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

被引:2
作者
Nakamura, Mashio [1 ]
Fukuda, Ikuo [2 ]
Yamada, Norikazu [3 ]
Takayama, Morimasa [4 ]
Maeda, Hideaki [5 ]
Yamashita, Takeshi [6 ]
Ikeda, Takanori [7 ]
Mo, Makoto [8 ]
Yamazaki, Tsutomu [9 ]
Okumura, Yasuo [10 ]
Hirayama, Atsushi [11 ]
机构
[1] Nakamura Med Clin, 7-1510 Hidamarinooka, Kuwana 5110867, Japan
[2] Keimeikai Yokawa Hosp, Dept Cardiol, Miki, Japan
[3] Kuwana City Med Ctr, Dept Cardiol, Kuwana, Japan
[4] Sakakibara Heart Inst, Dept Cardiol, Fuchu, Japan
[5] Ukima Cent Hosp, Dept Heart & Vasc Ctr, Tokyo, Japan
[6] Cardiovasc Inst, Dept Cardiovasc Med, Tokyo, Japan
[7] Toho Univ, Fac Med, Dept Cardiovasc Med, Tokyo, Japan
[8] Yokohama Minami Kyosai Hosp, Dept Cardiovasc Surg, Yokohama, Kanagawa, Japan
[9] Int Univ Hlth & Welf, Innovat & Res Support Ctr, Tokyo, Japan
[10] Nihon Univ, Sch Med, Dept Med, Div Cardiol, Tokyo, Japan
[11] Osaka Police Hosp, Dept Cardiol, Osaka, Japan
关键词
Deep vein thrombosis; Pulmonary embolism; Real-world survey; Rivaroxaban; Venous thromboembolism; ORAL RIVAROXABAN; STANDARD THERAPY;
D O I
10.1253/circrep.CR-23-0008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:144 / 151
页数:8
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