Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis
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2018-07-01
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taverne
Abstract
While many studies evaluate predictors of ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy (ARVC), a systematic review consolidating this evidence is currently lacking. Therefore, we searched MEDLINE and Embase for studies analyzing predictors of ventricular arrhythmias (sustained ventricular tachycardia/fibrillation (VT/VF), appropriate implantable cardioverter-defibrillator therapy, or sudden cardiac death) in patients with definite ARVC, patients with borderline ARVC, and ARVC-associated mutation carriers. In the case of multiple publications on the same cohort, the study with the largest population was included. This yielded 45 studies with a median cohort size of 70 patients (interquartile range 60 patients) and a median follow-up of 5.0 years (interquartile range 3.3 - 6.7 years). The average proportion of arrhythmic events observed was 10.6%/y in patients with definite ARVC, 10.0%/y in patients with borderline ARVC, and 3.7%/y with mutation carriers. Predictors of ventricular arrhythmias were population dependent: consistently predictive risk factors in patients with definite ARVC were male sex, syncope, T-wave inversion in lead >V3, right ventricular dysfunction, and prior (non)sustained VT/VF; in patients with borderline ARVC, 2 additional predictors—inducibility during electrophysiology study and strenuous exercise—were identified; and with mutation carriers, all aforementioned predictors as well as ventricular ectopy, multiple ARVC-related pathogenic mutations, left ventricular dysfunction, and palpitations/presyncope determined arrhythmic risk. Most evidence originated from small observational cohort studies, with a moderate quality of evidence. In conclusion, the average risk of ventricular arrhythmia ranged from 3.7 to 10.6%/y depending on the population with ARVC. Male sex, syncope, T-wave inversion in lead >V3, right ventricular dysfunction, and prior (non)sustained VT/VF consistently predict ventricular arrhythmias in all populations with ARVC.
Keywords
Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia/cardiomyopathy, Meta-analysis, Prognosis, Risk stratification, Sudden cardiac death, Systematic review, Ventricular arrhythmias, Humans, Risk Factors, Arrhythmogenic Right Ventricular Dysplasia/diagnosis, Electrocardiography, Risk Assessment/methods, Cardiac Resynchronization Therapy Devices, Taverne, Cardiology and Cardiovascular Medicine, Physiology (medical), Research Support, Non-U.S. Gov't, Meta-Analysis, Journal Article
Citation
Bosman, L P, Sammani, A, James, C A, Cadrin-Tourigny, J, Calkins, H, van Tintelen, J P, Hauer, R N W, Asselbergs, F W & te Riele, A S J M 2018, 'Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy : A systematic review and meta-analysis', Heart Rhythm, vol. 15, no. 7, pp. 1097-1107. https://doi.org/10.1016/j.hrthm.2018.01.031