Apparatus and method for treating ventricular tachyarrhythmias

• US 8,046,068 B2
• Filed: 04/20/2009
• Issued: 10/25/2011
• Est. Priority Date: 04/30/1997
• Status: Expired due to Fees

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Krig, David B., Dreher, Robert D., Wald, Jan D., Gilkerson, James O., Linder, William J., Zimmer, William L.
• Primary Examiner(s): EVANISKO, GEORGE ROBERT
• Application Number:
  US12/386,567
• Publication Number:
  US 20090234400A1
• Time in Patent Office: 918 Days
• Field of Search: 607/4, 607/5, 607/9, 607/14, 600515-518
• US Class Current: 607/14
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/395 for treating atrial fibrillation
• CPC Class Codes: A61N 1/39622 Pacing therapy

Abstract

A system and method for selectively treating a ventricular tachycardia based on sensed atrial and ventricular intervals from the patient'"'"'s heart. A detection window of the ten most recent atrial and ventricular intervals are analyzed for the occurrence of either tachycardia or fibrillation. When a majority of the sensed intervals are satisfied, the apparatus starts a duration time interval. Ventricular intervals and atrial intervals are compare, ventricular interval greater than the atrial interval by a bias factor the system delivers tachycardia therapy to the heart. Alternatively, the method withholds tachycardia therapy to the heart when the atrial rate is classified as atrial fibrillation and the ventricular response is unstable.

Claims

1. A method, comprising:

sensing atrial and ventricular events representative of cardiac rhythms;

determining ventricular intervals using the sensed ventricular events;

detecting a ventricular tachyarrhythmia using the ventricular intervals and predetermined rate zones;

starting a first time interval in response to the ventricular tachyarrhythmia being detected in a predetermined tachycardia rate zone of the predetermined rate zones;

determining whether at least a predetermined percentage of the ventricular intervals during a detection window are classified as fast ventricular intervals in the predetermined tachycardia rate zone;

analyzing the cardiac rhythms during the first time interval to assess an origin of the ventricular tachyarrhythmia;

resetting the first time interval in response to the at least the predetermined percentage of the ventricular intervals during the detection window not being classified as the fast ventricular intervals; and

delaying or inhibiting a ventricular tachycardia therapy at an end of the first time interval if the origin of the ventricular tachyarrhythmia is in an atrium.

2. The method of claim 1, wherein analyzing the cardiac rhythms includes:

determining an average atrial rate from the sensed atrial events and determining an average ventricular rate from sensed ventricular events; and

determining whether the average ventricular rate is not greater than the average atrial rate by at least a bias factor during the first time interval.

3. The method of claim 1, wherein analyzing the cardiac rhythms includes:

determining a ventricular rate from sensed ventricular events;

determining an onset rate, the onset rate being the rate of transition of a ventricular rate from a slower sinus rate to a tachycardia rate; and

determining whether the onset rate is equal to or greater than an onset threshold value.

4. The method of claim 1, wherein analyzing the cardiac rhythms includes:

determining a ventricular rate from sensed ventricular events; and

determining whether the ventricular rate is unstable, wherein the ventricular rate is unstable when an average variance of ventricular intervals exceeds a stability interval threshold value.

5. The method of claim 4, wherein analyzing the cardiac rhythms further includes determining an occurrence of atrial fibrillation from the sensed atrial events.

6. The method of claim 1, further comprising starting the first time interval programmed for a duration associated with the predetermined tachycardia rate zone.

7. The method of claim 1, further comprising

delivering ventricular tachycardia therapy at the end of the first time interval if the origin of the ventricular tachyarrhythmia is in a ventricle and if the at least the predetermined percentage of the ventricular intervals during the detection window are within the predetermined tachycardia rate zone during the first time interval.

8. An implantable cardioverter-defibrillator, comprising:

sensing circuitry adapted to sense atrial and ventricular events representative of cardiac rhythms;

therapy delivery circuitry adapted to apply or inhibit a ventricular tachycardia therapy; and

control circuitry coupled to the sensing circuitry and therapy circuitry, the control circuitry adapted to;

determine ventricular intervals using the sensed ventricular events;

detect a ventricular tachyarrhythmia using the ventricular intervals and predetermined rate zones;

start a first time interval in response to the ventricular tachyarrhythmia being detected using a predetermined tachycardia rate zone of the predetermined rate zones;

determine whether at least a predetermined percentage of the ventricular intervals during a detection window are fast ventricular intervals in the predetermined tachycardia rate zone;

reset the first time interval in response to a determination that the at least the predetermined percentage of the ventricular intervals during the detection window are not the fast ventricular intervals;

analyze the cardiac rhythms during the first time interval to assess an origin of the ventricular tachyarrhythmia; and

delay or inhibit the ventricular tachycardia therapy at an end of the first time interval if the origin of the ventricular tachyarrhythmia is in an atrium.

9. The implantable cardioverter-defibrillator of claim 8, wherein the control circuitry is adapted to:

determine an average atrial rate from the sensed atrial events;

determine an average ventricular rate from the sensed ventricular events; and

determine whether the average ventricular rate is not greater than the average atrial rate by at least a bias factor.

10. The implantable cardioverter-defibrillator of claim 9, wherein the therapy delivery circuitry is adapted to inhibit the ventricular tachycardia therapy if the average ventricular rate is not greater than the average atrial rate by at least the bias factor.

11. The implantable cardioverter-defibrillator of claim 8, wherein the control circuitry is adapted to determine whether an onset rate is gradual during the first time interval, wherein the onset rate is the rate of transition of a ventricular rate from a slower sinus rate to a tachycardia rate and the onset rate is gradual when the onset rate is equal to or greater than an onset threshold value, and wherein the therapy delivery circuitry is adapted to inhibit the ventricular tachycardia therapy when the onset rate is gradual.

12. The implantable cardioverter-defibrillator of claim 8, wherein the control circuitry is adapted to determine whether the ventricular rate is unstable, wherein the ventricular rate is unstable when an average variance of ventricular intervals exceeds a stability interval threshold value, and wherein the therapy delivery circuitry is adapted to inhibit the ventricular tachycardia therapy when the ventricular rate is unstable.

13. The implantable cardioverter-defibrillator of claim 12, wherein the control circuitry is adapted to determine an occurrence of atrial fibrillation from the sensed atrial events, and wherein the therapy delivery circuitry is adapted to inhibit the ventricular tachycardia therapy if the ventricular rate is unstable and atrial fibrillation is occurring.

14. The implantable cardioverter-defibrillator of claim 8,

wherein the therapy delivery circuitry is adapted to deliver the ventricular tachycardia therapy at the end of the first time interval if the origin of the a ventricular tachyarrhythmia is in a ventricle and if the at least the predetermined percentage of the ventricular intervals during the detection window are within the predetermined tachycardia rate zone during the first time interval.