Low-Dose Aspirin for Preventing Recurrent Venous Thromboembolism

被引:390
|
作者
Brighton, Timothy A. [1 ]
Eikelboom, John W. [5 ]
Mann, Kristy [2 ]
Biostat, M.
Mister, Rebecca [2 ]
Gallus, Alexander [3 ]
Ockelford, Paul [6 ]
Gibbs, Harry [4 ]
Hague, Wendy [2 ]
Xavier, Denis [7 ]
Diaz, Rafael [8 ]
Kirby, Adrienne [2 ]
Simes, John [2 ]
机构
[1] Prince Wales Hosp, SEALS, Dept Haematol, Sydney, NSW, Australia
[2] Univ Sydney, Natl Hlth & Med Res Council, Clin Trials Ctr, Sydney, NSW 2006, Australia
[3] SA Pathol Flinders Med Ctr, Dept Haematol, Adelaide, SA, Australia
[4] Alfred Hosp, Gen Med Unit, Melbourne, Vic, Australia
[5] McMaster Univ, Populat Hlth Res Inst, Hamilton, ON, Canada
[6] Auckland City Hosp, Thrombosis Unit, Auckland, New Zealand
[7] St Johns Med Coll & Res Inst, Bangalore, Karnataka, India
[8] Estudios Clin Latinoamer ECLA Int, Rosario, Argentina
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2012年 / 367卷 / 21期
基金
英国医学研究理事会;
关键词
ORAL ANTICOAGULANT-THERAPY; PULMONARY-EMBOLISM; 1ST EPISODE; THROMBOSIS; EVENTS;
D O I
10.1056/NEJMoa1210384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Patients who have had a first episode of unprovoked venous thromboembolism have a high risk of recurrence after anticoagulants are discontinued. Aspirin may be effective in preventing a recurrence of venous thromboembolism. METHODS We randomly assigned 822 patients who had completed initial anticoagulant therapy after a first episode of unprovoked venous thromboembolism to receive aspirin, at a dose of 100 mg daily, or placebo for up to 4 years. The primary outcome was a recurrence of venous thromboembolism. RESULTS During a median follow-up period of 37.2 months, venous thromboembolism re-curred in 73 of 411 patients assigned to placebo and in 57 of 411 assigned to aspirin (a rate of 6.5% per year vs. 4.8% per year; hazard ratio with aspirin, 0.74; 95% confidence interval [CI], 0.52 to 1.05; P = 0.09). Aspirin reduced the rate of the two prespecified secondary composite outcomes: the rate of venous thromboembolism, myocardial infarction, stroke, or cardiovascular death was reduced by 34% (a rate of 8.0% per year with placebo vs. 5.2% per year with aspirin; hazard ratio with aspirin, 0.66; 95% CI, 0.48 to 0.92; P = 0.01), and the rate of venous thromboembolism, myocardial infarction, stroke, major bleeding, or death from any cause was reduced by 33% (hazard ratio, 0.67; 95% CI, 0.49 to 0.91; P = 0.01). There was no significant between-group difference in the rates of major or clinically relevant nonmajor bleeding episodes (rate of 0.6% per year with placebo vs. 1.1% per year with aspirin, P = 0.22) or serious adverse events. CONCLUSIONS In this study, aspirin, as compared with placebo, did not significantly reduce the rate of recurrence of venous thromboembolism but resulted in a significant reduction in the rate of major vascular events, with improved net clinical benefit. These results substantiate earlier evidence of a therapeutic benefit of aspirin when it is given to patients after initial anticoagulant therapy for a first episode of unprovoked venous thromboembolism. (Funded by National Health and Medical Research Council [Australia] and others; Australian New Zealand Clinical Trials Registry number, ACTRN12605000004662.)
引用
收藏
页码:1979 / 1987
页数:9
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