US20060224141A1 - Method and system for providing integrated medication infusion and analyte monitoring system - Google Patents

Method and system for providing integrated medication infusion and analyte monitoring system Download PDF

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Publication number
US20060224141A1
US20060224141A1 US11/386,915 US38691506A US2006224141A1 US 20060224141 A1 US20060224141 A1 US 20060224141A1 US 38691506 A US38691506 A US 38691506A US 2006224141 A1 US2006224141 A1 US 2006224141A1
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Prior art keywords
analyte
infusion
fluid
infusion device
unit
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US11/386,915
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English (en)
Inventor
Benjamin Rush
Christopher Reggiardo
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Abbott Diabetes Care Inc
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Abbott Diabetes Care Inc
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Priority to US11/386,915 priority Critical patent/US20060224141A1/en
Publication of US20060224141A1 publication Critical patent/US20060224141A1/en
Assigned to ABBOTT DIABETES CARE, INC. reassignment ABBOTT DIABETES CARE, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: REGGIARDO, CHRISTOPHER V, RUSH, BENJAMIN M.
Priority to US12/625,518 priority patent/US8343092B2/en
Priority to US12/643,970 priority patent/US8029459B2/en
Priority to US12/643,971 priority patent/US8029460B2/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14546—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring analytes not otherwise provided for, e.g. ions, cytochromes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/48—Other medical applications
    • A61B5/4836—Diagnosis combined with treatment in closed-loop systems or methods
    • A61B5/4839—Diagnosis combined with treatment in closed-loop systems or methods combined with drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A61B5/6848—Needles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
    • A61K9/0009—Galenical forms characterised by the drug release technique; Application systems commanded by energy involving or responsive to electricity, magnetism or acoustic waves; Galenical aspects of sonophoresis, iontophoresis, electroporation or electroosmosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142—Pressure infusion, e.g. using pumps
    • A61M5/14244—Pressure infusion, e.g. using pumps adapted to be carried by the patient, e.g. portable on the body
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/172—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic
    • A61M5/1723—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic using feedback of body parameters, e.g. blood-sugar, pressure
    • A61M2005/1726—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic using feedback of body parameters, e.g. blood-sugar, pressure the body parameters being measured at, or proximate to, the infusion site
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/35—Communication
    • A61M2205/3546—Range
    • A61M2205/3561—Range local, e.g. within room or hospital
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/35—Communication
    • A61M2205/3546—Range
    • A61M2205/3569—Range sublocal, e.g. between console and disposable
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/35—Communication
    • A61M2205/3576—Communication with non implanted data transmission devices, e.g. using external transmitter or receiver
    • A61M2205/3592—Communication with non implanted data transmission devices, e.g. using external transmitter or receiver using telemetric means, e.g. radio or optical transmission

Definitions

  • the present invention relates to methods and systems for integrating infusion systems and analyte monitoring systems. More specifically, the present invention relates to methods and systems for integrating insulin infusion devices with continuous analyte monitoring systems.
  • Type 1 diabetics must periodically be administered with insulin to sustain their physiological conditions. Typically, these patients administer doses of either fast acting or slow acting insulin using needle type syringes, for example, prior to meals, and/or at a suitable time during the course of each day contemporaneously with the blood glucose level testing using fingerstick testing, for example. If insulin is not suitably administered, the diabetic patients risk serious if not fatal damage to the body.
  • the patient inserts a cannula which is connected to as infusion tubing attached to an external pump, and insulin is administered based on a preprogrammed basal profiles.
  • the external infusion devices include computational capability to determined suitable bolus doses such as carbohydrate bolus and correction bolus, for example, to be administered in conjunction with the infusion device executing the patient's basal profile.
  • the basal profiles are generally determined by the patients' physician or caretaker and are based on a number of factors including the patient's insulin sensitivity and physiological condition which are diagnosed by the patient's physician, for example, and are typically intended to as accurately estimate the patient's glucose levels over a predetermined time period during which the patient is infusing insulin.
  • the glucose levels may be estimated based on the patient's periodic discrete testing using a test strip and a blood glucose meter such as Freestyle® Glucose Meter available from Abbott Diabetes Care, Inc., of Alameda, Calif. Such estimations are, however, prone to error, and do not accurately mirror the patient's actual physiological condition.
  • an integrated system combining the functionalities of an infusion device such as insulin infusion pumps, and analyte monitoring systems such as continuous glucose monitoring systems.
  • FIG. 1 illustrates an integrated infusion device and analyte monitoring system in accordance with one embodiment of the present invention
  • FIG. 2 illustrates an integrated infusion device and analyte monitoring system in accordance with another embodiment of the present invention
  • FIG. 3 illustrates an integrated infusion device and analyte monitoring system in accordance with yet another embodiment of the present invention
  • FIG. 4 illustrates an integrated infusion device and analyte monitoring system in accordance with still another embodiment of the present invention
  • FIG. 5 illustrates an integrated infusion device and analyte monitoring system in accordance with still a further embodiment of the present invention
  • FIG. 6 illustrates an integrated infusion device and monitoring system in accordance with yet still a further embodiment embodiment of the present invention
  • FIG. 7A illustrates the integrated infusion device and monitoring system shown in FIGS. 6 in further detail in one embodiment of the present invention
  • FIGS. 7A-7B illustrate the analog front end circuitry located at the patient interface and the pump assembly, respectively, of the integrated infusion device and monitoring system shown in FIG. 7A in accordance with one embodiment of the present invention
  • FIGS. 8A-8C illustrate a passive sensor configuration for use in a continuous analyte monitoring system, and two embodiments of an active sensor configuration for use at the patient interface in the integrated infusion device and monitoring system, respectively, in accordance with one embodiment of the present invention
  • FIG. 9 illustrates an integrated infusion device and analyte monitoring system with the infusion device and the monitoring system transmitter integrated into a single patch worn by the patient in accordance with one embodiment of the present invention
  • FIG. 10 is a detailed view of the infusion device cannula integrated with analyte monitoring system sensor electrodes in accordance with one embodiment of the present invention.
