Whitbeck Matthew G, Applegate Robert J
Wake Forest School of Medicine, Section of Cardiology, Winston-Salem, NC.
Clin Med Insights Cardiol. 2013 Jul 23;7:115-26. doi: 10.4137/CMC.S11516. Print 2013.
Everolimus-eluting stents (EES) represent the next generation of drug-eluting stents (DES). Important design modifications include thin strut stent backbones, less inflammatory and more biocompatible polymers, and lower drug dosing. The cobalt chromium EES fluoropolymer XIENCE V stent has been the most extensively studied of such stents. In animal models, this stent demonstrated minimal vessel inflammation, a biologically active endothelium with strut coverage similar to a bare metal stent, and inhibition of intimal hyperplasia comparable to that seen with sirolimus-eluting stents. The SPIRIT family of clinical trials demonstrated low rates of late loss, and clinical restenosis, as well as low rates of very late stent thrombosis. These excellent clinical outcomes addressed limitations of the 1st generation DES, and substantiated widespread clinical use of the EES platform.
依维莫司洗脱支架(EES)代表了下一代药物洗脱支架(DES)。重要的设计改进包括薄支架梁的支架主体、炎症性更低且生物相容性更高的聚合物以及更低的药物剂量。钴铬EES含氟聚合物XIENCE V支架是此类支架中研究最为广泛的。在动物模型中,这种支架显示出最小程度的血管炎症、具有类似于裸金属支架的支架梁覆盖的生物活性内皮,以及与西罗莫司洗脱支架相当的内膜增生抑制作用。SPIRIT系列临床试验表明晚期管腔丢失率、临床再狭窄率较低,以及极晚期支架血栓形成率也较低。这些出色的临床结果解决了第一代DES的局限性,并证实了EES平台在临床上的广泛应用。