Pugliese Daniel N, Reiffel James A
Department of Medicine, Division of Cardiology, Columbia University Irving Medical Center, New York, NY, USA.
J Innov Card Rhythm Manag. 2019 Oct 15;10(10):3860-3864. doi: 10.19102/icrm.2019.101002. eCollection 2019 Oct.
This is a report of a patient with a history of hypertension and myocardial infarction and a left ventricular ejection fraction of 35% who suffered a syncopal event. Her admitting electrocardiogram was compatible with her old myocardial infarction, an anteroseptal left ventricular aneurysm, left ventricular hypertrophy, and short-QT syndrome. The present report discusses how each of these might contribute individually and to some extent synergistically to producing syncope. She was treated with an implantable cardioverter-defibrillator (ICD), though she did not meet strict Multicenter Automatic Defibrillator Implantation Trial (MADIT), MADIT II, and Multicenter Unsustained Tachycardia Trial (MUSTT) patient characteristics. Her implant, however, was consistent with the 2014 Heart Rhythm Society/American College of Cardiology/American Heart Association consensus document regarding patients who do not match clinical trial enrollees but for whom ICD consideration is appropriate.
这是一份关于一名有高血压和心肌梗死病史且左心室射血分数为35%的患者发生晕厥事件的报告。她入院时的心电图与陈旧性心肌梗死、前间隔左心室室壁瘤、左心室肥厚及短QT综合征相符。本报告讨论了这些因素如何分别在一定程度上协同作用导致晕厥。她接受了植入式心脏复律除颤器(ICD)治疗,尽管她不符合严格的多中心自动除颤器植入试验(MADIT)、MADIT II及多中心非持续性心动过速试验(MUSTT)的患者特征。然而,她的植入情况符合2014年心律协会/美国心脏病学会/美国心脏协会关于不符合临床试验入选标准但适合考虑植入ICD的患者的共识文件。