Cardiovascular Diseases Institute "Prof. Dr. George I.M. Georgescu", "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
"C. I. Parhon" University Hospital, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Biomed Res Int. 2020 Apr 19;2020:6126534. doi: 10.1155/2020/6126534. eCollection 2020.
Cardiogenic shock is associated with high mortality, despite new strategies for reperfusion therapy. Short-term circulatory support devices may provide adequate support for appropriate myocardial and organ perfusion.
This review is aimed at evaluating the impact on survival when using venoarterial extracorporeal membrane oxygenation (V-A ECMO) in patients with cardiogenic shock due to acute myocardial infarction (AMI).
We performed a systematic review that included studies using V-A ECMO in patients with cardiogenic shock. Time on ECMO, side effects, and the number of deceased patients, transplanted or upgraded to durable assist devices were analysed. Literature search was done using PubMed/MEDLINE (inception (1969) to January 10, 2019), ProQuest (inception (January 14, 1988) to January 10, 2019), and clinicaltrials.gov (inception (September 12, 2005) to January 10, 2019), by 2 authors. This protocol is registered with PROSPERO (no. CRD42019123982).
We included 9 studies with a total of 1,998 adult patients receiving V-A ECMO for AMI-induced cardiogenic shock. Survival rate varied from 30.0% to 79.2% at discharge and from 23.2% to 36.1% at 12 months. Time on ECMO varied between 1.96 and 6.0 days. Reported serious adverse events were gastrointestinal bleeding (3.6%) and peripheral complications (8.5%).
The use of V-A ECMO among patients with AMI-induced cardiogenic shock may provide survival benefits. However, V-A ECMO treatment effects are inconclusive because of limitations in cohort design and reporting.
尽管有新的再灌注治疗策略,心源性休克仍与高死亡率相关。短期循环支持设备可能为适当的心肌和器官灌注提供足够的支持。
本综述旨在评估急性心肌梗死(AMI)所致心源性休克患者使用静脉动脉体外膜肺氧合(V-A ECMO)对生存率的影响。
我们进行了一项系统综述,其中包括使用 V-A ECMO 治疗心源性休克患者的研究。分析 ECMO 时间、副作用以及死亡、移植或升级为耐用辅助设备的患者数量。文献检索使用了 PubMed/MEDLINE(1969 年 1 月 1 日至 2019 年 1 月 10 日)、ProQuest(1988 年 1 月 14 日至 2019 年 1 月 10 日)和 clinicaltrials.gov(2005 年 9 月 12 日至 2019 年 1 月 10 日),由 2 位作者进行。本方案已在 PROSPERO(编号:CRD42019123982)注册。
我们纳入了 9 项研究,共纳入 1998 例成人患者,因 AMI 引起的心源性休克接受 V-A ECMO 治疗。出院时的生存率为 30.0%至 79.2%,12 个月时为 23.2%至 36.1%。ECMO 时间为 1.96 至 6.0 天。报告的严重不良事件有胃肠道出血(3.6%)和外周并发症(8.5%)。
AMI 引起的心源性休克患者使用 V-A ECMO 可能带来生存获益。但是,由于队列设计和报告的局限性,V-A ECMO 的治疗效果尚无定论。