Apparatus and method for controlling multiple sensitivities in arrhythmia control system including post therapy packing delay

• US 4,940,054 A
• Filed: 04/29/1988
• Issued: 07/10/1990
• Est. Priority Date: 04/29/1988
• Status: Expired due to Term

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Telectronics Incorporated
• Inventors: Gilli, Norma L., Grevis, Richard
• Primary Examiner(s): Jaworski, Francis
• Assistant Examiner(s): Manuel, George
• Application Number:
  US07/187,797
• Time in Patent Office: 802 Days
• Field of Search: 128/419 PT, 128/419 P, 128/419 D, 128/419 PG
• US Class Current: 607/4
• CPC Class Codes: A61N 1/3621 for treating or preventing abnormally high heart rate
• CPC Class Codes: A61N 1/3704 Circuits specially adapted therefor, e.g. for sensitivity control
• CPC Class Codes: A61N 1/39622 Pacing therapy

Abstract

An apparatus and method for tachyarrhythmia reversion uses multiple sensitivities programmed for automatic operation. A first (medium) sensitivity is used normally for the detection of sinus rhythm and ventricular tachycardia. A second (higher) sensitivity is designed for differentiating ventricular fibrillation from asystole. A third (lower) sensitivity can also be programmed into the device to differentiate between R-waves and high amplitude current of injury T-waves which may occur post shock. Following the delivery of antitachycardia therapy in the form of either antitachycardia pacing therapy or cardioversion shock therapy, there is a pause, or post therapy pacing delay for a period of time prior to the commencement of bradycardia support pacing. The magnitude of the delay period is substantially greater than the normal bradycardia support pacing standby interval.

Claims

1. An apparatus for administering electrotherapy to the heart comprising:

a detector responsive to an electrical signal from the heart, said detector providing an output signal in response to said electrical signal;

sensitivity control means connected to said detector for controlling the sensitivity of said detector to said electrical signal, said sensitivity control means controlling said sensitivity to a first sensitivity level at a first time;

tachyarrhythmia detection means for receiving said output signal from said detector set at said first sensitivity level to determine if a tachyarrhythmia is sensed at said first time;

tachyarrhythmia confirmation means for receiving said output signal from said detector set at said first sensitivity level to confirm the presence of said tachyarrhythmia at a second time after said first time;

tachyarrhythmia therapy means for delivering tachyarrhythmia therapy to the heart if said tachyarrhythmia confirmation means confirms the presence of tachyarrhythmia at said second time;

said sensitivity control means controlling said sensitivity of said detector to a second sensitivity level if a tachyarrhythmia is not sensed by said detector at said second time, said second sensitivity level being higher than said first sensitivity level; and

said tachyarrhythmia therapy means delivering tachyarrhythmia therapy if said detector, at said second sensitivity level, detects tachyarrhythmia.

2. The apparatus of claim 1, wherein said second sensitivity level is sufficient so that said detector provides an output if tachyarrhythmia is present but provides no output during asystole.

3. The apparatus of claim 1, further comprising:

bradycardia detection means responsive to the output of said detector; and

bradycardia pacing means for supplying bradycardia pacing to the heart when said bradycardia detecting means detects bradycardia.

4. The apparatus of claim 3, further comprising delay means for delaying delivery of bradycardia pacing pulses by said bradycardia pacing means, after said tachyarrhythmia therapy means delivers tachyarrhythmia therapy.

5. The apparatus of claim 4, wherein said delay means delays said delivery of bradycardia therapy for a predetermined time interval.

6. The apparatus of claim 5, further comprising programming means connected to said delay means for programming said predetermined time interval.

7. The apparatus of claim 4, wherein said tachyarrhythmia therapy means delivers a first kind of tachyarrhythmia therapy and a second kind of tachyarrythmia therapy, said delay means having a first delay interval generation means for delay after said first kind of therapy, and a second delay, interval generation means for delay after said second kind of therapy.

8. The apparatus of claim 7, wherein delay of said first delay interval generation means and of said second delay interval generation means are independently programmable.

9. The apparatus of claim 1, wherein said sensitivity control means controls said sensitivity to change from said second sensitivity level to said first sensitivity level when said tachyarrhythmia detection means fails to detect a tachyarrhythmia when said detector is at said second sensitivity level.

10. The apparatus of claim 9, further comprising:

bradycardia detection means responsive to the output of said detector, when said sensitivity control means controls said detector sensitivity to return to said first sensitivity level; and

bradycardia pacing means for supplying bradycardia pacing when said bradycardia detection means detects bradycardia.

11. The apparatus of claim 1, wherein said tachyarrhythmia therapy means includes at least one of:

a tachyarrhythmia pacing means, and

a cardioversion means.

12. The apparatus of claim 1, further comprising programming means operatively connected to said sensitivity control means for programming at least one of said first sensitivity level and said second sensitivity level.

13. The apparatus of claim 1, wherein after tachyarrhythmia therapy has been delivered to the heart by said tachyarrhythmia therapy means, said sensitivity control means controls the sensitivity of said detector to a third level, said third sensitivity level being of lower sensitivity than said first level.

