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体外生命支持治疗并发急性心肌梗死后心源性休克患者的转归:ECLS-Shock 研究的 1 年结果。

Outcome of patients treated with extracorporeal life support in cardiogenic shock complicating acute myocardial infarction: 1-year result from the ECLS-Shock study.

机构信息

Department of Medicine I, Munich University Hospital, Ludwig-Maximilian-University, Marchioninistr. 15, 81377, Munich, Germany.

Department of Cardiac Surgery, Munich University Hospital, Ludwig-Maximilian-University, Marchioninistr. 15, 81377, Munich, Germany.

出版信息

Clin Res Cardiol. 2021 Sep;110(9):1412-1420. doi: 10.1007/s00392-020-01778-8. Epub 2020 Nov 12.

DOI:10.1007/s00392-020-01778-8
PMID:33180150
Abstract

BACKGROUND

Treatment with extracorporeal life support (ECLS) in acute myocardial infarction (AMI) complicated by cardiogenic shock (CS) fell short of improving myocardial recovery measured by 30 day ejection fraction in the ECLS-SHOCK trial. However, to date, no data regarding impact of ECLS on long-term outcomes exist.

METHODS

In this randomized, controlled, prospective, open-label trial, 42 patients with CS complicating AMI were randomly assigned to ECLS (ECLS group, n = 21) or no ECLS (control group, n = 21). The primary endpoint was left ventricular ejection fraction (LVEF) after 30 days. Secondary endpoints included mortality and neurological outcome after 12 months. Evaluation of neurological outcome used the modified Rankin Scale.

RESULTS

The 12-month all-cause mortality was 19% in the ECLS group versus 38% in the control group (p = 0.31). Only one patient (control group) died after the initial 30 days. Three patients underwent elective percutaneous coronary intervention (PCI) during follow-up (one in the control and two in the ECLS group). Favorable neurological outcome (modified Rankin Score ≤ 2) was seen in 61.9% of patients in the ECLS group versus 57.1% in the control group (p = 1).

CONCLUSION

This pilot study showed that randomized studies with ECLS in CS patients are feasible and safe. Small numbers of included patients impede meaningful conclusions about mortality and neurological outcome. Our findings of numerical differences in mortality and survival with severe neurological impairment give an urgent call for larger multi-centric randomized trials assessing the endpoint of all-cause mortality but also considering the effects on neurological outcome measures.

摘要

背景

在体外生命支持(ECLS)治疗急性心肌梗死(AMI)并发心源性休克(CS)的 ECLS-SHOCK 试验中,未能改善 30 天射血分数测量的心肌恢复。然而,迄今为止,尚无关于 ECLS 对长期结果影响的数据。

方法

在这项随机、对照、前瞻性、开放标签试验中,42 例 AMI 并发 CS 的患者被随机分为 ECLS(ECLS 组,n=21)或无 ECLS(对照组,n=21)。主要终点为 30 天后的左心室射血分数(LVEF)。次要终点包括 12 个月时的死亡率和神经结局。神经结局评估采用改良 Rankin 量表。

结果

ECLS 组的 12 个月全因死亡率为 19%,对照组为 38%(p=0.31)。只有一名患者(对照组)在最初的 30 天后死亡。在随访期间,有 3 名患者接受了选择性经皮冠状动脉介入治疗(PCI)(对照组 1 例,ECLS 组 2 例)。ECLS 组有 61.9%的患者神经结局良好(改良 Rankin 评分≤2),对照组为 57.1%(p=1)。

结论

这项初步研究表明,在 CS 患者中进行 ECLS 的随机研究是可行且安全的。纳入患者的数量较少,限制了对死亡率和神经结局的有意义的结论。我们发现死亡率和严重神经功能障碍存活率的数值差异,迫切需要进行更大规模的多中心随机试验,评估全因死亡率的终点,同时也考虑对神经结局测量的影响。

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