System and method for diagnosing and monitoring congestive heart failure
A system for diagnosing and monitoring congestive heart failure for automated remote patient care is presented. A database stores a plurality of monitoring sets relating to patient information recorded on a substantially continuous basis. A server retrieving and processing the monitoring sets includes a comparison module determining patient status changes by comparing at least one recorded measure from one of the monitoring sets to at least one other recorded measure from another of the monitoring sets with both recorded measures relating to a type of patient information, and an analysis module testing each patient status change for one of an absence, an onset, a progression, a regression, and a status quo of congestive heart failure against a predetermined indicator threshold corresponding to a type of patient information as the recorded measures. The indicator threshold corresponds to a quantifiable physiological measure of a pathophysiology indicative of congestive heart failure.
1. A non-transitory computer-readable storage medium storing code for remote automated congestive heart failure patient management, comprising:
code for receiving information to identify a patient enrolled in automated patient care, the information comprising at least one of treatment profile and patient medical history;
code for receiving collected device measures recorded by a medical device as raw physiometry for the patient;
code for deriving device measures as derivative physiometry based on the collected device measures;
code for comparing at least one of the derived device measures to at least one other of the derived device measures
code for determining a pathophysiology indicative of at least one of a change and a status quo of congestive heart failure;
code for receiving hysteresis parameters as a temporally-defined threshold for changes in the pathophysiology; and
code for adapting the hysteresis parameters depending upon patient medical history and peer-group guidelines.
2. A non-transitory computer-readable storage medium according to claim 1 , further comprising:
code for receiving evaluation parameters for the pathophysiology in terms of at least one of a cardiovascular and cardiopulmonary disease; and
code for determining a wellness indicator analyzing one or more of the derived device measures against the evaluation parameters.
3. A non-transitory computer-readable storage medium according to claim 2 , further comprising:
code for determining a patient comprising code for evaluating the wellness indicator to identify at least one of a change and a status quo of congestive heart failure.
4. A non-transitory computer-readable storage medium according to claim 2 ,
wherein the code for determining the wellness indicator further comprises code for analyzing one or more of the derived device measures against the hysteresis parameters.
5. A non-transitory computer-readable storage medium according to claim 1 , further comprising:
code for receiving quality of life measures as qualified voice feedback data, wherein the voice feedback data is electronically recorded by the patient contemporaneous to recordation of the collected device measures.
6. A non-transitory computer-readable storage medium according to claim 1 , wherein one or more of the derived device measures are selected from the group comprising self referencing, peer group, and general population physiometric measures.
7. A non-transitory computer-readable storage medium according to claim 1 , further comprising:
code for generating reprogramming parameters for the medical device; and
code for applying the programming parameters before the medical device has recorded the collected device measures.
8. A non-transitory computer-readable storage medium according to claim 1 , wherein the medical device comprises one of an implantable medical device and an external medical device.
9. A non-transitory computer-readable storage medium according to claim 1 , further comprising:
code for receiving structured data for the patient enrolled in the automated patient care, the structured data comprising at least one of the derived device measures.
10. A non-transitory computer-readable storage medium according to claim 9 , further comprising:
code for determining a wellness indicator comprising code for analyzing one or more of the collected and derived device measures against evaluation parameters that define a threshold for the pathophysiology in terms of at least one of a cardiovascular and cardiopulmonary disease.
11. A non-transitory computer-readable storage medium according to claim 9 , further comprising:
code for receiving quality of life measures as qualified voice feedback data, wherein the voice feedback data is electronically recorded by the patient contemporaneous to recordation of the collected device measures.
12. A non-transitory computer-readable storage medium according to claim 9 , further comprising:
code for receiving reprogramming parameters for the medical device; and
code for applying the reprogramming parameters before the medical device has recorded the collected device measures.
13. A non-transitory computer-readable storage medium according to claim 9 , wherein the medical device comprises one of an implantable medical device and an external medical device.