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大城市公立医院中无聚合物生物雷帕霉素洗脱支架在ST段抬高型急性心肌梗死患者中的血管造影和临床性能:BESAMI MUCHO研究

Angiographic and clinical performance of polymer-free biolimus-eluting stent in patients with ST-segment elevation acute myocardial infarction in a metropolitan public hospital: The BESAMI MUCHO study.

作者信息

Sgueglia Gregory A, D'Errico Fabrizio, Gioffrè Gaetano, De Santis Antonella, Summaria Francesco, Piccioni Fabiana, Gaspardone Achille

机构信息

Sant'Eugenio Hospital, Rome, Italy.

出版信息

Catheter Cardiovasc Interv. 2018 Apr 1;91(5):851-858. doi: 10.1002/ccd.27206. Epub 2017 Aug 2.

Abstract

OBJECTIVES

This study aimed at assessing the performance of a new generation polymer-free biolimus-eluting stent (BES) in real-world patients with ST-segment elevation myocardial infarction (STEMI).

BACKGROUND

Polymers components of early-generation drug-eluting stents have been implicated in the pathogenesis of delayed arterial healing, vessel remodeling, and delayed stent thrombosis. Recently, a novel polymer-free BES has shown excellent clinical performance in clinical trial setting.

METHODS

Overall, 175 consecutive patients (64 ± 14 years, 141 men) treated with the BioFreedom (Biosensors Europe, Morges, Switzerland) polymer-free BES because of STEMI were included in this study. The primary endpoint was the rate of major adverse cardiac events (MACE), a composite of cardiac death, recurrent myocardial infarction, and ischemia-driven target vessel revascularization at 1 year follow-up. A subgroup of patients underwent 6-month angiographic follow-up. Dual antiplatelet therapy was prescribed for 12 months after STEMI.

RESULTS

At 1 year, the cumulative rate of MACE was 4.6%. One patient (0.6%) had an arrhythmic cardiac death and five (2.9%) had ischemia-driven target vessel revascularization, although only three (1.7%) had target lesion revascularization. Two (1.1%) patients had acute stent thrombosis yielding nonfatal myocardial infarction. In 70 patients (63 ± 14 years, 61 men), quantitative coronary angiography at 6-month follow-up revealed diameter stenosis of 24.1 ± 13.7% and minimal lumen diameter of 2.29 ± 0.56 mm, yielding a late lumen loss of 0.13 ± 0.14 mm.

CONCLUSIONS

In real-world setting, implantation of a new-generation polymer-free BES during STEMI is associated with favorable clinical and angiographic results, pointing toward the overall efficacy and safety of the device in complex clinical scenarios.

摘要

目的

本研究旨在评估新一代无聚合物生物雷帕霉素洗脱支架(BES)在ST段抬高型心肌梗死(STEMI)真实世界患者中的性能。

背景

早期药物洗脱支架的聚合物成分与延迟动脉愈合、血管重塑和延迟支架血栓形成的发病机制有关。最近,一种新型无聚合物BES在临床试验中显示出优异的临床性能。

方法

本研究共纳入175例因STEMI接受BioFreedom(瑞士莫尔日的Biosensors Europe公司)无聚合物BES治疗的连续患者(64±14岁,141例男性)。主要终点是主要不良心脏事件(MACE)发生率,MACE是1年随访时心脏死亡、再发心肌梗死和缺血驱动的靶血管血运重建的复合终点。一组亚组患者接受了6个月的血管造影随访。STEMI后双联抗血小板治疗持续12个月。

结果

1年时,MACE累积发生率为4.6%。1例患者(0.6%)发生心律失常性心脏死亡,5例患者(2.9%)发生缺血驱动的靶血管血运重建,尽管只有3例患者(1.7%)发生靶病变血运重建。2例患者(1.1%)发生急性支架血栓形成,导致非致命性心肌梗死。在70例患者(63±14岁,61例男性)中,6个月随访时的定量冠状动脉造影显示直径狭窄为24.1±13.7%,最小管腔直径为2.29±0.56 mm,晚期管腔丢失为0.13±0.14 mm。

结论

在真实世界中,STEMI期间植入新一代无聚合物BES与良好的临床和血管造影结果相关,表明该装置在复杂临床情况下的总体有效性和安全性。

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