Comparative effectiveness and safety of edoxaban, rivaroxaban, and apixaban in patients with venous thromboembolism: A cohort study

被引:5
|
作者
Fukasawa, Toshiki [1 ,2 ]
Seki, Tomotsugu [1 ,3 ]
Nakashima, Masayuki [1 ]
Kawakami, Koji [1 ]
机构
[1] Kyoto Univ, Grad Sch Med & Publ Hlth, Dept Pharmacoepidemiol, Yoshidakonoe cho Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Med & Publ Hlth, Dept Digital Hlth & Epidemiol, Kyoto, Japan
[3] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Dept Cardiovasc Med, Kyoto, Japan
关键词
apixaban; edoxaban; factor Xa inhibitors; hemorrhage; rivaroxaban; venous thromboembolism; DIRECT ORAL ANTICOAGULANTS; PROPENSITY SCORE; DABIGATRAN; WARFARIN; ASSOCIATION;
D O I
10.1111/jth.15799
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Although several studies have compared the effectiveness and safety of rivaroxaban and apixaban in patients with venous thromboembolism (VTE), direct comparison of these drugs with edoxaban is lacking. Objective We compared the effectiveness and safety of edoxaban, rivaroxaban, and apixaban in patients with VTE. Patients/Methods In this retrospective cohort study using a Japanese hospital administrative database, we identified three mutually exclusive groups of patients with VTE beginning treatment with edoxaban, rivaroxaban, or apixaban. Primary effectiveness outcome was recurrent VTE, and principal safety outcome was a composite of intracranial hemorrhage and gastrointestinal bleeding. Subjects were followed for up to 180 days. Baseline characteristics among groups were balanced using propensity score matching weights. Results Three thousand three hundred sixty-nine edoxaban, 1592 rivaroxaban, and 1998 apixaban initiators were identified. There were no significant differences among the three drugs in the prevention of recurrent VTE (adjusted incidence rate ratio [aIRR], 0.77; 95% confidence interval [CI], 0.45-1.30 for edoxaban vs. rivaroxaban; aIRR, 0.92; 95% CI, 0.54-1.56 for edoxaban vs. apixaban; and aIRR, 1.20; 95% CI, 0.69-2.10 for rivaroxaban vs. apixaban), or in the risk of intracranial hemorrhage or gastrointestinal bleeding (aIRR, 1.57, 95% CI, 0.85-2.90 for edoxaban vs. rivaroxaban; aIRR, 1.30, 95% CI, 0.76-2.23 for edoxaban vs. apixaban; and aIRR, 0.83, 95% CI, 0.42-1.64 for rivaroxaban vs. apixaban). Conclusions In routine care, edoxaban, rivaroxaban, and apixaban appear to have similar effectiveness and safety in the treatment of VTE.
引用
收藏
页码:2083 / 2097
页数:15
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