Taylor Caroline, Stambler Bruce S
Cardiac Electrophysiology, Piedmont Heart Institute Atlanta, GA.
US Cardiol. 2021 May 20;15:e08. doi: 10.15420/usc.2021.02. eCollection 2021.
Congenital long QT syndrome (LQTS) is a primary genetic and electrical disorder that increases risk for torsades de pointes, syncope, and sudden death. Post-pubertal women with LQTS require specialized multidisciplinary management before, during, and after pregnancy involving cardiology and obstetrics to reduce risk for cardiac events in themselves and their fetuses and babies. The risk of potentially life-threatening events is lower during pregnancy but increases significantly during the 9-month postpartum period. Treatment of women with LQTS with a preferred β-blocker at optimal doses along with close monitoring are indicated throughout pregnancy and during the high-risk postpartum period.
先天性长QT综合征(LQTS)是一种原发性遗传和电紊乱疾病,会增加发生尖端扭转型室速、晕厥和猝死的风险。患有LQTS的青春期后女性在怀孕前、孕期和产后需要心脏病学和产科学的专业多学科管理,以降低自身及其胎儿和婴儿发生心脏事件的风险。危及生命事件的风险在孕期较低,但在产后9个月期间会显著增加。在整个孕期和高风险的产后期间,建议对患有LQTS的女性使用最佳剂量的首选β受体阻滞剂进行治疗,并密切监测。