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Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings
The approved dose of oral anticoagulant rivaroxaban for patients with non-valvular atrial fibrillation (NVAF) in Japan is 15 mg once daily (od) in patients whose creatinine clearance is ≥ 50 mL/min, but recent real-world studies have demonstrated that these patients often received less than the reco...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800859/ https://www.ncbi.nlm.nih.gov/pubmed/31432451 http://dx.doi.org/10.1007/s11239-019-01934-6 |
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author | Ikeda, Takanori Ogawa, Satoshi Kitazono, Takanari Nakagawara, Jyoji Minematsu, Kazuo Miyamoto, Susumu Murakawa, Yuji Iwashiro, Sanghun Kidani, Yoko Okayama, Yutaka Sunaya, Toshiyuki Sato, Shoichiro Yamanaka, Satoshi |
author_facet | Ikeda, Takanori Ogawa, Satoshi Kitazono, Takanari Nakagawara, Jyoji Minematsu, Kazuo Miyamoto, Susumu Murakawa, Yuji Iwashiro, Sanghun Kidani, Yoko Okayama, Yutaka Sunaya, Toshiyuki Sato, Shoichiro Yamanaka, Satoshi |
author_sort | Ikeda, Takanori |
collection | PubMed |
description | The approved dose of oral anticoagulant rivaroxaban for patients with non-valvular atrial fibrillation (NVAF) in Japan is 15 mg once daily (od) in patients whose creatinine clearance is ≥ 50 mL/min, but recent real-world studies have demonstrated that these patients often received less than the recommended dose due to bleeding concerns. The effect of under-dosing on safety and effectiveness outcomes remains unclear. We used 1-year follow-up data from the XAPASS, a real-world Japanese prospective, single-arm, observational study. Of the 11,308 patients, 6521 patients who completed a 1-year follow-up and had a creatinine clearance ≥ 50 mL/min were included in this sub-analysis. Primary endpoints were any bleeding and a composite of stroke/non-central nervous system systemic embolism (non-CNS SE)/myocardial infarction (MI). Among the 6521 patients, 4185 (64.2%; mean CHADS(2) score: 1.8) received the 15 mg od (recommended dose), whereas 2336 (35.8%; mean CHADS(2) score: 2.3) received 10 mg od (under-dose). After adjusting for patient characteristics by propensity scoring and inverse probability of treatment weighting, incidence rates of major bleeding were comparable between under-dosed patients and patients who received the recommended dose (1.34 vs. 1.63 events/100 patient-years, p = 0.197), although the incidence rates of stroke/non-CNS SE/MI were higher in under-dosed patients than in those who received the recommended dose (2.15 vs. 1.48 events/100 patient-years, p = 0.009). In Japanese clinical practice, some NVAF patients receive rivaroxaban doses inconsistent with the recommendation. Considering the total clinical benefit, the recommended dose may be preferable in terms of balance of safety and effectiveness. Clinicaltrials.gov NCT01582737. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11239-019-01934-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6800859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-68008592019-11-01 Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings Ikeda, Takanori Ogawa, Satoshi Kitazono, Takanari Nakagawara, Jyoji Minematsu, Kazuo Miyamoto, Susumu Murakawa, Yuji Iwashiro, Sanghun Kidani, Yoko Okayama, Yutaka Sunaya, Toshiyuki Sato, Shoichiro Yamanaka, Satoshi J Thromb Thrombolysis Article The approved dose of oral anticoagulant rivaroxaban for patients with non-valvular atrial fibrillation (NVAF) in Japan is 15 mg once daily (od) in patients whose creatinine clearance is ≥ 50 mL/min, but recent real-world studies have demonstrated that these patients often received less than the recommended dose due to bleeding concerns. The effect of under-dosing on safety and effectiveness outcomes remains unclear. We used 1-year follow-up data from the XAPASS, a real-world Japanese prospective, single-arm, observational study. Of the 11,308 patients, 6521 patients who completed a 1-year follow-up and had a creatinine clearance ≥ 50 mL/min were included in this sub-analysis. Primary endpoints were any bleeding and a composite of stroke/non-central nervous system systemic embolism (non-CNS SE)/myocardial infarction (MI). Among the 6521 patients, 4185 (64.2%; mean CHADS(2) score: 1.8) received the 15 mg od (recommended dose), whereas 2336 (35.8%; mean CHADS(2) score: 2.3) received 10 mg od (under-dose). After adjusting for patient characteristics by propensity scoring and inverse probability of treatment weighting, incidence rates of major bleeding were comparable between under-dosed patients and patients who received the recommended dose (1.34 vs. 1.63 events/100 patient-years, p = 0.197), although the incidence rates of stroke/non-CNS SE/MI were higher in under-dosed patients than in those who received the recommended dose (2.15 vs. 1.48 events/100 patient-years, p = 0.009). In Japanese clinical practice, some NVAF patients receive rivaroxaban doses inconsistent with the recommendation. Considering the total clinical benefit, the recommended dose may be preferable in terms of balance of safety and effectiveness. Clinicaltrials.gov NCT01582737. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11239-019-01934-6) contains supplementary material, which is available to authorized users. Springer US 2019-08-20 2019 /pmc/articles/PMC6800859/ /pubmed/31432451 http://dx.doi.org/10.1007/s11239-019-01934-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Ikeda, Takanori Ogawa, Satoshi Kitazono, Takanari Nakagawara, Jyoji Minematsu, Kazuo Miyamoto, Susumu Murakawa, Yuji Iwashiro, Sanghun Kidani, Yoko Okayama, Yutaka Sunaya, Toshiyuki Sato, Shoichiro Yamanaka, Satoshi Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title | Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title_full | Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title_fullStr | Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title_full_unstemmed | Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title_short | Outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world Japanese clinical settings |
title_sort | outcomes associated with under-dosing of rivaroxaban for management of non-valvular atrial fibrillation in real-world japanese clinical settings |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800859/ https://www.ncbi.nlm.nih.gov/pubmed/31432451 http://dx.doi.org/10.1007/s11239-019-01934-6 |
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