Defibrillation/cardioversion system with multiple evaluation of heart condition prior to shock delivery

• US 5,179,945 A
• Filed: 01/17/1991
• Issued: 01/19/1993
• Est. Priority Date: 01/17/1991
• Status: Expired due to Term

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Huntwork, Daniel, Van Hofwegen, Lloyd, Hsung, Jean-Cheui
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US07/642,337
• Time in Patent Office: 733 Days
• Field of Search: 128/419 D
• US Class Current: 607/5
• CPC Class Codes: A61N 1/3621 for treating or preventing abnormally high heart rate
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• 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

An automatic implantable defibrillator/cardioverter having a non-committed defibrillation/cardioversion algorithm. The defibrillator/cardioverter includes an ECG amplifier with automatic gain control (AGC) which detects the electrical activity of the heart for analysis by a cardiac condition detector. Logic is provided which receives input from the ECG amplifier and the cardiac condition detector for analyzing the heart activity. The non-committed defibrillation algorithm sensing begins upon the determination of an arrhythmia. The capacitor is charged while the heart activity is simultaneously monitored. After the capacitor is charged, a check is made on the duration of the last detected R-R interval while so charging the capacitor, and a comparison is made between this R-R interval and a preset value. If the last R-R interval is greater than the preset value, a non-committing period is entered which lasts approximately 2 seconds. The purpose of the non-committing period is to allow detection to monitor the arrhythmia further before making the decision to discharge the capacitor or dump the charge internally. If any R-R interval detected during this interval is less than PCLL, this indicates that the arrhythmia has not reverted and the capacitor charge is delivered to the patients, synchronously with the second R-wave of the fast R-R interval. If no rapid interval is detected during this time, a post intervention (PI) monitoring routine is entered at the end of the non-committing period to further monitor cardiac activity and shock if necessary.

Claims

1. A method for defibrillating/cardioverting the heart comprising the steps of:

(a) sensing the electrical activity of the heart including the interval between successive R-waves of the ECG;

(b) comparing the interval between successive R-waves with a preset value corresponding to an interval indicative of a heart arrhythmia, to detect heart arrhythmias;

(c) charging a defibrillation capacitor to a predetermined voltage level upon detecting an arrhythmia of the heart;

(d) storing the interval between successive R-waves during the step of charging the defibrillation capacitor;

(e) providing a first delay of a first predetermined period of time subsequent to said capacitor being charged to said predetermined level;

(f) comparing the stored interval between successive R-waves detected during the charging step with said preset value after said first delay;

(g) providing a second delay of a second predetermined period of time if said stored interval between successive R-waves is greater than said preset value as determined in step (f);

(h) comparing intervals between successive R-waves detected during the second delay with said preset value; and

(i) discharging said defibrillation capacitor through the heart if any interval between successive R-waves detected during the second delay is less than said preset value as determined in step (h).

2. The method of claim 1, wherein said step (i) of discharging further comprises the step of synchronizing discharge with the second of the R-waves that define the first R-R interval less than said preset value, if such an interval occurs.

3. The method of claim 1, and further comprising the steps of:

(j) determining a time interval between the last R-wave detected during the step of charging and the end of said first delay if said stored interval is not greater than said preset value as determined in step (f);

(k) comparing said time interval of step (j) with a preset time interval; and

(l) performing steps (g) - (i) if said time interval of step (j) exceeds said preset time interval as determined in step (k).

4. The method of claim 3, and further comprising the steps of:

(m) determining whether the detected arrhythmia has reverted if no interval between successive R-waves is less than said preset value as determined in step (h) or after the step (i) of discharging;

(n) diverting said predetermined voltage level of said defibrillation capacitor to an internal load if the arrhythmia has reverted as determined in step (m);

(o) providing a synchronization time window of a third predetermined period of time if a detected arrhythmia has not reverted as determined in step (m);

(p) detecting an R-wave during said synchronization time window;

(q) discharging said defibrillation capacitor at the occurrence of a detected R-wave in step (p); and

(r) discharging said defibrillation capacitor at the end of said synchronization time window if no R-wave is detected during the synchronization time window.

