3-Year Clinical Outcomes in the Randomized SORT OUT III Superiority Trial Comparing Zotarolimus- and Sirolimus-Eluting Coronary Stents

被引:29
|
作者
Maeng, Michael [1 ]
Tilsted, Hans-Henrik [2 ]
Jensen, Lisette Okkels [3 ]
Kaltoft, Anne [1 ]
Kelbk, Henning [4 ]
Abildgaard, Ulrik [5 ]
Villadsen, Anton B. [2 ]
Krusell, Lars Romer [1 ]
Ravkilde, Jan [2 ]
Hansen, Knud Norregaard [3 ]
Christiansen, Evald Hoj [1 ]
Aaroe, Jens [2 ]
Jensen, Jan Skov [5 ]
Kristensen, Steen Dalby [1 ]
Botker, Hans Erik [1 ]
Madsen, Morten [6 ]
Thayssen, Per [3 ]
Sorensen, Henrik Toft [6 ]
Thuesen, Leif [1 ]
Lassen, Jens Flensted [1 ]
机构
[1] Aarhus Univ Hosp, Dept Cardiol, DK-8000 Aarhus N, Denmark
[2] Aalborg Hosp, Aarhus Univ Hosp, Dept Cardiol, Aalborg, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Dept Cardiol, Copenhagen, Denmark
[4] Gentofte Univ Hosp, Dept Cardiol, Gentofte, Denmark
[5] Aarhus Univ Hosp, Dept Clin Epidemiol, DK-8000 Aarhus N, Denmark
[6] Odense Univ Hosp, Dept Cardiol, DK-5000 Odense, Denmark
关键词
coronary; drug-eluting; randomized clinical trial; sirolimus; stent; zotarolimus; BARE-METAL STENTS; FOLLOW-UP; PACLITAXEL; ENDEAVOR; EFFICACY; LESIONS; SAFETY; THROMBOSIS; SYSTEM; CYPHER;
D O I
10.1016/j.jcin.2012.04.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to examine the 3-year clinical outcomes in patients treated with the Endeavor (Medtronic, Santa Rosa, California) zotarolimus-eluting stent (ZES) or the Cypher (Cordis, Johnson & Johnson, Warren, New Jersey) sirolimus-eluting stent (SES) in routine clinical practice. Background The long-term clinical outcome in patients treated with ZES in comparison with SES is unclear. Methods The authors randomized 2,332 patients to ZES (n = 1,162) or SES (n = 1,170) implantation. Endpoints included major adverse cardiac events (MACE), a composite of cardiac death, myocardial infarction, or target vessel revascularization; the individual endpoints of MACE; and definite stent thrombosis. Results At 3-year follow-up, the MACE rate was higher in patients treated with ZES than in patients treated with SES (148 [12.9%] vs. 116 [10.1%]; hazard ratio [HR]: 1.33, 95% confidence interval [CI]: 1.04 to 1.69; p = 0.022). Target vessel revascularization was more frequent in the ZES group compared with the SES group (103 [9.1%] vs. 76 [6.7%]; HR: 1.40, 95% CI: 1.04 to 1.89; p = 0.025), whereas the occurrence of myocardial infarction (3.8% vs. 3.3%) and cardiac death (2.8% vs. 2.8%) did not differ significantly. Although the rate of definite stent thrombosis was similar at 3-year follow-up (1.1% vs. 1.4%), very late (12 to 36 months) definite stent thrombosis occurred in 0 (0%) patients in the ZES group versus 12 (1.1%) patients in the SES group (p = 0.0005). Conclusions Although the 3-year MACE rate is higher in patients treated with ZES versus SES, our data highlight a late safety problem concerning definite stent thrombosis with the use of SES. This finding underscores the importance of long-term follow-up in head-to-head comparisons of drug-eluting stents. (Randomized Clinical Comparison of the Endeavor and the Cypher Coronary Stents in Non-selected Angina Pectoris Patients [SORT OUT III]; NCT00660478) (J Am Coll Cardiol Intv 2012; 5: 812-8) (C) 2012 by the American College of Cardiology Foundation
引用
收藏
页码:812 / 818
页数:7
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