Sudden cardiac death in the young: A strategy for prevention by targeted evaluation

被引:64
作者
Sen-Chowdhry, Srijita
McKenna, William J.
机构
[1] UCL, Ctr Cardiol Young, Heart Hosp, London W1G 8PH, England
[2] Imperial Coll, Natl Heart & Lung Inst, London, England
关键词
arrhythmia; cardiomyopathy; genetics; sudden death;
D O I
10.1159/000091640
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The annual incidence of sudden cardiac death (SCD) in the general population is estimated as 1 in a 1,000. Since survival rates from out-of-hospital cardiac arrests are poor, primary prevention is key to reducing the burden of SCD in the community. Prominent causes of SCID include ischaemic heart disease, anomalous coronary arteries, and the primary myocardial diseases: hypertrophic cardiomyopathy, dilated cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy (ARVC). In 4% of sudden deaths in the 16-64 age group, postmortem examination fails to identify a cause, yielding a default diagnosis of sudden arrhythmic death syndrome (SADS). The inherited arrhythmia syndromes (long QT, short QT, and Brugada syndromes, and familial catecholaminergic polymorphic ventricular tachycardia) may be implicated in SAIDS, owing to their propensity for producing ventricular tachyarrhythmia in the structurally normal heart. Monogenic disorders therefore predominate as causes of SCID in the young. The advent of effective therapies for these diseases, particularly implantable cardioverter defibrillators, has prompted calls for universal screening to enable timely diagnosis of occult cardiac disease. Since prospective cardiac assessment of the general population is not feasible, the solution may be to target high-risk subgroups, namely, patients with cardiac symptoms, relatives of SCID victims, and competitive athletes. The recommended preliminary work-up includes a 12-lead ECG, signal-averaged ECG, transthoracic echocardiogram, exercise test, and ambulatory ECG monitoring. Cardiovascular magnetic resonance is a useful adjunct in patients with suspected ARVC or anomalous coronary arteries. Provocative challenge with a sodium challenge blocker may be of value in unmasking the Brugada syndrome. Identification of disease-causing mutations in affected individuals facilitates cascade screening of families. Copyright (c) 2006 S. Karger AG, Basel
引用
收藏
页码:196 / 206
页数:11
相关论文
共 65 条
  • [51] Rakocevic-Stojanovic V, 1999, PANMINERVA MED, V41, P27
  • [52] Short QT syndrome
    Schimpf, R
    Wolpert, C
    Gaita, F
    Giustetto, C
    Borggrefe, M
    [J]. CARDIOVASCULAR RESEARCH, 2005, 67 (03) : 357 - 366
  • [53] Schwartz PJ, 2001, CIRCULATION, V103, P89
  • [54] Genetics of right ventricular cardiomyopathy
    Sen-Chowdhry, S
    Syrris, P
    McKenna, WJ
    [J]. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2005, 16 (08) : 927 - 935
  • [55] Arrhythmogenic right ventricular cardiomyopathy: Clinical presentation, diagnosis, and management
    Sen-Chowdhry, S
    Lowe, MD
    Sporton, SC
    McKenna, WJ
    [J]. AMERICAN JOURNAL OF MEDICINE, 2004, 117 (09) : 685 - 695
  • [56] Desmoplakin disease in arrhythmogenic right ventricular cardiomyopathy: early genotype-phenotype studies
    Sen-Chowdhry, S
    Syrris, P
    McKenna, WJ
    [J]. EUROPEAN HEART JOURNAL, 2005, 26 (16) : 1582 - 1584
  • [57] The incidence of sudden cardiac death in the general population
    Straus, SMJM
    Bleumink, GS
    Dieleman, JP
    van der Lei, J
    Stricker, BHC
    Sturkenboom, MCJM
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 2004, 57 (01) : 98 - 102
  • [58] Circumstances of death and gross and microscopic observations in a series of 200 cases of sudden death associated with arrhythmogenic right ventricular cardiomyopathy and/or dysplasia
    Tabib, A
    Loire, R
    Chalabreysse, L
    Meyronnet, D
    Miras, A
    Malicier, D
    Thivolet, F
    Chevalier, P
    Bouvagnet, P
    [J]. CIRCULATION, 2003, 108 (24) : 3000 - 3005
  • [59] The failing heart
    Towbin, JA
    Bowles, NE
    [J]. NATURE, 2002, 415 (6868) : 227 - 233
  • [60] EFFECTS OF EXERCISE ON HEART-RATE, QT, QTC AND QT QS2 IN THE ROMANO-WARD INHERITED LONG QT SYNDROME
    VINCENT, GM
    JAISWAL, D
    TIMOTHY, KW
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (05) : 498 - 503