Implantable automatic and haemodynamically responsive cardioverting/defibrillating pacemaker with means for minimizing bradycardia support pacing voltages

• US 5,105,810 A
• Filed: 07/24/1990
• Issued: 04/21/1992
• Est. Priority Date: 07/24/1990
• Status: Expired due to Term

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Telectronics Pacing Systems, Inc (Abbott Laboratories Incorporated)
• Inventors: Maker, Philip J., Collins, Kenneth A.
• Primary Examiner(s): Kamm, William E.
• Assistant Examiner(s): Getzow, Scott M.
• Application Number:
  US07/557,248
• Time in Patent Office: 637 Days
• Field of Search: 128/419 PT, 128/419 D, 128/419 PG
• US Class Current: 607/9
• CPC Class Codes: A61N 1/3712 Auto-capture, i.e. automatic adjustment of the stimulation threshold
• CPC Class Codes: A61N 1/39622 Pacing therapy

Abstract

An implantable, battery-operated cardioverting/defibrillating pacemaker device with the ability to sense and respond to haemodynamic compromise is described. The ventricular pressure (VP) and electrical activity of the heart are sensed via one or more transvenous or epicardial devices. The filtered peak-to-peak amplitude (VFPPA) and a peak pressure function (VPPF) based upon the right and/or left VP waveform(s) are derived. One of the VFPPA and VPPF, and electrically derived heart rate information, are used in the diagnosis of arrhythmic states. Bradycardia support pacing is initiated and terminated by reference to the VP signal, and the pacing pulse voltage used during bradycardia support pacing is optimized in order to extend battery life of the device. This is done by using the haemodynamic sensor to confirm the presence of an appropriate haemodynamic response to the delivery of bradycardia support pacing, and adjusting the pacing voltage to its lowest efficacious level. In the preferred embodiment the high pass filtered right ventricular pressure is monitored to confirm pacing capture.

Claims

1. An implantable, battery-operated device for the treatment of a malfunctioning heart, said device including a first sensing modality for sensing an electrical function of a patient'"'"'s heart and providing a first signal representative of said electrical function, a second sensing modality for sensing an haemodynamic function of the patient'"'"'s heart and providing a second signal representative of said haemodynamic function, first means responsive to said first signal for analyzing the state of the heart'"'"'s function and providing any required electrical shock pacing therapy to the heart at an initial predetermined energy level high enough to ensure prompt pacing capture of the heart, and second means responsive to said second signal and operative when evoked haemodynamic responses from said pacing therapy are sensed to cause the energy level of said pacing therapy provided by said first means to be reduced from said initial predetermined level to a lower level, at which pacing capture of the heart can be maintained and battery life of the device is increased relative to the battery life obtainable at said predetermined energy level.

2. A device according to claim 1, wherein said second signal comprises the filtered peak-to-peak amplitude of a ventricular pressure waveform of the heart.

3. A device according to claim 2, wherein said second signal comprises the filtered and rectified integration of a ventricular pressure waveform of the heart.

4. A device according to any one of claims 1-3, wherein said ventricular pressure waveform of the heart is the right ventricular pressure waveform of the heart.

5. A device according to any one of claims 1-3, wherein said device comprises a dual chamber, cardioverting/defibrillating pacemaker.

6. An implantable, programmable, battery-operated device for sensing malfunctions in a patient'"'"'s heart and initiating therapy therefor based on the heart'"'"'s electrical and haemodynamic functions, comprising:

first means for calculating both the filtered and rectified integration of the pressure waveform of the right ventricle of the heart and the filtered peak-to-peak amplitude of such pressure waveform;

second means for determining haemodynamic compromise based upon at least one of said calculations of said first means;

third means for initiating appropriate electrical therapy for the heart based on the determination by said second means that haemodynamic compromise exists; and

,

fourth means operative following initiation of bradycardia support pacing therapy at a predetermined voltage level, and based on a sensing of the presence of bradycardia-support-pacing-evoked-responses in the right ventricular pressure, for lowering the level of the voltage utilized in said bradycardia support pacing to prolong the battery life of the device.

7. A device according to claim 6, wherein said fourth means progressively reduces said bradycardia support pacing voltage level until pacing capture of the heart is lost, and then progressively increases said voltage level until pacing recapture of the heart occurs.

8. A device according to any one of claims 6 or 7, wherein said device comprises a dual chamber cardioverting/defibrillating pacemaker.

9. A method of optimizing bradycardia support pacing voltages delivered to a patient'"'"'s heart, comprising the steps of:

(A) Delivering a chain of bradycardia support pacing pulses at a predetermined voltage level to the heart;

(B) Monitoring the ventricular pressure waveform of the heart to assess whether or not pacing capture of the heart occurs during delivery of said chain of pulses;

(C) If pacing capture of the heart occurs during step (B), decreasing the level of the bradycardia support pacing voltage delivered in step (A) to a minimum level at which pacing capture is lost, and then raising the level of said voltage to an intermediate level at which effective pacing capture is again achieved; and

,

(D) If pacing capture does not occur during steps (A) and (B), increasing the level of the bradycardia support pacing voltage delivered under step (A) until pacing capture of the heart occurs under step (B).

