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OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice
INTRODUCTION AND HYPOTHESIS: In randomized clinical trials onabotulinumtoxinA was demonstrated to be an effective and well-tolerated treatment for overactive bladder (OAB) with urinary incontinence (UI). However, data reporting onabotulinumtoxinA use in everyday clinical practice are limited. Here,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788019/ https://www.ncbi.nlm.nih.gov/pubmed/32719964 http://dx.doi.org/10.1007/s00192-020-04423-0 |
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author | Hamid, Rizwan Lorenzo-Gomez, Maria-Fernanda Schulte-Baukloh, Heinrich Boroujerdi, Amin Patel, Anand Farrelly, Elisabeth |
author_facet | Hamid, Rizwan Lorenzo-Gomez, Maria-Fernanda Schulte-Baukloh, Heinrich Boroujerdi, Amin Patel, Anand Farrelly, Elisabeth |
author_sort | Hamid, Rizwan |
collection | PubMed |
description | INTRODUCTION AND HYPOTHESIS: In randomized clinical trials onabotulinumtoxinA was demonstrated to be an effective and well-tolerated treatment for overactive bladder (OAB) with urinary incontinence (UI). However, data reporting onabotulinumtoxinA use in everyday clinical practice are limited. Here, we present the results from a large, first-of-its-kind real-world study in patients with OAB. METHODS: This was a prospective, observational, multinational study (GRACE; ClinicalTrials.gov, NCT02161159) performed in four European countries. Patients (N = 504) aged ≥ 18 years with OAB inadequately managed with ≥ 1 anticholinergic received onabotulinumtoxinA per their physician’s normal clinical practice. RESULTS: Physicians primarily used rigid cystoscopes for onabotulinumtoxinA injection; anesthesia/analgesia was utilized during most treatment procedures. Significant reductions in UI episodes/day from baseline to weeks 1 and 12 were observed as well as in micturition, urgency, and nocturia episodes/day. These improvements in urinary symptoms corresponded to higher scores on the treatment benefit scale at week 12. The use of other OAB medications dropped from baseline to weeks 1 and 12 and was sustained to week 52, which paralleled a reduction in the number of incontinence products used during that time frame. Adverse reactions were reported in 2.6% of patients throughout the study. CONCLUSIONS: In this real-world study, significant improvements in urinary symptoms were seen following onabotulinumtoxinA treatment as early as week 1 and sustained to at least week 12. This was accompanied by a reduced reliance upon incontinence products and reduction in concomitant OAB medication use. OnabotulinumtoxinA was well tolerated with no new safety signals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00192-020-04423-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7788019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-77880192021-01-14 OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice Hamid, Rizwan Lorenzo-Gomez, Maria-Fernanda Schulte-Baukloh, Heinrich Boroujerdi, Amin Patel, Anand Farrelly, Elisabeth Int Urogynecol J Original Article INTRODUCTION AND HYPOTHESIS: In randomized clinical trials onabotulinumtoxinA was demonstrated to be an effective and well-tolerated treatment for overactive bladder (OAB) with urinary incontinence (UI). However, data reporting onabotulinumtoxinA use in everyday clinical practice are limited. Here, we present the results from a large, first-of-its-kind real-world study in patients with OAB. METHODS: This was a prospective, observational, multinational study (GRACE; ClinicalTrials.gov, NCT02161159) performed in four European countries. Patients (N = 504) aged ≥ 18 years with OAB inadequately managed with ≥ 1 anticholinergic received onabotulinumtoxinA per their physician’s normal clinical practice. RESULTS: Physicians primarily used rigid cystoscopes for onabotulinumtoxinA injection; anesthesia/analgesia was utilized during most treatment procedures. Significant reductions in UI episodes/day from baseline to weeks 1 and 12 were observed as well as in micturition, urgency, and nocturia episodes/day. These improvements in urinary symptoms corresponded to higher scores on the treatment benefit scale at week 12. The use of other OAB medications dropped from baseline to weeks 1 and 12 and was sustained to week 52, which paralleled a reduction in the number of incontinence products used during that time frame. Adverse reactions were reported in 2.6% of patients throughout the study. CONCLUSIONS: In this real-world study, significant improvements in urinary symptoms were seen following onabotulinumtoxinA treatment as early as week 1 and sustained to at least week 12. This was accompanied by a reduced reliance upon incontinence products and reduction in concomitant OAB medication use. OnabotulinumtoxinA was well tolerated with no new safety signals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00192-020-04423-0) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-07-27 2021 /pmc/articles/PMC7788019/ /pubmed/32719964 http://dx.doi.org/10.1007/s00192-020-04423-0 Text en © The Author(s) 2020 Open Access This 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/. |
spellingShingle | Original Article Hamid, Rizwan Lorenzo-Gomez, Maria-Fernanda Schulte-Baukloh, Heinrich Boroujerdi, Amin Patel, Anand Farrelly, Elisabeth OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title | OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title_full | OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title_fullStr | OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title_full_unstemmed | OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title_short | OnabotulinumtoxinA is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
title_sort | onabotulinumtoxina is a well tolerated and effective treatment for refractory overactive bladder in real-world practice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788019/ https://www.ncbi.nlm.nih.gov/pubmed/32719964 http://dx.doi.org/10.1007/s00192-020-04423-0 |
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