Arrhythmia control system employing arrhythmia recognition algorithm

• US 5,086,772 A
• Filed: 07/30/1990
• Issued: 02/11/1992
• Est. Priority Date: 07/30/1990
• Status: Expired due to Fees

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Telectronics Pacing Systems, Inc (Abbott Laboratories Incorporated)
• Inventors: Routh, Andre G., Larnard, Donald J.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US07/559,295
• Time in Patent Office: 561 Days
• Field of Search: 128/419 D, 128/419 PG, 128/205, 128/206
• US Class Current: 607/4
• CPC Class Codes: A61N 1/3621 for treating or preventing abnormally high heart rate
• CPC Class Codes: A61N 1/39622 Pacing therapy

Abstract

An arrhythmia control method and device are disclosed which monitor the cardiac state of a patient, utilize an arrhythmia recognition algorithm to detect and distinguish among bradycardia, sinus rhythm, supraventricular tachycardia and ventricular fibrillation, and deliver therapy in the form of electrical energy to cardiac tissue to revert selected arrhythmias and restore normal sinus rhythm. In its preferred form the device is an implantable combined dual chamber pacing and cardioverting device that is adapted to be electrically connected to the atrium and ventricle for sensing the atrial and ventricular waveforms and deliverying shock therapy thereto as required. The arrhythmia recognition algorithm utilizes the sensed atrial and ventricular waveform data for, among other things, distinguishing between ventricular tachycardia and supraventricular tachycardia.

Claims

1. A cardioverting device for reverting tachycardia in a patient'"'"'s heart, said device including means for sensing the ventricular waveform of the heart, means for storing data corresponding to said waveform, and means for delivering cardioversion shock therapy to the heart, said device further comprising:

means for detecting event peaks in said waveform and establishing event data windows extending for predetermined time periods relative to each of said event peaks;

means responsive to the detection of an event peak in said waveform for determining the morphology of that portion of said waveform which occurs within said event data window;

means for classifying each of said events based on said morphology, said means outputting in real time at least one of a plurality of different values corresponding to at least one of a plurality of different heart rate categories, including at least a normal rate, a tachycardia rate and a ventricular fibrillation rate;

means for summing the output of said event classifying means during a predetermined number of events, said means outputting in real time at least one of a plurality of different rhythm signals based on said summing and corresponding at least to a non-pathological rhythm, a pathological ventricular tachycardia rhythm and a pathological ventricular fibrillation rhythm; and

,

means responsive to said output summing means for delivering appropriate therapy to the heart when said rhythm signal corresponds to one of said pathological rhythms.

2. A device according to claim 1, further including means for providing antitachycardia pacing to said heart.

3. A device according to claim 2, further including means for providing bradycardia support pacing to said heart.

7. A device according to any one of claims 1 and 4-6, wherein said device includes a microprocessor having a pulse clock timing mechanism therein, wherein said event data windows extend on opposite sides of and for predetermined time periods both before and after each of said event peaks, wherein said predetermined time period of the portion of said event data window occurring after said event peak is about fifty percent longer than said predetermined time period of the portion of said event data window occurring before said event peak, and wherein said predetermined time periods are timed by said pulse clock timing mechanism.

8. A device according to any one of claims 1 and 4-7, wherein said morphology determining means determines the widths and polarities of the R-waves of the heart, and the intervals between such R-waves.

9. A device according to claim 8, wherein said event classifying means utilizes said R-wave width, polarity and interval information to distinguish between ventricular fibrillation signals and noise signals occurring in the ventricular waveform.

10. A device according to anyone of claims 1 and 4-6, wherein the range of values required to be summed by said summing means during said predetermined number of events to output each of said rhythm signals is different from and non-overlapping with the range of values required to be summed during said predetermined number of events for the others of said rhythm signals.

4. An implantable combined dual chamber pacing and cardioverting device adapted to be electrically connected to the atrium and ventricle of a patient'"'"'s heart for the reversion of tachycardias, said device including means for sensing the atrial and ventricular waveforms of the heart, means for storing data relating to said waveforms, and means for delivering cardioversion shock therapy to the heart, said device further comprising:

means for detecting event peaks in said ventricular waveform and establishing event data windows extending for predetermined time periods relative to each of said event peaks;

means responsive to the detection of an event peak in said waveform for determining the morphology of that portion of said ventricular waveform which occurs within said event data window;

means for classifying each of said events based on said morphology, said means outputting in real time at least one of a plurality of different values corresponding to at least one of a plurality of different heart rate categories, including at least a normal rate, a tachycardia rate and a ventricular fibrillation rate;

means for summing the outputs of said event classifying means during a predetermined number of events, said means outputting in real time at least one of a plurality of different rhythm signals based on said summing and corresponding to nonpathological rhythm, a pathological ventricular tachycardia rhythm and a pathological ventricular fibrillation rhythm; and

means responsive to said output summing means for delivering appropriate therapy to the heart when said rhythm signal corresponds to one of said pathological rhythms.

