including overlaid virtual objects in the real surgical field received from the imaging module 38, the device/instrument display 39, and/or other visualization system 58. Hub display 65 may also display data received from devices connected to modular control tower 23 in combination with the image and the overlay image.

Fig. 6 shows a surgical hub 56 that includes a plurality of modules coupled to the modular control tower 23. The modular control tower 23 includes a modular communication hub 53 (e.g., a network connectivity device) and a computer system 60 to provide, for example, enhanced local processing, visualization, and imaging of surgical information. Modular communication hub 53 may be hierarchically configured to connect to extend the number of modules (e.g., devices) that may be connected to modular communication hub 53 and to transmit data associated with the modules to computer system 60, cloud computing resources, or both. Each of the hubs 57/switches 59 in the modular communications hub 53 may include three downstream ports and one upstream port. The upstream hub 57/switch 59 is connected to the processor 31 to provide a communication connection with cloud computing resources and a local display 67. Communication with cloud 54 may be through a wired or wireless communication channel.

The computer system 60 includes a processor 31 and a network interface 37. The processor 31 is coupled to a communication module 41, a storage device 45, a memory 46, a non-volatile memory 47 and an input/output interface 48 via a system bus. The system bus may be any of several types of bus structures including a memory bus or memory controller, a peripheral bus or external bus, and/or a local bus using any of a variety of available bus architectures.

The processor 31 includes enhancementsThe reality modeler (e.g., as shown in fig. 10) and may be implemented as a single-core or multi-core processor, such as those provided by texas instruments (Texas Instruments) under the trade name ARM Cortex. In one aspect, the processor may be an on-chip memory from, for example, texas instruments (Texas Instruments) LM4F230H5QR ARM Cortex-M4F processor core including 256KB of single-cycle flash memory or other non-volatile memory (up to 40 MHz), a prefetch buffer for improving execution above 40MHz, 32KB single-cycle Sequential Random Access Memory (SRAM), loaded withInternal read-only memory (ROM) of software, 2KB electrically erasable programmable read-only memory (EEPROM), and/or one or more Pulse Width Modulation (PWM) modules, one or more Quadrature Encoder Inputs (QEI) analog, one or more 12-bit analog-to-digital converters (ADC) with 12 analog input channels, the details of which can be seen in the product data sheet.

The system memory includes volatile memory and nonvolatile memory. A basic input/output system (BIOS), containing the basic routines to transfer information between elements within the computer system, such as during start-up, is stored in nonvolatile memory. For example, the non-volatile memory may include ROM, programmable ROM (PROM), electrically Programmable ROM (EPROM), EEPROM, or flash memory. Volatile memory includes Random Access Memory (RAM), which acts as external cache memory. Further, the RAM may be available in various forms such as SRAM, dynamic RAM (DRAM), synchronous DRAM (SDRAM), double data rate SDRAM (DDR SDRAM) Enhanced SDRAM (ESDRAM), synchronous Link DRAM (SLDRAM), and Direct Rambus RAM (DRRAM).

Computer system 60 also includes removable/non-removable, volatile/nonvolatile computer storage media such as, for example, magnetic disk storage. Disk storage includes, but is not limited to, devices such as magnetic disk drives, floppy disk drives, tape drives, jaz drives, zip drives, LS-60 drives, flash memory cards, or memory sticks. In addition, the disk storage can include storage media separately or in combination with other storage media including, but not limited to, an optical disk drive such as a compact disk ROM device (CD-ROM), compact disk recordable drive (CD-R drive), compact disk rewritable drive (CD-RW drive) or a digital versatile disk ROM drive (DVD-ROM). To facilitate connection of the disk storage devices to the system bus, a removable or non-removable interface may be used.

In various aspects, the computer system 60 of fig. 6, the imaging module 38 and/or the visualization system 58 and/or the processor module 15 of fig. 4-6 may include an image processor, an image processing engine, a Graphics Processing Unit (GPU), a media processor, or any special-purpose Digital Signal Processor (DSP) for processing digital images. The image processor may employ parallel computation with single instruction, multiple data (SIMD) or multiple instruction, multiple data (MIMD) techniques to increase speed and efficiency. The digital image processing engine may perform a series of tasks. The image processor may be a system on a chip having a multi-core processor architecture.

Fig. 7 shows an Augmented Reality (AR) system 263 that includes an intermediate signal combiner 64 positioned in the communication path between the imaging module 38 and a surgical hub display 67. The signal combiner 64 combines audio and/or image data received from the imaging module 38 and/or the AR device 66. The surgical hub 56 receives the combined data from the combiner 64 and superimposes the data provided to the display 67 on which the superimposed data is displayed. Imaging device 68 may be a digital video camera and audio device 69 may be a microphone. The signal combiner 64 may include a wireless heads-up display adapter to couple to an AR device 66 placed in the communication path of the display 67 to the console, allowing the surgical hub 56 to superimpose data on the display 67.

Fig. 8 illustrates an Augmented Reality (AR) system including an intermediate signal combiner positioned in a communication path between an imaging module and a surgical hub display. Fig. 8 shows AR device 66 worn by surgeon 73 to transmit data to surgical hub 56. Peripheral information of AR device 66 does not include active video. Instead, the peripheral information includes only the device settings or signals that do not have the same refresh rate requirements. The interaction may augment the surgeon's 73 information based on linking with preoperative Computed Tomography (CT) or other data linked in the surgical hub 56. The AR device 66 may identify structures, such as querying whether the instrument is contacting a nerve, vessel, or adhesion. The AR device 66 may include preoperative scan data, optical views, tissue interrogation features obtained throughout the procedure, and/or processing in the surgical hub 56 for providing answers. The surgeon 73 may dictate notes to the AR device 66 for storage in the hub storage device 45 with the patient data for later reporting or follow-up.

The AR device 66 worn by the surgeon 73 is linked to the surgical hub 56 with audio and visual information to avoid the need for superposition and to allow the display information to be customized around the perimeter of the field of view. The AR device 66 provides a signal from the device (e.g., instrument), answers queries about device settings or location information linked to the video to identify quadrants or locations. The AR device 66 has audio control and audio feedback from the AR device 66. The AR device 66 is able to interact with all other systems in the operating room and has feedback and interaction available wherever the surgeon 73 looks. For example, the AR device 66 may receive voice or gesture initiated commands and inquiries from the surgeon, and the AR device 66 may provide feedback in the form of one or more modalities including audio, visual, or tactile touches.

Fig. 9 shows a surgeon 73 wearing AR device 66, a patient 74, and a camera 96 may be included in operating room 75. The AR device 66 worn by the surgeon 73 may be used to present virtual objects superimposed on a real-time image of the surgical field to the surgeon 73 via an augmented reality display 89 or via a hub-connected display 67. The real-time image may include a portion of the surgical instrument 77. The virtual object may not be visible to other people (e.g., surgical assistants or nurses) within the operating room 75, although they may also be wearing the AR device 66. Even if another person is viewing operating room 75 using AR device 66, that person may not see the virtual object or be able to see the virtual object in the augmented reality shared with surgeon 73, or be able to see a modified version of the virtual object (e.g., according to a unique customization to surgeon 73) or be able to see a different virtual object.

The virtual objects and/or data may be configured to appear on a portion of the surgical instrument 77 or in a surgical field captured by the imaging module 38, by the imaging device 68 during a minimally invasive surgical procedure, and/or by the camera 96 during an open surgical procedure. In the illustrated example, the imaging module 38 is a laparoscopic camera that provides real-time feeding of the surgical field during a minimally invasive surgical procedure. The AR system may present a virtual object that is fixed to a real object regardless of the perspective of one or more observers (e.g., surgeon 73) of the AR system. For example, the virtual object may be visible to an observer of the AR system inside the operating room 75, and not visible to an observer of the AR system outside the operating room 75. When an observer enters operating room 75, the virtual object may be displayed to the observer outside operating room 75. The augmented image may be displayed on the surgical hub display 67 or the augmented reality display 89.

The AR device 66 may include one or more screens or lenses, such as a single screen or two screens (e.g., one screen for each eye of the user). The screen may allow light to pass through the screen such that aspects of the real environment are visible when the virtual object is displayed. The virtual object may be made visible to the surgeon 73 by projected light. The virtual object may appear to have some degree of transparency or may be opaque (i.e., occlude aspects of the real environment).

The AR system may be viewable to one or more observers and may include differences between views available to one or more observers while maintaining some aspects common between views. For example, the heads-up display may change between two views, while virtual objects and/or data may be fixed to real objects or regions in the two views. Aspects, such as color, illumination, or other changes of the object, may be changed between views without changing the fixed location of the at least one virtual object.

The user may consider virtual objects and/or data presented in the AR system as opaque or as including a degree of transparency. In one example, a user may interact with a virtual object, such as by moving the virtual object from a first location to a second location. For example, the user may move the object with his own hand. This may be accomplished virtually in an AR system by determining that a hand has moved to a location coincident with or adjacent to the object (e.g., using one or more cameras that may be mounted on the AR device 66, such as AR device camera 79 or a separate camera 96, and which may be static or controllable to move) and causing the object to move in response. The virtual aspect may comprise a virtual representation of the real world object or may comprise a visual effect, such as a lighting effect or the like. The AR system may include rules that govern the behavior of the virtual object, such as subjecting the virtual object to gravity or friction, or may include other predefined rules that exclude real world physical constraints (e.g., floating objects, perpetuation, etc.). The AR device 66 may include a camera 79 (not confused with camera 96, separate from the AR device 66) located on the AR device 66. The AR device camera 79 or camera 96 may include an infrared camera, an infrared filter, a visible light filter, multiple cameras, a depth camera, and the like. The AR device 66 may project the virtual item on a representation of the real environment so as to be viewable by the user.

The AR device 66 may be used in an operating room 75 during a surgical procedure, for example, performed on a patient 74 by a surgeon 73. The AR device 66 may project or display virtual objects such as virtual objects during a surgical procedure to enhance the vision of the surgeon. The surgeon 73 may view the virtual object using the AR device 66, a remote control for the AR device 66, or may interact with the virtual object, such as using a hand to "interact" with the virtual object or a gesture recognized by a camera 79 of the AR device 66. The virtual object may augment a surgical tool, such as surgical instrument 77. For example, the virtual object may appear (to the surgeon 73 viewing the virtual object through the AR device 66) to be coupled to or maintained a fixed distance from the surgical instrument 77. In another example, the virtual object may be used to guide a surgical instrument 77 and may appear to be fixed to the patient 74. In some examples, the virtual object may react to movement of other virtual objects or real world objects in the surgical field of view. For example, the virtual object may be changed while the surgeon is manipulating a surgical instrument that is proximate to the virtual object.

The augmented reality display system imaging device 38 captures a real image of the surgical field during the surgical procedure. The augmented reality displays 89, 67 present a superposition of the operational aspects of the surgical instrument 77 over the real image of the surgical field. Surgical instrument 77 includes communication circuitry 231 to communicate operational aspects and functional data from surgical instrument 77 to AR device 66 via communication circuitry 233 on AR device 66. Although surgical instrument 77 and AR device 66 are shown as RF wireless communication between circuits 231, 233 as indicated by arrow B, C, other communication techniques (e.g., wired, ultrasonic, infrared, etc.) may be employed. The overlay is related to the operational aspects of the active visualization of the surgical instrument 77. The overlay combines aspects of tissue interaction in the surgical field with functional data from the surgical instrument 77. The processor portion of AR device 66 is configured to receive operational aspects and functional data from surgical instrument 77, determine overlays relating to the operation of surgical instrument 77, and combine tissue aspects in the surgical field with functional data from surgical instrument 77. The enhanced image indicates warnings regarding device performance considerations, warnings of incompatible usage, warnings regarding incomplete capture. Incompatible uses include tissue out of range conditions and tissue not properly balanced within the jaws of the end effector. The additional enhanced image provides an indication of an incident, including an indication of tissue tension and an indication of foreign object detection. Other enhanced image indicates device status overlay and instrument indication.

Fig. 10 illustrates a system 83 for enhancing a surgical field image with information using an AR display 89 in accordance with at least one aspect of the present disclosure. The system 83 may be used to perform the techniques described below, for example, by using the processor 85. The system 83 includes one aspect of the AR device 66 that may communicate with a database 93. The AR device 66 includes a processor 85, a memory 87, an AR display 89, and a camera 79. The AR device 66 may include a sensor 90, a speaker 91, and/or a haptic controller 92. Database 93 may include an image store 94 or a pre-operative plan store 95.

The processor 85 of the AR device 66 includes an augmented reality modeler 86. The augmented reality modeler 86 may be used by the processor 85 to create an augmented reality environment. For example, the augmented reality modeler 86 may receive an image of an instrument in a surgical field of view, such as from the camera 79 or the sensor 90, and create an augmented reality environment to fit within a displayed image of the surgical field of view. In another example, physical objects and/or data may be superimposed on the surgical field of view and/or the surgical instrument image, and the augmented reality modeler 86 may use the physical objects and data to present an augmented reality display of the virtual objects and/or data in the augmented reality environment. For example, the augmented reality modeler 86 may use or detect an instrument at a surgical site of a patient and present virtual objects and/or data on the surgical instrument and/or images of the surgical site in a surgical field captured by the camera 79. The AR display 89 may display an AR environment superimposed on a real environment. Display 89 may display virtual objects and/or data using AR device 66, such as a fixed location in an AR environment.

The AR device 66 may include a sensor 90, such as an infrared sensor. The camera 79 or sensor 90 may be used to detect movements, such as gestures by a surgeon or other user, which the processor 85 may interpret as user attempts or intended interactions with the virtual target. The processor 85 may identify objects in the real environment, such as by using the processing information received by the camera 79. In other aspects, the sensor 90 may be a tactile, auditory, chemical, or thermal sensor to generate corresponding signals that may be combined with various data feeds to create an enhanced environment. The sensors 90 may include binaural audio sensors (spatial sound), inertial measurement sensors (accelerometers, gyroscopes, magnetometers), environmental sensors, depth camera sensors, hand-eye tracking sensors, and voice command recognition functions.

For example, during a surgical procedure, the AR display 89 may present virtual features corresponding to physical features hidden by anatomical aspects of the patient, such as within the surgical field, while allowing the surgical field to be viewed through the AR display 89. The virtual feature may have a virtual position or orientation corresponding to a first physical position or orientation of the physical feature. In one example, the virtual position or orientation of the virtual feature may include an offset from a first physical position or orientation of the physical feature. The offset may include a predetermined distance from the augmented reality display, a relative distance from the augmented reality display to an anatomical aspect, and the like.

In one example, the AR device 66 may be a single AR device. In one aspect, AR device 66 may be a Hololens 2AR device manufactured by Microsoft corporation of Redmond, wash. The AR device 66 includes goggles with lenses and binaural audio features (spatial sound), inertial measurement devices (accelerometers, gyroscopes, magnetometers), environmental sensors, depth and video cameras, hand-eye tracking, and voice command recognition functions. It provides an improved field of view with high resolution by using a mirror to guide the waveguide in front of the wearer's eye. The image can be magnified by changing the angle of the mirror. It also provides eye tracking to identify the user and adjust the lens width for the particular user.

In another example, the AR device 66 may be a Snapchat Spectacles 3AR device. The AR device is able to capture paired images and recreate a 3D depth map, add virtual effects, and replay 3D video. The AR device includes two HD cameras to capture 3D photos and videos at 60fps while four built-in microphones record immersive high-fidelity audio. The images from the two cameras combine to build a geometric map around the user's real world, providing a new perception of depth. The photos and videos may be synchronized to the external display device wirelessly.

