Safety and Effectiveness of the Endeavor Zotarolimus-Eluting Stent in Real-World Clinical Practice 12-Month Data From the E-Five Registry

被引:58
作者
Lotan, Chaim [1 ]
Meredith, Ian T.
Mauri, Laura [2 ,3 ]
Liu, Minglei [4 ]
Rothman, Martin T. [5 ]
机构
[1] Hadassah Hebrew Univ Med Ctr, Inst Heart, IL-91120 Jerusalem, Israel
[2] Brigham & Womens Hosp, Boston, MA 02115 USA
[3] Harvard Clin Res Inst, Boston, MA USA
[4] Medtron Cardio Vasc, Santa Rosa, CA USA
[5] Barts & London NHS Trust, London Chest Hosp, London, England
关键词
coronary artery lesion; drug-eluting stent; multicenter registry; restenosis; stent thrombosis; CORONARY-ARTERY-DISEASE; UNSELECTED POPULATION; OUTCOMES; THROMBOSIS; EFFICACY; MULTICENTER; THERAPY; TRIALS;
D O I
10.1016/j.jcin.2009.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The E-Five registry was designed to evaluate the safety and effectiveness of the Endeavor zotarolimus-eluting stent (ZES) (Medtronic CardioVascular, Santa Rosa, California) for the treatment of coronary artery stenosis across a wide range of patients treated in real-world clinical practice settings. Background Early clinical trials with the Endeavor ZES have demonstrated low rates of target lesion revascularization with a favorable safety profile including low late stent thrombosis with up to 4 years of follow-up. A clinical registry was designed to complement controlled trial data by examining a large patient population, including high-risk patient subsets. Methods The E-Five registry is a prospective, nonrandomized, multicenter global registry conducted at 188 centers worldwide. Adult patients (n = 8,314) with coronary artery disease who underwent single-vessel or multivessel percutaneous coronary intervention were enrolled. The primary end point was the rate of major adverse cardiac events (MACE) at 12 months. A secondary analysis stratified patients by standard versus extended-use clinical and lesion characteristics. Results Overall 12-month outcome rates were MACE 7.5%; cardiac death 1.7%; myocardial infarction (all) 1.6%; target lesion revascularization 4.5%; and stent thrombosis (Academic Research Consortium definite and probable) 1.1%. The 12-month MACE rates were 4.3% and 8.6% for standard- and extended-use patients, respectively (p < 0.001). Conclusions This large, international multicenter registry provides important information regarding the long-term safety and efficacy of the Endeavor ZES across standard and extended-use patients in the real-world setting. Rates of MACE and measures of safety including cardiac death, myocardial infarction, and stent thrombosis were low and consistent with pooled results of clinical trials. (E-Five Registry: A World-Wide Registry With The Endeavor Zotarolimus Eluting Coronary Stent [eFive Registry]; NCT00623441) (J Am Coll Cardiol Intv 2009;2:1227-35) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:1227 / 1235
页数:9
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