Literature DB >> 21835319

Electrocardiographic comparison of ventricular arrhythmias in patients with arrhythmogenic right ventricular cardiomyopathy and right ventricular outflow tract tachycardia.

Kurt S Hoffmayer1, Orlando N Machado, Gregory M Marcus, Yanfei Yang, Colleen J Johnson, Simon Ermakov, Eric Vittinghoff, Ulhas Pandurangi, Hugh Calkins, David Cannom, Kathleen C Gear, Crystal Tichnell, Young Park, Wojciech Zareba, Frank I Marcus, Melvin M Scheinman.   

Abstract

OBJECTIVES: The purpose of this study was to evaluate whether electrocardiographic characteristics of ventricular arrhythmias distinguish patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) from those with right ventricular outflow tract tachycardia (RVOT-VT).
BACKGROUND: Ventricular arrhythmias in RVOT-VT and ARVD/C-VT patients can share a left bundle branch block/inferior axis morphology.
METHODS: We compared the electrocardiographic morphology of ventricular tachycardia or premature ventricular contractions with left bundle branch block/inferior axis pattern in 16 ARVD/C patients with that in 42 RVOT-VT patients.
RESULTS: ARVD/C patients had a significantly longer mean QRS duration in lead I (150 ± 31 ms vs. 123 ± 34 ms, p = 0.006), more often exhibited a precordial transition in lead V(6) (3 of 17 [18%] vs. 0 of 42 [0%] with RVOT-VT, p = 0.005), and more often had at least 1 lead with notching (11 of 17 [65%] vs. 9 of 42 [21%], p = 0.001). The most sensitive characteristics for the detection of ARVD/C were a QRS duration in lead I of ≥120 ms (88% sensitivity, 91% negative predictive value). QRS transition at V(6) was most specific at 100% (100% positive predictive value, 77% negative predictive value). The presence of notching on any QRS complex had 79% sensitivity and 65% specificity of (55% positive predictive value, 85% negative predictive value). In multivariate analysis, QRS duration in lead I of ≥120 ms (odds ratio [OR]: 20.4, p = 0.034), earliest onset QRS in lead V(1) (OR: 17.0, p = 0.022), QRS notching (OR: 7.7, p = 0.018), and a transition of V(5) or later (OR: 7.0, p = 0.030) each predicted the presence of ARVD/C.
CONCLUSIONS: Several electrocardiographic criteria can help distinguish right ventricular outflow tract arrhythmias originating from ARVD/C compared with RVOT-VT patients.
Copyright © 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21835319     DOI: 10.1016/j.jacc.2011.05.017

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


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Review 4.  Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges.

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Review 6.  Mechanism, diagnosis, and treatment of outflow tract tachycardia.

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7.  Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes.

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8.  Update on Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C).

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Review 9.  Right Ventricular Outflow Tract Arrhythmias: Benign Or Early Stage Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia?

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Journal:  J Atr Fibrillation       Date:  2014-12-31

Review 10.  Which Is The Appropriate Arrhythmia Burden To Offer RF Ablation For RVOT Tachycardias?

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