reversal agent

逆转剂
  • 文章类型: Systematic Review
    背景:颅内出血是抗凝治疗的严重且可能致命的后果。Idarucizumab用于达比加群治疗的颅内出血(ICH)患者,以逆转达比加群的抗凝作用。缺乏对这些患者现实生活中死亡率的系统评价。目标:对所有已发表的与达比加群相关的ICH病例进行了综述。我们旨在估计这些患者的住院死亡率。方法:我们搜索了PubMed和Scopus在2021年5月15日之前在idarucizumab/dabigatran治疗的患者中所有已发表的ICH病例。评估的结果是院内死亡率。结果:我们确定了6项符合条件的研究(病例系列),其中386例患者和54例单病例报告。在病例系列中,住院死亡率为11.4%,在病例报告中为9.7%。结论:我们的分析提供了关于idarucizumab/dabigatran治疗的ICH患者院内死亡率的临床相关定量数据,估计为9.7-11.4%。
    Background: Intracranial hemorrhage is a severe and possibly fatal consequence of anticoagulation therapy. Idarucizumab is used in dabigatran-treated patients suffering from intracranial hemorrhage (ICH) to reverse the anticoagulant effect of dabigatran. Systematic review of real-life mortality in these patients is missing. Objectives: A review of all published dabigatran-related ICH cases treated with idarucizumab was performed. We aimed to estimate in-hospital mortality rate in these patients. Method: We searched PubMed and Scopus for all published cases of ICH in idarucizumab/dabigatran-treated patients until May 15, 2021. The assessed outcome was in-hospital mortality. Results: We identified six eligible studies (case series) with 386 patients and 54 single case reports. In-hospital mortality rate was 11.4% in the case series and 9.7% in the case reports. Conclusions: Our analysis provides clinically relevant quantitative data regarding in-hospital mortality in idarucizumab/dabigatran-treated patients with ICH, which is estimated to be 9.7-11.4%.
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  • 文章类型: Case Reports
    We report the case of an 81-year-old man taking dabigatran etexilate (dabigatran) for chronic atrial fibrillation, who presented with acute-onset hemoptysis and hypoxia. Chest high-resolution computed tomography showed bilateral ground grass opacities. After admission, his respiratory failure progressed rapidly and bronchoalveolar lavage was performed immediately, which showed copious amounts of bloody fluid and hemosiderin-laden macrophages with Prussian blue staining. He was diagnosed as having diffuse alveolar hemorrhage (DAH). We therefore stopped dabigatran and initiated multimodality therapy including idarucizumab, which is a reversal agent for dabigatran. Clinical and radiological improvement was observed and he was discharged without any impairment. There has been no relapse of DAH since then. No abnormalities were detected on further investigation; finally, we concluded that his DAH was caused by dabigatran. This is the first known case of idarucizumab use for severe DAH caused by dabigatran. Our case suggested that dabigatran can cause life-threatening DAH; in such cases, administering idarucizumab could be an effective treatment option.
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