Method and apparatus for delivering defibrillation shocks with improved effectiveness

• US 5,531,767 A
• Filed: 05/25/1995
• Issued: 07/02/1996
• Est. Priority Date: 03/29/1994
• Status: Expired due to Term

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Ventritex Incorporated (Abbott Laboratories Incorporated)
• Inventors: Fain, Eric S.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US08/450,168
• Time in Patent Office: 404 Days
• Field of Search: 607/5, 607/7
• US Class Current: 607/5
• CPC Class Codes: A61N 1/3956 Implantable devices for applying electric shocks to the heart, e.g. for cardioversion
• CPC Class Codes: A61N 1/3987 characterised by the timing or triggering of the shock

Abstract

A method for defibrillating a patient'"'"'s heart with an implantable defibrillator having defibrillation synchronized to the fibrillation waveform is disclosed. The defibrillator is used to detect fibrillation in a patient'"'"'s heart, monitor at least one far-field fibrillation voltage across two spaced-apart electrodes while the high voltage capacitors are charging, then deliver a high energy shock during a period of ventricular fibrillation when the absolute values of the peak and trough voltages exceed a threshold based on a desired percentage greater than a running average of the absolute values of the peaks and troughs of the fibrillation voltages monitored during and after capacitor charging. The shock is then delivered synchronous with the next significant cardiac complex. The defibrillator also includes a safety timer so that if the threshold is not reached within a specified safe time limit, the high energy shock will be delivered without further delay.

Claims

1. A method for defibrillating a patient'"'"'s heart with an implantable defibrillator having first and second implanted electrodes spaced apart from each other by at least 4 centimeters, comprising the steps of:

(a) detecting fibrillation in said patient'"'"'s heart;

(b) monitoring a fibrillation voltage across said first and second implanted electrodes, a waveform of said fibrillation voltage including peaks and troughs;

(c) determining absolute value amplitudes of the peaks and troughs of said fibrillation voltage;

(d) averaging a portion of said absolute value amplitudes to provide an average amplitude;

(e) comparing said average amplitude with the absolute values of the peaks and troughs of said fibrillation voltage to determine if a measure of the absolute values of the peaks and troughs of said fibrillation voltage exceeds said average amplitude determined in step (d) by a predetermined amount; and

(f) delivering a defibrillation shock to said patient'"'"'s heart during a period of ventricular fibrillation when the measure of the absolute values of the peaks and troughs of said fibrillation voltage exceeds said average amplitude determined in step (d) by said predetermined amount.

2. The method of claim 1 wherein said step of delivering said defibrillation shock includes delivering said shock synchronous with a peak or trough of said fibrillation voltage having an amplitude exceeding a threshold set as a function of said average amplitude.

3. The method of claim 1, wherein said implantable defibrillator includes a third electrode and wherein said step (a) of detecting fibrillation includes the step of sensing an electrical signal from said patient'"'"'s heart with said first and third electrodes.

4. The method of claim 1, wherein step (f) of delivering a defibrillation shock includes the step of delivering said defibrillation shock using at least one of said first and second spaced apart electrodes used to monitor said fibrillation voltage in step (b).

5. The method of claim 1, and further including the step of implanting said first and second spaced apart electrodes for monitoring fibrillation respectively in the right ventricle of said patient'"'"'s heart and in a subcutaneous pectoral region.

6. The method of claim 1, wherein said implantable defibrillator includes a third implanted spaced apart electrode and wherein step (b) includes monitoring a first and a second of said fibrillation voltages, said first and second spaced apart electrodes forming a first electrode pair for monitoring said first fibrillation voltage, and said first and third spaced apart electrodes forming a second electrode pair for monitoring said second fibrillation voltage.

7. The method of claim 1, and further including the steps of charging a high voltage capacitor in said implantable defibrillator following detection of fibrillation in said patient'"'"'s heart and of setting a safety timer upon completion of said charging step and delivering said defibrillation shock when said safety timer times out if said measure of the absolute values of the peaks and troughs of said fibrillation voltage has not exceeded said average amplitude by said predetermined amount.

8. The method of claim 1 wherein said step of averaging a portion of said absolute value amplitudes includes sequentially calculating the average using a running sequence of windows, each window including a defined time duration of said fibrillation voltage, whereby newer windows are included in said averaging and older windows are excluded from said averaging.

9. An implantable defibrillator comprising:

(a) a pulse generator including a battery, a high voltage capacitor and a charging circuit for charging said capacitor from said battery;

(b) bipolar fibrillation sensing means;

(c) unipolar sensing means for monitoring a fibrillation voltage and determining a relative measure of the strength of peaks and troughs of said fibrillation voltage measured during a running sequence of windows monitored following fibrillation detection;

(d) electrode means for delivering a defibrillation shock from said capacitor, during a period of ventricular fibrillation after said capacitor is charged when a measure of the absolute values of the peaks and troughs of said fibrillation voltage exceeds by a predetermined percentage said relative measure;

wherein said unipolar sensing means comprises at least two of the following;

(aa) a right ventricular pacing electrode;

(bb) a subcutaneous defibrillation electrode;

(cc) an electrically active portion of the implantable defibrillator case;

(dd) a superior vena cava defibrillation electrode;

(ee) a right ventricular defibrillation electrode.

10. The implantable defibrillator of claim 9 wherein said unipolar sensing means comprises at least three electrodes.

11. The implantable defibrillator of claim 9, wherein said unipolar sensing means comprises a first electrode and a second electrode, and wherein said electrode means for delivering a defibrillation shock includes said first electrode.

12. The implantable defibrillator of claim 11, wherein said electrode means for delivering a defibrillation shock further includes said second electrode.

13. A method for defibrillating a patient'"'"'s heart with an implantable defibrillator having first and second implanted electrodes spaced apart from each other by at least 4 centimeters, comprising the steps of:

(a) detecting fibrillation in said patient'"'"'s heart;

(b) monitoring a fibrillation voltage across said first and second implanted electrodes, a waveform of said fibrillation voltage including peaks and troughs;

(c) determining absolute value amplitudes of the peaks and troughs of said fibrillation voltage;

(d) calculating a measure of said amplitudes for a sequence of predefined duration portions of said fibrillation voltage;

(e) calculating an average of said measures for a predetermined number of said portions;

(f) comparing said average measure with at least one of said measures for one of said portions in said sequence subsequent to said predetermined number of said portions to determine if said measure for said subsequent portion exceeds said average measure calculated in step (e) by a predetermined amount; and

(g) delivering a defibrillation shock to said patient'"'"'s heart during a period of ventricular fibrillation when said measure for said subsequent portion exceeds said average measure by said predetermined amount.

14. The method of claim 13 wherein step (d) includes adding said amplitudes for each predefined duration portion to calculate each of said measures.

15. The method of claim 13 wherein step (d) includes averaging said amplitudes for each predefined duration portion to calculate each of said measures.