Arrhythmogenic right ventricular cardiomyopathy 2012: Diagnostic challenges and treatment

Frank I. Marcus, Aiden Abidov

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

ARVC 2012. The most common presentation of arrhythmogenic right ventricular cardiomyopathy (ARVC) is palpitations or ventricular tachycardia (VT) of left bundle branch morphology in a young or middle-aged individual. The 12-lead electrocardiogram may be normal or have T-wave inversion beyond V1 in an otherwise healthy person who is suspected of having ARVC. The most frequent imaging abnormalities are an enlarged right ventricle, decrease in right ventricular (RV) function, and localized wall motion abnormalities. Risk factors for implantable cardioverter defibrillator include a history of aborted sudden death, syncope, young age, decreased left ventricular function, and marked decrease in RV function. Recent results of treatment with epicardial ablation are encouraging.

Original languageEnglish (US)
Pages (from-to)1149-1153
Number of pages5
JournalJournal of cardiovascular electrophysiology
Volume23
Issue number10
DOIs
StatePublished - Oct 1 2012

Keywords

  • RV dysplasia
  • arrhythmogenic right ventricular cardiomyopathy
  • implantable cardioverter defibrillator
  • sudden death
  • ventricular tachycardia

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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