Pacemaker system and method for measuring and monitoring cardiac activity and for determining and maintaining capture

• US 4,686,988 A
• Filed: 10/19/1984
• Issued: 08/18/1987
• Est. Priority Date: 10/19/1984
• Status: Expired due to Term

• Current Assignee: Pacesetter AB (Abbott Laboratories)
• Original Assignee: Siemens-Elema AB (Siemens AG)
• Inventors: Sholder, Jason A.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US06/662,723
• Time in Patent Office: 1,033 Days
• Field of Search: 128/419 PG, 128/419 PT, 128/697
• US Class Current: 607/28
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• CPC Class Codes: A61N 1/368 comprising more than one electrode co-operating with different heart regions A61N1/3622, A61N1/3627 take precedence
• CPC Class Codes: A61N 1/3712 Auto-capture, i.e. automatic adjustment of the stimulation threshold
• CPC Class Codes: A61N 1/3714 Atrial capture
• CPC Class Codes: A61N 1/3716 with reduction of residual polarisation effects

Abstract

A system for determining P-wave and R-wave capture in response to pacemaker supplied electrical stimuli. One embodiment includes a conventional bipolar atrial lead having a tip electrode, connected to a P-wave pace/sense amplifier and pulse output circuits within an implantable pacemaker, and a ring electrode, spaced apart from the tip electrode, connected to a P-wave sensing EGM amplifier within the pacemaker. The bandpass characteristics of the P-wave pace/sense amplifier allow detection of P-wave frequencies in the absence of atrial stimulation pulses. The bandpass characteristics of the P-wave sensing EGM amplifier allow detection of all electrical frequencies in the atrium within the bandpass chosen. Output signals from these two amplifiers are selectively telemetered to an external receiver, where the occurrence of atrial stimulation pulses and P-waves can be monitored. In operation, if constant time intervals between the monitored atrial stimulation pulses and P-wave occurrences are present, P-wave capture has occurred. In the event of variable time intervals, capture has not occurred and the magnitude of the atrial stimulation pulses can be increased until P-wave capture does occur. An alternative embodiment measures this time differential and makes the stimulation pulse adjustment automatically. Other embodiments use the same manual or automatic systems to determine R-wave capture.

Claims

1. A system for determining atrial capture comprising:

heart pacing means for generating stimulation pulses;

electrically conductive lead means including

a first electrically conductive electrode connected to said heart pacing means, and

a second electrically conductive electrode spaced apart from said first electrode; and

means for sensing atrial capture of said stimulation pulses, said atrial capture sensing means including

a first amplifier connected to receive signals sensed by said first electrode, said first amplifier including first receiving means for receiving only those signals indicative of a naturally occurring or intrinsic atrial P-wave, said first amplifier further having means for generating a first output signal in response to the receipt of a signal by said first receiving means,

a second amplifier connected to receive signals sensed by said second electrode, said second amplifier including second receiving means for receiving signals indicative of any atrial P-wave sensed by said second electrode, said second amplifier further having means for generating a second output signal indicative of the sensing of at least a P-wave that occurs in response to a stimulation pulse applied to said first electrode by said heart pacing means, and

means responsive to the absence of the first output signal and the presence of said second output signal and said heart pacing means for determining whether atrial capture has occurred.

2. The system recited in claim 1 wherein said first and second electrodes are spaced apart at least one-half inch.

3. The system recited in claim 1 wherein said means for determining atrial capture comprises means for comparing successive time intervals between atrial stimulation pulses applied to said first electrode by said heart pacing means and the generation of the second output signal by said second amplifier in response to the occurrence of a P-wave sensed at said second electrode.

4. The system recited in claim 1 wherein said first and second electrically conductive electrodes comprise a single bipolar lead.

5. The system recited in claim 1 wherein there is further included:

at least a third electrode as part of said lead means spaced apart a distance from said first electrode different than the distance between said second electrode and said first electrode; and

wherein said means for sensing the atrial capture of said stimulation pulses also includes at least said third electrode.

6. The system recited in claim 1 wherein the second amplifier includes means for amplifying frequencies within the range of 3 to 125 Hz, which frequency range includes frequencies of substantially all atrial electrical activity.

