DATA ANALYTICS AND GENERATION OF RECOMMENDATIONS FOR CONTROLLING GLYCEMIC OUTCOMES ASSOCIATED WITH TRACKED EVENTS

• US 20170049383A1
• Filed: 08/18/2016
• Published: 02/23/2017
• Est. Priority Date: 08/21/2015
• Status: Active Grant

• Current Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Inventors: McMahon, Chantal M., Agrawal, Pratik, Zhong, Yuxiang, Jiang, Boyi, Neemuchwala, Huzefa F., Rushi, Amit J.
• Granted Patent: US 10,664,569 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61B 5/0022 Monitoring a patient using a global network, e.g. telephone networks, internet
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14542 for measuring blood gases A61B5/14551 takes precedence
• CPC Class Codes: A61B 5/4848 Monitoring or testing the effects of treatment, e.g. of medication
• CPC Class Codes: A61B 5/486 Bio-feedback A61B5/375 takes precedence
• CPC Class Codes: A61B 5/7275 Determining trends in physiological measurement data; Predicting development of a medical condition based on physiological measurements, e.g. determining a risk factor
• CPC Class Codes: A61B 5/7282 Event detection, e.g. detecting unique waveforms indicative of a medical condition A61B5/4094, A61B5/4818, A61B5/349, A61B5/0823 take precedence
• CPC Class Codes: A61B 5/7405 using sound
• CPC Class Codes: A61B 5/742 using visual displays A61B5/339 takes precedence
• CPC Class Codes: A61B 5/743 Displaying an image simultaneously with additional graphical information, e.g. symbols, charts, function plots
• CPC Class Codes: A61B 5/746 Alarms related to a physiological condition, e.g. details of setting alarm thresholds or avoiding false alarms alarms per se G08B
• CPC Class Codes: A61M 2005/1402 Priming
• CPC Class Codes: A61M 2205/18 with alarm
• CPC Class Codes: A61M 2205/3584 using modem, internet or bluetooth
• CPC Class Codes: A61M 2205/502 User interfaces, e.g. screens or keyboards
• CPC Class Codes: A61M 2205/52 with memories providing a history of measured variating parameters of apparatus or patient
• CPC Class Codes: A61M 5/003 Kits for diabetics
• CPC Class Codes: A61M 5/142 Pressure infusion, e.g. using pumps
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00
• CPC Class Codes: G06Q 10/109 Time management, e.g. calendars, reminders, meetings or time accounting
• CPC Class Codes: G09B 19/0092 : Nutrition
• CPC Class Codes: G09B 5/125 : the stations being mobile
• CPC Class Codes: G16H 40/63 : for local operation
• CPC Class Codes: G16H 40/67 : for remote operation
• CPC Class Codes: G16H 50/20 : for computer-aided diagnosis, e.g. based on medical expert systems
• CPC Class Codes: G16H 70/00 : ICT specially adapted for the handling or processing of medical references
• CPC Class Codes: G16H 70/60 : relating to pathologies
• CPC Class Codes: G16H 80/00 : ICT specially adapted for facilitating communication between medical practitioners or patients, e.g. for collaborative diagnosis, therapy or health monitoring

Abstract

A computer-implemented system and related method of reporting glucose information for a user of a diabetes management device are presented here. An embodiment of the method obtains input data for the user of the diabetes management device, and identifies a tracked glycemic response event. One or more recommended glycemic control parameters are calculated based on an analysis of the obtained input data. The glycemic control parameters are calculated to extend a time period during which the user remains within a target glucose range following the tracked glycemic response event. The method continues by generating an output message that includes at least some of the recommended glycemic control parameters, and delivering the generated output message to a user device operated by the user of the diabetes management device.

Claims

1. A method of reporting glucose information for a user of a diabetes management device, the method comprising:

obtaining input data for the user of the diabetes management device;

identifying a glycemic response event;

calculating one or more recommended glycemic control parameters based on an analysis of the obtained input data, wherein the one or more glycemic control parameters are calculated to extend a time period during which the user remains within a target glucose range following the glycemic response event;

generating an output message that includes at least some of the recommended glycemic control parameters; and

delivering the generated output message to a user device operated by the user of the diabetes management device.

