Buka Richard J, Krishna Mamidipudi T, Sutton David J
Institute of Cardiovascular Sciences University of Birmingham Birmingham UK.
Institute of Immunology and Immunotherapy University of Birmingham Birmingham UK.
EJHaem. 2024 Jun 22;5(4):829-832. doi: 10.1002/jha2.959. eCollection 2024 Aug.
Andexanet alfa is a recombinant, modified factor Xa (FXa) molecule that is used for the reversal of the anticoagulant effect of oral anti-FXa anticoagulants in patients with major haemorrhage. Here, we present a case of an 85-year-old man taking rivaroxaban for atrial fibrillation, who presented with an acute, upper gastrointestinal bleed. He was stabilised with red cell transfusion and then received a 400 mg bolus of andexanet alfa. Within minutes of this, he developed chest tightness, shortness of breath, ischaemic electrocardiographic changes and then cardiac arrest from which he could not be resuscitated. The onset of symptoms was clearly temporally related to andexanet alfa administration and the differential diagnosis includes anaphylaxis with Kounis syndrome, or myocardial infarction. Although infusion site reactions have been reported and are relatively common, this is to date the first case of a fatal drug reaction andexanet alfa. This knowledge can be factored into physicians' risk-benefit decisions when treating patients with oral anti-FXa anticoagulant-associated major haemorrhage.
安多凝血酶原是一种重组修饰的Xa因子(FXa)分子,用于在大出血患者中逆转口服抗FXa抗凝剂的抗凝作用。在此,我们报告一例85岁男性,因心房颤动服用利伐沙班,出现急性上消化道出血。经红细胞输注病情稳定后,他接受了400mg安多凝血酶原推注。在此之后几分钟内,他出现胸闷、气短、缺血性心电图改变,随后心脏骤停,未能复苏。症状的发作在时间上与安多凝血酶原的给药明显相关,鉴别诊断包括伴有库尼斯综合征的过敏反应或心肌梗死。虽然已经报道了输注部位反应且相对常见,但这是迄今为止安多凝血酶原致死性药物反应的首例。在治疗口服抗FXa抗凝剂相关大出血患者时,这一知识可纳入医生的风险效益决策中。