Dual-chamber implantable pacemaker having an adaptive AV interval that prevents ventricular fusion beats and method of operating same

• US 5,334,220 A
• Filed: 11/13/1992
• Issued: 08/02/1994
• Est. Priority Date: 11/13/1992
• Status: Expired due to Term

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Siemens Pacesetter, Inc. (Abbott Laboratories)
• Inventors: Sholder, Jason A.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US07/976,153
• Time in Patent Office: 627 Days
• Field of Search: 128/419 PG
• US Class Current: 607/9
• CPC Class Codes: A61N 1/3627 for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy
• CPC Class Codes: A61N 1/36585 controlled by two or more physical parameters
• CPC Class Codes: A61N 1/3682 with a variable atrioventricular delay

Abstract

A dual-chamber implantable pacemaker automatically adjusts its AV interval so that any ventricular stimulation pulses generated by the pacemaker at the conclusion of the pacemaker-defined AV interval occur at a time in the cardiac cycle that avoids fusion with the natural ventricular depolarization of a patient'"'"'s heart. The AV interval is set using a search sequence that sets the AV interval value to be on one side or the other of the natural conduction time of the heart, and incrementally changes the AV interval value until it crosses over the natural conduction time interval. The cross-over point is manifest by the occurrence of an R-wave, where an R-wave had previously been absent, or the absence of an R-wave, where an R-wave had previously been present. A final AV interval value is then set as the AV interval value at the cross-over point, adjusted by appending an AV margin thereto. The search sequence is automatically invoked whenever a prescribed search time has elapsed, or whenever the sudden presence or absence of a sensed R-wave indicates a sufficient change in the natural conduction time so as to have crossed over with the existing AV interval. If the search sequence is invoked too frequently, it is automatically suspended for a prescribed suspension period.

Claims

1. An implantable pacemaker comprising:

atrial sensing means for sensing an atrial depolarization (P-wave);

atrial pacing means for generating an atrial stimulation pulse (A-pulse);

ventricular sensing means for sensing a ventricular depolarization (R-wave), and;

ventricular pacing means for generating a ventricular stimulation pulse (V-pulse);

means for storing operating instructions and control parameters; and

controlling means coupled to said storing means, said atrial and ventricular sensing means and said atrial and ventricular pacing means for coordinating the operation of said atrial and ventricular sensing means, and said atrial and ventricular pacing means, in accordance with said operating instructions and said control parameters, said controlling means comprising;

first timing means for defining an AV interval;

second timing means for defining an atrial escape interval;

third timing means for measuring a conduction time interval, said conduction time interval comprising the time between atrial activity and sensing an R-wave, atrial activity comprising either of sensing a P-wave and generating an A-pulse;

first logic means for triggering said ventricular pacing means at the conclusion of said AV interval only in the event an R-wave is not sensed during said AV interval, said AV interval commencing with said atrial activity;

second logic means for triggering said atrial pacing means at the conclusion of said atrial escape interval only in the event a P-wave is not sensed during said atrial escape interval; and

adjustment means for automatically adjusting said AV interval to a value that is different than said conduction time interval;

whereby V-pulses that are generated by said pacemaker are generated at a time that is different than said conduction time, thereby avoiding fusion between said V-pulses and said R-waves.

2. The implantable pacemaker, as set forth in claim 1, having an existing AV interval value, wherein said control parameters include parameters stored therein defining a maximum AV interval value, a minimum AV interval value, an adjustment time period value, an initial AV adjustment value, and an incremental difference value, and wherein said adjustment means further comprises:

first means for changing the value of said AV interval from said existing AV interval value to said initial AV adjustment value for said adjustment time period;

second means for changing the value of said AV interval in stair-step fashion, with said AV interval assuming a new AV interval value that differs from the preceding AV interval value by said incremental difference value for each of a plurality of subsequent adjustment time periods, said initial AV adjustment value and new AV interval values always being within the range defined by said maximum AV interval value and said minimum AV interval value;

means for determining if there is a change in the type of ventricular activity that occurred in the most recent adjustment time period compared to the type of ventricular activity that occurred in the adjustment time period just prior to the most recent adjustment time period; and

means for setting a final AV adjustment value as a function of the AV interval value used in the most recent adjustment time period for which a change was detected in the type of ventricular activity that occurred.

3. The implantable pacemaker, as set forth in claim 2, wherein said pacemaker is programmably configurable to operate in at least a first mode and a second mode, said setting means further comprising:

first mode means setting said final AV adjustment value to a value that is greater than said conduction time interval by a specified amount, said first mode means active when said pacemaker is programmably configured to operate in said first mode, whereby an R-wave will normally occur before the termination of said AV interval; and

second mode means setting said final AV adjustment value to a value that is less than said conduction time interval by a specified amount, said second mode means active when said pacemaker is programmably configured to operate in said second mode, whereby a V-pulse will normally be generated prior to occurrence of an R-wave.

