Method and apparatus to optimally measure cardiac depolarization/repolarization instability

• US 6,850,796 B1
• Filed: 08/08/2000
• Issued: 02/01/2005
• Est. Priority Date: 08/31/1999
• Status: Expired due to Fees

• Current Assignee: Mortara Instrument, Inc. (Baxter International Inc.)
• Original Assignee: David W. Mortara
• Inventors: Mortara, David W.
• Primary Examiner(s): EVANISKO, GEORGE ROBERT
• Application Number:
  US09/634,271
• Time in Patent Office: 1,638 Days
• Field of Search: 600/512, 600/508, 600/509, 600/515, 600/517, 600/518
• US Class Current: 600/517
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle

Abstract

A method of identifying and measuring altemans in an electrocardiographic (ECG) signal representative of the electric activity of a heart of a patient. The ECG signals from the patient are divided into individual cardiac cycles and the amplitude of four segments of the repolarization portion and the depolarization portion of each cardiac cycle are measured. The amplitude for each of the repolarization segments are measured from a reference baseline that is determined by a first base segment occurring immediately prior to the repolarization portion of the present cardiac cycle and a second base segment occurring immediately before the depolarization portion of the next cardiac cycle in the sequence. Based upon the amplitude measurements over the repolarization and the depolarization portions of each cardiac cycle, digital signal processing is applied to the measurements to generate eigenvariables. A spectral density is calculated for each of the eigenvariables, which spectral densities can be used to determine both the presence of altemans and the respiratory frequency.

Claims

1. A method for identifying and measuring electrocardiographic altemans from at least one electrocardiographic (ECG) signal representative of the electric activity of a heart of a patient, the method comprising the steps of:

obtaining the ECG signal over a predetermined number of cardiac cycles of the patient'"'"'s heart;

dividing the ECG signal into its individual cardiac cycles, each cardiac cycle having a depolarization portion and a repolarization portion;

dividing the repolarization portion of each cardiac cycle into a plurality of repolarization segments;

separately measuring the amplitude of each of the plurality of repolarization segments contained in the repolarization portion during each cardiac cycle, the amplitude of each repolarization segment for each cardiac cycle being measured from a repolarization reference baseline drawn between a first base segment occurring immediately prior to the repolarization portion of the present cardiac cycle and a second base segment occurring immediately prior to the depolarization portion of the subsequent cardiac cycle; and

digitally processing the amplitude measurements for the repolarization segments to determine the presence of alternans in the physiologic signals.

2. The method of claim 1 wherein the step of obtaining the ECG signal includes:

obtaining a twelve lead ECG signal over the predetermined number of cardiac cycles; and

reducing the twelve lead ECG signal to an orthogonal 3-dimensional lead set.

3. The method of claim 2 wherein the step of reducing the twelve lead ECG signal to the 3-dimensional set includes the steps of:

deriving eight orthogonal leads from the twelve lead ECG signal where the eight orthogonal leads are linear combinations of the twelve ECG signal leads; and

selecting the three leads of the eight orthogonal lead ECG signal that have the largest mean-square amplitude.

4. The method of claim 1 further comprising the step of measuring the amplitude of a plurality of depolarization segments contained in the depolarization portion of each cardiac cycle, the amplitude of each depolarization segment being measured from a second reference baseline defined by a third base segment occurring immediately prior to the depolarization portion of the present cardiac cycle and the second base segment occurring immediately prior to the depolarization portion of the subsequent cardiac cycle.

5. The method of claim 4 wherein the ECG signal includes three ECG signals taken from three leads and the amplitude of the repolarization portion of each cardiac cycle is measured at four repolarization segments for each of the three leads, such that twelve amplitude measurements are taken over the repolarization portion of each cardiac cycle.

6. The method of claim 5 wherein the digital processing of the twelve amplitude measurements for the repolarization segments includes:

filtering the amplitude measurements to remove the low frequency portion of each measurement;

transforming the twelve amplitude measurements into eigenvariables by using singular value decomposition; and

calculating a spectral density from each of the eigenvariables, wherein the spectral density for each of the eigenvariables are used to locate alternans.

7. The method of claim 5 wherein the ECG signal includes three ECG signals taken from three leads and the amplitude of the depolarization of each cardiac cycle is measured at four depolarization segments for each of the three leads, such that twelve amplitude measurements are taken over the depolarization portion of each cardiac cycle.

8. The method of claim 7 wherein the digital processing of the twelve amplitude measurements of the depolarization portion of each cardiac cycle includes:

filtering the amplitude measurements to remove the low frequency portion of each amplitude measurement;

transforming the twelve amplitude measurements of the depolarization portion into eigenvariables by using singular value decomposition;

calculating a spectral density from each of the eigenvariables; and

determining the respiration frequency from the maximum spectral density of the first eigenvariable calculated from the depolarization portion of the cardiac cycle.

9. A method for identifying and measuring electrocardiographic altemans from at least one electrocardiographic (ECG) signal representative of the electric activity of a heart of a patient, the method comprising the steps of:

obtaining the ECG signal over a predetermined number of cardiac cycles of a patient'"'"'s heart;

dividing the ECG signal into its individual cardiac cycles, each cardiac cycle having a depolarization portion and a repolarization portion;

dividing the repolarization portion of each cardiac cycle into a plurality of repolarization segments;

separately measuring the amplitude of the plurality of repolarization segments contained in the repolarization portion during each cardiac cycle, the amplitude of each repolarization segment being measured from a repolarization reference baseline calculated from the ECG signal for only the present cardiac cycle; and

digitally processing the amplitude measurements from the plurality of repolarization segments for each cardiac cycle to determine the presence of alternans in the physiologic signals.

10. The method of claim 9 wherein the repolarization reference baseline is drawn between a first base segment occurring immediately prior to the repolarization portion of the present cardiac cycle and a second base segment occurring immediately prior to the depolarization portion of the subsequent cardiac cycle.

11. The method of claim 9 wherein the ECG signal includes three ECG signals taken from three leads and the amplitude of the repolarization portion of each cardiac cycle is measured at four repolarization segments for each of the three leads, such that twelve amplitude measurements are taken over the repolarization portion of each cardiac cycle.

12. The method of claim 11 wherein the digital processing of the twelve amplitude measurements for the repolarization segments includes:

filtering the amplitude measurements to remove the low frequency portion of each measurement;

transforming the twelve amplitude measurements into eigenvariables by using singular value decomposition; and

calculating a spectral density from each of the eigenvariables, wherein the spectral density for each of the eigenvariables are used to locate alternans.

13. The method of claim 9 wherein the step of obtaining the ECG signal includes:

obtaining a twelve lead ECG signal over the predetermined number of cardiac cycles; and

reducing the twelve lead ECG signal to an orthogonal 3-dimensional lead set.

14. The method of claim 13 wherein the step of reducing the twelve lead ECG signal to the 3-dimensional set includes the steps of:

deriving eight orthogonal leads from the twelve lead ECG signal where the eight orthogonal leads are linear combinations of the twelve ECG signal leads; and

selecting the three leads of the eight orthogonal lead ECG signal that have the largest mean-square amplitude.

15. The method of claim 9 further comprising the step of separately measuring the amplitude of a plurality of depolarization segments contained in the depolarization portion during each cardiac cycle, the amplitude of each depolarization segment being measured from a second reference baseline.

16. The method of claim 15 wherein the second reference baseline is drawn between by a third base segment occurring immediately prior to the depolarization portion of the present cardiac cycle and a second base segment occurring immediately prior to the depolarization portion of the subsequent cardiac cycle.