Methods and means for non-invasive, dynamic tracking of cardiac vulnerability by simultaneous analysis of heart rate variability and T-wave alternans

• US 5,265,617 A
• Filed: 09/22/1992
• Issued: 11/30/1993
• Est. Priority Date: 02/20/1991
• Status: Expired due to Term

• Current Assignee: Georgetown University
• Original Assignee: Georgetown University
• Inventors: Nearing, Bruce D., Verrier, Richard L.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US07/948,529
• Time in Patent Office: 434 Days
• Field of Search: 128/702-705
• US Class Current: 600/517
• CPC Class Codes: A61B 5/02405 Determining heart rate variability
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/35 by template matching
• CPC Class Codes: A61B 5/355 Detecting T-waves
• CPC Class Codes: A61B 5/361 Detecting fibrillation
• CPC Class Codes: A61B 5/4035 Evaluating the autonomic nervous system
• CPC Class Codes: A61B 5/7275 Determining trends in physiological measurement data; Predicting development of a medical condition based on physiological measurements, e.g. determining a risk factor
• CPC Class Codes: G06F 2218/12 Classification; Matching

Abstract

A method and apparatus for the non-invasive, dynamic tracking and diagnosing of cardiac vulnerability to ventricular fibrillation are disclosed. T-wave alternans and heart rate variability are simultaneously evaluated. T-wave alternation is an absolute predictor of cardiac electrical instability. Heart rate variability is a measure of autonomic influence, a major factor in triggering cardiac arrythmias. By simultaneously analyzing both phenomena, the extent and cause of cardiac vulnerability can be assessed. The method includes the following steps. An ECG signal is sensed from a heart. The T-wave portions of the ECG signal are analyzed to estimate an amplitude of beat-to-beat alternation. The amplitude of beat-to-beat alternation represents cardiac electrical instability. The R-R intervals are analyzed to estimate a magnitude of a high frequency component of heart rate variability and to estimate a magnitude of a low frequency component of heart rate variability. The high frequency component indicates parasympathetic activity. The low frequency component indicates combined sympathetic activity and parasympathetic activity. The amplitude of beat-to-beat alternation, the high frequency component of heart rate variability, and the low frequency component of heart rate variability are simultaneously analyzed to diagnose cardiac electrical instability.

Claims

1. A method of tracking and diagnosing cardiac vulnerability comprising the steps of:

sensing an ECG signal from a heart, said ECG signal having a plurality of R-R intervals, each R-R interval including an R-wave and a T-wave;

analyzing said T-waves to estimate an amplitude of beat-to-beat alternation, said amplitude of beat-to-beat alternation representing cardiac electrical instability;

analyzing said R-R intervals to estimate a magnitude of a high frequency component of heart rate variability and to estimate a magnitude of a low frequency component of heart rate variability, said magnitude of said high frequency component indicating parasympathetic neural influence on the heart, said low frequency component indicating combined sympathetic and parasympathetic neural influence on the heart; and

analyzing said amplitude of beat-to-beat alternation, said magnitude of said high frequency component of heart rate variability, and said magnitude of said low frequency component of heart rate variability to diagnose said cardiac electrical instability.

2. The method of claim 1 wherein said step of sensing an ECG signal comprises the following steps:

placing a precordial ECG lead on the surface of a subject'"'"'s body proximate to the subject'"'"'s heart to sense said ECG signal;

amplifying said ECG signal;

low-pass filtering said ECG signal; and

sampling said ECG signal.

3. The method of claim 2, wherein said step of analyzing said T-waves comprises the following steps:

predicting the location in said ECG signal of the T-wave in each R-R interval;

partitioning each T-wave in said ECG signal into a plurality of time divisions;

summing the samples in each of said time divisions of said ECG signal;

forming a time series for each of said time divisions, each time series including corresponding sums from corresponding time divisions from successive ones of said T-waves; and

performing dynamic estimation on each said time series to estimate the amplitude of beat-to-beat alternation for each said time division.

4. The method of claim 3, wherein said step of performing dynamic estimation includes performing complex demodulation on each said time series.

