US2018325437A1PendingUtilityA1
Analyte sensor
Est. expiryAug 1, 2023(expired)· nominal 20-yr term from priority
C12Q 1/001A61B 5/14735A61B 5/6849A61B 5/412A61B 5/1486G16H 40/40C12Q 1/006A61B 5/150992A61M 5/14A61B 5/14532G16H 20/17A61B 5/14535G16H 10/40A61B 5/14542A61B 5/1495A61B 5/4839A61M 2230/201A61M 2005/14296A61B 5/157A61M 5/1723A61B 5/743A61B 2562/085A61B 5/14546A61B 5/155A61B 2560/0223A61B 5/14865A61M 5/16804A61B 5/0031A61B 5/15003A61B 2560/04A61B 5/7275A61B 5/14539A61B 5/6848Y02A90/26G16H 40/63Y02A90/10
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Claims
Abstract
Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes a vascular access device, a sensor and sensor electronics, the system being configured for insertion into communication with a host's circulatory system.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for evaluating a change in a sensitivity of an implanted analyte sensor over a predetermined time period, comprising:
receiving sensor data from an analyte sensor implanted in a host, wherein the implanted sensor is configured to generate sensor data, wherein the sensor data comprises one or more sensor analyte values measured in a biological sample of a host; intermittently calculating a sensitivity of the analyte sensor; and evaluating, using an electronic device, a change in sensitivity by evaluating a plurality of time-spaced sensitivity calculations over a predetermined time period, wherein evaluating a change in sensitivity is based at least in part on using a priori sensitivity information throughout a sensor session, wherein the plurality of time spaced sensitivity calculations are not based on a blood-glucose measurement.
2 . The method of claim 1 , wherein the predetermined time period is less than or equal to about 30 minutes.
3 . The method of claim 1 , wherein the predetermined time period is less than or equal to about 20 minutes.
4 . The method of claim 1 , wherein the predetermined time period is less than or equal to about 10 minutes.
5 . The method of claim 1 , wherein evaluating a change in sensitivity comprises evaluating at least two sensitivity measurements during the predetermined time period.
6 . The method of claim 5 , further comprising averaging and/or filtering the at least two sensitivity measurements prior to evaluating the at least two sensitivity measurements.
7 . The method of claim 1 , wherein evaluating a change in sensitivity comprises comparing the change in sensitivity with one or more criteria.
8 . The method of claim 7 , further comprising using a most recent sensitivity calculation evaluated to calibrate the analyte sensor when the change in sensitivity meets one or more criteria.
9 . The method of claim 7 , further comprising not using a most recent sensitivity calculation evaluated to calibrate the analyte sensor when the change in sensitivity does not meet one or more criteria.
10 . The method of claim 1 , wherein evaluating a change in sensitivity is iteratively performed on the plurality of time-spaced sensitivity calculations over the predetermined time period.
11 . The method of claim 1 , wherein the predetermined time period is at least about 30 minutes.
12 . The method of claim 1 , wherein the predetermined time period is at least about 60 minutes.
13 . The method of claim 1 , wherein the predetermined time period is at least about 120 minutes.
14 . The method of claim 1 , wherein evaluating a change in sensitivity is iteratively performed on the plurality of time-spaced sensitivity calculations over the predetermined time period.
15 . The method of claim 1 , wherein evaluating a change in sensitivity comprises evaluating all sensitivity calculations over a sensor session.
16 . The method of claim 1 , wherein the a priori sensitivity information defines a range of acceptable change in sensitivity.
17 . A method for evaluating a change in a sensitivity of an implanted analyte sensor over a predetermined time period, comprising:
receiving sensor data from an analyte sensor implanted in a host, wherein the implanted sensor is configured to generate sensor data, wherein the sensor data comprises one or more sensor analyte values measured in a biological sample of a host; intermittently, using an electronic device, calculating a sensitivity of the analyte sensor; measuring a change in sensitivity by evaluating a parameter indicative of a change in solute transport of a membrane of the analyte sensor; and auto-calibrating the analyte sensor responsive to measurement of the change in sensitivity.
18 . A method for evaluating a change in a sensitivity of an analyte sensor over a predetermined time period, the method comprising:
receiving sensor data from an analyte sensor, wherein the sensor data comprises one or more sensor analyte values measured in a biological sample of a host; intermittently calculating a sensitivity of the analyte; filtering at least two sensitivity values, whereby filtered sensitivity values are obtained; and evaluating, using an electronic device, a change in sensitivity by evaluating the filtered sensitivity values over a predetermined time period, wherein evaluating a change in sensitivity is based at least in part on using a priori sensitivity information throughout a sensor session.Join the waitlist — get patent alerts
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