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低剂量阿哌沙班或利伐沙班作为上肢深静脉血栓形成的二级预防。

Low-dose apixaban or rivaroxaban as secondary prophylaxis of upper extremity deep vein thrombosis.

机构信息

Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Via Benevento 6, Rome, 00161, Italy.

出版信息

J Thromb Thrombolysis. 2023 Aug;56(2):323-326. doi: 10.1007/s11239-023-02842-6. Epub 2023 Jun 21.

Abstract

Upper extremity deep vein thrombosis (UEDVT) may occur without inciting factor or may be secondary to malignancy, surgery, trauma, central venous catheter or related to thoracic outlet syndrome (TOS). International guidelines recommend anticoagulant treatment for at least three months, in particular the use of vitamin K antagonists (VKAs) and direct oral anticoagulants (DOACs). No data on extended anticoagulant therapy and reduced dose of DOACs have been reported in patients affected by UEDVT with persistent thrombotic risk (active cancer, major congenital thrombophilia) or without affected vein recanalization. In our retrospective observational study, including 43 patients, we treated secondary UEDVT with DOACs. In the acute phase of thrombosis (median time of 4 months), we used therapeutic dose of DOACs; the 32 patients with permanent thrombotic risk factors or without recanalization of the UEDVT were shifted to low-dose DOACs (apixaban 2.5 mg twice daily or rivaroxaban 10 mg daily). During therapy with full-dose DOACs, 1 patient presented recurrence of thrombosis; no thromboembolic events were observed during treatment with low-dose DOACs. During full-dose treatment, 3 patients presented minor hemorrhagic complications; no hemorrhagic events were observed during DOACs at low dose. We think our preliminary data could support the indication to extend the anticoagulation with dose reduction of DOACs in patients affected by UEDVT and no-transient thrombotic risk. These data should be confirmed in randomized controlled prospective study.

摘要

上肢深静脉血栓形成(UEDVT)可无诱因发生,也可继发于恶性肿瘤、手术、创伤、中心静脉导管或与胸廓出口综合征(TOS)有关。国际指南建议抗凝治疗至少 3 个月,特别是使用维生素 K 拮抗剂(VKAs)和直接口服抗凝剂(DOACs)。对于上肢深静脉血栓形成伴持续性血栓形成风险(活动性癌症、主要先天性血栓形成倾向)或静脉未再通的患者,尚未报道延长抗凝治疗和减少 DOAC 剂量的数据。在我们的回顾性观察性研究中,包括 43 名患者,我们使用 DOAC 治疗继发性 UEDVT。在血栓形成的急性期(中位数时间为 4 个月),我们使用 DOAC 的治疗剂量;32 名具有永久性血栓形成危险因素或上肢深静脉血栓形成未再通的患者转为低剂量 DOAC(阿哌沙班 2.5mg 每日 2 次或利伐沙班 10mg 每日 1 次)。在使用全剂量 DOAC 治疗期间,1 名患者出现血栓形成复发;在低剂量 DOAC 治疗期间未观察到血栓栓塞事件。在全剂量治疗期间,3 名患者出现轻微出血并发症;在低剂量使用 DOACs 期间未观察到出血事件。我们认为我们的初步数据可以支持在无暂时性血栓形成风险的上肢深静脉血栓形成患者中延长抗凝治疗并减少 DOAC 剂量的适应证。这些数据应在随机对照前瞻性研究中得到证实。

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