In yet another example, AR device 66 may be a Google Glass 2AR device. The AR device provides inertial measurement (accelerometer, gyroscope, magnetometer) information superimposed on the lens (outside the field of view) to supplement the information.

In another example, the AR device 66 may be Amazon's Echo Frames AR device. The AR device has no camera/display. The microphone and speaker are connected to Alexa. The AR device provides less functionality than a heads-up display.

In yet another example, AR device 66 may be a North (Google) Focals AR device. The AR device provides notification push/smart watch simulation; inertial measurement, screen overlay of information (weather, calendar, messages), voice control (Alexa) integration. The AR device provides a basic heads-up display function.

In another example, the AR device 66 may be an Nreal AR device. The AR device includes spatial sound, two ambient cameras, photo cameras, IMU (accelerometer, gyroscope), ambient light sensor, proximity sensor functions. Nebula projects application information onto the lens.

In various other examples, AR device 66 may be any of the following commercially available AR devices: magic Leap 1, epson Moverio, vuzix Blade AR, zenFone AR, microsoft AR eyeglass prototype, eyeTap to generate light collinear with ambient light directly into the retina. For example, the beam splitter makes the same light seen by the eye available for computer processing and superimposing information. AR visualization systems include HUDs, contact lenses, glasses, virtual Reality (VR) headphones, virtual retinal displays, operating room displays, and/or smart contact lenses (biomimetic lenses).

The multi-user interface for AR device 66 includes a virtual retinal display (such as a raster display drawn directly on the retina rather than on a screen in front of the eye), a smart television, a smart phone, and/or a spatial display (such as a Sony spatial display system).

Other AR technologies may include, for example, AR capture devices and software applications, AR creation devices and software applications, and AR cloud devices and software applications. The AR capture device and software applications include, for example, apple polycyam application u binary 6 (Mirrorworld using display. Land app), the user can scan and obtain 3D images of the real world (to create a 3D model). AR creation devices and software applications include, for example, adobe Aero, vuforia, ARToolKit, google ARCore, apple arcet, MAXST, aurasma, zappar, blippar. AR cloud devices and software applications include, for example, facebook, google (world geometry, object recognition, predictive data), amazon AR cloud (business), microsoft Azure, samsung Project Whare, niantic, magic Leap.

Situational awareness refers to 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 being the subject of the procedure. Using background information related to the surgical procedure, the surgical system can, for example, improve the manner in which the surgical system controls a modular device (e.g., robotic arm and/or robotic surgical tool) connected thereto, and provide the surgeon with background information or advice during the course of the surgical procedure.

Fig. 11 shows a time axis of a situational awareness surgical procedure. Fig. 11 shows a timeline 5200 of an exemplary surgical procedure and context information that the surgical hub 5104 can derive from data received from the data source 5126 at each step of the surgical procedure. The time axis 5200 depicts typical steps that nurses, surgeons and other medical personnel will take during a segmental lung resection procedure, starting from the establishment of an operating room and until the patient is transferred to a post-operative recovery room. The situation aware surgical hub 5104 receives data from the data source 5126 throughout the surgical procedure, including data generated each time a medical professional utilizes the modular device 5102 paired with the surgical hub 5104. The surgical hub 5104 can receive this data from the paired modular device 5102 and other data sources 5126 and continually derive inferences about the ongoing procedure (i.e., background information) such as which step of the procedure to perform at any given time as new data is received. The situational awareness system of the surgical hub 5104 can, for example, record data related to a procedure for generating a report, verify steps that a medical professional is taking, provide data or prompts (e.g., via a display screen) that may be related to particular procedure steps, adjust the modular device 5102 based on context (e.g., activate a monitor, adjust the FOV of a medical imaging device, or change the energy level of an ultrasonic surgical instrument or RF electrosurgical instrument), and take any other such action described herein.

First 5202, a hospital staff member retrieves the patient's EMR from the hospital's EMR database. Based on the patient data selected in the EMR, the surgical hub 5104 determines that the procedure to be performed is a chest procedure.

Second 5204, the staff member scans the incoming medical supplies for the procedure. The surgical hub 5104 cross-compares the scanned supplies with the list of supplies utilized in the various types of protocols and confirms that the combination of supplies corresponds to the chest protocol. In addition, the surgical hub 5104 can also determine that the procedure is not a wedge procedure (because the incoming supplies lack certain supplies required for, or otherwise do not correspond to, a chest wedge procedure).

Third 5206, the medical personnel scans the patient belt via a scanner 5128 communicatively connected to the surgical hub 5104. The surgical hub 5104 may then confirm the identity of the patient based on the scanned data.

Fourth 5208, the medical staff opens the auxiliary equipment. The auxiliary devices utilized may vary depending on the type of surgical procedure and the technique to be used by the surgeon, but in this exemplary case they include smoke evacuators, insufflators and medical imaging devices. When activated, the ancillary equipment as the modular device 5102 may automatically pair with the surgical hub 5104 located in a specific vicinity of the modular device 5102 as part of its initialization process. The surgical hub 5104 can then derive background information about the surgical procedure by detecting the type of modular device 5102 paired therewith during this pre-operative or initialization phase. In this particular example, the surgical hub 5104 determines that the surgical procedure is a VATS procedure based on this particular combination of paired modular devices 5102. Based on a combination of data from the patient's EMR, a list of medical supplies to be used in the procedure, and the type of modular device 5102 connected to the hub, the surgical hub 5104 can generally infer the particular procedure that the surgical team will perform. Once the surgical hub 5104 knows the particular procedure being performed, the surgical hub 5104 can retrieve the steps of the procedure from memory or the cloud and then cross-reference the data it subsequently receives from the connected data sources 5126 (e.g., the modular device 5102 and the patient monitoring device 5124) to infer the steps of the surgical procedure being performed by the surgical team.

Fifth 5210, the staff attaches EKG electrodes and other patient monitoring devices 5124 to the patient. The EKG electrode and other patient monitoring device 5124 can be paired with the surgical hub 5104. As the surgical hub 5104 begins to receive data from the patient monitoring device 5124, the surgical hub 5104 thus confirms that the patient is in the operating room.

Sixth 5212, medical personnel induce anesthesia in patients. The surgical hub 5104 may infer that the patient is under anesthesia based on data (including EKG data, blood pressure data, ventilator data, or a combination thereof) from the modular device 5102 and/or the patient monitoring device 5124. Upon completion of the sixth step 5212, the preoperative portion of the lung segmental resection procedure is complete and the operative portion begins.

Seventh 5214, collapse of the lungs of the patient being operated on (while ventilation is switched to the contralateral lung). The surgical hub 5104 may infer from the ventilator data that the patient's lungs have collapsed. The surgical hub 5104 can infer that the surgical portion of the procedure has begun, as it can compare the detection of the patient's lung collapse to the expected steps of the procedure (which can be previously accessed or retrieved), thereby determining that collapsing the lung is a surgical step in that particular procedure.

Eighth 5216, a medical imaging device 5108 (e.g., an endoscope) is inserted and video from the medical imaging device is activated. The surgical hub 5104 receives medical imaging device data (i.e., still image data or live streaming video in real time) through its connection with the medical imaging device. After receiving the medical imaging device data, the surgical hub 5104 can determine that the laparoscopic portion of the surgical procedure has begun. In addition, the surgical hub 5104 may determine that the particular procedure being performed is a segmental resection, rather than a pneumonectomy (note that the surgical hub 5104 has excluded a wedge-shaped procedure based on the data received at the second step 5204 of the procedure). The data from the medical imaging device 124 (fig. 2) can be used to determine background information related to the type of procedure being performed in a number of different ways, including by determining the angle of the visual orientation of the medical imaging device relative to the patient's anatomy, monitoring the number of medical imaging devices utilized (i.e., activated and paired with the surgical hub 5104), and monitoring the type of visualization device utilized.

For example, one technique for performing a vat lobectomy places the camera in the lower anterior corner of the patient's chest over the septum, while one for performing a vat segmented resection places the camera in an anterior intercostal position relative to the segmented slit. For example, using pattern recognition or machine learning techniques, the situational awareness system may be trained to recognize the positioning of the medical imaging device from the visualization of the patient anatomy. As another example, one technique for performing a vat lobectomy utilizes a single medical imaging apparatus, while another technique for performing a vat segmented excision utilizes multiple cameras. As another example, a technique for performing vat segmental resections utilizes an infrared light source (which may be communicatively coupled to a surgical hub as part of a visualization system) to visualize segmental slots that are not used in vat pulmonary resections. By tracking any or all of this data from the medical imaging device 5108, the surgical hub 5104 can thus determine the particular type of surgical procedure being performed and/or the technique for the particular type of surgical procedure.

Ninth 5218, the surgical team begins the anatomic steps of the procedure. The surgical hub 5104 can infer that the surgeon is in the process of dissecting to mobilize the patient's lungs because it receives data from the RF generator or ultrasound generator indicating that the energy instrument is being fired. The surgical hub 5104 can cross-reference the received data with a retrieval step of the surgical procedure to determine that the energy instrument fired at that point in the method (i.e., after the previously discussed procedure steps are completed) corresponds to an anatomical step.

Tenth 5220, the surgical team proceeds to the ligation step of the procedure. The surgical hub 5104 can infer that the surgeon is ligating arteries and veins because it receives data from the surgical stapling and severing instrument indicating that the instrument is being fired. Similar to the previous steps, the surgical hub 5104 can derive the inference by cross-referencing the receipt of data from the surgical stapling and severing instrument with the retrieval steps in the method.

Eleventh 5222, a segmental resection portion of the procedure is performed. The surgical hub 5104 infers that the surgeon is transecting soft tissue based on data from the surgical instrument, including data from the staple cartridge. The cartridge data may correspond to the size or type of staples fired by the instrument. The cartridge data may indicate the type of tissue being stapled and/or transected for different types of staples employed in different types of tissue. The type of staples being fired is used for soft tissue or other tissue types to enable the surgical hub 5104 to infer that a segmental resection procedure is being performed.

Twelfth 5224, the node dissection step is performed. The surgical hub 5104 may infer that the surgical team is dissecting a node and performing a leak test based on data received from the generator indicating that an RF or ultrasonic instrument is being fired. For this particular procedure, the use of an RF or ultrasound instrument after transecting the soft tissue corresponds to a node dissection step, which allows the surgical hub 5104 to make this inference. It should be noted that the surgeon switches back and forth between surgical stapling/cutting instruments and surgical energy (i.e., RF or ultrasonic) instruments periodically, depending on the particular steps in the procedure, as the different instruments are better suited for the particular task. Thus, the particular sequence in which the stapling/severing instrument and the surgical energy instrument are used may dictate the steps of the procedure that the surgeon is performing. At the completion of the twelfth step 5224, the incision is closed and the post-operative portion of the procedure begins.

Thirteenth 5226, the patient is reversed from anesthesia. For example, the surgical hub 5104 may infer that the patient is waking from anesthesia based on ventilator data (i.e., the patient's respiration rate begins to increase).

Finally, fourteenth 5228, the medical personnel remove various patient monitoring devices 5124 from the patient. Thus, when the surgical hub 5104 loses EKG, BP and other data from the patient monitoring device 5124, the hub can infer that the patient is being transferred to the recovery room. The surgical hub 5104 can determine or infer when each step of a given surgical procedure occurs from data received from various data sources 5126 communicatively coupled to the surgical hub 5104.

In addition to using patient data from the EMR database to infer the type of surgical procedure to be performed, the situational awareness surgical hub 5104 may also use patient data to generate control adjustments for the paired modular device 5102, as shown in a first step 5202 of the timeline 5200 shown in fig. 86.

The surgical displays (e.g., displays 7, 9, 19, 35, 62, 65, 66, 67, and 89) play an important role in the operating room by providing useful information to the clinician (e.g., surgeon, surgical staff) that can be used to evaluate the progress of the surgical procedure, determine the subsequent steps to be taken in the surgical procedure, monitor patient vital signs, and the like. The display needs to be large enough so that the information provided can be seen, but not so large as to be too conspicuous and interfere with workflow or movement in a crowded operating room.

For example, an imaging device (such as one of many imaging devices described elsewhere herein) is used to capture a live stream of a surgical field of view during a surgical procedure. The display displays this live stream captured by the imaging device so that the clinician can view the surgical field during the surgical procedure.

During the surgical procedure, information related or associated with the surgical procedure may be superimposed on the live stream on the display. For example, an Electrocardiogram (EKG) monitors the heart rate of a patient during a surgical procedure, and the monitored heart rate is superimposed on a live stream so that a clinician can ensure that the patient's condition is stable.

Various other sensors, detectors, modules, etc. monitor other parameters during the surgical procedure, and information related to these parameters may also be superimposed on the display. However, some superimposed information may be more important than other superimposed information. For example, when a clinician manipulates tissue with an end effector of a surgical instrument, information regarding how much force is applied to the tissue with the end effector is relevant to monitoring to ensure that the tissue is not unintentionally damaged.

However, due to the amount of information superimposed on the display, the clinician may ignore or miss more important information, such as the force applied to the tissue. Such a large amount of competitive information can lead to the surgeon being overwhelmed with information that can affect his ability to adequately perform the surgical procedure, which can be costly for the patient. Accordingly, there is a need to prioritize, control and/or limit the amount of data superimposed on a display.

Fig. 12 illustrates a surgical visualization system 6000 in accordance with at least one aspect of the present disclosure. The various components of the surgical visualization system 6000 are similar in many respects to the components of other systems described elsewhere in this disclosure, and thus, for brevity, are not repeated here at the same level of detail. In some implementations, the system 6000 is a stand-alone system. In other implementations, the system 6000 is integrated into or used in conjunction with the computer-implemented interactive surgical system 1.

The surgical visualization system 6000 includes a control module 6001 configured to be able to perform the various techniques described herein, for example, through the use of one or more processors or processing circuitry, such as processor 85. In some implementations, the system 6000 may include, be used in conjunction with, or be in communication with, for example, the augmented reality device 84. The system 6000 may also include storage media (such as, for example, memory 6003), imaging devices 6004 (such as, for example, cameras 88), and a display 6005. The system 6000 may also include one or more speakers 91, haptic controllers 92, and/or sensors 90 (see fig. 10). Display 6005 may include, for example, AR display 89, VR display, projector, heads-up display, screen, and/or any other suitable device for depicting visual content.

In some implementations, the system 6000 is incorporated into, for example, a computer-implemented interactive surgical system 50. In some implementations, the system 6000 is in operable communication with one or more hubs, systems, networks, servers, and/or databases that may deliver surgical data to the system 6000. For example, the system 6000 may be in operative communication with the cloud 54 including the remote server 63, the robotic hub 72, the surgical hub 56, the devices/instruments 21, and/or the modular control tower 23 via wired or wireless communication standards or protocols as described herein. In some implementations, the system 6000 includes a situational awareness module 6006 similar to that described in connection with the surgical hub 5104. The situational awareness module 6006 can be trained to infer contextual information about the surgical procedure based on a large amount of perioperative data received via sensor input and/or user input.

Fig. 13 is a flowchart illustrating operation of an exemplary method 6010 for determining a display arrangement for competing surgical data presented on a display, such as display 6005. Method 6010 includes detecting 6011 surgical data, assigning 6012 a display priority value or a display priority status to the surgical data, and determining 6013 a display arrangement of the surgical data on a display based on the display priority value. Method 6010 may further include presenting 6014 a visual representation of the surgical data, for example, according to a display arrangement by displaying or overlaying the live stream over the surgical field of view.