2. The method of claim 1, wherein the input data comprises:

a first amount of data provided by the diabetes management device; and

a second amount of data provided by a source other than the diabetes management device.

3. The method of claim 1, wherein the input data comprises data provided by a mobile device operated by the user.

4. The method of claim 1, wherein the input data comprises at least some of:

carbohydrate amount;

bolus information;

insulin to carbohydrate ratio;

insulin sensitivity factor;

active insulin amount;

time of day;

basal rate;

temporary basal use;

consecutive boluses;

insulin suspension;

reservoir rewind time;

reservoir priming time;

pump alarms and associated alarm times;

sensor alerts and associated alert times;

blood glucose readings and associated measurement times;

user demographic information;

meal times and corresponding meal content;

exercise times and corresponding exercise content or type;

medication type, dosage, and time;

sleep time and quality;

stress time;

electronic medical records; and

medical lab test data.

5. The method of claim 1, wherein the recommended glycemic control parameters are calculated based on historical input data collected for the user.

6. The method of claim 1, wherein the identifying step comprises:

obtaining user-entered information that indicates the glycemic response event.

7. The method of claim 1, wherein the recommended glycemic control parameters include recommendations related to ingestion of meals, timing of meals, insulin bolus size, timing of insulin boluses, food portion size, meal content, sleep duration, sleep timing, activity type, activity duration, or activity timing.

8. The method of claim 1, wherein the generated output message comprises a text-based message, graphics, video content, or audio content.

9. The method of claim 1, wherein the delivering step delivers the generated output message prior to an occurrence of the glycemic response event.

10. A computer-implemented glucose reporting system comprising:

at least one processor device; and

a non-transitory processor-readable medium operatively associated with the at least one processor device, the processor-readable medium comprising executable instructions configurable to cause the at least one processor device to perform a method comprising;

obtaining input data for a user of a diabetes management device;

identifying a glycemic response event;

calculating one or more recommended glycemic control parameters based on an analysis of the obtained input data, wherein the one or more glycemic control parameters are calculated to extend a time period during which the user remains within a target glucose range following the glycemic response event;

generating an output message that includes at least some of the recommended glycemic control parameters; and

delivering the generated output message to a user device operated by the user of the diabetes management device.

11. The system of claim 10, wherein the input data comprises:

a first amount of data provided by the diabetes management device; and

a second amount of data provided by a source other than the diabetes management device.

12. The system of claim 10, wherein the input data comprises data provided by a mobile device operated by the user of the diabetes management device.

13. The system of claim 10, wherein the input data comprises at least some of:

carbohydrate amount;

bolus information;

insulin to carbohydrate ratio;

insulin sensitivity factor;

active insulin amount;

time of day;

basal rate;

temporary basal use;

consecutive boluses;

insulin suspension;

reservoir rewind time;

reservoir priming time;

pump alarms and associated alarm times;

sensor alerts and associated alert times;

blood glucose readings and associated measurement times;

user demographic information;

meal times and corresponding meal content;

exercise times and corresponding exercise content or type;

medication type, dosage, and time;

sleep time and quality;

stress time;

electronic medical records; and

medical lab test data.

14. The system of claim 10, wherein the recommended glycemic control parameters are calculated based on historical input data collected for the user.

15. The system of claim 10, wherein the identifying step comprises:

obtaining user-entered information that indicates the glycemic response event.

16. The system of claim 10, wherein the recommended glycemic control parameters include recommendations related to ingestion of meals, timing of meals, insulin bolus size, timing of insulin boluses, food portion size, meal content, sleep duration, sleep timing, activity type, activity duration, or activity timing.

17. The system of claim 10, wherein the generated output message comprises a text-based message, graphics, video content, or audio content.

18. The system of claim 10, wherein the delivering step delivers the generated output message prior to an occurrence of the glycemic response event.