Department of Cardiology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milano, Italy.
Department of Cardiology, Ospedale di Cremona, Cremona, Italy.
Future Cardiol. 2020 Jul;16(4):251-261. doi: 10.2217/fca-2019-0093. Epub 2020 Apr 24.
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.
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。