In some implementations, 6011 surgical data is detected by the control module 6001. Surgical data may be detected 6011 by receiving the surgical data from one or more sources (such as, for example, components of computer-implemented interactive surgical system 1) via one or more wireless and/or wired communication interfaces. In at least one example, the surgical data may include data received from one or more surgical instruments 21. In another example, the surgical data includes contextual information determined by situational awareness module 6006.

In certain examples, the surgical data includes control data, biomarker measurements, and/or other operational indications of the operation and/or results associated with the surgical instrument 21. In some examples, the surgical data may be any data indicative of malformed staples and poorly sealed tissue with a high likelihood. In some cases, the surgical data may be associated with tissue flow, clamping force, firing force, and other tissue and/or instrument parameters that may be monitored and displayed to the clinician in real-time in a variety of ways to enable adjustment of the firing process or to alert the surgeon to the possible presence of malformed staple areas.

In some implementations, the display priority value is assigned based on surgical data and/or contextual information regarding the surgical procedure developed by situational awareness module 6006. In some implementations, the display priority value is assigned based on a trigger event, condition, or characteristic of the surgical data. In some implementations, assigning 6012 a display priority value includes changing a previously assigned display priority value. For example, detection of a trigger event, condition, and/or characteristic of the surgical data may cause a previously assigned display priority value to change to a higher value or a lower value.

In some examples, the processor 85 employs a predetermined equation and/or formula in determining the display priority value of the surgical data. Various relevant factors may be considered and assigned different weights when calculating the display priority value. Additionally or alternatively, in assigning the display priority values, the processor 85 may utilize one or more databases or tables listing surgical data and corresponding display priority values.

In various implementations, the assigned 6012 display priority values include various display priority levels, such as, for example, a low display priority level, a medium display priority level, and/or a high display priority level. In some implementations, the display priority value is a display priority state, such as, for example, a high priority state, a neutral priority state, and/or a low priority state.

Fig. 14 is a flowchart illustrating the operation of an exemplary method 6020 for determining a display priority value of surgical data of 6011 detected according to method 6010 of fig. 13. In some implementations, the display priority value is dependent on the surgical data. In the illustrated example, the display priority value is assigned based on a proximity of a surgical instrument utilized in the surgical procedure to a critical anatomical structure associated with the surgical procedure. The display priority value is based on a relationship between the received proximity data and a predetermined proximity threshold. For example, if 6021 the distance between the surgical instrument and the anatomy is greater than a predetermined threshold, 6022 assigns a low display priority value to the proximity data. However, if 6021 distance is less than or equal to the predetermined proximity threshold, 6023 assigns a high display priority value to the proximity data.

In some implementations, the system 6000 employs a situational awareness module 6006 to identify the type of surgical procedure to be performed. The type of surgical procedure may be determined, for example, from user input. Alternatively or additionally, the type of surgical procedure may be determined from an inventory list of devices selected for the surgical procedure that are unique to or characteristic of the surgical procedure type. The system 6000 may also identify key structures associated with the surgical procedure, for example, from a database and/or user input. In some implementations, the system 6000 can detect critical structures in the live stream of the surgical field captured by the imaging device. In addition, the system 6000 may also detect surgical instruments 21 in the surgical field and may track the proximity of the surgical instruments 21 to critical structures. The display priority value of the proximity data may be determined as discussed in connection with fig. 14.

In some implementations, identification of critical structures and/or surgical instruments in the live stream of the surgical field may be accomplished through a variety of suitable object recognition, object tracking, object marking, and/or other image processing techniques, such as those discussed in U.S. patent application publication No. END9228USNP1/190580-1M, entitled "STRUCTURED MULTI SPECTRAL COMPUTATIONAL ANALYSIS," which is incorporated herein by reference in its entirety. For example, previously stored images of surgical instruments and/or critical structures may be utilized to identify surgical instruments and/or critical structures in a surgical field of view.

low-Level Anterior Resection (LAR) surgical procedures are common surgical procedures for rectal cancer. The procedure involves excision of the rectum. The colon is then attached to the remaining segment of the rectum to achieve normal bowel movement. Circular staplers are commonly used in low LAR procedures. Initially, as the surgeon begins to build structure to form an anastomosis, certain parameters (such as parameters of tissue tension and anastomotic tissue pressure) are irrelevant and may be distracting if superimposed or emphasized too quickly on the live stream. In some cases, such parameters are superimposed and/or emphasized according to method 6010 in a display arrangement on display 6005 in order to avoid distraction and/or reduce the display space available for the live stream.

In some implementations, display priority values are assigned to parameters of tissue tension and anastomotic tissue pressure based on trigger events associated with correlations of the parameters with surgical procedures. The triggering event may be, for example, detection of a connection of the circular stapler anvil to the circular stapler trocar. For example, detection may be achieved automatically by employing one or more object recognition, object tracking, object marking, and/or other image processing algorithms of the live stream and/or by one or more sensors in the anvil and/or the trocar triggered by the connection or proximity of the anvil to the trocar.

In some implementations, the triggering event is associated with an increased criticality or risk level. In some cases, the trigger event may generate a warning and/or immediately pause the surgical activity, such as, for example, pausing the staple firing of the surgical instrument 21. The triggering event may cause a transition to a pending failure mode, such as providing a series of instructions to remedy or reduce the cause of the failure. As described in detail below, the trigger event may be, for example, buttress excavation, cutting tissue without sealing the tissue, and/or breaking the anvil. In some implementations, these trigger events are automatically detected visually, such as by object recognition, object tracking, object marking, and/or other suitable image processing techniques of image frames of a live stream, or by various suitable wired and/or wireless communication schemes.

In some implementations, the failure mode is caused by buttress mining, which is a condition that may occur when using a buttress in a tissue stapling by surgical instrument 21. In response to detecting buttress mining, the control module 6001, for example, causes the surgical instrument 21 to stop a firing sequence of the surgical instrument. For example, the control module 6001 can communicate a firing stop command to the surgical instrument 21 via a wireless or wired interface. Additionally, the control module 6001 can cause a warning and/or a series of instructions to remedy the failure by applying tension to the tissue during firing, such as being displayed or superimposed on the live stream of the surgical field.

Alternatively, a malfunction may be caused by detecting that the tissue is cut without sealing the tissue. For example, as the cutting member of the surgical instrument 21 advances, the control module 6001 may detect a failure of a staple to be deployed into tissue grasped by the end effector of the surgical instrument 21, which results in a cutting tissue failure that occurs without sealing the tissue. In response to detecting the fault, the control module 6001 can cause a series of instructions to alert and/or remedy the fault to be displayed or superimposed on the live stream of the surgical field. These instructions may suggest clamping the surrounding blood supply, preparing the hemostatic material, and then releasing the tissue from the jaws of the end effector of the surgical instrument 21.

Fig. 15 is a flowchart illustrating operation of an exemplary method 6030 for determining display priority values for tissue tension and/or pressure parameters within a surgical anastomosis. Method 6030 includes receiving 6031 tissue parameters and assigning a display priority value to the parameters based on a triggering event, such as detection of a connection between an anvil and a trocar of a circular stapler. For example, if 6032 does not detect a trocar-anvil connection, 6033 assigns a low display priority value to the parameter. However, if 6032 does not detect a trocar-anvil connection, 6034 assigns a high display priority value to the parameter.

While the example provided by method 6030 utilizes detection of the connection of components of a circular stapler as a trigger event for determining a display priority value, the connection of other components of other instruments 21 may also be used as a trigger event for determining a display priority value. For example, the attachment of the cartridge reload, end effector, and/or shaft may represent a trigger event for determining a display priority value. In some implementations, components of a surgical instrument component, a surgical robot component, and/or any suitable surgical system may be used as trigger events for determining a display priority value.

Fig. 16 is a flow chart illustrating the operation of an exemplary method 6040 for determining a display priority value based on a trigger event. In the illustrated example, the trigger event is activation of the surgical instrument 21 prior to receiving parameters required to perform an adjustment of the settings of the surgical instrument for optimal operation of the surgical instrument 21. In some implementations, the system 6000 may be configured to detect the surgical instrument 21 in the live stream of the surgical field and await user input of the desired parameters.

In some implementations, the parameter may be a desired user input. The parameter may be associated with a tissue characteristic or a disease state. Prior to treating tissue with certain devices, the device settings may be adjusted based on the tissue condition and/or disease state. These adjustments may include reducing the firing rate of the surgical stapling instrument to better ensure sealing. For surgical energy devices, the surgeon may adjust the power in response to new tissue characteristics, for example, to provide better tissue sealing.

As shown in fig. 16, method 6040 includes detecting 6041 a user attempt to activate surgical instrument 21. If the required parameters are received (6042), a low display priority value 6043 is assigned. However, if 6042 does not detect a trocar-anvil connection, 6044 assigns a high display priority value to the parameter.

In some implementations, the parameter is a sensor parameter, which may be an internal sensor of the surgical instrument 21 or any other sensor configured to measure a parameter required for proper operation of the surgical procedure. Detection of a trigger event, such as activating surgical instrument 21 prior to receiving a parameter, may cause system 6000 to assign a high priority value to visual content, e.g., in the form of a superposition, requesting permission to ignore or proceed without the missing parameter, or requesting input of the missing parameter, for example.

In some implementations, the triggering event is a sensor parameter that deviates from an acceptable predetermined range or threshold. The sensor parameter may be a tissue impedance parameter that is measurable by a surgical instrument holding tissue in a surgical field, such as by performing impedance spectroscopy measurements. If the grasped tissue is highly saturated with saline, the measured tissue impedance will deviate from an acceptable predetermined range or threshold, triggering the system 6000 to assign a high display priority value to an alert regarding the detected deviation, user override request, and/or user override request.

In some implementations, the triggering event can be detection of a mismatch between the selected surgical instrument 21 and the surgical procedure to be performed by the surgical instrument 21. For example, a mismatch may be detected by the system 6000 and/or the computer implemented interactive surgical system 1. The type of surgical procedure and inventory list of surgical instruments 21 to be used in the surgical procedure may be entered through a user interface and/or may be detected through other suitable image processing techniques such as object recognition, object tracking, object marking, and/or image frames of a live stream or through various suitable wired and/or wireless communication schemes. The situation awareness module 6006 can compare the inventory list detected or entered by the user to a previously stored inventory list historically associated with the type of surgical procedure detected or entered by the user. The detection of a mismatch causes the system 6000 to assign a high display priority value to the alert, user override request and/or confirmation request regarding the mismatch.

In at least one example, detection of selection of a circular stapler for hysterectomy causes system 6000 to assign a high display priority value to the alert, user override request, and/or confirmation request regarding the mismatch. The system 6000 may require the staff to confirm that a circular stapler is needed or to eliminate or correct procedure plan mismatch from the currently active list.

In some implementations, the triggering event may be detection of an incompatible component of the surgical instrument assembly. The various surgical instruments 21 utilize interchangeable components such as, for example, interchangeable cartridges, reloads, end effectors, shafts, handles, motors, and/or batteries. The use of incompatible components may result in the surgical instrument 21 being malfunctioning, which may cause injury to the patient and/or interfere with the surgical procedure results. The system 6000 may assign display priority values based on the detection of incompatible components.

The computer-implemented interactive surgical system 1 may detect incompatible components through an authenticity check or an integrity check. Unsuccessful authenticity and/or integrity verification may indicate incompatible components. In some implementations, the various components are equipped with appropriately connected sensors that can detect appropriate connections that indicate appropriate compatibility between the connected components. In such implementations, a sensor signal or no sensor signal may indicate an incompatible component.

In at least one example, upon installation of the interchangeable component in the surgical instrument 21, the surgical instrument 21 may interrogate the interchangeable component for identification information that may be compared with recognized identification information stored, for example, in a database. The database may be stored on a storage medium such as the surgical instrument 21, hub 22, and/or remote server 13 of the cloud-based system 4. Failure to verify the identification information causes the system 6000 to assign a high display priority value to the alert, user override request, and/or confirmation request regarding the incompatible component. The computer-implemented interactive surgical system 1 may also disable certain capabilities of the surgical instrument 21, or lock the surgical instrument 21, to protect the patient and/or the surgical procedure results.

In some implementations, the trigger event is the detection of a tissue condition (such as a biological abnormality) that can adversely affect the proper use of the surgical instrument 21 in a surgical procedure at a standard setting. For example, an extremely high body mass index "BMI" may be required to adjust the various settings of the surgical instrument 21 during sleeve gastrectomy. BMI levels may be detected by situational awareness module 6006, for example, from perioperative data.

Detection of a BMI level that deviates from an acceptable predetermined threshold may cause the system 6000 to assign a high display priority value to an alert, user override request, and/or confirmation request regarding the BMI level. In addition, the system 6000 may also assign a high display priority value to recommended surgical instrument settings, such as, for example, a lower firing rate of a surgical stapler used in sleeve gastrectomy. The system 6000 and/or the computer-implemented interactive surgical system 1 may be configured to automatically determine recommended surgical instrument settings based on perioperative data.

In various aspects, determining 6013 the display arrangement of the surgical data on the display 6005 includes changing a characteristic of the visual representation of the surgical data. In some implementations, the surgical data may be in the form of sensor readings that may be superimposed on the live stream of the surgical field of view of the display 6005. The sensor readings may be highlighted in a color that varies according to the importance of the sensor parameter readings to the surgical procedure. In some implementations, the sensor reading may be visually represented in a first color when the sensor reading is within normal limits of the predetermined criteria, and the sensor reading may be visually represented in a second color different from the first color when the sensor reading is outside of the normal limits.

For example, the sensor reading may be a temperature reading, which may be visually represented as green when the temperature reading is less than or equal to a predetermined temperature threshold. If the temperature reading exceeds a predetermined threshold, the temperature reading may be visually represented, for example, in yellow or red, indicating the importance of the current temperature surgical procedure.

In some implementations, the characteristic change of the visual representation of the surgical data can be gradual. For example, the temperature reading may gradually transition from yellow to red as the temperature increases to reflect the severity of the temperature change. In some implementations, other characteristics of the visual representation may also vary, such as, for example, size, shape, display time, display location, display three-dimensional arrangement (e.g., foreground, background), display blinking, highlighting, and/or font.

In various aspects, determining 6013 the display arrangement of the surgical data on the display 6005 includes, for example, removing or changing a characteristic of the visual representation of the surgical data in a manner that reflects a reduced significance and/or inactive state. In some implementations, the surgical data includes a temperature of a surgical energy device used to seal tissue in a surgical field of view of the surgical procedure. In response to activation of the surgical energy device, a visual representation of temperature is superimposed on the live stream of the surgical field of view on display 6005. The visual representation means that the surgical energy device is "hot" to alert individuals to careful operation while the surgical energy device is active. In some implementations, the visual representation may include characteristics that indicate a high priority status to ensure that attention is drawn to a clinician and/OR other OR personnel using the surgical energy device.

When the clinician uses the surgical energy device, a visual representation of temperature may be assigned a lower priority status even though the surgical energy device is still hot. This is to reduce distraction to the clinician and/or to divert the clinician's attention to another visual representation of higher priority surgical data. For example, visual representations of temperature may be changed to neutral colors, smaller sizes, and/or to different shapes.

