Dual chamber pacemaker

• US 4,539,991 A
• Filed: 02/11/1983
• Issued: 09/10/1985
• Est. Priority Date: 02/11/1983
• Status: Expired due to Term

• Current Assignee: Vitatron Medical BV
• Original Assignee: Vitafin N.V.
• Inventors: Wittkampf, Frederik H. M., van Arragon, Gerrit W., Boute, Wim
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US06/465,890
• Time in Patent Office: 942 Days
• Field of Search: 128/419 PG
• US Class Current: 607/9
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions

Abstract

An improved cardiac pacemaker adapted to be programmed into one of a plurality of given modes of operation, including dual chamber modes, and in particular synchronous operation for pacing the patient'"'"'s ventricle following detection of natural atrial heartbeats. The pacemaker has means for monitoring the time relationship between delivered ventricular stimulus pulses and next succeeding atrial heartbeats, for determining the occurrence of pacemaker induced retrograde P waves, or pacemaker caused tachycardia. The timing, and thus the rate of sensed P signals is processed to determine the desirability of establishing a special P sense window for looking for the occurrence of P signals at rates above a normal maximum operating rate, in which event the stability of the V-A timing is monitored in accordance with predetermined criteria to determine the existence of pacemaker mediated tachycardia, which may be broken up by skipping a ventricular stimulus. During detection of atrial beats at a rate higher then the predetermined maximum operating rate, the synchronous ventricular stimulus rate is maintained at an average at or below the maximum rate, while maintaining a substantially constant A-V interval.

Claims

1. A cardiac pacemaker having atrial terminal means for connection thereto of P signals representing atrial heartbeats and ventricular terminal means for connection thereto of generated ventricular stimulus Vst pulses, ventricular pulse generating means for generating and connecting said Vst pulses to said ventricular terminal means, atrial sensing means for sensing P signals connected to said atrial terminal means from the patient'"'"'s heart,

measuring means for measuring when a sensed P signal follows a connected Vst pulse by a V-A time which is within a predetermined range,

counting means for counting the number of successive P signals having a V-A time within said predetermined range, and

skipping means for causing skipping of sensing of the next P signal within said predetermined range following sensing of a P signal which is counted as the nth successive P signal by said counting means, where n is a predetermined number.

2. The pacemaker as described in claim 1, further comprising P rate means for determining a measure of the rate of sensed P signals, wherein said means for counting further comprises initiating means for initiating counting only when said P signal rate is determined to meet at least a predetermined criterion.

3. The pacemaker as described in claim 1, wherein said measuring means comprises window logic means for measuring when a sensed P signal occurs within a time window W corresponding to said predetermined range, and enabling means for enabling said window logic means as a function of a sensed physiological P signal within a physiological time window corresponding to a lower range of rates then that of said window W.

4. The pacemaker as defined in claim 3, having pacemaker timing means for timing out pacemaker cycles, said timing means being re-cycled to initiate a new pacing cycle normally upon the occurrence of each atrial signal, and means for modifying said timing means to initiate a new cycle only at the end of said time window W when a P signal is sensed within said time window W.

5. The pacemaker as described in claim 4, comprising means for normally timing out an A-V interval T_AV following sensing of a P signal, and means for causing said ventricular pulse generating means to generate a stimulating pulse at the end of the timed out T_AV, further comprising means for reducing T_AV to less than said normal T_AV following the sensing of a P signal within said time window W.

6. The pacemaker as described in claim 5, wherein T_AV is reduced by about one-half the time of said time window W when it is reduced.

7. The pacemaker as described in claim 3, comprising means for detecting the occurrence of a PVC, and means for disabling said window logic means following the occurrence of a PVC.

8. The pacemaker as described in claim 1, comprising means for processing sensed P signals having rates below a predetermined maximum rate corresponding to the end of the normal atrial refractory period, and further having means for adjusting said maximum rate as a predetermined function of such sensed processed P signal rates.

9. The pacemaker as described in claim 1, comprising second window means for timing out an evaluation window, and wherein said initiating means comprises means for determining when a sensed P signal appears within said evaluation window.

