PRESSURE MEASUREMENT-BASED ISCHEMIA DETECTION

• US 20080287818A1
• Filed: 04/19/2007
• Published: 11/20/2008
• Est. Priority Date: 04/19/2007
• Status: Abandoned Application

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Inventors: Shelchuk, Anne M., Gutfinger, Dan E.
• Application Number:
  US11/737,650
• Publication Number:
  US 20080287818A1
• Time in Patent Office: Days
• US Class Current: 600/509
• CPC Class Codes: A61B 5/0215 by means inserted into the body catheters A61M25/00
• CPC Class Codes: A61B 5/352 Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• CPC Class Codes: A61N 1/36564 controlled by blood pressure
• CPC Class Codes: A61N 1/36585 controlled by two or more physical parameters
• CPC Class Codes: A61N 1/3684 for stimulating the heart at multiple sites of the ventricle or the atrium

Abstract

In some aspects ischemia is indicated based on cardiac pressure measurements. For example, ischemia may be indicated based on an increase in an intraventricular electromechanical delay where mechanical contractions are detected by measuring pressure in a cardiac chamber. Ischemia detection also may involve obtaining timing information relating to a mechanical contraction of at least one ventricle to identify an intraventricular dyssynchrony. In this case, pressure measurements may be used to identify the timing of the mechanical contraction. Ischemia may be indicated based on a change in a time interval associated with a systolic interval of a ventricle. Ischemia also may be indicated based on an intracardiac electrogram-based indication of ischemia in conjunction with an increase in mean left atrial pressure and/or an increase in the size of a v-wave.

Claims

1. A method of generating an indication of ischemia associated with a heart of a patient, comprising:

determining an electrical depolarization to mechanical contraction delay for a ventricle of a heart;

determining whether the delay is more than an expected delay; and

generating an indication of ischemia in accordance with a determination that the delay is more than the expected delay.

2. The method of claim 1, wherein determining whether the delay is more than the expected delay comprises comparing the delay to a baseline delay value.

3. The method of claim 2, further comprising adjusting the baseline delay value in accordance with an activity level and/or a position of the patient.

4. The method of claim 1, wherein determining whether the delay is more than the expected delay comprises determining that electrical depolarization to mechanical contraction delay for the ventricle has increased.

5. The method of claim 1, wherein determining whether the delay is more than the expected delay comprises determining whether there has been an increase in a percentage of a cardiac cycle associated with electrical depolarization to mechanical contraction delay for the ventricle.

6. The method of claim 1, wherein determining the electrical depolarization to mechanical contraction delay comprises measuring a delay between an R-wave and an upslope of a pressure wave for the ventricle.

7. The method of claim 1, wherein determining the electrical depolarization to mechanical contraction delay comprises measuring left atrial pressure.

8. The method of claim 1, wherein the ventricle comprises a right ventricle or a left ventricle.

9. The method of claim 1, wherein generating the indication of ischemia further comprises corroborating an intracardiac electrogram-based indication of ischemia.

10. A method of generating an indication of ischemia associated with a heart of a patient, comprising:

determining timing of an onset of mechanical contraction for at least one ventricle of a heart by measuring pressure associated with the at least one ventricle;

identifying an intraventricular dyssynchrony in accordance with the timing of the onset of mechanical contraction for the at least one ventricle; and

generating an indication of ischemia in accordance with the identification of an intraventricular dyssynchrony.

11. The method of claim 10, wherein determining timing of the onset of mechanical contraction for at least one ventricle comprises determining that contraction of a left ventricle follows contraction of a right ventricle by a time interval that is greater than an expected time interval.

12. The method of claim 10, wherein determining timing of the onset of mechanical contraction for at least one ventricle comprises determining whether there is an increase in a percentage of a cardiac cycle associated with a time period between contraction of a left ventricle and contraction of a right ventricle.

13. The method of claim 10, wherein determining timing of the onset of mechanical contraction for at least one ventricle comprises obtaining pressure information associated with a right ventricle and obtaining pressure information associated with a left ventricle.

14. The method of claim 10, wherein:

the at least one ventricle comprises a first ventricle; and

identifying the intraventricular dyssynchrony further comprises determining that a time interval between an electrical depolarization of a second ventricle and the onset of mechanical contraction for the first ventricle is greater than an expected time interval.

15. The method of claim 10, wherein generating the indication of ischemia further comprises corroborating an intracardiac electrogram-based indication of ischemia.

16. A method of generating an indication of ischemia associated with a heart of a patient, comprising:

generating an intracardiac electrogram-based indication of ischemia;

detecting a change in left atrial pressure; and

generating an indication of ischemia in accordance with the intracardiac electrogram-based indication of ischemia and the change in left atrial pressure.

17. The method of claim 16, wherein detecting the increase in mean left atrial pressure comprises:

obtaining a mean left atrial pressure value; and

comparing the mean left atrial pressure value to a baseline mean left atrial pressure.

18. The method of claim 16, wherein detecting the increase in mean left atrial pressure comprises determining that there has been an increase in a relative mean left atrial pressure associated with a first time interval and a second time interval.

19. The method of claim 18, wherein the first time interval corresponds to a time period when a v-wave is not present.

20. The method of claim 18, wherein the second time interval corresponds to a time period when a v-wave is present.