Al-Obeidi Arshed, Garavito Draia, Smalley Sierra, John Kayla, Jones Lee Ann, Key Nigel, Strohm Tamara
Department of Medicine, Division of Hematology, University of North Carolina, Chapel Hill, NC, USA.
Department of Neurology, Division of Neurocritical Care, University of North Carolina, Chapel Hill, NC, USA.
Neurohospitalist. 2025 Jan 21:19418744251314534. doi: 10.1177/19418744251314534.
BACKGROUND/OBJECTIVES: There is currently no consensus regarding the optimal strategy for reversal of anticoagulation in life-threatening hemorrhage associated with factor XIa (FXIa) inhibitors.
For this clinical case report, informed consent was obtained from surrogate.
Here, we present the case of an 82-year-old female who sustained a large subdural hematoma after a fall. Her aPTT on admission was elevated at 90.4 s and remained persistently prolonged at 90.9 s 12-hour after receiving an adequate dose of 4-factor prothrombin complex concentrate (PCC). She was found to have received a factor XIa inhibitor in a clinical trial, and subsequently received recombinant activated factor VII (rFVIIa) 2 mg (45 mcg/kg) as a one-time dose, and tranexamic acid (TXA) 1 g intravenously for reversal given her intracranial bleeding in the setting of trauma complicated by recent factor XIa inhibitor use. However, given her clinical decline and high surgical risk, the patient's family elected to withdraw care and she expired three days later. Reversal of FXIa inhibitors is challenging but may best be achieved using a combination of rFVIIa and TXA.
Clinicians should consider administration of low dose recombinant activated factor VII (rFVIIa) in conjunction with an anti-fibrinolytic inhibitor such as tranexamic acid (TXA) for reversal of life-threatening hemorrhage in bleeding patients with exposure to novel factor XIa inhibitors that are currently in clinical trials.
背景/目的:目前,对于与因子 XIa(FXIa)抑制剂相关的危及生命的出血,抗凝逆转的最佳策略尚无共识。
对于本临床病例报告,已获得替代者的知情同意。
在此,我们报告一例 82 岁女性,跌倒后发生大量硬膜下血肿。入院时她的活化部分凝血活酶时间(aPTT)升高至 90.4 秒,在接受足量的 4 因子凝血酶原复合物浓缩物(PCC)12 小时后仍持续延长至 90.9 秒。发现她在一项临床试验中接受了因子 XIa 抑制剂治疗,随后鉴于其在近期使用因子 XIa 抑制剂的创伤背景下发生颅内出血,给予一次性剂量的重组活化因子 VII(rFVIIa)2 毫克(45 微克/千克),并静脉注射氨甲环酸(TXA)1 克以进行逆转。然而,鉴于其临床状况恶化和手术风险高,患者家属选择放弃治疗,她在三天后死亡。FXIa 抑制剂的逆转具有挑战性,但使用 rFVIIa 和 TXA 的联合治疗可能最有效。
临床医生应考虑给予低剂量重组活化因子 VII(rFVIIa)并联合抗纤溶抑制剂如氨甲环酸(TXA),以逆转暴露于目前正在临床试验中的新型因子 XIa 抑制剂的出血患者的危及生命的出血。