Once the surgical energy device is inactive, if the temperature is at or above a predetermined threshold, the high priority state is reassigned to the temperature, causing its visual representation to change, thereby providing a warning to draw attention or highlight that the surgical energy device is still above a temperature threshold that may cause injury even if inactive. In response to the temperature falling below the predetermined threshold, the visual representation of the temperature again changes to a lower priority state. In some implementations, the temperature of the surgical energy device may be monitored using one or more temperature sensors located on or near an end effector of the surgical energy device. The sensor readings may be transmitted to the system 6000 wirelessly or by wired communication.

In various aspects, determining 6013 a display arrangement of the surgical data includes transmitting a visual representation of the surgical data between the first display and the second display. This transfer allows the system 6000 to present the surgical data to the appropriate user at the appropriate time and location in a timely manner. In some implementations, the first display is a setup display, a nurse display, or a preparation display, and the second display is a surgical field or surgeon display, such as, for example, display 6005. In such implementations, the transfer may be triggered by detecting that the setup is complete. In some cases, the user input may indicate that the setting is complete, which triggers the transfer. The setting may include checking the surgical device against the inventory list to ensure that there are surgical devices necessary to perform the surgical procedure. Setting may also include testing the surgical device to ensure successful wireless communication operation and/or any other suitable testing.

In some implementations, the control module 6001 is configured to assign a high display priority value to surgical data at a first display and a low display priority value to the same surgical data at a second display until a trigger event is detected. In response to the detection, the control module 6001 is configured to assign a low display priority value to surgical data at the first display and a high display priority value to the same surgical data at the second display. The switching of the priorities causes surgical data to be transferred to the second display. In some implementations, the switching causes the visual representation of the surgical data to darken at the first display and appear at the second display. Then, after the predetermined period of time has elapsed, the visual representation of the surgical data may be completely removed from the first display.

In various aspects, the determined 6013 display arrangement may require additional processing power, such as, for example, processing power that involves forming a spectral view and/or tracking a surgical end effector in a surgical field of view and superimposing surgical data on the surgical end effector. Fig. 17 is a flowchart illustrating operation of an exemplary method 60600 for responding to a need for additional processing speed during a surgical procedure performed by the computer-implemented interactive surgical system 1. The control module 6001 can utilize a Field Programmable Gate Array (FPGA) where additional processing power 6061 is required. For example, as shown in method 6060 in fig. 17, in advanced visualization mode 6063, additional high-speed calculations for key variables may be assigned to the FPGA. When advanced visualization mode 6063 is enabled, the FPGA is dynamically reused to maximize visualization (e.g., spectral) processing power. After completing the high-speed computation, the FPGA may return to normal operation in conventional visualization mode 6062.

In some implementations, the transition between the conventional visualization mode 6062 and the advanced visualization mode 6063 can be triggered by a surgical task. The control module 6001 can detect an upcoming or current surgical task based on the contextual information generated by the situational awareness module 6006. The control module 6001 can consult a database that can be stored in memory 6003 for a visualization mode associated with a surgical task. If the surgical task requires advanced visualization mode 6063, control module 6001 then uses the FPGA to facilitate the high-speed computations associated with advanced visualization mode 6063. When the surgical task is completed, the control module 6001 then triggers a return to the conventional visualization mode 6062, effectively switching the FPGA to perform the conventional task.

In some implementations, detecting 6011 surgical data includes receiving two separate surgical data competing for user attention. For example, detecting 6011 surgical data may include receiving first surgical data and second surgical data, wherein the first surgical data and the second surgical data are both related to a current surgical task and/or associated with one or more active surgical devices. In such implementations, method 6010 may include assigning 6012 a priority value to the first surgical data and the second surgical data based on the relative criticality of the first surgical data and the second surgical data to the success of the procedure and/or the severity of the failure that may result from ignoring them. For example, if the first surgical data includes a higher criticality than the second surgical data, method 6010 assigns 6012 a higher display priority value to the first surgical data than the second surgical data. Additionally or alternatively, if a first fault associated with the first surgical data is more severe than a second fault associated with the second surgical data, method 6010 assigns 6012 a higher display priority value to the first surgical data than the second surgical data.

In some implementations, the display priority values and corresponding criticality and/or fault severity associated with the various surgical data may be stored in any suitable format (e.g., table or database) in a storage medium such as memory 6003. The processor 85 of the control module 6001 can be configured to assign 6012 a display priority value based on such stored information.

Additionally or alternatively, 6012 display priority values may be assigned based on predetermined user preferences and/or user-specific surgical contexts. In some implementations, surgical data associated with the active surgical instrument 21 may be selectively displayed on a display associated with a clinician using the surgical instrument 21. Thus, method 6010 may include assigning 6012 different display priority values to the same surgical data for different displays.

In one example, surgical data associated with a first surgical device utilized by a clinician is simultaneously assigned 6012 a high display priority value relative to a first display selected by or otherwise associated with the clinician and a low display priority value relative to other displays not selected by or associated with the clinician. In another example, first surgical data associated with a first surgical device utilized by a clinician is assigned a high display priority value relative to a first display selected by or otherwise associated with the clinician, while second surgical data associated with a second surgical device not utilized by the clinician is assigned a low display priority value relative to the first display.

In various cases, the control module 6001 receives context information from the situational awareness module 6006, which can be used in the aforementioned pairing of surgical data for a particular surgical device with a display associated with a clinician using the surgical device. Context information may be generated by situational awareness module 6006 based on perioperative data.

In some implementations, a database or table may store pairing information. In other cases, the clinician may wear a unique identifier that can be detected by the surgical device while holding the surgical device. When a positive identification is made, the control module 6001 can then assign a high display priority value to surgical data associated with the surgical device relative to a display selected by or otherwise associated with the clinician. In one example, the unique identifier may be an RFID in a clinician's glove that is detected by a corresponding RFID scanner in the surgical device handle.

In some cases, such as during a colorectal procedure, the system 6000 is configured to automatically switch a display (e.g., display 6005) from a first live stream displaying a first surgical field of view to a second live stream displaying a second surgical field of view. The automatic switching may be triggered by completion of a surgical task in the surgical procedure. In one example, a predetermined surgical cue indicating completion of a surgical task may be used as a trigger for automatic switching between streams of conditions. The predetermined surgical cue may include, for example, detecting completion of a staple being fired into tissue by the surgical instrument 21, detecting completion of sealing tissue by the surgical instrument 21, and/or detecting release of tissue from the jaws of the end effector of the surgical instrument 21, such as by opening the jaws.

The predetermined surgical cue may also include detecting activation of the surgical instrument 21, followed by detecting deactivation of the surgical instrument 21, which indicates that the surgical instrument 21 is completing a surgical task. In some implementations, the control module 6001 utilizes readings from one or more sensors of the surgical instrument 21 and/or other components of the computer-implemented interactive surgical system 1 to detect predetermined surgical cues. In some examples, the predetermined surgical cue is detected based on context information generated by situational awareness module 6006.

In colorectal procedures, a clinician uses a circular stapler and a linear stapler to accomplish various tasks of the procedure. Colorectal procedures involve operating in two discrete surgical fields, an internal surgical field in which diseased tissue is resected and an external surgical field with a circular stapler. In some implementations, the first live stream is focused on an inner portion where tissue ablation occurs and the second live stream is focused on an outer portion where a circular stapler is applied. In such implementations, the automatic switching may be triggered by completion of tissue resection by the linear stapler, which may be detected, for example, by deactivating the linear stapler and/or removing the linear stapler from the first surgical field. The control module 6001 can employ various object recognition, object tracking and/or object marking algorithms, and/or other image processing techniques of image frames of the live stream, for example, to detect removal of the linear stapler from the surgical field.

Fig. 18 is a flow chart illustrating operation of an exemplary method 6070 of automatically switching between live streams for a surgical field in a surgical procedure. In some implementations, the method 6070 may be performed, for example, by the computer-implemented interactive surgical system 1. The method 6070 includes presenting 6071 the first live stream of the first surgical field on a display (e.g., display 6005). If 6072 detects a predetermined surgical cue indicating completion of a surgical task at a first surgical field, 6073 automatically switches from presenting a first live stream of the first surgical field on the display to presenting a second live stream of the second surgical field on the display. In some examples, the second surgical field is associated with a second surgical task subsequent to the first surgical task in the surgical procedure.

During a surgical procedure, various components of the computer-implemented interactive surgical system 1 may compete for available system resources, such as power, current, and/or processing resources. Additionally or alternatively, the operation of certain components of the computer-implemented interactive surgical system 1 may interfere with or adversely affect the operation of other components of the computer-implemented interactive surgical system 1. Various methods and systems are described herein that ensure component functionality is successful by maintaining a balance of system resources and/or component operations.

Fig. 19 is a flowchart illustrating operation of an exemplary method 6050 for balancing system resources during a surgical procedure performed by the computer-implemented interactive surgical system 1. The method 6050 includes detecting 6051 a failure of a system resource to meet competing demands of different components of the computer-implemented interactive surgical system 1. The method 6050 further includes displaying a resource allocation control of the system resource in response to detecting the fault, such as 6052 by superimposing the resource allocation control over a live stream of the surgical field of view of the surgical procedure. Additionally, the method 6050 may further comprise displaying recommended adjustments to the resource allocation control.

In addition to the above, the method 6050 further comprises adjusting 6053 the power consumption of one or more of the different components based on the resource allocation control adjustment by the user. The method 6050 may also include returning 6055 to a default resource allocation or removing a resource consumption limit when the failure is no longer detected. The method 6050 may further include 6054 displaying visual content representing an effect of the adjustment of the resource allocation and/or 6056 displaying visual content representing a return to a default mode, for example by superimposing the visual content on a live stream of the surgical field on a display of the computer-implemented interactive surgical system 1.

In some implementations, 6051 detecting the fault includes reaching and/or exceeding a predetermined threshold, such as, for example, a power threshold, a current threshold, a process threshold, and/or a maximum utilization threshold. The predetermined threshold may be selected to ensure that 6051 detection of a fault is achieved before reaching a point where the power consumption exceeds the available power resources to avoid a fault during the surgical procedure. In some implementations, the predetermined threshold is stored in a storage medium, such as memory 6003, that is accessed by the processor 85 and compared to the monitored value (e.g., total consumption, rate of consumption).

In some implementations, 6051 detects a fault when the control module 6001 detects competing tasks that are performed at a total estimated resource consumption (e.g., power consumption) or resource consumption rate that is equal to or greater than a predetermined threshold during a surgical procedure. In some implementations, 6051 detects a fault when control module 6001 detects multiple components of computer-implemented interactive surgical system 1 concurrently with an overall estimated resource consumption (e.g., power consumption) or resource consumption rate that is equal to or greater than a predetermined threshold. In one example, a database stored in memory 6003, for example, can include a list of resource consumption estimates associated with various components of the computer-implemented interactive surgical procedure system 1 and/or various tasks performed by the computer-implemented interactive surgical procedure system 1. The processor 85 may calculate a resource consumption value based on information in the database and compare the calculated value to a predetermined threshold to determine if a fault 6051 is detected.

In some implementations, the system resource is power and the component of the computer-implemented interactive surgical system 1 competing for the power resource is the system 6000 or any other visualization system of the computer-implemented interactive surgical system 1 and the generator 27. For example, during a surgical tissue sealing procedure, the computer-implemented interactive surgical system 1 may be configured to perform two tasks that together require power consumption that meets or exceeds a predetermined threshold. The first task may be, for example, a visualization task that provides a spectral view of the surgical field of view, and the second task may be, for example, energizing the surgical energy device to seal tissue grasped by the surgical energy device in the surgical field of view. The generator module 27 may be configured to supply power to the surgical energy device to seal the tissue by applying therapeutic energy to the tissue.

In such implementations, the fault is detected by monitoring the power consumption 6051 of the system 6000 and the generator module 27. If the power consumption reaches and/or exceeds a predetermined threshold, the control module 6001 issues a user alert by superimposing 6052 the power distribution control over the live stream of the surgical field on the display 6005. The control module 6001 can then adjust power consumption based on user adjustments to the power allocation control.

In some cases, control module 6001 reduces the power requirements of one or more systems to implement user adjustments. For example, control module 6001 can reduce the brightness of display 6005 in response to a user input selecting to reduce the power allocation to system 6000 to facilitate maintaining the power allocation to generator module 27. Additionally or alternatively, the control module 6001 may slow down, delay, or pause certain tasks performed by the system 6000, such as secondary image processing tasks, in response to a selection to reduce power allocation to the system 6000 to facilitate maintaining user input to the power allocation to the generator module 27.

In some cases, user adjustment of the power allocation control may be more biased toward the system 6000 for power allocation relative to the generator module 27. This may occur where the user is in a critical step requiring optimal visualization (e.g., sealing a blood vessel), and where proper operation of the energy device can still be achieved at a lower power level (possibly by extending the tissue sealing time). In this case, control module 6001 can cause surgical energy device and/or generator module 27 to adjust one or more of its settings to reduce the power draw in favor of system 6000.

In some implementations, the control module 6001 automatically coordinates to make power allocation adjustments in response to detecting a fault without user input. In such implementations, the control module 6001 only alerts the user of changes caused by automatic changes in power consumption. For example, the control module 6001 may superimpose an alert of a change in brightness of the display 6005 on a live stream on the display 6005 and/or a temporary pause in the superimposition of visual content, such as surgical data superimposition, for example, due to the temporary pause in image processing producing the superimposition. The stack may be reintroduced when the surgical energy device completes tissue sealing. Alternatively, the overlay may be displayed intermittently rather than continuously to reduce power consumption of the system 6000 to facilitate the generator module 27.

In some implementations, user adjustment of the power distribution control is implemented via one or more active discrete current limiting circuits configured to be able to, for example, prevent one or more systems from exceeding a maximum fuse limit threshold.

In some implementations, the system resource is power and the component of the computer-implemented interactive surgical system 1 that competes for the power resource is a system 6000 or any other visualization system of the computer-implemented interactive surgical system 1 and the smoke evacuation module 26 (fig. 3). For example, during a surgical tissue sealing procedure, the computer-implemented interactive surgical system 1 may be configured to perform two tasks that together require power consumption that meets or exceeds a predetermined threshold. The first task may be, for example, a visualization task that provides a spectral view of the surgical field of view, and the second task may be, for example, extracting smoke from the surgical field of view. Smoke is a byproduct of the tissue sealing process performed by the energy device.

In such implementations, if 6051 detects a fault, control module 6001 may then issue a user alert, for example by having power distribution control superimposed 6052 on the live stream of the surgical field on display 6005, as previously discussed. The control module 6001 can then adjust power consumption based on user adjustments to the power allocation control. In some cases, control module 6001 may recommend adjusting smoke evacuation module 26 to a lower setting, such as by overlaying visual content representing the recommended adjustment on a live stream of the surgical field of view on display 6005. In addition, the control module 6001 may superimpose visual content indicating a decrease in smoke rate. Presenting such visual content in the indicated manner provides the user of the surgical energy device with an opportunity to slow the sealing process by adjusting the surgical energy device to a lower setting that generates less smoke. When the further power requirements of the system 6000 are stopped, for example due to the completion of the image processing associated with the spectral views, the control module 6001 causes the superposition of visual content representing an alert to inform the user that the smoke evacuation module 26 is returning to its initial setting.

In various circumstances, methods similar to method 6050 may be implemented to address other faults, such as overheating and/or noise, that may adversely affect a surgical procedure performed using computer-implemented interactive surgical system 1. In this case, fault detection may be achieved based on readings of one or more internal and/or external sensors of one or more components of the computer-implemented interactive surgical system 1. The sensor readings may then be compared to a predetermined threshold to detect a fault. For example, if one or more temperature sensor readings are at or above a predetermined temperature threshold, an overheat fault may be detected. In response to the fault, the control module 6001 can superimpose virtual control over the live stream of the surgical field of view of the surgical procedure on the display 6005, presenting the user with an opportunity to change the settings of one or more components of the computer-implemented interactive surgical system 1 to address overheating. A similar approach may be used to address noise levels.

