Gatzoulis M A, Balaji S, Webber S A, Siu S C, Hokanson J S, Poile C, Rosenthal M, Nakazawa M, Moller J H, Gillette P C, Webb G D, Redington A N
Department of Paediatrics, Royal Brompton Hospital and the National Heart and Lung Institute, London, UK.
Lancet. 2000 Sep 16;356(9234):975-81. doi: 10.1016/S0140-6736(00)02714-8.
Ventricular arrhythmia and sudden cardiac death late after repair of tetralogy of Fallot are devastating complications in adult survivors of early surgery, but their prediction remains difficult.
We examined surgical, electrocardiographic, and late haemodynamic data, and their relation to clinical arrhythmia and sudden death occurring over 10 years, in a multicentre cohort of patients with repaired tetralogy, who were alive in 1985.
Of 793 patients (mean age at repair 8.2 years [SD 8], mean time from repair 21.1 years [8.7]) who entered the study, 33 patients developed sustained monomorphic ventricular tachycardia, 16 died suddenly, and 29 had new-onset sustained atrial flutter or fibrillation. Electrocardiographic markers (QRS duration, QRS rate of change between 1985 and 1995) were significantly greater in the ventricular tachycardia and sudden-death groups. Older age at repair was associated with a higher risk of sudden death and atrial tachyarrhythmia. Pulmonary regurgitation was the main underlying haemodynamic lesion for patients with ventricular tachycardia and sudden death, whereas tricuspid regurgitation was for those with atrial flutter/fibrillation. Despite adverse haemodynamics, no patient who died suddenly had undergone late reoperation.
Arrhythmia and sudden death are important late sequelae for patients after repair of tetralogy of Fallot. The electrophysiological and haemodynamic substrate of sudden death resembled that of sustained ventricular tachycardia, with pulmonary regurgitation being the predominant haemodynamic lesion. Preservation or restoration of pulmonary valve function may thus reduce the risk of sudden death. Furthermore, electrocardiographic markers can help to identify patients at risk.
法洛四联症修复术后晚期出现的室性心律失常和心源性猝死是早期手术成年幸存者的严重并发症,但对其进行预测仍然困难。
我们在一个多中心队列研究中,对1985年时存活的法洛四联症修复患者的手术、心电图和晚期血流动力学数据,以及它们与10年间发生的临床心律失常和猝死的关系进行了研究。
在进入研究的793例患者中(修复时平均年龄8.2岁[标准差8],距修复平均时间21.1年[8.7]),33例发生持续性单形性室性心动过速,16例猝死,29例出现新发持续性心房扑动或心房颤动。室性心动过速和猝死组的心电图指标(QRS波时限、1985年至1995年间QRS波变化率)显著更高。修复时年龄较大与猝死和房性快速性心律失常风险较高相关。肺动脉反流是室性心动过速和猝死患者的主要潜在血流动力学病变,而三尖瓣反流是心房扑动/颤动患者的主要病变。尽管存在不良血流动力学情况,但没有猝死患者接受过晚期再次手术。
心律失常和猝死是法洛四联症修复术后患者重要的晚期后遗症。猝死的电生理和血流动力学基础与持续性室性心动过速相似,肺动脉反流是主要的血流动力学病变。因此,保留或恢复肺动脉瓣功能可能会降低猝死风险。此外,心电图指标有助于识别有风险的患者。