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Circulation· 2013Q1

Treatment of Acute Venous Thromboembolism With Dabigatran or Warfarin and Pooled Analysis

Sam Schulman, Ajay K. Kakkar, Samuel Z. Goldhaber, Sebastian Schellong et al.

Short summary

Dabigatran (2.3% VTE recurrence) showed similar efficacy to warfarin (2.2% VTE recurrence) in treating acute venous thromboembolism (VTE), but with significantly less overall bleeding (15.6% vs. 22.1%).

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

Key points

  • Dabigatran and warfarin had similar rates of recurrent symptomatic VTE over 6 months (2.3% vs. 2.2%).
  • Dabigatran showed a significantly lower rate of any bleeding compared to warfarin (15.6% vs. 22.1%).
  • Major bleeding rates were numerically lower with dabigatran (1.2%) than warfarin (1.7%), though not statistically significant in this trial.
  • Pooled analysis of two trials confirmed similar VTE recurrence and reduced overall bleeding with dabigatran.

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

Abstract

BACKGROUND: Dabigatran and warfarin have been compared for the treatment of acute venous thromboembolism (VTE) in a previous trial. We undertook this study to extend those findings. METHODS AND RESULTS: In a randomized, double-blind, double-dummy trial of 2589 patients with acute VTE treated with low-molecular-weight or unfractionated heparin for 5 to 11 days, we compared dabigatran 150 mg twice daily with warfarin. The primary outcome, recurrent symptomatic, objectively confirmed VTE and related deaths during 6 months of treatment occurred in 30 of the 1279 dabigatran patients (2.3%) compared with 28 of the 1289 warfarin patients (2.2%; hazard ratio, 1.08; 95% confidence interval [CI], 0.64-1.80; absolute risk difference, 0.2%; 95% CI, -1.0 to 1.3; P<0.001 for the prespecified noninferiority margin for both criteria). The safety end point, major bleeding, occurred in 15 patients receiving dabigatran (1.2%) and in 22 receiving warfarin (1.7%; hazard ratio, 0.69; 95% CI, 0.36-1.32). Any bleeding occurred in 200 dabigatran (15.6%) and 285 warfarin (22.1%; hazard ratio, 0.67; 95% CI, 0.56-0.81) patients. Deaths, adverse events, and acute coronary syndromes were similar in both groups. Pooled analysis of this study RE-COVER II and the RE-COVER trial gave hazard ratios for recurrent VTE of 1.09 (95% CI, 0.76-1.57), for major bleeding of 0.73 (95% CI, 0.48-1.11), and for any bleeding of 0.70 (95% CI, 0.61-0.79). CONCLUSION: Dabigatran has similar effects on VTE recurrence and a lower risk of bleeding compared with warfarin for the treatment of acute VTE. CLINICAL TRIAL REGISTRATION URL: www.clinicaltrials.gov. Unique identifiers: NCT00680186 and NCT00291330.

The authors' abstract, as published at the source. Circulation, 2013 · DOI ↗

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Field: Internal Medicine

Internal MedicineMedicine