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Ultimaster 冠状动脉支架系统:5 年全球经验。

The Ultimaster coronary stent system: 5-year worldwide experience.

机构信息

Department of Cardiology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milano, Italy.

Department of Cardiology, Ospedale di Cremona, Cremona, Italy.

出版信息

Future Cardiol. 2020 Jul;16(4):251-261. doi: 10.2217/fca-2019-0093. Epub 2020 Apr 24.

Abstract

Newer generation drug-eluting stents have significantly improved outcomes in patients undergoing percutaneous coronary intervention by reducing the risk of restenosis and stent thrombosis. In comparison with first-generation ones, contemporary drug-eluting stents have thinner struts and more biocompatible polymers, which reduce inflammation, promote endothelialization and decrease neointimal proliferation. The Ultimaster™/Ultimaster™ Tansei™ coronary stent system is a cobalt-chromium, biodegradable polymer, sirolimus-eluting stent (Terumo, Tokyo, Japan) that received the Conformitè Européenne mark approval for clinical use in 2014/2018. This device has been the object of intense clinical evaluation in controlled randomized studies and observational registries. In this article, we analytically reviewed the available clinical data with a focus on the latest real-world evidence that demonstrates excellent performance in all of the clinical subsets.

摘要

新一代药物洗脱支架通过降低再狭窄和支架内血栓形成的风险,显著改善了经皮冠状动脉介入治疗患者的预后。与第一代药物洗脱支架相比,当代药物洗脱支架具有更薄的支架梁和更具生物相容性的聚合物,从而减少炎症、促进内皮化和减少新生内膜增殖。Ultimaster™/Ultimaster™ Tansei™ 冠状动脉支架系统是一种钴铬、可生物降解聚合物、西罗莫司洗脱支架(日本东京 Terumo),于 2014/2018 年获得临床使用的欧洲合格认证标志批准。该器械在对照随机研究和观察性注册研究中受到了广泛的临床评估。在本文中,我们对现有临床数据进行了分析性综述,重点关注最新的真实世界证据,这些证据表明该器械在所有临床亚组中均表现出色。

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