Andexanet Alfa versus Four-Factor Prothrombin Complex Concentrate for the Reversal of Factor Xa (FXa) Inhibitor-Associated Intracranial Hemorrhage: A Systematic Review of Retrospective Studies

Author:

Ferreira Luan Oliveira1ORCID,Oldemburg Ricardo Andres León1,Leitão Filho João Monteiro1,Cerveira Rodrigo Arcoverde23ORCID,Vasconcelos Victoria Winkler1,da Costa Giovana Escribano1,Rodrigues Roseny dos Reis45,Lopes Dielly Catrina Favacho6ORCID

Affiliation:

1. Department of Anesthesiology, João de Barros Barreto University Hospital, Belém 66073-000, Brazil

2. Division of Immunology & Allergy, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, SE-171 76 Stockholm, Sweden

3. Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, SE-171 76 Stockholm, Sweden

4. Department of Anesthesiology, São Paulo University, São Paulo 05403-010, Brazil

5. Intensive Care Department, Albert Einstein Hospital, São Paulo 05652-900, Brazil

6. Laboratory of Experimental Neuropathology, Federal University of Pará, Belém 66073-000, Brazil

Abstract

Background/Objectives: There are limited data on the risks and benefits of using Andexanet alfa (AA) compared with four-factor prothrombin complex concentrate (4F-PCC) for the reversal of factor Xa inhibitor-associated intracranial hemorrhage (ICH). Our aim was to describe a compilation of the information available in the literature to date. Methods: PubMed, Embase, Web of Science (Clarivate Analytics) and the Cochrane Central Register of Controlled Trials were searched until December 2023. Following the “Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)” guidelines, our systematic literature review included studies that were retrospective in design and evaluated both drugs to control bleeding and complications (death and thromboembolic events). Two researchers re-examined the studies for relevance, extracted the data and assessed the risk of bias. No meta-analyses were performed for the results. Results: In this limited patient sample, we found no differences between published articles in terms of neuroimaging stability or thrombotic events. However, some studies show significant differences in mortality, suggesting that one of the AAs may be superior to 4F-PCC. Conclusions: Our qualitative analysis shows that AA has a better efficacy profile compared with 4F-PCC. However, further studies monitoring these patients and a multicenter collaborative network dedicated to this topic are needed.

Funder

PROPESP-UFPA

Publisher

MDPI AG

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