5. The method of claim 4, and further comprising the step of ensuring that the charge on said defibrillation capacitor is at an appropriate voltage level if a detected arrhythmia has not reverted as determined in step (m).

6. The method of claim 4, wherein said third predetermined period of time is 2 seconds.

7. The method of claim 1, and further comprising the step of diverting said predetermined voltage level of said capacitor to an internal load during said first delay should an operator desire to prevent discharge to the heart of a patient.

8. The method of claim 1, wherein said first predetermined period of time is 200 milliseconds and said second predetermined period of time is 2 seconds.

9. The method of claim 1, wherein said step of storing includes storing successive R-R intervals and retaining only the last interval detected.

10. A system for defibrillating/cardioverting the heart comprising:

means for sensing the electrical activity of the heart including the interval between successive R-waves of the ECG;

means for detecting an arrhythmia of the heart;

means for storing the interval between successive R-waves;

defibrillation capacitor means;

means for charging said defibrillation capacitor means to a predetermined voltage level upon detecting an arrhythmia of the heart using said means for detecting;

means for triggering the discharge of said defibrillation capacitor means; and

logic means including means for providing a first delay of a first predetermined period of time subsequent to said capacitor being charged to said predetermined level means for providing a second delay of a second predetermined period of time subsequent to said first delay;

means for comparing the stored interval between successive R-waves detected during charging of the defibrillation capacitor means with a preset value during said first delay;

means for entering said second delay of said second predetermined period of time if said stored interval between successive R-waves is greater than said preset value; and

means for discharging said defibrillation capacitor to the heart if any interval between successive R-waves is less than said preset value during said second delay.

11. The system of claim 10, wherein said logic means further comprises means for determining a variable time interval between the last R-wave detected while charging the defibrillation capacitor means and the end of said first delay of said first predetermined period of time if said stored interval of successive R-waves is not greater than said preset value during said first delay, and compares said variable time interval with a preset time interval to enter said second delay if said variable time interval exceeds said preset time interval.

12. The system of claim 11, and further comprising an internal load, and wherein said logic means further comprises means for determining if a detected arrhythmia has reverted if no R-R interval detected during the second delay is less than said preset value or after discharge of the defibrillation capacitor means if an R-R interval is less than said preset value, and operates the means for triggering to divert said predetermined voltage level of said defibrillation capacitor to said internal load if the arrhythmia has reverted, the logic means further providing a synchronization time window of a third predetermined period of time if a detected arrhythmia has not reverted, said means for sensing detecting an R-wave during said third predetermined period of time and said logic means operating the means for triggering to effect discharge of said defibrillation capacitor at the occurrence of a detected R-wave during said synchronization time window or effecting discharge of said defibrillation capacitor at the end of said synchronization time window if no R-wave is detected during said third predetermined period of time.

13. The system of claim 12, wherein said logic means further comprises means for triggering said means for charging to charge said defibrillation capacitor means to an appropriate voltage level if a detected arrhythmia has not reverted after said second delay and charge on the defibrillation capacitor means has leaked to below the predetermined voltage level.

14. The system of claim 12, and further comprising memory means for programming said logic means wherein said first predetermined period of time is 200 milliseconds and said second predetermined period of time is 2 seconds.

15. The system of claim 12, wherein said third predetermined period of time is two seconds.

16. A method of non-committed defibrillation/cardioversion of the heart comprising the steps of:

(a) sensing the electrical activity of the heart including the interval between successive R-waves of the ECG;

(b) comparing the interval between successive R-waves with a first preset value and a second preset value, each of said first and second preset values corresponding to an interval indicative of a heart arrhythmia, to detect heart arrhythmias;

(c) charging a defibrillation capacitor to a predetermined voltage level upon detecting an arrhythmia of the heart;

(d) storing the interval between successive R-waves during the step of charging the defibrillation capacitor;

(e) comparing the stored interval between successive R-waves detected during the charging step with said first preset value;

(f) providing a non-committing period of a first predetermined period of time if said stored interval between successive R-waves is greater than said first preset value as determined in step (e);

(g) comparing intervals between successive R-waves detected during the non-committing period with the second preset value; and

(h) discharging said defibrillation capacitor through the heart if any interval between successive R-waves detected during the non-committing period is less than said second preset value as determined in step (g).

