System and method for managing respiratory insufficiency through remote patient care
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61B-005/08
A61B-005/02
A61B-005/00
출원번호
US-0789387
(2007-04-23)
등록번호
US-8747329
(2014-06-10)
발명자
/ 주소
Bardy, Gust
출원인 / 주소
Cardiac Pacemakers, Inc.
대리인 / 주소
Pauly, DeVries Smith & Deffner LLC
인용정보
피인용 횟수 :
0인용 특허 :
141
초록▼
A system and method for managing respiratory insufficiency through remote patient care is described. A patient enrolled in remote patient care is identified with information including at least one of treatment profile and medical history. Collected device measures are received to record raw physiome
A system and method for managing respiratory insufficiency through remote patient care is described. A patient enrolled in remote patient care is identified with information including at least one of treatment profile and medical history. Collected device measures are received to record raw physiometry for a patient, wherein the patient is regularly monitored by a medical device. Derived device measures are generated to provide derivative physiometry based on the collected device measures. A patient status indicator is determined by analyzing the collected and derived device measures to diagnose a pathophysiology indicative of respiratory insufficiency.
대표청구항▼
1. A computer-usable storage medium having program code stored thereon for determining a pathophysiology indicative of respiratory insufficiency through remote patient care, the computer-usable medium comprising program code for causing: identifying a patient enrolled under remote patient care with
1. A computer-usable storage medium having program code stored thereon for determining a pathophysiology indicative of respiratory insufficiency through remote patient care, the computer-usable medium comprising program code for causing: identifying a patient enrolled under remote patient care with information comprising at least one of treatment profile and medical history;recording raw physiometry for the patient, wherein the patient is regularly monitored by a medical device and the raw physiometry comprises collected device measures;providing derivative physiometry based on the collected device measures, wherein the derivative physiometry comprises derived device measures;detecting respiratory distress and reduced exercise capacity using indicator thresholds; anddetermining a wellness indicator by analyzing the collected and derived device measures against the indicator thresholds to determine a pathophysiology indicative of respiratory insufficiency. 2. The computer usable storage medium of claim 1, further comprising program code for causing one or more of: identifying a patient status by evaluating the collected and derived device measures for at least one of a change and a status quo of respiratory insufficiency; andreprogramming parameters for the medical device, wherein the collected device measures are recorded subsequent to application of the reprogramming parameters. 3. The computer-useable storage medium of claim 1, further comprising program code for causing: receiving quality of life measures to provide qualified voice feedback data electronically recorded by the patient contemporaneous to recordation of the collected device measures. 4. The computer-useable storage medium of claim 1, further comprising program code for causing: quantifying baseline data based on those of the collected and derived device measures associated with a fixed time period. 5. The computer-useable storage medium of claim 1, further comprising program code for causing: providing feedback data selected from the group comprising an interpretive pathophysiology, a medical diagnosis patient notification, a medical diagnosis caregiver notification, and reprogramming instructions for the medical device. 6. A device for managing respiratory insufficiency through remote patient care, comprising: memory comprising: at least one of treatment profile and medical history for a patient enrolled under remote patient care;collected device measures to record raw physiometry for the patient, wherein the patient is regularly monitored by a medical device;derived device measures to provide derivative physiometry based on the collected device measures; andindicator thresholds to detect respiratory distress and reduced exercise capacity; anda processor to determine a wellness indicator by analyzing the collected and derived data measures against the indicator thresholds to determine a pathophysiology of respiratory insufficiency. 7. A device according to claim 6, the memory further comprising: baseline data quantified by those of the collected and derived device measures associated with a fixed time period. 8. An analysis system for managing respiratory insufficiency through remote patient care, comprising: a database, comprising: information to identify a patient enrolled in remote patient care comprising at least one of treatment profile and medical history;collected device measures to record raw physiometry for the patient, wherein the patient is regularly monitored by a medical device;derived device measures to provide derivative physiometry based on the collected device measures; andstored indicator thresholds to detect respiratory distress and reduced exercise capacity; andan analysis module to determine a wellness indicator by analyzing one or more of the collected and derived device measures against the indicator thresholds;an interface to receive the collected device measures; anda processing module, comprising: a processor to generate derived device measures from the collected device measures; anda determination module to use the wellness indicator to determine a pathophysiology indicative of respiratory insufficiency. 