  • FIG. 11A illustrates a component perspective view of the infusion device cannula integrated with analyte monitoring system sensor electrodes in accordance with another embodiment of the present invention
  • FIG. 11B illustrates a top planar view of the analyte monitoring system transmitter unit integrated with infusion device in accordance with one embodiment of the present invention
  • FIG. 12A-12C each illustrate a cross sectional view of the infusion device cannula integrated with continuous analyte monitoring system sensor electrodes of FIG. 10 in accordance with the various embodiments respectively, of the present invention.
  • FIG. 13 is a timing chart for illustrating the temporal spacing of blood glucose measurement and insulin delivery by the integrated infusion device and monitoring system in one embodiment.
  • FIG. 1 illustrates an integrated infusion device and analyte monitoring system in accordance with one embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 100 in one embodiment of the present invention includes an infusion device 110 connected to an infusion tubing 130 for liquid transport or infusion, and which is further coupled to a cannula 170 .
  • the cannula 170 is configured to be mountably coupled to a transmitter unit 150 , where the transmitter unit 150 is also mountably coupled to an analyte sensor 160 .
  • an analyte monitor unit 120 which is configured to wirelessly communicate with the transmitter unit over a communication path 140 .
  • the transmitter unit 150 is configured for unidirectional wireless communication over the communication path 140 to the analyte monitor unit 120 .
  • the analyte monitor unit 120 may be configured to include a transceiver unit (not shown) for bidirectional communication over the communication path 140 .
  • the transmitter unit 150 in one embodiment may be configured to periodically and/or intermittently transmit signals associated with analyte levels detected by the analyte sensor 160 to the analyte monitor unit 120 .
  • the analyte monitor unit 120 may be configured to receive the signals from the transmitter unit 150 and in one embodiment, is configured to perform data storage and processing based on one or more preprogrammed or predetermined processes.
  • the analyte monitor unit 120 is configured to store the received signals associated with analyte levels in a data storage unit (not shown).
  • the analyte monitor unit 120 may be configured to process the signals associated with the analyte levels to generate trend indication by, for example, visual display of a line chart or an angular icon based display for output display on its display unit 121 . Additional information may be output displayed on the display unit 121 of the analyte monitor unit 120 including, but not limited to, the substantially contemporaneous and real time analyte level of the patient received from the transmitter unit 150 as detected by the sensor 160 .
  • the real time analyte level may be displayed in a numeric format or in any other suitable format which provides the patient with the accurate measurement of the substantially real time analyte level detected by the sensor 160 .
  • Additional analytes that may be monitored or determined by the sensor 160 include, for example, acetyl choline, amylase, bilirubin, cholesterol, chorionic gonadotropin, creatine kinase (e.g., CK-MB), creatine, DNA, fructosamine, glucose, glutamine, growth hormones, hormones, ketones, lactate, peroxide, prostate-specific antigen, prothrombin, RNA, thyroid stimulating hormone, and troponin.
  • concentration of drugs such as, for example, antibiotics (e.g., gentamicin, vancomycin, and the like), digitoxin, digoxin, drugs of abuse, theophylline, and warfarin, may also be determined.
  • the sensor 160 may include a short term (for example, 3 day, 5 day or 7 day use) analyte sensor which is replaced after its intended useful life.
  • the sensor 160 is configured to be positioned subcutaneous to the skin of the patient such that at least a portion of the analyte sensor is maintained in fluid contact with the patient's analyte such as, for example, interstitial fluid or blood.
  • the cannula 170 which is configured to similarly be positioned under the patient's skin is connected to the infusion tubing 130 of the infusion device 110 so as to deliver medication such as insulin to the patient.
  • the cannula 170 is configured to be replaced with the replacement of the sensor 160 .
  • the cannula 170 and the sensor 160 may be configured to be subcutaneously positioned under the skin of the patient using an insertion mechanism (not shown) such as an insertion gun which may include, for example, a spring biased or loaded insertion mechanism to substantially accurately position the cannula 170 and the sensor 160 under the patient's skin.
  • an insertion mechanism such as an insertion gun which may include, for example, a spring biased or loaded insertion mechanism to substantially accurately position the cannula 170 and the sensor 160 under the patient's skin.
  • the cannula 170 and the sensor 160 maybe subcutaneously positioned with substantially little or no perceived pain by the patient.
  • the cannula 170 and/or the sensor 160 may be configured to be manually inserted by the patient through the patient's skin.
  • an adhesive layer 180 which is configured to adhere to the skin of the patient for the duration of the time period during which the sensor 160 and the cannula 170 are subcutaneously positioned.
  • the transmitter unit 150 may be mounted after the subcutaneous positioning of the sensor 160 and the cannula 150 so as to be in electrical contact with the sensor electrodes.
  • the infusion tubing 130 may be configured to operatively couple to the housing of the transmitter unit 150 so as to be in accurately positioned for alignment with the cannula 170 and to provide a substantially water tight seal. Additional detailed description of the analyte monitoring system including the sensor 160 , transmitter unit 150 and the analyte monitor unit 120 is provided in U.S. Pat. No. 6,175,752, assigned to the assignee of the present invention, Abbott Diabetes Care, Inc.
  • the infusion device 110 may include capabilities to program basal profiles, calculation of bolus doses including, but not limited to correction bolus, carbohydrate bolus, extended bolus, and dual bolus, which maybe performed by the patient using the infusion device 110 , and maybe based on one or more factors including the patient's insulin sensitivity, insulin on board, intended carbohydrate intake (for example, for the carbohydrate bolus calculation prior to a meal), the patient's measured or detected glucose level, and the patient's glucose trend information.
  • the bolus calculation capabilities may also be provided in the analyte monitor unit 120 .
  • the analyte monitor unit 120 is configured with a substantially compact housing that can be easily carried by the patient.
  • the infusion device 110 similarly may be configured as a substantially compact device which can be easily and conveniently worn on the patient's clothing (for example, housed in a holster or a carrying device worn or clipped to the patient's belt or other parts of the clothing).
  • the analyte monitor unit 120 and/or the infusion device 110 may include a user interface such as information input mechanism by the patient as well as data output including, for example, the display unit 121 on the analyte monitor unit 120 , or similarly a display unit 111 on the infusion device 110 .
  • One or more audio output devices such as, for example, speakers or buzzers may be integrated with the housing of the infusion device 110 and/or the analyte monitor unit 120 so as to output audible alerts or alarms based on the occurrence of one or more predetermined conditions associated with the infusion device 110 or the analyte monitor unit 120 .
