Intravesical injections of botulinum neurotoxin A to treat overactive bladder and/or detrusor overactivity related to multiple sclerosis: 5-Year continuation rate and specific risk factors for discontinuation—A study from the neuro-urology committee of the French Association of Urology

Background: While intravesical injections of botulinum neurotoxin A (BoNT-A) are currently recommended for patients experiencing refractory neurogenic overactive bladder and/or detrusor overactivity (OAB/DO), it is unclear how much this therapy is effective and sustainable in the long-term in patien...

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Veröffentlicht in:Multiple sclerosis 2023-07, Vol.29 (8), p.1024-1032
Hauptverfasser: Delaval, Stéphanie, Dequirez, Pierre-Luc, Hentzen, Claire, Baron, Maximilien, Mille, Eva, Tariel, François, Peyronnet, Benoit, Perrouin-Verbe, Marie-Aimée, Pierache, Adeline, Chartier-Kastler, Emmanuel, Capon, Grégoire, Cornu, Jean-Nicolas, Castel-Lacanal, Evelyne, Gamé, Xavier, Karsenty, Gilles, Ruffion, Alain, Denys, Pierre, Even, Alexia, Joussain, Charles, Amarenco, Gérard, Phé, Véronique, Biardeau, Xavier
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container_end_page 1032
container_issue 8
container_start_page 1024
container_title Multiple sclerosis
container_volume 29
creator Delaval, Stéphanie
Dequirez, Pierre-Luc
Hentzen, Claire
Baron, Maximilien
Mille, Eva
Tariel, François
Peyronnet, Benoit
Perrouin-Verbe, Marie-Aimée
Pierache, Adeline
Chartier-Kastler, Emmanuel
Capon, Grégoire
Cornu, Jean-Nicolas
Castel-Lacanal, Evelyne
Gamé, Xavier
Karsenty, Gilles
Ruffion, Alain
Denys, Pierre
Even, Alexia
Joussain, Charles
Amarenco, Gérard
Phé, Véronique
Biardeau, Xavier
description Background: While intravesical injections of botulinum neurotoxin A (BoNT-A) are currently recommended for patients experiencing refractory neurogenic overactive bladder and/or detrusor overactivity (OAB/DO), it is unclear how much this therapy is effective and sustainable in the long-term in patients with multiple sclerosis (MS). Objectives: To assess the mid-term continuation rate of BoNT-A injections to treat neurogenic OAB/DO in MS patients and to investigate MS-specific risk factors for discontinuation. Methods: This retrospective study involved 11 French university hospital centers. All MS patients who received BoNT-A to treat neurogenic OAB/DO between 2008 and 2013 and were subsequently followed up for at least 5 years were eligible. Results: Of the 196 MS patients included, 159 (81.1%) were still under BoNT-A 5 years after the first injection. The combination of the Expanded Disability Status Scale (EDSS < 6 or ⩾ 6) and of the MS type (relapsing–remitting vs progressive) predicted the risk of discontinuation. This risk was 5.5% for patients with no risk factor, whereas patients presenting with one or two risk factors were 3.3 and 5.7 times more likely to discontinue, respectively. Conclusion: BoNT-A is a satisfying mid-term neurogenic OAB/DO therapy for most MS patients. Combining EDSS and MS type could help predict BoNT-A discontinuation.
doi_str_mv 10.1177/13524585231174580
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Objectives: To assess the mid-term continuation rate of BoNT-A injections to treat neurogenic OAB/DO in MS patients and to investigate MS-specific risk factors for discontinuation. Methods: This retrospective study involved 11 French university hospital centers. All MS patients who received BoNT-A to treat neurogenic OAB/DO between 2008 and 2013 and were subsequently followed up for at least 5 years were eligible. Results: Of the 196 MS patients included, 159 (81.1%) were still under BoNT-A 5 years after the first injection. The combination of the Expanded Disability Status Scale (EDSS &lt; 6 or ⩾ 6) and of the MS type (relapsing–remitting vs progressive) predicted the risk of discontinuation. This risk was 5.5% for patients with no risk factor, whereas patients presenting with one or two risk factors were 3.3 and 5.7 times more likely to discontinue, respectively. Conclusion: BoNT-A is a satisfying mid-term neurogenic OAB/DO therapy for most MS patients. Combining EDSS and MS type could help predict BoNT-A discontinuation.