静脉血栓栓塞患者初始强化利伐沙班治疗的持续时间——J' xely研究的亚分析。

Mashio Nakamura, Ikuo Fukuda, Norikazu Yamada, Morimasa Takayama, Hideaki Maeda, Takeshi Yamashita, Takanori Ikeda, Makoto Mo, Tsutomu Yamazaki, Yasuo Okumura, Atsushi Hirayama
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引用次数: 0

摘要

背景:利伐沙班是一种直接口服抗凝剂,被用作预防静脉血栓栓塞(VTE)的一线治疗,包括深静脉血栓形成(DVT)和肺栓塞(PE)。然而,21天是否为最佳初始治疗时间还没有研究。方法和结果:在前瞻性多中心观察性J' xtly研究的亚分析中,包括1039名日本急性症状/无症状DVT/PE患者,他们服用利伐沙班,对667名接受利伐沙班强化治疗(15mg,每日两次),短(1-8天),中期(9-16)或标准(17-24)时间的患者进行静脉血栓栓塞复发率和出血并发症发生率的评估。与标准治疗时间组相比,短治疗时间组有静脉血栓栓塞复发/加重增加的趋势(6.10% vs 2.60% /患者年)。中等治疗时间组出血事件发生率高于标准治疗时间组(9.34% vs 2.16% /患者-年),两组患者特征无明显差异。结论:在日本急性有症状/无症状DVT/PE患者的静脉血栓栓塞治疗和预防的真实世界观察性研究的亚分析中,标准的初始强化利伐沙班治疗时间(17-24天)似乎是安全有效的,为利伐沙班初始治疗时间在该人群中的临床结果提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Duration of Initial Intensive Rivaroxaban Therapy for Patients With Venous Thromboembolism - Subanalysis of the J'xactly Study.

Duration of Initial Intensive Rivaroxaban Therapy for Patients With Venous Thromboembolism - Subanalysis of the J'xactly Study.

Duration of Initial Intensive Rivaroxaban Therapy for Patients With Venous Thromboembolism - Subanalysis of the J'xactly Study.

Duration of Initial Intensive Rivaroxaban Therapy for Patients With Venous Thromboembolism - Subanalysis of the J'xactly Study.

Background: Rivaroxaban, a direct oral anticoagulant, is used as a first-line treatment to prevent venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE). However, whether 21 days is optimal for the initial treatment duration has not been investigated. Methods and Results: In this subanalysis of the prospective multicenter observational J'xactly study, which included 1,039 Japanese patients with acute symptomatic/asymptomatic DVT/PE who were prescribed rivaroxaban, the VTE recurrence rate and incidence of bleeding complications were assessed in 667 patients who underwent intensive rivaroxaban treatment (15 mg, twice daily) for a short (1-8 days), intermediate (9-16), or standard (17-24) duration. The short treatment duration group showed a tendency for increased VTE recurrence/aggravation compared with the standard treatment duration group (6.10% vs. 2.60% per patient-year). The intermediate treatment duration group showed a higher incidence of bleeding events than the standard treatment duration group (9.34% vs. 2.16% per patient-year), without major differences in patient characteristics between the groups. Conclusions: In this subanalysis of the real-world observational J'xactly study of VTE treatment and prevention in Japanese patients with acute symptomatic/asymptomatic DVT/PE, the standard initial intensive rivaroxaban treatment duration (17-24 days) appeared to be safe and effective, providing important insights into the clinical outcomes of the initial rivaroxaban treatment duration in this population.

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