Pundi Kavitha N, Bos J Martijn, Cannon Bryan C, Ackerman Michael J
Department of Pediatric and Adolescent Medicine, Division of Pediatric Cardiology, Mayo Clinic, Rochester, Minnesota.
Department of Pediatric and Adolescent Medicine, Division of Pediatric Cardiology, Mayo Clinic, Rochester, Minnesota; Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, Minnesota.
Heart Rhythm. 2015 Apr;12(4):776-81. doi: 10.1016/j.hrthm.2015.01.002. Epub 2015 Jan 7.
Long QT syndrome (LQTS) is a potentially lethal yet highly treatable cardiac channelopathy. A comprehensive LQTS-directed treatment program often includes an automated external defibrillator (AED).
The purpose of this study was to determine the incidence of AED rescues among children evaluated, risk-stratified, and treated in an LQTS specialty center.
We performed a retrospective review of the electronic medical records to identify 1665 patients evaluated in our Genetic Heart Rhythm Clinic (1999-2013). Subset analysis was performed on 291 children managed without an implantable cardioverter-defibrillator (ICD).
The average age at diagnosis was 8.3 ± 5.7 years with an average. QTc of 463 ± 40 ms (17% ≥500 ms). The represented LQTS genotypes included type 1 (LQT1) in 52%, type 2 (LQT2) in 35%, and type 3 (LQT3) in 7%. During follow-up, 3 of 291 children (1%) had a cardiac arrest with an appropriate AED rescue (2/51 symptomatic, 1/240 asymptomatic). The first AED rescue occurred during exercise in a symptomatic 3-year-old boy with compound LQT1 treated with beta-blocker and videoscopic left cardiac sympathetic denervation (LCSD). The second AED rescue occurred in a remotely symptomatic 14-year-old boy with high-risk LQT2 (QTc >550 ms) on a beta-blocker who previously declined a prophylactic ICD. The third AED rescue involved an asymptomatic 17-year-old girl with LQT3 on mexiletine who collapsed in school.
An AED should seldom be necessary in an appropriately treated child with LQTS. Nevertheless, despite only 3 AED rescues in more than 1700 patient-years, an AED can be a lifesaving and cost-effective part of an LQTS patient's comprehensive sudden death prevention program.
长QT综合征(LQTS)是一种潜在致命但可高度治疗的心脏通道病。一个全面的LQTS定向治疗方案通常包括一台自动体外除颤器(AED)。
本研究的目的是确定在一个LQTS专科中心接受评估、风险分层和治疗的儿童中AED抢救的发生率。
我们对电子病历进行了回顾性审查,以识别在我们的遗传性心律诊所(1999 - 2013年)接受评估的1665例患者。对291例未植入心脏复律除颤器(ICD)的儿童进行了亚组分析。
诊断时的平均年龄为8.3±5.7岁,平均QTc为463±40毫秒(17%≥500毫秒)。所代表的LQTS基因型包括1型(LQT1)占52%,2型(LQT2)占35%,3型(LQT3)占7%。在随访期间,291例儿童中有3例(1%)发生心脏骤停并通过适当的AED抢救成功(2例有症状,51例中有2例;1例无症状,240例中有1例)。第一次AED抢救发生在一名有症状的3岁复合LQT1男孩运动期间,该男孩接受了β受体阻滞剂和电视辅助左心交感神经去神经术(LCSD)治疗。第二次AED抢救发生在一名有轻微症状的14岁高危LQT2(QTc>550毫秒)男孩身上,该男孩服用β受体阻滞剂,此前拒绝接受预防性ICD。第三次AED抢救涉及一名无症状的17岁LQT3女孩,她在服用美西律期间在学校晕倒。
对于接受适当治疗的LQTS儿童,很少需要使用AED。然而,尽管在超过1700患者年中仅有3次AED抢救,但AED可以成为LQTS患者全面猝死预防方案中挽救生命且具有成本效益的一部分。