Volume 42, Issue 7 pp. 1499-1505
CLINICAL ARTICLE

Predictors for adverse events following intravesical botulinum toxin injections in men

Luis Ribeiro

Corresponding Author

Luis Ribeiro

Department of Urology, St George's University Hospital Foundation Trust, London, UK

Correspondence Luis Ribeiro, Department of Urology, St George's University Hospital Foundation Trust, London, UK.

Email: [email protected]

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Lap Yan Leung

Lap Yan Leung

Department of Urology, Epsom & St Helier Hospital Foundation Trust, London, UK

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Nataniel Tan

Nataniel Tan

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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Zhi-Yang Low

Zhi-Yang Low

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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Mathura Nagarajah

Mathura Nagarajah

Department of Urology, Epsom & St Helier Hospital Foundation Trust, London, UK

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Ghazia Ahmed

Ghazia Ahmed

Department of Urology, Epsom & St Helier Hospital Foundation Trust, London, UK

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Mikaela Carey

Mikaela Carey

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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Samer Sabbagh

Samer Sabbagh

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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Davendra Sharma

Davendra Sharma

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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Roger Walker

Roger Walker

Department of Urology, Epsom & St Helier Hospital Foundation Trust, London, UK

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Tharani Nitkunan

Tharani Nitkunan

Department of Urology, Epsom & St Helier Hospital Foundation Trust, London, UK

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Jai Seth

Jai Seth

Department of Urology, St George's University Hospital Foundation Trust, London, UK

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First published: 29 June 2023

[Correction added on 25 August 2023, after first online publication: Roger Walker and Tharani Nitkunan have been added as co-authors in this version.]

Abstract

Introduction

Intravesical botulinum toxin A (BTX-A) has been long established as treatment for overactive bladder and neurogenic bladder dysfunction. However, most published data are reported among a female cohort. Adverse events such as intermittent self-catheterization (ISC) and urinary tract infections (UTIs) play a large role in discontinuation of therapy. There is currently limited information regarding predictive factors to appropriately counsel male patients.

Materials and Methods

We retrospectively collected data on male patients undergoing their first intravesical BTX-A therapy from January 2016 to July 2021 in two high-volume centers. Data included demographics, past medical and surgical history, and urodynamic parameters. Patients were excluded if they had a long-term catheter or ISC before initiation of therapy.

Results

A total of 69 men were included in the study with a median age of 66 years. There were 18 patients with neurogenic bladder dysfunction. Thirty men had urge incontinence secondary to radical prostatectomy or bladder outflow surgery. Overall rates of ISC were 43.5%. Predictors for ISC included a baseline postvoid residual (PVR) ≥ 50 mL (odds ratio [OR]: 4.2, 95% confidence interval [CI]: 1.36–13.03, p = 0.01), BTX-A dose >100 units (OR: 4.2, 95% CI: 1.36–13.0, p = 0.01). Stress urinary incontinence was protective against ISC (OR: 0.20, 95% CI: 0.04–1.00, p = 0.049) as well as history of prostatectomy/bladder outflow obstruction (BOO) surgery (OR: 0.16, 95% CI: 0.05–0.47, p < 0.001). A multivariable logistic regression model with these factors yielded a c-statistic of 0.80 (optimism-adjusted = 0.75). An enlarged prostate was the only predictor for UTI among our male cohort (OR: 8.0, 95% CI: 2.03–31.5, p = 0.003).

Conclusions

This is the first study assessing risk factors of adverse events among men following BTX-A injection. High PVR and BTX-A dose of >100U were predictors of requiring ISC after BTX-A. Stress incontinence, previous radical prostatectomy, and BOO surgery were all protective against needing ISC post-BTX-A. An enlarged prostate was associated with development of UTI. These factors can be used to assist in counseling male patients regarding their risk of ISC and UTI.

CONFLICT OF INTEREST STATEMENT

The authors declare no conflict of interest.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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