ECG signal power vector detection of ischemia or infarction

• US 7,567,836 B2
• Filed: 01/30/2006
• Issued: 07/28/2009
• Est. Priority Date: 01/30/2006
• Status: Expired due to Fees

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Zhang, Yi
• Primary Examiner(s): Layno; Carl H
• Assistant Examiner(s): Porter, Jr.; Gary A
• Application Number:
  US11/275,800
• Publication Number:
  US 20070179392A1
• Time in Patent Office: 1,275 Days
• Field of Search: 600/508, 600/512, 600/517
• US Class Current: 600/512
• CPC Class Codes: A61B 5/341 Vectorcardiography [VCG]
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/7207 of noise induced by motion artifacts
• CPC Class Codes: A61B 5/7285 for synchronising or triggering a physiological measurement or image acquisition with a physiological event or waveform, e.g. an ECG signal A61B6/5205, A61B6/541, A61B8/5207, A61B8/543 take precedence

Abstract

A system comprising a processor that includes a cardiac signal vector module and an ischemia detection module. The cardiac signal vector module is configured to measure a first dominant vector corresponding to a direction and magnitude of maximum signal power of a first segment of at least one cardiac cycle of a subject and at least a second dominant vector corresponding to a direction and magnitude of maximum signal power of a second segment of the cardiac cycle from an electrical cardiac signal. The ischemia detection module is configured to measure a change in the first dominant vector, to form a difference by subtracting a measured change in the second dominant vector from a measured change in the first dominant vector, and to declare whether an ischemic event occurred using the difference.

Claims

1. A system comprising:

a processor including;

a cardiac signal vector module configured to measure, from an electrical cardiac signal, a first dominant vector corresponding to a direction and magnitude of maximum signal power of an ST-T first segment of at least one cardiac cycle of a subject and at least a second dominant vector corresponding to a direction and magnitude of maximum signal power of a P-QRS second segment of the cardiac cycle, wherein the P-QRS segment includes the P-wave and extends to and includes the S-wave; and

an ischemia detection module configured to measure a change in the first dominant vector and the second dominant vector, to form a difference by subtracting a measured change in the second dominant vector from the measured change in the first dominant vector, and to declare whether an ischemic event occurred using the difference.

2. The system of claim 1, wherein the ischemia detection module reduces noise due to posture of the subject by the subtracting the measured change in the second dominant vector from the measured change in the first dominant vector.

3. The system of claim 1, wherein the cardiac signal vector module is further configured to establish first and second baseline vectors for the first and second dominant vectors, and wherein the ischemia detection module is further configured to measure a change in a dominant vector relative to a baseline vector.

4. The system of claim 3, wherein the ischemia detection module is further configured to:

subtract the first baseline vector from a later-measured first dominant vector to obtain a first change representative of a change due to posture during the first segment;

subtract the second baseline vector from a later-measured second dominant vector to obtain a second change representative of a change due to posture and ischemia during the second segment; and

subtract the first change from the second change to obtain a third change representative of a change due to ischemia.

5. The system of claim 3, wherein the ischemia detection module is configured to measure a change in a dominant vector by measuring at least one of a change in angle, a change in magnitude, a variance of the angle or the magnitude, a power spectral density, a rate of change of the angle, a rate of change of the magnitude, and a rate of change of the variance of the angle or the magnitude.

6. The system of claim 3, wherein the processor is operable to calculate trend data of measured subsequent changes from at least one baseline vector, and wherein the system includes a memory circuit coupled to the processor to store the trend data.

7. The system of claim 6, further including an ischemia indicator stored in the memory circuit, wherein the processor is operable to establish a value of the ischemia indicator using the trend data.

8. The system of claim 1, wherein the ischemia detection module declares that an ischemic event occurred when the difference exceeds a specified threshold value.

9. The system of claim 8, wherein the ischemia detection module declares that an ischemic event occurred if the difference exceeds a specified threshold value in X of Y consecutive cardiac cycles, wherein X and Y are integers and X is less than or equal to Y.

10. The system of claim 1, wherein the processor is included in an implantable medical device (IMD) and wherein the IMD further includes:

a plurality of implantable electrodes adapted for spatial distribution within the subject; and

at least one cardiac signal sensing circuit in communication with the electrodes, the cardiac signal sensing circuit operable to produce the electrical cardiac signal representative of cardiac activity of the subject, and wherein the processor is coupled to the cardiac signal sensing circuit.

11. The system of claim 10, wherein the plurality of implantable electrodes includes at least a first electrode and a second electrode adapted for placement to sense a cardiac signal approximating a surface electrocardiogram (ECG).

12. The system of claim 1, further including:

an implantable medical device (IMD) comprising;

a plurality of implantable electrodes adapted for spatial distribution within the subject;

at least one cardiac signal sensing circuit in communication with the electrodes, the cardiac signal sensing circuit operable to produce the electrical cardiac signal representative of cardiac activity of the subject;

a controller circuit coupled to the cardiac signal sensing circuit; and

a communication circuit coupled to the controller circuit; and

an external device, wherein the IMD is operable to communicate information to the external device and wherein the processor is included in the external device.

13. The system of claim 12, wherein the external device includes an IMD programmer.

14. The system of claim 12, wherein the external device includes a display configured to display a change in at least one of a magnitude and a direction of a computed vector.

15. The system of claim 1, wherein the processor is configured to activate an alarm indicative of a deemed ischemic event.

16. The system of claim 1, further including:

an implantable medical device (IMD) comprising;

a plurality of implantable electrodes adapted for spatial distribution within the subject;

at least one cardiac signal sensing circuit in communication with the electrodes, the cardiac signal sensing circuit operable to produce the electrical cardiac signal representative of cardiac activity of the subject;

a controller circuit coupled to the cardiac signal sensing circuit; and

a communication circuit coupled to the controller circuit;

an external device, wherein the IMD is operable to communicate information to the external device; and

a server in communication with a network, wherein the server includes the processor, and wherein the external device is operable to communicate with the server via the network.

17. The system of claim 16, wherein the server initiates at least one dominant vector measurement.

18. The system of claim 1, wherein the ischemia detection module is configured to deem whether an ischemic event occurred from whether the difference exceeds a specified threshold value in combination with a measured output provided from one or more sensors.

19. The system of claim 18, wherein the ischemia detection module is configured to deem whether an ischemic event occurred by blending the output provided by the censor and the difference according to at least one rule.

20. The system of claim 18, wherein the sensor includes at least one of a intracardiac impedance sensor, a transthoracic impedance sensor, and a blood pressure sensor.