Calculation of the atrioventricular delay for an active implantable metal device

• US 8,233,981 B2
• Filed: 11/18/2009
• Issued: 07/31/2012
• Est. Priority Date: 11/19/2008
• Status: Active Grant

• Current Assignee: Sorin CRM SAS (MicroPort Scientific Corp.)
• Original Assignee: Sorin CRM SAS (MicroPort Scientific Corp.)
• Inventors: Casset, Cyrille
• Primary Examiner(s): Gedeon, Brian T
• Application Number:
  US12/621,314
• Publication Number:
  US 20100125308A1
• Time in Patent Office: 986 Days
• Field of Search: 607/4, 607/9, 607/19, 607/18, 607/27, 607/28, 600/508, 600/509
• US Class Current: 607/9
• CPC Class Codes: A61N 1/368 comprising more than one electrode co-operating with different heart regions A61N1/3622, A61N1/3627 take precedence
• CPC Class Codes: A61N 1/3682 with a variable atrioventricular delay
• CPC Class Codes: A61N 1/3688 configured for switching the pacing mode, e.g. from AAI to DDD
• 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 including circuits for calculating an atrio ventricular delay (AVD) period. The device is able to detect the atrial and ventricular events; calculate an AVD and to start the AVD on detection of a spontaneous or paced atrial event. The device is able to deliver a low energy ventricular stimulation pulse at the expiration of the AVD in the absence of a detected spontaneous ventricular event. To calculate the AVD, the device uses an acceleration sensor to deliver an endocardiac acceleration (EA) signal representative of the movements produced by the contractions of the atrial cavity; and analyzes the EA signal to identify and isolate in the EA signal a component corresponding to the fourth peak of endocardiac acceleration (PEA4) associated to the atrial activity, and to calculate the AVD based on a parameter of this component.

Claims

1. An active implantable medical device of the cardiac stimulation, resynchronization, cardioversion and/or defibrillation type, comprising:

means for detecting spontaneous and stimulated atrial events;

means for detecting ventricular events;

means for calculating an atrio-ventricular delay AVD, said AVD starting on the detection of one of a spontaneous and a stimulated atrial event;

an acceleration sensor having an output signal that is an EA signal representative of the movements produced by the contractions of the atrial cavity;

means for analyzing the EA signal to identify and isolate in the EA signal an EA4 component corresponding to the fourth peak of endocardiac acceleration associated to the atrial activity, and means for calculating the value of the AVD based upon the EA4 component; and

means for pacing the ventrical with a low energy stimulation pulse, in response to an expiration of the calculated AVD and in the absence of a detected spontaneous ventricular event,

wherein the means for calculating the value of the AVD further comprises means for determining a parameter of the EA4 component as a function of an end time of the EA4 component, and calculating the value of the AVD as a function of said determined parameter.

2. The device of claim 1, wherein the value of the AVD is calculated so that the end of the AVD is at least concurrent with or subsequent to the end time of the EA4 component.

3. The device of claim 2, wherein the end of the AVD is defined by the end time of the EA4 component.

4. The device of claim 1 wherein the end of the AVD is calculated so that the end of the AVD is subsequent to the end time of the EA4 component.

5. The device of claim 1, wherein:

the means for analyzing the EA signal further comprises means for recognizing and isolating in the EA signal an EA1 component corresponding to a first endocardial acceleration peak associated with the ventricular activity and for determining a start time of said EA1 component, and

the value of the AVD is calculated based on the determined start time of the EA1 component.

6. The device of claim 5, wherein the value of the AVD is calculated based on the time interval between the end time of the EA4 component and the start time of the EA1 component immediately following.

7. The device of claim 6, wherein the value of the AVD is calculated so that the end time of the EA4 component matches the start time of the immediately following EA1 component.

8. The device of claim 6, wherein the value of the AVD is calculated so that the end time of the EA4 component precedes the start time of the immediately following EA1 component by a predetermined duration.

9. The device of claim 1, wherein the means for analyzing the EA signal further comprises means for quantifying a parameter (I) of the EA signal within at least one analysis time window (W) having a predetermined length, said window being triggered after the detection of the atrial event (P), and ending on another specific event.

10. The device of claim 9 wherein said another specific event is an event selected from among the group consisting of a ventricular detection, a ventricular stimulation, a detection of an EA1 signal, and a fixed period.

11. The device of claim 9 wherein the quantified parameter (I) is the energy of the EA signal integrated over the duration of the window (W).

12. The device of claim 9, wherein the means for analyzing the EA signal further comprises means for quantifying the parameter (I1 . . . In) inside each of a plurality of temporally successive windows (W1 . . . Wn).

13. The device of claim 12, wherein the temporally successive windows (W1 . . . Wn) are windows overlapping in time.

14. The device of claim 12, wherein the means for analyzing the EA signal further comprises means for comparing the quantified parameters (I1 . . . In) to a given threshold (S) and defining the end time of the EA4 component in response to the quantified parameters of successive windows crossing downward of said threshold.

15. The device of claim 14, wherein the threshold (S) is selected from among the group consisting of a fixed threshold;

a parameterizable threshold;

an adaptive threshold recalculated at regular intervals; and

an adaptive threshold recalculated on each cycle comprising a valid atrial event.

16. The device of claim 1, wherein the acceleration sensor is selected from among the group consisting of an endocardial sensor;

an epicardial sensor; and

an external sensor.