17. The method of claim 16, wherein the first preset value and the second preset value are equal.

18. The method of claim 17, wherein the first preset value and the second preset value are equal to a tachycardia primary rate cycle length limit which corresponds to a threshold cardiac rate at which the heart is deemed to be in tachycardia.

19. The method of claim 16, wherein said step (h) of discharging further comprises the step of synchronizing discharge with the second of the R-waves that define a first interval of successive R-waves less than said second preset value, if such an interval occurs.

20. The method of claim 16, and further comprising the steps of:

(i) providing a synchronization time window of a second predetermined period of time if said stored interval of successive R-waves is not greater than said first preset value as determined in step (e);

(j) detecting an R-wave during said synchronization time window; and

(k) discharging said defibrillation capacitor synchronized to a detected R-wave in step (j) and otherwise discharging the defibrillation capacitor at the end of the synchronization time window if no R-wave is detected.

21. The method of claim 16, and further comprising the steps of:

(l) determining whether the detected arrhythmia has reverted if no interval between successive R-waves is less than said second preset value as determined in step (g) and after the step (h) of discharging;

(m) diverting said predetermined voltage level of said defibrillation capacitor to an internal load if the arrhythmia has reverted as determined in step (l);

(n) providing a synchronization time window of a second predetermined period of time if a detected arrhythmia has not reverted as determined in step (l);

(o) detecting an R-wave during said synchronization time window;

(p) discharging said defibrillation capacitor at the occurrence of a detected R-wave in step (o); and

(q) discharging said defibrillation capacitor at the end of said synchronization time window if no R-wave is detected during the synchronization time window.

22. The method of claim 16, wherein said step of storing includes storing successive R-R intervals and retaining only the last interval detected.

23. A method for defibrillating/cardioverting the heart, according to the existence of first and second predetermined conditions of the heart, said method comprising the steps of:

(a) sensing a physiological indicator of an arrhythmia;

(b) detecting an arrhythmia of the heart based on the physiological indicator;

(c) charging a defibrillation capacitor to a predetermined voltage level upon detecting an arrhythmia of the heart;

(d) storing data related to the cardiac function of the heart during the step of charging;

(e) detecting whether the first predetermined condition of the heart occurs during the step of charging;

(f) providing a non-committing period of a first predetermined period of time if the first predetermined condition of the heart does not occur during the step of charging as determined in step (e);

(g) detecting whether the second predetermined condition of the heart occurs during said non-committing period based on the physiological indicator; and

(h) discharging said defibrillation capacitor through the heart if said second predetermined condition of the heart is detected during said non-committing period as determined in step (g).

24. The method of claim 23, and wherein said first predetermined condition comprises a time interval of consecutive R-waves being less than a preset value corresponding to a time interval indicative of a heart arrhythmia.

25. The method of claim 23, wherein said second predetermined condition comprises a time interval of consecutive R-waves occurring during the non-committing period being less than a preset value corresponding to a time interval indicative of a heart arrhythmia.

26. The method of claim 23, and further comprising the steps of:

(i) providing a synchronization time window of a second predetermined period of time if said first predetermined condition is detected as determined in step (e);

(j) detecting an R-wave during said synchronization time window; and

(k) discharging said defibrillation capacitor synchronized to a detected R-wave in step (j) and otherwise discharging the defibrillation capacitor at the end of the synchronization time window if no R-wave is detected.

27. The method of claim 23, and further comprising the steps of:

(l) determining whether the detected arrhythmia has reverted if the second predetermined condition is not detected as determined in step (g) and after the step (h) of discharging;

(m) diverting said predetermined voltage level of said defibrillation capacitor to an internal load if the arrhythmia has reverted as determined in step (l);

(n) providing a synchronization time window of a second predetermined period of time if a detected arrhythmia has not reverted as determined in step (l);

(o) detecting an R-wave during said synchronization time window;

(p) discharging said defibrillation capacitor at the occurrence of a detected R-wave in step (o); and

(q) discharging said defibrillation capacitor at the end of said synchronization time window if no R-wave is detected during the synchronization time window.