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直接口服抗凝剂在急性脑卒中的特异性逆转剂。

Specific Reversal Agents for Direct Oral Anticoagulants in Acute Stroke.

机构信息

Department of Vascular Neurology, University Medical Center Ljubljana, Ljubljana, Slovenia.

Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Clin Appl Thromb Hemost. 2024 Jan-Dec;30:10760296241279545. doi: 10.1177/10760296241279545.

DOI:10.1177/10760296241279545
PMID:39183537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348480/
Abstract

Direct oral anticoagulants (DOACs) changed stroke prevention and decreased the risk of ischemic and hemorrhagic complications in patients on oral anticoagulation (OAC) therapy. The numbers of patients prescribed DOACs has increased rapidly. Availability of specific reversal agents opened new avenues in the prevention and management of DOAC complications. An ideal specific reversal agent for a DOAC in acute stroke is an agent which lacks safety concerns and immediately reverses DOAC anticoagulation activity, thereby enabling effective treatment. Reversal of anticoagulant activity is mandatory in patients with acute ischemic stroke (AIS) before performing therapeutic procedures such as intravenous thrombolysis (IVT) and neurosurgery in intracranial hemorrhage (ICH) in order to improve clinical outcomes. In this manuscript we pursue an interdisciplinary approach in discussing advantages and concerns of specific reversal agents in acute stroke DOAC-treated patients in everyday clinical practice.

摘要

直接口服抗凝剂(DOACs)改变了卒中预防策略,并降低了口服抗凝治疗(OAC)患者的缺血性和出血性并发症风险。处方 DOAC 的患者数量迅速增加。特异性逆转剂的出现为预防和管理 DOAC 并发症开辟了新途径。对于急性卒中患者的 DOAC,理想的特异性逆转剂应该是一种没有安全性问题且能立即逆转 DOAC 抗凝活性的药物,从而实现有效的治疗。在进行治疗性操作(如急性缺血性卒中(AIS)患者的静脉溶栓(IVT)和颅内出血(ICH)患者的神经外科手术)之前,有必要逆转抗凝活性,以改善临床结局。在本文中,我们采用跨学科方法讨论了在日常临床实践中,特异性逆转剂在急性卒中 DOAC 治疗患者中的优势和关注点。

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本文引用的文献

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Idarucizumab in dabigatran-treated patients with acute stroke: a review and clinical update.达比加群治疗的急性卒中患者使用依达赛珠单抗:综述与临床进展
Front Neurol. 2024 May 16;15:1389283. doi: 10.3389/fneur.2024.1389283. eCollection 2024.
2
Andexanet for Factor Xa Inhibitor-Associated Acute Intracerebral Hemorrhage.依达赛珠单抗治疗因子 Xa 抑制剂相关急性脑出血。
N Engl J Med. 2024 May 16;390(19):1745-1755. doi: 10.1056/NEJMoa2313040.
3
Andexanet alfa versus PCC products for factor Xa inhibitor bleeding: A systematic review with meta-analysis.依达赛珠单抗对比凝血因子 Xa 抑制剂相关出血的 PCC 产品:系统评价与荟萃分析。
Pharmacotherapy. 2024 May;44(5):394-408. doi: 10.1002/phar.2925. Epub 2024 May 9.
4
Trial of Early Minimally Invasive Removal of Intracerebral Hemorrhage.早期微创清除脑出血的试验。
N Engl J Med. 2024 Apr 11;390(14):1277-1289. doi: 10.1056/NEJMoa2308440.
5
Andexanet Alfa: What We Have Learned from Clinical Trials and Real-World Data.依达赛珠单抗:临床试验和真实世界数据的经验总结。
CNS Drugs. 2024 Mar;38(3):163-168. doi: 10.1007/s40263-024-01071-6. Epub 2024 Feb 23.
6
Swiss trial of decompressive craniectomy versus best medical treatment of spontaneous supratentorial intracerebral haemorrhage (SWITCH): an international, multicentre, randomised-controlled, two-arm, assessor-blinded trial.瑞士去骨瓣减压术与自发性幕上脑内出血最佳药物治疗的比较试验(SWITCH):一项国际性、多中心、随机对照、双臂、评估者设盲的试验。
Eur Stroke J. 2024 Sep;9(3):781-788. doi: 10.1177/23969873241231047. Epub 2024 Feb 12.
7
Prothrombin Complex Concentrate vs Conservative Management in ICH Associated With Direct Oral Anticoagulants.凝血酶原复合物浓缩剂与直接口服抗凝剂相关脑出血的保守治疗对比
JAMA Netw Open. 2024 Feb 5;7(2):e2354916. doi: 10.1001/jamanetworkopen.2023.54916.
8
Andexanet alfa versus non-specific treatments for intracerebral hemorrhage in patients taking factor Xa inhibitors - Individual patient data analysis of ANNEXA-4 and TICH-NOAC.依达赛珠单抗对比非特异性治疗用于服用因子 Xa 抑制剂的颅内出血患者:ANNEXA-4 和 TICH-NOAC 的个体患者数据分析。
Int J Stroke. 2024 Jun;19(5):506-514. doi: 10.1177/17474930241230209. Epub 2024 Mar 8.
9
Code ICH: A Call to Action.编码 ICH:行动呼吁。
Stroke. 2024 Feb;55(2):494-505. doi: 10.1161/STROKEAHA.123.043033. Epub 2023 Dec 15.
10
Case report: First treatment of acute ischaemic stroke in a patient on active rivaroxaban therapy using andexanet alfa and rtPA combined with early complete recovery.病例报告:在一名正在接受利伐沙班治疗的患者中,首次使用andexanet alfa和rtPA联合治疗急性缺血性卒中并实现早期完全康复。
Front Neurol. 2023 Oct 25;14:1269651. doi: 10.3389/fneur.2023.1269651. eCollection 2023.