Managing Nonoperable Intracranial Bleeding Associated With Apixaban: A Series of 2 Cases

Author:

Faust Andrew C.1,Tran Dang M.2,Lo Catherine2,Lai Sophia2,Sheperd Lyndsay1,Liu Mary1,Denetclaw Tina34

Affiliation:

1. Department of Pharmacy, Texas Health Presbyterian Hospital Dallas, Dallas, TX, USA

2. School of Pharmacy, University of California, San Francisco, CA, USA

3. School of Pharmacy, Department of Clinical Pharmacy, University of California, San Francisco, CA, USA

4. Marin General Hospital, Greenbrae, CA, USA

Abstract

Objective: To report 2 cases of nonoperable intracranial bleeding associated with apixaban managed by 3-factor prothrombin complex concentrate (PCC3). Case Summaries: Case 1 presented with a 1.3-cm left parieto-occipital hemorrhage and a thin subdural hematoma (SDH) on the left tentorium of the brain about 6 hours after his last dose of apixaban. Case 2 presented with a 4-mm left parafalcine SDH with time of most recent apixaban dose unknown. The patients received 24.9 to 25.5 U/kg of PCC3 with none to 1 U fresh frozen plasma (FFP) and demonstrated minimal or no progression in lesions measured by repeat computed tomography (CT) after treatment. One patient was discharged to a skilled nursing facility after 8 days; the other patient was discharged to home after 18 days. Discussion: Apixaban has no specific antidote. Current bleeding management strategies are based on expert opinion. The risks and benefits for differing strategies are unclear, and little clinical experience for managing apixaban-associated intracranial bleeding has been reported to date. These cases describe the clinical use of PCC3 to manage parieto-occipital and subdural hemorrhage associated with apixaban in events not requiring surgical intervention. Conclusion: In these 2 cases, 25 U/kg PCC3, with none to one unit FFP, ceased apixaban-associated intracranial bleeding without apparent thrombogenic complications.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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