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/13524585231174580</identifier><identifier>PMID: 37264947</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Administration, Intravesical ; Botulinum toxin type A ; Botulinum Toxins, Type A - adverse effects ; Humans ; Life Sciences ; Multiple sclerosis ; Multiple Sclerosis - chemically induced ; Multiple Sclerosis - complications ; Neuromuscular Agents - adverse effects ; Retrospective Studies ; Risk factors ; Treatment Outcome ; Urinary Bladder, Neurogenic - drug therapy ; Urinary Bladder, Neurogenic - etiology ; Urinary Bladder, Overactive - complications ; Urinary Bladder, Overactive - etiology ; Urology</subject><ispartof>Multiple sclerosis, 2023-07, Vol.29 (8), p.1024-1032</ispartof><rights>The Author(s), 2023</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c354t-4ce3112b6fb6949d39b7187efbd78aed3efff7beacf07e01adfea9403662c12c3</cites><orcidid>0000-0003-0921-1253 ; 0000-0002-8999-8326 ; 0000-0003-0512-3459</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/13524585231174580$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/13524585231174580$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37264947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://normandie-univ.hal.science/hal-04142840$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Delaval, Stéphanie</creatorcontrib><creatorcontrib>Dequirez, Pierre-Luc</creatorcontrib><creatorcontrib>Hentzen, Claire</creatorcontrib><creatorcontrib>Baron, Maximilien</creatorcontrib><creatorcontrib>Mille, Eva</creatorcontrib><creatorcontrib>Tariel, François</creatorcontrib><creatorcontrib>Peyronnet, Benoit</creatorcontrib><creatorcontrib>Perrouin-Verbe, Marie-Aimée</creatorcontrib><creatorcontrib>Pierache, Adeline</creatorcontrib><creatorcontrib>Chartier-Kastler, Emmanuel</creatorcontrib><creatorcontrib>Capon, Grégoire</creatorcontrib><creatorcontrib>Cornu, Jean-Nicolas</creatorcontrib><creatorcontrib>Castel-Lacanal, Evelyne</creatorcontrib><creatorcontrib>Gamé, Xavier</creatorcontrib><creatorcontrib>Karsenty, Gilles</creatorcontrib><creatorcontrib>Ruffion, Alain</creatorcontrib><creatorcontrib>Denys, Pierre</creatorcontrib><creatorcontrib>Even, Alexia</creatorcontrib><creatorcontrib>Joussain, Charles</creatorcontrib><creatorcontrib>Amarenco, Gérard</creatorcontrib><creatorcontrib>Phé, Véronique</creatorcontrib><creatorcontrib>Biardeau, Xavier</creatorcontrib><title>Intravesical injections of botulinum neurotoxin A to treat overactive bladder and/or detrusor overactivity related to multiple sclerosis: 5-Year continuation rate and specific risk factors for discontinuation—A study from the neuro-urology committee of the French Association of Urology</title><title>Multiple sclerosis</title><addtitle>Mult Scler</addtitle><description>Background: While intravesical injections of botulinum neurotoxin A (BoNT-A) are currently recommended for patients experiencing refractory neurogenic overactive bladder and/or detrusor overactivity (OAB/DO), it is unclear how much this therapy is effective and sustainable in the long-term in patients with multiple sclerosis (MS). Objectives: To assess the mid-term continuation rate of BoNT-A injections to treat neurogenic OAB/DO in MS patients and to investigate MS-specific risk factors for discontinuation. Methods: This retrospective study involved 11 French university hospital centers. All MS patients who received BoNT-A to treat neurogenic OAB/DO between 2008 and 2013 and were subsequently followed up for at least 5 years were eligible. Results: Of the 196 MS patients included, 159 (81.1%) were still under BoNT-A 5 years after the first injection. The combination of the Expanded Disability Status Scale (EDSS &lt; 6 or ⩾ 6) and of the MS type (relapsing–remitting vs progressive) predicted the risk of discontinuation. This risk was 5.5% for patients with no risk factor, whereas patients presenting with one or two risk factors were 3.3 and 5.7 times more likely to discontinue, respectively. Conclusion: BoNT-A is a satisfying mid-term neurogenic OAB/DO therapy for most MS patients. 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Dequirez, Pierre-Luc ; Hentzen, Claire ; Baron, Maximilien ; Mille, Eva ; Tariel, François ; Peyronnet, Benoit ; Perrouin-Verbe, Marie-Aimée ; Pierache, Adeline ; Chartier-Kastler, Emmanuel ; Capon, Grégoire ; Cornu, Jean-Nicolas ; Castel-Lacanal, Evelyne ; Gamé, Xavier ; Karsenty, Gilles ; Ruffion, Alain ; Denys, Pierre ; Even, Alexia ; Joussain, Charles ; Amarenco, Gérard ; Phé, Véronique ; Biardeau, Xavier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-4ce3112b6fb6949d39b7187efbd78aed3efff7beacf07e01adfea9403662c12c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Administration, Intravesical</topic><topic>Botulinum toxin type A</topic><topic>Botulinum Toxins, Type A - adverse effects</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - chemically induced</topic><topic>Multiple Sclerosis - complications</topic><topic>Neuromuscular Agents - adverse effects</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Treatment Outcome</topic><topic>Urinary Bladder, Neurogenic - drug therapy</topic><topic>Urinary