5. The method of claim 2, wherein said step of analyzing said R-R intervals comprises the following steps:

locating the peak amplitude in each R-R interval to find the apex of each R-wave;

computing the time between successive R-waves to determine a magnitude of each said R-R interval;

forming a time series with said magnitudes of said R-R intervals;

performing dynamic estimation on said time series to estimate said magnitude of said high frequency component of heart rate variability and to estimate said magnitude of said low frequency component of heart rate variability; and

forming a ratio of said magnitudes of said low frequency and said high frequency components of heart rate variability, said ratio indicating sympathetic activity.

6. The method of claim 5, wherein said step of performing dynamic estimation includes performing complex demodulation on said time series.

7. The method of any of claims 3-6, further comprising the step of comparing each R-R interval with a standard criteria to eliminate premature beats.

8. The method of claim 7, further comprising the step of detrending each said time series prior to performing dynamic estimation in order to eliminate the effects of drift and DC bias.

9. A method of tracking and diagnosing cardiac vulnerability comprising the steps of:

sensing an ECG signal from a heart, said ECG signal including a plurality of R-R intervals and a plurality of T-waves;

analyzing said T-waves to estimate an amplitude of beat-to-beat alternation, said amplitude of beat-to-beat alternation representing cardiac electrical instability.

analyzing said R-R intervals to characterize heart rate variability;

estimating the magnitude of a high frequency component of heart rate variability, said magnitude of said high frequency component indicating parasympathetic activity;

estimating the magnitude of a low frequency component of heart rate variability;

forming a ratio of said low frequency and said high frequency components of heart rate variability, said ratio indicating sympathetic activity; and

analyzing said amplitude of beat-to-beat alternation, said magnitude of said low frequency component of heart rate variability, and said ratio of said low frequency and said high frequency components of heart rate variability to diagnose said cardiac electrical instability.

10. The method of claim 9, wherein said step of sensing an ECG signal comprises the following steps:

placing a precordial ECG lead on the surface of a subject'"'"'s body proximate to the subject'"'"'s heart to sense said ECG signal;

amplifying said ECG signal;

low-pass filtering said ECG signal; and

sampling said ECG signal.

11. The method of claim 10, wherein said step of analyzing said T-waves comprises the following steps:

predicting the location in said ECG signal of the T-wave in each R-R interval;

partitioning each T-wave in said ECG signal into a plurality of time divisions;

summing the samples in each of said time divisions of said ECG signal;

forming a time series for each of said time divisions, each time series including corresponding sums from corresponding time divisions from successive ones of said T-waves; and

performing dynamic estimation on each said time series to estimate the amplitude of beat-to-beat alternation for each said time division.

12. The method of claim 11, wherein said step of performing dynamic estimation includes performing complex demodulation on each said time series.

13. The method of claim 10, wherein said step of analyzing said R-R intervals comprises the following steps:

locating the peak amplitude in each R-R interval to find the apex of each R-wave;

computing the time between successive R-waves to determine a magnitude of each said R-R interval; and

forming a time series with said magnitudes of said R-R intervals.

14. The method of claim 13 wherein said steps of estimating the magnitude of low and high frequency components of heart rate variability are performed using complex demodulation.

15. An apparatus for dynamically tracking and diagnosing cardiac vulnerability by simultaneously analyzing T-wave alternation and heart rate variability in an ECG having a plurality of R-R intervals, said apparatus comprising:

means for sampling the ECG;

means for predicting the location in the ECG signal of the T-wave in each R-R interval;

means for analyzing said T-waves to determine an amplitude of beat-to-beat alternation;

means for computing the magnitude of each R-R interval to determine a heart rate;

means for analyzing said heart rate to determine a variability therein, for computing a magnitude of a high frequency component of said variability indicative of parasympathetic neural influence on a heart and a magnitude of a low frequency component of said variability indicative of combined sympathetic and parasympathetic neural influence on said heart, and for computing a ratio of said low frequency component to said high frequency component, said ratio indicating sympathetic neural influence on said heart; and

means for presenting said amplitude of beat-to-beat alternation, said high frequency component of said variability and said ratio to a user.