Meta-Analysis of Reversal Agents for Severe Bleeding Associated With Direct Oral Anticoagulants

J Am Coll Cardiol. 2021 Jun 22;77(24):2987-3001. doi: 10.1016/j.jacc.2021.04.061.

Abstract

Background: Direct oral anticoagulants (DOACs) have shown a positive benefit-risk balance in both clinical trials and real-world data, but approximately 2% to 3.5% of patients experience major bleeding annually. Many of these patients require hospitalization, and the administration of reversal agents may be required to control bleeding.

Objectives: The aim of this study was to investigate clinical outcomes associated with the use of 4-factor prothrombin complex concentrates, idarucizumab, or andexanet for reversal of severe DOAC-associated bleeding.

Methods: The investigators systematically searched for studies of reversal agents for the treatment of severe bleeding associated with DOAC. Mortality rates, thromboembolic events, and hemostatic efficacy were meta-analyzed using a random effects model.

Results: The investigators evaluated 60 studies in 4,735 patients with severe DOAC-related bleeding who were treated with 4-factor prothrombin complex concentrates (n = 2,688), idarucizumab (n = 1,111), or andexanet (n = 936). The mortality rate was 17.7% (95% confidence interval [CI]: 15.1% to 20.4%), and it was higher in patients with intracranial bleedings (20.2%) than in patients with extracranial hemorrhages (15.4%). The thromboembolism rate was 4.6% (95% CI: 3.3% to 6.0%), being particularly high with andexanet (10.7%; 95% CI: 6.5% to 15.7%). The effective hemostasis rate was 78.5% (95% CI: 75.1% to 81.8%) and was similar regardless of the reversal agent considered. The rebleeding rate was 13.2% (95% CI: 5.5% to 23.1%) and 78% of rebleeds occurred after resumption of anticoagulation. The risk of death was markedly and significantly associated with failure to achieve effective hemostasis (relative risk: 3.63; 95% CI: 2.56 to 5.16). The results were robust regardless of the type of study or the hemostatic scale used.

Conclusions: The risk of death after severe DOAC-related bleeding remains significant despite a high rate of effective hemostasis with reversal agents. Failure to achieve effective hemostasis strongly correlated with a fatal outcome. Thromboembolism rates are particularly high with andexanet. Comparative clinical trials are needed.

Keywords: andexanet alfa; bleeding; direct oral anticoagulants; idarucizumab; reversal agents.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Administration, Oral
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Anticoagulants / administration & dosage
  • Anticoagulants / adverse effects*
  • Blood Coagulation / drug effects*
  • Blood Coagulation / physiology
  • Blood Coagulation Factors / pharmacology
  • Blood Coagulation Factors / therapeutic use
  • Factor Xa / pharmacology
  • Factor Xa / therapeutic use
  • Hemorrhage / blood
  • Hemorrhage / chemically induced*
  • Hemorrhage / drug therapy*
  • Hemostasis / drug effects*
  • Hemostasis / physiology
  • Humans
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use
  • Retrospective Studies

Substances

  • Antibodies, Monoclonal, Humanized
  • Anticoagulants
  • Blood Coagulation Factors
  • PRT064445
  • Recombinant Proteins
  • prothrombin complex concentrates
  • idarucizumab
  • Factor Xa