System and method for managing respiratory insufficiency in conjunction with heart failure assessment
A system and method for evaluating a patient status from sampled physiometry for use in respiratory insufficiency management and heart failure assessment is presented. Physiological measures are stored and include direct measures regularly recorded on a substantially continuous basis by a medical device for a patient or measures derived from the direct measures. The physiological measures are sampled, which each relate to a same type of physiometry, and those of the physiological measures, which each relate to a different type of physiometry. A status is determined through analysis of those sampled physiological measures assembled from a plurality of recordation points. The sampled physiological measures are evaluated. Any trends are identified and include one of a status quo and a change, which might affect cardiac performance or respiratory performance. Each such trend is compared to applicable indications of worsening heart failure and respiratory insufficiency to generate a notification of parameter violations.
1. A system for managing respiratory insufficiency in conjunction with heart failure assessment, comprising:
a data module to assemble physiological measures, which were directly recorded as data on a substantially continuous basis by a medical device for a patient or indirectly derived from the data;
a status module to determine a wellness indicator for the patient through sampling and analysis of the physiological measures over a plurality of data assembly points; and
an evaluation module to evaluate the physiological measures relative to the wellness indicator, comprising:
an analysis module to analyze a patient status trend comprising one of a status quo and a change in at least one of cardiac performance and respiratory performance; and
a comparison module to compare the patient status trend to applicable indications of worsening heart failure and respiratory insufficiency, wherein the evaluation module further evaluates a time span over which the patient status trend occurs;
an indicator module to define stickiness indicators comprising a temporal bound on change of one or more of the physiological measures, and
a revision module to revise patient treatment in a manner corresponding to a rate of the patient status trend over the time span.
2. A system according to claim 1 , wherein the patient status relates to at least one of a finding of reduced exercise capacity and respiratory distress.
3. A system according to claim 2 , wherein the finding of reduced exercise capacity is selected from the group comprising decreased cardiac output, decreased mixed venous oxygen score, decreased patient activity score and decreased exercise tolerance.
4. A system according to claim 2 , wherein the finding of respiratory distress is selected from the group comprising a spike in patient activity score, a spike in pulmonary artery pressure, a spike in right ventricular pressure, a spike in transthoracic impedance, increased respiratory rate, increased minute ventilation, increased temperature, decreased QT interval, decreased arterial oxygen and decreased arterial carbon dioxide.
5. A system according to claim 1 , further comprising:
a quality of life module to associate quality of life measures chronicled by the patient with the physiological measures.
6. A system according to claim 1 , wherein the change in at least one of cardiac performance and respiratory performance is selected from the group comprising an onset, progression, and regression of either a cardiac performance or a respiratory performance parameter.
7. A system according to claim 1 , wherein the worsening heart failure indications are selected from the group comprising pulmonary artery pressure, left atrial pressure, dyspnea, orthopnea, pulmonary edema, peripheral edema, and fatigue.
8. A system according to claim 1 , further comprising:
a measurement module to measure one or more of pulmonary artery pressure, heart rate, heart sounds, intrathoracic impedance, respiration, posture, lung fluid, activity, weight, and physiological response to activity.
9. A system according to claim 1 , further comprising:
a reprogramming module to reprogram a medical device based on evaluation of the physiological measures.
10. A system according to claim 9 , wherein either the worsening heart failure indications or the respiratory insufficiency are factored into the reprogramming.
11. A system according to claim 1 , wherein respiration rate is tracked through the medical device, further comprising:
a notification module to generate a notification triggered by a parameter assigned to the respiration rate.
12. A system according to claim 11 , wherein the parameter comprises one or more of an upper limit parameter applied over a short term and a counter parameter applied over a long term.
13. A system according to claim 1 , wherein the medical device comprises one of an implantable medical device and an external medical device.
14. A method for managing respiratory insufficiency in conjunction with heart failure assessment, comprising:
assembling physiological measures, which were directly recorded as data on a substantially continuous basis by a medical device for a patient or indirectly derived from the data;
determining a patient status indicator for the patient through sampling and analysis of the physiological measures over a plurality of data assembly points; and
evaluating the physiological measures relative to the patient status indicator for determining a patient status trend comprising one of a status quo and a change in at least one of cardiac performance and respiratory performance and comparing the patient status trend to applicable indications of worsening heart failure and respiratory insufficiency;
defining stickiness indicators comprising a temporal bound on change of one or more of the physiological measures;
evaluating a time span of the patient status change; and
revising patient treatment in a manner corresponding to a rate of the patient status trend over the time span.
15. A method according to claim 14 , wherein the patient status chance relates to at least one of a finding of reduced exercise capacity and respiratory distress.
