Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation?

被引:36
作者
Priori, SG
Napolitano, C
Grillo, M
机构
[1] Fondaz Salvatore Maugeri, I-27100 Pavia, Italy
[2] Univ Pavia, Dept Cardiol, I-27100 Pavia, Italy
关键词
arrhythmia (mechanisms); long QT syndrome; ventricular arrhythmias; sudden death;
D O I
10.1016/S0008-6363(01)00224-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In similar to6-10% of survivors of cardiac arrest no cardiac abnormality can be identified despite extensive clinical evaluation. Autopsy data confirm that in a similar percentage of victims of sudden death no structural heart disease can be identified at post mortem evaluation. Occurrence of cardiac arrest in the absence of a substrate is defined 'idiopathic ventricular fibrillation' thus admitting that the cause for the arrhythmic event has remained unknown. We present data supporting the hypothesis that incompletely penetrant genetic defects may underlie at least some of these unexplained deaths. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:218 / 223
页数:6
相关论文
共 29 条
[1]   Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning [J].
Ackerman, MJ ;
Tester, DJ ;
Porter, CJ ;
Edwards, WD .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (15) :1121-1125
[2]  
[Anonymous], 1992, HEART DIS TXB CARDIO
[3]  
Bowker T. J., 1996, HEART, V75, P80
[4]  
Brugada J, 1998, CIRCULATION, V97, P457
[5]   Sodium channel blockers identify risk for sudden death in patients with ST-Segment elevation and right bundle branch block but structurally normal hearts [J].
Brugada, R ;
Brugada, J ;
Antzelevitch, C ;
Kirsch, GE ;
Potenza, D ;
Towbin, JA ;
Brugada, P .
CIRCULATION, 2000, 101 (05) :510-515
[6]  
Coumel P., 1978, BRIT HEART J, V40, P28
[7]   THE LONG QT SYNDROME IN CHILDREN - AN INTERNATIONAL STUDY OF 287 PATIENTS [J].
GARSON, A ;
DICK, M ;
FOURNIER, A ;
GILLETTE, PC ;
HAMILTON, R ;
KUGLER, JD ;
VANHARE, GF ;
VETTER, V ;
VICK, GW .
CIRCULATION, 1993, 87 (06) :1866-1872
[8]   Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy [J].
Kamisago, M ;
Sharma, SD ;
DePalma, SR ;
Solomon, S ;
Sharma, P ;
McDonough, B ;
Smoot, L ;
Mullen, MP ;
Woolf, PK ;
Wigle, ED ;
Seidman, JG ;
Seidman, CE .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (23) :1688-1696
[9]   SHORT-COUPLED VARIANT OF TORSADE-DE-POINTES - A NEW ELECTROCARDIOGRAPHIC ENTITY IN THE SPECTRUM OF IDIOPATHIC VENTRICULAR TACHYARRHYTHMIAS [J].
LEENHARDT, A ;
GLASER, E ;
BURGUERA, M ;
NURNBERG, M ;
MAISONBLANCHE, P ;
COUMEL, P .
CIRCULATION, 1994, 89 (01) :206-215
[10]   CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR-TACHYCARDIA IN CHILDREN - A 7-YEAR FOLLOW-UP OF 21 PATIENTS [J].
LEENHARDT, A ;
LUCET, V ;
DENJOY, I ;
GRAU, F ;
DONGOC, D ;
COUMEL, P .
CIRCULATION, 1995, 91 (05) :1512-1519