Real world use of idarucizumab for dabigatran reversal in Aragón (Spain)

O. Sebastián, J. Calvo, Manuela Dobón-Rebollo, Irene Amarilla, Nuria Fernández, Luis Ignacio Sancho, I. Cuesta, E. Franco-García, A. Pérez, L. Lacalle
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Abstract

Background: Idarucizumab is the only reversal agent specifically targeting dabigatran anticoagulation effect. Real-world evidence for idarucizumab in Spain is limited. Objectives: To assess idarucizumab management and results according to the routine clinical practice in emergency situations in Aragon (Spain). Methods: Observational, retrospective, multicentre study in Aragon (Spain). All patients that received idarucizumab (January 2016 - October 2019) for urgent reversal (major bleeding or emergency surgery) were included. Reversal effect was based on the activated Partial Thromboplastin Time (aPTT) in the first 24h. Results: During the study period, thirty patients needed idarucizumab reversal in Aragon: 22 (73.3%) emergency surgeries, 7 (23.3%) major bleedings and 1 off-label use. Most patients were male (63.3%), aged (70.0% ≥75y-o) and showed mild/moderate renal impairment (80.0%). A high proportion of patients (66.7%) used dabigatran 110 mg (twice daily). Complete reversal (aPTT ≤40 seconds) was shown in 70.0% of the patients (85.7% major bleeding; 63.6% emergency surgery). Haemostasis was restored mainly in aged patients (81% in patients ≥75y-o), female (81.8%) and dabigatran reduced dose users (75.0%). Adverse events were shown in two patients (6.7%), none of them thrombosis-related. Since no thromboembolism was shown, according to clinical criteria, all patients could be considered as successfully reverted. Conclusions: Idarucizumab demonstrated effective reversal of dabigatran in ≥70% of the emergency situations linked to anticoagulation reversal need in Aragon (Spain). The clinical use of idarucizumab was safe and conducted according to the authorized label, although it would be recommendable the development of standardized hospital protocols to guarantee an optimal drug use.
idarucizumab在Aragón(西班牙)用于达比加群逆转的现实世界使用
背景:Idarucizumab是唯一专门针对达比加群抗凝作用的逆转药物。idarucizumab在西班牙的实际证据有限。目的:根据西班牙阿拉贡的常规临床实践,评估依达鲁珠单抗在紧急情况下的管理和结果。方法:在西班牙阿拉贡进行观察性、回顾性、多中心研究。所有接受idarucizumab紧急逆转(大出血或紧急手术)的患者(2016年1月至2019年10月)均被纳入。逆转效果基于前24小时激活的部分凝血活素时间(aPTT)。结果:在研究期间,阿拉贡有30例患者需要idarucizumab逆转:22例(73.3%)急诊手术,7例(23.3%)大出血,1例超说明书使用。患者以男性(63.3%)、年龄(70.0%≥75 - 0岁)、轻中度肾功能损害(80.0%)为主。高比例的患者(66.7%)使用达比加群110 mg(每日2次)。70.0%的患者出现完全逆转(aPTT≤40秒)(85.7%为大出血;63.6%急诊手术)。止血恢复主要见于老年患者(≥75岁占81%)、女性患者(81.8%)和达比加群减量使用者(75.0%)。2例患者出现不良事件(6.7%),均与血栓形成无关。由于没有血栓栓塞的表现,根据临床标准,所有患者都可以认为是成功恢复。结论:在阿拉贡(西班牙),Idarucizumab在与抗凝逆转需求相关的≥70%的紧急情况下显示有效逆转达比加群。idarucizumab的临床使用是安全的,并根据授权的标签进行,尽管建议制定标准化的医院方案以保证最佳的药物使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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