4. The implantable pacemaker, as set forth in claim 3, wherein said initial AV adjustment value comprises said minimum AV interval value when said pacemaker is programmably configured to operate in said first mode;

and comprises said maximum AV interval value when said pacemaker is programmably configured to operate in said second mode.

5. The implantable pacemaker, as set forth in claim 3, wherein said final AV adjustment value is set by said setting means to be the AV interval value used in the most recent adjustment time period for which a change was detected in the type of ventricular activity that occurred plus:

(1) a positive AV margin for a pacemaker configured in said first mode, whereby the final AV adjustment value is longer than the AV interval value used in the most recent adjustment time period, and (2) a negative AV margin for a pacemaker configured in said second mode, whereby the final AV adjustment value is shorter than the AV interval value used in the most recent adjustment time period.

6. (amended) implantable pacemaker, as set forth in claim 5, wherein said AV margin comprises a multiple of said incremental difference value.

7. The implant able pacemaker, as set forth in claim 6, wherein said AV margin comprises one said incremental difference value.

8. The implantable pacemaker, as set forth in claim 2, wherein said adjustment means adjusts the AV interval value whenever each of the following occurs:

(1) there is a change in the type of ventricular activity that occurs at a time when the AV interval value is not being adjusted, and (2) a search interval, T_S, times-out;

said search interval, T_S, beginning upon the setting of said AV interval value to its initial AV adjustment value by said first changing means, and concluding a programmable search time interval thereafter.

9. The implantable pacemaker, as set forth in claim 8, wherein said search interval, T_s, comprises 1-72 hours.

10. The implantable pacemaker, as set forth in claim 2, wherein said adjustment means further comprises:

means for monitoring the time interval between successive changings by said first changing means of the AV interval value; and

means for automatically changing the final AV adjustment value to increase the difference between it and the conduction time in the event the time interval between said successive changings is less than a prescribed threshold.

11. The implantable pacemaker, as set forth in claim 10, wherein said prescribed threshold comprises 10-30 cardiac cycles, where a cardiac cycle comprises the time interval between consecutive ventricular activity.

12. The implantable pacemaker, as set forth in claim 2, wherein said prescribed adjustment time period comprises at least one cardiac cycle, a cardiac cycle comprising the time interval between consecutive ventricular activity.

13. The implantable pacemaker, as set forth in claim 12, wherein the prescribed adjustment time period comprises one cardiac cycle.

14. An implantable dual-chamber pacemaker that automatically adjusts its AV interval and avoids fusion between the generation of a ventricular stimulation pulse (V-pulse), at the conclusion of said AV interval, and the occurrence of natural ventricular depolarization, as evidenced by the occurrence of an R-wave, said pacemaker comprising:

means for sensing atrial activity in an atrial channel;

means for sensing an R-wave and generating said V-pulse; and

first control means for defining said AV interval as the longest time interval the pacemaker will allow from the occurrence of atrial activity until the generation of a V-pulse, the occurrence of an R-wave during said AV interval causing the generation of a V-pulse to be inhibited;

second control means for recognizing a need to adjust said AV interval from its present value to a new value;

third control means for adjusting said AV interval from its present value to an intermediate value, when an adjustment in the AV interval is needed, following a prescribed adjustment sequence;

forth control means for determining when in the adjustment sequence the AV interval crosses over an AR interval, said AR interval comprising the time interval between atrial activity and sensing an R-wave, and thereby representing a measure of the natural conduction time of a heart to which said pacemaker is coupled; and

fifth control means for setting the new AV value of said pacemaker to a value that is a prescribed difference from said AR interval;

whereby a V-pulse and an R-wave will not occur at the same time, thereby avoiding fusion, even though the AV interval is automatically adjusted when needed.

15. The dual-chamber pacemaker, as set forth in claim 14, wherein said pacemaker further comprises a sixth control means for defining a programmable search interval, T_S, that begins upon the starting of said prescribed adjustment sequence, and wherein said control means begins said prescribed adjustment sequence whenever either one of two events occur;

the first event comprising a change in the type of ventricular activity, i.e., an R-wave or a that occurs during a current cardiac cycle as compared to the type of ventricular activity that occurred during an immediately preceding cardiac cycle, where a cardiac cycle comprises the time interval between consecutive ventricular activity;

the second event comprising the timing out of said search interval, T_S.

16. The dual-chamber pacemaker, as set forth in claim 15, wherein said programmable search interval comprises at least 30 minutes.

