2-Year Clinical Follow-Up From the Randomized Comparison of Biolimus-Eluting Stents With Biodegradable Polymer and Sirolimus-Eluting Stents With Durable Polymer in Routine Clinical Practice

被引:29
作者
Klauss, Volker [2 ]
Serruys, Patrick W. [5 ]
Pilgrim, Thomas [1 ]
Buszman, Pawel [11 ]
Linke, Axel [4 ]
Ischinger, Thomas [3 ]
Eberli, Franz [9 ]
Corti, Roberto [10 ]
Wijns, William [12 ]
Morice, Marie-Claude [13 ]
di Mario, Carlo [14 ]
van Geuns, Robert Jan [5 ]
van Es, Gerrit-Anne [6 ]
Kalesan, Bindu [1 ,7 ]
Wenaweser, Peter [1 ]
Jueni, Peter [7 ,8 ]
Windecker, Stephan [1 ,8 ]
机构
[1] Univ Hosp Bern, Dept Cardiol, CH-3010 Bern, Switzerland
[2] Univ Hosp Munich Innenstadt, Dept Cardiol, Munich, Germany
[3] Hosp Bogenhausen, Dept Cardiol, Munich, Germany
[4] Herzzentrum Leipzig, Leipzig, Germany
[5] Erasmus Univ, Thoraxctr, NL-3000 DR Rotterdam, Netherlands
[6] Cardialysis, Rotterdam, Netherlands
[7] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[8] Univ Hosp Bern, Clin Trials Unit Bern, CH-3010 Bern, Switzerland
[9] Triemli Spiral, Dept Cardiol, Zurich, Switzerland
[10] Univ Hosp, Dept Cardiol, Zurich, Switzerland
[11] Med Univ Silesia, Dept Cardiol, Katowice, Poland
[12] Onze Lieve Vrouw Hosp, Dept Cardiol, Aalst, Belgium
[13] Inst Cardiovasc Paris Sud, Dept Cardiol, Paris, France
[14] Royal Brompton Hosp, Dept Cardiol, London SW3 6LY, England
关键词
restenosis; stems; thrombosis; CORONARY-ARTERY-DISEASE; BARE-METAL STENTS; OFF-LABEL; CLOPIDOGREL USE; DRUG; THROMBOSIS; OUTCOMES; IMPLANTATION; TRIAL; REVASCULARIZATION;
D O I
10.1016/j.jcin.2011.03.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to investigate safety and efficacy of biolimus-eluting stents (BES) with biodegradable polymer as compared with sirolimus-eluting stents (SES) with durable polymer through 2 years of follow-up. Background BES with a biodegradable polymer provide similar efficacy and safety as SES with a durable polymer at 9 months. Clinical outcomes beyond the period of biodegradation of the polymer used for drug release and after discontinuation of dual antiplatelet therapy are of particular interest. Methods A total of 1,707 patients were randomized to unrestricted use of BES (n = 857) or SES (n = 850) in an all-comers patient population. Results At 2 years, BES remained noninferior compared with SES for the primary endpoint, which was a composite of cardiac death, myocardial infarction, or clinically indicated target vessel revascularization (BES 12.8% vs. SES 15.2%, hazard ratio [HR]: 0.84, 95% confidence interval [CI]: 0.65 to 1.08, P(noninferiority) < 0.0001, p(superiority =) 0.18). Rates of cardiac death (3.2% vs. 3.9%, HR: 0.81, 95% CI: 0.49 to 1.35, p = 0.42), myocardial infarction (6.3% vs. 5.6%, HR: 1.12, 95% CI: 0.76 to 1.65, p = 0.56), and clinically indicated target vessel revascularization (7.5% vs. 8.6%, HR: 0.86, 95% CI: 0.62 to 1.20, p = 0.38) were similar for BES and SES. The rate of definite stent thrombosis through 2 years was 2.2% for BES and 2.5% for SES (p = 0.73). For the period between 1 and 2 years, event rates for definite stent thrombosis were 0.2% for BES and 0.5% for SES (p = 0.42). After discontinuation of dual antiplatelet therapy, no very late definite stent thrombosis occurred in the BES group. Conclusions At 2 years of follow-up, the unrestricted use of BES with a biodegradable polymer maintained a similar safety and efficacy profile as SES with a durable polymer. (Limus Eluted From a Durable Versus Erodable Stent Coating [LEADERS]; NCT00389220) (J Am Coll Cardiol Intv 2011;4: 887-95) (C) 2011 by the American College of Cardiology Foundation
引用
收藏
页码:887 / 895
页数:9
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