10. A method according to claim 9, including the further step of:

(E) providing a warning signal in the event that the level of the bradycardia support pacing voltage delivered during step (D) reaches a predetermined maximum level.

11. A method according to claim 9, wherein the voltage level decrease of step (C) and the voltage level increases of steps (C) and (D) are incremental and progressive.

12. A method according to claim 11, wherein the ventricular pressure waveform monitored in step (B) is the right ventricular pressure waveform.

13. A method according to claim 12, wherein the right ventricular pressure waveform is monitored during step (B), and wherein a filtered peak-to-peak amplitude is derived from said right ventricular pressure waveform to assess whether or not pacing capture of the heart occurs during step (B).

14. A method according to claim 13, including the further step of:

(E) providing a warning signal in the event that the level of the bradycardia support pacing voltage delivered during step (D) reaches a predetermined maximum level.

15. A method of determining whether or not pacing capture of a heart occurs during the application of bradycardia support pacing therapy to the heat, comprising the steps of providing bradycardia support pacing to the heart;

monitoring the ventricular pressure waveform response for a programmed predetermined time period after a bradycardia support pacing pulse has been delivered to the heart; and

, deeming pacing capture to have occurred in the event that the pressure waveform crosses a threshold value within said predetermined time.

17. A method according to any one of claims 15 or 16, wherein the right ventricular pressure waveform of the heart is passed through a high-pass filter and digitized to provide a derived right ventricular peak-to-peak amplitude signal which is monitored for said programmed predetermined time to determine whether or not said threshold value has been crossed.

16. A method of determining whether or not pacing capture of a heart occurs during the application of support pacing therapy to the heart, comprising the steps of pacing the heart and monitoring the ventricular pressure waveform response for a programmed predetermined time period after a pacing pulse has been delivered to the heart;

and, deeming pacing capture to have occurred in the event that the pressure waveform crosses a threshold value a predetermined number of times in response to an equal or a predetermined larger number of pacing pulses.

18. A method for determining the need for bradycardia support pacing of a patient'"'"'s heart, comprising the steps of:

(A) continuously monitoring a signal derived from a haemodynamic pressure waveform of the patient;

(B) comparing said monitored signal with a predetermined threshold value;

(C) detecting when said threshold value is crossed by said monitored signal to determine when heart contractions have occurred; and

,

(D) initiating bradycardia support pacing in the event a heart contraction does not occur within a predetermined time period following a last-detected heart contraction.

21. A method according to any one of claims 18-20, wherein said signal is derived from a ventricular pressure waveform of the heart.

22. A method according to claim 21, wherein said signal comprises a high-pass-filtered, digitized representation of the right ventricular pressure waveform of the heart.

23. A method according to claim 21, wherein said signal comprises a rectified, integration of a high-pass-filtered, digitized representation of the right ventricular pressure waveform of the heart.

19. A method for determining the need for bradycardia support pacing of a patient'"'"'s heart, comprising the steps of:

(A) continuously monitoring a signal derived from a haemodynamic pressure waveform of the heart;

(B) comparing said monitored signal with a predetermined threshold value;

(C) detecting when said threshold value is crossed by said monitored signal to determine when heart contractions have occurred; and

,

(D) initiating bradycardia support pacing in the event a threshold crossing does not occur within a predetermined time period following the time at which the last-detected threshold crossing occurred.

20. A method for determining the need for continuing ongoing bradycardia support pacing of a patient'"'"'s heart, comprising the steps of:

(A) continuously monitoring a signal derived from a haemodynamic pressure waveform of the patient during the application to the heart of bradycardia support pacing pulses;

(B) comparing said monitored signal with a predetermined threshold value;

(C) noting when said threshold value is crossed by said monitored signal to determine when heart contractions have occurred and;

(D) initiating a subsequent bradycardia support pacing pulse in the event a threshold crossing does not occur within a predetermined time period after a last-previous bradycardia support pacing pulse has been delivered.

24. A method for terminating ongoing bradycardia support pacing of a patient'"'"'s heart, comprising the steps:

(A) continuously monitoring both a first signal derived from a haemodynamic pressure waveform of the patient and a second signal representing electrical activity of the heart during the application to the heart of bradycardia support pacing pulses;

(B) comparing said monitored first signal with a predetermined threshold value and said monitored second signal with a predetermined QRS-wave complex; and

,

(C) terminating said bradycardia support pacing if, within a first predetermined time after a last-previous bradycardia support pacing pulse has been delivered, either said first signal crosses a predetermined threshold value or said second signal displays a QRS-wave pattern within said predetermined QRS-wave complex.

25. A method according to claim 24, wherein said first signal is derived from a ventricular pressure waveform of the heart.

26. A method according to claim 25, wherein said first signal comprises a high-pass-filtered, digitized representation of the right ventricula pressure waveform of the heart.

27. A method according to claim 25, wherein said first signal comprises a rectified, integration of a high-pass-filtered, digitized representation of the right ventricular pressure waveform of the heart, and said second signal comprises an ECG waveform of the heart.

28. A method according to any one of claims 24-27, wherein pacing capture of the heart is determined during a programmed second predetermined time period after a bradycardia support pacing pulse has been delivered, and wherein said first predetermined time period elapses before the start of said second predetermined time period.