3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Reversal of apixaban and rivaroxaban with andexanet alfa prior to invasive or surgical procedures

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Outcomes following andexanet alfa reversal of factor Xa inhibitors in patients requiring urgent or emergent invasive procedures are lacking. This study aimed to describe efficacy and safety outcomes following andexanet alfa administration within 24 h of an invasive procedure.

          Methods

          This single‐center, observational, retrospective study included patients who received andexanet alfa within 24 h of an invasive or surgical procedure. The primary outcome was hemostatic efficacy graded as excellent, good, or poor using similar definitions to the ANNEXA‐4 criteria. Secondary outcomes included hospital discharge disposition, intensive care unit (ICU) and hospital length of stay, 30‐day mortality, 30‐day thromboischemic event rates, and serum coagulation assay changes pre‐ and postreversal.

          Results

          Forty‐four patients met inclusion criteria; of these, 27 (62.8%) received apixaban and 16 (37.2%) were treated with rivaroxaban prior to admission. The indications for reversal were categorized as intracranial ( n = 20 [45.5%]) or extracranial ( n = 24 [54.5%]) sites. Majority of patients required emergent operative procedures (18 [40.9%]), followed by invasive device placement (10 [22.7%]) or arterial embolization (9 [20.5%]). Thirty‐eight (86.4%) patients were able to be adequately graded for hemostatic efficacy. Overall, 30 (78.9%) patients achieved excellent or good hemostasis within 24 h after periprocedural administration of andexanet alfa (19 [82.6%] apixaban vs. 11 [78.6%] rivaroxaban; 12 [80.0%] intracranial events vs. 18 [78.3%] extracranial events). Discharge disposition was most often to a short‐ or long‐term care facilities (27 [61.4%]). Thirty‐day mortality and thromboischemic complications occurred in 15 (34.1%) and 12 (27.3%) patients, respectively. Prothrombin time and antifactor Xa assay results were significantly decreased after andexanet alfa administration ( p < 0.05) while thromboelastogram assay values (reaction time, kinetic time, and activated clotting time) showed nonsignificant changes pre‐ versus postreversal.

          Conclusion

          Andexanet alfa may be used for urgent or emergent reversal of apixaban and rivaroxaban peri‐procedurally with promising hemostatic outcomes. Further prospective, comparative clinical research is warranted.

          Related collections

          Most cited references31

          • Record: found
          • Abstract: not found
          • Article: not found

          2019 AHA/ACC/HRS Focused Update of the 2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Antithrombotic Therapy for VTE Disease: CHEST Guideline and Expert Panel Report.

            We update recommendations on 12 topics that were in the 9th edition of these guidelines, and address 3 new topics.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Full Study Report of Andexanet Alfa for Bleeding Associated with Factor Xa Inhibitors

              Andexanet alfa is a modified recombinant inactive form of human factor Xa developed for reversal of factor Xa inhibitors.
                Bookmark

                Author and article information

                Contributors
                paige.bradshaw@uchealth.com
                Journal
                Pharmacotherapy
                Pharmacotherapy
                10.1002/(ISSN)1875-9114
                PHAR
                Pharmacotherapy
                John Wiley and Sons Inc. (Hoboken )
                0277-0008
                1875-9114
                23 September 2022
                October 2022
                : 42
                : 10 ( doiID: 10.1002/phar.v42.10 )
                : 780-791
                Affiliations
                [ 1 ] Department of Pharmacy UC Health – University of Cincinnati Medical Center Cincinnati Ohio USA
                [ 2 ] University of Cincinnati James L. Winkle College of Pharmacy Cincinnati Ohio USA
                [ 3 ] Department of Surgery, Division of Trauma University of Cincinnati Cincinnati Ohio USA
                [ 4 ] Department of Emergency Medicine University of Washington School of Medicine Seattle Washington USA
                Author notes
                [*] [* ] Correspondence

                Paige Garber Bradshaw, UC Medical Center, 3188 Bellevue Avenue, Cincinnati, Ohio 45219, USA.

                Email: paige.bradshaw@ 123456uchealth.com

                Author information
                https://orcid.org/0000-0002-8030-7269
                https://orcid.org/0000-0002-4338-1021
                https://orcid.org/0000-0002-0962-1001
                Article
                PHAR2727 06-22-0311.R1
                10.1002/phar.2727
                9826450
                36073083
                54b11e05-8ad4-44b0-87b4-63612a6487cc
                © 2022 The Authors. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy published by Wiley Periodicals LLC on behalf of Pharmacotherapy Publications, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 19 August 2022
                : 30 June 2022
                : 22 August 2022
                Page count
                Figures: 2, Tables: 4, Pages: 12, Words: 6933
                Categories
                Original Research Article
                Original Research Articles
                Custom metadata
                2.0
                October 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.3 mode:remove_FC converted:08.01.2023

                anticoagulation reversal,anticoagulation reversal agents,factor xa,factor xa inhibitors,general surgery,recombinant proteins

                Comments

                Comment on this article