7. The system recited in claim 1 wherein there is further included means for stimulating the ventricle and means for sensing in the ventricle of the heart.

8. The system recited in claim 1 wherein there is included means for transmitting information in said pacing means concerning the P-wave capture to an external receiver.

9. The system recited in claim 1 wherein there is further included:

means for measuring the time delays between successive atrial stimulation pulses and sensed atrial P-waves;

means for controlling the magnitude of the atrial stimulation pulses of said heart pacing means in accordance with the means for sensing atrial capture; and

wherein said means for controlling the magnitude includes means for reducing the magnitude of said atrial stimulation pulses until time delays between successive atrial stimulation pulses and sensed atrial P-waves are unequal and then increasing the magnitude of said stimulation pulses until the time delays are equal, whereby atrial capture of atrial stimulation pulses is determined.

10. The system recited in claim 9 wherein there is included means for excluding time delays between atrial stimulation pulses and sensed intrinsic atrial P-waves.

11. The system recited in claim 1 wherein there is included means for controlling the magnitude of the atrial stimulation pulses of said heart pacing means in accordance with the means for sensing atrial capture.

12. The system recited in claim 11 wherein is included means for automatically periodically adjusting the magnitude of said atrial stimulation pulses.

13. The system recited in claim 11 wherein there is further included means for optimally adjusting stimulation pulse magnitude so as to maintain atrial capture at a minimum power drain level.

14. In a heart pacing device including atrial stimulation means for stimulating the atrium of a heart with atrial stimulation pulses, and atrial capture sensing means for sensing atrial capture, a means for maintaining atrial capture comprising:

means for measuring the time delay between successive atrial stimulation pulses and the resulting P-waves; and

means for adjusting the magnitude of the atrial stimulation pulses of said atrial stimulation means until the time delay between successive atrial stimulation pulses and sensed atrial P-waves are equal.

15. In combination with means for stimulating and means for sensing in the atrium of the heart, a means for indicating the successful stimulation of the atrium comprising:

comparison means for comparing successive time intervals between the application of stimulation pulses by said stimulating means and sensed electrical activity as sensed by said atrial sensing means; and

means responsive to said comparison means for indicating when said successive time intervals are the same.

16. A system for determining capture in response to pacemaker supplied electrical stimuli comprising:

first lead means having at its distal end a first exposed electrically conductive electrode, a second exposed electrically conductive electrode spaced apart and electrically isolated from said first electrode, and first and second terminals, near the proximal end of said lead means, electrically connected to said first and second electrodes, respectively, the distal end of said first lead means being positionable in a first chamber of a heart; and

pacemaker means comprising

first pulse output means for generating stimulation pulses,

first connector means electrically connected to said first pulse output means and including means for engagingly receiving said first terminal of said lead means,

first sense/pace amplifier means for sensing electrical waves generated by spontaneous cardiac action, the input of said sense/pace amplifier means being electrically connected to said first connector means,

second sensing amplifier means for sensing electrical waves generated by spontaneous and stimulated cardiac action,

second connector means electrically connected to the input of said second sensing amplifier means and including means for engagingly receiving said second terminal of said lead means, and

means for monitoring the output of said first and second sensing amplifier means for the purpose of determining if spontaneous or stimulated cardiac action has occurred and whether capture due to said stimulation pulses has occurred.

17. The system of claim 16 wherein said means for monitoring comprises:

a receiving device external from said pacemaker means;

telemetering means for transmitting signals to said receiving device from said pacemaker means; and

means for connecting the output of said second sensing amplifier means to said telemetry means.

18. The system of claim 16 wherein

said second connector means comprises switch means for selectively connecting said telemetry means to the output of said second amplifier means or the output of said first sense/pace amplifier means.

19. The system of claim 18 wherein said telemetry means further comprises:

a transmitting device external from said pacemaker means;

receiving means within said pacemaker means for receiving signals from said transmitting device, said pacemaker means further including means responsive to signals transmitted by said transmitting device and received by said receiving means for controlling said switch means.

