论文部分内容阅读
Background TARGET Ⅰ randomized controlled trial demonstrated that the novel abluminal groove-filled biodegradable polymer sirolimus-eluting stent FIREHAWK (MicroPort Medical,Shanghai,China) was non-inferior to the everolimus-eluting stent with respect to in-stent late loss at 9 months for the treatment of single de novo coronary lesions.The choice of revascularization strategy in multivessel coronary disease (MVD) remains a critical issue in cardiology.The aim of this study was to evaluate the clinical safety and effectiveness of FIREHAWK in patients with MVD from TARGET Clinical Program (TARGET Ⅰ and Ⅱ trials).