Evidence map›Paper›PMID 42682053›Full record

ArticleThe Canadian journal of urology2026

Clinical and urodynamic indicators of non-response to OnabotulinumtoxinA in idiopathic overactive bladder.

Samer Shamout, Hani Kabbara, Claudia Covarrubias, Jacques Corcos, Lysanne Campeau

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Article in The Canadian journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Samer ShamoutDivision of Urology, Department of Surgery, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Hani KabbaraStatistical Research and Analysis Consultancy Firm (Statrac), Montreal, QC, Canada.
Claudia CovarrubiasLady Davis Institute, Jewish General Hospital, Montreal, QC, Canada.
Jacques CorcosDivision of Urology, Department of Surgery, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Lysanne CampeauDivision of Urology, Department of Surgery, Jewish General Hospital, McGill University, Montreal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOnabotulinum toxin-A (BoNT/A) intradetrusor injection is an established, effective, and safe treatment for overactive bladder (OAB) refractory to anticholinergics. Although primary non-response to BoNT/A is infrequent, it remains clinically relevant. We investigated whether baseline clinical, demographic, or urodynamic characteristics could predict non-responders prior to treatment.

methodsA Retrospective analysis of 65 consecutive refractory idiopathic OAB (I-OAB) male and female patients treated with 100 U BoNT/A at Jewish General Hospital between 2005 and 2015 was conducted. Response defined as >30% increase in maximum cystometric bladder capacity (MCBC) at 12 weeks, confirmed clinically and through urodynamic studies (UDS). Non-response was verified by lack of improvement after the second intradetrusor injection.

resultsA total of 13 men and 52 women with a mean age of 70 years (range 21 to 94) were studied. At 12 weeks, 63% (41/65) of patients demonstrated a significant response in both symptoms and UDS (p < 0.05), while 37% (24/65) were non-responders. Non-responders exhibited significantly higher baseline first desire to void volume (FDV) and postvoid residual urine (PVR) (p < 0.05), with a trend toward greater bladder compliance (18.8 ± 15.1 vs. 13.3 ± 9.4 cmH2O, p = 0.09). Multivariate logistic regression identified no independent predictors of response.

conclusionsElevated baseline FDV and PVR are associated with poor response to 100 U BoNT/A in refractory I-OAB patients.

Indexed as

Acetylcholine Release InhibitorsBotulinum Toxins, Type ANeuromuscular AgentsUrinary Bladder, OveractiveUrodynamicsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment FailureYoung AdultAcetylcholine Release InhibitorsBotulinum Toxins, Type ANeuromuscular Agentsonabotulinum toxin ABotoxBotulinum toxinidiopathic overactive bladderpredictorsurodynamic study

Identifiers

PMID42682053

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.