摘要

The advent of drug-eluting stents (DES) has revolutionized the field of interventional cardiology and witnessed dramatic restenotic advantages over prior bare-metal stents (BMS) [1,2]. In the first generation DESs, stainless steel was widely used as the stent platform. Recently, several second-generation DESs have been developed by using cobalt-chromium stent platforms to further facilitate the procedure and improve the long-term DES safety [3]. As compared to the stainless steel, cobalt-chromium is stronger and more radio-opaque, therefore allowing to reduce the strut thickness while maintaining radial strength and to make the stent platforms more flexible and deliverable [4,5]. The FOCUS registry was a large-scale, prospective, nonrandomized, observational, multi-center, web-based program, designed to evaluate the safety and efficacy of a second-generation cobalt-chromium sirolimus-eluting stent (CoCr-SES) in routine treatment of patients with coronary artery diseases (CAD) [6,7]. The present report described the 2-year clinical outcomes of unrestricted use of CoCr-SES in patients from the FOCUS registry.

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