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Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)

BACKGROUND: We assessed the efficacy and safety of mirabegron, a β(3)-adrenoceptor agonist, in older adults (≥ 80 years old) with overactive bladder (OAB). METHODS: OAB patients aged ≥ 80 years were enrolled in this prospective, single-arm observational study. OAB was diagnosed based on the OAB symp...

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Autores principales: Nakagomi, Hiroshi, Mitsui, Takahiko, Shimura, Hiroshi, Ihara, Tatsuya, Kira, Satoru, Sawada, Norifumi, Takeda, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939141/
https://www.ncbi.nlm.nih.gov/pubmed/35313873
http://dx.doi.org/10.1186/s12894-022-00989-7
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author Nakagomi, Hiroshi
Mitsui, Takahiko
Shimura, Hiroshi
Ihara, Tatsuya
Kira, Satoru
Sawada, Norifumi
Takeda, Masayuki
author_facet Nakagomi, Hiroshi
Mitsui, Takahiko
Shimura, Hiroshi
Ihara, Tatsuya
Kira, Satoru
Sawada, Norifumi
Takeda, Masayuki
author_sort Nakagomi, Hiroshi
collection PubMed
description BACKGROUND: We assessed the efficacy and safety of mirabegron, a β(3)-adrenoceptor agonist, in older adults (≥ 80 years old) with overactive bladder (OAB). METHODS: OAB patients aged ≥ 80 years were enrolled in this prospective, single-arm observational study. OAB was diagnosed based on the OAB symptom score (OABSS); i.e., a total score of ≥ 3 points and an urgency score of ≥ 2 points. Patients who received 50 mg mirabegron once daily were evaluated at the baseline and at 4, 8, and 12 weeks. The changes from the baseline in the OABSS, International Prostate Symptom Score (IPSS), OAB questionnaire (OAB-q) score, and Vulnerable Elders Survey (VES-13) score were determined. Adverse events, laboratory tests, 12-lead electrocardiography, the QT interval according to Fridericia’s formula (QTcF), uroflowmetry, the post-void residual urine volume (PVR), and the Mini-Mental State Examination (MMSE) score were used to assess safety. RESULTS: Forty-three patients (median age: 84 years, range: 80–96 years) were examined. They had high rates of comorbidities and polypharmacy. Mirabegron significantly improved in total score of the OABSS, including urgency and urge incontinence. The total IPSS, IPSS quality-of-life (QOL) index, and OAB-q scores also significantly improved. Mirabegron improved in the VES-13 score. There were no significant changes in laboratory test values, uroflowmetry findings, PVR, the QTcF, or MMSE score. Two patients (4.7%) withdrew from the study after experiencing adverse events. CONCLUSIONS: Mirabegron was well tolerated and significantly improved in OAB symptoms, and QOL in older patients. Trial registration The present clinical study was approved by University of Yamanashi Institutional Review Board prior to study initiation (ID1447) and was retrospectively registered with the UMIN Clinical Trials Registry (UMIN-CTR), Japan (UMIN000045996) on Nov 6, 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-022-00989-7.
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spelling pubmed-89391412022-03-23 Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study) Nakagomi, Hiroshi Mitsui, Takahiko Shimura, Hiroshi Ihara, Tatsuya Kira, Satoru Sawada, Norifumi Takeda, Masayuki BMC Urol Research Article BACKGROUND: We assessed the efficacy and safety of mirabegron, a β(3)-adrenoceptor agonist, in older adults (≥ 80 years old) with overactive bladder (OAB). METHODS: OAB patients aged ≥ 80 years were enrolled in this prospective, single-arm observational study. OAB was diagnosed based on the OAB symptom score (OABSS); i.e., a total score of ≥ 3 points and an urgency score of ≥ 2 points. Patients who received 50 mg mirabegron once daily were evaluated at the baseline and at 4, 8, and 12 weeks. The changes from the baseline in the OABSS, International Prostate Symptom Score (IPSS), OAB questionnaire (OAB-q) score, and Vulnerable Elders Survey (VES-13) score were determined. Adverse events, laboratory tests, 12-lead electrocardiography, the QT interval according to Fridericia’s formula (QTcF), uroflowmetry, the post-void residual urine volume (PVR), and the Mini-Mental State Examination (MMSE) score were used to assess safety. RESULTS: Forty-three patients (median age: 84 years, range: 80–96 years) were examined. They had high rates of comorbidities and polypharmacy. Mirabegron significantly improved in total score of the OABSS, including urgency and urge incontinence. The total IPSS, IPSS quality-of-life (QOL) index, and OAB-q scores also significantly improved. Mirabegron improved in the VES-13 score. There were no significant changes in laboratory test values, uroflowmetry findings, PVR, the QTcF, or MMSE score. Two patients (4.7%) withdrew from the study after experiencing adverse events. CONCLUSIONS: Mirabegron was well tolerated and significantly improved in OAB symptoms, and QOL in older patients. Trial registration The present clinical study was approved by University of Yamanashi Institutional Review Board prior to study initiation (ID1447) and was retrospectively registered with the UMIN Clinical Trials Registry (UMIN-CTR), Japan (UMIN000045996) on Nov 6, 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-022-00989-7. BioMed Central 2022-03-21 /pmc/articles/PMC8939141/ /pubmed/35313873 http://dx.doi.org/10.1186/s12894-022-00989-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Nakagomi, Hiroshi
Mitsui, Takahiko
Shimura, Hiroshi
Ihara, Tatsuya
Kira, Satoru
Sawada, Norifumi
Takeda, Masayuki
Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title_full Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title_fullStr Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title_full_unstemmed Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title_short Mirabegron for overactive bladder in frail patients 80 years or over (HOKUTO study)
title_sort mirabegron for overactive bladder in frail patients 80 years or over (hokuto study)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939141/
https://www.ncbi.nlm.nih.gov/pubmed/35313873
http://dx.doi.org/10.1186/s12894-022-00989-7
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