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Background: Andexanet alfa, an anti-Xa inhibitor antagonist, induces heparin resistance. Here, we report a case of successful management of cardiopulmonary bypass with andexanet alfa-induced heparin resistance using nafamostat mesylate.
Case Presentation: An 84-year-old female, with Stanford type A acute aortic dissection, underwent an emergency surgery for total aortic arch replacement. Andexanet alfa 400 mg was administered preoperatively to antagonize edoxaban, an oral Xa inhibitor. Heparin 300 IU/kg was administered before cardiopulmonary bypass, and the activated clotting time (ACT) was 291 s. The ACT was 361 s after another administration of heparin 200 IU/kg. According to our routine therapy for heparin resistance, an initial dose of nafamostat mesylate 10 mg was administered intravenously, followed by a continuous infusion of 20-30 mg/h. The ACT was prolonged to 500 s, and cardiopulmonary bypass was successfully established thereafter.
Conclusions: This case report presents the successful management of cardiopulmonary bypass with andexanet alfa-induced heparin resistance using nafamostat mesilate. This report presents the successful management of cardiopulmonary bypass with andexanet alfa-induced heparin resistance using nafamostat mesilate.
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http://dx.doi.org/10.1186/s40981-024-00690-8 | DOI Listing |
Thromb Res
August 2025
Institute for Clinical and Experimental Transfusion Medicine, Tuebingen, Germany; Center for Clinical Transfusion Medicine, University Hospital of Tuebingen, Tuebingen, Germany.
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View Article and Find Full Text PDFBMJ Case Rep
August 2025
Pulmonary and Critical Care Division, Internal Medicine Department, American University of Beirut Medical Center, Beirut, Lebanon
The use of enoxaparin is generally not recommended in patients with end-stage renal disease (ESRD) and undergoing haemodialysis. We describe the administration of high-dose enoxaparin in a haemodialysis patient with heparin resistance and recurrent deep vein thrombosis (DVT) outlining a novel dosing regimen along an innovative method for monitoring antifactor Xa activity. As a last resort of his recurrent DVT, a critically ill intensive care unit patient undergoing dialysis was prescribed high-dose enoxaparin, administered exclusively after dialysis, on dialysis days for a period of 2 months.
View Article and Find Full Text PDFJ Cardiothorac Vasc Anesth
August 2025
Department of Anesthesiology, University of Oklahoma Health,Oklahoma City, OK. Electronic address:
Res Sq
August 2025
School of Biomedical Engineering, Colorado State University, Fort Collins, CO 80526, USA.
This research introduces carboxymethyl kappa-carrageenan-chitosan polyelectrolyte multilayers as a promising and sustainable alternative to heparin, used in surface treatments for blood-contacting medical devices. The polysaccharide-based surface coatings have good cytocompatibility and resist microbial adhesion of both Pseudomonas aeruginosa and Staphylococcus aureus. The blood compatibility of surfaces containing carboxymethyl-kappa-carrageenan was directly compared to similar polyelectrolyte multilayers containing heparin.
View Article and Find Full Text PDFPancreatic ductal adenocarcinoma (PDAC) stands to become the second most deadly cancer by 2030. The small GTPase, KRAS, is mutated in over 90% of PDAC patients and considered the primary driver mutation. Despite being an almost ubiquitous event, KRAS mutations have been difficult to target therapeutically, particularly KRAS , the most common mutation in PDAC.
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