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直接口服抗凝剂逆转新兴可能性的药理学综述

Review of the Pharmacology of the Emerging Possibilities of the Direct Oral Anticoagulants' Reversal.

作者信息

Samos Matej, Stanciakova Lucia, Skornova Ingrid, Bolek Tomas, Kovar Frantisek, Stasko Jan, Galajda Peter, Mokan Marian, Kubisz Peter

机构信息

Department of Internal Medicine I, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Kollarova 2, 036 59 Martin. Slovakia.

National Centre of Hemostasis and Thrombosis, Department of Hematology and Blood Transfusion, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin. Slovakia.

出版信息

Curr Drug Metab. 2017;18(7):643-650. doi: 10.2174/1389200218666170413155351.

Abstract

BACKGROUND

Direct oral anticoagulants (DOACs) offer consistent and predictable anticoagulation, oral administration with good patient compliance and a good safety profile. Dabigatran - a direct thrombin inhibitor, apixaban and rivaroxaban - direct factor Xa inhibitors are now largely used for anticoagulation in patients with nonvalvular atrial fibrillation and in patients with venous thromboembolism. These agents have emerged as an expediential clinical choice in long-term anticoagulation for an increasing number of patients. Despite their advantages, concerns persist about a lack of rapid reversal agents in urgent clinical situations.

METHODS

This review is focused on the pharmacology of nonspecific and target-specific reversal agents for DOACs-induced anticoagulation. A systemic review of preclinical and clinical studies published in peer-reviewed scientific journals was performed.

RESULTS AND CONCLUSIONS

Fresh frozen plasma and coagulation factors concentrates might be considered in bleeding emergencies; however, there is a lack of larger studies confirming the efficacy of coagulation factors concentrates for the reversal of DOACs-induced anticoagulation, and a particular risk of coagulation factors concentrates-induced thrombosis. Recently, idarucizumab has been approved commercially for acute reversal of dabigatran in emergencies as a first target-specific reversal agent. Moreover, andexanet alpha and aripazine are being extensively studied in several phase II and III clinical studies. It is likely that more target-specific agents for reversal of DOACs-induced anticoagulation will be introduced to clinical practice in near future.

摘要

背景

直接口服抗凝剂(DOACs)可提供持续且可预测的抗凝效果,口服给药,患者依从性良好,安全性也较好。达比加群——一种直接凝血酶抑制剂,阿哌沙班和利伐沙班——直接因子Xa抑制剂,目前在非瓣膜性心房颤动患者和静脉血栓栓塞患者的抗凝治疗中广泛应用。这些药物已成为越来越多患者长期抗凝治疗的便捷临床选择。尽管它们具有诸多优势,但在紧急临床情况下缺乏快速逆转剂的问题仍然存在。

方法

本综述聚焦于DOACs诱导抗凝的非特异性和靶向特异性逆转剂的药理学。对同行评审科学期刊上发表的临床前和临床研究进行了系统综述。

结果与结论

在出血紧急情况下可考虑使用新鲜冷冻血浆和凝血因子浓缩物;然而,缺乏大型研究证实凝血因子浓缩物对逆转DOACs诱导的抗凝效果,且存在凝血因子浓缩物诱发血栓形成的特殊风险。最近,艾达赛珠单抗已获商业批准,作为首个靶向特异性逆转剂用于紧急情况下达比加群的急性逆转。此外,andexanet alpha和阿利哌嗪正在多项II期和III期临床研究中进行广泛研究。在不久的将来,可能会有更多用于逆转DOACs诱导抗凝的靶向特异性药物引入临床实践。

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