In various cases, according to method 6010, a display arrangement includes segments of display 6005 to accommodate a visual representation of surgical data. The size, shape, display time, display location, display three-dimensional arrangement (e.g., foreground, background), display blinking, highlighting, and/or fonts of the simultaneously displayed segments may depend on a variety of factors, including the nature, complexity, and/or criticality of the surgical data. In some implementations, pairing information for surgical data configured to be simultaneously displayable may be provided in a database or table stored on a storage medium such as memory 6003. The processor 85 of the control module 6001 can determine whether to display multiple surgical data simultaneously based on the stored information.

In some implementations, visual representations of two different surgical data are configured to be simultaneously displayed on the display 6005 in a segmented mode, but only one visual representation is ready to be displayed. In such implementations, the visual representation that is not ready may represent a blank area in the segment to which it is assigned. In addition, as described above, the control module 6001 can be configured to be able to re-use the FPGA for additional processing speeds to help prepare the visual representation of the lack of readiness. Alternatively, the visual representation that is not ready may be displayed at a lower quality to ensure that the surgical data is displayed simultaneously.

In some cases, the visual representations of the plurality of surgical data are configured to be simultaneously displayed on the display 6005, for example, in a segmented mode, but the system 6000 does not have sufficient processing power to simultaneously display all of the different surgical data. In response to detecting an insufficient processing power thereof, the system 6000 may prioritize the display of higher priority surgical data over lower priority surgical data, e.g., based on the assigned display priority value of the surgical data.

In other cases, the display problem may be that there is insufficient display area on the display 6005 to simultaneously display a visual representation of multiple surgical data in a segmented mode. In this case, the display arrangement implemented by the control module 6001 can include a picture-in-picture type display arrangement in which the first visual representation is displayed inside the second visual representation. In other words, the first visual representation may appear in the foreground and may be smaller in size than the second visual representation appearing in the background. Additionally, through any suitable user interface 6007, a clinician may switch between the two visual representations by selectively moving one of the visual representations to the foreground and the other to the background.

The control module 6001 can be configured to detect whether there is a lack of sufficient display area based on a predetermined display size of the display 6005 and a calculated display size of the visual representation of the surgical data. In some implementations, a predetermined equation may be utilized in the calculation. In other cases where the visual representations are the same or similar in size, a lack of adequate display is detected when the number of visual representations of the surgical data is equal to or greater than a predetermined threshold.

In various cases, according to method 6010, the display arrangement includes transitions between display modes, such as, for example, a static or passive display mode and a dynamic or active display mode. In some implementations, the control module 6001 is configured to transition the visual representation of the surgical data from a static mode to a dynamic mode. The control module 6001 can be configured to effect a transition in response to a predetermined trigger, such as, for example, a change in priority, criticality and/or risk associated with surgical data. For example, 6012 surgical data initially assigned a low display priority value may be displayed or superimposed on a live stream of the surgical field in a static display mode that later transitions to an active display mode as the display priority value of the surgical data increases to a higher display priority value.

In addition to the above, in some implementations, the static mode includes displaying or overlaying a static visual representation of surgical data associated with the surgical instrument 21 on, for example, a side or corner of the display 6005. Conversely, the active mode may include, for example, superimposing an active visual representation of the surgical data on a portion of the surgical instrument 21 in the live stream of the surgical field of view and/or moving a highlighted region in the static visual representation. In various implementations, the static display mode differs from the active display mode in one or more of, for example, size, shape, display time, display location, display three-dimensional arrangement (e.g., foreground, background), display blinking, highlighting, and/or font.

In some implementations, the transition from the static display mode to the active display mode is based on actuation or activation of the surgical instrument 21, meaning that this is a technically sensitive step requiring a real-time dynamic display. For example, during firing of subsequent staples into tissue (which requires a particular firing angle relative to a previous firing), actuation or activation of the surgical instrument 21 may trigger a transition to the active display mode. First, certain display elements, such as visual representations of surgical data (e.g., various firing parameters and/or tissue parameters) may be displayed or overlaid in a static display mode. Then, in response to actuation or activation of the surgical instrument 21, in a subsequent firing, the control module 6001 causes a transition to a dynamic display mode, wherein display elements are highlighted and/or moved, for example. In various instances, the subsequent firing of the trigger transition involves staple firing that also deploys tissue appendages (e.g., tissue thickness compensators).

In some implementations, the control module 6001 is configured to be able to cause display elements in the static display mode to become smaller in size, less prominent, and/or disappear over time. The various operating parameters of the surgical instrument 21 may initially be presented in a dynamic display mode and then transition to a static display mode as the importance level of these parameters changes. In some examples, certain display elements are assigned to predetermined locations on the display 6005, for example, in a static display mode, and then change these predetermined locations in an active display mode.

In some implementations, the visual representation of the surgical data (e.g., the biomarker) is presented in a static display mode, such as a solid color that is not highlighted, while the value associated with the biomarker remains within a predetermined range or below a predetermined threshold. However, if the value moves beyond a predetermined range or beyond a predetermined threshold, the visual representation of the surgical data may transition to a dynamic display mode by, for example, causing certain display elements of the visual representation to change in size, shape, display time, display location, display three-dimensional arrangement (e.g., foreground, background), display blinking, highlighting, and/or font.

Fig. 19A is a flowchart illustrating operation of an exemplary method 6110 for transitioning between a static display mode and an active display mode based on surgical data. In some implementations, the method 6110 may be performed, for example, by the computer-implemented interactive surgical system 1. In the illustrated example, the surgical data includes tissue parameters. The tissue parameter is tissue impedance. Other tissue parameters may be similarly presented, such as, for example, tissue thickness, tissue pressure, tissue conductivity, and/or tissue compression.

In addition to the above, the method 6110 further includes 6111 detecting tissue between jaws of an end effector of the surgical instrument 21. In some cases, the tissue detection 6111 may be automatically implemented, for example, by object recognition, object tracking, and/or object tagging algorithms, and/or other image processing techniques of image frames of the live stream. Alternatively, the surgical instrument 21 can be configured to 61111 detect the presence of tissue between the jaws based on signal readings from one or more sensors in the jaws. For example, tissue 6111 may be detected when a non-therapeutic signal flowing through the tissue produces an acceptable tissue impedance.

In response to detecting the tissue 6111, the method 6110 presents the tissue parameter in a static display mode 6112, such as by displaying or superimposing a visual representation of the tissue parameter on a live stream of the surgical field. However, if the tissue parameter 6113 meets or exceeds the predetermined threshold, or becomes outside of the predetermined range, the method 6110 further causes the one or more display elements 6115 of the visual representation of the tissue parameter to transition to the active display mode.

In some implementations, the surgical instrument 21 is an energy device configured to seal tissue grasped by an end effector of the surgical instrument 21. At the beginning of treatment, when 6111 detects tissue, the tissue impedance is presented in a static display mode. Surgical instrument 21 may communicate surgical data indicative of tissue impedance to control module 6001 via a wired or wireless interface to be displayed on display 6005, for example, in a static display mode. As energy is initially applied to the tissue, the tissue impedance changes. However, if the tissue impedance reaches or exceeds a predetermined threshold, or becomes outside a predetermined range, this may be an indication that the end effector is immersed in fluid, electrically shorted, or only low impedance tissue. In any event, a transition 6115 to the active display mode is triggered to alert the clinician to conduct the survey.

In various circumstances, the control module 6001 determines various surgical information related to the surgical procedure, such as, for example, the steps of the surgical procedure, the surgical instrument 21 to be used in each step, and various risks and/or techniques associated with each step. Such determination may be based, for example, on context information generated by situational awareness module 6006. The control module 6001 can then display or overlay surgical information over the surgical field of view of the surgical procedure in a display arrangement using one or more methods described in this disclosure. For example, the current step, surgical instrument 21 associated with the current step, risk associated with the current step, and/or technique associated with the current step may be presented in an active display mode, while previous and/or subsequent steps are presented in a static display mode. When the next step is changed to the current step, it is transitioned to the active display mode.

In addition to the above, the transition 6115 from the static display mode to the active display mode may be used to reflect changes to the protocol plan, such as reflecting a new layout. In various circumstances, surgical information may be divided by the control module 6001 into stages, such as accessing, separating and/or moving, resecting and/or repairing and/or adding relevant data to a surgeon for presentation.

In various instances, the transition of the visual representation of the surgical data between the static display mode and the active display mode is based on a change in the use of the surgical instrument 21 linked or associated with the surgical data. Surgical data may be initially presented in a static display mode. However, if a predetermined change is detected in the use of the surgical instrument 21, the transition of the visual representation of the surgical data to the active display mode is affected.

FIG. 19B is a flowchart illustrating the operation of an exemplary method 6120 for transitioning a visual representation of surgical data between a static display mode and an active display mode. The transition is based on a change in or triggered by the use of the surgical instrument 21 linked or associated with the surgical data. In some implementations, the method 6120 may be performed, for example, by the computer-implemented interactive surgical system 1.

In the illustrated example, the surgical instrument 21 is an ultrasonic surgical instrument configured to coagulate tissue grasped by its end effector during a surgical procedure. The surgical instrument 21 is used with a generator that employs a preset generator setting that is received 6121 by the control module 6001 for display or overlay on the surgical field of view of the surgical procedure. The method 6120 further includes presenting 6122 the preset generator settings in a static display mode. However, if 6123 detects that the end effector is immersed in blood during a surgical procedure due to, for example, a semi-immersion of the blood vessel attempting to coagulate, the new generator setting is presented in an active display mode. The new generator set-up may include increasing the transducer power level in response to the end effector being immersed in blood. The display of new generator settings or the superposition on the live stream of the surgical field alerts the user of the surgical instrument 21 and provides the user with an opportunity to adjust the position of the end effector if an increased power level is disadvantageous.

In some implementations, detecting immersion of the end effector in blood is accomplished by one or more sensors. In one example, a non-therapeutic current may flow. If a short circuit is detected, the short circuit is an indication of immersion in blood. In response, the surgical data indicating the infusion is transmitted to the control module 6001 wirelessly or through a wired interface.

In various cases, the display arrangement according to method 6010 includes initially presenting a visual representation of surgical data in a static display mode. Then, method 6010 causes a change in one or more display elements of the visual representation (such as, for example, values associated with the surgical data) in response to a change in the state of surgical instrument 21 associated with the surgical data. These variations include, for example, encountering cartridge lockout, activation of the advanced energy device, transition between an open configuration and a closed configuration of the end effector of the surgical instrument 21.

As previously described, the change in one or more values associated with the surgical data may be performed in a static display mode. Alternatively, in some implementations, the change may be accompanied by a transition from a static display mode to an active display mode to provide additional warning. Such implementations include, for example, various adaptation techniques such as, for example, pausing to allow tissue creep and/or tissue compression, detecting unbalanced tissue in the jaws of the end effector of the surgical instrument 21, and/or detecting that clamping of the jaws is inducing undue tissue tension.

In various cases, the display arrangement according to method 6010 includes a transition from a first dynamic display mode to a second dynamic display mode, wherein the second dynamic display mode includes or represents a higher priority, risk, and/or criticality than the first dynamic display mode. In one example, the blood pressure is tracked during the surgical procedure via a blood pressure monitoring device, which may communicate readings to the control module 6001, for example, using a wireless or wired interface. Then, due to the importance of the blood pressure data, a visual representation of the blood pressure may be presented in a first dynamic display mode. However, if an increase in blood pressure data is detected during the surgical procedure that exceeds an acceptable limit, a transition is made to raise the blood pressure data to a second dynamic display mode, e.g., to ensure that an appropriate alert is delivered.

In various implementations, one or more characteristics of the visual representation of the surgical data, such as, for example, the size, shape, display time, display location, display three-dimensional arrangement (e.g., foreground, background), display blinking, highlighting, and/or font of the visual representation, may be based on the 6012 assigned display priority value. In some cases, 6012 assigned display priority values may result in a display arrangement with display conflicts. For example, determining a display arrangement based on the assigned display priority value may result in more than one visual representation of surgical data having the same location on the display 6005, for example.

Fig. 20 is a flowchart illustrating the operation of an exemplary method 6010' for resolving display conflicts in a display arrangement. Method 6010' is similar in many respects to method 6010. For the sake of brevity, common details between the two methods are not repeated here. In some cases, as shown in fig. 20, a display conflict detected by 6080 may resolve the conflict by 6081 changing one or more display times of the competitive visual representation. Alternatively, the clinician may be made aware of the conflict and a selection may be provided on the display 6005 to select 6082 between different surgical data. Alternatively, selection 6083 may be made automatically based on predetermined preferences of the clinician, which may be based on user input or context information generated by a situational awareness module (e.g., 6006).

In some implementations, 6080 detecting a display conflict between the first surgical data and the second surgical data includes retrieving, for example, by the processor 85, display priority information for the first surgical data and the second surgical data from, for example, the memory 6003. The processor 85 may then compare the display priority information of the first surgical data and the second surgical data to determine whether a display conflict 6080 is detected.

In some implementations, the control module 6001 is configured to be able to respond to the detected display conflict 6080, for example, by concurrently displaying visual representations of competing surgical data that are smaller in size than a default size. Allowing the clinician to select between visual representations, for example, through user interface 6007. In response, the control module 6001 removes the unselected visual representations and increases the size of the selected visual representations to a default size.

In some implementations, the display conflict detected 6080 can be resolved by automatically setting priority 6084 based on a resolution order determined from the surgical data presenting the display conflict. In some implementations, the order of resolution is determined based on the order of surgical steps associated with the surgical data and/or the risk reported by the surgical data and/or the urgency of the problem.

In some examples, 6080 detects a display conflict between the first surgical data and the second surgical data, both presenting a high priority problem and/or risk. Furthermore, the second solution associated with the second surgical data cannot be executed until the first solution associated with the first surgical data is implemented. In such examples, the first visual representation of the first surgical data automatically prioritizes the second visual representation 6084 of the second surgical data based on the order of resolution.

In some examples, a display conflict may occur between the first surgical data associated with locking to prevent actuation of the surgical instrument 21 and the second surgical data associated with a suboptimal tissue thickness of tissue being treated by the surgical instrument. In such examples, a predetermined resolution order may be employed to resolve conflicts that favor locking, as tissue thickness issues, despite high priority, cannot be resolved while the surgical instrument 21 is in the locked state.

In some cases, the resolution order may be stored on a storage medium (e.g., memory 6003) in the form of a database, table, or any other suitable form. The stored information may list various surgical data and corresponding resolution orders. The processor 85 may refer to the stored information to identify a resolution order between competing surgical data to resolve the display conflict. In some implementations, the order of resolution is based on the order of surgical tasks to be initiated or completed according to competitive surgical data.

In some examples, the control module 6001 can receive first surgical data indicating that a detected staple cartridge (e.g., a staple cartridge loaded onto the surgical instrument 21) has been previously fired. The controller of the surgical instrument 21 may interrogate the staple cartridge, for example, by requesting firing information stored on the chip of the staple cartridge, and may determine whether the staple cartridge has been previously fired based on the retrieved firing information. The first surgical data including the firing information may then be transmitted to the control module 6001 wirelessly or by wireless communication. In addition, the control module 6001 can receive second surgical data associated with closing an end effector of the surgical instrument 21 onto tissue being stapled in a surgical procedure involving the surgical instrument 21 loaded with a previously fired staple cartridge. For example, the second surgical data can relate to tissue thickness and/or tissue position between jaws of the end effector.

