THERAPY MANAGEMENT SYSTEM

• US 20100274592A1
• Filed: 06/25/2010
• Published: 10/28/2010
• Est. Priority Date: 06/03/2005
• Status: Abandoned Application

• Current Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Inventors: Cortina, Gabe, Plummer, Jon, Glidden, Matt, Nitzan, Tamir, Marcus, Alan O., Goldsmith, Joel, Hayes, Andrew C., Mastrototaro, John J.
• Application Number:
  US12/823,888
• Publication Number:
  US 20100274592A1
• 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 50/50 for simulation or modelling of medical disorders

Abstract

A diabetes data management system selects variable parameters and one or more devices with data that are utilized in a report. The diabetes data management system analyzes data during a selected period. The system generates reports which highlight data from one or more device during the selected period including carbohydrate, insulin, and glucose data, reports which highlight data around and during meal events and other user-defined events, reports which overlay multiple data based on time of day and other factors, and automatically prepared logbook reports.

Claims

1. A computing device to generate a diabetes management report for a patient, comprising:

a processor for executing computer instructions;

a database including infusion pump information, wherein the infusion pump information includes bolus event information and priming event information;

a display for displaying a report including information presented in a plurality of separately identifiable regions, a first region including a representation of the bolus event information and a second region including a representation of the priming event information; and

a computer readable storage medium containing executable computer program instructions, which when executed by the processor cause the report to be generated on the display.

2. The computing device of claim 1, wherein the bolus event information includes at least one type of information selected from the group consisting of manual bolus event information and correction bolus event information.

3. The computing device of claim 2, wherein the bolus event information further includes at least one type of information selected from the group consisting of bolus wizard event information and bolus with food event information.

4. The computing device of claim 1, wherein the priming event information includes at least one type of information selected from the group consisting of rewind information, fixed priming information, manual priming information, prime volume information, and suspend duration information.

5. The computing device of claim 4, wherein the infusion pump information further includes glucose information indicating the number of glucose readings taken during a report time period and the display includes a third region indicating a representation of the glucose information.

6. A program code storage device, comprising:

a computer-readable storage medium;

computer-readable program code, the computer-readable program code including instructions, which when executed cause a computing device to;

receive medical information including infusion pump information, wherein the infusion pump information includes bolus event information and priming event information; and

display a report including information presented in a plurality of separately identifiable regions, a first region including a representation of the bolus event information and a second region including a representation of the priming event information.

7. The program code storage device of claim 6, wherein the bolus event information includes at least one type of information selected from the group consisting of manual bolus event information and correction bolus event information.

8. The program code storage device of claim 6, wherein the bolus event information further includes at least one type of information selected from the group consisting of bolus wizard event information and bolus with food event information.

9. The program code storage device of claim 8, wherein the priming event information includes at least one type of information selected from the group consisting of rewind information, fixed priming information, manual priming information, prime volume information, and suspend duration information.

10. The program code storage device of claim 6, wherein the infusion pump information further includes glucose information indicating the number of glucose readings taken during a report time period, and the display includes a third region indicating a representation of the glucose information.