17. The dual-chamber pacemaker, as set forth in claim 15, wherein said prescribed adjustment sequence comprises a multi-step sequencing means, wherein said AV interval assumes a prescribed value during each step, and wherein each step lasts a prescribed time interval.

18. The dual-chamber pacemaker, as set forth in claim 17, wherein said multi-step sequencing means comprises a stair-step sequencing means wherein said AV interval assumes an initial starting value, and thereafter assumes in each step a succeeding value that is a prescribed difference from the AV interval value of the prior step.

19. The dual-chamber pacemaker, as set forth in claim 15, wherein said pacemaker further comprises a seventh control means for automatically increasing the prescribed difference between the new AV interval of an adjustment sequence and said AR interval in the event said adjustment sequence begins a second time within a defined time period.

20. A method of operating a dual-chamber pacemaker to avoid fusion between a ventricular stimulus (V-pulse) and an R-wave, said pacemaker having means for sensing atrial activity, means for sensing an R-wave and means for generating said V-pulse;

and control means for defining said AV interval as the longest time interval the pacemaker will allow from the occurrence of atrial activity until the generation of a V-pulse, the occurrence of an R-wave during said AV interval causing the generation of a V-pulse to be inhibited;

said method comprising the steps of;

(a) generating an A-pulse in the atrium in the absence of said sensed atrial activity;

(b) adjusting said AV interval from its present value to an adjustment start value;

(c) incrementally adjusting the value of said AV interval from its adjustment start value in a direction back towards said first value in prescribed increments, with each prescribed increment comprising a specified change in the duration of said AV interval in the adjustment direction, and with each adjusted value of said AV interval being used in a specified incremental time period that includes at least one cardiac cycle;

(d) monitoring for ventricular activity during each of said specified incremental time periods, said activity comprising either an R-wave and the presence of a V-pulse;

(e) detecting the approximate duration of an AR interval from the monitoring performed in step (d), said AR interval defining the time period between atrial activity and the occurrence of an R-wave;

(f) setting the final value of said AV interval to be different from the AR interval detected in step (e); and

(g) generating a V-pulse in the absence of a sensed R-wave during said AV interval;

whereby said AV interval is automatically adjusted to a value that avoids fusion between said V-pulse and said R-wave.

21. The method, as set forth in claim 20, wherein step (e) comprises detecting whether said ventricular activity during the most recent incremental time period is different from said ventricular activity from the incremental time period immediately preceding said most recent incremental time period, whereby the approximate value of said AR interval is known to lie between the value of the AV interval used in the most recent incremental time period and the value of the AV interval used in the immediately preceding incremental time period when said detecting indicates a difference.

22. The method, as set forth in claim 21, wherein step (f) comprises setting the final value of the AV interval to be equal to the AV interval value used in the most recent incremental time period modified by a prescribed margin value.

23. A method of adjusting the AV interval of a dual-chamber pacemaker, said pacemaker including atrial pulse generation means for generating an atrial stimulation pulse (A-pulse), ventricular pulse generation means for generating a ventricular stimulation pulse (V-pulse), atrial sensing means for sensing a natural atrial depolarization (P-wave), ventricular sensing means for sensing a natural ventricular depolarization (R-wave), and control means for controlling said atrial and ventricular pulse generation means in response to timed intervals, including an AV interval, generated by said control means, and in response to said atrial and ventricular sensing means;

said AV interval comprising a pacemaker-defined time period that starts with atrial activity, comprising an A-pulse or a P-wave, whichever occurs first, and ends with the generation of a V-pulse providing an R-wave does not occur prior to the termination of said AV interval;

said method comprising the steps of;

(a) generating an A-pulse in the absence of said sensed atrial activity;

(b) changing said AV interval from its present first value, AV₀, to a prescribed adjustment starting value, AV₁ ;

(c) incrementally adjusting said AV interval from the prescribed adjustment starting value AV₁ back towards the first value AV₀ value in prescribed step sizes;

(d) making a determination after each incremental adjustment of the AV interval in step (c) as to whether an R-wave is thereafter sensed by the ventricular sensing means prior to the termination of the AV interval; and

(e) stopping the adjustment of said AV interval as soon as the determination made in step (d) indicates a change in said determination, said change comprising one of either;

(1) determining that an R-wave is sensed after the most recent adjustment of the AV interval when an R-wave was not previously sensed prior to the most recent adjustment of the AV interval, and (2) determining that an R-wave is not sensed after the most recent adjustment of the AV interval when an R-wave was previously sensed prior to the most recent adjustment of the AV interval;

(f) generating a V-pulse in the absence of a sensed R-wave during said AV interval;

whereby said AV interval is adaptively changed to a value that is close to, but not the same as, the time period between atrial activity and an R-wave;

whereby fusion between an R-wave and a V-pulse is avoided.