  • the infusion device 110 may be configured to output an audible alarm or alert to the patient upon detection of an occlusion in the infusion tubing 130 or the occurrence of a timed event such as a reminder to prime the infusion tubing upon replacement of the cannula 170 , and the like.
  • the analyte monitor unit 120 may be similarly be configured to output an audible alarm or alert when a predetermined condition or a pre-programmed event occurs, such as, for example, a reminder to replace the sensor 160 after its useful life (of 3 days, 5 days or 7 days), or one or more alerts associated with the data received from the transmitter unit 150 corresponding to the patient's monitored analyte levels.
  • alerts or alarms may include a warning alert to the patient that the detected analyte level is beyond a predetermined threshold level, or the trend of the detected analyte levels within a given time period is indicative of a significant condition such as potential hyperglycemia or hypoglycemia, which require attention or corrective action.
  • audible alarms and/or alerts are described above for illustrative purposes only, that within the scope of the present invention, other events or conditions may be programmed into the infusion device 110 or the analyte monitor unit 120 or both, so as to alert or notify the patient of the occurrence or the potential occurrence of such events or conditions.
  • audible alarms may be output alone, or in combination with one or more of a visual alert such as an output display on the display unit 111 , 121 of the infusion device 110 or the analyte monitor unit 120 , respectively, or vibratory alert which would provide a tactile indication to the patient of the associated alarm and/or alert.
  • a visual alert such as an output display on the display unit 111 , 121 of the infusion device 110 or the analyte monitor unit 120 , respectively, or vibratory alert which would provide a tactile indication to the patient of the associated alarm and/or alert.
  • analyte monitor unit 120 and one transmitter unit 150 are shown, within the scope of the present invention, additional analyte monitor units or transmitter units may be provided such that, for example, the transmitter unit 150 may be configured to transmit to multiple analyte monitor units substantially simultaneously.
  • multiple transmitter units coupled to multiple sensors concurrently in fluid contact with the patient's analyte may be configured to transmit to the analyte monitor unit 120 , or to multiple analyte monitor units.
  • an additional transmitter unit coupled to an additional sensor may be provided in the integrated infusion device and analyte monitoring system 100 which does not include the cannula 170 , and which may be used to perform functions associated with the sensor 160 such as sensor calibration, sensor data verification, and the like.
  • the transmitter unit 150 is configured to transmit the sampled data signals received from the sensor 160 without acknowledgement from the analyte monitor unit 120 that the transmitted sampled data signals have been received.
  • the transmitter unit 150 may be configured to transmit the encoded sampled data signals at a fixed rate (e.g., at one minute intervals) after the completion of the initial power on procedure.
  • the analyte monitor unit 120 may be configured to detect such transmitted encoded sampled data signals at predetermined time intervals.
  • the transmitter unit 150 and the analyte monitor unit 120 may be configured for bi-directional communication over the communication path 140 .
  • the analyte monitor unit 120 may include two sections.
  • the first section of the analyte monitor unit 120 may include an analog interface section that is configured to communicate with the transmitter unit 150 via the communication path 140 .
  • the analog interface section may include an RF receiver and an antenna for receiving and amplifying the data signals from the transmitter unit 150 , which are thereafter, demodulated with a local oscillator and filtered through a band-pass filter.
  • the second section of the analyte monitor unit 120 may include a data processing section which is configured to process the data signals received from the transmitter unit 150 such as by performing data decoding, error detection and correction, data clock generation, and data bit recovery, for example.
  • the analyte monitor unit 120 is configured to detect the presence of the transmitter unit 150 within its range based on, for example, the strength of the detected data signals received from the transmitter unit 150 or a predetermined transmitter identification information. Upon successful synchronization with the transmitter unit 150 , the analyte monitor unit 120 is configured to begin receiving from the transmitter unit 150 data signals corresponding to the patient's detected analyte, for example glucose, levels.
  • the analyte monitor unit 120 or the infusion device 110 may be configured to further communicate with a data processing terminal (not shown) which may include a desktop computer terminal, a data communication enabled kiosk, a laptop computer, a handheld computing device such as a personal digital assistant (PDAs), or a data communication enabled mobile telephone, and the like, each of which may be configured for data communication via a wired or a wireless connection.
  • a data processing terminal for example may include physician's terminal and/or a bedside terminal in a hospital environment, for example.
  • the communication path 140 for data communication between the transmitter unit 150 and the analyte monitor unit 120 of FIG. 1 may include an RF communication link, Bluetooth communication link, infrared communication link, or any other type of suitable wireless communication connection between two or more electronic devices.
  • the data communication link may also include a wired cable connection such as, for example, but not limited to an RS232 connection, USB connection, or serial cable connection.
  • the analyte monitor unit 120 or the infusion device 110 may also include a test strip port configured to receive a blood glucose test strip for discrete sampling of the patient's blood for glucose level determination.
  • a test strip port configured to receive a blood glucose test strip for discrete sampling of the patient's blood for glucose level determination.
  • An example of the functionality of blood glucose test strip meter unit may be found in Freestyle® Blood Glucose Meter available from the assignee of the present invention, Abbott Diabetes Care, Inc.
  • the cannula 170 for infusing insulin or other suitable medication is integrated with the adhesive patch 180 for the sensor 160 and the transmitter unit 150 of the analyte monitoring system. Accordingly, only one on-skin patch can be worn by the patient (for example, on the skin of the abdomen) rather than two separate patches for the infusion device cannula 170 , and the analyte monitoring system sensor 160 (with the transmitter unit 150 ).
  • the Type-1 diabetic patient may conveniently implement infusion therapy in conjunction with real time glucose monitoring while minimizing potential skin irritation on the adhesive patch 180 site on the patient's skin, and thus provide more insertion sites with less irritation.
  • the integrated infusion device and analyte monitoring system 100 as shown in FIG. 1 maybe configured such that the infusion tubing 130 may be disconnected from the infusion device 110 as well as from the housing of the transmitter 150 (or the adhesive patch 180 ) such that, optionally, the patient may configure the system as continuous analyte monitoring system while disabling the infusion device 110 functionality.
