Active implantable medical device comprising means for the diagnosis of heart failure

Patent metadata

Field	Value
Publication number	US-8938286-B2
Application number	US-201313755519-A
Country	US
Kind code	B2
Filing date	Jan 31, 2013
Priority date	Jan 31, 2012
Publication date	Jan 20, 2015
Grant date	Jan 20, 2015

Abstract

Methods, devices, and processor-readable storage media are provided for the diagnosis of heart failure. A method in this context includes collecting, using an implantable device, reference episodes, the reference episodes comprising, at least one of: electrical activity signals of a myocardium; myocardium hemodynamic activity signals, or indicators reflecting variation of physical parameters, variation of activity, and variation of hemodynamic phases between phases of effort and phases of recovery; generating an in-suspicion model-cycle and an off-suspicion model-cycle based on the reference episodes; and determining whether to generate an early heart failure alert, based on a difference between the in-suspicion model-cycle and the off-suspicion model-cycle.

First claim

What is claimed is:

1. A method of diagnosis of heart failure, the method comprising:
collecting, using an implantable device, a plurality of reference episodes, the reference episodes comprising at least one of: electrical activity signals of a myocardium; myocardium hemodynamic activity signals, or indicators reflecting variation of parameters between phases of effort and phases of recovery, wherein the parameters comprise at least one of physical parameters, activity parameters, or hemodynamic phase parameters between phases of effort and phases of recovery;
analysing, using the implantable device, the plurality of reference episodes based on predefined criteria to assign each of the reference episodes an in-suspicion marker or an off-suspicion marker, wherein the in-suspicion marker indicates a suspicion that the reference episode is associated with cardiac decompensation, wherein the off-suspicion marker indicates a suspicion that the reference episode is not associated with cardiac decompensation, and wherein the reference episodes assigned the in-suspicion marker and the reference episodes assigned the off-suspicion marker are interspersed within the plurality of reference episodes;
generating, using the implantable device, an in-suspicion model-cycle based on data associated with a plurality of in-suspicion reference episodes to which the in-suspicion marker has been assigned;
generating, using the implantable device, an off-suspicion model-cycle based on data associated with a plurality of off-suspicion reference episodes to which the off-suspicion marker has been assigned; and
determining, using the implantable device, whether to generate an early heart failure alert based on a difference between the in-suspicion model-cycle and the off-suspicion model-cycle.

2. The method of claim 1 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one endocardial electrogram beat recorded during an episode fulfilling predetermined conditions of heart rate and patient activity.

3. The method of claim 1 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one beat of an endocardiac acceleration signal recorded during an episode fulfilling predetermined conditions of heart rate and patient activity.

4. The method of claim 1 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one minute ventilation versus heart-rate characteristic pattern that was recorded during an episode comprising an effort phase followed by a recovery phase of the patient.

5. The method of claim 1 , further comprising:
updating the in-suspicion model-cycle and off-suspicion model-cycle; and
storing the updated in-suspicion model-cycle and updated off-suspicion model-cycle.

6. The method of claim 5 , wherein each of the in-suspicion model-cycle and the off-suspicion model-cycle is a combination of a previous model-cycle with at least one older model-cycle.

7. The method of claim 1 , wherein generating the early heart failure alert comprises:
generating at least one index of a clinical condition of a patient, based on the difference between the in-suspicion model-cycle and the off-suspicion model-cycle; and
generating an early heart failure alert based on the at least one index.

8. The method of claim 7 , wherein the at least one index of a clinical condition is updated periodically.

9. The method of claim 7 , wherein the at least one index is calculated based on an average of model-cycles.

10. A device for the diagnosis of heart failure, comprising:
a processor, configured to:
collect data relating to a plurality of reference episodes, the reference episodes comprising at least one of: electrical activity signals of a myocardium; myocardium hemodynamic activity signals, or indicators reflecting variation of parameters between phases of effort and phases of recovery, wherein the parameters comprise at least one of physical parameters, activity parameters, or hemodynamic phase parameters between phases of effort and phases of recovery;
analyze the plurality of reference episodes based on predefined criteria to assign each of the reference episodes an in-suspicion marker or an off-suspicion marker, wherein the in-suspicion marker indicates a suspicion that the reference episode is associated with cardiac decompensation, wherein the off-suspicion marker indicates a suspicion that the reference episode is not associated with cardiac decompensation, and wherein the reference episodes assigned the in-suspicion marker and the reference episodes assigned the off-suspicion marker are interspersed within the plurality of reference episodes;
generate an in-suspicion model-cycle based on data associated with a plurality of in-suspicion reference episodes to which the in-suspicion marker has been assigned;
generate an off-suspicion model-cycle based on data associated with a plurality of off-suspicion reference episodes to which the off-suspicion marker has been assigned; and
determine whether to generate an early heart failure alert based on a difference between the in-suspicion model-cycle and the off-suspicion model-cycle.

11. The device of claim 10 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one endocardial electrogram beat recorded during an episode fulfilling predetermined conditions of heart rate and patient activity.

12. The device of claim 10 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one beat of an endocardiac acceleration signal recorded during an episode fulfilling predetermined conditions of heart rate and patient activity.

13. The device of claim 10 , wherein the in-suspicion model-cycle or off-suspicion model-cycle comprises at least one minute ventilation versus heart-rate characteristic pattern that was recorded during an episode comprising an effort phase followed by a recovery phase of the patient.

14. The device of claim 10 , further comprising:
a memory;
wherein the processor is further configured to:
update the in-suspicion model-cycle and off-suspicion model-cycle; and
store, in the memory, the updated in-suspicion model-cycle and updated off-suspicion model-cycle.

15. The device of claim 14 , wherein each of the in-suspicion model-cycle and the off-suspicion model-cycle is a combination of a previous model-cycle with at least one older model-cycle.

16. The device of claim 10 , wherein generating the early heart failure alert comprises:
generating at least one index of a clinical condition of a patient, based on the difference between the in-suspicion model-cycle and the off-suspicion model-cycle; and
generating an early heart failure alert based on the at least one index.

17. The device of claim 16 , wherein the at least one index of a clinical condition is updated periodically.

18. The device of claim 16 , wherein the at least one index is calculated based on an average of model-cycles.

19. The device of claim 10 , wherein the device is a pacing, resynchronization, or defibrillation device or an implant for diagnostic purposes.

20. A processor-readable, non-transitory storage medium having instructions stored thereon that, when executed by a processor, cause the processor to:
collect data relating to a plurality of reference episodes, the reference episodes comprising at least one of: electrical activity signals of a myocardium; myocardium hemodynamic activity signals, or indicators reflecting variation of parameters between phases of

Assignees

• Sorin Crm Sas

Inventors

• Dumont Jérôme
• Giorgis Lionel

Classifications

• A61B5/02 Primary

  Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow · CPC title

• A61B5/7221

  Determining signal validity, reliability or quality (preventing, reducing or removing noise induced by motion artefacts A61B5/7207; noise originating from a therapeutic or surgical apparatus A61B5/7217) · CPC title

• A61B5/7275

  Determining trends in physiological measurement data; Predicting development of a medical condition based on physiological measurements, e.g. determining a risk factor · CPC title

• A61B5/0402

  Human Necessities · mapped topic

• A61B5/0205 Primary

  Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition · CPC title