Suzuki Yasuhito, Kikura Mutsuhito, Kawashima Shingo, Kimura Tetsuro, Nakajima Yoshiki
Department of Anesthesiology and Intensive Care, Hamamatsu University School of Medicine, Shizuoka, Japan.
Department of Anesthesiology, Hamamatsu Rosai Hospital, Japan Organization of Occupational Health and Safety, Shizuoka, Japan.
JA Clin Rep. 2024 Jan 29;10(1):6. doi: 10.1186/s40981-024-00690-8.
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.
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.
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.
抗Xa抑制剂拮抗剂andexanet alfa可诱导肝素抵抗。在此,我们报告一例使用甲磺酸萘莫司他成功处理andexanet alfa诱导的肝素抵抗并进行体外循环的病例。
一名84岁女性,患有A型斯坦福急性主动脉夹层,接受了全主动脉弓置换急诊手术。术前给予andexanet alfa 400mg以拮抗口服Xa抑制剂依度沙班。体外循环前给予肝素300IU/kg,活化凝血时间(ACT)为291秒。再次给予肝素200IU/kg后,ACT为361秒。根据我们针对肝素抵抗的常规治疗方法,静脉注射首剂甲磺酸萘莫司他10mg,随后以20 - 30mg/h持续输注。ACT延长至500秒,此后成功建立了体外循环。
本病例报告展示了使用甲磺酸萘莫司他成功处理andexanet alfa诱导的肝素抵抗并进行体外循环的过程。本报告展示了使用甲磺酸萘莫司他成功处理andexanet alfa诱导的肝素抵抗并进行体外循环的过程。