Apparatus for reversal of myocardial remodeling with pre-excitation

• US 8,046,066 B2
• Filed: 06/15/2009
• Issued: 10/25/2011
• Est. Priority Date: 04/27/2001
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Spinelli, Julio C., Kramer, Andrew P., KenKnight, Bruce H., Salo, Rodney W.
• Primary Examiner(s): Layno; Carl H
• Assistant Examiner(s): SARCIONE, JESSICA LYNN
• Application Number:
  US12/484,882
• Publication Number:
  US 20090254141A1
• Time in Patent Office: 862 Days
• Field of Search: 607/9, 607 13- 14, 607 17- 18, 607/25
• US Class Current: 607/9
• CPC Class Codes: A61N 1/3627 for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• CPC Class Codes: A61N 1/36542 controlled by body motion, e.g. acceleration
• CPC Class Codes: A61N 1/36585 controlled by two or more physical parameters
• CPC Class Codes: A61N 1/368 comprising more than one electrode co-operating with different heart regions A61N1/3622, A61N1/3627 take precedence

Abstract

An apparatus for reversing ventricular remodeling with electro-stimulatory therapy. A ventricle is paced by delivering one or more stimulatory pulses in a manner such that a stressed region of the myocardium is pre-excited relative to other regions in order to subject the stressed region to a lessened preload and afterload during systole. The unloading of the stressed myocardium over time effects reversal of undesirable ventricular remodeling.

Claims

1. A cardiac pacing device, comprising:

a sensing amplifier and pulse generator for incorporating into one or more sensing/pacing channels including a pacing electrode for disposition at a first pacing site in proximity to a stressed region of the myocardium;

an exertion level sensor;

a controller for controlling the delivery of pacing pulses;

wherein the controller is programmed to deliver pacing therapy to the first pacing site in a manner such that the stressed region of the myocardium is excited before other regions of the myocardium in order to subject the stressed region to less mechanical stress when the myocardium contracts;

wherein the controller is programmed to measure the patient'"'"'s exertion level with the exertion level sensor; and

,

wherein the controller is programmed to alternate between a pulse output sequence that pre-excites the stressed region and a pulse output sequence that does not in accordance with the exertion level measurement such that pre-excitation of the stressed region is discontinued during periods of increased exertion.

2. The device of claim 1 wherein the exertion level sensor is an accelerometer.

3. The device of claim 1 wherein the exertion level sensor is a minute ventilation sensor.

4. The device of claim 1 further comprising means for adjusting a pacing pulse output sequence in accordance with measurements of myocardial mass.

5. The device of claim 1 wherein the controller is programmed to deliver pacing therapy to the stressed region in an atrial tracking or AV sequential pacing mode with an AV delay interval shorter than the patient'"'"'s measured intrinsic AV delay interval by a specified pre-excitation interval.

6. The device of claim 5 wherein the controller is programmed to vary the AV delay interval dynamically with a measured heart rate.

7. The device of claim 5 wherein the controller is programmed to vary the AV delay interval dynamically with a measured exertion level.

8. The device of claim 1 wherein:

the controller is programmed to measure an intrinsic conduction delay between the first pacing site and an earlier excited ventricular site during an intrinsic heartbeat referred to as a V-V interval; and

,

the controller is programmed to deliver pacing pulses to the pacing site in accordance with a programmed pacing mode, wherein the pacing pulses are delivered after an AV pacing delay interval following an atrial sense or pace which is set in accordance with the measured V-V interval.

9. The device of claim 8 wherein the AV pacing delay interval is set to equal a linear function of the V-V interval subtracted from a measured intrinsic AV delay interval.

10. The device of claim 1 wherein the controller is programmed to alternately switch between delivering paces to the first pacing site in proximity to the stressed region and a second pacing site disposed elsewhere.

11. The device of claim 10 wherein the controller is programmed to switch between delivering paces to the first pacing site in proximity to the stressed region and a second pacing site disposed elsewhere in accordance with a the exertion level measurement.

12. The device of claim 1 wherein the controller is programmed to delivering pacing pulses to a plurality of pacing sites as defined by a specified pulse output configuration and in accordance with a defined pulse output sequence such that the stressed region is excited before other regions of the myocardium.

13. The device of claim 12 wherein the pulse output sequence specifies that the paces are delivered after an AV delay interval following an atrial sense or pace.

14. The device of claim 12 wherein the controller is programmed to adjust the pulse output sequence in accordance with measurements of conduction delays that reflect regional variations in myocardial mass.

15. The device of claim 12 wherein the controller is programmed to adjust the pulse output sequence in accordance with impedance measurements that reflect regional variations in myocardial mass.

16. The device of claim 12 wherein the controller is programmed to adjust the pulse output sequence in accordance with impedance measurements that reflect variations in contraction sequence.

17. The device of claim 12 wherein the controller is programmed to adjust the pulse output sequence used to pre-excite the stressed region in accordance with detected changes in the remodeling process.

18. A system, comprising:

means for identifying a stressed region of a patient'"'"'s myocardium;

a pacing device with one or more electrodes including a pacing electrode for disposition at a first pacing site in proximity to the stressed region;

wherein the pacing device is programmed to deliver pacing therapy to the first pacing site in a manner such that the stressed region of the myocardium is excited before other regions of the myocardium in order to subject the stressed region to less mechanical stress when the myocardium contracts;

wherein the pacing device is programmed to measure the patient'"'"'s exertion level with an accelerometer or minute ventilation sensor; and

,

wherein the pacing device is programmed to alternate between a pulse output sequence that pre-excites the stressed region and a pulse output sequence that does not in accordance with the exertion level measurement such that pre-excitation of the stressed region is discontinued during periods of increased exertion.

19. The system of claim 18 wherein the means for identifying a stressed region of the myocardium is capable of identifying a hypertrophied region.

20. The system of claim 18 the means for identifying a stressed region of the myocardium is capable of identifying an infarcted region.