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Comparison of Zotarolimus-Eluting Stents With Sirolimus- and Paclitaxel-Eluting Stents for Coronary Revascularization

Objectives The aim of this study was to evaluate the relative efficacy and safety of zotarolimus-eluting stents (ZES) in comparison with the established and widely used sirolimus- (SES) and paclitaxel-eluting stents (PES) in routine clinical practice. Background Whether ZES might provide similar cli...

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Published in:Journal of the American College of Cardiology 2010-10, Vol.56 (15), p.1187-1195
Main Authors: Park, Duk-Woo, MD, Kim, Young-Hak, MD, Yun, Sung-Cheol, PhD, Kang, Soo-Jin, MD, Lee, Seung-Whan, MD, Lee, Cheol-Whan, MD, Park, Seong-Wook, MD, Seong, In-Whan, MD, Lee, Jae-Hwan, MD, Tahk, Seung-Jea, MD, Jeong, Myung-Ho, MD, Jang, Yangsoo, MD, Cheong, Sang-Sig, MD, Yang, Joo-Young, MD, Lim, Do-Sun, MD, Seung, Ki-Bae, MD, Chae, Jei-Keon, MD, Hur, Seung-Ho, MD, Lee, Sang-Gon, MD, Yoon, Junghan, MD, Lee, Nae-Hee, MD, Choi, Young-Jin, MD, Kim, Hyun-Sook, MD, Kim, Kee-Sik, MD, Kim, Hyo-Soo, MD, Hong, Taeg-Jong, MD, Park, Hun-Sik, MD, Park, Seung-Jung, MD
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Language:English
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Summary:Objectives The aim of this study was to evaluate the relative efficacy and safety of zotarolimus-eluting stents (ZES) in comparison with the established and widely used sirolimus- (SES) and paclitaxel-eluting stents (PES) in routine clinical practice. Background Whether ZES might provide similar clinical and angiographic outcomes in a broad spectrum of patients compared with SES or PES is undetermined. Methods We performed a single-blind, multicenter, prospectively randomized trial to compare ZES with SES and PES in 2,645 patients undergoing percutaneous coronary intervention. The primary end point was a composite of major adverse cardiac events (MACE) (death, myocardial infarction, and ischemia-driven target vessel revascularization) at 12 months. A noninferiority comparison (ZES vs. SES) and a superiority comparison (ZES vs. PES) were performed for the primary end point. Results Baseline clinical and angiographic characteristics were similar in the 3 groups. At 12 months, the ZES group showed noninferior rates of MACE compared with the SES group (10.2% vs. 8.3%, p for noninferiority = 0.01, p for superiority = 0.17) and significantly fewer MACE than the PES group (10.2% vs. 14.1%, p for superiority = 0.01). The incidence of death or myocardial infarction was similar among the groups (ZES vs. SES vs. PES, 5.8% vs. 6.9% vs. 7.6%, respectively, p = 0.31). The incidence of stent thrombosis was significantly lower in the SES group (ZES vs. SES vs. PES, 0.7% vs. 0% vs. 0.8%, respectively, p = 0.02). Conclusions In this large-scale, practical randomized trial, the use of ZES resulted in similar rates of MACE compared with SES and in fewer MACE compared with PES at 12 months. (Comparison of the Efficacy and the Safety of Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting Stent for Coronary Lesions; NCT00418067 )
ISSN:0735-1097
1558-3597
DOI:10.1016/j.jacc.2010.03.086