Authors
Rosa Talerico, Chiara Cavallaro, Michela Iorio, Maria Alessandra Capparella, Francesco Bossi, Angelo Porfidia, Koichiro Abe, Mario Biglietto, Antonio Chistolini, Anders Holt, Lies Lahousse, Roberto Pola, Cecilia Becattini, Maria Cristina Vedovati
Published in
Thrombosis research. Volume 263. Pages 109752. Jun 16, 2026. Epub Jun 16, 2026.
Abstract
Direct oral anticoagulants (DOACs) and corticosteroids are frequently co-prescribed in clinical practice. While both drug classes independently increase bleeding risk, the impact of their concurrent use remains unclear.
To systematically review the literature on bleeding outcomes associated with combined DOAC and corticosteroid use.
We conducted a systematic review following PRISMA guidelines. PubMed, Web of Science, and Scopus were searched for studies reporting bleeding in patients receiving both DOACs and corticosteroids. Cumulative incidences of any bleeding and major bleeding (MB) were estimated using a random-effects model, and study quality assessed using the Newcastle-Ottawa Scale and the Cochrane RoB2. Subgroup analyses were performed for patients treated for atrial fibrillation (AF) and venous thromboembolism (VTE).
Nine studies including 87,209 patients were included. The weighted cumulative incidence of any bleeding was 7.0% (95% CI 3.96-12.01%), and of MB 6.6% (95% CI 6.21-6.97%). Heterogeneity was high for any bleeding in the overall and in the AF populations, likely reflecting differences in patient characteristics, corticosteroid exposure, follow-up duration, and study design, whereas heterogeneity was minimal in the VTE subgroup. Variability in bleeding definitions, limited reporting of corticosteroid dose and duration, and absence of stratification by DOAC type/dose or bleeding site further contributed to differences in observed incidences.
Available evidence suggests a clinically relevant incidence of bleeding among patients receiving concomitant DOAC and corticosteroid therapy. Clinicians should carefully evaluate the risk-benefit profile, monitor patients closely, and consider preventive strategies. Future studies are needed to improve risk characterization in this common clinical scenario.
CRD420251045710.
PMID:
42320245
Bibliographic data and abstract were imported from PubMed on 20 Jun 2026.
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