Oral Rivaroxaban for Symptomatic Venous Thromboembolism
Abstract
Rivaroxaban, an oral factor Xa inhibitor, may provide a simple, fixed-dose regimen for treating acute deep-vein thrombosis (DVT) and for continued treatment, without the need for laboratory monitoring.
We conducted an open-label, randomized, event-driven, noninferiority study that compared oral rivaroxaban alone (15 mg twice daily for 3 weeks, followed by 20 mg once daily) with subcutaneous enoxaparin followed by a vitamin K antagonist (either warfarin or acenocoumarol) for 3, 6, or 12 months in patients with acute, symptomatic DVT. In parallel, we carried out a double-blind, randomized, event-driven superiority study that compared rivaroxaban alone (20 mg once daily) with placebo for an additional 6 or 12 months in patients who had completed 6 to 12 months of treatment for venous thromboembolism. The primary efficacy outcome for both studies was recurrent venous thromboembolism. The principal safety outcome was major bleeding or clinically relevant nonmajor bleeding in the initial-treatment study and major bleeding in the continued-treatment study.
Citation impact
- FWCI
- 140.52
- Percentile
- 100%
- References
- 20
Authors
1- TEThe EINSTEIN InvestigatorsCorresponding
Topics & keywords
- Rivaroxaban
- Medicine
- Vitamin K antagonist
- Edoxaban
- Warfarin
- Venous thrombosis
- Placebo
- Anesthesia
- Good health and well-being