Elevated on-treatment D-dimer level is associated with major bleeding during extended anticoagulation for venous thromboembolism
Assessing optimal anticoagulant duration in venous thromboembolism (VTE) requires balancing the risks of recurrent VTE and anticoagulant-associated bleeding with fixed-duration or indefinite anticoagulation. In unprovoked VTE, elevated on-treatment D-dimer level is a predictor of recurrent thromboembolism after anticoagulant cessation, but its impact on anticoagulant-associated bleeding is unknown. We performed a post-hoc pooled analysis of two prospective cohorts (BLEEDRISK and REVERSE-2 studies) that enrolled unprovoked VTE patients who continued anticoagulation after ≥3 months of initial treatment. We calculated incidence rates of major bleeding, intracranial hemorrhage and fatal bleeding by D-dimer quartiles, then determined hazard ratios with the lowest D-dimer quartile as reference. Among 3,337 participants, incidence rates of anticoagulant-associated major bleeding from the lowest to highest D-dimer quartile were 0.45, 0.91, 1.43 and 2.20 events per 100 person-years respectively. Accounting for age, sex and anticoagulant type, individuals in the highest D-dimer quartile had a 2.7-fold higher risk of anticoagulant-associated major bleeding compared to the lowest quartile (adjusted hazard ratio [aHR] 2.70, 95% CI 1.35 - 5.41, p=0.005). This association remained robust after additional adjustment for hemoglobin, creatinine and concurrent anti-platelet use in the BLEEDRISK cohort. We did not observe differences in risks of intracranial hemorrhage or fatal bleeding by D-dimer quartiles. Elevated on-treatment D-dimer levels predicted higher risks of major bleeding during indefinite anticoagulation. Given the established relationship between elevated on-treatment D-dimer levels and recurrent VTE after time-limited anticoagulation, our findings underscore the need for additional risk stratification tools in this population to personalize anticoagulant treatment that maximizes its net clinical benefit.
Authors
- David R. Anderson (ORCID: https://orcid.org/0000-0003-0845-1722)
- R Mallick
- A Lazo-Langner
- Antoine Élias (ORCID: https://orcid.org/0000-0002-1337-1826)
- Jeannot Schmidt (ORCID: https://orcid.org/0000-0003-3424-337X)
- Thomas L. Ortel (ORCID: https://orcid.org/0000-0001-6193-4585)
- MSc Marc A. Rodger
- Harry Wang
- Marc Carrier
- Lana A. Castellucci
- Philip S. Wells
- Susan R. Kahn
- Grégoire Le Gal
- Menno V. Huisman
- Michael J. Kovacs
- Yan Xu
- Marc Righini
Institutions
- Western University (CA)
- Dalhousie University (CA)
- University of Ottawa (CA)
- Duke University (US)
- Leiden University Medical Center (NL)
- Ottawa Hospital (CA)
- Centre Hospitalier Universitaire de Clermont-Ferrand (FR)
- Ottawa Public Health (CA)
- Centre Hospitalier Intercommunal Toulon-La Seyne-sur-Mer (FR)
- Ottawa Hospital Research Institute (CA)
- McGill University (CA)
- Geneva College (US)
Publication Details
- Journal
- Haematologica
- Published
- 2026-07-16
- DOI
- https://doi.org/10.3324/haematol.2026.300589
- Primary Topic
- Venous Thromboembolism Diagnosis and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Bristol-Myers Squibb
- Pfizer
- Sanofi
- Heart and Stroke Foundation of Canada
- University of Ottawa
- McGill University
- Ottawa Hospital Research Institute
- Bayer HealthCare
- Servier
- LEO Pharma
- Canadian Institutes of Health Research