Bladder, Neurogenic - etiology</topic><topic>Urinary Bladder, Overactive - complications</topic><topic>Urinary Bladder, Overactive - etiology</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delaval, Stéphanie</creatorcontrib><creatorcontrib>Dequirez, Pierre-Luc</creatorcontrib><creatorcontrib>Hentzen, Claire</creatorcontrib><creatorcontrib>Baron, Maximilien</creatorcontrib><creatorcontrib>Mille, Eva</creatorcontrib><creatorcontrib>Tariel, François</creatorcontrib><creatorcontrib>Peyronnet, Benoit</creatorcontrib><creatorcontrib>Perrouin-Verbe, Marie-Aimée</creatorcontrib><creatorcontrib>Pierache, Adeline</creatorcontrib><creatorcontrib>Chartier-Kastler, Emmanuel</creatorcontrib><creatorcontrib>Capon, Grégoire</creatorcontrib><creatorcontrib>Cornu, Jean-Nicolas</creatorcontrib><creatorcontrib>Castel-Lacanal, Evelyne</creatorcontrib><creatorcontrib>Gamé, Xavier</creatorcontrib><creatorcontrib>Karsenty, Gilles</creatorcontrib><creatorcontrib>Ruffion, Alain</creatorcontrib><creatorcontrib>Denys, Pierre</creatorcontrib><creatorcontrib>Even, Alexia</creatorcontrib><creatorcontrib>Joussain, Charles</creatorcontrib><creatorcontrib>Amarenco, Gérard</creatorcontrib><creatorcontrib>Phé, Véronique</creatorcontrib><creatorcontrib>Biardeau, Xavier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Multiple sclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delaval, Stéphanie</au><au>Dequirez, Pierre-Luc</au><au>Hentzen, Claire</au><au>Baron, Maximilien</au><au>Mille, Eva</au><au>Tariel, François</au><au>Peyronnet, Benoit</au><au>Perrouin-Verbe, Marie-Aimée</au><au>Pierache, Adeline</au><au>Chartier-Kastler, Emmanuel</au><au>Capon, Grégoire</au><au>Cornu, Jean-Nicolas</au><au>Castel-Lacanal, Evelyne</au><au>Gamé, Xavier</au><au>Karsenty, Gilles</au><au>Ruffion, Alain</au><au>Denys, Pierre</au><au>Even, Alexia</au><au>Joussain, Charles</au><au>Amarenco, Gérard</au><au>Phé, Véronique</au><au>Biardeau, Xavier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravesical injections of botulinum neurotoxin A to treat overactive bladder and/or detrusor overactivity related to multiple sclerosis: 5-Year continuation rate and specific risk factors for discontinuation—A study from the neuro-urology committee of the French Association of Urology</atitle><jtitle>Multiple sclerosis</jtitle><addtitle>Mult Scler</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>29</volume><issue>8</issue><spage>1024</spage><epage>1032</epage><pages>1024-1032</pages><issn>1352-4585</issn><eissn>1477-0970</eissn><abstract>Background: While intravesical injections of botulinum neurotoxin A (BoNT-A) are currently recommended for patients experiencing refractory neurogenic overactive bladder and/or detrusor overactivity (OAB/DO), it is unclear how much this therapy is effective and sustainable in the long-term in patients with multiple sclerosis (MS). Objectives: To assess the mid-term continuation rate of BoNT-A injections to treat neurogenic OAB/DO in MS patients and to investigate MS-specific risk factors for discontinuation. Methods: This retrospective study involved 11 French university hospital centers. All MS patients who received BoNT-A to treat neurogenic OAB/DO between 2008 and 2013 and were subsequently followed up for at least 5 years were eligible. Results: Of the 196 MS patients included, 159 (81.1%) were still under BoNT-A 5 years after the first injection. The combination of the Expanded Disability Status Scale (EDSS &lt; 6 or ⩾ 6) and of the MS type (relapsing–remitting vs progressive) predicted the risk of discontinuation. This risk was 5.5% for patients with no risk factor, whereas patients presenting with one or two risk factors were 3.3 and 5.7 times more likely to discontinue, respectively. Conclusion: BoNT-A is a satisfying mid-term neurogenic OAB/DO therapy for most MS patients. 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subjects Administration, Intravesical
Botulinum toxin type A
Botulinum Toxins, Type A - adverse effects
Humans
Life Sciences
Multiple sclerosis
Multiple Sclerosis - chemically induced
Multiple Sclerosis - complications
Neuromuscular Agents - adverse effects
Retrospective Studies
Risk factors
Treatment Outcome
Urinary Bladder, Neurogenic - drug therapy
Urinary Bladder, Neurogenic - etiology
Urinary Bladder, Overactive - complications
Urinary Bladder, Overactive - etiology
Urology
title Intravesical injections of botulinum neurotoxin A to treat overactive bladder and/or detrusor overactivity related to multiple sclerosis: 5-Year continuation rate and specific risk factors for discontinuation—A study from the neuro-urology committee of the French Association of Urology
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