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Real-World Retention Rates After Intravesical OnabotulinumtoxinA for Idiopathic Overactive Bladder
Daniel Liberman1, Olufenwa Milhouse, Marta Johnson-Mitchell
1From Metro Urology, Woodbury, MN.
Symptomatic urinary retention requiring catheterization after onabotulinumtoxinA (BoNT-A) for overactive bladder occurred in 20.3% of patients in a private practice. This rate is higher than in clinical trials, necessitating careful patient counseling on BoNT-A risks.
Area of Science:
- Urology
- Pharmacology
Background:
- Intravesical onabotulinumtoxinA (BoNT-A) is used for idiopathic overactive bladder.
- Incomplete bladder evacuation requiring catheterization is a known risk of BoNT-A, but reported rates vary and are generally low in clinical trials.
Purpose of the Study:
- To evaluate the rate of symptomatic acute urinary retention requiring catheterization after initial intravesical BoNT-A in a private practice setting for patients with idiopathic overactive bladder.
Main Methods:
- Retrospective study of 103 patients with idiopathic overactive bladder receiving their first intravesical BoNT-A from 2010 to 2014.
- Data collected included demographics, baseline postvoid residual (PVR), urodynamic findings, and BoNT-A dose.
- Urinary retention defined as symptomatic and requiring catheterization for PVR ≥ 200 mL.
Main Results:
- 20.3% (21/103) of patients developed symptomatic retention requiring catheterization.
- No significant differences in baseline characteristics or injected BoNT-A dose were found between groups.
- The retention group had a higher incidence of bacteriuria and symptomatic urinary tract infections.
Conclusions:
- The rate of catheterization due to urinary retention after initial intravesical BoNT-A appears higher in a private practice setting compared to clinical trials.
- This finding is crucial for accurately counseling patients on the potential risks and benefits of BoNT-A therapy.
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