  • the patient may better manage the physiological conditions associated with diabetes by having substantially continuous real time-glucose data, trend information based on the substantially continuous real time glucose data, and accordingly, modify or adjust the infusion levels delivered by the infusion device 110 from the pre-programmed basal profiles that the infusion device 110 is configured to implement.
  • FIG. 2 illustrates an integrated infusion device and analyte monitoring system in accordance with another embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 200 in one embodiment of the present invention includes an integrated infusion device and analyte monitor unit 210 which is coupled to an infusion tubing 220 connected to the cannula 260 .
  • a transmitter unit 240 which is in electrical contact with an analyte sensor 250 , where the cannula 260 and the analyte sensor 250 are subcutaneously positioned under the skin of the patient, and retained in position by an adhesive layer or patch 270 .
  • the integrated infusion device and analyte monitor unit 210 is configured to wirelessly communicate with the transmitter unit 240 over a communication path 230 such as an RF communication link.
  • a communication path 230 such as an RF communication link.
  • the transmitter unit 240 may be configured to transmit signals corresponding to the detected analyte levels received from the analyte sensor 250 to the integrated infusion device and analyte monitor unit 210 for data analysis and processing.
  • the patient may conveniently receive real time glucose levels from the transmitter unit 240 and accordingly, determine whether to modify the existing basal profile(s) in accordance with which insulin is delivered to the patient.
  • the functionalities of the analyte monitor unit may be integrated within the compact housing of the infusion device to provide additional convenience to the patient by, for example, by providing the real time glucose data as well as other relevant information such as glucose trend data to the user interface of the infusion device, so that the patient may readily and easily determine any suitable modification to the infusion rate of the insulin pump.
  • each component shown in FIG. 2 including the cannula 260 , the analyte sensor 250 , the transmitter unit 240 , the adhesive layer 270 , the communication path 230 , as well as the infusion tubing 220 and the functionalities of the infusion device and the analyte monitor are substantially similar to the corresponding respective component as described above in conjunction with FIG. 1 .
  • the additional convenience may be provided to the patient in maintaining and enhancing diabetes management by, for example, having a single integrated device such as the integrated infusion device and analyte monitor unit 210 which would allow the patient to easily manipulate and manage insulin therapy using a single user interface system of the integrated infusion device and analyte monitor unit 210 .
  • the patient may be provided with the additional convenience in managing diabetes and improving insulin therapy.
  • FIG. 3 illustrates an integrated infusion device and analyte monitoring system in accordance with yet another embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 300 in one embodiment of the present invention includes an infusion device 310 connected to an infusion tubing 340 coupled to a cannula 370 .
  • the cannula 380 is configured to be positioned subcutaneously under the patient's skin and substantially retained in position by and adhesive layer 380 .
  • an analyte sensor 360 also positioned subcutaneously under the patient's skin and maintained in fluid contact with the patient's analyte.
  • a transmitter unit 350 is provided so as to be electrically coupled to the analyte sensor 360 electrodes. Also, as can be seen from FIG. 3 , in one embodiment, the infusion tubing 340 is connected to the housing of the transmitter unit 350 so as to connect to the cannula 370 disposed under the patient's skin.
  • an analyte monitor unit 320 configured to wirelessly communicate with the transmitter unit 350 to receive data therefrom associated with the analyte levels of the patient detected by the analyte sensor 360 .
  • the infusion device 310 does not include a user interface such as a display unit and/or an input unit such as buttons or a jog dial.
  • the user interface and control mechanism is provided on the analyte monitoring unit 320 such that the analyte monitoring unit 320 is configured to wirelessly control the operation of the infusion device 310 and further, to suitably program the infusion device 310 to execute pre-programmed basal profile(s), and to otherwise control the functionality of the infusion device 310 .
  • all of the programming and control mechanism for the infusion device 310 is provided in the analyte monitoring unit 320 such that when the patient is wearing the infusion device 310 , it may be worn discreetly under clothing near the infusion site on the patient's skin (such as abdomen), while still providing convenient access to the patient for controlling the infusion device 310 through the analyte monitoring unit 320 .
  • each component shown in FIG. 3 including the cannula 380 , the analyte sensor 360 , the transmitter unit 350 , the adhesive layer 380 , the communication path 320 , as well as the infusion tubing 340 and the functionalities of the infusion device and the analyte monitoring unit 320 are substantially similar to the corresponding respective component as described above in conjunction with FIG. 1 .
  • the infusion device 310 in the embodiment shown in FIG. 3 is configured with a transceiver or an equivalent communication mechanism to communicate with the analyte monitoring unit 320 .
  • configuration of the infusion device 310 without a user interface provides a smaller and lighter housing and configuration for the infusion device 310 which would enhance the comfort in wearing and/or carrying the infusion device 310 with the patient.
  • the control and programming functions of the infusion device 310 is provided on the analyte monitoring unit 320 , the patient may conveniently program and/or control the functions and operations of the infusion device 310 without being tethered to the infusion tubing 340 attached to the cannula 370 which is positioned under the patient's skin.
  • the programming and control of the infusion device 310 is remotely performed on the analyte monitoring unit 320 , the infusion tubing 304 may be shorter and thus less cumbersome.
  • FIG. 4 illustrates an integrated infusion device and analyte monitoring system in accordance with still another embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 400 in one embodiment of the present invention includes an infusion device 410 configured to wirelessly communicate with an analyte monitoring unit 420 over a communication path 430 such as an RF (radio frequency) link.
  • the infusion device 410 is connected to an infusion tubing 440 which has provided therein integral wires connected to the analyte sensor electrodes.
  • the measured analyte levels of the patient is received by the infusion device 410 via the infusion tubing 440 and transmitted to the analyte monitoring unit 420 for further processing and analysis.
  • the integrated infusion device and analyte monitoring system 400 includes a patch 450 provided with a cannula 470 and an analyte sensor 460 .
  • the cannula 470 is configured to deliver or infuse medication such as insulin from the infusion device 410 to the patient. That is, in one embodiment, the cannula 470 and the analyte sensor 460 are configured to be positioned subcutaneous to the patient's skin.
  • the analyte sensor 460 is configured to be positioned to be in fluid contact with the patient's analyte.
  • the analyte sensor 460 is electrically coupled to integral wires provided within the infusion tubing 440 so as to provide signals corresponding to the measured or detected analyte levels of the patient to the infusion device 410 .
