Method and apparatus for tissue protection against ischemia using remote conditioning

• US 8,874,207 B2
• Filed: 12/08/2010
• Issued: 10/28/2014
• Est. Priority Date: 12/23/2005
• Status: Active Grant

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Sih, Haris J., Baynham, Tamara Colette, Wagner, Darrell O.
• Primary Examiner(s): PATTON, AMANDA K
• Application Number:
  US12/963,224
• Publication Number:
  US 20110077701A1
• Time in Patent Office: 1,420 Days
• Field of Search: 607 2- 3
• US Class Current: 607/3
• CPC Class Codes: A61N 1/3627 for treating a mechanical deficiency of the heart, e.g. congestive heart failure or cardiomyopathy

Abstract

A stimulation system delivers stimulation to protect an ischemic region of a body from tissue damage caused by ischemia. The stimulation is delivered to one or more stimulation sites remote from the ischemic region to elicit a physiological effect that protects the ischemic region from the tissue damage caused by ischemia. In one embodiment, the stimulation system delivers cardioprotective stimulation to one or more stimulation sites remote from the heart to protect the heart from injuries associated with cardiac ischemic events. In another embodiment, the stimulation system delivers remote conditioning stimulation to one or more stimulation sites in or on the heart to protect a non-cardiac region from injuries associated with non-cardiac ischemic events.

Claims

1. A method for operating an implantable medical device to stimulate at least one stimulation site in a body having a heart, the at least one stimulation site remote from the heart, the method comprising:

detecting an end of a cardiac ischemic event;

producing a cardioprotective stimulation signal in response to a detection of the end of the cardiac ischemic event;

timing a cardioprotective stimulation sequence in response to the cardioprotective stimulation signal, the cardioprotective stimulation sequence including alternating stimulation and non-stimulation periods, the stimulation periods each having a stimulation duration during which one or more non-cardiac stimuli are delivered, the non-stimulation periods each having a non-stimulation duration during which no non-cardiac stimulus is delivered; and

delivering the one or more non-cardiac stimuli from the implantable medical device to the at least one stimulation site remote from the heart during each of the stimulation period, the one or more non-cardiac stimuli creating a physiologic stress at the at least one stimulation site without causing myocardial contraction in the heart, the physiologic stress capable of eliciting a cardioprotective effect that protects the heart from tissue damage caused by cardiac ischemia.

2. The method of claim 1, further comprising:

sensing at least one stress-indicating signal indicative of a level of the physiologic stress; and

adjusting the delivery of the one or more non-cardiac stimuli using the at least one stress-indicating signal.

3. The method of claim 2, wherein sensing the at least one stress-indicating signal comprises sensing an exertion level signal.

4. The method of claim 3, wherein sensing the exertion level signal comprises sensing a pH value.

5. The method of claim 3, wherein sensing the exertion level signal comprises sensing an oximetry or plethysmography signal.

6. The method of claim 3, wherein sensing the exertion level signal comprises sensing a respiratory signal.

7. The method of claim 3, wherein sensing the exertion level signal comprises sensing one or more cardiac time intervals.

8. The method of claim 3, wherein sensing the exertion level signal comprises sensing one or more of body temperature, blood temperature, and myocardial temperature.

9. The method of claim 2, wherein sensing the at least one stress-indicating signal comprises sensing an electrogram.

10. The method of claim 2, wherein sensing the at least one stress indicating signal comprises sensing a degree of chemical reaction to the non-cardiac stimili.

11. The method of claim 1, wherein delivering the one or more non-cardiac stimuli comprises delivering one or more of electrical stimuli, chemical stimuli, biologic stimuli, mechanical stimuli, optical stimuli, thermal stimuli, and acoustic stimuli.

12. The method of claim 11, wherein delivering the one or more non-cardiac stimuli comprises delivering electrical stimulation pulses.

13. The method of claim 12, wherein delivering the electrical stimulation pulses comprises delivering the electrical stimulation pulses to skeletal muscles in a pectoral area of the body.

14. The method of claim 1, wherein producing the cardioprotective stimulation signal comprises producing a postconditioning signal in response to the detection of the cardiac ischemic event, and wherein timing the cardioprotective stimulation sequence in response to the cardioprotective stimulation signal comprises timing a postconditioning stimulation sequence in response to the postconditioning signal.

15. The method of claim 14, wherein producing the postconditioning signal in response to the detection of the cardiac ischemic event comprises producing the postconditioning signal when a post-ischemia time interval expires, the post-ischemia time interval starting when an end of the cardiac ischemic event is detected and is up to approximately 10 minutes.

16. The method of claim 14, wherein producing the cardioprotective stimulation signal further comprises producing a plurality of preconditioning signals in response to the detection of the cardiac ischemic event, and wherein timing the cardioprotective stimulation sequence in response to the cardioprotective stimulation signal comprises timing a preconditioning stimulation sequence in response to each of the preconditioning signals.

17. The method of claim 16, wherein producing the plurality of preconditioning signals comprises producing the plurality of preconditioning signals on a periodic basis using a predetermined period in a range of approximately 24 hours to 72 hours.

18. The method of claim 1, further comprising:

detecting a cardioprotective stimulation command; and

producing the cardioprotective stimulation signal in response to the detection of the cardioprotective stimulation command.

19. The method of claim 18, wherein producing the cardioprotective stimulation signal comprises producing a postconditioning signal and a plurality of preconditioning signals in response to the detection of the cardioprotective stimulation command.

20. The method of claim 18, wherein producing the cardioprotective stimulation signal comprises producing a postconditioning signal when the detected cardioprotective stimulation command is a postconditioning command and producing a preconditioning signal when the detected cardioprotective stimulation command is a preconditioning command.