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New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA

In the last few years, much new information has been generated on the pathophysiology, possible therapeutic targets, and pharmacologic treatment of overactive bladder (OAB). Antimuscarinic drugs are still first-line pharmacologic treatment for OAB and often have good initial response rates, but adve...

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Autor principal: Andersson, Karl-Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634323/
https://www.ncbi.nlm.nih.gov/pubmed/23637536
http://dx.doi.org/10.2147/TCRM.S33052
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author Andersson, Karl-Erik
author_facet Andersson, Karl-Erik
author_sort Andersson, Karl-Erik
collection PubMed
description In the last few years, much new information has been generated on the pathophysiology, possible therapeutic targets, and pharmacologic treatment of overactive bladder (OAB). Antimuscarinic drugs are still first-line pharmacologic treatment for OAB and often have good initial response rates, but adverse effects and decreasing efficacy cause long-term compliance problems, prompting a search for new therapeutic alternatives. Mirabegron and onabotulinumtoxinA, two drugs with different mechanisms of action, and with adverse effect profiles different from those of antimuscarinics, were recently approved for treatment of OAB. However, their place in the treatment of this disorder has not yet been established. In this short review, the mechanisms of action, clinical efficacy, and safety profiles of these drugs are discussed and compared with those of the current gold standard, antimuscarinic agents.
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spelling pubmed-36343232013-05-01 New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA Andersson, Karl-Erik Ther Clin Risk Manag Review In the last few years, much new information has been generated on the pathophysiology, possible therapeutic targets, and pharmacologic treatment of overactive bladder (OAB). Antimuscarinic drugs are still first-line pharmacologic treatment for OAB and often have good initial response rates, but adverse effects and decreasing efficacy cause long-term compliance problems, prompting a search for new therapeutic alternatives. Mirabegron and onabotulinumtoxinA, two drugs with different mechanisms of action, and with adverse effect profiles different from those of antimuscarinics, were recently approved for treatment of OAB. However, their place in the treatment of this disorder has not yet been established. In this short review, the mechanisms of action, clinical efficacy, and safety profiles of these drugs are discussed and compared with those of the current gold standard, antimuscarinic agents. Dove Medical Press 2013 2013-04-18 /pmc/articles/PMC3634323/ /pubmed/23637536 http://dx.doi.org/10.2147/TCRM.S33052 Text en © 2013 Andersson, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Andersson, Karl-Erik
New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title_full New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title_fullStr New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title_full_unstemmed New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title_short New developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxinA
title_sort new developments in the management of overactive bladder: focus on mirabegron and onabotulinumtoxina
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634323/
https://www.ncbi.nlm.nih.gov/pubmed/23637536
http://dx.doi.org/10.2147/TCRM.S33052
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