  • the infusion device 410 is configured to perform data analysis and storage, such that the infusion device 410 may be configured to display the real time measured glucose levels to the patient on it display unit 411 .
  • the infusion device 410 is configured to wirelessly transmit the received signals from the analyte sensor 460 to the analyte monitoring unit 420 for data analysis, display, and/or storage and the analyte monitoring unit 420 may be configured to remotely control the functions and features of the infusion device 410 providing additional user convenience and discreteness.
  • the patch 450 may be configured to be substantially small without a transmitter unit mounted thereon, and provided with a relatively small surface area to be attached to the patient's skin.
  • the patient may be provided with added comfort in having a substantially compact housing mounted on the skin (attached with an adhesive layer, for example), to infuse medication such as insulin, and for continuous analyte monitoring with the analyte sensor 460 .
  • FIG. 5 illustrates an integrated infusion device and analyte monitoring system in accordance with still a further embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 500 of FIG. 5 includes an integrated infusion device and analyte monitoring unit 510 .
  • one user interface is provided to the user including the display unit 511 and input buttons 512 provided on the housing of the integrated infusion device and analyte monitoring unit 510 .
  • an adhesive patch 530 is provided to retain the subcutaneous position of a cannula 550 and the analyte sensor 540 in the desired positions under the patient's skin.
  • the integrated infusion device and analyte monitoring unit 510 may be provided with wireless or wired communication capability so to communicate with a remote terminal such as a physician's computer terminal over a wireless communication path such as RF communication link, or over a cable connection such as a USB connection, for example.
  • a remote terminal such as a physician's computer terminal
  • a wireless communication path such as RF communication link
  • a cable connection such as a USB connection
  • FIG. 6 illustrates an integrated infusion device and monitoring system in accordance with yet still a further embodiment embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 600 is provided with an infusion device without a user interface, and configured to wirelessly communicate with an analyte monitoring unit 620 over a communication path 630 such as an RF link.
  • the infusion device 610 which may be provided in a compact housing since it does not incorporate the components associated with a user interface, is connected to an infusion tubing 640 having disposed therein integral wires correspondingly connected to the electrodes of analyte sensor 660 in fluid contact with the patient's analyte.
  • the compact adhesive patch 650 in one embodiment is configured to retain cannula 670 and the analyte sensor 660 in the desired position under the skin of the patient.
  • the analyte monitoring unit 620 is configured to control and program the infusion device 610 over the communication link 630 . In this manner, the control and programming functions of the infusion device 610 may be remotely performed by the analyte monitoring unit 620 , providing convenience to the patient.
  • FIG. 7A illustrates the integrated infusion device and monitoring system shown in FIGS. 6 in further detail in one embodiment of the present invention
  • FIGS. 7A-7B illustrate the analog front end circuitry located at the patient interface and the pump assembly, respectively, of the integrated infusion device and monitoring system shown in FIG. 7A in accordance with one embodiment of the present invention.
  • an infusion device 710 connected to an infusion tubing 720 with integral wires provided therein for connection to the electrodes of the analyse sensor is shown.
  • the infusion tubing 720 is further connected to an adhesive patch 730 which is configured to retain cannula 750 and analyte sensor 740 in the desired subcutaneous position under the skin of the patient.
  • the infusion device 710 may be provided with a first analog front end circuitry unit 711
  • the adhesive patch may be provided with a second analog front end circuitry unit 731
  • the integral wires from the analyte sensor 740 is configured to extend from the infusion device 710 to the adhesive layer 730 via the infusion tubing 720 . Since the analyte sensor 740 in one embodiment is a passive component, the signals on the working electrode and the reference electrodes of the analyte sensors are subject to noise given the high impendence of the electrodes and the length of the integral wires (in excess of a few centimeters). The noise in turn may potentially adversely affect the signals on the working and reference electrodes which may distort the measured analyte levels detected by the analyte sensor 740 .
  • the signals from the working and reference electrodes may be converted to low impedance signals to minimize adverse impact from the noise.
  • the infusion device 710 may be provided with a first analog front end circuitry unit 711
  • the adhesive patch 730 may be provided with a second analog front end circuitry unit 731 as discussed in further detail below in conjunction with FIGS. 7B and 7C .
  • the second analog front end circuitry unit 731 disposed on the adhesive patch 730 on the patient's skin in one embodiment includes an a trans-impedance amplifier (current to voltage converter or “I-to-V”) 73 1 A configured to convert the working electrode (W) current to a voltage (Vw), and to provide a guard signal (G), and a servo segment 731 B to drive the counter electrode (C) voltage (Vc) based on the reference electrode (R) voltage. Also shown in FIG.
  • LPF Low-Pass Filter
  • ⁇ C microcontroller
  • the second analog front end circuitry unit 731 may be implemented by a pair of operational amplifiers ( 731 A and 731 B), four resistors (R 1 , R 2 , R 3 , Rf), and a bypass capacitor (Cb).
  • the I-to-F stage using operational amplifier 731 A is generated by the action of the input current from the working electrode (W) flowing through the feedback resistor (Rf) and creating a voltage differential that is driven by the operational amplifier 731 A as the low impedance signal Vw.
  • the offset for the Vw signal is established by the resistor divider comprised of R 1 , R 2 and R 3 which also creates the voltage of the guard signal (G)—a signal that is at the same potential or voltage as the working electrode (W).
  • the servo drives the counter electrode (C) voltage to the sensor so that the reference electrode (R) is at the second value set by the resistor divider comprised of resistors R 1 , R 2 and R 3 .
  • This maintains the working electrode (W) voltage above the reference electrode (R) by a set amount known as the “Poise Voltage” (i.e 40 mV).
  • the bypass capacitor (Cb) may be a small, low equivalent series resistance (ESR) capacitor, such as a 0.1 uF (100 nF) multi-layer ceramic (MLC) capacitor, that acts to provide local energy and reduce noise on the circuit.
  • ESR equivalent series resistance
  • the voltage source for this circuit may be provided by the potential difference between V+ and V ⁇ where, for example, V+ may be 5V and V ⁇ may be ground (GND) or V+ may be +3V and V ⁇ may be ⁇ 3V.
