System and method for medical evaluation and monitoring

• US 20080071580A1
• Filed: 09/12/2007
• Published: 03/20/2008
• Est. Priority Date: 06/03/2005
• Status: Abandoned Application

• Current Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Inventors: Brooke, Julie, Qamar, Osman, Perry, Brenda, Marcus, Alan, Shin, John
• Application Number:
  US11/900,464
• Publication Number:
  US 20080071580A1
• Time in Patent Office: Days
• US Class Current: 705/3
• CPC Class Codes: G16H 15/00 ICT specially adapted for medical reports, e.g. generation or transmission thereof
• CPC Class Codes: G16H 20/17 delivered via infusion or injection
• CPC Class Codes: G16H 20/60 relating to nutrition control, e.g. diets
• CPC Class Codes: G16H 40/67 for remote operation
• CPC Class Codes: G16H 50/30 for calculating health indices; for individual health risk assessment

Abstract

A diabetes data management system (DDMS) and corresponding method assist a health-care professional in monitoring and evaluating the progress of a diabetic patient by generating various types of reports that are indicative of periodic trends in the patient'"'"'s behavior, including compliance with a prescribed course of therapy. Specifically, input data, including carbohydrate, insulin, and glucose data are uploaded by the patient into the DDMS, which then generates periodic (e.g., weekly), patient-specific output data in the form of box plot graphs, bar graphs, etc. over an extended period of time (e.g., several months). By studying the trends indicated by the output data, the health-care professional can modify the patient'"'"'s therapy in accordance with a set of goals for that patient. Output data may include insulin delivery effectiveness, bolus/basal delivery effectiveness, carbohydrate intake, usage of bolus wizard, bolus wizard compliance, Glucose alert response, frequency of infusion set replacement, and sensor usage.

Claims

1. A method for assisting a health-care professional to evaluate a diabetic patient'"'"'s progress during a given course of diabetes therapy, comprising:

obtaining a plurality of daily values for a first input related to the patient'"'"'s therapy, each said daily value corresponding to a given day within a first time period;

calculating a first output based on a first subset of said daily values representing consecutive daily values in a second time period within said first time period;

calculating at least a second output based on a second subset of said daily values representing consecutive daily values in a third time period within said first time period; and

generating a report that displays said first output and said at least second output as a function of time, thereby allowing the health-care professional to evaluate the patient'"'"'s progress based on a comparison of the first output and the at least second output over said first time period.

2. The method of claim 1, wherein said first time period is at least 2 weeks long, the second time period is one week within the first time period, and the third time period is another week subsequent to the second time period.

3. The method of claim 1, wherein:

the first input is selected from the group consisting of the patient'"'"'s carbohydrate intake, the number of bolus wizard events, the number of failures to recover from a hyper or hypo alert, and the total number of infusion set manual primes;

the first output is calculated as the average of the daily values over the second time period; and

the second output is calculated as the average of the daily values over the third time period.

4. The method of claim 3, wherein each of said first and second outputs is displayed on said report as a statistical spread including a minimum value, a maximum value, a mean value, and a median value.

5. The method of claim 1, wherein the first input is the number of hours a sensor is worn by the patient.

6. The method of claim 1, wherein said report further displays a baseline value against which the first output and the at least second output can be compared.

7. A method for assisting a health-care professional to evaluate a diabetic patient'"'"'s progress during a given course of diabetes therapy, comprising:

obtaining a plurality of daily values for first and second inputs related to the patient'"'"'s therapy, each said daily value corresponding to a given day within a first time period;

calculating a first output based on a first subset of said daily values representing consecutive daily values in a second time period within said first time period;

calculating at least a second output based on a second subset of said daily values representing consecutive daily values in a third time period within said first time period; and

generating a report that displays said first output and said at least second output as a function of time, thereby allowing the health-care professional to evaluate the patient'"'"'s progress based on a comparison of the first output and the at least second output over said first time period.

8. The method of claim 7, wherein said first time period is at least 2 weeks long, the second time period is one week within the first time period, and the third time period is another week subsequent to the second time period.

9. The method of claim 7, wherein said report further displays a baseline value against which the first output and the at least second output can be compared.

10. The method of claim 7, wherein:

the first output is calculated as the average, for all days in the second time period, of the daily ratio of the first-input value to the second-input value; and

the second output is calculated as the average, for all days in the third time period, of the daily ratio of the first-input value to the second-input value.

11. The method of claim 10, wherein the first input is the average of a daily sensor glucose and the second input is a daily total insulin.

12. The method of claim 10, wherein the first input is the average of a peak sensor glucose for a plurality of daily peak periods, and the second input is a daily total bolus.

13. The method of claim 10, wherein the first input is the mean sensor glucose from midnight to 6 am, and the second input is 25% of a daily total insulin.

14. The method of claim 10, wherein the first input is the total number of boluses and the second input is the total number of bolus wizard events.

15. The method of claim 10, wherein each of said first and second outputs is displayed on said report as a statistical spread including a minimum value, a maximum value, a mean value, and a median value.

16. A method for assisting a health-care professional to evaluate a diabetic patient'"'"'s progress during a given course of diabetes therapy, comprising:

obtaining a plurality of daily values for a plurality of inputs related to the patient'"'"'s therapy, each said daily value corresponding to a given day within a given time period;

calculating a plurality of outputs based on said daily values; and

generating a report that indicates whether, for the given time period, each of said plurality of outputs falls within a predefined acceptable range.

17. The method of claim 16, wherein said given time period is a week.

18. The method of claim 16, wherein each of said plurality of inputs is a member selected from the group consisting of the patient'"'"'s carbohydrate intake, the number of bolus wizard events, the number of failures to recover from a hyper or hypo alert, the total number of infusion set manual primes, the average of a daily sensor glucose, a daily total insulin, the average of a peak sensor glucose for a plurality of daily peak periods, a daily total bolus, the mean sensor glucose from midnight to 6 am, and combinations thereof.

19. The method of claim 16, wherein each of said plurality of outputs is calculated so as to be indicative of a member selected from the group consisting of insulin delivery effectiveness, bolus delivery effectiveness, basal delivery effectiveness, carbohydrate intake, usage of bolus wizard, bolus wizard compliance, Glucose alert response, frequency of infusion set replacement, and sensor usage by the patient.

20. The method of claim 16, wherein said obtaining and calculating steps are repeated for a multiplicity of time periods, and the report indicates whether, for each of the multiplicity of time periods, each of said plurality of outputs falls within a predefined acceptable range.

21. The method of claim 20, wherein said multiplicity of time periods are consecutive weeks.