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The old and new: PCCs, VIIa, and long-lasting clotting factors for hemophilia and other bleeding disorders

机译:新旧:血友病和其他出血性疾病的PCC,VIIa和持久凝血因子

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摘要

What is the correct use of established clotting factors, prothrombin complex concentrates (PCCs), and activated factor VII in bleeding complications of trauma, surgery, and old and new oral anticoagulants? How will new clotting factors, specifically the long-acting factors, change the hemostatic management of coagulation deficiency disorders? From bench to bedside, comparative coagulation studies and clinical trials of modified clotting factors are providing insights to help guide hemostatic management of congenital and acquired bleeding disorders. Comparative thrombin-generation studies and preclinical and clinical trials suggest that PCCs and fresh-frozen plasma are effective in reversing the anticoagulant effects of warfarin, yet there are few data to guide reversal of the new oral anticoagulants dabigatran and rivaroxaban. Although coagulation studies support the use of PCCs to reverse new oral anticoagulants, correlation with clinical response is variable and clinical trials in bleeding patients are needed. For congenital bleeding disorders, exciting new technologies are emerging from the bench. Data from clinical trials of molecularly modified coagulation factors with extended half-lives suggest the possibility of fewer infusions, reduced bleeds, and better quality of life in persons with hemophilia. Preclinical studies of other novel prohemostatic approaches for hemophilia and other congenital coagulation disorders include RNA interference silencing of antithrombin, monoclonal anti-tissue factor pathway inhibitor (anti-antibody, anti-tissue factor pathway inhibitor) aptamer, bispecific anti-IXa/X antibody, and fucoidans. Understanding the comparative coagulation studies of established prohemostatic agents, the pharmacokinetics of new long-acting clotting factors, and their correlation with bleeding outcomes will provide opportunities to optimize the hemostatic management of both congenital and acquired hemostatic disorders.
机译:在创伤,手术以及新旧口服抗凝剂的出血并发症中,正确使用已建立的凝血因子,凝血酶原复合物浓缩物(PCC)和活化的VII因子是正确的吗?新的凝血因子,特别是长效因子如何改变凝血缺乏症的止血方法?从工作台到床头,比较凝血研究和改良凝血因子的临床试验为指导先天性和获得性出血性疾病的止血管理提供了见识。凝血酶生成的比较研究以及临床前和临床试验表明,PCC和新鲜冷冻的血浆可有效逆转华法林的抗凝作用,但尚无指导新的口服抗凝剂达比加群和利伐沙班逆转的数据。尽管凝血研究支持使用PCC逆转新的口服抗凝剂,但其与临床反应的相关性还是可变的,因此需要在出血患者中进行临床试验。对于先天性出血性疾病,令人兴奋的新技术正在不断涌现。分子修饰的凝血因子具有延长的半衰期的临床试验数据表明,血友病患者可以减少输注,减少流血和改善生活质量。其他针对血友病和其他先天性凝血疾病的新止血方法的临床前研究包括抗凝血酶的RNA干扰沉默,单克隆抗组织因子途径抑制剂(抗抗体,抗组织因子途径抑制剂),双特异性抗IXa / X抗体,和岩藻依聚糖。了解已建立的止血剂的比较凝血研究,新的长效凝血因子的药代动力学以及它们与出血结果的相关性,将为优化先天性和获得性止血疾病的止血管理提供机会。

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