Clinical profile of arrhythmogenic right ventricular cardiomyopathy in Chinese patients

被引:18
作者
Fung, WH [1 ]
Sanderson, JE [1 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Div Cardiol, Hong Kong, Hong Kong, Peoples R China
关键词
arrhythmogenic right ventricular cardiomyopathy; Chinese;
D O I
10.1016/S0167-5273(01)00519-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To study the clinical profile of Chinese patients with arrhythmogenic right ventricular cardiomyopathy (ARVC). Patients: Chinese patients who fulfilled the diagnostic criteria of ARVC proposed by the Task Force of the European Society of Cardiology and of the scientific council on cardiomyopathy of the International Society and Federation of Cardiology were recruited for analysis. Methods: Clinical data of patients with ARVC including age, sex, family history, presenting symptoms, electrocardiograph (ECG), echocardiography, cardiac catheterization, magnetic resonance imaging (MRI), electrophysiology study (EPS) and therapeutic intervention were analyzed. Results: Eleven patients (seven males) were diagnosed with ARVC. Mean age at clinical presentation was 42.6 +/- 14.8 years. Two patients (18.1%) had positive family history of ARVC or premature sudden cardiac death. The commonest presenting symptoms were palpitation (73%) and dizziness (46%). Spontaneous ventricular tachycardia (VT) was the presenting arrhythmia in 54% and 1 (9%) with ventricular fibrillation and cardiac arrest. Seven patients (64%) had the ECG abnormality as defined by the Task Force. Echocardiography showed right ventricular (RV) dilatation in five patients (46%) and all patients had normal left ventricular function. Nine patients (90%) had RV wall thinning or fibrofatty replacement on MRI examination. Inducible monomorphic VT was detected in four out of nine patients at EPS. All eight patients had normal coronary arteries and left ventriculogram. but RV dilatation and global hypokinesia was seen in three patients. Implantable cardioverter defibrillators were implanted in five patients and two of them had shocks delivered during the follow-up period. Conclusion: In this study, familial incidence of premature sudden death in patients with ARVC appears to be low and left ventricular involvement in affected individuals is uncommon. MRI is still the best investigation for ARVC. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 18
页数:10
相关论文
共 23 条
[11]   Electrocardiographic and morphometric features in patients with ventricular tachycardia of right ventricular origin [J].
Kazmierczak, J ;
De Sutter, J ;
Tavernier, R ;
Cuvelier, C ;
Dimmer, D ;
Jordaens, L .
HEART, 1998, 79 (04) :388-393
[12]   RIGHT VENTRICULAR DYSPLASIA - A REPORT OF 24 ADULT CASES [J].
MARCUS, FI ;
FONTAINE, GH ;
GUIRAUDON, G ;
FRANK, R ;
LAURENCEAU, JL ;
MALERGUE, C ;
GROSGOGEAT, Y .
CIRCULATION, 1982, 65 (02) :384-398
[13]  
MCKENNA WJ, 1994, BRIT HEART J, V71, P215
[14]   Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease) [J].
McKoy, G ;
Protonotarios, N ;
Crosby, A ;
Tsatsopoulou, A ;
Anastasakis, A ;
Coonar, A ;
Norman, M ;
Baboonian, C ;
Jeffery, S ;
McKenna, WJ .
LANCET, 2000, 355 (9221) :2119-2124
[15]   Arrhythmogenic Right Ventricular Dysplasia: cardiomyopathy current opinions on diagnostic and therapeutic aspects [J].
Naccarella, F ;
Naccarelli, G ;
Fattori, R ;
Nava, A ;
Martini, B ;
Corrado, D ;
Masotti, A .
CURRENT OPINION IN CARDIOLOGY, 2001, 16 (01) :8-16
[16]   Signal-averaged electrocardiogram in patients with arrhythmogenic right ventricular cardiomyopathy and ventricular arrhythmias [J].
Nava, A ;
Folino, AF ;
Bauce, A ;
Turrini, P ;
Buja, GF ;
Daliento, L ;
Thiene, G .
EUROPEAN HEART JOURNAL, 2000, 21 (01) :58-65
[17]   Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy [J].
Nava, A ;
Bauce, B ;
Basso, C ;
Muriago, M ;
Rampazzo, A ;
Villanova, C ;
Daliento, L ;
Buja, G ;
Corrado, D ;
Danieli, GA ;
Thiene, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (07) :2226-2233
[18]   FAMILIAL OCCURRENCE OF RIGHT VENTRICULAR DYSPLASIA - A STUDY INVOLVING 9 FAMILIES [J].
NAVA, A ;
THIENE, G ;
CANCIANI, B ;
SCOGNAMIGLIO, R ;
DALIENTO, L ;
BUJA, G ;
MARTINI, B ;
STRITONI, P ;
FASOLI, G .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1988, 12 (05) :1222-1228
[19]   SIGNAL-AVERAGED ELECTROCARDIOGRAPHY IN FAMILIAL FORM OF ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY [J].
OSELLADORE, L ;
NAVA, A ;
BUJA, G ;
TURRINI, P ;
DALIENTO, L ;
LIVOLSI, B ;
THIENE, G .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (15) :1038-1041
[20]  
PROTONOTARIOS N, 1986, BRIT HEART J, V56, P321