Clopidogrel and aspirin versus aspirin alone for the prevention of atherothrombotic events

被引:1990
作者
Bhatt, DL
Fox, KAA
Hacke, W
Berger, PB
Black, HR
Boden, WE
Cacoub, P
Cohen, EA
Creager, MA
Easton, JD
Flather, MD
Haffner, SM
Hamm, CW
Hankey, GJ
Johnston, SC
Mak, KH
Mas, JL
Montalescot, G
Pearson, TA
Steg, PG
Steinhubl, SR
Weber, MA
Brennan, DM
Fabry-Ribaudo, L
Booth, J
Topol, EJ
Frye, RL
Amarenco, P
Brass, LM
Buyse, M
Cohen, LS
DeMets, DL
Fuster, V
Hart, RG
Marler, JR
McCarthy, C
Schoemig, A
Lincoff, AM
Brener, SJ
Sila, CA
Albuquerque, A
Aroutiounov, G
Artemiev, D
Atkeson, BG
Bartel, T
Basart, DCG
Lima, AB
Belli, G
Bordalo e Sa, AL
Bosch, X
机构
[1] Case Western Reserve Univ, Dept Genet, Cleveland, OH 44106 USA
[2] Cleveland Clin, Cleveland, OH 44106 USA
[3] Univ & Royal Infirm Edinburgh, Edinburgh, Midlothian, Scotland
[4] Heidelberg Univ, Heidelberg, Germany
[5] Duke Univ, Durham, NC USA
[6] Rush Med Coll, Chicago, IL 60612 USA
[7] Hartford Hosp, Hartford, CT 06115 USA
[8] Hop La Pitie Salpetriere, Paris, France
[9] Hop St Anne, F-75674 Paris, France
[10] CHU Pitie Salpetriere, Inst Cardiol, Paris, France
[11] Hop Bichat Claude Bernard, F-75877 Paris, France
[12] Sunnybrook & Womens Coll Hlth Sci Ctr, Toronto, ON, Canada
[13] Brigham & Womens Hosp, Boston, MA 02115 USA
[14] Harvard Univ, Sch Med, Boston, MA USA
[15] Rhode Isl Hosp, Providence, RI USA
[16] Brown Univ, Providence, RI 02912 USA
[17] Royal Brompton Hosp, London SW3 6LY, England
[18] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
[19] Kerckhoff Klin Ctr, Bad Nauheim, Germany
[20] Univ Western Australia, Royal Perth Hosp, Perth, WA 6009, Australia
[21] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
[22] Univ Calif San Francisco, San Francisco, CA 94143 USA
[23] Gleneagles Med Ctr, Singapore, Singapore
[24] Univ Rochester, Sch Med, Rochester, NY USA
[25] Univ Kentucky, Lexington, KY USA
[26] Suny Downstate Med Ctr, Brooklyn, NY 11203 USA
关键词
D O I
10.1056/NEJMoa060989
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Dual antiplatelet therapy with clopidogrel plus low-dose aspirin has not been studied in a broad population of patients at high risk for atherothrombotic events. METHODS: We randomly assigned 15,603 patients with either clinically evident cardiovascular disease or multiple risk factors to receive clopidogrel (75 mg per day) plus low-dose aspirin (75 to 162 mg per day) or placebo plus low-dose aspirin and followed them for a median of 28 months. The primary efficacy end point was a composite of myocardial infarction, stroke, or death from cardiovascular causes. RESULTS: The rate of the primary efficacy end point was 6.8 percent with clopidogrel plus aspirin and 7.3 percent with placebo plus aspirin (relative risk, 0.93; 95 percent confidence interval, 0.83 to 1.05; P=0.22). The respective rate of the principal secondary efficacy end point, which included hospitalizations for ischemic events, was 16.7 percent and 17.9 percent (relative risk, 0.92; 95 percent confidence interval, 0.86 to 0.995; P=0.04), and the rate of severe bleeding was 1.7 percent and 1.3 percent (relative risk, 1.25; 95 percent confidence interval, 0.97 to 1.61 percent; P=0.09). The rate of the primary end point among patients with multiple risk factors was 6.6 percent with clopidogrel and 5.5 percent with placebo (relative risk, 1.2; 95 percent confidence interval, 0.91 to 1.59; P=0.20) and the rate of death from cardiovascular causes also was higher with clopidogrel (3.9 percent vs. 2.2 percent, P=0.01). In the subgroup with clinically evident atherothrombosis, the rate was 6.9 percent with clopidogrel and 7.9 percent with placebo (relative risk, 0.88; 95 percent confidence interval, 0.77 to 0.998; P=0.046). CONCLUSIONS: In this trial, there was a suggestion of benefit with clopidogrel treatment in patients with symptomatic atherothrombosis and a suggestion of harm in patients with multiple risk factors. Overall, clopidogrel plus aspirin was not significantly more effective than aspirin alone in reducing the rate of myocardial infarction, stroke, or death from cardiovascular causes.
引用
收藏
页码:1706 / 1717
页数:12
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