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Intravesical treatment of overactive bladder
1Department of Uro-Neurology, National Hospital for Neurology and Neurosurgery, UCLH, Institute of Neurology, University College London, London, United Kingdom.
Urology
|April 18, 2000
Summary
Intravesical agents offer a targeted approach for overactive bladder, particularly neurogenic detrusor hyperreflexia (DH). These treatments aim to reduce bladder overactivity by blocking nerve signals or de-afferenting the bladder.
Area of Science:
- Urology
- Pharmacology
- Neuroscience
Background:
- Intravesical agents are primarily used for neurogenic bladder disorders with severe detrusor hyperreflexia (DH) and incomplete emptying.
- Patients often perform intermittent self-catheterization due to residual urine, making intravesical medication suitable.
- Current strategies focus on reducing parasympathetic efferent activity or de-afferenting the bladder.
Purpose of the Study:
- To review the use and potential of intravesical agents for treating detrusor hyperreflexia (DH).
- To explore mechanisms of action, including cholinergic blockade and afferent nerve modulation.
- To evaluate specific agents like oxybutynin, atropine, local anesthetics, capsaicin, and resiniferatoxin (RTX).
Main Methods:
- Review of existing literature on intravesical treatments for overactive bladder and detrusor hyperreflexia (DH).
- Discussion of pharmacological mechanisms, including cholinergic transmission blockade and afferent pathway targeting.
- Comparison of different intravesical agents based on efficacy, duration, and side effect profiles.
Main Results:
- Intravesical oxybutynin shows effectiveness in resistant DH, potentially via local anesthetic and cholinergic blockade.
- Intravesical atropine may increase bladder capacity, but clinical utility for DH requires further study.
- Capsaicin and its analog RTX target capsaicin-sensitive bladder afferents, with RTX offering a non-irritant profile.
Conclusions:
- Intravesical agents provide an alternative to oral medications for overactive bladder and DH.
- These agents offer the potential for targeted therapy by selectively affecting implicated end organs.
- Further research is needed to fully establish the clinical role of agents like atropine, capsaicin, and RTX.