急性冠状动脉综合征经皮冠状动脉介入治疗前单次大剂量他汀类药物的疗效:系统综述和荟萃分析

Bryan Gervais de Liyis, Gusti Ngurah Prana Jagannatha, Anastasya Maria Kosasih, I. Kadek Susila Surya Darma, I. Made Junior Rina Artha
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引用次数: 0

摘要

单次大剂量他汀类药物预处理对接受经皮冠状动脉介入治疗(PCI)患者的影响尚未得到充分研究。本研究旨在评估单次大剂量他汀预处理对急性冠脉综合征(ACS)患者术后的影响。荟萃分析回顾了 Cochrane、PubMed 和 Medline 数据库中对接受 PCI 的 ACS 患者进行的单次大剂量阿托伐他汀或罗苏伐他汀与安慰剂的比较研究。主要终点包括主要不良心血管事件(MACE)、心肌梗死(MI)、全因死亡率和三个月后靶血管血运重建(TVR)。次要终点是 TIMI 血流 3 级和左心室射血分数 (LVEF)。对 15 项 RCT 进行了综合分析,共涉及 6207 名患者(3090 对 3117 名患者)。汇总结果显示,与对照组相比,在PCI术前服用单次大剂量他汀类药物可显著降低PCI术后三个月的MACE发生率(OR 0.50,95%CI 0.35-0.71,P = 0.0001)。与对照组相比,他汀类药物单次高剂量组的 MI(OR 0.57,95%CI 0.42-0.77,p = 0.0002)、全因死亡率(OR 0.56,95%CI 0.39-0.81,p = 0.0002)和 TVR(OR 0.56,95%CI 0.35-0.92,p = 0.02)发生率显著降低。对 TIMI 血流 3 级(OR 1.20,95%CI 0.94-1.53,p = 0.14)或左室射血分数(OR 2.19,95%CI - 0.97 至 5.34,p = 0.17)无明显影响。亚组分析显示,单次服用80毫克阿托伐他汀(OR 0.66,95%CI 0.54-0.81,p < 0.0001)和40毫克罗伐他汀(OR 0.19,95%CI 0.07-0.54,p = 0.002)可降低MACE发生率。ACS患者在PCI术前服用单次大剂量他汀类药物可显著降低PCI术后三个月的MACE、MI、全因死亡率和TVR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of single high-dose statin prior to percutaneous coronary intervention in acute coronary syndrome: a systematic review and meta-analysis
The impacts of single high-dose statin preloading in patients undergoing percutaneous coronary intervention (PCI) have not been fully examined. This study aims to evaluate post-procedure impacts of single high-dose statin pretreatment with acute coronary syndrome (ACS). The meta-analysis reviewed Cochrane, PubMed, and Medline databases for studies comparing single high-dose atorvastatin or rosuvastatin to placebo in ACS patients undergoing PCI. The primary endpoints included major adverse cardiovascular events (MACE), myocardial infarction (MI), all-cause mortality, and target vessel revascularization (TVR) at three months. Secondary endpoints examined were the TIMI flow grade 3 and left ventricular ejection fraction (LVEF). Comprehensive analysis was conducted on fifteen RCTs, encompassing a total of 6,207 patients (3090 vs 3117 patients). The pooled results demonstrated that a single high-dose of statin administered prior to PCI led to a significant decrease in the incidence of MACE at three months post-PCI compared to the control group (OR 0.50, 95%CI 0.35–0.71, p = 0.0001). The occurrence of MI (OR 0.57, 95%CI 0.42–0.77, p = 0.0002), all-cause mortality (OR 0.56, 95%CI 0.39–0.81, p = 0.0002), and TVR (OR 0.56, 95%CI 0.35–0.92, p = 0.02) was significantly lower in the statin single high-dose group compared to the control group. No significant effects on TIMI flow grade 3 (OR 1.20, 95%CI 0.94–1.53, p = 0.14) or left ventricular ejection fraction (OR 2.19, 95%CI − 0.97 to 5.34, p = 0.17) were observed. Subgroup analysis demonstrated reduced incidence of MACE with a single dose of 80 mg atorvastatin (OR 0.66, 95%CI 0.54–0.81, p < 0.0001) and 40 mg rosuvastatin (OR 0.19, 95%CI 0.07–0.54, p = 0.002). Single high-dose statin before PCI in patients with ACS significantly reduces MACE, MI, all-cause mortality, and TVR three months post-PCI.
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