依维莫司洗脱支架:当前临床研究的最新进展。

IF 1.3 Q4 ENGINEERING, BIOMEDICAL Medical Devices-Evidence and Research Pub Date : 2011-01-01 Epub Date: 2011-07-26 DOI:10.2147/MDER.S22043
Dominic J Allocco, Anita A Joshi, Keith D Dawkins
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引用次数: 0

摘要

依维莫司洗脱支架(EES)已成为全球最常植入的冠状动脉支架。本综述描述并分析了支持使用 EES 的临床数据,主要侧重于已发表的随机对照试验。与早一代紫杉醇洗脱支架(PES)相比,依维莫司洗脱支架的再狭窄、支架血栓形成和围手术期心肌梗死的发生率较低。与 PES 相比,EES 在所有亚组中的不良事件发生率普遍较低,但糖尿病患者明显例外。将 EES 与西罗莫司洗脱支架或佐他洛利莫司洗脱支架进行比较的随机临床试验较少,但在已进行的试验中观察到 EES 取得了非常好的效果。最近的临床试验数据表明,下一代 EES 在机械性能和放射能力方面都有所改进,因此能保持出色的安全性和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Everolimus-eluting stents: update on current clinical studies.

Everolimus-eluting stents (EES) have become the most commonly implanted coronary stents worldwide. This review describes and analyzes the clinical data supporting the use of EES, focusing primarily on published, randomized, controlled trials. Everolimus-eluting stents have been shown to have less restenosis, stent thrombosis, and periprocedural myocardial infarction compared with earlier generation paclitaxel-eluting stents (PES). Lower rates of adverse events for EES compared with PES were generally seen in all subgroups, with the notable exception of patients with diabetes mellitus. There have been fewer, randomized, clinical trials comparing EES with either sirolimus-eluting stents or zotarolimus-eluting stents, although very good results with EES have been observed in the trials that have been performed. Recent clinical trial data suggest that this excellent safety and efficacy profile is maintained in a next-generation EES designed to have improved mechanical properties and radiopacity.

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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
0.00%
发文量
41
审稿时长
16 weeks
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