AI Article Synopsis

  • Intravesical injections of botulinum neurotoxin A (BoNT-A) are used to treat neurogenic overactive bladder and/or detrusor overactivity in patients with multiple sclerosis, but their long-term effectiveness is unclear.
  • A study involving 196 MS patients assessed the mid-term continuation rate and identified specific risk factors for discontinuation, finding that 81.1% continued treatment after 5 years.
  • The research indicated that the Expanded Disability Status Scale and the type of MS significantly influenced the likelihood of discontinuation, with those having one or more risk factors being more prone to stop treatment.

Article 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 < 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.

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Source
http://dx.doi.org/10.1177/13524585231174580DOI Listing

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