Andexanet Alfa 及其临床应用。

IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Heart International Pub Date : 2020-06-19 eCollection Date: 2020-01-01 DOI:10.17925/HI.2020.14.1.20
Fauve A Noordergraaf, Marco Alings
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引用次数: 0

摘要

因子 Xa(FXa)抑制剂被广泛用于预防非瓣膜性心房颤动患者中风,以及治疗和预防深静脉血栓和肺栓塞。与华法林相比,单个 FXa 抑制剂的大出血风险较低。尽管如此,出血仍然是任何抗凝疗法都担心的并发症。尽管 FXa 抑制剂的安全性已得到证实,但在临床实践中的应用可能因缺乏特效解毒剂而受到限制。不过,最近美国食品药品管理局和欧洲药品管理局批准了安赛乐α,用于对接受利伐沙班或阿哌沙班治疗但出现危及生命或无法控制的出血的患者进行抗凝逆转。本综述将讨论 andexanet alfa 的作用模式、使用指征和疗效,重点关注其在临床实践中的合理使用。应避免不必要的使用,因为这可能会危及患者安全。由多学科团队对潜在的合适患者进行评估、根据机构协议使用和集中储存都有助于正确使用 andexanet alfa。本文提出了一种实用工具来指导如何合理使用安赛蜜α。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Andexanet Alfa and its Clinical Application.

Factor Xa (FXa) inhibitors are widely used for stroke prevention in patients with nonvalvular atrial fibrillation, and for the treatment and prevention of deep venous thrombosis and pulmonary embolism. Compared with warfarin, individual FXa inhibitors are associated with a lower risk of major bleeding. Nevertheless, bleeding remains a feared complication of any anticoagulant therapy. Despite their demonstrated safety, implementation of FXa inhibitors in clinical practice may have been limited by the lack of a specific antidote. Recently, however, the United States Food and Drug Administration and the European Medicines Agency approved andexanet alfa for reversal of anticoagulation in patients treated with rivaroxaban or apixaban who have life-threatening or uncontrolled bleeding. This review will discuss andexanet alfa's mode of action, indication for use and efficacy, with a focus on its appropriate use in clinical practice. Unnecessary usage should be prevented as this may compromise patient safety. Assessment of potentially suitable patients by a multidisciplinary team, use according to the institutional protocol and central storage, all contribute to proper use of andexanet alfa. A practical tool to direct appropriate use of andexanet alfa is proposed.

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来源期刊
Heart International
Heart International Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.90
自引率
0.00%
发文量
9
审稿时长
7 weeks
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