In addition to the above, the control module 6001 detects a display conflict 6080 because both the first surgical data (previously fired cartridge) and the second surgical data (end effector closed onto tissue) include high priority status. For example, to determine the arrangement of the visual representations of the first surgical data and the second surgical data on the display 6005, the processor 85 examines the resolution order information stored on a storage medium (e.g., memory 6003) in a database, table, or any other suitable form. In this example, a first problem presented by the first surgical data (previously fired staple cartridge) must be addressed before a second problem presented by the second surgical data (end effector closed onto tissue). This is because it is not important to address the problem of closing the end effector onto tissue if the previously fired staple cartridge is not available for treating tissue.

Once the display conflict is resolved, method 6010 'continues to display visual representations of the first surgical data and the second surgical data according to the display arrangement 6014' selected based on the resolution order. For example, the first visual representation of the first surgical data may be displayed before the second visual representation of the second surgical data. Other suitable display arrangements may be employed as described elsewhere in this disclosure.

In various aspects, the surgical procedure involves stapling tissue using a surgical instrument 21, such as, for example, a surgical stapler. The surgical procedure generally includes positioning an end effector of the surgical instrument 21 in a surgical field and actuating the end effector to grasp tissue between jaws of the end effector. The jaws place the grasped tissue under compression. As the tissue contains water, the grasped tissue gradually changes in response to compression by the jaws of the end effector in a process known as tissue creep until the tissue reaches a steady state. In addition, the gap between the jaws and the thickness of the tissue may also vary until the tissue reaches a steady state. Furthermore, tissue flow or tissue movement may also occur until the tissue reaches a steady state. In some implementations, to successfully suture, the tissue is allowed to wait for a certain time to reach steady state. Parameters associated with the previously described tissue changes, such as latency parameters, tissue thickness parameters, and/or instrument clearance parameters, are important for properly assessing when tissue homeostasis is reached.

Fig. 21 is a flow chart illustrating operation of an exemplary method 6090 for accounting for tissue changes (e.g., tissue creep, tissue flow, tissue compression) in a surgical procedure employing a surgical instrument 21. In some implementations, the method 6090 includes 6091 detecting tissue between jaws of an end effector of the surgical instrument 21. In some cases, tissue detection 6091 may be automatically and visually implemented, for example, by object recognition, object tracking, and/or object tagging algorithms, and/or other image processing techniques of image frames of a live stream. Alternatively, the surgical instrument 21 can be configured to detect 6091 the presence of tissue between the jaws based on signal readings of one or more sensors in the jaws. For example, tissue 6091 may be detected when a non-therapeutic signal flowing through the tissue produces an acceptable tissue impedance.

In response to 6091 detecting tissue, method 6090 may display or superimpose at least one parameter of tissue change (e.g., tissue creep, tissue flow, tissue compression) and/or parameters of surgical instrument gap distance between jaws of an end effector and/or latency 6092 on a live stream of a surgical field. In certain implementations, the method 6090 further includes alerting 6094 to a user of the surgical instrument 21 to initiate tissue treatment when steady state is reached. In some cases, steady state 6093 is detected based on one or more of the tissue variation parameters and/or one or more of the surgical instrument parameters. For example, steady state 6093 may be detected when one or more of tissue flow, tissue creep, tissue thickness, tissue compression, gap distance between jaws of an end effector, and/or latency is at or above a predetermined threshold. Alternatively, steady state 6093 may be detected if the rate of change of one or more of tissue flow, tissue creep, tissue thickness, tissue compression, gap distance between jaws of the end effector, and/or latency is less than or equal to a predetermined threshold. Additionally or alternatively, steady state 6093 may be automatically visually detected based on object recognition, object tracking, and/or object marking algorithms, and/or other image processing techniques that may monitor, for example, changes in tissue.

In some implementations, the method 6090 further includes automatically visually monitoring tissue changes during application of the treatment by the surgical instrument 21, for example, by utilizing one or more suitable object recognition, object tracking, and/or object marking algorithms, and/or other image processing techniques of image frames of the live stream. In some cases, the treatment may be, for example, firing staples into the grasped tissue. If 6095 tissue changes reach excessive levels during firing, the method 6090 may further include displaying or overlaying a warning 6096 to the clinician. In some cases, the method 6090 includes 6097 displaying or overlaying a visual representation of the location and/or size of the excess tissue variation, for example as shown in fig. 26. In some implementations, tissue changes are automatically visually monitored by, for example, tracking the size, location, color, and/or movement of one or more tissue targets in the grasped tissue.

The method 6090 may further include 6098 displaying or overlaying the recommended solution, such as, for example, adjusting one or more parameters of the surgical instrument 21, such as one or more closure parameters (e.g., jaw grip, jaw pressure, distal tip load) and/or firing parameters (e.g., firing speed, ion beam speed). In some cases, the recommended solution may be additional latency. In some cases, the surgical instrument 21 is an ultrasonic instrument and the recommended solution is a solution to reduce the distal tip load of the end effector. In other cases, the surgical instrument 21 is a surgical stapler and the recommended solution is a solution to increase the distal tip load of the end effector.

In various circumstances, tissue changes (e.g., tissue flow) are at least partially affected by the tension experienced by the tissue grasped between the jaws. In some cases, tissue tension is due to movement such as rotation of the end effector from a neutral position while grasping tissue. In this case, the 6098 overlay solution may be in the form of a recommended adjustment to the rotational position of the end effector. Excess tissue tension may be automatically observed, for example, by utilizing one or more suitable object recognition, object tracking, and/or object marking algorithms, and/or other image processing techniques of image frames of the live stream.

In some implementations, one or more sensors including accelerometers, gyroscopes, relative position sensors, and/or three-dimensional magnetic sensors may be used to determine the position and/or orientation of the end effector. In some implementations, the sensor may generate location information characterizing one or more location changes. The location information may be transmitted to the control module 6001 via a wired or wireless interface.

In some implementations, the accelerometer may be a single axis, dual axis, or tri-axis accelerometer. Accelerometers may be used to measure the appropriate acceleration, which is not necessarily a coordinate acceleration (rate of change of speed). In contrast, an accelerometer may observe accelerations associated with weight phenomena experienced by the test mass when the reference frame of the accelerometer is stationary. Additionally or alternatively, the position and/or orientation of the end effector may be automatically observed, for example, by utilizing one or more suitable object recognition, object tracking and/or object marking algorithms, and/or other image processing techniques of image frames of the live stream.

In response to detecting tissue tension in tissue grasped by the jaws of the end effector, the control module 6001 may display a visual representation of the tissue tension, the magnitude of the tissue tension, and/or the rotational orientation responsible for the tissue tension, or superimpose them on the live stream of the surgical field. In some implementations, as shown in fig. 22A-22C, visual representations 6100, 6101, 6102 of tissue tension can provide positional information of an end effector in three-dimensional space, for example. In some implementations, the positional information of the end effector is represented by a first axis (e.g., an x-axis) extending longitudinally through the end effector from the center, a second axis (e.g., a y-axis) perpendicular to the first axis and extending in a first plane with the first axis, and a third axis (z-axis) perpendicular to the first axis and extending in a second plane with the first axis, wherein the first plane intersects the second plane at the first axis.

Each of the coordinate axes may be presented in a first form (e.g., color, shape, size) while the end effector is in a neutral state relative to the coordinate axes, as shown in fig. 22A. In response to detecting an excessive deviation from the neutral state with respect to one or more coordinate axes, the control module 6001 causes the one or more coordinate axes to change to a second form that is different from the first form. In other cases, for example, the excessive deviation from the neutral state may be a first deviation and may be based on a first predetermined threshold or range, while the second deviation may be more excessive than the first deviation and may be based on a second predetermined threshold or range that is different from the first predetermined threshold or range. In this case, the neutral state may be presented in a first form, the first excessive deviation may be presented in a second form, and the second excessive deviation may be presented in a third form different from the first and second forms. In certain implementations, the first form includes green, the second form includes yellow, and the third form includes red.

In the illustrated example, a first excessive deviation from neutral is detected about the y-axis. In response, the control module 6001 causes the y-axis to switch from the first to the second form while the x-axis and z-axis remain in the first form, as shown in fig. 22B. In the illustrated example, the first excessive deviation is greater than or equal to a first predetermined threshold. Then, as shown in fig. 22C, a second excessive deviation greater than or equal to the second predetermined threshold value is detected around the x-axis, while the first excessive deviation around the x-axis has been corrected. In response, the control module 6001 returns the Y-axis to the first form and changes the x-axis to the third form.

In various cases, different deviations from neutral (e.g., a first excessive deviation and a second excessive deviation) may include different severity, and may indicate different forms of presentation of severity. For example, a first excessive deviation may be represented as yellow, while a second excessive deviation that is more severe than the first excessive deviation may be represented as red. In some implementations, the deviation from the neutral state is determined based on a range of rotation angles around one or more of the coordinate axes. For example, the neutral state with respect to the first axis is detected in the case where the rotation angle of the end effector with respect to the first axis satisfies the range of about ±a°, the first excessive deviation is detected in the case where the rotation angle of the end effector with respect to the first axis satisfies the range of about ±b°, and the second excessive deviation is detected in the case where the rotation angle of the end effector with respect to the first axis satisfies the range of about ±c°. In the illustrated example, A, B and C are integers, where a is less than B and B is less than C.

23A-23B, in some implementations, the visual representations 6104, 6105 of tissue tension may also include tissue tension measurements 6104a, 6105a associated with each of the coordinate axes. The control module 6001 can cause the tissue tension measurements to change form (e.g., color, size, and/or shape) in response to excessive deviation in tissue tension (e.g., from 2.0 pounds to 7.0 pounds).

In some implementations, the control module 6001 can also cause the recommendation to be displayed or superimposed on the live stream of the surgical field to address excessive tissue tension issues. In some examples, as shown in fig. 24, the recommendation includes a visual representation 2106 showing the surgical instrument 21 with an arrow 6107 indicating a recommended rotation to transition the end effector of the surgical instrument 21 to a neutral state.

Fig. 24-30 illustrate various display arrangements 6013 determined based on detected surgical data 6011 according to methods 6010 of the present disclosure and/or any other suitable methods. The display arrangement shown in fig. 24-30 is shown in the context of a surgical instrument 21 configured to suture and cut tissue. However, in other implementations, one or more of the display arrangements shown in fig. 24-30 may be similarly used with other surgical instruments in other types of surgical procedures.

The various display arrangements described in this disclosure relate to superimposing various visual representations of surgical data on a live stream of a surgical field of view displayed on a display, such as display 6005. As used herein, the term overlay includes semi-transparent overlays, partial overlays, and/or moving overlays. Further, the superimposed layers may be positioned on or at least partially on or near objects in the surgical field such as, for example, end effectors and/or critical surgical structures. Some display arrangements may include changes in one or more display elements of the superimposed layers, including changes in color, size, shape, display time, display location, display frequency, highlighting, or combinations thereof, based on changes in display priority values.

Fig. 25 shows a display arrangement 6117 comprising a mixed reality view presented by the control module 6001, for example on a display 6005. The display 6005 shows a live stream of the surgical field during a surgical procedure utilizing the surgical instrument 21 to staple and cut tissue T grasped by the end effector 6119 of the surgical instrument 21. In the illustrated example, the display arrangement 6117 overlays a transection progress line 6118 or staple firing progress line on the channel of the end effector 6119. In addition, the display arrangement 6117 superimposes the distance D traveled by the firing or cutting member on the path of the end effector 6119 to assist the clinician in tracking the firing process of the surgical instrument 21.

In some implementations, the control module 6001 detects a change in one or more parameters of tissue grasped by the end effector 6119 and/or parameters of the surgical instrument 21 that exceed a predetermined threshold or range, for example. In at least one implementation, the parameter change is a change in firing rate equal to or less than a predetermined threshold. For example, the control module 6001 can receive surgical data indicative of a parameter change via a wired or wireless communication interface with the surgical instrument 21 and/or surgical hub 6 (fig. 1). In response to detecting a parameter change, the control module 6001 can cause a change in the cross-cut progress line 6118 or staple firing progress line on the channel of the end effector 6119, including a change in color, size, shape, display time, display position, display frequency, highlighting, or a combination thereof.

Additionally or alternatively, in response to detecting a parameter change, the control module 6001 can cause a superposition of virtual channels to be superimposed on the end effector 6119 to change at least one of color, size, shape, display time, display position, display frequency, highlighting, or a combination thereof, according to a magnitude of the change, according to a value of the parameter, or according to a risk level associated with the parameter change.

Fig. 26 shows a display arrangement 6114 presented by the control module 6001, e.g. on a display 6005, e.g. according to the method of the present disclosure. The display 6005 shows a live stream of the surgical field during a surgical procedure utilizing the surgical instrument 21 to staple and cut tissue T grasped by the end effector 6119 of the surgical instrument 21. In the illustrated example, the display arrangement 6117 superimposes tissue markers 6116 on the tissue T that indicate tissue flow. For example, as described in connection with method 6090 of fig. 21, excessive tissue flow may be detected. In the illustrated example, the display arrangement 6114 combines the superposition of the transection progress line 6118 and the tissue marker 6116. Other display arrangements may include only tissue markers 6116.

27A-27C illustrate a display arrangement 6130 providing a visual representation 6131 of surgical data, according to at least one aspect of the present disclosure. In some implementations, the display arrangement 6130 is presented by the control module 6001, for example, on the display 6005, for example, in accordance with methods of the present disclosure. In the illustrated example, the display arrangement 6130 presents a visual representation 6132 in the form of a semi-transparent overlay 6133, indicating tissue flow during the firing sequence of the surgical instrument 21. During a firing sequence, the surgical instrument 21 is configured to deploy staples into tissue T grasped by an end effector of the surgical instrument 21 and cut the tissue T in parallel. In the illustrated example, the display arrangement 6130 is presented in a dynamic display mode, where changes in display elements 6132 (fig. 27A), 6133 '(fig. 27B), 6133' (fig. 27C) of the visual representation 6131 are depicted.

The display element may track tissue flow across the width of the end effector. The different locations may be presented in different forms (e.g., colors, shapes, and/or sizes), where the different forms represent different levels of tissue flow in the different locations. In the illustrated example, the display element 6132 represents an acceptable tissue flow condition, and the display element 6132' represents a low risk tissue flow condition. In contrast, display element 6132' "represents a high risk tissue flow condition.

Referring to fig. 28 and 29, in some implementations, a display arrangement 6140 is presented by the control module 6001, for example, on the display 6005, for example, in accordance with methods of the present disclosure. The display 6005 shows a live stream of the surgical field during a surgical procedure utilizing the surgical instrument 21 to staple and cut tissue T grasped by the end effector 6141 of the surgical instrument 21. In the illustrated example, the display arrangement 6140 superimposes the performance parameter profile 6142 (fig. 29) with the historical trace according to firing member, cutting member, and/or knife position. For example, the curve 6142 overlaps adjacent to the end effector 6141.

The curve 6142 presents risk severity associated with one or more parameters 6146, such as, for example, anvil gap, tissue load, firing speed, and/or motor speed, monitored during the firing sequence of the surgical instrument 21. Further, the curve 6142 also provides a plurality of thresholds (e.g., three thresholds 6143, 6144, 6145), each representing a severity level (e.g., low, medium, high), to provide a visual indicator to the clinician of the severity of the risk associated with the measured parameter 6146.

