Method and apparatus for advanced tachyarrhythmia discrimination

• US 5,891,170 A
• Filed: 06/17/1997
• Issued: 04/06/1999
• Est. Priority Date: 06/18/1996
• Status: Expired due to Term

• Current Assignee: Sorin CRM SAS (MicroPort Scientific Corp.)
• Original Assignee: Ela Medical S.A. (LivaNova Plc)
• Inventors: Iscolo, Nicolas, Limousin, Marcel, Nitzsche, Remi, Bonnet, Jean-Luc
• Primary Examiner(s): Kamm, William E.
• Assistant Examiner(s): SCHAETZLE, KENNEDY
• Application Number:
  US08/877,039
• Time in Patent Office: 658 Days
• Field of Search: 607/14, 607/4, 607/5, 600/518, 600/519, 600/515-517
• US Class Current: 607/4
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/395 for treating atrial fibrillation
• CPC Class Codes: A61N 1/3956 Implantable devices for applying electric shocks to the heart, e.g. for cardioversion

Abstract

An active implantable medical device of the defibrillator/cardiovertor type with advanced tachycardia discrimination in which the device monitors the atrial and ventricular activity, suspects and confirms the presence of tachycardia episodes in the monitored activity, and operates a classification algorithm to discriminate between ventricular tachycardias and supra-ventricular tachycardias according to predetermined criteria and a given adjustment of these criteria, and to authorize the releasing of a shock therapy defibrillation, and/or cardioversion and/or anti-tachycardia ventricular stimulation in the presence ventricular tachycardias and to inhibit delivery of a shock therapy in the presence of a supra-ventricular tachycardias, or instead to release an atrial therapy. The advanced discrimination modifies the classification operation by being able to add temporarily one or more criterion and/or to modify temporarily the adjustment of an existing (predetermined) criterion in case of a suspected atrial fibrillation. Added criterion include particularly a supplementary research criterion of short and/or long RR intervals, which are significantly distanced from a zone of RR interval stability, which significantly distanced zones are, for example, separated from the RR interval stability zone by a predetermined width interval, which width interval is identical on both sides of the RR interval stability zone.

Claims

1. An active implantable medical device of the defibrillator/cardiovertor type, comprising:

means for delivering a shock therapy;

means for monitoring atrial and ventricular activity;

means for suspecting and confirming the presence of a tachycardia episode in the monitored activity;

means of classification, operable to discriminate a suspected tachycardia episode as between a ventricular tachycardia and a supra-ventricular tachycardia according to a predetermined criteria and a given adjustment of said predetermined criteria, and to authorize delivery of a shock therapy in the presence of a ventricular tachycardia and to inhibit delivery of a shock therapy in the presence of a supra-ventricular tachycardia and said classification means further comprising means for modifying said discrimination operation, in response to a supra-ventricular tachycardia, by one of adding temporarily at least one criterion and modifying temporarily the adjustment of a predetermined criterion.

2. The device of claim 1, wherein the added criterion further comprises a supplementary research criterion of at least one of a short RR interval range and a long RR interval range, said one RR interval range being significantly distanced from an RR interval stability zone.

3. The device of claim 2, wherein the RR interval stability zone further comprises a first limit and a second limit defining said RR interval stability zone, and the research criterion further comprises a long RR interval range and a short RR interval range respectively separated from the first and second limits by a predetermined width interval on each side of the RR interval stability zone.

4. The device of claim 1, in which the added criterion comprises a supplementary counting and comparison criterion corresponding to a number of atrial events relative to a number of ventricular events during a given duration.

5. The device of claim 1, in which the modifiable adjustment comprises a majority parameter and means for evaluating the majority parameter over a number of given cycles and determining the presence of a percentage, greater than or equal to a given threshold, of the RR intervals situated outside of a predetermined RR interval stability zone.

6. The device of claim 5, in which the modifiable adjustment comprises a duration parameter of tachycardia persistence.

7. The device of claim 5, in which the modifiable adjustment comprises a width parameter of an RR interval stability zone.

8. The device of claim 1, in which the predetermined criteria and/or parameters of the classification means are restored in response to an absence of a confirmed supra-ventricular tachycardia episode in the monitored activity.

9. The device of claim 1, further comprising means for determining if one or more criterion are temporarily adjusted and/or the temporarily modified adjustment is in use a determined number of times in the course of a predetermined period, and for applying the addition and/or modification in a permanent manner.

10. The device of claim 1 further comprising means for releasing an atrial therapy in response to a detected supra-ventricular tachycardia.

11. A method for discriminating tachycardia episodes in an active implantable medical device of the defibrillator/cardiovertor type for delivering a shock therapy, comprising:

monitoring atrial and ventricular activity;

identifying a tachycardia episode occurring in the monitored activity;

classifying said tachycardia episode as between one of a ventricular tachycardia and a supra-ventricular tachycardia according to a predetermined criteria and a given adjustment of said predetermined criteria;

authorizing delivery of a shock therapy in response to a classified ventricular tachycardia and inhibiting delivery of a shock therapy in response to a classified supra-ventricular tachycardia, and

modifying said classifying step, in response to a discriminated atrial fibrillation, by one of adding temporarily at least one criterion and modifying temporarily the adjustment of a predetermined criterion to confirm said discriminated atrial fibrillation as one of genuine and not genuine.

12. The method of claim 11, wherein modifying said discrimination step further comprises providing a supplementary research criterion of at least one of a short RR interval range and a long RR interval range, said one RR interval range being significantly distanced from an RR interval stability zone.

13. The method of claim 12, further comprising defining said RR interval stability zone as having a first limit and a second limit and wherein providing the research criterion further comprises providing a long RR interval range and a short RR interval range respectively separated from the first and second limits by a predetermined interval width on each side of the RR stability zone.

14. The method of claim 11, wherein providing the added criterion further comprises providing a supplementary counting and comparison criterion corresponding to a number of atrial events relative to a number of ventricular events during a given duration.

15. The method of claim 11, wherein providing the modifiable adjustment further comprises providing a majority parameter, evaluating the majority parameter over a number of predetermined cycles, identifying an RR interval and determining the presence of a percentage, greater than or equal to a given threshold, of the identified RR intervals situated outside of a predetermined RR interval stability zone.

16. The method of claim 15, wherein providing the modifiable adjustment further comprises providing a duration parameter of tachycardia persistence.

17. The method of claim 15, wherein providing the modifiable adjustment further comprises providing a width parameter of an RR interval stability zone.

18. The method of claim 11, further comprising restoring the criteria and/or parameters of the classification steps in response to an absence of a classified supra-ventricular tachycardia episode in the monitored activity.

19. The method of claim 11, further comprising determining if one or more criterion are temporarily adjusted and/or the temporarily modified adjustment is in use a determined number of times in the course of a given period, and applying the addition and/or modification in a permanent manner.

20. The method of claim 11 further comprising authorizing an atrial therapy in response to a classified supra-ventricular tachycardia.