Intermittent stress augmentation pacing for cardioprotective effect

• US 7,979,123 B2
• Filed: 10/08/2007
• Issued: 07/12/2011
• Est. Priority Date: 01/06/2005
• Status: Expired due to Fees

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Cornelussen, Richard, Prinzen, Frits, Vanagt, Ward, Spinelli, Julio C., Pastore, Joseph M.
• Primary Examiner(s): Layno; Carl H
• Assistant Examiner(s): PATEL, NATASHA
• Application Number:
  US11/868,767
• Publication Number:
  US 20080027495A1
• Time in Patent Office: 1,373 Days
• Field of Search: 607/9, 607/17, 607/27, 600/510, 600/515, 600/516, 600/517
• US Class Current: 607/17
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions

Abstract

A device and method for delivering electrical stimulation to the heart in a manner which provides a protective effect against subsequent ischemia is disclosed. The protective effect is produced by configuring a cardiac pacing device to intermittently switch from a normal operating mode to a stress augmentation mode in which the spatial pattern of depolarization is varied to thereby subject a particular region or regions of the ventricular myocardium to increased mechanical stress.

Claims

1. A cardiac rhythm management device, comprising:

a pulse generator for delivering pacing pulses to a selected ventricular myocardial site through a pacing channel;

a controller for controlling the delivery of pacing pulses in accordance with a programmed pacing mode,

wherein the controller is programmed to operate in either a normal operating mode or a stress augmentation mode in which a particular region or regions of the ventricular myocardium are subjected to increased mechanical stress as compared with the stress experienced by those regions during the normal operating mode; and

,

wherein the controller is further programmed to intermittently switch from the normal operating mode to the stress augmentation mode for a specified stress augmentation time period according to a defined schedule.

2. The device of claim 1 wherein the normal operating mode is a primary pacing mode for delivering ventricular pacing therapy and wherein stress augmentation mode causes a different depolarization pattern than the primary pacing mode.

3. The device of claim 2 wherein the stress augmentation mode excites the ventricular myocardium at a site or sites different from the primary pacing mode.

4. The device of claim 2 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from bipolar pacing to unipolar pacing or vice-versa.

5. The device of claim 2 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching which electrode of a bipolar pacing lead is the cathode and which electrode is the anode.

6. The device of claim 2 further comprising:

multiple pulse generators for delivering pacing pulses to a plurality of ventricular pacing sites through multiple pacing channels; and

,

wherein the stress augmentation mode uses at least one pacing channel not used in the primary pacing mode.

7. The device of claim 6 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from left ventricle-only pacing to right ventricular pacing or vice-versa.

8. The device of claim 6 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from biventricular pacing to single ventricular pacing or vice-versa.

9. The device of claim 1 further comprising an exertion level sensor and wherein the controller is programmed such that the switch from a normal operating mode to a stress augmentation mode is inhibited if the measured exertion level is above a specified limit value.

10. The device of claim 1 further comprising a sensing amplifier for incorporation into a cardiac sensing channel and wherein the controller is programmed to detect cardiac ischemia from an electrogram morphology analysis and further wherein the controller is programmed such that the switch from a normal operating mode to a stress augmentation mode is inhibited if cardiac ischemia is detected.

11. A method for operating a cardiac rhythm management device, comprising:

delivering pacing therapy in either a normal operating mode or a stress augmentation mode in which a particular region or regions of the ventricular myocardium are subjected to increased mechanical stress as compared with the stress experienced by those regions during the normal operating mode;

intermittently switching from the normal operating mode to the stress augmentation mode for a specified stress augmentation time period according to a defined schedule.

12. The method of claim 11 wherein the normal operating mode is a primary pacing mode for delivering ventricular pacing therapy and wherein stress augmentation mode causes a different depolarization pattern than the primary pacing mode.

13. The method of claim 12 wherein the stress augmentation mode excites the ventricular myocardium at a site or sites different from the primary pacing mode.

14. The method of claim 12 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from bipolar pacing to unipolar pacing or vice-versa.

15. The method of claim 12 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching which electrode of a bipolar pacing lead is the cathode and which electrode is the anode.

16. The method of claim 12 wherein the device is equipped with multiple pacing channels and further wherein the stress augmentation mode uses at least one pacing channel not used in the primary pacing mode.

17. The method of claim 16 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from left ventricle-only pacing to right ventricular pacing or vice-versa.

18. The method of claim 16 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching from biventricular pacing to single ventricular pacing or vice-versa.

19. The method of claim 11 further comprising measuring a patient'"'"'s exertion level inhibiting the switch from a normal operating mode to a stress augmentation mode if the measured exertion level is above a specified limit value.

20. The method of claim 11 further comprising detecting cardiac ischemia from an electrogram morphology analysis and inhibiting the switch from a normal operating mode to a stress augmentation mode if cardiac ischemia is detected.