Department of Cardiothoracic Transplantation and Mechanical Circulatory Support, Harefield Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Department of Cardiology, Harefield Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Interact Cardiovasc Thorac Surg. 2021 Jan 22;32(2):298-305. doi: 10.1093/icvts/ivaa259.
Left ventricular assist device (LVAD) implantation for end-stage heart failure patients has been on the rise, providing a reliable long-term option. For some LVAD patients, longer term LV unloading leads to recovery; hence, the need for evaluating potential myocardial recovery and weaning eligibility has emerged.
All patients who underwent contemporary LVAD explantation at our institution between 2009 and 2020 were included in the study. Patients in New York Heart Association I, left ventricular ejection fraction >40%, a cardiac index >2.4 l/min and a peak oxygen intake >50% predicted underwent a 4-phase weaning assessment. A minimally invasive approach using a titanium plug was the surgery of choice in the most recent explants. Kaplan-Meier curves were used to estimate the survival at 1 and 5 years.
Twenty-six patients (17 HeartMate II, 9 HeartWare) underwent LVAD explantation after a median 317 days of support [IQ (212-518)], range 131-1437. Mean age at explant was 35.8 ± 12.7 years and 85% were males. Idiopathic dilated cardiomyopathy was the underlying diagnosis in 70% of cases. Thirteen (48%) patients were on short-term mechanical circulatory support and 60% required intensive care unit admission prior to the LVAD implantation. At 1 year, Kaplan-Meier estimated survival was 88%, whereas at 6 years, it was 77%. The average left ventricular ejection fraction at 1 year post-explant was 44.25% ± 8.44.
The use of a standardized weaning protocol (echocardiographic and invasive) and a minimally invasive LVAD explant technique minimizes periprocedural complications and leads to good long-term device-free survival rates.
左心室辅助装置(LVAD)植入治疗终末期心力衰竭患者的数量不断增加,为患者提供了一种可靠的长期治疗选择。对于一些 LVAD 患者,长期的 LV 卸载可导致心肌恢复;因此,评估潜在的心肌恢复和脱机资格的需求已经出现。
本研究纳入了 2009 年至 2020 年期间在我院接受当代 LVAD 取出术的所有患者。纽约心脏协会(NYHA)心功能分级 I 级、左心室射血分数(LVEF)>40%、心指数(CI)>2.4 L/min 和峰值摄氧量(peak oxygen intake, VO2)>预测值 50%的患者进行了 4 期脱机评估。最近的 LVAD 取出术采用了钛制塞子的微创方法。使用 Kaplan-Meier 曲线估计 1 年和 5 年的生存率。
26 例患者(17 例使用 HeartMate II,9 例使用 HeartWare)在中位 317 天的支持后接受了 LVAD 取出术[中位数(范围):212-518],支持时间范围为 131-1437 天。取出术时的平均年龄为 35.8±12.7 岁,85%为男性。70%的患者基础诊断为特发性扩张型心肌病。13 例(48%)患者接受了短期机械循环支持,60%的患者在植入 LVAD 前需要入住重症监护病房。1 年时,Kaplan-Meier 估计的生存率为 88%,而 6 年时为 77%。LVAD 取出后 1 年的平均 LVEF 为 44.25%±8.44%。
使用标准化的脱机方案(超声心动图和有创性)和微创的 LVAD 取出技术可最大程度地减少围手术期并发症,并导致良好的长期无设备生存率。