SYSTEMS AND METHODS FOR MONITORING AND REPORTING LAB RESULTS

• US 20110046974A1
• Filed: 08/20/2010
• Published: 02/24/2011
• Est. Priority Date: 08/21/2009
• Status: Abandoned Application

• Current Assignee: Ascend Clinical LLC
• Original Assignee: Ascend Clinical LLC
• Inventors: Beyer, Paul, Gindraux, Olivier, Vizethann, Jeff, Burks, Greg
• Application Number:
  US12/860,571
• Publication Number:
  US 20110046974A1
• Time in Patent Office: Days
• US Class Current: 705/2
• CPC Class Codes: G06Q 99/00 Subject matter not provided for in other groups of this subclass
• CPC Class Codes: G16H 10/40 for data related to laboratory analysis, e.g. patient specimen analysis
• CPC Class Codes: G16H 15/00 ICT specially adapted for medical reports, e.g. generation or transmission thereof
• CPC Class Codes: G16H 40/67 for remote operation

Abstract

The invention provides systems and methods for monitoring and/or reporting laboratory data. One or more laboratory facility may communicate with a data management center. Medical laboratory data, which may include renal data, may be provided to the data management center. In some instances, some of the data from a laboratory facility may be compared to a reference value, or a goal to assess the performance of the laboratory facility. Data may be displayed to a user of the system in a report. Financial tools may also be provided to assess costs associated with bundling various laboratory tests.

Claims

1. A system for managing medical laboratory data, said system comprising:

a telecommunications network;

at least one remote laboratory facility with laboratory equipment for gathering medical laboratory data from a plurality of subjects; and

a data management center for receiving medical laboratory data from the at least one remote laboratory facility via the telecommunications network, wherein the data management center compares the received medical laboratory data to a reference medical laboratory data to assess performance of the at least one remote laboratory facility.

2. The system of claim 1, wherein the medical laboratory data includes renal or dialysis data from the plurality of subjects.

3. The system of claim 1, wherein the reference medical laboratory data is based on at least one of the following:

another laboratory facility, a mathematical calculation from the data management center based on a plurality of laboratory facilities, or generated theoretical reference data from the data management center.

4. The system of claim 1, wherein the data management center generates a report based on the comparison of the received medical laboratory data with the reference medical laboratory data.

5. The system of claim 4, wherein the report content and/or format is customized by a user of the system.

6. The system of claim 5, wherein the user chooses a report template and one or more report parameters.

7. The system of claim 4, wherein individual patient level data can be accessed from the report.

8. The system of claim 1, wherein the received medical laboratory data is analyzed based on a selected focus criteria.

9. The system of claim 8, wherein the selected focus criteria includes at least one of the following:

schedule, days in dialysis, age, gender, nephrologist, race, diabetic status, or facility.

10. A method for managing medical laboratory data, said method comprising:

receiving medical data from at least one laboratory facility;

establishing at least one laboratory result goal for the at least one laboratory facility; and

determining, based on the medical data, whether the at least one laboratory result goal was met by the at least one laboratory facility.

11. The method of claim 10, wherein the at least one laboratory goal includes an acceptable range of values for a laboratory result from one or more subjects at the laboratory facility.

12. The method of claim 11, wherein a plurality of laboratory result goals are established for the at least one laboratory facility.

13. The method of claim 10, wherein the at least one laboratory facility or an entity affiliated with the at least one laboratory facility defines its own at least one laboratory goal.

14. The method of claim 10, wherein the medical data is received at a remote command center via a telecommunication network.

15. The method of claim 10, further comprising creating a report displaying information related to the laboratory result goal.

16. The method of claim 15, wherein the report includes distribution and trend data.

17. The method of claim 15, wherein the report can be filtered depending on whether the laboratory facility does or does not meet the at least one laboratory result goal.

18. The method of claim 10, wherein the at least one laboratory facility or an entity affiliated with the at least one laboratory facility creates and manages groupings based on at least one selected filter.

19. The method of claim 18, wherein the selected filter includes at least one of:

schedule, days in dialysis, age, gender, nephrologist, race, diabetic status, or facility.

20. The method of claim 10, wherein the at least one laboratory goal is inherited from a parent entity, such that if the parent entity updates a goal, the corresponding laboratory goal is automatically updated.

21. The method of claim 10, wherein the at least one laboratory goal is copied from a parent entity, such that if the parent entity updates a goal, the corresponding laboratory goal is not automatically updated.

22. A graphical user interface for facility performance assessment, said graphical user interface comprising:

a list with a plurality of laboratory result types;

a plurality of comparison methods, wherein each comparison method is visually mapped to the corresponding laboratory result type;

a plurality of goal values, wherein each goal value is visually mapped to the corresponding laboratory result type; and

a plurality of acceptable range values, wherein the acceptable range values denote an acceptable range for a laboratory result as compared to the corresponding goal values, and wherein each acceptable range value is visually mapped to the corresponding laboratory result type.

23. The method of claim 22, further comprising at least one user interactive feature that provides access to edit at least one of:

a goal value, comparison method, or acceptable range values.

24. A graphical user interface for performing bundling analytics for Medicare bundling, comprising:

a list of one or more tests to be included within a medical service bundle;

at least one cost value for the test, visually mapped to the test;

a frequency selection zone for the test, indicating how often the test is to be performed; and

an average cost per patient estimated over a selected time period.

25. The method of claim 24 further comprising an occurrence entry zone configured to indicate the percentage of patients that may utilize the associated test.