Non-invasive dynamic tracking of cardiac vulnerability by analysis of T-wave alternans

• US 5,148,812 A
• Filed: 09/30/1991
• Issued: 09/22/1992
• Est. Priority Date: 02/20/1991
• Status: Expired due to Term

• Current Assignee: Georgetown University
• Original Assignee: Georgetown University
• Inventors: Verrier, Richard L., Nearing, Bruce D.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US07/768,054
• Time in Patent Office: 358 Days
• Field of Search: 128/702-704, 128/710, 346/413.06
• US Class Current: 600/517
• 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 5/361 Detecting fibrillation
• CPC Class Codes: A61B 5/4035 Evaluating the autonomic nervous system

Abstract

A non-invasive method for dynamic tracking of cardiac vulnerability to ventricular fibrillation is disclosed. A heart is monitored to sense an ECG signal. The sensed ECG signal is then amplified and low-pass filtered before it is digitally sampled and stored. The location of the T-wave in each R-R interval (pulse) of the ECG is estimated and each T-wave is partitioned into a plurality of time divisions. The sampled ECG signal in each of the time divisions is summed together and a time series is formed for each of the time divisions such that each time series includes corresponding sums from corresponding time divisions from successive T-waves. Each time series is detrended in order to eliminate the effects of drift and DC bias, and then a method of dynamic estimation is performed on each time series to estimate the amplitude of alternation for each time division. The methods of dynamic estimation include Complex Demodulation, Estimation by Subtraction, Least Squares Estimation, Auto Regressive Estimation, and Auto Regressive Moving Average Estimation. In this manner, the cycle-to-cycle alternation in the T-wave of the ECG can be determined for dynamic tracking of cardiac vulnerability. In one embodiment of the invention, the ECG is sensed non-invasively via the precordial or chest leads. In alternate embodiments, the ECG is sensed via a catheter inserted into the apex of either the left or right ventricles of the heart.

Claims

1. A method of analyzing an ECG having a plurality of R-R intervals for dynamic tracking of cardiac vulnerability, comprising the steps of:

sampling said ECG signal;

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.

2. The method of claim 1, wherein said step of performing dynamic estimation includes performing complex demodulation on each said time series.

3. The method of claim 1, wherein said step of performing dynamic estimation includes performing estimation by subtraction on each said time series.

4. The method of claim 1, wherein said step of performing dynamic estimation includes performing least squares estimation on each said time series.

5. The method of claim 1, wherein said step of performing dynamic estimation includes performing auto-regressive estimation on each said time series.

6. The method of claim 1, wherein said step of performing dynamic estimation includes performing auto-regressive moving average estimation on each said time series.

7. The method of any of claims 1-6, 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.

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

9. The method of claim 8, wherein predicting the location in said ECG signal of the T-wave in each R-R interval includes identifying in said ECG signal the location of the R-wave in each R-R interval and predicting the location of the T-wave with respect to the location of the R-wave.

10. A method for dynamic tracking of 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;

sampling said ECG signal;

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.

11. The method of claim 10, wherein said step of performing dynamic estimation includes performing complex demodulation on each said time series.

12. The method of claim 10, wherein said step of performing dynamic estimation includes performing estimation by subtraction on each said time series.

13. The method of claim 10, wherein said step of performing dynamic estimation includes performing least squares estimation on each said time series.

14. The method of claim 10, wherein said step of performing dynamic estimation includes performing auto-regressive estimation on each said time series.

15. The method of claim 10, wherein said step of performing dynamic estimation includes performing auto-regressive moving average estimation on each said time series.

16. The method of any of claim 10-15, 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.

17. The method of any of claim 16, further comprising the step of comparing each R-R interval with a standard criteria to eliminate premature beats.

18. The method of claim 17, wherein predicting the location in said ECG signal of the T-wave in each R-R interval includes identifying in said ECG signal the location of the R-wave in each R-R interval and predicting the location of the T-wave with respect to the location of the R-wave.

19. The method of any of claims 10-15 wherein said ECG signal is sensed via a precordial surface lead.

20. The method of claim 18, wherein said ECG signal is sensed via a precordial surface lead.

21. A method for non-invasive, dynamic tracking of cardiac vulnerability in a live subject, comprising the steps of:

(a) placing a precordial ECG lead on the surface of the subject'"'"'s body proximate to the subject'"'"'s heart to sense an ECG signal, said ECG signal having a plurality of R-R intervals, each R-R interval including an R-wave and a T-wave;

(b) amplifying said ECG signal;

(c) low-pass filtering said ECG signal;

(d) sampling said ECG signal;

(e) identifying in said ECG signal the location of the R-wave in each R-R interval;

(f) comparing each R-R interval with a standard criteria to eliminate premature beats;

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

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

(i) summing the sampled ECG signal in each of said time divisions;

(j) 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;

(k) detrending each said time series; and

(l) performing dynamic estimation of the amplitude of beat-to-beat alternation for each said time division on each detrended time series.

22. The method of 21, wherein said precordial ECG lead of step (a) is lead V₅ when alternans originate from the left-hand side of the heart and wherein said precordial ECG lead is lead V₂ when alternans originate for the right-hand side of the heart.

23. An apparatus for dynamically tracking cardiac vulnerability by analyzing alternans in the T-waves of a plurality of R-R intervals of an ECG, 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 partitioning each T-wave in said ECG signal into a plurality of time divisions;

means for summing the samples of the ECG signal in each of said time divisions and for 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

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

24. The apparatus of claim 23, further comprising means for detrending each said time series prior to performing dynamic estimation in order to eliminate the effects of drift and DC bias.

25. The apparatus of claim 24, further comprising means for comparing each R-R interval with a standard criteria to eliminate premature beats.

26. An apparatus for the non-invasive, dynamic tracking of cardiac vulnerability through analysis of alternans in the T-waves of an ECG signal, said ECG signal having a plurality of R-to-R intervals, said apparatus comprising:

means for non-invasively sensing the ECG signal from a living subject;

means for high-pass filtering the ECG signal to eliminate DC components;

means for amplifying the ECG signal;

means for low-pass filtering the ECG signal to eliminate noise;

means for sampling the ECG signal to produce a sampled ECG signal;

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

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

means for summing the samples of the ECG signal in each of said time divisions and for 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

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

27. The apparatus of claim 26, further comprising means for detrending each said time series prior to performing dynamic estimation in order to eliminate the effects of drift and DC bias.

28. The apparatus of claim 27, further comprising means for comparing each R-R interval with a standard criteria to eliminate premature beats.