4.6 Article

Repeated Botulinum Toxin Type A Injections for Refractory Overactive Bladder: Medium-Term Outcomes, Safety Profile, and Discontinuation Rates

Journal

EUROPEAN UROLOGY
Volume 61, Issue 4, Pages 834-839

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.eururo.2011.12.011

Keywords

OnabotulinumtoxinA; Idiopathic detrusor overactivity; Overactive bladder; Repeated injections; Botulinum toxin A; Discontinuation rates

Funding

  1. Allergan Ltd. Sahai
  2. Department of Health via the National Institute for Health Research (NIHR) comprehensive Biomedical Research Centre
  3. NHS Foundation Trust with King's College London
  4. MRC Centre for Transplantation
  5. Medical Research Council [MR/J006742/1, G0600698] Funding Source: researchfish
  6. MRC [G0600698] Funding Source: UKRI

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Background: Efficacy and safety of botulinum toxin type A (BoNTA) injection is supported by level 1 evidence, but data regarding repeated injections are limited in patients with refractory overactive bladder (OAB) and idiopathic detrusor overactivity (IDO). Objectives: Describe medium-term outcomes and discontinuation rates for patients adopting repeated BoNTA as a management strategy for IDO. Design, setting, and participants: Prospective data from a single centre were collected from the first 100 patients. Intervention: Bladder injection of BoNTA (predominantly 200 U onabotulinumtoxinA; Allergan Ltd., Marlow, Buckinghamshire, UK) in an outpatient setting. Measurements: OAB symptoms, quality of life, discontinuation rates, interinjection interval, and adverse events were recorded. Data comparisons were performed using a generalised linear model or a chi-square test where appropriate. Results and limitations: Two hundred seven injections were performed in 100 patients. All patients had 1 injection, 53 had a total of 2, 20 had 3, 13 had 4, 10 had 5, 5 had 6, 3 had 7, 1 had 8, 1 had 9, and 1 had 10 injections. Statistics were applied up to five repeated injections. A statistically significant reduction in frequency, urgency, and urge urinary incontinence were seen following the first BoNTA injection compared to baseline. This improvement was maintained after repeated injections and was not statistically different when comparing differences between injections. Thirty-seven patients stopped treatment after the first two injections; thereafter, dropouts were rare. The most common reasons for discontinuing treatment were poor efficacy (13%) and clean intermittent self-catheterisation (CISC)-related issues (11%). The incidence of CISC after the first injection was 35%. Bacteriuria was detected in 21% of patients. The mean interinjection interval was 322 d. Limitations included the concurrent use of antimuscarinic drugs in some patients. Conclusions: BoNTA can provide a safe and effective medium-term management option for patients with refractory IDO. The most common reasons cited for stopping treatment were poor efficacy and CISC-related issues. (C) 2011 European Association of Urology. Published by Elsevier B.V. All rights reserved.

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