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急性心肌梗死患者中雷帕霉素洗脱支架与金属裸支架的 3 年随访结果。

Three-year follow-up of sirolimus-eluting stents vs. bare metal stents for acute myocardial infarction.

机构信息

Department of Cardiology, Hiroshima City Hospital, Hiroshima, Japan.

出版信息

Circ J. 2012;76(1):65-70. doi: 10.1253/circj.cj-11-0300. Epub 2011 Oct 29.

Abstract

BACKGROUND

The long-term safety and efficacy of drug-eluting stents for patients with acute myocardial infarction (AMI) remain controversial.

METHODS AND RESULTS

A total of 143 consecutive patients who presented between August 2004 and July 2006 with AMI and who underwent primary percutaneous coronary intervention (PCI) using sirolimus-eluting stents (SES), were compared with a historical control cohort of 129 consecutive patients who presented between August 2002 and July 2004 and who underwent primary PCI using bare metal stents (BMS). The rate of major adverse cardiovascular events at 3 years was significantly lower in the SES group than in the BMS group (20.3% vs. 33.1%, respectively; P=0.01). This reduction was mainly driven by a decrease in the rate of target vessel revascularization (12.3% vs. 22.4%, respectively; P=0.02). There was no significant difference in the rate of cardiovascular death (4.5% vs. 5.7%, respectively; P=0.67), non-fatal myocardial infarction (4.5% vs. 9.2%, respectively; P=0.16), coronary artery bypass grafting (2.3% vs. 2.5%, respectively; P=0.93), stroke (2.4% vs. 0.8%, respectively; P=0.35), and stent thrombosis (2.9% vs. 2.3%, respectively; P=0.80) between the 2 groups.

CONCLUSIONS

SES can be used safely and effectively in patients with AMI.

摘要

背景

药物洗脱支架治疗急性心肌梗死(AMI)患者的长期安全性和疗效仍存在争议。

方法和结果

共有 143 例连续患者于 2004 年 8 月至 2006 年 7 月期间因 AMI 就诊,并接受雷帕霉素洗脱支架(SES)的直接经皮冠状动脉介入治疗(PCI),与 2002 年 8 月至 2004 年 7 月期间就诊并接受裸金属支架(BMS)直接 PCI 的 129 例连续患者的历史对照队列进行比较。SES 组的主要不良心血管事件发生率在 3 年内显著低于 BMS 组(分别为 20.3%和 33.1%,P=0.01)。这种降低主要是由于靶血管血运重建率的降低(分别为 12.3%和 22.4%,P=0.02)。心血管死亡(分别为 4.5%和 5.7%,P=0.67)、非致命性心肌梗死(分别为 4.5%和 9.2%,P=0.16)、冠状动脉旁路移植术(分别为 2.3%和 2.5%,P=0.93)、卒中和支架血栓形成(分别为 2.4%和 0.8%,P=0.35)的发生率在两组之间无显著差异。

结论

SES 可安全有效地用于 AMI 患者。

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