9. An analysis system according to claim 8, further comprising: an analysis module to identify a patient status by evaluating the collected and derived device measures for at least one of a change and a status quo of respiratory insufficiency. 10. An analysis system according to claim 8, further comprising: recorded quality of life measures to provide qualified voice feedback data electronically recorded by the candidate patient contemporaneous to recordation of the collected device measures. 11. An analysis system according to claim 8, further comprising: reprogramming parameters for the medical device, wherein the collected device measures are recorded subsequent to application of the reprogramming parameters. 12. An analysis system according to claim 8, further comprising: an analysis module to define a baseline quantified by those of the collected and derived device measures associated with a fixed time period. 13. An analysis system according to claim 8, further comprising a feedback module to determine feedback selected from the group comprising an interpretive pathophysiology, a medical diagnosis patient notification, a medical diagnosis caregiver notification, and reprogramming instructions for the medical device. 14. A computer-usable storage medium having program code stored thereon for determining a pathophysiology indicative of respiratory insufficiency through remote patient care, comprising program code for causing: providing structured data for a patient enrolled in remote patient care, comprising at least one of: identifying the patient using information comprising at least one of treatment profile and medical history;recording raw physiometry for the patient, wherein the patient is regularly monitored by a medical device and the raw physiometry comprises collected device measures; andproviding derivative physiometry based on the collected device measures, wherein the derivative physiometry comprises derived device measures;detecting respiratory distress and reduced exercise capacity using indicator thresholds;determining a wellness indicator by analyzing the collected and derived device measures against the indicator thresholds to determine a pathophysiology indicative of respiratory insufficiency. 15. The computer-usable storage medium of claim 14, further comprising program code for causing: receiving quality of life measures to provide qualified voice feedback data electronically recorded by the patient contemporaneous to recordation of the collected device measures. 16. The computer-usable storage medium of claim 14, further comprising program code for causing: quantifying a baseline by those of the collected and derived device measures associated with a fixed time period. 17. A method for managing respiratory insufficiency through remote patient care with a server system, comprising: identifying a patient enrolled in remote patient care with information comprising at least one of treatment profile and medical history;receiving collected device measures to record raw physiometry for a patient, wherein the patient is regularly monitored by a medical device;generating, with a processor, derived device measures to provide derivative physiometry based on the collected device measures;defining, with the processor indicator thresholds to detect respiratory distress and reduced exercise capacity;determining, with the processor a wellness indicator by analyzing one or more of the collected and derived device measures against the indicator thresholds; anddetermining, with the processor, a pathophysiology indicative of respiratory insufficiency based on the wellness indicator. 18. A method according to claim 17, further comprising: identifying a patient status by evaluating the collected and derived device measures for at least one of a change and a status quo of respiratory insufficiency. 19. A method according to claim 17, further comprising: receiving quality of life measures to provide qualified voice feedback data electronically recorded by the candidate patient contemporaneous to recordation of the collected device measures. 20. A method according to claim 17, further comprising: generating reprogramming parameters for the medical device, wherein the collected device measures are recorded subsequent to application of the reprogramming parameters. 21. A method according to claim 17, further comprising: defining a baseline quantified by those of the collected and derived device measures associated with a fixed time period. 22. A method according to claim 17, further comprising determining feedback selected from the group comprising an interpretive pathophysiology, a medical diagnosis patient notification, a medical diagnosis caregiver notification, and reprogramming instructions for the medical device.
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