Length of hospitalization and mortality for bleeding during treatment with warfarin, dabigatran, or rivaroxaban

PLoS One. 2018 Mar 28;13(3):e0193912. doi: 10.1371/journal.pone.0193912. eCollection 2018.

Abstract

Background: Different outcomes among patients hospitalized for bleeding after starting anticoagulation could influence choice of anticoagulant. We compared length of hospitalization, proportion of Intensive Care Unit (ICU) admissions, ICU length of stay, and 30- and 90-day mortality for adults with atrial fibrillation hospitalized for bleeding after starting warfarin, dabigatran, or rivaroxaban.

Methods: An US commercial database of 38 million members from 1 November 2010 to 31 March 2014 was used to examine adults with atrial fibrillation hospitalized for bleeding after starting warfarin (2,446), dabigatran (442), or rivaroxaban (256). Outcomes included difference in mean total length of hospitalization, proportion of ICU admissions, mean length of ICU stay, and all-cause 30- and 90-day mortality.

Results: Warfarin users were older and had more comorbidities. Multivariable regression modeling with propensity score weighting showed warfarin users were hospitalized 2.0 days longer (95% CI 1.8-2.3; p < 0.001) than dabigatran users and 2.6 days longer (95% CI 2.4-2.9; p < 0.001) than rivaroxaban users. Dabigatran users were hospitalized 0.6 days longer (95% CI 0.2-1.0; p = 0.001) than rivaroxaban users. There were no differences in the proportion of ICU admissions. Among ICU admissions, warfarin users stayed 3.0 days (95% CI 1.9-3.9; p < 0.001) longer than dabigatran users and 2.4 days longer (95% CI 0.9-3.7; p = 0.003) than rivaroxaban users. There was no difference in ICU stay between dabigatran and rivaroxaban users. There were no differences in 30- and 90-day all-cause mortality.

Conclusions: Rivaroxaban and dabigatran were associated with shorter hospitalizations; however, there were no differences in 30- and 90-day mortality. These findings suggest bleeding associated with the newer agents is not more dangerous than bleeding associated with warfarin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anticoagulants / adverse effects*
  • Anticoagulants / therapeutic use
  • Atrial Fibrillation / drug therapy
  • Blood Coagulation / drug effects
  • Dabigatran / adverse effects*
  • Dabigatran / therapeutic use
  • Female
  • Hemorrhage / chemically induced*
  • Hemorrhage / mortality*
  • Hospitalization
  • Humans
  • Intensive Care Units
  • Length of Stay
  • Male
  • Propensity Score
  • Retrospective Studies
  • Rivaroxaban / adverse effects*
  • Rivaroxaban / therapeutic use
  • Warfarin / adverse effects*
  • Warfarin / therapeutic use

Substances

  • Anticoagulants
  • Warfarin
  • Rivaroxaban
  • Dabigatran

Grants and funding

Blake Charlton was supported by the Outstanding Resident Research Award, Resident ResearchFunding Grant, and Resident Research Travel Grant--all from the Clinical & Translational Science Institute, University of California San Francisco. These awards and grants provided funding for statistical consultation and travel to the American Heart Association’s 2015 conference, where this project was presented as a scientific poster. Gboyega Adeboyeje and John J Barron were employed by HealthCore, a wholly-owned and independently operated subsidiary of Anthem, Inc. HealthCore provided support in the form of salaries for the Gboyega Adeboyeje and John J Barron but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. Anthem has no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of all authors are articulated in the ‘author contributions’ section.