System and method for far-field R-wave detection

• US 6,934,585 B1
• Filed: 06/21/2002
• Issued: 08/23/2005
• Est. Priority Date: 06/21/2002
• Status: Expired due to Fees

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Inventors: Mai, Junyu, Schloss, Harold C.
• Primary Examiner(s): Getzow, Scott M.
• Application Number:
  US10/176,554
• Time in Patent Office: 1,159 Days
• Field of Search: 607 4- 30
• US Class Current: 607/9
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/37 Monitoring; Protecting

Abstract

A system and corresponding method are disclosed for discriminating between far field R-waves and actual atrial events that are sensed on an atrial sense channel. In one embodiment, such information is used to prevent mode switching. In another embodiment, the information is used to extend an atrial blanking period so that the far field R-waves are no longer sensed on an atrial channel.

Claims

1. In an implantable cardiac stimulation device, a method comprising:

sensing a plurality of ventricular events and atrial events;

calculating a plurality of ventricular-to-atrial interval values based on the sensed ventricular and atrial events;

processing the interval values to determine if the interval values are substantially constant; and

initiating a predetermined action if the interval values are substantially constant;

wherein initiating a predetermined action comprises preventing mode switching.

2. In an implantable cardiac stimulation device, a method comprising:

sensing a plurality of ventricular events and atrial events;

calculating a plurality of ventricular-to-atrial interval values based on the sensed ventricular and atrial events;

processing the interval values to determine if the interval values are substantially constant;

initiating a predetermined action if the interval values are substantially constant; and

determining if the patient is at an increased activity level, and performing the acts of sensing, calculating, processing, and initiating only if the patient is at an increased activity level.

3. The method of claim 2, wherein sensing ventricular events comprises sensing intrinsic ventricular events.

4. The method of claim 2, wherein sensing ventricular events comprises monitoring for ventricular pacing pulses.

5. The method of claim 2, wherein processing the interval values comprises calculating an averaged deviation value based on the plurality of interval values.

6. The method of claim 2, wherein sensing atrial events comprises defining a detection window based on a sensed ventricular event, and monitoring for an atrial event occurring within the detection window.

7. The method of claim 2, wherein calculating interval values comprises calculating interval values for at least four pairs of ventricular and atrial events.

8. The method of claim 2, wherein initiating a predetermined action comprises extending an atrial blanking period.

9. The method of claim 2, wherein calculating interval values comprises calculating interval values for all pairs of ventricular and atrial events occurring within a predetermined duration.

10. The method of claim 2, further comprising storing the interval values as diagnostic data, and transmitting the diagnostic data to an external device.

11. The method of claim 2, wherein processing comprises calculating an averaged deviation for the interval values, and comparing the averaged deviation with a threshold value.

12. The method of claim 11, wherein the threshold value is on the order of approximately 20 milliseconds.

13. In an implantable cardiac stimulation device, a method comprising:

sensing a plurality of ventricular events and subsequent atrial events;

calculating interval values between the ventricular events and subsequent atrial events for a plurality of pairs of events;

processing the interval values to determine if the interval values are substantially constant;

extending an atrial blanking period if the interval values are substantially constant; and

stopping an ongoing mode switch if the interval values are substantially constant.

14. The method of claim 13, wherein sensing ventricular events comprises sensing intrinsic ventricular events.

15. The method of claim 13, wherein extending an atrial blanking period comprises extending an atrial blanking period following intrinsic ventricular events.

16. The method of claim 13, wherein sensing ventricular events comprises monitoring for ventricular pacing pulses.

17. The method of claim 16, wherein extending an atrial blanking period comprises extending an atrial blanking period following ventricular pacing pulses.

18. The method of claim 13, wherein processing the interval values comprises calculating an averaged deviation value based on the plurality of interval values, and comparing the averaged deviation with a predetermined threshold value.

19. The method of claim 18, wherein the threshold value is on the order of approximately 20 milliseconds.

20. The method of claim 13, wherein sensing subsequent atrial events comprises defining a detection window based on a sensed ventricular event, and monitoring for an atrial event occurring within the detection window.

21. The method of claim 13, wherein calculating interval values comprises calculating interval values for at least four pairs of ventricular and atrial events.

22. The method of claim 13, wherein calculating interval values comprises calculating interval values for all pairs of ventricular and atrial events occurring within a predetermined duration of time.

23. The method of claim 22, wherein calculating interval values comprises calculating interval values for all pairs of ventricular and atrial events occurring within a period of about ten seconds.

