Literature DB >> 20816873

Beat-to-beat three-dimensional ECG variability predicts ventricular arrhythmia in ICD recipients.

Larisa G Tereshchenko1, Lichy Han, Alan Cheng, Joseph E Marine, David D Spragg, Sunil Sinha, Darshan Dalal, Hugh Calkins, Gordon F Tomaselli, Ronald D Berger.   

Abstract

BACKGROUND: Methodological difficulties associated with QT measurements prompt the search for new electrocardiographic markers of repolarization heterogeneity.
OBJECTIVE: We hypothesized that beat-to-beat 3-dimensional vectorcardiogram variability predicts ventricular arrhythmia (VA) in patients with structural heart disease, left ventricular systolic dysfunction, and implanted implantable cardioverter-defibrillators (ICDs).
METHODS: Baseline orthogonal electrocardiograms were recorded in 414 patients with structural heart disease (mean age 59.4 ± 12.0; 280 white [68%] and 134 black [32%]) at rest before implantation of ICD for primary prevention of sudden cardiac death. R and T peaks of 30 consecutive sinus beats were plotted in 3 dimensions to form an R peaks cloud and a T peaks cloud. The volume of the peaks cloud was calculated as the volume within the convex hull. Patients were followed up for at least 6 months; sustained VA with appropriate ICD therapies served as an end point.
RESULTS: During a mean follow-up time of 18.4 ± 12.5 months, 61 of the 414 patients (14.73% or 9.6% per person-year of follow-up) experienced sustained VA with appropriate ICD therapies: 41 of them were white and 20 were black. In the multivariate Cox model that included inducibility of VA and use of beta-blockers, the highest tertile of T/R peaks cloud volume ratio significantly predicted VA (hazard ratio 1.68, 95% confidence interval 1.01 to 2.80; P = .046) in all patients. T peaks cloud volume and T/R peaks cloud volume ratio were significantly smaller in black subjects (median 0.09 [interquartile range 0.04 to 0.15] vs. median 0.11 [interquartile range 0.06 to 0.22], P = .002).
CONCLUSION: A relatively large T peaks cloud volume is associated with increased risk of VA in patients with structural heart disease and systolic dysfunction.
Copyright © 2010 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20816873      PMCID: PMC2990972          DOI: 10.1016/j.hrthm.2010.08.022

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


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