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Use of Idarucizumab for dabigatran reversal: Emergency department experience in two cases with subdural haematoma

机译:依达西珠单抗逆转达比加群:硬膜下血肿两例急诊科经验

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Introduction Idarucizumab is the first effective humanized monoclonal antibody fragment developed specifically as a reversal agent for dabigatran, a Direct Oral Anticoagulant. Despite recent trials demonstrating reversal of clinically relevant bleeding, there is a paucity of data on use outside the trial setting. This manuscript describes the use of Idarucizumab to reverse dabigatran in two patients presenting to the emergency department of a major tertiary hospital with acute traumatic subdural haematomas (SDH). Methods Patients were identified through retrospective review of medication dispensing systems and electronic medical records. Results Two cases of Idarucizumab use were identified. Case 1 was of a 63-year-old male who presented following a motorcycle crash. Case 2 was of a 77-year-old male who presented with a 3-week history of ataxia and recurrent falls. Both patients were taking dabigatran for atrial fibrillation (AF). CT Brain revealed acute SDH with clinical indications for urgent surgical evacuation. Serum dabigatran levels were obtained on arrival in the emergency department with levels of 155ng/ml and 110ng/ml (reference range 117–275ng/ml). Idarucizumab for dabigatran reversal was commenced; Case 1 received 5g Idarucizumab as an intravenous bolus dose, while Case 2 received 5g Idarucizumab as two 2.5g intravenous infusions. Serum dabigatran levels for Cases 1 and 2 were 0ng/ml at 75min and 340min post Idarucizumab administration respectively. Both patients proceeded to craniotomy with evacuation of the SDH. There was no extension of the SDH in either case. Anticoagulation was withheld until outpatient clinic review, and both patients transferred for rehabilitation prior to discharge home. Conclusion Idarucizumab was clinically effective for reversing dabigatran, resulting in undetectable serum levels, and should be considered in patients presenting to hospital with clinically significant bleeding associated with dabigatran therapy.
机译:引言伊达珠单抗是第一个有效的人源化单克隆抗体片段,专门开发为达比加群(一种直接口服抗凝剂)的逆转剂。尽管最近有试验证明了临床相关出血的逆转,但在试验环境外使用的数据很少。这份手稿描述了在一家大型三级硬膜下硬膜下血肿(SDH)的三级大医院急诊科就诊的两名患者中使用依达珠单抗逆转达比加群的情况。方法通过回顾性分析药物分配系统和电子病历来识别患者。结果确定了2例使用依达珠单抗的病例。案例1是一名63岁的男性,在摩托车坠毁后出现。案例2是一名77岁的男性,他有3周的共济失调和反复跌倒史。两名患者均服用达比加群用于房颤(AF)。 CT脑部显示急性SDH,并有紧急手术后撤的临床指征。到达急诊室时的血清达比加群水平为155ng / ml和110ng / ml(参考范围为117-275ng / ml)。开始进行达比加群逆转的依达珠单抗;案例1接受5克依达珠单抗静脉推注,而案例2接受5克依达珠单抗作为两次2.5克静脉输注。依达西单抗给药后第75分钟和第340分钟,病例1和2的血清达比加群水平分别为0ng / ml。两名患者均进行了开颅手术,并撤出了SDH。在这两种情况下,SDH都没有扩展。直到门诊患者接受抗凝治疗为止,两名患者出院前均已转移以进行康复治疗。结论伊达珠单抗在临床上可逆转达比加群,从而导致血清水平无法检测,因此在就诊时出现达比加群治疗相关的临床上明显出血的患者应考虑使用。

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