24. In an implantable cardiac stimulation device, a method comprising:

sensing a plurality of ventricular events and subsequent atrial events;

calculating interval values between the ventricular events and subsequent atrial events for a plurality of pairs of events;

processing the interval values to determine if the interval values are substantially constant; and

extending an atrial blanking period if the interval values are substantially constant; and

determining if the patient is at an increased activity level, and performing the acts of sensing, calculating, processing, and extending only if the patient is at an increased activity level.

25. In an implantable cardiac stimulation device, a method comprising:

sensing a plurality of ventricular events and subsequent atrial events;

calculating interval values between the ventricular events and subsequent atrial events for a plurality of pairs of events;

processing the interval values to determine if the interval values are substantially constant; and

preventing mode switching if the interval values are substantially constant.

26. The method of claim 25, wherein sensing ventricular events comprises sensing intrinsic ventricular events.

27. The method of claim 25, further comprising extending an atrial blanking period if the interval values are substantially constant.

28. The method of claim 25, wherein sensing ventricular events comprises sensing paced ventricular events.

29. The method of claim 25, wherein processing the interval values comprises calculating an averaged deviation value based on the plurality of interval values, and comparing the averaged deviation value with a predetermined threshold value.

30. The method of claim 29, wherein the threshold value is on the order of approximately 20 milliseconds.

31. The method of claim 25, further comprising determining if the patient is at an increased activity level, and performing the acts of sensing, calculating, processing, and preventing only if the patient is at an increased activity level.

32. The method of claim 25, wherein sensing subsequent atrial events comprises defining a detection window based on a sensed ventricular event, and monitoring for an atrial event occurring within the detection window.

33. The method of claim 25, wherein calculating interval values comprises calculating interval values for at least four pairs of ventricular and atrial events.

34. The method of claim 25, wherein calculating interval values comprises calculating interval values for all pairs of ventricular and atrial events occurring within a predetermined duration.

35. The method of claim 34, wherein calculating interval values comprises calculating interval values for all pairs of ventricular and atrial events occurring within a period of about ten seconds.

36. An implantable cardiac stimulation device comprising:

sensing circuitry that is operative to sense a plurality of ventricular events and subsequent atrial events; and

control circuitry that is operative to calculate interval values, between a ventricular event and a subsequent atrial event, for a plurality of pairs of events, to compare the plurality of interval values to determine if the interval values are substantially stable, and to take predetermined action if a stable interval exists;

wherein the control circuitry is operative to determine if the patient is at an increased activity level, and is responsive to the patient not being at the increased activity level to ignore the interval values.

37. The device of claim 36, wherein the sensing circuitry is operative to sense intrinsic ventricular events.

38. The device of claim 36, wherein the control circuitry is operative to calculate an averaged deviation value based on the plurality of interval values, and to compare the averaged deviation value with a predetermined threshold value.

39. The device of claim 38, wherein the threshold value is on the order of approximately 20 milliseconds.

40. The device of claim 36, wherein the control circuitry is operative to define a detection window based on a sensed ventricular event, and monitor for an atrial event occurring within the detection window.

41. The device of claim 36, wherein the control circuitry is operative to calculate interval values for at least four pairs of ventricular and atrial events.

42. The device of claim 36, wherein the control circuitry is operative to extend an atrial blanking period if far-field sensing exists.

43. The device of claim 36, wherein the control circuitry is operative to calculate interval values for all pairs of ventricular and atrial events occurring within a predetermined duration.

44. The device of claim 36, wherein the control circuitry is further operative to generate diagnostic data from the sensed events, and further comprising telemetry circuitry that is operative to transmit the diagnostic data to an external device.

45. An implantable cardiac stimulation device comprising:

sensing circuitry that is operative to sense a plurality of ventricular events and subsequent atrial events; and

control circuitry that is operative to calculate interval values, between a ventricular event and a subsequent atrial event, for a plurality of pairs of events, to compare the plurality of interval values to determine if the interval values are substantially stable, and to take predetermined action if a stable interval exists;

wherein the control circuitry is operative to prevent mode switching if far-field sensing exists.

46. An implantable cardiac device comprising:

means for sensing ventricular and atrial events;

means for calculating a plurality of ventricular-to-atrial interval values;

means for ignoring the interval values if the patient is not at an increased activity level;

means for determining if the interval values are substantially constant; and

means for initiating a predetermined action if the interval values are substantially constant.