New England Journal of Medicine· 2012Q1
Low-Dose Aspirin for Preventing Recurrent Venous Thromboembolism
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- 2012year
Short summary
Low-dose aspirin (100 mg daily) did not significantly reduce recurrent venous thromboembolism (VTE) but did significantly reduce major vascular events by 34% (HR 0.66) and overall major vascular events or death by 33% (HR 0.67) in patients who completed initial anticoagulant therapy for unprovoked VTE.
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Key points
- Low-dose aspirin (100 mg daily) did not significantly reduce the primary outcome of recurrent venous thromboembolism (VTE) in patients who completed initial anticoagulant therapy for unprovoked VTE (HR 0.74, P=0.09).
- Aspirin significantly reduced the rate of VTE, myocardial infarction, stroke, or cardiovascular death by 34% (HR 0.66, P=0.01).
- Aspirin significantly reduced the rate of VTE, myocardial infarction, stroke, major bleeding, or death from any cause by 33% (HR 0.67, P=0.01).
- There were no significant differences in major or clinically relevant nonmajor bleeding episodes between aspirin and placebo groups.
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Abstract
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 recurred 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.).
The authors' abstract, as published at the source. New England Journal of Medicine, 2012 · DOI ↗
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Field: Internal Medicine
Internal MedicineMedicine