Kirtane Ajay J, Leon Martin B
Center for Interventional Vascular Therapy, Columbia University Medical Center, New York, NY 10032, USA.
Cardiovasc Drug Rev. 2007 Winter;25(4):316-32. doi: 10.1111/j.1527-3466.2007.00024.x.
Drug-eluting stents, or intracoronary stents that combine the local delivery of antirestenotic pharmacologic therapies while maintaining the mechanical advantage of bare metal stents over balloon angioplasty alone, are a highly complex technology that have profoundly affected the practice of percutaneous coronary intervention over the last 5 years. These devices were designed specifically to treat the neointimal hyperplasia occurring after conventional bare metal stent placement, and have been remarkably successful in this regard. However, recent concerns have been raised regarding the long-term safety of these devices, particularly when used outside of the specific patient and lesion subsets studied in the pivotal randomized trials that led to device approval by regulatory bodies within the United States and abroad. This review aims to present a brief description of the sirolimus-eluting stent device platform and its mechanism of action, followed by an overview of current data regarding efficacy and safety regarding the clinical use of sirolimus-eluting stent technology.
药物洗脱支架,即冠状动脉内支架,它在保持裸金属支架相对于单纯球囊血管成形术的机械优势的同时,实现抗再狭窄药物治疗的局部递送,是一项高度复杂的技术,在过去5年中对经皮冠状动脉介入治疗的实践产生了深远影响。这些装置专门设计用于治疗传统裸金属支架置入后发生的新生内膜增生,在这方面取得了显著成功。然而,最近人们对这些装置的长期安全性提出了担忧,特别是当它们用于美国和国外监管机构批准该装置的关键随机试验所研究的特定患者和病变亚组之外时。本综述旨在简要描述西罗莫司洗脱支架装置平台及其作用机制,随后概述有关西罗莫司洗脱支架技术临床应用的疗效和安全性的当前数据。