Key result
DOACs linked to lower risk of major events and kidney transplant rejection vs VKA in AF.
Why the study?
The risk-benefit profile of direct oral anticoagulants in kidney transplant recipients with atrial fibrillation remains under-investigated.
Does DOAC use reduce the composite of all-cause death, thromboembolic events, and major bleeding compared to VKAs in kidney transplant recipients with atrial fibrillation?
Cohort (n=1,367)
Yes
Does DOAC use reduce the composite of all-cause death, thromboembolic events, and major bleeding compared to VKAs in kidney transplant recipients with atrial fibrillation?
Answers are grounded in this paper and cite their sources.
In kidney transplant recipients with atrial fibrillation, DOACs were associated with a significantly lower risk of adverse clinical outcomes and transplant rejection compared to VKAs.
BACKGROUND: The risk-benefit profile of direct oral anticoagulants (DOACs) in kidney transplant recipients (KTRs) with atrial fibrillation (AF) remains under-investigated. PURPOSE: To evaluate the safety and efficacy of DOACs compared with vitamin K antagonists (VKAs) in KTRs with AF. METHODS: Retrospective analysis from TriNetX network. Adult KTRs with AF were included. Patients with mechanical valves, antiphospholipid syndrome, or an estimated eGFR <15 mL/min/1.73 m² were excluded. Anticoagulated patients were stratified into two cohorts (DOACs versus VKAs) . The first 3 months post-transplant were excluded, and follow-up for outcomes started at 9 months post-transplant and continued for 12 months thereafter. Propensity score matching (1:1) balanced baseline characteristics. The primary outcome was a composite of all-cause death, thromboembolic events, major bleeding. Secondary outcomes included each component of the composite outcome and kidney transplant rejection. RESULTS: Of the 1367 KTRs with AF, 695 received DOACs (65.0 ± 10.0 years, 30.5% female), while 672 received VKAs (64.0 ± 10.1 years, 29.9% female). After matching, each cohort included 553 patients. At one-year follow-up, compared with VKAs, DOACs were associated with a lower risk of the composite outcome (HR 0.66, 95%CI 0.50-0.87), and kidney transplant rejection (HR 0.46, 95%CI 0.30-0.71). A non-significant trend was observed toward a lower risk of all-cause death (HR 0.64, 95%CI 0.41-1.01), major bleeding (HR 0.66, 95%CI 0.43-1.01), thromboembolic events (HR 0.68, 95%CI 0.43-1.07). CONCLUSION: In this real-world cohort of KTRs with AF, DOACs use was associated with lower risk of the composite outcome and kidney transplant rejection.
No takes yet. Share an insight, caveat, or question.
Rossi et al. (2026) conducted a cohort in Kidney transplant recipients with atrial fibrillation (n=1,367). Direct oral anticoagulants (DOACs) vs. Vitamin K antagonists (VKAs) was evaluated on Composite of all-cause death, thromboembolic events, major bleeding (HR 0.66, 95% CI 0.50-0.87). In kidney transplant recipients with atrial fibrillation, DOACs were associated with a lower risk of the primary composite outcome compared with VKAs (HR 0.66; 95% CI 0.50-0.87).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: