直接(新)口服抗凝剂(DOACs):缺点、出血和逆转。

Ozgur Karcioglu, Sehmus Zengin, Bilgen Ozkaya, Eylem Ersan, Sarper Yilmaz, Goksu Afacan, Derya Abuska, Mandana Hosseinzadeh, Selman Yeniocak
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引用次数: 7

摘要

背景和目的:直接(新型)口服抗凝剂(DOACs)已成为治疗血栓形成和静脉血栓栓塞(VTE)的一种当代和有前途的选择,同时保护凝血级联免受不良出血事件的影响。它们用于静脉血栓栓塞(VTE)和其他血栓性疾病的管理和预防。这些药物最突出的并发症是出血。与华法林相比,这些药物有相似或更低的颅内大出血率,但它们有更高的胃肠道大出血风险。本文旨在修订和更新文献发现,概述DOACs在各种临床情况下的副作用。方法:对目前发表的研究进行叙述性回顾。对2021年7月之前发表的临床试验进行在线数据库检索,研究抗凝治疗的疗效和不良反应,特别是DOACs。通过电子数据库进行了文献检索,从使用西方语文论文中的代理开始。搜索词最初包括直接(新型)口服抗凝剂、达比加群、利伐沙班、阿哌沙班、依多沙班、依达鲁单抗、和德沙奈、凝血酶原复合物浓缩物和新鲜冷冻血浆。论文在被纳入之前已经过方法学上的检验。结果:严重出血发作需要积极的干预才能成功管理。因此,出血的评估应特别考虑出血的位置和速度,以及失血量。患者的年龄、体重和器官功能障碍(如肾/肝衰竭或慢性呼吸系统疾病)直接影响过量用药的临床病程。结论:与DOAC使用相关的出血的管理建议不同,取决于罪魁祸首的类别(直接凝血酶抑制剂vs. FXa抑制剂),患者的临床状态(轻度/中度vs.严重/危及生命),以及机构的能力。如果可能,可以使用特异性逆转药物(即idarucizumab和anddexanet alfa),而凝血酶原复合物浓缩物、新鲜冷冻血浆和/或氨甲环酸也可以作为非特异性替代药物用于doac相关出血的管理。
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Direct (New) Oral Anticoagulants (DOACs): Drawbacks, Bleeding and Reversal.

Background and objective: Direct (new) Oral Anticoagulants (DOACs) have emerged as a contemporary and promising option in the treatment of thromboses and VTE, while protecting the coagulation cascade against untoward bleeding events. They are used in the management and prophylaxis of Venous Thromboembolism (VTE) and other thrombotic diseases. The most prominent complication of these agents is bleeding. These agents have similar or lower rates of major intracranial hemorrhages, while they had a higher risk of major gastrointestinal bleeding when compared to warfarin. This manuscript is aimed to revise and update the literature findings to outline the side effects of DOACs in various clinical scenarios.

Methods: A narrative review of currently published studies was performed. Online database searches were performed for clinical trials published before July 2021, on the efficacy and adverse effects attributed to the anticoagulant treatment, especially DOACs. A literature search via electronic databases was carried out, beginning with the usage of the agents in the Western Languages papers. The search terms initially included direct (new) oral anticoagulants, dabigatran, rivaroxaban, apixaban, edoxaban, idarucizumab, andexanet, prothrombin complex concentrates, and fresh frozen plasma. Papers were examined for methodological soundness before being included.

Results: Severe bleeding episodes require aggressive interventions for successful management. Therefore, bleeding should be evaluated in special regard to the location and rate of hemorrhage, and total volume of blood loss. Patient's age, weight and organ dysfunctions (e.g., kidney/liver failure or chronic respiratory diseases) directly affect the clinical course of overdose.

Conclusion: Management recommendations for hemorrhage associated with DOAC use vary, depending on the class of the culprit agent (direct thrombin inhibitor vs. FXa inhibitor), the clinical status of the patient (mild/ moderate vs. severe/life-threatening), and capabilities of the institution. Specific reversal agents (i.e., idarucizumab and andexanet alfa) can be used if available, while prothrombin complex concentrates, fresh frozen plasma and/ or tranexamic acid can also be employed as nonspecific replacement agents in the management of DOAC-related bleeding diathesis.

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来源期刊
Cardiovascular and Hematological Agents in Medicinal Chemistry
Cardiovascular and Hematological Agents in Medicinal Chemistry Medicine-Cardiology and Cardiovascular Medicine
CiteScore
2.70
自引率
0.00%
发文量
34
期刊介绍: Cardiovascular & Hematological Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new Cardiovascular & Hematological Agents. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of current topics in Cardiovascular & Hematological medicinal chemistry. Cardiovascular & Hematological Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in cardiovascular & hematological drug discovery.
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