Institute of Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, 91120, Israel.
J Control Release. 2012 Jul 20;161(2):703-12. doi: 10.1016/j.jconrel.2012.02.010. Epub 2012 Feb 17.
Coronary stenting has revolutionized current perspective of coronary artery disease management. Bare-metal stents (BMS) were introduced in 1994, but long-term results have been shattered by the dual problems of in-stent restenosis (ISR) and stent thrombosis associated with BMS. Though stent thrombosis became much less frequent after the introduction of antiplatelet therapy, restenosis however remained as a significant problem. Intense work on stent development has successfully led to the introduction of drug-eluting stents (DES) in 2002, as an effort to address restenosis problem. First generation DES (sirolimus and paclitaxel eluting) were introduced first and found to be more effective than BMS. The use of first generation DES dealt with the problem of restenosis. But, despite early successes, uncertainty remains on the overall safety, especially for late adverse clinical events such as stent thrombosis. Thus, the second generation (everolimus and zotarolimus eluting) stents were developed and introduced with lower thrombosis rates. Today, in the search for improving the performance of available DES various developments and clinical studies are ongoing. Research and developments is primarily centred on increasing the long-term safety and efficacy of stents.
经皮冠状动脉介入治疗(PCI)已彻底改变了冠心病的治疗模式。裸金属支架(BMS)于 1994 年问世,但由于 BMS 相关的支架内再狭窄(ISR)和支架内血栓形成的双重问题,长期结果并不理想。虽然抗血小板治疗的引入使支架内血栓形成的发生率大大降低,但再狭窄仍然是一个重要问题。经过对支架开发的深入研究,药物洗脱支架(DES)于 2002 年问世,旨在解决再狭窄问题。第一代 DES(西罗莫司和紫杉醇洗脱)首先问世,被发现比 BMS 更有效。第一代 DES 的使用解决了再狭窄问题。但是,尽管早期取得了成功,但对于晚期不良临床事件(如支架内血栓形成)的总体安全性仍存在不确定性。因此,第二代(依维莫司和佐他莫司洗脱)支架的开发和引入降低了血栓形成的发生率。如今,为了提高现有 DES 的性能,正在进行各种开发和临床研究。研究和开发主要集中在提高支架的长期安全性和疗效上。