Differential Neutralization of Unfractionated Heparin and Enoxaparin by Andexanet Alfa. (May 2022)

• Record Type: Journal Article
• Authors: Lewis, Joseph; Iqbal, Omer; Jeske, Walter; Hoppensteadt, Debra; Siddiqui, Fakiha; Fareed, Jawed
• Is Part Of: Clinical and applied thrombosis/hemostasis. Volume 28(2022)
• Publication Date: 2022-05
• Subjects: neutralization -- andexanet alfa -- UFH -- LMWH -- thrombelastography -- activated clotting time; Hemostasis -- Periodicals; Thrombosis -- Periodicals; 616.13
• DOI: 10.1177/10760296221099934
• Languages: English
• ISSNs: 1076-0296

Abstract

Introduction: Andexanet alfa (andexanet) is an approved antidote used to reverse the bleeding effects of Direct Oral Anticoagulant (Direct-Xa agents) agents because it reverses anti-Xa activity. Unfractionated heparin (UFH) and low molecular weight heparins (LMWHs) exhibit anti-Xa activity. The purpose is to investigate the neutralization of UFH and LMWH by andexanet in activated clotting time (ACT), thrombelastography (TEG), and anti-Xa due to the protamine sulfate shortage. Methods: UFH and LMWH were studied with andexanet, PS, or saline as potential reversal agents/controls at varying concentrations in ACT, TEG, and anti-Xa and compared to each other. Results: Andexanet partially neutralized both drugs several TEG parameters at high andexanet concentrations, but it was not as effective as protamine sulfate in any of the assays used. Most TEG parameters were correlated with andexanet concentration. In ACT, significant neutralization was demonstrated at many andexanet concentrations for UFH, but not LMWH. UFH was completely neutralized by PS in ACT, while LMWH was partially neutralized by PS in ACT. Andexanet alfa was a less effective neutralization agent than the protamine sulfate as it only partially neutralized UFH in ACT and was ineffective at neutralizing LMWH when tested at the same concentration as PS (10 ug/mL). Conclusion: Andexanet partially neutralized UFH and LMWH with variability between assays, necessitating investigation into assay-dependent differences.