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轻度低温作为ST段抬高型心肌梗死患者辅助治疗的影响:一项随机对照试验的荟萃分析和试验序贯分析

Impact of Mild Hypothermia As Adjunctive Therapy in Patients With ST-Elevation Myocardial Infarction: A Meta-Analysis and Trial Sequential Analysis of Randomized Controlled Trials.

作者信息

Laborante Renzo, Paglianiti Donato Antonio, Galli Mattia, Patti Giuseppe, D'Amario Domenico

机构信息

Department of Cardiovascular Science, Fondazione Policlinico Agostino Gemelli IRCCS, Rome, Italy.

Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.

出版信息

Catheter Cardiovasc Interv. 2025 Feb;105(3):543-556. doi: 10.1002/ccd.31351. Epub 2024 Dec 15.

Abstract

BACKGROUND

The prevention of reperfusion injury remains an unmet need in ST-elevation myocardial infarction (STEMI) patients. Several randomized controlled trials (RCTs) evaluated mild hypothermia as adjunctive therapy during STEMI, with conflicting results.

AIMS

To summarize the evidence about the efficacy and safety of mild hypothermia in patients with STEMI, as well as its conclusiveness through a trial sequential analysis (TSA).

METHODS

PubMed and Scopus electronic databases were screened for eligible studies until August 12, 2024. Efficacy endpoints were all-cause death, infarct size (IS), left ventricular ejection fraction (LVEF), the occurrence of microvascular obstruction (MVO), thrombolysis in myocardial infarction (TIMI) flow grade 3, and the resolution of ST-segment elevation (i.e., > 50-70% from baseline) after the procedure. Safety endpoints included: the incidence of atrial fibrillation (AF), infections, any bleeding, major bleeding, acute and subacute stent thrombosis (STh), cardiogenic shock/pulmonary oedema, and ventricular fibrillation/tachycardia. "Door-to-balloon time" was indicated as the procedural endpoint. Two pre-specified subgroup analyses were planned according to the mean ischemic time and the site of hypothermia induction (intra-coronary vs. extra-coronary). A TSA was run to explore whether the effect estimate of each efficacy outcome could be influenced by further studies.

RESULTS

Ten RCTs were included. Hypothermia did not provide a benefit for any of the specified efficacy endpoints. Furthermore, it enhanced the risk of infection, the risk of STh in patients with a mean ischemic time of less than 4 h, and the risk of AF in patients undergoing extra-coronary hypothermia. Finally, it was also associated with an increased "door-to-balloon time", and a trend toward an increased risk of any bleeding. No significant difference was found for the other endpoints. TSA showed conclusive evidence of an absence of benefit of hypothermia on IS, MVO, LVEF, and TIMI three flow.

CONCLUSIONS

Mild hypothermia is not beneficial and causes relevant delays in clinical management of STEMI patients, raising safety issues mainly related to the occurrence of STh, AF, and infections.

摘要

背景

在ST段抬高型心肌梗死(STEMI)患者中,预防再灌注损伤仍是一项未满足的需求。多项随机对照试验(RCT)评估了轻度低温作为STEMI辅助治疗的效果,结果相互矛盾。

目的

总结关于轻度低温对STEMI患者疗效和安全性的证据,以及通过试验序贯分析(TSA)得出的结论性结果。

方法

检索PubMed和Scopus电子数据库,查找截至2024年8月12日的符合条件的研究。疗效终点包括全因死亡、梗死面积(IS)、左心室射血分数(LVEF)、微血管阻塞(MVO)的发生、心肌梗死溶栓(TIMI)血流3级以及术后ST段抬高的缓解情况(即较基线降低>50-70%)。安全终点包括:房颤(AF)发生率、感染、任何出血、大出血、急性和亚急性支架血栓形成(STh)、心源性休克/肺水肿以及室颤/室速。“门球时间”被指定为手术终点。根据平均缺血时间和低温诱导部位(冠状动脉内与冠状动脉外)计划进行两项预先设定的亚组分析。进行TSA以探讨每项疗效结果的效应估计是否会受到进一步研究的影响。

结果

纳入了10项RCT。低温对任何指定的疗效终点均无益处。此外,它增加了感染风险、平均缺血时间少于4小时患者的STh风险以及接受冠状动脉外低温治疗患者的AF风险。最后,它还与“门球时间”延长以及任何出血风险增加的趋势相关。其他终点未发现显著差异。TSA显示有确凿证据表明低温对IS、MVO、LVEF和TIMI 3级血流无益处。

结论

轻度低温无益,且会导致STEMI患者临床管理出现相关延误,引发主要与STh、AF和感染发生相关的安全问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a823/11831718/ebf71ac24fcb/CCD-105-543-g003.jpg

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