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Cardiol J ; 17(2): 172-8, 2010.
Article in English | MEDLINE | ID: mdl-20544617

ABSTRACT

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a disorder that involves replacement of the right ventricular myocardium with fibro-fatty tissue. Ventricular tachycardia is a main presenting feature. There are no known reports of this disease from the Arab countries in the Middle East. This is the first report of 34 patients from Iraq. METHODS: Thirty four patients with ARVC/D diagnosed from January 2003 to May 2007 according to the International Task Force criteria were included in this study. RESULTS: All patients presented with ventricular tachycardia of left bundle branch block morphology. The following findings were seen on the 12-lead electrocardiography during sinus rhythm: T wave inversion V1-V3 or beyond in 80%, epsilon wave in 28%, and parietal block in 48%. Right ventricular enlargement by echocardiography was seen in 69%. Twenty two per cent had a family history of sudden cardiac death. All patients were treated with implanted cardioverter-defibrillators. CONCLUSIONS: ARVC/D is a disease seen in Iraq. It requires a high diagnostic suspicion with verification using the international task force criteria.


Subject(s)
Arrhythmogenic Right Ventricular Dysplasia/epidemiology , Adult , Arrhythmogenic Right Ventricular Dysplasia/diagnosis , Arrhythmogenic Right Ventricular Dysplasia/therapy , Bundle-Branch Block/epidemiology , Death, Sudden, Cardiac/epidemiology , Defibrillators, Implantable , Echocardiography , Electric Countershock/instrumentation , Electrocardiography , Electrophysiologic Techniques, Cardiac , Female , Humans , Iraq/epidemiology , Male , Predictive Value of Tests , Tachycardia, Ventricular/epidemiology , Treatment Outcome , Young Adult
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