Key result
ARVD requires multidisciplinary management to prevent sudden cardiac death.
Why the study?
Arrhythmogenic right ventricular dysplasia is a rare inherited heart disorder associated with ventricular arrhythmias and sudden cardiac death, requiring a comprehensive overview of its pathophysiology, clinical manifestations, diagnosis, and management.
Design
Review
Authors
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May warrant multidisciplinary teams for suspected ARVD; leaves open higher-quality studies to optimize SCD prevention.
This comprehensive review outlines the pathophysiology, clinical manifestations, diagnostic criteria, and multifaceted management strategies for Arrhythmogenic Right Ventricular Dysplasia.
Cruz et al. (2024) conducted a review in Arrhythmogenic Right Ventricular Dysplasia (ARVD). Arrhythmogenic Right Ventricular Dysplasia is a rare, potentially life-threatening inherited cardiomyopathy requiring a multidisciplinary approach for diagnosis and management to prevent sudden cardiac death.