Akwaa Frank, Spyropoulos Alex C
University of Rochester, Rochester, NY, 14611, USA.
Curr Treat Options Cardiovasc Med. 2013 Jun;15(3):288-98. doi: 10.1007/s11936-013-0238-5.
Major bleeding in patients taking oral anticoagulants for stroke prevention can progress to catastrophic bleeding if it is not controlled. This is especially of concern if the bleeding is related to the use of a novel oral anticoagulant (NOAC) such as dabigatran or rivaroxaban, given the dearth of literature addressing the reversal of their anticoagulant effects. The goal of treatment is to prevent progression to catastrophic hemorrhage or exsanguination, and decrease bleeding-related morbidity and mortality. Clinical decisions in such instances should be made in a timely fashion to address the necessity for intervention. Animal models have shown potential for the use of 'fresh frozen plasma (FFP) or prothrombin complex concentrate (PCC) in reversing bleeding related to novel oral anticoagulants. However, there is paucity of clinical trials assessing the efficacy of these agents in humans in such clinical scenarios. Hence, there are no guidelines or ideal agents to use in such a scenario. We do not recommend the use of FFP for bleeding related to NOACs. In the setting of early overdose of dabigatran (within 3-4 hours), activated charcoal may be given, and hemodialysis may be used if there is evidence of critical organ bleeding. In our opinion, 4-factor PCC or 3-factor PCC at a dose of about 50 U/kg may be given in an emergency setting to manage bleeding related to factor Xa inhibitors such as rivaroxaban or apixaban, but not direct thrombin inhibitors such as dabigatran. We are also of the opinion that aPCC (FEIBA®) would not be helpful for management of direct thrombin inhibitor (dabigatran)-related bleeding, based on current available efficacy data in humans. We reserve the use of Novoseven® as a last resort, given the lack of pre-clinical or clinical data supporting its ability to reverse the anticoagulant effects of NOACs, except in one case report where it was used in combination with hemodialysis.
服用口服抗凝剂预防中风的患者若大出血得不到控制,可能会发展为灾难性出血。鉴于针对新型口服抗凝剂(如达比加群或利伐沙班)抗凝作用逆转的文献匮乏,若出血与这类药物的使用有关,尤其令人担忧。治疗目标是防止进展为灾难性出血或失血过多,并降低出血相关的发病率和死亡率。在此类情况下应及时做出临床决策,以确定是否有干预的必要。动物模型显示,使用新鲜冷冻血浆(FFP)或凝血酶原复合物浓缩剂(PCC)有可能逆转与新型口服抗凝剂相关的出血。然而,缺乏评估这些药物在人类此类临床场景中疗效的临床试验。因此,在这种情况下没有可用的指南或理想药物。我们不建议使用FFP来治疗与新型口服抗凝剂相关的出血。在达比加群早期过量(3 - 4小时内)的情况下,可给予活性炭,若有重要器官出血的证据,可进行血液透析。我们认为,在紧急情况下,对于与利伐沙班或阿哌沙班等Xa因子抑制剂相关的出血,可给予剂量约为50 U/kg的4因子PCC或3因子PCC进行处理,但对于达比加群等直接凝血酶抑制剂相关的出血则无效。基于目前人类可用的疗效数据,我们还认为活化PCC(FEIBA®)对治疗直接凝血酶抑制剂(达比加群)相关出血没有帮助。鉴于缺乏临床前或临床数据支持诺其(Novoseven®)逆转新型口服抗凝剂抗凝作用的能力,我们仅在一个与血液透析联合使用的病例报告中见到过,故将其作为最后手段保留使用。