5. An implantable combined dual chamber pacing and cardioverting device adapted to be electrically connected to the atrium and ventricle of a patient'"'"'s heart for the reversion of tachycardias, said device including means for sensing the atrial and ventricular waveforms of the heart, means for storing data relating to said waveforms, and means for delivering cardioversion shock therapy to the heart, said device further comprising:

means for detecting event peaks in said ventricular waveform and establishing event data windows extending for predetermined time periods relative to each of said event peaks;

means responsive to the detection of an event peak in said waveform for determining the morphology of that portion of said ventricular waveform which occurs within said event data window;

means for classifying each of said events based on said morphology, said means outputting in real time at least one of a plurality of different values corresponding to at least one of a plurality of different heart rate categories, including at least a normal rate, a tachycardia rate and a ventricular fibrillation rate;

means for summing the outputs of said event classifying means during a predetermined number of events, said means outputting in real time at least one of a plurality of different rhythm signals based on said summing and corresponding to a non-pathological rhythm, a pathological ventricular tachycardia rhythm and a pathological ventricular fibrillation rhythm; and

,

means responsive to said output summing means for delivering appropriate therapy to the heart when said rhythm signal corresponds to one of said pathological rhythms.

6. A device according to claim 5, further including means for providing bradycardia support pacing to both the atrium and the ventricle.

11. A device according to any one of claims 5-6, wherein said morphology determining means determines the widths and polarities of the R-waves of the heart, the intervals between such R-waves, and the intervals between the P-waves of the heart and the R-waves of the heart.

12. A device according to claim 11, wherein said event classifying means utilizes the information with respect to the interval between the P-wave and the R-wave to distinguish between ventricular tachycardia and supraventricular tachycardia.

13. A device according to claim 12, wherein said event classifying means utilizes said R-wave width, polarity and interval information to distinguish between ventricular fibrillation signals and noise signals occurring in the ventricular waveform.

14. A device according to claim 12, wherein said means for classifying each of the events based on morphology also outputs a value corresponding to a bradycardia rate.

15. A device according to claim 14, wherein said means for summing the outputs of said event classifying means also outputs a rhythm signal based on said summing which corresponds to a bradycardia rate.

16. A device according to claim 12, wherein said means for classifying each of the events based on morphology also outputs a value corresponding to a bradycardia rate.

17. A device according to claim 16, wherein said means for summing the outputs of said event classifying means also outputs a rhythm signal based on said summing which corresponds to a bradycardia rate.

18. A method of reverting tachycardia in the heart of a patient, comprising the following steps:

sensing the ventricular waveform of the heart;

storing data corresponding to said ventricular waveform;

detecting event peaks in said ventricular waveform and establishing event data windows extending for predetermined time periods with respect to each of said event peaks;

in response to the detection of an event peak in said waveform, determining the morphology of that portion of said ventricular waveform which occurs within said event data window;

classifying each of said events based on said morphology and providing in real time a plurality of different rate signals corresponding to at least one of a plurality of different heart rate categories, including at least a normal rate, a tachycardia rate and a ventricular fibrillation rate;

summing said rate signals during a predetermined number of events and providing in real time at least one of a plurality of different rhythm signals based on said summing and corresponding at least to a non-pathological rhythm, a pathological ventricular tachycardia rhythm and a pathological ventricular fibrillation rhythm; and

delivering appropriate electrical shock therapy to the heart when said rhythm signal corresponds to one of said pathological signals.

19. A method according to claim 18, wherein each of said event data windows extends for a predetermined time period both before and after each of said event peaks.

20. A method according to claim 19, wherein the electrical shock therapy is delivered to the ventricle.

21. A method according to claim 20, wherein during the step of determining the morphology of the ventricular waveform, the widths and polarities of the the R-waves of the heart, and the intervals between said such R-waves, are determined.

22. A method according to claim 18, including the steps of sensing the atrial waveform of the patient'"'"'s heart and storing data corresponding to said atrial waveform.

23. A method according to claim 22, wherein each of said event data windows extends for a predetermined time period both before and after each of said event peaks.

24. A method according to claim 23, wherein the electrical shock therapy is delivered to both the atrium and the ventricle.

25. A method according to claim 24, wherein during the step of determining the morphology of the ventricular waveform, the widths and polarities of the R-waves of the heart, the intervals between said R-waves, and the intervals between the P-waves and the R-waves of the heart are determined.

26. A method according to any one of claims 21 and 25, wherein during the step of classifying each of the events based on morphology, said R-wave width, polarity and interval information is utilized to distinguish between ventricular fibrillation signals and noise signals occurring in said ventricular waveform.

27. A method according to claim 25, wherein during the step of classifying each of the events based on morphology, said information with respect to the interval between the P-wave and the R-wave of the patient'"'"'s heart is utilized to distinguish between ventricular tachycardia and supraventricular tachycardia.

28. A method according to claim 27, wherein during the step of classifying each of the events based on morphology, said R-wave width, polarity and interval information is utilized to distinguish between ventricular fibrillation signals and noise signals occurring in said ventricular waveform.

29. A method according to any one of claims 18-25, 27 and 28, wherein during the step of providing a plurality of different rate signals corresponding to different heart rate categories, a rate signal corresponding to a bradycardia rate is also provided.

30. A method according to claim 29, wherein during said step of providing a plurality of different rhythm signals based on the summing of said rate signals, a rhythm signal corresponding to a bradycardia rhythm is also provided.

31. A method according to any one of claims 18-25, 27 and 28, wherein the range of rate signals required to be summed during said predetermined number of events to provide each of said rhythm signals is different from and non-overlapping with the range of rate signals required to be summed during said predetermined number of events for the others of said rhythm signals.