TRACKING DIRECT REPORTED ADVERSE EVENTS

• US 20100179821A1
• Filed: 01/09/2009
• Published: 07/15/2010
• Est. Priority Date: 01/09/2009
• Status: Abandoned Application

• Current Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Original Assignee: Cerner Innovation, Inc. (Oracle Corporation)
• Inventors: GRIFFIN, SARA JANE, GEDEON, HANNA MINA
• Application Number:
  US12/351,628
• Publication Number:
  US 20100179821A1
• Time in Patent Office: Days
• US Class Current: 705/2
• CPC Class Codes: G16H 10/60 for patient-specific data, e.g. for electronic patient records
• CPC Class Codes: G16H 15/00 ICT specially adapted for medical reports, e.g. generation or transmission thereof
• CPC Class Codes: G16H 20/10 relating to drugs or medications, e.g. for ensuring correct administration to patients

Abstract

Systems, methods, and computer readable media are described for communicating an adverse event report directly to an end-user receiving party and tracking one or more adverse event reports. An adverse event may be detected manually or automatically by a system and an electronic adverse event reporting form presented to a user with one or more data fields pre-populated with data from a patient'"'"'s electronic health record (EHR). The user may enter and edit data in the electronic form and may submit the data in the electronic form directly to an end-user receiving party such as the U.S. Food and Drug Administration. One or more receipts may be received from the receiving party and indicia from the receipts recorded to one or more records. The submitted adverse event reports may be tracked, accessed, and interacted with through a user interface and additional information may be provided to a user therein.

Claims

1. A method in a medical information computing environment for tracking one or more adverse event reports, the method comprising:

communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties;

receiving one or more received receipts from the one or more end-user receiving parties for each of the one or more communicated electronic forms;

recording indicia corresponding to the one or more received receipts in one or more records associated with the one or more communicated electronic forms;

querying the status of one or more adverse event reports communicated to the one or more end-user receiving parties as an electronic form; and

providing a user interface on a display to allow a user to at least one of view, query, audit, and create reports for one or more data corresponding to the one or more adverse event reports.

2. The method of claim 1, wherein the one or more data in the one or more electronic adverse event reporting forms are communicated as electronic mail messages.

3. The method of claim 1, wherein the one or more received receipts comprises at least one of a successful transmission receipt and a transmission failure receipt.

4. The method of claim 3, wherein the successful transmission receipt is a message delivery notification (MDN) receipt.

5. The method of claim 1, wherein a unique identifier is assigned to each of the one or more adverse event reports by the one or more end-user receiving parties.

6. The method of claim 5, further comprising:

receiving one or more unique identifiers from the one or more end-user receiving parties; and

recording the one or more unique identifiers in the one or more records associated with the one or more communicated electronic forms.

7. The method of claim 6, wherein the one or more unique identifiers are a mail disposition notification (MDN) and the one or more end-user receiving parties are comprised of at least the United States Food and Drug Administration.

8. The method of claim 1, wherein the one or more received receipts comprises at least an acknowledgment receipt.

9. The method of claim 8, wherein the acknowledgement receipt is an ACK acknowledgement character.

10. The method of claim 1, wherein a receipt notification is sent to the one or more end-user receiving parties after the steps of receiving.

11. The method of claim 1, wherein the one or more records associated with the one or more electronic forms comprise one or more of a patient'"'"'s electronic health record, a quality control record, and a clinician'"'"'s records.

12. The method of claim 1, further comprising the step of providing a user interface on a display to present to a user one or more of statistics, related reports, safety warnings, notices, and related data based on at least one of the groups of all, and a subset of all, adverse event reports communicated to the one or more end-user receiving parties by one or more users.

13. A system in a medical information computing environment for facilitating the tracking of one or more adverse event reports, the system comprising:

a communication component for communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties;

a receiving component for receiving at least one of a receipt and a unique identifier;

a recording component for recording the at least one of receipts and identifiers in one or more records associated with each of the one or more adverse event reports; and

a displaying component for presenting on a display one or more data corresponding to the one or more adverse event reports.

14. The system of claim 13, wherein the receipt comprises one or more of an acknowledgement receipt, a successful transmission receipt, and a transmission failure receipt.

15. The system of claim 13, wherein the displaying component provides to a user one or more functionalities from the group of:

viewing, sorting, querying, auditing, and generating reports from the data.

16. The system of claim 13, wherein the displaying component provides to a user one or more of statistics, related reports, safety warnings, notices, and related data based on at least one of the groups of all, and a subset of all, adverse event reports communicated to the one or more end-user receiving parties by one or more users.

17. The system of claim 13, wherein the acknowledgment receipt is an ACK acknowledgment character, the successful transmission receipt is a mail disposition notification (MDN), and the MDN contains the unique identifier.

18. The system of claim 13, wherein the one or more records comprise at least one of a patient'"'"'s electronic health record, a quality control record, and a clinician'"'"'s records.

19. The system of claim 13, wherein the one or more data in the one or more electronic forms is communicated as one or more electronic mail messages via an electronic mail server.

20. A method in a medical information computing environment for tracking one or more adverse event reports, the method comprising:

communicating one or more data in one or more electronic adverse event reporting forms to one or more end-user receiving parties as an electronic mail message;

receiving one of a successful transmission receipt and a transmission failure receipt for each of the one or more communicated electronic forms;

receiving a unique identifier for each of the one or more electronic forms from one or more of the one or more end-user receiving parties;

receiving an acknowledgment receipt for each of the one or more communicated electronic forms;

recording indicia corresponding to one or more of the acknowledgment receipt, the one of successful transmission receipt and transmission failure receipt, and the unique identifier in one or more records associated with the one or more communicated electronic forms;

querying the status of one or more adverse event reports communicated to the one or more end-user receiving parties as an electronic form;

providing a user interface on a display to allow a user to at least one of view, query, audit, and create reports for one or more data corresponding to the one or more adverse event reports; and

providing a user interface on a display to present to a user one or more of statistics, related reports, safety warnings, notices and related data based on at least one of the groups of all, and a subset of all, adverse event reports communicated to the one or more end-user receiving parties by one or more users.