Efficacy of Antibiotic Prophylaxis in Botulinum Toxin Injections into the Bladder Wall Under Local Anaesthesia: A Comparison of a Single Dose of Ciprofloxacin vs. a Full Course of Trimethoprim

Farag A1, Manandhar A1

Research Type

Clinical

Abstract Category

Overactive Bladder

Abstract 495
Open Discussion ePosters
Scientific Open Discussion Session 104
Friday 19th September 2025
10:45 - 10:50 (ePoster Station 2)
Exhibition
Overactive Bladder Clinical Trial Detrusor Overactivity
1. University Hospitals of Birmingham NHS Trust
Presenter
Links

Abstract

Hypothesis / aims of study
This study aims to evaluate and directly compare the efficacy of a single dose of Ciprofloxacin (500 mg) with a full course of Trimethoprim (5 days) as antibiotic prophylaxis following botulinum toxin injections into the bladder wall under local anaesthesia.
Study design, materials and methods
A cohort of patients referred between October 2022 and April 2023 was included in the study. Follow-up assessments were conducted at 2 weeks post-procedure. Inclusion criteria comprised patients undergoing botulinum toxin injections, while exclusion criteria involved individuals with intermittent self-catheterization (ISC), long-term catheters (LTC), known hypersensitivity to Ciprofloxacin, or those with microorganisms resistant to Ciprofloxacin in prior mid-stream urine (MSU) cultures
Results
Fifty-six patients (37 females, 19 males) were included in the study, receiving a single dose of Ciprofloxacin (500 mg) immediately post-procedure. Of these, 5 patients (3 females, 2 males) developed a urinary tract infection (UTI), representing 8.9% of the cohort. Notably, 4 of these 5 patients had previously received a 5-day course of Trimethoprim after prior botulinum toxin injections and did not experience UTIs.

In a second cohort of 40 patients (29 females, 11 males) with a history of prior botulinum toxin injections into the bladder wall, a 5-day course of Trimethoprim was administered post-procedure. Of these, 3 patients (2 females, 1 male) developed a UTI, corresponding to 7.5% of the cohort. None of these 3 patients had a UTI after receiving Ciprofloxacin post-procedure in the prior intervention.
Interpretation of results
The results suggest that both a single dose of Ciprofloxacin and a 5-day course of Trimethoprim are effective in preventing UTIs following botulinum toxin injections into the bladder wall. The incidence of UTIs observed in both groups (8.9% for Ciprofloxacin and 7.5% for Trimethoprim) was comparable, indicating that a single dose of Ciprofloxacin may be just as effective as a prolonged course of Trimethoprim. These findings imply that a single dose of Ciprofloxacin could be a viable alternative to a full course of Trimethoprim, potentially offering a more convenient and cost-effective option for antibiotic prophylaxis in this clinical setting.
Concluding message
A single dose of Ciprofloxacin (500 mg) administered post-procedure demonstrated comparable efficacy to a 5-day course of Trimethoprim in preventing post-procedural UTIs following botulinum toxin injections into the bladder wall under local anaesthesia. Neither regimen showed superiority or inferiority over the other in terms of UTI prevention.
Disclosures
Funding no funding Clinical Trial Yes Public Registry No RCT No Subjects Human Ethics Committee UHB NHS Trust Audit Committe Helsinki Yes Informed Consent No
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