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Emergencies on direct oral anticoagulants: Management, outcomes, and laboratory effects of prothrombin complex concentrate

机译:直接口服抗凝血剂的紧急情况:凝血酶体复合物浓缩物的管理,结果和实验室作用

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Background In the initial absence of specific reversal agents for factor Xa inhibitors (FXa‐Is), prothrombin complex concentrate (PCC) as a hemostatic agent has been recommended by guidelines. Since 2017, idarucizumab has been registered for dabigatran reversal. Still, data on the clinical outcome of direct oral anticoagulant (DOAC)‐related emergencies (major bleeding or urgent interventions) is scarce. In addition, it is unknown to what extent PCC restores thrombin generation in FXa‐I–related emergencies. Our aim was to describe management and clinical outcomes of DOAC‐related emergencies and to assess the laboratory effect of PCC in patients with FXa‐I emergencies. Methods In this prospective cohort study in 5 Dutch hospitals, patients presenting with DOAC‐related emergencies were eligible. The primary outcome was effective hemostasis according to the ISTH definition. Safety outcomes were 30‐day mortality and thromboembolic rate. In patients treated with PCC, additional blood samples were taken to assess the effect on thrombin generation. Results We included 101 patients with major bleeding (FXa‐I, 76; dabigatran, 25) and 21 patients requiring an urgent intervention (FXa‐I, 16; dabigatran, 5). Of patients with major bleeding, 67% were treated with PCC or idarucizumab. Effective hemostasis, 30‐day mortality, and thromboembolism rate were 67%, 22%, and 1%, respectively. In a subset of bleeding patients on FXa‐I managed with PCC, thrombin generation increased, with 96% immediately after PCC administration. In patients requiring an urgent intervention, effective hemostasis, 30‐day mortality, and thromboembolic rate were 95%, 14%, and 5%. Conclusions Effective hemostasis was achieved in the majority of patients?presenting with DOAC‐related emergencies;, thromboembolic complications were rare, and mortality was quite high.
机译:背景技术在最初不存在于因子Xa抑制剂(的FXa-IS),凝血酶原复合物浓缩物(PCC)作为止血剂特定逆转剂已被推荐的指导方针。 2017年以来,idarucizumab已注册达比加群逆转。尽管如此,直接口服抗凝药的临床结果(DOAC)数据 - 相关突发事件(主要出血或紧急干预)是稀少。此外,目前还不清楚到什么程度PCC恢复凝血酶一代的FXa-I相关的紧急情况。我们的目的是描述DOAC有关的紧急情况的管理和临床疗效,并评估PCC的患者的FXa-I紧急实验室效果。方法在5家荷兰医院的前瞻性队列研究中,患者DOAC有关的紧急情况提出资格。主要的结果是根据ISTH定义有效的止血。安全终点为30天死亡率和血栓栓塞率。与PCC治疗的患者,取额外的血样以评估对凝血酶产生的影响。结果我们包括101例大出血(的FXa-I,76;达比加群,25)和21名患者需要紧急干预(的FXa-I,16;达比加群,5)。患者的主要出血,67%用PCC或idarucizumab处理。有效的止血,30天的死亡率,和血栓栓塞率分别为67%,22%,和1%之间。在对出血患者的一个子集的FXa-I与PCC管理,凝血酶的产生PCC给药后增加,96%,立即。在需要的紧急干预的患者,有效止血,30天死亡率和血栓栓塞率分别为95%,14%和5%。结论止血效果好于多数患者实现?有DOAC有关的紧急情况呈现;,血栓栓塞并发症是罕见的,而且死亡率也相当高。
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