10. The pacemaker as described in claim 9, wherein said measuring means comprises first window means for timing out a first time window corresponding to said predetermined range, said second time window following said first time window.

11. A dual chamber cardiac pacemaker, having means for sensing atrial heartbeats and means for delivering ventricular stimulus pulses, comprising

monitoring means for monitoring the time relationships between said ventricular stimulus pulses and the respective succeeding atrial heartbeats of the patient, means for storing data reflective of a plurality of said monitored time relationships, and means for determining the occurrence of pacemaker mediated tachycardia in accordance with said data, and

means for altering pacer operation in response to the determining of a said occurrence.

12. The dual chamber pacemaker as described in claim 11, wherein said means for altering normal pacer operation inhibits delivery of a ventricular stimulus pulse at the normal A-V time following a sensed atrial heartbeat signal when there has been a determination of pacemajer mediated tachycardia.

13. A cardiac pacemaker having cyclical means for cyclically sensing P signals representative of a patient'"'"'s atrial heartbeats and generating stimulus pulses for delivery to a patient'"'"'s ventricle, further comprising

means for measuring the stability of the V-A intervalbetween a delivered ventricular stimulus pulse and the next succeeding atrial heartbeat and for determining the existence of tachycardia as a predetermined criteria of said measured V-A internal stability, said means for measuring including means for measuring the occurrence of a plurality of P signals each occurring within a predetermined time window following a respective prior ventricular stimulus pulse, and

means for changing the operation of said cyclical means over at least a portion of a cycle following determination of the existence of tachycardia.

14. The pacemaker as described in claim 13, wherein said means for changing controls said cyclical means to skip generation of a stimulus pulse which would normally be generated following sensing of a P signal.

15. The pacemaker as described in claim 13, wherein said means for changing controls said cyclical means to disable sensing of the next normally due P signal if it occurs at a V-A interval with a predetermined time range.

16. The cardiac pacemaker as described in claim 13, in combination with an atrial lead for connnection directly to a patient'"'"'s atrium, and a ventricular lead for connection directly to the patient'"'"'s ventricle.

17. The cardiac pacemaker as described in claim 16, comprising control means for operating in A-V synchronous operation and having program means for receiving program signals to place said pacemaker into A-V synchronous operation.

18. The cardiac pacemaker as described in claim 13, wherein said means for measuring stability of the V-A interval comprises means for measuring said interval over a plurality of successive cycles of operation.

19. The cardiac pacemaker as described in claim 18, wherein said means for measuring includes means for determining the average value of said V-A interval over a predetermined number of cycles of operation.

20. The cardiac pacemaker as described in claim 17, wherein said means for measuring comprises means for determining the occurrence of V-A intervals within a predetermined time range corresponding to pacemaker mediated tachycardia.

21. A dual chamber cardiac pacemaker for pacing a patient in at least an A-V synchronous mode, having means for sensing P signals, A-V timeout means for timing out an A-V delay following a sensed P signal, said A-V delay normally being a predetermined time T_AV, and means for generating a ventricular stimulus pulse for delivery to the patient at the time out of a said A-V delay,

further comprising means for timing out an atrial refractory period following each sensed P signal, which atrial refractory period corresponds to a predetermined maximum heartbeat rate;

and

control means for controlling said A-V timeout means (i) to delay initiation of timing out said A-V delay to the end of said atrial refractory period whenever a P signal is sensed before the end of said atrial refractory period, and (ii) to reduce the length of said A-V delay to a time less than T_AV following each said delay of initiation.

22. The pacemaker as described in claim 21, wherein said control means establishes a P sense window for sensing said P signals from the patient'"'"'s heart during a predetermined time period W preceding the end of said atrial refractory period, and said A-V delay timeout is reduced to about one-half W so that the A-V delay equals about T_AV -W/2.

23. The pacemaker as described in claim 22, comprising stability means for monitoring the occurrence of P signals within said P sense window, and for determining the existence of patient tachycardia due to retrograde P waves as a function of said stability monitoring.

24. The pacemaker as described in claim 23, comprising process means for processing the sensed P signals which have rates lower than said predetermined maximum heartbeat rate, and for enabling said control means to reduce the length of said A-V delay as a function of said processing.