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Spatiotemporal heterogeneity of activation alternans in cardiomyopathy: Implications for risk stratification with
Nathan C Denham1, Adrian M Suszko1, Raja J Selvaraj2
1Division of Cardiology, Peter Munk Cardiac Center, University Health Network, Toronto, Canada.
Insights
Intracardiac activation alternans (AA) in cardiomyopathy patients are linked to ventricular arrhythmias (VA). Surface microvolt QRS alternans (QRSA) reflect these intracardiac changes, explaining their predictive value for VA.
Area of Science:
- Cardiology
- Electrophysiology
- Biomedical Engineering
Background:
- Microvolt QRS alternans (QRSA) on the surface ECG predicts ventricular arrhythmia (VA) in cardiomyopathy (CM) patients.
- The precise intracardiac origin of QRSA remains undefined.
Purpose of the Study:
- To investigate the spatiotemporal characteristics of intracardiac activation alternans (AA).
- To correlate intracardiac AA with surface QRSA and subsequent VA risk.
Main Methods:
- Recorded unipolar electrograms from left ventricular epicardium and right ventricular endocardium in 10 CM patients.
- Quantified AA and QRSA using spectral methods during atrial pacing at varying rates.
- Utilized a heart model to simulate AA and assess its relationship with surface QRSA.
- Followed patients for 5 years to record VA events.
Main Results:
- AA was more prevalent in the left ventricular epicardium and late QRS complex.
- AA prevalence and magnitude increased with heart rate, with an earlier onset than QRSA.
- Simulated AA correlated with surface QRSA magnitude.
- Patients with AA at 75 bpm had a significantly higher incidence of VA (100% vs. 0%).
Conclusions:
- Intracardiac AA displays significant spatiotemporal heterogeneity and heart rate dependency in CM.
- Surface QRSA is a noninvasive indicator of intracardiac AA.
- This relationship likely underlies the prognostic significance of QRSA for VA.
Background:
Microvolt QRS alternans (QRSA) on the surface electrocardiogram is a strong predictor of ventricular arrhythmia (VA) in patients with cardiomyopathy (CM); however, its intracardiac origin has not been defined.
Objective:
This study aimed to assess the spatiotemporal features of intracardiac activation alternans (AA) in relation to body surface QRSA and VA.
Methods:
Unipolar electrograms were recorded from the great cardiac vein (left ventricular epicardium) and the right ventricular endocardium in 10 patients with CM (age 59 ± 16 years; left ventricular ejection fraction 32% ± 9%). Unipolar AA and surface QRSA were quantified using the spectral method during consecutive atrial pacing at 75, 100, and 120 beats per minute. AA was simulated with a 1500-node heart model to assess the relationship with surface QRSA. Patients were followed for VA over 5 years.
Results:
AA was more prevalent in the left ventricular epicardium than the right ventricular endocardium (25% vs 5% of recording electrodes; P = .01) and more prevalent in the late QRS than early QRS (92% vs 69%; P < .01). AA and QRSA were equally prevalent (62% vs 46%; P = .12) but AA had greater magnitude (43 [0-90] vs 0 [0-6] μV; P < .01). AA prevalence and magnitude increased with rate but had a lower heart rate onset than QRSA. Simulated activation time alternans of 2-5 ms in a 1 cm node produced surface QRSA of similar magnitude to patients with AA. Patients with AA at 75 beats per minute were more likely to have VA in follow-up (100% vs 0%; P = .048).
Conclusion:
AA exhibits substantial spatiotemporal heterogeneity in patients with CM and is dependent on heart rate. Surface microvolt QRSA is the noninvasive manifestation of intracardiac AA, which may explain its prognostic utility.
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