14. The apparatus of claim 13, wherein said third sensitivity level is sufficiently high so that said detector detects sinus rhythm, but is sufficiently low so that said detector does not detect a current of injury T-wave.

15. The apparatus of claim 13, wherein said sensitivity control means controls said sensitivity to said third level for at least a period of time sufficient to detect the presence of sinus rhythm.

16. The apparatus of claim 15, wherein if sinus rhythm is not detected at said third sensitivity level, said sensitivity control means controls the sensitivity of said detector to change from said third sensitivity level to said second sensitivity level.

17. The apparatus of claim 15, wherein said period of time is predetermined.

18. The apparatus of claim 15, further comprising programing means operative connected to said sensitivity control means for programming duration of said period of time.

19. The apparatus of claim 13, further comprising sensitivity programming means for programming at least one of said first sensitivity level, said second sensitivity level and said third sensitivity level.

20. The apparatus of claim 13, further comprising sensitivity programming means for independently programming at least one of said first sensitivity level, said second sensitivity level and said third sensitivity level.

21. An apparatus for treating tachyarrhythmias comprising:

sensing means for sensing the presence of a patient tachyarrhythmia, tachyarrhythmia therapy delivery means for delivering tachyarrhythmia therapy, programming means for programming at least two sensitivity levels, a detector means programmable to said sensitivity levels for producing output signals at each of said sensitivity levels, a first sensitivity level being for sensing of sinus, VF and VT, and a second sensitivity level being a higher level of sensitivity than said first sensitivity level, said second sensitivity level being for differentiating VF not detected at said first sensitivity level from an asystole condition, and switching means for switching from said first sensitivity level to said second sensitivity, level when there is an absence of output signals from said detector means at the first sensitivity level.

22. The apparatus of claim 21, wherein said switching means switches back to the first sensitivity level following the delivery of one of tachyarrhythmia therapy, a sensed sinus event and a paced event.

23. The apparatus of claim 21, wherein said programming means also programs third sensitivity level for distinguishing between (a) post-therapy R-waves and (b) current of injury T-waves and far field R-waves.

24. A medical device as claimed in claim 23, wherein said switching means switches interchangeably to and from said third sensitivity level.

25. A method for administering electrotherapy to the heart comprising the steps of:

setting the sensitivity of a detector to an electrical signal from the heart to a first sensitivity level;

detecting the presence of a tachyarrhythmia with said detector, at a first time;

determining whether said tachyarrhythmia is detected by said detector at a second time, at said first sensitivity level, said second time being after said first time;

delivering tachyarrhythmia therapy if said tachyarrhythmia is detected at said second time;

changing said sensitivity to a second sensitivity level if said tachyarrhythmia is not detected at said second time, said second sensitivity level being higher than said first sensitivity level;

determining whether said tachyarrhythmia is detected at said second sensitivity level at a third time, said third time being later than said second time; and

delivering tachyarrhythmia therapy if said tachyarrhythmia is detected at said third time.

26. The method of claim 25, further comprising the step of:

changing said sensitivity back to said first sensitivity level if said tachyarrhythmia is not detected at said third time.

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

detecting the presence of bradycardia after said step of changing said sensitivity back to said second level, and

delivering bradycardia pacing when bradycardia is detected

28. The method of claim 27, further comprising the step of delaying the delivering of bradycardia pacing by a predetermined period of time after delivery of said tachyarrhythmia therapy

29. The method of claim 28, wherein said tachyarrythmia therapy is of a first type of therapy and a second type of therapy, said first type of therapy being delayed for a first delay interval and said second type of therapy being delayed for a second delay interval.

30. The method of claim 29, further comprising the step of independently programming said first delay interval and said second delay interval.

31. The method of claim 28, further comprising the step of programming said predetermined period of time.

32. The method of claim 25, wherein said tachyarrhythmia therapy includes at least one of pacing and cardioversion.

33. The method of claim 25, further comprising the step of programming at least one of said first sensitivity level and said second sensitivity level.

34. The method of claim 25, wherein at least one of said first sensitivity level and said second sensitivity level is programmed to a fixed level.

35. The method of claim 25, further comprising the steps of:

setting said sensitivity of said detector to a third level after the delivery of tachyarrhythmia therapy, for a period of time sufficient to detect the presence of sinus rhythm, said third level being lower than said first level;

determining whether sinus rhythm is detected by said detector at said third sensitivity level;

maintaining said sensitivity at said third level for a predetermined period of time if sinus rhythm is detected; and

changing said sensitivity to said second level if sinus rhythm is not detected.

36. The method of claim 35, wherein said third sensitivity level is sufficiently high to detect sinus rhythm and insufficiently high to detect a current of injury T-wave.

37. The method of claim 35, further comprising the step of programming said first sensitivity level, said second sensitivity level and said third sensitivity level.

38. The method of claim 35, further comprising the step of independently programming said first sensitivity level, said second sensitivity level and said third sensitivity level.

39. The method of claim 35, further comprising the step of programming a duration of said predetermined period of time.