Additionally or alternatively, the display arrangement 6140 may be configured to utilize the colored curve 6147 to present surgical data associated with tissue parameters of the tissue T (e.g., tissue pressure, tissue compression, tissue flow, tissue thickness). The tissue parameter values may be represented in different colors (e.g., green, yellow, red or light shade, medium shade, dark shade) according to a value relationship to one or more predetermined thresholds. In the illustrated example, green represents tissue portions with acceptable values, yellow represents tissue portions with low risk values, and red represents tissue portions with high risk values. For example, the color profile 6147 provides a convenient and fast risk assessment tool that helps the clinician determine whether to begin and/or continue the firing sequence.

In various implementations, the tissue parameter values are measured by sensors dispersed at multiple locations, for example, across the width of the end effector 6141 and along the length of the end effector. The tissue parameter values are then represented by colored (e.g., green, yellow, red or light shading, medium shading, dark shading) areas on a colored curve 6147 commensurate with the position of the sensor on the end effector 6141, for example.

Fig. 30 illustrates a display arrangement 6150 that provides a visual representation of surgical data in accordance with at least one aspect of the present disclosure. In some implementations, the display arrangement 6150 is presented by the control module 6001, for example, on the display 6005, for example, in accordance with methods of the present disclosure. In some implementations, the display arrangement 6150 is superimposed on the live stream of the surgical field of view of the surgical procedure for stapling and cutting tissue with the surgical instrument 21.

In some implementations, the display arrangement 6150 includes a simulated cross-sectional overlay 6152 of the end effector 6153 of the surgical instrument 21, which in effect displays and matches, for example, the position and movement of one or more end effector components. The enhanced visualization may help the clinician better understand the current state and risk-based feedback from the surgical instrument 21 (e.g., clamping load is too high, force is too great, latency is required, etc.).

In the illustrated example, the simulated stack 6152 shows the staples 6156, the staple drivers 6154, and a firing member (e.g., sled 6155) configured to push the staple drivers 6154 to deploy the staples 6156 into tissue. The position of the firing member in the simulated stack 6152 reflects the position of the firing member in the end effector 6153 and indicates the progress of the firing sequence in real time. Further, in the illustrated example, simulated overlay 6152 shows Simulated Tissue (ST), which may be presented in a manner that reflects tissue flow in the region where tissue flow is detected. Although the illustrated example shows only one row of staples 6156, in other examples, multiple rows of staples may be shown.

In some implementations, the firing sequence is shown by analog overlay 6152 in dynamic display mode. Further, in some cases, staple formation may be predicted based on one or more determined parameters, such as, for example, tissue type, patient parameters, tissue flow, closing force, tissue creep stability, anvil gap, and the like. For example, the control module 6001 can employ predetermined formulas, databases, and/or tables to predict staple formation.

In the illustrated example, the display arrangement 6150 also includes a staple forming superimposed layer 6157. The control module 6001 can be configured to be able to predict staple formation and update the staple formation draping layer 6157 in real time, for example.

Fig. 31 is a flowchart illustrating an exemplary method 6160 for manipulating a display arrangement based on risk during a surgical procedure, in accordance with at least one aspect of the present disclosure. In some implementations, the method 6120 may be performed, for example, by the computer-implemented interactive surgical system 1. In some implementations, the method 6160 is performed by a surgical system including a surgical instrument 21 configured to suture and cut tissue in a surgical field of view of a surgical procedure. The surgical system further includes a control module 6001, an imaging device 6004 and a display 6005 configured to display a live stream of a surgical field of view. For example, live streams are captured by imaging device 6004.

In some implementations, the method 6160 includes detecting 6161 a surgical risk, assigning 6162 a severity to the surgical risk, and determining 6163 a display arrangement based on the severity, wherein displaying the arrangement includes superimposing a warning feature on the live stream. In some implementations, the method 6160 further includes presenting 6164 a visual representation of the surgical risk according to the display arrangement.

In some implementations, 6161 surgical risk is detected by the control module 6001. The surgical risk may be detected 6161 based on one surgical data received from one or more sources (such as, for example, components of the computer-implemented interactive surgical system 1) via one or more wireless and/or wired communication interfaces. In at least one example, the surgical data may include data received from one or more surgical instruments 21. In another example, the surgical data includes contextual information determined by situational awareness module 6006.

In certain examples, the surgical data includes control data, biomarker measurements, and/or other operational indications of the operation and/or results associated with the surgical instrument 21. In some examples, the surgical data may be any data indicative of a highly likely malformed nail and/or well-sealed tissue. In some cases, the surgical data may be associated with tissue flow, clamping force, firing force, and other tissue and/or instrument parameters that may be monitored and displayed to the clinician in real-time in a variety of ways to enable adjustment of the firing sequence or alert the surgeon that a malformed staple area may be present.

In some examples, the processor 85 employs a predetermined equation and/or formula in determining the severity of the surgical risk. Various relevant factors may be considered and may be assigned different weights when calculating severity. Additionally or alternatively, in assigning 6162 the severity level, the processor 85 may utilize one or more databases or tables listing surgical data and corresponding severity levels. In various implementations, the assigned severity level of 6162 includes, for example, a low severity level, a medium severity level, or a high severity level.

Fig. 32 illustrates a specific implementation of a display arrangement 6170 in accordance with at least one aspect of the present disclosure. In some implementations, the display arrangement 6170 is determined based on, for example, the severity of the surgical risk detected at 6161 in method 6160. In the illustrated example, the display arrangement 6170 includes superimposing a warning feature 6171 by the control module 6001 in response to 6161 detecting a surgical risk. During a surgical procedure, the warning feature 6171 is superimposed on the live stream of the surgical field 6179. In the illustrated example, the live stream of the surgical field 6179 shows the end effector 6172 of the surgical instrument 21 configured to manipulate the surgical structure 6178.

In the illustrated example, the warning feature 6171 is superimposed on the live stream in corner areas away from the end effector 6172 and/or away from any critical surgical structures so as not to obstruct the clinician's view of the surgical field. In other examples, the warning feature 6171 may be moved to or initially superimposed on a central region of the live stream, closer to the end effector 6172 and/or any critical surgical structures, for example, to represent a higher severity surgical risk.

In addition to the above, the display arrangement 6170 also includes a change in the alert feature 6171 responsive to the user's reaction. In the illustrated example, the change to the alert feature 6171 includes replacing the alert feature 6171 with information 6173 associated with the surgical risk. Information 6173 may include details regarding surgical risk and/or recommended solutions.

In the illustrated example, the user reaction is a transition of the end effector 6172 between the open configuration and the closed configuration. In other implementations, the user reaction may include any other suitable gesture or movement of the end effector 6172. In still other implementations, the user response may include, for example, a hand gesture or motion and/or an eye gesture or motion.

In other examples, the user response may be a composite user response or a multi-factor response to ensure that the user's incidental actions will not be interpreted by the control module 6001 as a user response for manipulating the alert feature 6171. In some implementations, the user response that can be recognized by the control module 6001 can include two components, such as, for example, an end effector gesture or motion, followed by the user's eye movement moving the user's hand movement.

In some implementations, as shown in fig. 33, a display arrangement 6170' that is similar in many respects to the display arrangement 6170 includes a different user response. In the illustrated example, the user reaction includes hovering the end effector 6172 over the alert feature 6171.

In some implementations, the user response is automatically detected, for example, by object recognition, object tracking, object marking, and/or other suitable image processing techniques of image frames of the live stream, or by various suitable wired and/or wireless communication schemes. Additionally or alternatively, the user response may be automatically detected by receiving information indicative of the user response via a suitable wired and/or wireless communication scheme. For example, the camera may monitor the user's body movements or body gestures, such as, for example, waving a hand, gazing, or blinking twice. In another example, a clinician's glove may be tracked via one or more suitable sensors positioned on the glove. Sensor readings indicative of a predetermined hand motion, indicative of a predetermined user reaction, may be communicated to the control module 6001.

In some implementations, the display arrangement 6170 includes changing the alert feature 6171 based on a change in severity of the surgical risk. The change may be implemented, for example, in a dynamic display mode. In some examples, the change to the alert feature 6171 includes changing at least one of a color, a size, a shape, a display time, a display location, a display frequency, a highlighting, or a combination thereof, according to a severity of the surgical risk. In some implementations, the alert feature 6171 is in the form of an alert icon that changes color, for example, based on the severity of the surgical risk.

In some implementations, as shown in fig. 34, a display arrangement 6170 "similar in many respects to the display arrangement 6170 positions the warning feature 6171 in a position that interferes with the clinician's view of the critical surgical structure 6178, for example, to represent a high severity surgical risk. Nonetheless, the display arrangement 6170 "allows the user to remove the warning feature 6171 from the critical surgical structure 6178 by hovering the end effector 6172 over the warning feature 6171. In response to detecting that the end effector 6172 and the warning feature 6171 occupy the same position, the control module 6001 causes the warning feature to move to a different position on the live stream, e.g., the surgical field 6179.

In other examples, a predetermined user reaction (such as, for example, closing and opening the jaws of the end effector 6172 once or twice) simulates the grasping alert feature 6171. Further, the end effector 6172 may be moved to a corner of the display 6005, for example, such that the captured warning feature 6171 moves therewith. A pause in the new location may indicate that the alert feature is discarded at the new location. Other suitable gestures and/or motions may be employed to represent a user reaction to move the warning feature 6171 away from the critical surgical structure 6178. In some implementations, the control module 6001 can automatically cause the alert feature 6171 to move away from the end effector 6172 and/or critical surgical structure 6178 after being determined to be less than or equal to, for example, the initial deployment of the end effector 6172 and/or critical surgical structure 6178, such as in a dynamic mode.

In various implementations, the pose and/or motion of the end effector 6172 may be automatically observed, for example, by other image processing techniques utilizing one or more suitable object recognition, object tracking, and/or object marking algorithms, and/or image frames of the live stream of the surgical field 6179. In various cases, the end effector 6172 is visually identified based on the characteristic reflectivity, color, and/or shape. Additionally or alternatively, the pose and/or movement of the end effector 6172 may be detected by sensor readings of sensors in the surgical instrument 21.

In some implementations, the change in the alert feature 6171 in response to the user reaction includes movement of the alert feature 6171 away from the end effector 6172 and/or critical surgical structure 6178. In some examples, the control module 6001 is configured to track the position of the end effector 6172 and/or critical surgical structure 6178 relative to the position of the warning feature 6171 on the display 6005, for example. Further, the control module 6001 is configured to automatically change the position of the warning feature 6171 based on at least one of the position of the end effector 6172 and the critical surgical structure 6178, for example, to facilitate clear viewing of the end effector 6172 and/or the critical surgical structure 6178.

In some implementations, the control module 6001 is configured, for example, to be able to correlate the alert feature 6171 with a risk source represented by the alert feature 6171. For example, the correlation provides an indication to the clinician of the nature of the risk without having to develop the warning feature 6171 to view details of the risk. The correlation may be achieved by a common display characteristic such as, for example, a common color highlighting and/or a common blink frequency. For example, where a risk is associated with a surgical instrument 21 that includes an end effector 6172 in the surgical field, both the warning feature 6171 and the end effector 6172 may be highlighted, for example, with a common color. Additionally or alternatively, the correlation may be achieved, for example, by having the surgical instrument 21 provide acoustic feedback and/or tactile feedback consistent with the presence of the alert feature 6171 on the display 6005. Additionally or alternatively, the correlation may be achieved by superimposing one or more color-coded bubbles and/or arrows that are separate from the warning feature 6171, directed to the end effector 6172, indicating that the risk represented by the warning feature 6171 is associated with the surgical instrument 21.

In some implementations, the display arrangement associated with a particular surgical instrument task or surgical step may be changed in response to detecting that the surgical instrument task or surgical step is complete. For example, a surgical procedure, such as a surgical sleeve procedure, involves a predetermined number of shots of the surgical instrument 21 configured to staple and cut tissue. Each firing in the firing sequence deploys staples from the staple cartridge into tissue. The staple cartridge is then replaced with a new staple cartridge for the next firing in the firing sequence. The control module 6001 can be configured to detect the number of firings of the surgical instrument 21 and continue to superimpose surgical data associated with firings of the surgical instrument 21 until a predetermined number of firings is reached. In response to detecting the completion of firing, the control module 6001 causes the superposition of surgical data associated with the firing of the surgical instrument 21 to be folded or removed from the display 6005.

In some implementations, detecting completion of a surgical instrument task or surgical step may be accomplished visually and automatically, such as by object recognition, object tracking, object marking, and/or other suitable image processing techniques of image frames of live streams, or by input from surgical instrument 21 and/or surgical hub 6, such as via various suitable wired and/or wireless communication schemes.

In various cases, one or more functions of the foregoing methods are performed by one or more components of the computer-implemented interactive surgical system 1 (such as, for example, one or more components of the surgical visualization system 6000). In some cases, components that perform one or more of the functions of the foregoing methods communicate via wireless and/or wired communication interfaces. In various cases, the memory (e.g., memory 6003) of the computer-implemented interactive surgical system 1 stores program instructions that, when executed by a processor (e.g., processor 85), cause the processor to implement one or more functions of the foregoing methods. Although the foregoing functions are described in a discrete method, in some implementations, some of the functions of the foregoing methods may be combined in any suitable manner to produce different methods for different program instructions that are executed by one or more components of, for example, the computer-implemented interactive surgical system 1.

In various cases, to perform tracking, an algorithm analyzes sequential video frames and outputs movement of a target between the frames in accordance with one or more aspects of the present disclosure. Exemplary algorithms include target representation and localization algorithms, and filtering and data correlation algorithms. The target representation and localization algorithms include kernel-based tracking and/or contour tracking, for example. Filtering and data correlation algorithms include, for example, kalman filtering and particle filtering.

Various additional aspects of the subject matter described herein are set forth in the following numbered embodiments:

embodiment 1. A surgical visualization system, the surgical visualization system comprising: an imaging device; a display configured to display a live stream of a surgical field of view of a surgical procedure, wherein the live stream is captured by the imaging device; and a control module configured to detect surgical data competing for presentation on the display, generate visual content based on the surgical data, and selectively superimpose the visual content onto a live stream of the surgical field of view based on the surgical data.

Embodiment 2. The surgical visualization system of embodiment 1, wherein the surgical data comprises a distance between a critical surgical structure and a surgical instrument in the surgical field.

Embodiment 3. The surgical visualization system of embodiments 1 or 2, wherein the surgical data includes detection of an assembly of components of a surgical instrument utilized in the surgical procedure.

Embodiment 4. The surgical visualization system of any of embodiments 1-3, wherein the surgical data comprises process speed data.

Embodiment 5. The surgical visualization system of any of embodiments 1-4, wherein the surgical data includes failure to detect receipt of a parameter associated with a setting of a surgical instrument utilized in the surgical procedure.

Embodiment 6. The surgical visualization system of any of embodiments 1-5, wherein selectively superimposing the visual content comprises a transition from a static display mode to a dynamic display mode.

Embodiment 7. The surgical visualization system of any of embodiments 1-6, wherein selectively superimposing the visual content includes selecting a color, a size, a shape, a display time, a display location, a display frequency, a highlighting, or a combination thereof for one or more display elements of the visual content.

Embodiment 8 the surgical visualization system of any of embodiments 1-7, further comprising a situational awareness module configured to generate context information based on perioperative data, wherein selectively superimposing the visual content is based on the context information.

