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Updated: Nov 1, 2025

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Published on: May 7, 2015
Less bleeding associated with apixaban versus other direct acting oral anticoagulation in solid organ transplant
David M Salerno1, Megan E Thornberg1,2, Nicholas W Lange1
1Department of Pharmacy, NewYork-Presbyterian Hospital, New York, New York, USA.
Background:
The purpose of this study was to evaluate outcomes of bleeding and thrombosis resulting from the use of direct oral anticoagulants (DOACs) in a large cohort of solid organ transplant (SOT) recipients.
Methods:
This was a single center, retrospective cohort study of adult kidney, heart, lung, and liver transplant recipients transplanted between August 2009 and May 2018. Patients were stratified into two groups: those who received apixaban (apixaban group) or those patients receiving either rivaroxaban or dabigatran (non-apixaban group). The primary endpoint was the cumulative incidence of bleeding while receiving DOAC therapy. The secondary endpoints were incidence of major bleeding and thrombosis at any time while receiving DOAC therapy.
Results:
A total of 106 patients were included; 70 patients received apixaban and 36 patients received non-apixaban anticoagulation. Cumulative incidence of any bleeding was lower in the apixaban group compared to the non-apixaban group at both 90 days (4.9% vs. 16.1%) and 180 days (11.4% vs. 24.9%, P = .034). Cumulative incidence of major bleeding (P = .686) and thrombosis (P = .515) were similar between groups. DOAC dosing congruent with the package insert(s) was associated with a lower risk of thrombosis.
Conclusion:
Apixaban-based anticoagulation was associated with a lower cumulative incidence of any bleeding compared to non-apixaban DOACs.
Insights
Direct oral anticoagulants (DOACs) in solid organ transplant (SOT) recipients showed apixaban was linked to less bleeding than other DOACs. Proper DOAC dosing also reduced thrombosis risk in these patients.
Area of Science:
- Transplantation Medicine
- Pharmacology
- Cardiovascular Research
Background:
- Solid organ transplant (SOT) recipients often require anticoagulation.
- Direct oral anticoagulants (DOACs) are increasingly used, but their outcomes in SOT populations require further study.
- Bleeding and thrombosis are significant concerns in SOT patients on anticoagulation.
Purpose of the Study:
- To evaluate bleeding and thrombosis outcomes associated with DOAC use in SOT recipients.
- To compare outcomes between apixaban and other DOACs (rivaroxaban, dabigatran) in this cohort.
- To identify factors influencing DOAC-related complications in SOT patients.
Main Methods:
- Retrospective cohort study of 106 adult SOT recipients (kidney, heart, lung, liver) between 2009-2018.
- Patients were divided into apixaban and non-apixaban (rivaroxaban or dabigatran) groups.
- Primary endpoint: cumulative incidence of any bleeding. Secondary endpoints: major bleeding and thrombosis.
Main Results:
- Apixaban use was associated with a significantly lower cumulative incidence of any bleeding at 90 days (4.9% vs 16.1%) and 180 days (11.4% vs 24.9%, P=.034).
- Incidence of major bleeding and thrombosis did not differ significantly between the apixaban and non-apixaban groups.
- Correct DOAC dosing, aligned with package inserts, correlated with a reduced risk of thrombosis.
Conclusions:
- Apixaban-based anticoagulation demonstrated a lower cumulative incidence of bleeding compared to non-apixaban DOACs in SOT recipients.
- DOACs can be used in SOT patients, with apixaban showing a favorable bleeding profile.
- Adherence to recommended DOAC dosing is crucial for mitigating thrombosis risk.
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