  • the operational amplifiers 731 A, 731 B may be acquired as a dual operational amplifier integrated circuit (IC) in a single, small 8-pin, surface mount technology (SMT) package such as the OPA2349 in a SOT23-8 package (3 mm by 3 mm). Similar dual operational amplifier products maybe available in even smaller ball-grid array (BGA) packages and as bare die that may be mounted directly to the circuit substrate, such as a printed circuit board (PCB) or flex circuit, using techniques such as “flip-chip” and wire-bond.
  • IC integrated circuit
  • SMT surface mount technology
  • Similar dual operational amplifier products maybe available in even smaller ball-grid array (BGA) packages and as bare die that may be mounted directly to the circuit substrate, such as a printed circuit board (PCB) or flex circuit, using techniques such as “flip-chip” and wire-bond.
  • PCB printed circuit board
  • flex circuit using techniques such as “flip-chip” and wire-bond.
  • FIGS. 8A-8C illustrate a passive sensor configuration for use in a continuous analyte monitoring system, and two embodiments of an active sensor configuration for use at the patient interface in the integrated infusion device and monitoring system, respectively, in accordance with one embodiment of the present invention.
  • analyte sensor 810 includes working electrode 811 , a guard trace 812 , a reference electrode 813 , and a counter electrode 814 .
  • the “tail” segment 815 of the analyte sensor 810 is configured to be positioned subcutaneously under the patient's skin so as to be in fluid contact with the patient.
  • analyte sensor 820 is provided with the analog front end portion 821 where the four contacts shown are V+, V ⁇ , Vw, and Vc signals in accordance with one embodiment in place of the working electrode 811 , a guard trace 812 , a reference electrode 813 , and a counter electrode 814 , respectively.
  • these signals of the active analyte sensor 820 are low impedance and thus less subject to noise than the passive sensor signals.
  • the analyte sensor 820 configuration may include a flex circuit.
  • an active sensor of similar construction to the active sensor 820 of FIG. 11B but with much smaller dimensions is shown. More specifically, analyte sensor 830 is provided with four contacts configured for direct wire bonding rather than a mechanical contact system as indicated by the large contact areas on the previous two sensor configurations shown in FIGS. 8A-8B . Since the shape of the analyte sensor 830 is reduced, the sensor 830 may be wrapped around the cannula (for example, cannula 470 of FIG. 4 ) and thus only a single entry site may be required for the patient analyte monitoring and insulin infusion. Moreover, within the scope of the present invention, additional sensor/cannula configurations may be provided where the sensor circuitry and cannula are created as a single assembly such as a cannula with the circuit 831 fabricated on the surface.
  • FIG. 9 illustrates an integrated infusion device and analyte monitoring system with the infusion device and the monitoring system transmitter integrated into a single patch worn by the patient in accordance with one embodiment of the present invention.
  • the integrated infusion device and analyte monitoring system 900 includes an integrated patch pump and transmitter unit 910 provided on an adhesive layer 960 , and which is configured to be placed on the skin of the patient, so as to securely position cannula 950 and analyte sensor 940 subcutaneously under the skin of the patient.
  • the housing of the integrated infusion pump and transmitter unit 910 is configured in one embodiment to include the infusion mechanism to deliver medication such as insulin to the patient via the cannula 950 .
  • the integrated patch pump and transmitter unit 910 is configured transmit signals associated with the detected analyte levels measured by the analyte sensor 940 , over a wireless communication path 930 such as an RF link.
  • the signals are transmitted from the on body integrated patch pump and transmitter unit 910 to a controller unit 920 which is configured to control the operation of the integrated patch pump and transmitter unit 910 , as well as to receive the transmitted signals from the integrated patch pump and transmitter unit 910 which correspond to the detected analyte levels of the patient.
  • the infusion mechanism of the integrated patch pump and transmitter unit 910 may includes the infusion device of the type described in U.S. Pat. No. 6,916,159 assigned to the assignee of the present invention Abbott Diabetes Care, Inc.
  • the wireless communication path 930 may be replaced by a set of wires to provide a wired connection to the controller unit 920 .
  • the integrated infusion device and analyte monitoring system 900 does not use an infusion tubing which may provide additional comfort and convenience to the patient by providing additional freedom from having to wear a cumbersome tubing.
  • FIG. 10 is a detailed view of the infusion device cannula integrated with analyte monitoring system sensor electrodes in accordance with one embodiment of the present invention.
  • infusion device cannula with analyte sensor electrodes 1020 disposed therein, and mounted to an adhesive patch 1010 so as to retain its position securely in the patient.
  • the cannula with analyte sensor electrodes 1020 include sensor electrodes 1021 , 1022 , 1023 (which may correspond to working, reference and counter electrodes, respectively) each of which are provided within the cannula tip 1020 , and further, positioned so as to maintain fluid contact with the patient's analyte.
  • FIG. 12A-12C each illustrate a cross sectional view of the infusion device cannula integrated with continuous analyte monitoring system sensor electrodes of FIG. 10 in accordance with the various embodiments respectively, of the present invention.
  • the wire and tubing are provided in parallel such that the tubing wall 1020 , the tube bore for insulin flow 1024 , the wire outer casing 1020 and the individual insulated wires 1021 , 1022 , 1023 are substantially provided as shown in FIG. 12A .
  • each of the three insulated wires are provided with an insulation layer 1020 of tubing wall individually surrounding each insulated wires 1021 , 1022 , 1023 , and further, where the three insulated wires 1021 , 1022 , 1023 are in turn surrounded by the tubing wall 1020 .
  • the insulated wires 1021 , 1022 , 1023 respectively connected to the sensor electrodes are co-extruded into tubing wall 1020 , with the tube bore 1024 for insulin delivery and the insulated wires 1021 , 1022 , 1023 configured substantially as shown in the FIG. 12B .
  • FIG. 12B Referring now to FIG. 12B in one embodiment of the present invention, the insulated wires 1021 , 1022 , 1023 respectively connected to the sensor electrodes are co-extruded into tubing wall 1020 , with the tube bore 1024 for insulin delivery and the insulated wires 1021 , 1022 , 1023 configured substantially as shown in the FIG. 12B .
  • each of the insulated wires 1021 , 1022 , 1023 are wrapped around the tubing 1020 and covered with a sheath 1210 , thus providing the tubing wall 1020 , the tubing bore 1024 for insulin delivery, the individual insulated wires 1021 , 1022 , 1023 , and the outer protective sheath 1210 , which may also serve as an electromagnetic shield to eliminate electronic noise as substantially shown in the Figure.