16. A method according to claim 15 , wherein the finding of reduced exercise capacity is selected from the group comprising decreased cardiac output, decreased mixed venous oxygen score, decreased patient activity score and decreased exercise tolerance.
17. A method according to claim 15 , wherein the finding of respiratory distress is selected from the group comprising a spike in patient activity score, a spike in pulmonary artery pressure, a spike in right ventricular pressure, a spike in transthoracic impedance, increased respiratory rate, increased minute ventilation, increased temperature, decreased QT interval, decreased arterial oxygen and decreased arterial carbon dioxide.
18. A method according to claim 14 , further comprising:
associating quality of life measures chronicled by the patient with the physiological measures.
19. A method according to claim 14 , wherein the patient status trend in at least one of cardiac performance and respiratory performance is selected from the group comprising an onset, progression, and regression of either a cardiac performance or a respiratory performance parameter.
20. A method according to claim 14 , wherein the worsening heart failure indications are selected from the group comprising pulmonary artery pressure, left atrial pressure, dyspnea, orthopnea, pulmonary edema, peripheral edema, and fatigue.
21. A method according to claim 14 , further comprising:
measuring one or more of pulmonary artery pressure, heart rate, heart sounds, intrathoracic impedance, respiration, posture, lung fluid, activity, weight, and physiological response to activity.
22. A method according to claim 14 , further comprising:
reprogramming a medical device based on evaluation of the physiological measures.
23. A method according to claim 22 , further comprising:
factoring either the worsening heart failure indications or the respiratory insufficiency into the reprogramming.
24. A method according to claim 14 , further comprising:
tracking respiration rate through the medical device; and
generating a notification triggered by a parameter assigned to the respiration rate.
25. A method according to claim 24 , wherein the parameter comprises one or more of an upper limit parameter applied over a short term and a counter parameter applied over a long term.
26. A method according to claim 14 , wherein the medical device comprises one of an implantable medical device and an external medical device.
27. A system for evaluating a patient status from sampled physiometry for use in respiratory insufficiency management and heart failure assessment, comprising:
a storage module to store physiological measures comprising at least one of direct measures regularly recorded on a substantially continuous basis by a medical device for a patient and measures derived from the direct measures;
a sampling module to sample at least one of those of the physiological measures, which each relate to a same type of physiometry, and those of the physiological measures, which each relate to a different type of physiometry;
a status module to determine a wellness indicator for the patient through analysis of those sampled physiological measures assembled from a plurality of recordation points; and
an evaluation module to evaluate the sampled physiological measures, comprising:
an analysis module to identify a patient status trend comprising one of a status quo and a change, which affects one or more of cardiac performance and respiratory performance of the patient, wherein the evaluation module further evaluates a time span over which the patient status trend occurs;
a comparison module to compare the patient status to applicable indications of worsening heart failure and respiratory insufficiency to generate a notification of parameter violations;
an indicator module to define stickiness indicators comprising a temporal bound on change of one or more of the physiological measures, and
a revision module to revise patient treatment in a manner corresponding to a rate of the patient status trend over the time span.
28. A system according to claim 27 , further comprising:
a reprogramming module to reprogram a medical device based on extended evaluation of the direct measures and the derived measures.
29. A system according to claim 27 , further comprising:
a tracking module to track respiration rate of the patient on a regular basis through the medical device; and
a notification module to generate a notification triggered by one or more of an upper limit parameter applied over a short term and a counter parameter applied over a long term.
30. A method for evaluating a patient status from sampled physiometry for use in respiratory insufficiency management and heart failure assessment, comprising:
storing physiological measures comprising at least one of direct measures regularly recorded on a substantially continuous basis by a medical device for a patient and measures derived from the direct measures;
sampling at least one of those of the physiological measures, which each relate to a same type of physiometry, and those of the physiological measures, which each relate to a different type of physiometry;
determining a wellness indicator for the patient through analysis of those sampled physiological measures assembled from a plurality of recordation points; and
evaluating the sampled physiological measures, comprising:
identifying a patient status trend comprising one of a status quo and a change, which affects one or more of cardiac performance and respiratory performance of the patient; and
comparing the patient status to applicable indications of worsening heart failure and respiratory insufficiency to generate a notification of parameter violations;
defining stickiness indicators comprising a temporal bound on change of one or more of the physiological measures;
evaluating a time span of the patient status change; and
revising patient treatment in a manner corresponding to a rate of the change over the time span.
31. A method according to claim 30 , further comprising:
reprogramming a medical device based on extended evaluation of the direct measures and the derived measures.
32. A method according to claim 30 , further comprising:
tracking respiration rate of the patient on a regular basis through the medical device; and
generating a notification triggered by one or more of an upper limit parameter applied over a short term and a counter parameter applied over a long term.