US2017188909A1PendingUtilityA1
Method and Apparatus for Providing Data Processing and Control in a Medical Communication System
Est. expiryMay 14, 2027(~0.8 yrs left)· nominal 20-yr term from priority
Inventors:Gary Alan HayterGeoffrey V. McgarraughAndrew H. NaegeliJohn Charles MazzaBenjamin J. Feldman
A61B 5/0004G01N 33/48A61B 5/14532A61B 5/1495G06F 19/3412A61B 5/1473G16Z 99/00A61B 5/7221G01D 18/008A61B 5/7275G16H 20/17G16H 40/40A61B 2560/0252A61B 2560/0223A61B 5/4839A61B 5/002G16H 15/00G16H 40/63
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Claims
Abstract
Methods and apparatus for providing data processing and control for use in a medical communication system are provided.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A method for calibrating sensor data generated by a continuous analyte sensor, comprising:
generating sensor data using a continuous analyte sensor; iteratively determining, with an electronic device, a sensitivity value of the continuous analyte sensor by applying a priori information comprising a sensitivity profile, wherein the sensitivity profile is a function of time, wherein the sensitivity profile comprises an initial sensitivity value associated with a correlation between a sensitivity determined from in vitro analyte concentration measurements and a sensitivity determined from in vivo analyte concentration measurements; and calibrating the sensor data based at least in part on the determined sensitivity value.
3 . The method of claim 2 , wherein the a priori information is associated with a calibration code.
4 . The method of claim 2 , wherein the a priori sensitivity information is stored in the sensor electronics prior to use of the sensor.
5 . The method of claim 2 , wherein calibrating the sensor data is performed iteratively throughout a substantially entire sensor session.
6 . The method of claim 2 , wherein iteratively determining a sensitivity value is performed at regular intervals or performed at irregular intervals, as determined by the a priori information.
7 . The method of claim 2 , wherein iteratively determining a sensitivity value is performed throughout a substantially entire sensor session.
8 . The method of claim 2 , wherein determining a sensitivity value is performed in substantially real time.
9 . The method of claim 2 , wherein the sensitivity value of the continuous analyte sensor is also a function of a second parameter that is not time.
10 . The method of claim 9 , wherein the third parameter is selected from the group consisting of: temperature or an analyte concentration of a fluid surrounding the continuous analyte sensor during startup of the sensor, and combinations thereof.
11 . The method of claim 2 , wherein calibrating the sensor data is performed without using reference blood glucose data.
12 . The method of claim 2 , further comprising receiving at least one calibration code, wherein the calibration code is associated with the sensitivity profile; and
applying the at least one calibration code to the electronic device at a predetermined time after start of the sensor session.
13 . The method of claim 2 , wherein the sensitivity profile is a function of a parameter associated with fabrication of the sensor.Join the waitlist — get patent alerts
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