Benefits and Risks of Extended Dual Antiplatelet Therapy After Everolimus-Eluting Stents

被引:53
|
作者
Hermiller, James B. [1 ]
Krucoff, Mitchell W. [2 ]
Kereiakes, Dean J. [3 ,4 ]
Windecker, Stephan [5 ]
Steg, P. Gabriel [6 ,7 ,8 ]
Yeh, Robert W. [9 ,10 ,11 ]
Cohen, David J. [12 ]
Cutlip, Donald E. [10 ,11 ,13 ]
Massaro, Joseph M. [11 ,14 ]
Hsieh, Wen-Hua [11 ]
Mauri, Laura [10 ,11 ,15 ]
机构
[1] St Vincent Heart Ctr, Indianapolis, IN USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Christ Hosp, Heart & Vasc Ctr, Cincinnati, OH 45219 USA
[4] Lindner Ctr Res & Educ, Cincinnati, OH USA
[5] Univ Hosp Bern, Dept Cardiol, CH-3010 Bern, Switzerland
[6] Univ Paris Diderot, INSERM, U1148, Paris, France
[7] Hop Bichat Claude Bernard, AP HP, Dept Hosp Univ FIRE, F-75877 Paris, France
[8] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Royal Brompton Hosp, London, England
[9] Beth Israel Deaconess Med Ctr, Smith Ctr Outcomes Res Cardiol, Boston, MA 02215 USA
[10] Harvard Univ, Sch Med, Boston, MA USA
[11] Harvard Clin Res Inst, Boston, MA USA
[12] Univ Missouri, Sch Med, Dept Cardiol, St Lukes Mid Amer Heart Inst, Kansas City, MO 64108 USA
[13] Beth Israel Deaconess Med Ctr, Dept Med, Div Cardiol, Boston, MA 02215 USA
[14] Boston Univ, Sch Med, Sch Publ Hlth, Boston, MA 02118 USA
[15] Brigham & Womens Hosp, Div Cardiovasc Med, 75 Francis St, Boston, MA 02115 USA
关键词
drug-eluting stent(s); dual antiplatelet therapy; everolimus; stent thrombosis; BARE-METAL; CORONARY STENTS; THROMBOSIS; OUTCOMES; METAANALYSIS;
D O I
10.1016/j.jcin.2015.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to characterize outcomes for everolimus-eluting stent (EES)-treated subjects according to treatment with continued thienopyridine plus aspirin versus aspirin alone 12 to 30 months after stenting. BACKGROUND In the DAPT (Dual Antiplatelet Therapy) study, continued thienopyridine plus aspirin beyond 1 year after coronary stenting reduced ischemic events. Given low rates of stent thrombosis and myocardial infarction (MI) for current drug-eluting stents, we examined outcomes among EES-treated subjects in the DAPT study. METHODS The DAPT study enrolled 25,682 subjects (11,308 EES-treated) after coronary stenting. Following 12 months of treatment with thienopyridine and aspirin, eligible subjects continued treatment with aspirin and 9,961 (4,703 with EES) were randomized to 18 months of continued thienopyridine or placebo. Stent type was not randomized, and the EES subset analysis was post hoc. RESULTS Among EES-treated patients, continued thienopyridine reduced stent thrombosis (0.3% vs. 0.7%, hazard ratio [HR]: 0.38, 95% confidence interval [CI]: 0.15 to 0.97; p = 0.04) and MI (2.1% vs. 3.2%, HR: 0.63, 95% CI: 0.44 to 0.91; p = 0.01) versus placebo but did not reduce a composite of death, MI, and stroke (4.3% vs. 4.5%, HR: 0.89, 95% CI: 0.67 to 1.18; p = 0.42), and increased moderate/severe bleeding (2.5% vs. 1.3%, HR: 1.79, 95% CI: 1.15 to 2.80; p = 0.01), and death (2.2% vs. 1.1%, HR: 1.80, 95% CI: 1.11 to 2.92; p = 0.02). Death due to cancer and not related to bleeding was increased (0.64% vs. 0.17%; p = 0.01). CONCLUSIONS In EES-treated subjects, significant reductions in stent thrombosis and MI and an increase in bleeding were observed with continued thienopyridine beyond 1 year compared with aspirin alone. (The Dual Antiplatelet Therapy Study [DAPT Study]); NCT00977938) (J Am Coll Cardiol Intv 2016; 9: 138-47) (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:138 / 147
页数:10
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