20. The system of claim 18 further comprising:

second lead means having at its distal end a third exposed electrically conductive electrode being electrically connected to a third terminal near the proximal end of said second lead means, said third conductive electrode being positionable in a second chamber of the heart; and

said pacemaker means further comprises

a third sense/pace amplifier means for sensing electrical waves generated by spontaneous and stimulated cardiac action,

second pulse output means for generating stimulation pulses,

third connector means electrically connected to said second pulse output means and the input of said third sense/pace amplifier means, said third connector means including means for engagingly receiving said third terminal of said second lead, and

said switch means further comprises means for selectively connecting the output of said third sense/pace amplifier means to said telemetry means.

21. The system of claim 16 wherein said second sensing amplifier means comprises bandpass amplifier means that is approximately flat between 31/2 Hz and 125 Hz.

22. The system of claim 16 wherein said first sense/pace amplifier means comprises bandpass amplifier means having a center frequency of approximately 60 Hz and 3 db points at approximately 10 Hz and 100 Hz.

23. The system of claim 16 wherein said first sense/pace amplifier means comprises bandpass amplifier means having a center frequency between 40 Hz and 80 Hz and 3 db points between 0.1 Hz and 500 Hz.

24. The system of claim 16 wherein said means for monitoring comprises:

means for determining a stimulation-response time between application of a stimulation pulse to said first heart chamber and the occurrence of a specified electrical wave in said first heart chamber, said specified electrical wave being indicative of a contraction of said first heart chamber;

comparing means for comparing one of said stimulation-response times with at least one other of said stimulation-response times; and

means responsive to said comparing means for altering the magnitude of the stimulation pulse.

25. The system of claim 16 wherein said first pulse output means comprises means for generating stimulation pulses having predetermined pulse width and pulse amplitude characteristics, and said pacemaker means further comprises:

means for determining a capture threshold for a plurality of stimulation pulse amplitudes and pulse widths; and

means for selecting a particular stimulation pulse amplitude/pulse width combination related to said capture thresholds obtained from said means for determining.

26. The system of claim 25 wherein said means for selecting includes means for selecting a stimulation pulse amplitude/pulse width combination that minimizes power consumption of said pacemaker means while still retaining capture.

27. The system of claim 26 wherein said means for selecting further comprises means for altering the amplitude of a selected stimulation pulse to a value higher than that of said selected pulse.

28. The system of claim 26 wherein said means for selecting further comprises means for altering the pulse width of a selected stimulation pulse to a value wider than that of said selected pulse.

29. The system of claim 26 wherein said means for selecting further comprises means for altering the amplitude of a selected pulse to a value higher than that of said selected pulse and a means for altering the width of a selected pulse to a value wider than that of said selected pulse.

30. An implantable cardiac pacing system comprising:

atrial lead means having first and second terminals at the lead proximal end, a first electrode at the lead distal end electrically connected to said first terminal, a second electrode near the lead distal end spaced from said first electrode and electrically connected to said second terminal; and

pacemaker means comprising

first connector means for electrically engaging said first terminal,

second connector means for electrically engaging said second terminal,

pulse generation means connected to said first connector means for providing an atrial stimulation pulse,

P-wave sense/pace amplifier means connected to said first connector means for sensing spontaneous atrial action,

P-wave sensing EGM amplifier means connected to said second connector means for sensing spontaneous and stimulated atrial action, and

means for monitoring the output of said P-wave sensing EGM amplifier means in the presence of atrial stimulation pulses for the purpose of determining if P-wave capture has occurred.

31. The system of claim 30 further including a receiving device external from said implanted pacemaker means, and wherein said means for monitoring comprises implanted telemetry means for telemetering a signal related to the output of said P-wave sensing ECG amplifier means to said receiving device.

32. The system of claim 30 wherein said pacemaker means comprises a portion of its case being electrically conductive and circuit means for connecting said case conductive to said pulse generation means, said conductive case portion being a portion of the electrical return path for said first electrode and said second electrode.

33. The system of claim 30 wherein said means for monitoring further comprises:

switch means for connecting the output of at least said P-wave sensing EGM amplifier means to said telemetry means; and

means responsive to signals from said telemetry means for controlling said switch means.

