Systems and methods for disrupting undesirable outcomes

• US 9,940,578 B1
• Filed: 07/10/2014
• Issued: 04/10/2018
• Est. Priority Date: 07/10/2013
• Status: Active Grant

• Current Assignee: Intego Software LLC (Tigerconnect Inc.)
• Original Assignee: Sphere3, LLC (Tigerconnect Inc.)
• Inventors: Govro, Kourtney, Rayson, Kristal, Mills, Steven Kent, Evans, Kyle, Govro, David, Kerns, Devon
• Primary Examiner(s): Chen, Alan S
• Application Number:
  US14/328,533
• Time in Patent Office: 1,370 Days
• Field of Search: None
• CPC Class Codes: G16H 40/20 for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
• CPC Class Codes: G16H 40/60 for the operation of medical equipment or devices
• CPC Class Codes: G16H 50/20 for computer-aided diagnosis, e.g. based on medical expert systems

Abstract

Systems and methods set forth herein may aid in identifying and disrupting undesirable outcomes. The system may include computer readable media; an electronic input device; an output device; a processor in data communication with the input device and the output device; and electronic instructions. The electronic instructions, when executed by the at least one processor, perform steps for: automatically storing event data from the electronic input device in the computer readable media; actuating the output device to graphically display the event data; determining if the event data qualifies as a critical event; storing the critical event data as outcome data in the computer readable media; accessing the event data and outcome data; determining at least one correlation between the event data and the outcome data; actuating the output device to display an intervention to aid in disrupting future critical events; and storing the intervention in the computer readable media.

Claims

1. A system for identifying and disrupting undesirable outcomes in a patient'"'"'s care, comprising:

a non-transitory computer readable medium; and

at least one processor programmed to perform the steps of;

receiving patient event data provided by a patient event device, wherein the patient event data comprises physiological data generated by the patient event device;

receiving patient action data manually input by at least one clinician associated with the patient'"'"'s care, wherein the patient action data is information related to an interaction between the at least one clinician and the patient during the patient'"'"'s care;

analyzing the patient event data and the patient action data and, based on the analysis, identifying a first critical event related to the patient'"'"'s care;

comparing the patient event data and the patient action data to the first critical event;

identifying, based on the comparison, a causal link from the patient event data and the patient action data that resulted in the first critical event;

determining, based on the identified causal link, a first intervention to aid in disrupting a second critical event;

wherein the first intervention provides at least one instruction to avoid the second critical event;

determining a second intervention, distinct from the first intervention, to aid in disrupting the second critical event, based on the identified causal link; and

determining a superior intervention based on the first intervention, the second intervention, and a determining factor.

2. The system of claim 1, wherein the patient event device includes at least one item selected from the group consisting of an interactive bed, a telemetry system, a ventilator system, an IV pump, a thermometer, a nurse call light system, an O2 saturation system, and a RTLS/RFID locating system.

3. The system of claim 2, wherein one of the first intervention, the second intervention, or the superior intervention identifies critical event data leading to the first critical event and provides instructions to avoid the second critical event in the future.

4. The system of claim 3, wherein the first critical event is determined based on predetermined criteria for recognizing undesirable outcomes.

5. The system of claim 2, wherein the action data comprises data not automatically input via the patient event device.

6. The system of claim 1, wherein the patient event data and the patient action data include corresponding location data to maintain a record of origin for the event and the action.

7. The system of claim 1, wherein one of the first intervention, the second intervention, or the superior intervention identifies the patient event data and the patient action data leading to the first critical event and provides instructions to avoid the second critical event in the future.

8. The system of claim 1, wherein the instructions provide information to prevent future patient falls.

9. The system of claim 1, wherein the instructions provide information to alter patient medication.

10. The system of claim 1, wherein the determining factor is a cost that is lower than the calculated cost of either the first intervention the second intervention, or the superior intervention.

11. The system of claim 1, wherein the determining factor is staff availability.

12. A system for identifying and disrupting undesirable outcomes in a patient'"'"'s care, comprising:

a non-transitory computer readable medium; and

at least one processor programmed to perform the steps of;

receiving patient event data provided by a patient event device, wherein the patient event data comprises physiological data generated by the patient event device;

receiving patient action data manually input by at least one clinician associated with the patient'"'"'s care, wherein the patient action data is information related to an interaction between the at least one clinician and the patient during the patient'"'"'s care;

analyzing the patient event data and the patient action data and, based on the analysis, identifying a first critical event related to the patient'"'"'s care;

comparing the patient event data and the patient action data to the first critical event and, based on the comparison, identifying a causal link from the patient event data and the patient action data that resulted in the first critical event;

based on the identified causal link, determining a first intervention to aid in disrupting a second critical event;

based on the identified causal link, determining a second intervention, distinct from the first intervention, to aid in disrupting the second critical event; and

determining a superior intervention based on the first intervention, the second intervention, and a determining factor,

wherein the superior intervention is determined by the at least one processor calculating a lower cost for the superior intervention than the cost of either the first intervention or the second intervention.

13. The system of claim 12, wherein the determining factor is staff availability.

14. The system of claim 12,

wherein the determining factor is a first determining factor,

wherein the step of determining the superior intervention is further based on a second determining factor.

15. The system of claim 14, wherein the second determining factor is a cost that is lower than the calculated cost of either the first intervention or the second intervention.

16. The system of claim 15, wherein the first intervention identifies critical event data leading to the first critical event and provides instructions to avoid the second critical event in the future.

17. The system of claim 12, wherein the patient event device includes at least one item selected from the group consisting of an interactive bed, a telemetry system, a ventilator system, an IV pump, a thermometer, a nurse call light system, an O2 saturation system, and a RTLS/RFID locating system.

18. The system of claim 17, wherein the first critical event is determined based on predetermined criteria for recognizing undesirable outcomes.