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直接口服抗凝剂治疗罕见部位静脉血栓形成:最新进展

Direct Oral Anticoagulants for the Treatment of Unusual-Site Venous Thrombosis: An Update.

作者信息

Franco-Moreno Anabel, Madroñal-Cerezo Elena, Martínez-Casa-Muñoz Ana, Ortiz-Sánchez Judith, Ancos-Aracil Cristina Lucía

机构信息

Venous Thromboembolism Unit, Department of Internal Medicine, Hospital Universitario Infanta Leonor, Avenida Gran Via del Este, 80, 28031 Madrid, Spain.

Venous Thromboembolism Unit, Department of Internal Medicine, Hospital Universitario de Fuenlabrada, Camino del Molino, 2, Fuenlabrada, 28942 Madrid, Spain.

出版信息

Pharmaceutics. 2025 Mar 7;17(3):342. doi: 10.3390/pharmaceutics17030342.

DOI:10.3390/pharmaceutics17030342
PMID:40143006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11944374/
Abstract

Direct oral anticoagulants (DOACs) have emerged as the preferred oral anticoagulant therapy for patients with deep vein thrombosis of the lower extremities and pulmonary embolism. DOACs offer several advantages over vitamin K antagonists, including fixed dosage, fewer drug interactions, faster onset of action, and a lower risk of major bleeding, especially intracranial. Although evidence on the use of DOACs in unusual-site venous thrombosis (USVT) is limited, their use in such cases is becoming increasingly common. This narrative review examines the evidence derived from randomized controlled trials, and large observational studies focused on the use of the DOACs in USVT, including cerebral, splanchnic, upper extremity, ovarian, renal, and retinal vein thrombosis. In addition, it also provides practical advice for their use in these clinical settings according to the updated scientific literature.

摘要

直接口服抗凝剂(DOACs)已成为下肢深静脉血栓形成和肺栓塞患者首选的口服抗凝治疗药物。与维生素K拮抗剂相比,DOACs具有多种优势,包括固定剂量、较少的药物相互作用、起效更快以及大出血风险较低,尤其是颅内出血风险。尽管关于DOACs在非寻常部位静脉血栓形成(USVT)中应用的证据有限,但它们在这类病例中的使用正变得越来越普遍。这篇叙述性综述考察了来自随机对照试验以及专注于DOACs在USVT中应用的大型观察性研究的证据,包括脑静脉、内脏静脉、上肢静脉、卵巢静脉、肾静脉和视网膜静脉血栓形成。此外,它还根据最新的科学文献为在这些临床环境中使用DOACs提供实用建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aee/11944374/eb863f0499ad/pharmaceutics-17-00342-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aee/11944374/eb863f0499ad/pharmaceutics-17-00342-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aee/11944374/eb863f0499ad/pharmaceutics-17-00342-g001.jpg

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Direct Oral Anticoagulants for the Treatment of Unusual-Site Venous Thrombosis: An Update.直接口服抗凝剂治疗罕见部位静脉血栓形成:最新进展
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本文引用的文献

1
Clinical course and neurological outcomes of cerebral venous sinus thrombosis: A single center retrospective observational study.脑静脉窦血栓形成的临床病程及神经学转归:一项单中心回顾性观察研究。
PLoS One. 2025 Jan 13;20(1):e0316849. doi: 10.1371/journal.pone.0316849. eCollection 2025.
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Direct Oral Anticoagulants Versus Traditional Anticoagulation in Cirrhotic Patients with Portal Vein Thrombosis: Updated Systematic Review.
直接口服抗凝剂与传统抗凝剂治疗肝硬化门静脉血栓形成患者的比较:更新的系统评价。
Clin Appl Thromb Hemost. 2024 Jan-Dec;30:10760296241303758. doi: 10.1177/10760296241303758.
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A 12-Year Review of Upper Extremity Deep Vein Thrombosis-Are They the Same as Lower Extremity Deep Vein Thrombosis?上肢深静脉血栓形成的12年回顾——它们与下肢深静脉血栓形成相同吗?
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Splanchnic vein thrombosis: management for the thrombosis specialist.内脏静脉血栓形成:血栓形成专家的管理方法
J Thromb Haemost. 2025 Feb;23(2):404-416. doi: 10.1016/j.jtha.2024.10.012. Epub 2024 Oct 21.
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Efficacy and safety of Apixaban in the treatment of cerebral venous sinus thrombosis: a multi-center study.阿哌沙班治疗脑静脉窦血栓形成的疗效和安全性:一项多中心研究。
Front Neurol. 2024 May 16;15:1404099. doi: 10.3389/fneur.2024.1404099. eCollection 2024.
8
Dabigatran etexilate versus warfarin in cerebral venous thrombosis in Chinese patients (CHOICE-CVT): An open-label, randomized controlled trial.达比加群酯与华法林治疗中国患者脑静脉血栓形成的疗效比较(CHOICE-CVT):一项开放标签的随机对照试验。
Int J Stroke. 2024 Jul;19(6):635-644. doi: 10.1177/17474930241234749. Epub 2024 Feb 26.
9
Rivaroxaban Prophylaxis in Noncirrhotic Portal Vein Thrombosis.利伐沙班预防非肝硬化门静脉血栓形成。
NEJM Evid. 2022 Dec;1(12):EVIDoa2200104. doi: 10.1056/EVIDoa2200104. Epub 2022 Nov 22.
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Evaluation of rivaroxaban versus warfarin for the treatment of cerebral vein thrombosis: A case-control blinded study.利伐沙班与华法林治疗脑静脉血栓形成的疗效评估:一项病例对照双盲研究。
Curr J Neurol. 2021 Jul 6;20(3):125-130. doi: 10.18502/cjn.v20i3.7687.