Methods and devices for prediction of hypoglycemic events

• US 20050119540A1
• Filed: 11/05/2004
• Published: 06/02/2005
• Est. Priority Date: 08/18/2000
• Status: Abandoned Application

• Current Assignee: Animas Technologies LLC (Johnson & Johnson)
• Original Assignee: Cygnus, Inc. (Johnson & Johnson)
• Inventors: Potts, Russell O., Tierney, Michael J.
• Application Number:
  US10/982,148
• Publication Number:
  US 20050119540A1
• Time in Patent Office: Days
• US Class Current: 600/315
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/7267 involving training the classification device
• CPC Class Codes: G01N 27/3271 Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood amperometry per se G01N27/49; aspects concerning the enzyme reagent C12Q1/001

Abstract

Described herein are methods, devices, and microprocessors useful for predicting a hypoglycemic event in a subject. The hypoglycemic predictive approach described herein utilizes information obtained from a data stream, e.g., frequently obtained glucose values (current and/or predicted), body temperature, and/or skin conductance, to predict incipient hypoglycemic events and to alert the user.

Claims

1. A method for predicting a hypoglycemic event in a subject, said method comprising,

determining (i) a threshold glucose value that corresponds to said hypoglycemic event, and (ii) a threshold skin conductance and/or temperature value that is correlated with said hypoglycemic event,

obtaining a series of glucose measurement values at selected time intervals using a method comprising

obtaining a raw signal specifically related to a glucose amount or concentration in the subject for a given time interval,

correlating the raw signal with a glucose measurement value indicative of the amount or concentration of glucose present in the subject in said given time interval,

repeating said obtaining and correlating to provide a series of glucose measurement values at selected time intervals,

predicting a glucose measurement value at a further time interval subsequent to said series of glucose measurement values, and

comparing said predicted glucose measurement value to said threshold glucose value, when the predicted glucose measurement value is less than or equal to the threshold glucose value a hypoglycemic is predicted;

measuring skin conductance and/or temperature of the subject concurrently simultaneously, or sequentially with said obtaining of the series of glucose measurement values to obtain a skin conductance and/or temperature value or trend of skin conductance and/or temperature values, and comparing said skin conductance and/or temperature value or trend of skin conductance and/or temperature values with said threshold skin conductance and/or temperature value to determine whether said skin conductance and/or temperature value or trend of skin conductance and/or temperature values indicates a hypoglycemic event;

predicting a hypoglycemic event in said subject when both (i) comparing the predicted glucose measurement value to said threshold glucose value indicates a hypoglycemic event at said further time interval and (ii) comparing said skin conductance and/or temperature value or trend of skin conductance and/or temperature values with said threshold skin conductance and/or temperature value indicates a hypoglycemic event and

providing an alert to the subject when a hypoglycemic event is predicted.

2. The method of claim 1, wherein the selected time intervals are evenly spaced.

3. The method of claim 1, wherein the series of lucose measurement values comprises three or more discrete glucose measurement values.

4. The method of claim 3, wherein the further time interval occurs one time interval after the series of glucose measurement values.

5. The method of claim 1, wherein the values or trend of values for both skin conductance readings and temperature are used to predict the likelihood of a hypoglycemic event.

6. The method of claim 3, wherein said predicting of the glucose measurement value at a further time interval is carried out using said series of three or more glucose measurement values in a series function represented by:

7. The method of claim 6, wherein the series function is used to predict the value of y_n+1 wherein time interval n+1 occurs one time interval after the series of glucose measurement values is obtained.

10. The method of claim 1, wherein sample comprising glucose is extracted from the subject into one or more collection reservoirs to obtain an amount or concentration of glucose in a reservoir.

11. The method of claim 10, wherein the one or more collection reservoirs are in contact with the skin or mucosal surface of the subject and the sample is extracted using an iontophoretic current applied to said skin or mucosal surface.

12. The method of claim 10, wherein at least one collection reservoir comprises an enzyme that reacts with the extracted glucose to produce an electrochemically detectable signal to provide said raw signal.

14. The method of claim 1, wherein said obtaining of the series of glucose measurement values is performed using a near-IR spectrometer.

