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The impact of Mirabegron on sexual function in women with idiopathic overactive bladder

BACKGROUND: Overactive bladder (OAB) can frequently exert a negative effect on female sexual function. Mirabegron, a β3 receptor agonist, improves OAB symptoms, but there are very few information about its role on female sexual dysfunction (FSD). Aim of the study was to assess the impact of Mirabegr...

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Autores principales: Gubbiotti, Marilena, Giannantoni, Antonella, Cantaluppi, Simona, Coluccia, Anna Chiara, Ghezzi, Fabio, Serati, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341751/
https://www.ncbi.nlm.nih.gov/pubmed/30665388
http://dx.doi.org/10.1186/s12894-019-0438-8
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author Gubbiotti, Marilena
Giannantoni, Antonella
Cantaluppi, Simona
Coluccia, Anna Chiara
Ghezzi, Fabio
Serati, Maurizio
author_facet Gubbiotti, Marilena
Giannantoni, Antonella
Cantaluppi, Simona
Coluccia, Anna Chiara
Ghezzi, Fabio
Serati, Maurizio
author_sort Gubbiotti, Marilena
collection PubMed
description BACKGROUND: Overactive bladder (OAB) can frequently exert a negative effect on female sexual function. Mirabegron, a β3 receptor agonist, improves OAB symptoms, but there are very few information about its role on female sexual dysfunction (FSD). Aim of the study was to assess the impact of Mirabegron on FSD in women affected by OAB. METHODS: Fifty sexually active women suffering from idiopathic OAB were included in the study. Patients were assessed by means of a urogynecologic physical examination and were asked to complete the 3-day voiding diary, the International Consultation on Incontinence Questionnaire- Short Form (ICIQ-SF), the Female Sexual Function Index (FSFI) questionnaire and VAS, before and 12 weeks after treatment with Mirabegron. In addition, at the same time points, patients underwent uroflowmetry with the measurement of post- void residual volume (PVR). RESULTS: At baseline all patients were affected by OAB symptoms, with 49/50 patients (98%) presenting with FSD. At 12- weeks follow- up, OAB symptoms improved significantly in all patients, with 59.5% of subjects achieving a complete urinary continence. FSFI Total Score significantly improved in 42/50 patients (84%) from 18.9 ± 4.3 to 21.8 ± 4.5 (p < 0.0001). Sixteen cases (32%) presented with no FSD. Also mean ± SD scores of ICIQ-SF and VAS significantly improved (from 17.1 ± 5 to 7.9 ± 4.8 and from 3.9 ± 1.2 to 6.9 ± 1.2 respectively, p < 0.000). CONCLUSIONS: Mirabegron not only is able to control urinary symptoms in women with OAB, but also induces a significant improvement in their sexual life.
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spelling pubmed-63417512019-01-24 The impact of Mirabegron on sexual function in women with idiopathic overactive bladder Gubbiotti, Marilena Giannantoni, Antonella Cantaluppi, Simona Coluccia, Anna Chiara Ghezzi, Fabio Serati, Maurizio BMC Urol Research Article BACKGROUND: Overactive bladder (OAB) can frequently exert a negative effect on female sexual function. Mirabegron, a β3 receptor agonist, improves OAB symptoms, but there are very few information about its role on female sexual dysfunction (FSD). Aim of the study was to assess the impact of Mirabegron on FSD in women affected by OAB. METHODS: Fifty sexually active women suffering from idiopathic OAB were included in the study. Patients were assessed by means of a urogynecologic physical examination and were asked to complete the 3-day voiding diary, the International Consultation on Incontinence Questionnaire- Short Form (ICIQ-SF), the Female Sexual Function Index (FSFI) questionnaire and VAS, before and 12 weeks after treatment with Mirabegron. In addition, at the same time points, patients underwent uroflowmetry with the measurement of post- void residual volume (PVR). RESULTS: At baseline all patients were affected by OAB symptoms, with 49/50 patients (98%) presenting with FSD. At 12- weeks follow- up, OAB symptoms improved significantly in all patients, with 59.5% of subjects achieving a complete urinary continence. FSFI Total Score significantly improved in 42/50 patients (84%) from 18.9 ± 4.3 to 21.8 ± 4.5 (p < 0.0001). Sixteen cases (32%) presented with no FSD. Also mean ± SD scores of ICIQ-SF and VAS significantly improved (from 17.1 ± 5 to 7.9 ± 4.8 and from 3.9 ± 1.2 to 6.9 ± 1.2 respectively, p < 0.000). CONCLUSIONS: Mirabegron not only is able to control urinary symptoms in women with OAB, but also induces a significant improvement in their sexual life. BioMed Central 2019-01-21 /pmc/articles/PMC6341751/ /pubmed/30665388 http://dx.doi.org/10.1186/s12894-019-0438-8 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gubbiotti, Marilena
Giannantoni, Antonella
Cantaluppi, Simona
Coluccia, Anna Chiara
Ghezzi, Fabio
Serati, Maurizio
The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title_full The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title_fullStr The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title_full_unstemmed The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title_short The impact of Mirabegron on sexual function in women with idiopathic overactive bladder
title_sort impact of mirabegron on sexual function in women with idiopathic overactive bladder
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341751/
https://www.ncbi.nlm.nih.gov/pubmed/30665388
http://dx.doi.org/10.1186/s12894-019-0438-8
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