| Literature DB >> 30416732 |
Frédéric Schnell1, Nathalie Behar2, François Carré1.
Abstract
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.Entities:
Keywords: Long QT syndrome; arrhythmia; athlete; sport; sudden death
Year: 2018 PMID: 30416732 PMCID: PMC6141947 DOI: 10.15420/aer.2018.39.3
Source DB: PubMed Journal: Arrhythm Electrophysiol Rev ISSN: 2050-3369