  • the embodiments shown in FIGS. 12A and 12C may have larger cross-sectional area (thus a larger hole needed to be punctured on the skin of the patient), but are likely easier to manufacture, more reliable and easier to make connection to the analyte sensor electronics).
  • an optical data transmission i.e. fiber optics
  • insulin delivery tubing between sensor and pump may be provided instead of integral wires as discussed above.
  • FIG. 11A illustrates a component perspective view of the infusion device cannula integrated with analyte monitoring system sensor electrodes in accordance with another embodiment of the present invention
  • FIG. 11B illustrates a top planar view of the analyte monitoring system transmitter unit integrated with infusion device in accordance with one embodiment of the present invention
  • integrated analyte sensor and infusion device cannula 1100 comprises five laminated layers including a top insulation layer 1101 , a conductive layer 1102 with electrode traces disposed thereon, followed by three layer substrate with integrated infusion cannula 1103 .
  • the three layer substrate with integrated infusion cannula 1103 includes a separation/insulation layer 1103 A to insulate the sensor electrodes from the infusion cannula, a channel layer 1103 B configured to guide the flow of the insulin or any other suitable medication, and an inlet/outlet layer 1103 C. Also shown in FIG. 11A is an assembled view of the integrated analyte sensor and infusion device cannula 1100 .
  • a patch pump as shown in one embodiment is provided with a transmitter unit 1110 and an insulin pump 1130 coupled to insulin reservoir 1120 , and operatively coupled or mounted to the transmitter unit 1110 .
  • the analyte sensor contacts 1140 which are configured to establish electrical contact with the respective electrodes of the integrated infusion cannula and analyte sensor 1100 .
  • insulin port 1150 which is connected to the channel layer 1103 B of the integrated infusion device cannula and analyte sensor 1100 .
  • the patch pump may be worn by the patient on skin and which includes the insulin infusion mechanism as well as the analyte sensor and transmitter unit.
  • FIG. 13 is a timing chart for illustrating the temporal spacing of blood glucose measurement and insulin delivery by the integrated infusion device and monitoring system in one embodiment. More specifically, insulin pumps typically deliver insulin in a periodic manner with the period of delivery in the range of 2 to 3 minutes and the duration of delivery at each period being on the order of a few seconds or less. The amount of insulin that is delivered each period may be varied depending on the overall insulin delivery rate that is desired.
  • the analyte data is collected continuously (as, for example, a continuous current of glucose oxidation) but is typically reported to the user periodically.
  • the analyte reporting period is typically 1 to 10 minutes and glucose oxidation current needs to be collected for 10 to 30 seconds in order to generate a reportable glucose value (to allow for filtering etc.).
  • analyte monitoring and insulin delivery may necessitate placement of a analyte sensor in close proximity to an insulin infusion cannula on the body.
  • Such close proximity engenders the possibility of insulin delivery interfering with the analyte measurements.
  • glucose measurement in this area would not be representative of the glucose concentration in the body as a whole. Accordingly, in one embodiment of the present invention, there is provided a method for temporal spacing of blood glucose measurements and insulin delivery to mitigate the possible interference between insulin infusion and glucose measurements.
  • the temporal spacing of analyte measurement and insulin delivery may include providing as large a temporal gap from after insulin delivery and before taking a analyte measurement. Since both analyte measurement and insulin delivery are performed periodically, a maximum spacing in time may be achieved if analyte measurement substantially immediately precedes insulin delivery. During the time between insulin delivery and the subsequent glucose measurement, infused insulin has time to diffuse and be transported away from the infusion site due to normal circulation of interstitial fluid. An example timeline of temporally spaced analyte measurement and insulin delivery is shown in FIG. 13 . If multiple analyte measurements are taken between insulin delivery points, there should always be a reading just prior to insulin delivery and as well just after insulin delivery to minimize the affect of injected insulin on the glucose measurement readings.
  • readings are typically taken periodically for simplicity in processing, a reading may be taken out of time with other readings and scaled appropriately for the overall reading average. Similarly, the insulin delivery point may be delayed slightly until after the reading with little or no affect as the readings typically occur much more frequently than the infusions, which are intended to act over longer periods of time.
  • other timing considerations may be considered depending on the environment in which the integrated infusion device and analyte monitoring system is used by the patient, within the scope of the present invention to minimize potential error on measured analyte levels and/or introduce noise or potential adverse effects to the infusion rates of the infusion device.
  • fluctuation in the power supplies of the infusion device and/or the analyte monitoring system including, for example, batteries or related power distribution circuitry may introduce electrical noise effects which may adversely affect the measured readings associated with the analyte monitoring system.
  • the analyte monitoring system when configured to be in an active state so as to be transmitting or receiving data, or when the pump cycle of the infusion device is active, the power supply may be affected by the load from the data transmission/reception, or the pumping cycle.
  • the adverse effect of the power supply in addition to noise from other components of the electronic circuitry may introduce undesirable noise and adversely affect the accuracy of the analyte sensor measurements.
  • the transmitter unit 150 may be configured to monitor the timing or occurrence of the measured analyte level received from the analyte sensor 160 and the data transmission timing of the transmitter unit 150 such that the two events do not substantially overlap or occur at the substantially the same time.
  • the analyte monitor unit 120 may be configured to compare the timing of the analyte sensor 160 measurement and the timing of the data transmission from the transmitter unit 150 , and to discard data analyte related data received from the transmitter unit 150 which coincide with the timing of the analyte measurements by the analyte sensor 160 .
  • air bubble detection in the insulin tubing may be provided, by monitoring fluid motion that would also detect the absence of fluid such as that due to an air bubble in the line.
  • the flow sensor may be configured to generate zero current when an air bubble was present.
  • colorization of insulin may be provided for air bubble detection in the tubing. Since pharmaceutical insulin is a clear colorless liquid, it is difficult to visually discriminate between insulin and air in tubing that carries insulin from the insulin pump to the cannula. By providing a color tint to the insulin it would be much easier to visually identify air bubbles in the tubing and be able to remove them before they cause problems.
  • An insulin tint in one embodiment is biocompatible and insulin compatible.