8-9. -9. (canceled)

13. The method of claim 4412 wherein said enzyme is glucose oxidase.

15. A glucose monitoring system for measuring glucose in a subject, said system comprising, in operative combination:

a sensing mechanism in operative contact with the subject or with a glucose-containing sample extracted from the subject, wherein said sensing mechanism obtains a raw signal specifically related to glucose amount or concentration in the subject;

a first device to obtain skin conductance readings or temperature readings from the subject, and

one or more microprocessors in operative communication with the sensing mechanism, wherein said microprocessors comprise programming to

(i) control the sensing mechanism to obtain a series of raw signals at selected time intervals,

(ii) correlate the raw signals with measurement values indicative of the amount or concentration of glucose present in the subject to obtain a series of glucose measurement values,

(iii) predict a glucose measurement value at a further time interval, subsequent to obtaining the series of glucose measurement values,

(iv) compare said predicted glucose measurement value to a threshold glucose value, wherein a predicted glucose measurement value less than or equal to the threshold glucose value is designated to be hypoglycemic,

(v) control the first device to measure skin conductance readings or temperature readings of the subject,

(vi) compare said skin conductance readings or temperature readings with a threshold skin conductance or temperature value or trend of skin conductance or temperature values to determine whether said skin conductance readings or temperature readings indicate a hypoglycemic event,

(vii) predict a hypoglycemic event in said subject when both (a) comparing said predicted glucose measurement value to said threshold glucose value indicates a hypoglycemic event at said further time intervals, and (b) comparing said skin conductance readings or temperature readings with a threshold skin conductance or temperature value or trend of skin conductance or temperature values indicates a hypoglycemic event; and

(viii) control providing an alert to the subject when a hypoglycemic event is predicted.

16. The monitoring system of claim 15, wherein the sensing mechanism comprises a biosensor having an electrochemical sensing element.

17. The monitoring system of claim 15, wherein the sensing mechanism comprises a near-IR spectrometer.

18. The monitoring system of claim 15, wherein said first device to obtain said skin conductance readings is a sweat probe.

19. The monitoring system of claim 15, wherein said first device to obtain said temperature readings is a temperature probe.

20. The monitoring system of claim 15, wherein the selected time intervals are evenly spaced.

21. The monitoring system of claim 15, wherein the series of lucose measurement values obtained comprises three or more discrete glucose measurement values.

22. The monitoring system of claim 21, wherein the further time interval occurs one time interval after the series of glucose measurement values.

24. The monitoring system of claim 21, wherein said predicting of glucose measurement value at a further time interval is carried out using said series of three or more glucose measurement values in a series function represented by:

25. The monitoring system of claim 24, wherein the series function is used to predict the value of y_n+1 wherein time interval n+1 occurs one time interval after the series of glucose measurement values is obtained.

35. The monitoring system of claim 15, further comprising a second device and wherein said first device comprises a sweat probe to obtain said skin conductance readings and said second device comprises a temperature probe to obtain said temperature readings.

23. The monitoring system of claim, wherein both skin conductance readings and temperature readings are used to predict the likelihood of a hypoglycemic event.

26. One or more microprocessors, comprising programming to:

(i) control a sensing mechanism to obtain a series of raw signals at selected time intervals, wherein each raw signal is related to an amount or concentration of glucose in a subjects

(ii) correlate the raw signals with glucose measurement values indicative of the amount or concentration of glucose present in the subject to obtain a series of glucose measurement values-,

(iii) predict a glucose measurement value at a further time interval, subsequent to obtaining the series of glucose measurement values;

(iv) compare said predicted glucose measurement value to a threshold lucose value, wherein a predicted lucose measurement value less than or equal to the threshold glucose value is designated to be hypoglycemic;

(v) control a first device to measure skin conductance readings or temperature readings of the subject;

(vi) compare said skin conductance readings or temperature readings with a threshold skin conductance or temperature value or trend of skin conductance or temperature values to determine whether said skin conductance readings or temperature readings indicate a hypoglycemic event; and

(vii) predict a hypoglycemic event in said subject when both (a) comparing said predicted glucose measurement value to said threshold glucose value indicates a hypoglycemic event at said further time interval, and (b) comparing said skin conductance readings or temperature readings with a threshold skin conductance or temperature value or trend of skin conductance or temperature values indicates a hypoglycemic event

(viii) control providing an alert to the subject when a hypoglycemic event is predicted.

27. The one or more microprocessors of claim 26, wherein the sensing mechanism comprises a biosensor having an electrochemical sensing element.

28. The one or more microprocessors of claim 26, wherein the sensing mechanism comprises a near-IR spectrometer.

29. The one or more microprocessors of claim 26, wherein the selected time intervals are evenly spaced.

30. The one or more microprocessors of claim 26, wherein the series of glucose measurement values obtained comprises three or more discrete glucose measurement values.

31. The one or more microprocessors of claim 26, wherein the further time interval occurs one time interval after the series of glucose measurement values.

32. The one or more microprocessors of claim 36, wherein both skin conductance readings and temperature readings are used to predict the likelihood of a hypoglycemic event.

33. The one or more microprocessors of claim 30, wherein the predicting the glucose measurement value at a further time interval is carried out using said series of three or more glucose measurement values in a series function represented by:

34. The one or more microprocessors of claim 33, wherein the series function is used to predict the value of y_n+1 wherein time interval n+1 occurs one time interval after the series of glucose measurement values is obtained.

36. The one or more microprocessors of claim 26, further comprising programming to control a second device, wherein said first device provides skin conductance readings and said second device provides temperature readings.