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New England Journal of Medicine· 2012Q1· Clinical trial

Oral Rivaroxaban for the Treatment of Symptomatic Pulmonary Embolism

The EINSTEIN–PE Investigators

Short summary

A fixed-dose oral rivaroxaban regimen proved noninferior to standard anticoagulant therapy for treating symptomatic pulmonary embolism, with a significantly lower rate of major bleeding.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Rivaroxaban was noninferior to standard therapy for symptomatic pulmonary embolism (2.1% vs 1.8% recurrent VTE).
  • Rivaroxaban significantly reduced major bleeding by nearly half (1.1% vs 2.2%).
  • The trial involved 4832 patients with acute symptomatic pulmonary embolism.
  • Rivaroxaban offers a simplified, fixed-dose oral treatment option.

AI-generated from the title and abstract; the full text is not read.

Abstract

BACKGROUND: A fixed-dose regimen of rivaroxaban, an oral factor Xa inhibitor, has been shown to be as effective as standard anticoagulant therapy for the treatment of deep-vein thrombosis, without the need for laboratory monitoring. This approach may also simplify the treatment of pulmonary embolism. METHODS: In a randomized, open-label, event-driven, noninferiority trial involving 4832 patients who had acute symptomatic pulmonary embolism with or without deep-vein thrombosis, we compared rivaroxaban (15 mg twice daily for 3 weeks, followed by 20 mg once daily) with standard therapy with enoxaparin followed by an adjusted-dose vitamin K antagonist for 3, 6, or 12 months. The primary efficacy outcome was symptomatic recurrent venous thromboembolism. The principal safety outcome was major or clinically relevant nonmajor bleeding. RESULTS: Rivaroxaban was noninferior to standard therapy (noninferiority margin, 2.0; P=0.003) for the primary efficacy outcome, with 50 events in the rivaroxaban group (2.1%) versus 44 events in the standard-therapy group (1.8%) (hazard ratio, 1.12; 95% confidence interval [CI], 0.75 to 1.68). The principal safety outcome occurred in 10.3% of patients in the rivaroxaban group and 11.4% of those in the standard-therapy group (hazard ratio, 0.90; 95% CI, 0.76 to 1.07; P=0.23). Major bleeding was observed in 26 patients (1.1%) in the rivaroxaban group and 52 patients (2.2%) in the standard-therapy group (hazard ratio, 0.49; 95% CI, 0.31 to 0.79; P=0.003). Rates of other adverse events were similar in the two groups. CONCLUSIONS: A fixed-dose regimen of rivaroxaban alone was noninferior to standard therapy for the initial and long-term treatment of pulmonary embolism and had a potentially improved benefit-risk profile. (Funded by Bayer HealthCare and Janssen Pharmaceuticals; EINSTEIN-PE ClinicalTrials.gov number, NCT00439777.).

The authors' abstract, as published at the source. New England Journal of Medicine, 2012 · DOI ↗

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Field: Internal Medicine

Internal MedicineMedicine