Schnell Frédéric, Behar Nathalie, Carré François
University of Rennes, Department of Sports Medicine University Hospital of Rennes, Inserm, LTSI-UMR 1099 Rennes, France.
University of Rennes, Department of Cardiology University Hospital of Rennes, Inserm, LTSI-UMR 1099 Rennes, France.
Arrhythm Electrophysiol Rev. 2018 Aug;7(3):187-192. doi: 10.15420/aer.2018.39.3.
Long QT syndrome (LQTS) is an inherited channelopathy which exposes athletes to a risk of sudden cardiac death. Diagnosis is more difficult in this population because: the QT interval is prolonged by training; and the extreme bradycardia frequently observed in athletes makes the QT correction formula less accurate. Based on limited clinical data which tend to demonstrate that exercise, especially swimming, is a trigger for cardiac events, participation in any competitive sports practice is not supported by 2005 European guidelines. However, based on recent retrospective studies and adopting a different medical approach, involving the patient-athlete in shared decision making, the 2015 US guidelines are less restrictive, especially in asymptomatic genotype-positive/phenotype-negative athletes. These guidelines also consider giving medical clearance to competitive sport participation in asymptomatic athletes with appropriate medical therapy.
长QT综合征(LQTS)是一种遗传性通道病,会使运动员面临心源性猝死风险。在这一人群中诊断更为困难,原因如下:训练会延长QT间期;运动员中经常观察到的极度心动过缓使QT校正公式的准确性降低。基于有限的临床数据,这些数据倾向于表明运动,尤其是游泳,是心脏事件的触发因素,2005年欧洲指南不支持参与任何竞技体育项目。然而,基于最近的回顾性研究并采用不同的医学方法,让患者运动员参与共同决策,2015年美国指南的限制较少,尤其是对于无症状的基因型阳性/表型阴性运动员。这些指南还考虑给予接受适当药物治疗的无症状运动员参加竞技运动的医学许可。