  • a system including an infusion device and an analyte monitoring unit in one embodiment of the present invention includes an infusion device, an on-body unit including a data transmission section, the on-body unit further coupled to the infusion device, the on-body unit configured to receive one or more signals corresponding to a respective one or more analyte levels, and further, the on-body unit configured to infuse a fluid received from the infusion device, and a receiver unit operatively coupled to the on-body unit, the receiver unit configured to receive data from the on-body unit, wherein the received data is associated with the analyte level.
  • the system may further include an analyte sensor at least a first portion of which is in fluid contact with an analyte of a patient, and further, where at a second portion of the analyte sensor is in signal communication with the data transmission section.
  • the data transmission section may in one embodiment be configured to transmit the one or more signals corresponding to a respective one or more analyte levels substantially periodically at one or more predetermined time intervals, where the one or more predetermined time intervals may include one or more of 30 seconds, one minute, or 90 seconds.
  • the on-body unit may include a cannula at least a portion of which is subcutaneously positioned under a skin layer, and further, may also include an infusion tubing connected to the infusion device to deliver the fluid to the on-body unit.
  • the infusion tubing and the on-body unit in a further aspect may be connected in a substantially water tight seal.
  • the infusion tubing may be configured to operatively couple to the cannula to deliver the fluid.
  • the on-body unit may be configured to wirelessly transmit the one or more signals corresponding to the respective one or more analyte levels to the receiver unit, where the on-body unit and the receiver maybe configured to wirelessly communicate over one or more of an RF communication link, a Bluetooth communication link, or an infrared communication link.
  • the infusion device in a further embodiment may be configured to control the delivery rate of the fluid based on the one or more signals corresponding to the respective one or more analyte levels received by the receiver unit, and further, where the infusion device may be configured to determine a modified delivery protocol for delivering fluid such as insulin based on information associated with the one or more signals corresponding to the respective one or more analyte levels.
  • the modified delivery protocol may include one or more of a correction bolus, a modified basal profile, a carbohydrate bolus, an extended bolus, or combinations thereof.
  • the receiver unit in one embodiment may be configured to wirelessly communicate with the infusion device.
  • the receiver unit maybe integrated into a housing of the infusion device.
  • a method of integrating analyte monitoring and fluid infusion in another embodiment of the present invention includes infusing a fluid at a predetermined delivery rate, detecting one or more analyte levels, transmitting one or more signals associated with the respective detected one or more analyte levels, and determining a modified delivery rate based on the transmitted one or more signals.
  • the one or more signals maybe transmitted substantially immediately after the associated respective one or more analyte levels are detected.
  • the transmitting step in one embodiment may include wirelessly transmitting the one or more signals which wirelessly transmitted over one or more of an RF communication link, a Bluetooth communication link, an infrared communication link, or combinations thereof
  • the method in a further aspect may also include the steps of receiving the transmitted one or more signals, and displaying the received one or more signals.
  • the method may also include the step of displaying the modified delivery rate.
  • the method may also include the step of implementing the modified delivery rate, where the predetermined delivery rate may include one or more basal delivery rates.
  • the modified delivery rate in a further embodiment may include one or more of a correction bolus, a modified basal profile, a carbohydrate bolus, an extended bolus, or combinations thereof.
  • An apparatus including an analyte sensor and a fluid delivery channel in yet another embodiment of the present invention includes a fluid delivery unit having an inner wall and an outer wall, and a plurality of electrodes disposed between the inner wall and the outer wall of the fluid delivery unit, where a portion of the of the fluid delivery unit and a portion of the plurality of electrodes are subcutaneously positioned under a skin layer.
  • the plurality of electrodes may comprise an analyte sensor, including, for example, one or more of a working electrode, a counter electrode, a reference electrode, or combinations thereof
  • the fluid delivery unit may include a channel for delivering a fluid such as insulin, the channel substantially formed by the inner wall.
  • An apparatus including an analyte sensor and a fluid delivery channel in accordance with still another embodiment of the present invention includes a first tubing having a first tubing channel, and a second tubing having a second tubing channel including a plurality of electrodes disposed within the second tubing channel, where at least a portion of the first tubing and at least a portion of the second tubing are subcutaneously positioned under a skin layer.
  • the plurality of the electrodes may be substantially and entirely insulated from each other.
  • first tubing and the second tubing may be integrally formed such that an outer surface of the first tubing is substantially in contact with an outer surface of the second tubing.
  • a system including an infusion device and an analyte monitoring unit in accordance with still another embodiment of the present invention includes an infusion and monitoring device, an on-body unit including a data transmission section, the on-body unit further coupled to the infusion and monitoring device, the on-body unit configured to receive one or more signals corresponding to a respective one or more analyte levels, and further, the on-body unit configured to infuse a fluid received from the infusion and monitoring device, and a connector coupled at a first end to the infusion device, and further, coupled at a second end to the on-body unit, the connector configured to channel the fluid from the infusion device to the on-body unit, and further, configured to provide the one or more signals corresponding to the respective one or more analyte levels to the infusion and monitoring device.
  • the infusion and monitoring device may be configured to execute fluid delivery to a patient, and further, to detect analyte levels of the patient over a predetermined time period.
  • the infusion and monitoring device may include a continuous glucose monitoring system.
  • the infusion and monitoring device may include an insulin pump.
  • a method of fluid delivery and analyte monitoring in accordance with still another embodiment of the present invention includes determining a delivery profile for fluid infusion, wherein the delivery profile including a plurality of predetermined discrete fluid infusion each temporally separated by a predetermined time period, and sampling an analyte level substantially immediately prior to each predetermined discrete fluid infusion.
  • the method may further include the step of sampling an analyte level substantially immediately after each predetermined discrete fluid infusion.

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US12/643,970 US8029459B2 (en) 2005-03-21 2009-12-21 Method and system for providing integrated medication infusion and analyte monitoring system
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JP2008535548A (ja) 2008-09-04
US20100100077A1 (en) 2010-04-22
US20100100076A1 (en) 2010-04-22
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AU2006226988A1 (en) 2006-09-28
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US20100076412A1 (en) 2010-03-25
US8029460B2 (en) 2011-10-04
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US8029459B2 (en) 2011-10-04
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US8343092B2 (en) 2013-01-01

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