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The Wearable Cardioverter-Defibrillator: Experience in 153 Patients and a Long-Term Follow-Up

机译:穿戴式心脏复律除颤器:153例患者的经验和长期随访

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摘要

Background: The wearable cardioverter-defibrillator (WCD) is available for patients at high risk for sudden cardiac death (SCD) when immediate implantable cardioverter-defibrillator (ICD) implantation is not possible or indicated. Patient selection remains challenging especially in primary prevention. Long-term data on these patients is still lacking. Methods: 153 patients were included in this study. They were prescribed the WCD between April 2012 and March 2019 at the University Medical Center, Mannheim, Germany. The mean follow-up period was 36.2 ± 15.6 months. Outcome data, including all-cause mortality, were analyzed by disease etiology and ICD implantation following WCD use. Results: We analyzed 56 patients with ischemic cardiomyopathy, 70 patients with non-ischemic cardiomyopathy, 16 patients with prior need for ICD/CRT-D (device for cardiac resynchronization therapy with defibrillator) explanation, 8 patients with acute myocarditis and 3 patients with congenital diseases. 58% of the patients did not need ICD/CRT-D implantation after WCD use. 4% of all patients suffered from appropriate WCD shocks. 2 of these patients (33%) experienced appropriate ICD shocks after implantation due to ventricular tachyarrhythmias. Long-term follow-up shows a good overall survival. All-cause mortality was 10%. There was no significant difference between patients with or without subsequent ICD implantation ( = 0.48). Patients with ischemic cardiomyopathy numerically showed a higher long-term mortality than patients with non-ischemic cardiomyopathy (14% vs. 6%, = 0.13) and received significantly more ICD shocks after implantation (10% of ischemic cardiomyopathy (ICM) patients versus 3% of non-ischemic cardiomyopathy (NICM) patients, = 0.04). All patients with ventricular tachyarrhythmias during WCD use or after ICD implantation survived the follow-up period. Conclusion: Following WCD use, ICD implantation could be avoided in 58% of patients. Long-term follow-up shows good overall survival. The majority of all patients did not suffer from WCD shocks nor did receive ICD shocks after subsequent implantation. Patient selection regarding predictive conditions on long-term risk of ventricular tachyarrhythmias needs further risk stratification.
机译:背景:当无法或不能立即植入可植入的心脏复律除颤器(ICD)时,可穿戴式心脏复律除颤器(WCD)适用于发生心脏猝死(SCD)的高风险患者。患者的选择仍然具有挑战性,尤其是在一级预防中。这些患者的长期数据仍然缺乏。方法:本研究纳入153例患者。他们于2012年4月至2019年3月在德国曼海姆大学医学中心接受了WCD处方。平均随访时间为36.2±15.6个月。使用WCD后,通过疾病病因和ICD植入分析结果数据,包括全因死亡率。结果:我们分析了56例缺血性心肌病患者,70例非缺血性心肌病患者,16例事先需要ICD / CRT-D(带除颤器的心脏再同步治疗设备)的患者说明,8例急性心肌炎和3例先天性疾病。使用WCD后58%的患者不需要ICD / CRT-D植入。所有患者中有4%遭受了适当的WCD冲击。这些患者中有2名(33%)由于室速过快而在植入后经历了适当的ICD休克。长期随访显示总体生存良好。全因死亡率为10%。植入或未植入ICD的患者之间无显着差异(= 0.48)。与非缺血性心肌病患者相比,缺血性心肌病患者的长期死亡率在数值上更高(分别为14%和6%,= 0.13),植入后接受ICD冲击的比例明显更高(缺血性心肌病(ICM)患者为10​​%,而3%)非缺血性心肌病(NICM)患者的百分比,%= 0.04)。在使用WCD期间或植入ICD后所有患有室性快速性心律失常的患者都存活了下来。结论:使用WCD后,可以避免58%的患者植入ICD。长期随访显示总体生存良好。所有患者中的大多数都没有遭受WCD冲击,也没有在随后的植入后接受ICD冲击。有关预测室速的长期风险的预测条件的患者选择还需要进一步的风险分层。

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