Management and outcomes of major bleeding during treatment with dabigatran or warfarin

Circulation. 2013 Nov 19;128(21):2325-32. doi: 10.1161/CIRCULATIONAHA.113.002332. Epub 2013 Sep 30.

Abstract

Background: The aim of this study was to compare the management and prognosis of major bleeding in patients treated with dabigatran or warfarin.

Methods and results: Two independent investigators reviewed bleeding reports from 1034 individuals with 1121 major bleeds enrolled in 5 phase III trials comparing dabigatran with warfarin in 27 419 patients treated for 6 to 36 months. Patients with major bleeds on dabigatran (n=627 of 16 755) were older, had lower creatinine clearance, and more frequently used aspirin or non-steroid anti-inflammatory agents than those on warfarin (n=407 of 10 002). The 30-day mortality after the first major bleed tended to be lower in the dabigatran group (9.1%) than in the warfarin group (13.0%; pooled odds ratio, 0.68; 95% confidence interval, 0.46-1.01; P=0.057). After adjustment for sex, age, weight, renal function, and concomitant antithrombotic therapy, the pooled odds ratio for 30-day mortality with dabigatran versus warfarin was 0.66 (95% confidence interval, 0.44-1.00; P=0.051). Major bleeds in dabigatran patients were more frequently treated with blood transfusions (423/696, 61%) than bleeds in warfarin patients (175/425, 42%; P<0.001) but less frequently with plasma (dabigatran, 19.8%; warfarin, 30.2%; P<0.001). Patients who experienced a bleed had shorter stays in the intensive care unit if they had previously received dabigatran (mean 1.6 nights) compared with those who had received warfarin (mean 2.7 nights; P=0.01).

Conclusions: Patients who experienced major bleeding on dabigatran required more red cell transfusions but received less plasma, required a shorter stay in intensive care, and had a trend to lower mortality compared with those who had major bleeding on warfarin.

Clinical trial registration url: http://www.ClinicalTrials.gov. Unique identifiers: NCT00262600, NCT00291330, NCT00680186, NCT00329238 and NCT00558259.

Keywords: anticoagulants; atrial fibrillation; hemorrhage; mortality; venous thrombosis.

Publication types

  • Clinical Trial, Phase III
  • Comparative Study
  • Meta-Analysis
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Anticoagulants / administration & dosage
  • Anticoagulants / adverse effects
  • Antithrombins / administration & dosage
  • Antithrombins / adverse effects
  • Atrial Fibrillation / drug therapy*
  • Atrial Fibrillation / mortality
  • Benzimidazoles / administration & dosage
  • Benzimidazoles / adverse effects*
  • Blood Transfusion / statistics & numerical data
  • Dabigatran
  • Female
  • Hemoglobins / metabolism
  • Hemorrhage / chemically induced*
  • Hemorrhage / mortality
  • Hemorrhage / therapy*
  • Humans
  • Length of Stay / statistics & numerical data
  • Male
  • Middle Aged
  • Risk Factors
  • Treatment Outcome
  • Venous Thromboembolism / drug therapy*
  • Venous Thromboembolism / mortality
  • Warfarin / administration & dosage
  • Warfarin / adverse effects*
  • beta-Alanine / administration & dosage
  • beta-Alanine / adverse effects
  • beta-Alanine / analogs & derivatives*

Substances

  • Anticoagulants
  • Antithrombins
  • Benzimidazoles
  • Hemoglobins
  • beta-Alanine
  • Warfarin
  • Dabigatran

Associated data

  • ClinicalTrials.gov/NCT00262600
  • ClinicalTrials.gov/NCT00291330
  • ClinicalTrials.gov/NCT00329238
  • ClinicalTrials.gov/NCT00558259
  • ClinicalTrials.gov/NCT00680186