Department of Internal Medicine II, Division of Cardiology and Pneumology, University of Bonn, Bonn, Germany.
ZOLL, Pittsburgh, Pennsylvania, United States of America.
PLoS One. 2018 Mar 22;13(3):e0194496. doi: 10.1371/journal.pone.0194496. eCollection 2018.
Patients with cardiac sarcoidosis are at increased risk of ventricular tachycardia/fibrillation.
We tested the hypothesis that the wearable cardioverter defibrillator can be used to mitigate the risk of sudden cardiac death among cardiac sarcoidosis patients.
A retrospective review of the commercial database identified cardiac sarcoidosis patients who wore the wearable cardioverter defibrillator. Evidence for cardiac sarcoidosis diagnosis as well as demographic, co-morbidity and left ventricular ejection fraction were provided by patient clinical records. Clinical data also included daily wearable cardioverter defibrillator wear, shock treatment and survival information.
The wearable cardioverter defibrillator was worn by 46 cardiac sarcoidosis patients, 24 (52%) male. The median age was 48 years and median left ventricular ejection fraction was 30%. The wearable cardioverter defibrillator was worn a median of 23.6 hours each day. There were 11 ventricular tachycardia/fibrillation episodes occurring in 10 (22%) patients. Ventricular tachycardia/fibrillation occurred over a range of 1 to 79 days, median 24 days. First-shock success for conversion of ventricular tachycardia/fibrillation was 100%. Patient survival 24 hours after shock treatment was 100%. Follow up to determine the reason for discontinuing wearable cardioverter defibrillator use indicated that among shocked patients 7 received an implantable cardioverter defibrillator, 1 patient was admitted to the hospital ending in death 2 weeks after discontinuing wearable cardioverter defibrillator use, and 2 patients were lost to follow up. Among the not shocked patients, there were 16 who received an implantable cardioverter defibrillator while 7 achieved improved left ventricular ejection fraction.
Management of sudden cardiac death among cardiac sarcoidosis patients was aided by the wearable cardioverter defibrillator resulting in successful termination of ventricular tachycardia/fibrillation upon delivery of shock.
患有心脏结节病的患者发生室性心动过速/颤动的风险增加。
我们检验了可穿戴式除颤器可用于降低心脏结节病患者发生心源性猝死风险的假说。
对商业数据库进行回顾性分析,确定佩戴可穿戴式除颤器的心脏结节病患者。患者临床记录提供了心脏结节病诊断的证据以及人口统计学、合并症和左心室射血分数。临床数据还包括可穿戴式除颤器佩戴时间、电击治疗和生存信息。
46 名心脏结节病患者佩戴了可穿戴式除颤器,其中 24 名(52%)为男性。中位年龄为 48 岁,中位左心室射血分数为 30%。可穿戴式除颤器的佩戴时间中位数为每天 23.6 小时。10 名(22%)患者发生 11 次室性心动过速/颤动事件。室性心动过速/颤动发生在 1 至 79 天之间,中位时间为 24 天。首次电击治疗成功转换为室性心动过速/颤动的比例为 100%。电击治疗后 24 小时患者存活率为 100%。随访确定停止使用可穿戴式除颤器的原因,结果表明在被电击的患者中,有 7 人接受了植入式心脏复律除颤器,1 名患者在停止使用可穿戴式除颤器后 2 周因医院治疗死亡,2 名患者失访。在未被电击的患者中,有 16 人接受了植入式心脏复律除颤器,而 7 人左心室射血分数得到改善。
可穿戴式除颤器有助于管理心脏结节病患者的心脏性猝死,电击治疗成功终止了室性心动过速/颤动。