Controlled delivery of intermittent stress augmentation pacing for cardioprotective effect

• US 20060253156A1
• Filed: 06/13/2005
• Published: 11/09/2006
• Est. Priority Date: 05/06/2005
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Spinelli, Julio C., Pastore, Joseph M.
• Granted Patent: US 7,366,568 B2
• Time in Patent Office: Days
• US Class Current: 607/9
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• CPC Class Codes: A61N 1/36557 controlled by chemical substances in blood
• CPC Class Codes: A61N 1/3684 for stimulating the heart at multiple sites of the ventricle or the atrium
• CPC Class Codes: A61N 1/36842 Multi-site stimulation in the same chamber
• CPC Class Codes: A61N 1/36843 Bi-ventricular stimulation
• CPC Class Codes: A61N 1/3688 configured for switching the pacing mode, e.g. from AAI to DDD
• CPC Class Codes: A61N 1/3702 Physiological parameters A61N1/365 takes precedence; evoked response A61N1/371

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

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

wherein the controller is programmed to switch from a normal operating mode to 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 programmed to switch to the stress augmentation mode for a specified time period upon expiration of a timer, where the timer is defined with an expiration which coincides with when the patient is expected to awaken from sleep.

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 form 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 pacing channels for delivering pacing pulses to a plurality of ventricular pacing sites; and

,

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

7. A cardiac rhythm management device, comprising:

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

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

a posture sensor interfaced to the controller;

wherein the controller is programmed to switch from a normal operating mode to 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 programmed to switch to the stress augmentation mode for a specified time period upon receiving a signal from the posture sensor indicating that the patient'"'"'s posture has changed from a supine position to an erect or sitting position.

8. The device of claim 7 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.

9. The device of claim 8 wherein the stress augmentation mode excites the ventricular myocardium at a site or sites different from the primary pacing mode.

10. The device of claim 8 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching form bipolar pacing to unipolar pacing or vice-versa.

11. The device of claim 8 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.

12. The device of claim 8 further comprising:

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

,

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

13. The device of claim 7 wherein the controller is further programmed to switch to the stress augmentation mode for a specified time period upon receiving a signal from the posture sensor indicating that the patient'"'"'s posture has changed from a supine position to an erect or sitting position and if the time of day is within a defined wakeup window as determined by a time stamp.

14. A cardiac rhythm management device, comprising:

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

a sensing channel for detecting intrinsic cardiac activity;

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

wherein the controller is programmed to determine an LF/HF ratio by analyzing data received from the sensing channel;

wherein the controller is programmed to switch from a normal operating mode to 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 programmed to switch to the stress augmentation mode for a specified time period when the LF/HF ratio is above a specified threshold value.

15. The device of claim 14 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.

16. The device of claim 15 wherein the stress augmentation mode excites the ventricular myocardium at a site or sites different from the primary pacing mode.

17. The device of claim 15 wherein the switch from a primary pacing mode to a stress augmentation mode involves switching form bipolar pacing to unipolar pacing or vice-versa.

18. The device of claim 15 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.

19. The device of claim 15 further comprising:

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

,

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