34. The system of claim 30 further comprising:

ventricle lead means having a third electrode at a distal end of said ventricle lead, said third electrode being connected to a third terminal at a proximal end of said ventricle lead;

said pacemaker means further comprises

third connector means for electrically engaging said third terminal,

R-wave sense/pace amplifier means connected to said third terminal; and

said means for monitoring comprises

telemetry means included within said pacemaker means for telemetering signals to and from said pacemaker means;

switch means for selectively connecting said telemetry means to one of the output of said P-wave sense/pace amplifier means, said P-wave sensing ECG amplifier means, or said R-wave sense/pace amplifier means, and

means responsive to signals from said telemetry means for controlling said switch means.

35. A method of determining capture of stimulation pulses comprising the steps of:

sensing electrical activity within a prescribed heart chamber at a location spaced apart from a stimulating location of said prescribed heart chamber;

measuring the time delay between the application of a stimulation pulse and a resulting electrical wave, said resulting electrical wave being indicative of a contraction of said prescribed heart chamber;

comparing successive time delays between stimulation pulses and the resulting electrical wave; and

adjusting the magnitude of the stimulation pulses until said time delays are the same, denoting captured atrial stimulation pulses.

36. The method recited in claim 35 wherein said adjusting step comprises reducing the magnitude of said atrial stimulation pulses until said time delays are not the same and then gradually increasing the magnitude of said stimulation pulses until said time delays are the same.

37. The method recited in claim 36 wherein said adjusting step comprises increasing the magnitude of the stimulation pulses to slightly more than necessary to effect the same time delays, whereby a margin of operability is obtained.

38. A method of determining the effectiveness of atrial stimulation of a heart, the steps comprising:

stimulating the atrium with stimulation pulses;

sensing atrial P-waves in said heart;

measuring the time intervals between the application of a stimulation pulse and a subsequent P-wave;

identifying those atrial P-waves which are not of intrinsic origin by comparing the measured time intervals, P-wave capture being present when the measured time intervals are the same; and

adjusting the magnitude of the stimulation pulses until atrial P-wave capture occurs.

39. A method for determining P-wave capture in response to pacemaker supplied atrial electrical stimuli comprising the steps of:

attaching an atrial lead means having first and second electrodes spaced-apart from each other to a pacemaker, said pacemaker including an atrial stimulation pulse generation means to which said first electrode is electrically connected, and a P-wave sensing EGM amplifier means to which said second electrode is electrically connected;

stimulating the atrium with pulses provided by said atrial stimulation pulse generation means; and

monitoring the output of said P-wave sensing EGM amplifier means for determining if P-wave capture has been effected by said atrial stimulation pulses.

40. The method of claim 39 wherein said pacemaker means includes telemetry means for transmitting signals to a receiver external from said pacemaker means, and wherein said monitoring step comprises:

telemetering a signal related to said P-wave sensing EGM amplifier means output signal to said receiving means; and

analyzing said signal telemetered in said telemetering step for determining if P-wave capture has been effected.

41. A method for effecting capture in response to pacemaker supplied electrical stimuli comprising the steps of:

attaching an lead having first and second electrodes spaced-apart from each other to a pacemaker means, said pacemaker means including a stimulation pulse generation means to which said first electrode is electrically connected, and a stimulated-wave sensing EGM amplifier means to which said second electrode is electrically connected;

stimulating a chamber of the heart with pulses provided by said stimulation pulse generation means;

measuring the time differential between at least two stimulation pulses and the next-occurring stimulated waves sensed by said EGM amplifier means;

determining if the measured time intervals are the same; and

increasing the amplitude of said stimulation pulses until the measured time intervals are the same.

42. The method of claim 41 further comprising the steps of:

repeating said stimulating step using stimulation pulses having a plurality of stimulation pulse widths, each stimulating step beginning with a stimulation pulse having an amplitude below that initially determined in said increasing step;

repeating said measuring step for each of said stimulating steps;

repeating said determining step for each of said measuring steps;

repeating said increasing step for each of said measuring steps;

determining the power consumed for each of the stimulation pulse amplitude/pulse width combinations having the same measured time intervals as determined in each of said increasing steps;

selecting in response to said determining steps the pulse amplitude/pulse width combination having a desired power consumption characteristics; and

setting the pulse width/pulse amplitude of the stimulation pulses provided by said stimulation pulse generation means to a value related to the value determined in said selecting step.