Embodiment 9. The surgical visualization system of any of embodiments 1-8, wherein the surgical visualization system comprises a communication interface, and wherein detecting the surgical data comprises receiving the surgical data via the communication interface.

Embodiment 10. The surgical visualization system of any of embodiments 1-9, wherein the surgical visualization system comprises a processor, and wherein selectively superimposing the visual content comprises automatically superimposing, by the processor, the visual content onto the live stream of the surgical field of view.

Embodiment 11. The surgical visualization system of any of embodiments 1-10, wherein the surgical visualization system comprises a processor and a memory, and wherein generating the visual content based on the surgical data comprises automatically populating, by the processor, values associated with the surgical data into templates stored in the memory.

Embodiment 12. A surgical visualization system, the surgical visualization system comprising: a surgical device; an imaging device; a display configured to display a live stream of a surgical field of view of a surgical procedure, wherein the live stream is captured by the imaging device; and a control module configured to detect surgical device data, generate visual content based on the surgical device data, and selectively adjust the visual content on a live stream of the surgical field of view.

While various forms have been illustrated and described, it is not the intention of the applicant to restrict or limit the scope of the appended claims to such detail. Many modifications, variations, changes, substitutions, combinations, and equivalents of these forms may be made by one skilled in the art without departing from the scope of the disclosure. Furthermore, the structure of each element associated with the described form may alternatively be described as a means for providing the function performed by the element. In addition, where materials for certain components are disclosed, other materials may be used. It is, therefore, to be understood that the foregoing detailed description and the appended claims are intended to cover all such modifications, combinations, and variations as fall within the scope of the disclosed forms of the invention. The appended claims are intended to cover all such modifications, variations, changes, substitutions, modifications and equivalents.

The foregoing detailed description has set forth various forms of the apparatus and/or methods via the use of block diagrams, flowcharts, and/or examples. Insofar as such block diagrams, flowcharts, and/or examples contain one or more functions and/or operations, it will be understood by those within the art that 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 thereof. Those skilled in the art will recognize that some aspects of the forms disclosed herein may be equivalently implemented in integrated circuits, as one or more computer programs running on one or more computers (e.g., as one or more programs running on one or more computer systems), as one or more programs running on one or more processors (e.g., as one or more programs running on one or more microprocessors), as firmware, or as virtually any combination thereof, and that designing the circuitry and/or writing the code for the software and/or hardware would be well within the skill of one of skill in the art in light of this disclosure. In addition, those skilled in the art will appreciate that the mechanisms of the subject matter described herein are capable of being distributed as a program product or products in a variety of forms, and that an illustrative form of the subject matter described herein applies regardless of the particular type of signal bearing media used to actually carry out the distribution.

Instructions for programming logic to perform the various disclosed aspects can be stored within a memory in a system, such as Dynamic Random Access Memory (DRAM), cache, flash memory, or other memory. Furthermore, the instructions may be distributed via a network or by other computer readable media. Thus, a machine-readable medium may include any mechanism for storing or transmitting information in a form readable by a machine (e.g., a computer), but is not limited to floppy diskettes, optical disks, compact disk read-only memories (CD-ROMs), and magneto-optical disks, read-only memories (ROMs), random Access Memories (RAMs), erasable programmable read-only memories (EPROMs), electrically erasable programmable read-only memories (EEPROMs), magnetic or optical cards, flash memory, or a tangible, machine-readable storage device for use in transmitting information over the internet via electrical, optical, acoustic, or other form of propagated signals (e.g., carrier waves, infrared signals, digital signals, etc.). Thus, a non-transitory computer-readable medium includes any type of tangible machine-readable medium suitable for storing or transmitting electronic instructions or information in a form readable by a machine (e.g., a computer).

As used in any aspect herein, the term "control circuitry" may refer to, for example, hardwired circuitry, programmable circuitry (e.g., a computer processor including one or more individual instruction processing cores, processing units, processors, microcontrollers, microcontroller units, controllers, digital Signal Processors (DSPs), programmable Logic Devices (PLDs), programmable Logic Arrays (PLAs), field Programmable Gate Arrays (FPGAs)), state machine circuitry, firmware storing instructions executed by the programmable circuitry, and any combination thereof. The control circuitry may be implemented collectively or individually as circuitry forming part of a larger system, such as an Integrated Circuit (IC), an Application Specific Integrated Circuit (ASIC), a system-on-a-chip (SoC), a desktop computer, a laptop computer, a tablet computer, a server, a smart phone, or the like. Thus, as used herein, "control circuitry" includes, but is not limited to, electronic circuitry having at least one discrete circuit, electronic circuitry having at least one integrated circuit, electronic circuitry having at least one application specific integrated circuit, electronic circuitry forming a general purpose computing device configured by a computer program (e.g., a general purpose computer configured by a computer program that at least partially implements the methods and/or apparatus described herein, or a microprocessor configured by a computer program that at least partially implements the methods and/or apparatus described herein), electronic circuitry forming a memory device (e.g., forming a random access memory), and/or electronic circuitry forming a communication device (e.g., a modem, communication switch, or optoelectronic device). Those skilled in the art will recognize that the subject matter described herein may be implemented in analog or digital fashion, or some combination thereof.

As used in any aspect herein, the term "logic" may refer to an application, software, firmware, and/or circuitry configured to be capable of performing any of the foregoing operations. The software may be embodied as software packages, code, instructions, instruction sets, and/or data recorded on a non-transitory computer readable storage medium. The firmware may be embodied as code, instructions or a set of instructions and/or data that are hard-coded (e.g., non-volatile) in a memory device.

As used in any aspect herein, the terms "component," "system," "module," and the like can refer to a control circuit, a computer-related entity, hardware, a combination of hardware and software, or software in execution.

As used in any aspect herein, an "algorithm" refers to an organized sequence of steps leading to a desired result, wherein "step" refers to the manipulation of physical quantities and/or logical states, which may, but need not, take the form of electrical or magnetic signals capable of being stored, transferred, combined, compared, and otherwise manipulated. Are often used to refer to signals such as bits, values, elements, symbols, characters, terms, numbers, or the like. These and similar terms may be associated with the appropriate physical quantities and are merely convenient labels applied to these quantities and/or conditions.

The network may comprise a packet switched network. The communication devices may be capable of communicating with each other using the selected packet switched network communication protocol. One exemplary communication protocol may include an ethernet communication protocol that may be capable of allowing communication using transmission control protocol/internet protocol (TCP/IP). The ethernet protocol may conform to or be compatible with the ethernet Standard and/or a higher version of the Standard, titled "IEEE 802.3Standard" published by the Institute of Electrical and Electronics Engineers (IEEE) at month 12 of 2008. Alternatively or additionally, the communication devices may be capable of communicating with each other using an x.25 communication protocol. The x.25 communication protocol may conform to or be compatible with standards promulgated by the international telecommunications union telecommunication standardization sector (ITU-T). Alternatively or additionally, the communication devices may be capable of communicating with each other using a frame relay communication protocol. The frame relay communication protocol may conform to or be compatible with standards promulgated by the international telegraph and telephone Consultation Committee (CCITT) and/or the American National Standards Institute (ANSI). Alternatively or additionally, the transceivers may be capable of communicating with each other using an Asynchronous Transfer Mode (ATM) communication protocol. The ATM communication protocol may conform to or be compatible with the ATM standard promulgated by the ATM forum at month 8 of 2001 under the name "ATM-MPLS Network Interworking 2.0" and/or a higher version of the standard. Of course, different and/or later developed connection oriented network communication protocols are likewise contemplated herein.

Unless specifically stated otherwise as apparent from the above disclosure, it is appreciated that throughout the above disclosure, discussions utilizing terms such as "processing," "computing," "calculating," "determining," "displaying" or the like, refer to the action and processes of a computer system, or similar electronic computing device, that manipulates and transforms data represented as physical (electronic) quantities within the computer system's registers and memories into other data similarly represented as physical quantities within the computer system memories or registers or other such information storage, transmission or display devices.

One or more components may be referred to herein as "configured to be capable of", "configurable to be capable of", "operable/operable", "adapted/adaptable", "capable of", "conformable/conformable", and the like. Those skilled in the art will recognize that "configured to be capable of" may generally encompass active and/or inactive and/or standby components unless the context indicates otherwise.

The terms "proximal" and "distal" are used herein with respect to a clinician manipulating a handle portion of a surgical instrument. The term "proximal" refers to the portion closest to the clinician, and the term "distal" refers to the portion located away from the clinician. It will also be appreciated that for simplicity and clarity, spatial terms such as "vertical," "horizontal," "upper," and "lower" may be used herein with respect to the drawings. However, surgical instruments are used in many orientations and positions, and these terms are not intended to be limiting and/or absolute.

Those skilled in the art will recognize that, in general, terms used herein, and particularly in the appended claims (e.g., bodies of the appended claims) are generally intended to be "open" terms (e.g., the term "including" should be construed as "including but not limited to," the term "having" should be construed as "having at least," the term "comprising" should be construed as "including but not limited to," etc.). It will be further understood by those with skill in the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases "at least one" and "one or more" to introduce claim(s). However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles "a" or "an" limits any particular claim containing such introduced claim recitation to claims containing only one such recitation, even when the same claim includes the introductory phrases "one or more" or "at least one" and indefinite articles such as "a" or "an" (e.g., "a" and/or "an" should typically be interpreted to mean "at least one" or "one or more"); the same holds true for the use of definite articles used to introduce claim recitations.

In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should typically be interpreted to mean at least the recited number (e.g., the bare recitation of "two recitations," without other modifiers, typically means at least two recitations, or two or more recitations). Moreover, in those instances where a convention analogous to "at least one of A, B and C, etc." is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., "a system having at least one of A, B and C" would include but not be limited to systems having only a, only B, only C, A and B together, a and C together, B and C together, and/or A, B and C together, etc.). In those instances where a convention analogous to "A, B or at least one of C, etc." is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., "a system having at least one of A, B or C" shall include but not be limited to systems having only a, only B, only C, 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 within the art that, in general, unless the context indicates otherwise, disjunctive words and/or phrases presenting two or more alternative terms in the detailed description, claims, or drawings should be understood to encompass the possibility of including one of the terms, either of the terms, or both. For example, the phrase "a or B" will generally be understood to include the possibility of "a" or "B" or "a and B".

For the purposes of the appended claims, those skilled in the art will understand that the operations recited therein can generally be performed in any order. Additionally, while various operational flow diagrams are set forth in one or more sequences, it should be understood that various operations may be performed in other sequences than the illustrated sequences, or may be performed concurrently. Examples of such alternative ordering may include overlapping, staggered, interrupted, reordered, incremental, preparatory, supplemental, simultaneous, reverse, or other altered ordering unless the context dictates otherwise. Moreover, unless the context dictates otherwise, terms such as "responsive to," "related to," or other past-type adjectives are generally not intended to exclude such variants.

It is worth mentioning that any reference to "an aspect", "an example" means that a particular feature, structure or characteristic described in connection with the aspect is included in at least one aspect. Thus, the appearances of the phrases "in one aspect," "in an example," and "in an example" in various places throughout this specification are not necessarily all referring to the same aspect. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more aspects.

Any patent application, patent, non-patent publication, or other disclosure material referred to in this specification and/or listed in any application data sheet is incorporated herein by reference, as if the incorporated material was not inconsistent herewith. Accordingly, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.

In summary, many of the benefits resulting from employing the concepts described herein have been described. The foregoing detailed description of one or more forms has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed. Modifications or variations of the present invention are possible in light of the above teachings. One or more of the forms selected and described are chosen to illustrate principles and practical application to thereby enable one of ordinary skill in the art to utilize various forms and various modifications as are suited to the particular use contemplated. The claims filed herewith are intended to define the full scope.

Claims (20)

1. A surgical visualization system for use in a surgical procedure, the surgical visualization system comprising:

an imaging device;

a display configured to display a live stream of a surgical field of view of the surgical procedure, wherein the live stream is captured by the imaging device; and

a control module configured to enable:

detecting surgical data competing for presentation on the display;

generating visual content based on the surgical data; and

the visual content is selectively superimposed onto the live stream of the surgical field based on the surgical data.

2. The surgical visualization system of claim 1, wherein the surgical data includes a distance between critical surgical structures and surgical instruments in the surgical field of view.

3. The surgical visualization system of claim 1, wherein the surgical data includes detection of an assembly of components of a surgical instrument utilized in the surgical procedure.

4. The surgical visualization system of claim 1, wherein the surgical data includes a processing speed.

5. The surgical visualization system of claim 1, wherein the surgical data includes detecting failure to receive parameters associated with settings of a surgical instrument utilized in the surgical procedure.

6. The surgical visualization system of claim 1, wherein selectively superimposing the visual content includes a transition from a static display mode to a dynamic display mode.

7. The surgical visualization system of claim 1, wherein selectively superimposing the visual content includes selecting a color, a size, a shape, a display time, a display location, a display frequency, a highlighting, or a combination thereof for one or more display elements of the visual content.

8. The surgical visualization system of claim 1, further comprising a situational awareness module configured to generate context information based on perioperative data, wherein selectively superimposing the visual content is based on the context information.

9. The surgical visualization system of claim 1, wherein the surgical visualization system comprises a communication interface, and wherein detecting the surgical data comprises receiving the surgical data via the communication interface.

10. The surgical visualization system of claim 1, wherein the surgical visualization system comprises a processor, and wherein selectively superimposing the visual content comprises automatically superimposing, by the processor, the visual content onto the live stream of the surgical field of view.

11. The surgical visualization system of claim 1, wherein the surgical visualization system comprises a processor and a memory, and wherein generating the visual content based on the surgical data comprises automatically populating, by the processor, values associated with the surgical data into templates stored in the memory.

12. A surgical visualization system for use in a surgical procedure, the surgical visualization system comprising:

a surgical instrument;

an imaging device;

a display configured to display a live stream of a surgical field of view of the surgical procedure, wherein the live stream is captured by the imaging device; and

a control module configured to enable:

detecting surgical device data;

generating visual content based on the surgical device data; and

the visual content on the live stream of the surgical field is selectively adjusted.

13. The surgical visualization system of claim 12, wherein the surgical data includes a distance between critical surgical structures and surgical instruments in the surgical field.

14. The surgical visualization system of claim 12, wherein the surgical data includes detection of an assembly of components of a surgical instrument utilized in the surgical procedure.

15. The surgical visualization system of claim 12, wherein the surgical data includes a processing speed.

16. The surgical visualization system of claim 12, wherein the surgical data includes detecting failure to receive parameters associated with settings at the surgical instrument.

17. The surgical visualization system of claim 12, wherein selectively superimposing the visual content includes a transition from a static display mode to a dynamic display mode.

18. The surgical visualization system of claim 12, wherein selectively superimposing the visual content includes selecting a color, a size, a shape, a display time, a display location, a display frequency, a highlighting, or a combination thereof for one or more display elements of the visual content.

19. A surgical visualization system for use in a surgical procedure, the surgical visualization system comprising:

an imaging device;

a display configured to display a live stream of a surgical field of view of the surgical procedure, wherein the live stream is captured by the imaging device; and

a control module configured to enable:

Receiving surgical data;

presenting a visual representation of the surgical data on the display according to a static display mode;

detecting a change in the surgical data greater than or equal to a predetermined threshold; and

in response to detecting the change, transitioning to displaying the visual representation according to a dynamic display mode.

20. The surgical visualization system of claim 19, wherein the surgical data includes tissue parameters.