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Efficacy and safety of febuxostat in elderly female patients

BACKGROUND: Maintenance of low serum urate levels is important for the management of gout. Achieving the recommended serum urate levels of less than 6.0 mg/dL is difficult in elderly (65 years of age or older) patients with renal impairment. Xanthine oxidase inhibitors allopurinol and febuxostat are...

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Autores principales: Mizuno, Tomohiro, Hayashi, Takahiro, Hikosaka, Sayo, Shimabukuro, Yuka, Murase, Maho, Takahashi, Kazuo, Hayashi, Hiroki, Yuzawa, Yukio, Nagamatsu, Tadashi, Yamada, Shigeki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158997/
https://www.ncbi.nlm.nih.gov/pubmed/25214776
http://dx.doi.org/10.2147/CIA.S70855
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author Mizuno, Tomohiro
Hayashi, Takahiro
Hikosaka, Sayo
Shimabukuro, Yuka
Murase, Maho
Takahashi, Kazuo
Hayashi, Hiroki
Yuzawa, Yukio
Nagamatsu, Tadashi
Yamada, Shigeki
author_facet Mizuno, Tomohiro
Hayashi, Takahiro
Hikosaka, Sayo
Shimabukuro, Yuka
Murase, Maho
Takahashi, Kazuo
Hayashi, Hiroki
Yuzawa, Yukio
Nagamatsu, Tadashi
Yamada, Shigeki
author_sort Mizuno, Tomohiro
collection PubMed
description BACKGROUND: Maintenance of low serum urate levels is important for the management of gout. Achieving the recommended serum urate levels of less than 6.0 mg/dL is difficult in elderly (65 years of age or older) patients with renal impairment. Xanthine oxidase inhibitors allopurinol and febuxostat are used for this purpose. Although febuxostat had been shown to be efficacious in elderly patients, its safety and efficacy in elderly female patients with hyperuricemia remain unclear. OBJECTIVE: The aim of this study was to assess the efficacy and safety of febuxostat in elderly female patients. METHODS: We studied a retrospective cohort study. The study included elderly Japanese patients (65 years of age or older) who were treated with febuxostat at Fujita Health University Hospital from January 2012 to December 2013. The treatment goal was defined as achievement of serum urate levels of 6.0 mg/dL or lower within 16 weeks; this was the primary endpoint in the present study. Adverse events of febuxostat were defined as more than twofold increases in Common Terminology Criteria for adverse events scores from baseline. RESULTS: We evaluated 82 patients treated with febuxostat during the observation period and classified them into male (n=53) and female (n=29) groups. The mean time to achievement of the treatment goal was significantly shorter in the female group (53 days) than in the male group (71 days). There were no significant differences in adverse events between the 2 groups. CONCLUSION: Our findings suggest that the efficacy of febuxostat in elderly female patients is superior to that in elderly male patients and that the safety is equivalent.
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spelling pubmed-41589972014-09-11 Efficacy and safety of febuxostat in elderly female patients Mizuno, Tomohiro Hayashi, Takahiro Hikosaka, Sayo Shimabukuro, Yuka Murase, Maho Takahashi, Kazuo Hayashi, Hiroki Yuzawa, Yukio Nagamatsu, Tadashi Yamada, Shigeki Clin Interv Aging Original Research BACKGROUND: Maintenance of low serum urate levels is important for the management of gout. Achieving the recommended serum urate levels of less than 6.0 mg/dL is difficult in elderly (65 years of age or older) patients with renal impairment. Xanthine oxidase inhibitors allopurinol and febuxostat are used for this purpose. Although febuxostat had been shown to be efficacious in elderly patients, its safety and efficacy in elderly female patients with hyperuricemia remain unclear. OBJECTIVE: The aim of this study was to assess the efficacy and safety of febuxostat in elderly female patients. METHODS: We studied a retrospective cohort study. The study included elderly Japanese patients (65 years of age or older) who were treated with febuxostat at Fujita Health University Hospital from January 2012 to December 2013. The treatment goal was defined as achievement of serum urate levels of 6.0 mg/dL or lower within 16 weeks; this was the primary endpoint in the present study. Adverse events of febuxostat were defined as more than twofold increases in Common Terminology Criteria for adverse events scores from baseline. RESULTS: We evaluated 82 patients treated with febuxostat during the observation period and classified them into male (n=53) and female (n=29) groups. The mean time to achievement of the treatment goal was significantly shorter in the female group (53 days) than in the male group (71 days). There were no significant differences in adverse events between the 2 groups. CONCLUSION: Our findings suggest that the efficacy of febuxostat in elderly female patients is superior to that in elderly male patients and that the safety is equivalent. Dove Medical Press 2014-09-04 /pmc/articles/PMC4158997/ /pubmed/25214776 http://dx.doi.org/10.2147/CIA.S70855 Text en © 2014 Mizuno et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Mizuno, Tomohiro
Hayashi, Takahiro
Hikosaka, Sayo
Shimabukuro, Yuka
Murase, Maho
Takahashi, Kazuo
Hayashi, Hiroki
Yuzawa, Yukio
Nagamatsu, Tadashi
Yamada, Shigeki
Efficacy and safety of febuxostat in elderly female patients
title Efficacy and safety of febuxostat in elderly female patients
title_full Efficacy and safety of febuxostat in elderly female patients
title_fullStr Efficacy and safety of febuxostat in elderly female patients
title_full_unstemmed Efficacy and safety of febuxostat in elderly female patients
title_short Efficacy and safety of febuxostat in elderly female patients
title_sort efficacy and safety of febuxostat in elderly female patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158997/
https://www.ncbi.nlm.nih.gov/pubmed/25214776
http://dx.doi.org/10.2147/CIA.S70855
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