Dosage escalation of intravesical oxybutynin in the treatment of neurogenic bladder patients

Citation
A. Haferkamp et al., Dosage escalation of intravesical oxybutynin in the treatment of neurogenic bladder patients, SPINAL CORD, 38(4), 2000, pp. 250-254
Citations number
21
Categorie Soggetti
Neurology
Journal title
SPINAL CORD
ISSN journal
13624393 → ACNP
Volume
38
Issue
4
Year of publication
2000
Pages
250 - 254
Database
ISI
SICI code
1362-4393(200004)38:4<250:DEOIOI>2.0.ZU;2-V
Abstract
Objective: We prospectively analyzed the dose dependent outcome and side ef fects of neurogenic bladder patients with intravesical application of oxybu tynin at our centre. Materials and methods: We examined the data of 32 patients with neurogenic bladders and detrusor hyperreflexia. We registered clinical outcome, contin ence situation, side effects and urodynamic data of patients with (A) stand ard dosages of intravesical oxybutynin (0.3 mg/kg bodyweight per day) and ( B) with increasing dosages in steps of 0.3 mg/kg bodyweight pur day up to 0 .9 mg/kg bodyweight per day. Results: We examined 32 patients aged 1 to 34 years, mean age 12 years. 21/ 33 patients became totally continent with the dosage (A). They showed a sig nificant (P<0.01) decrease in the median max detrusor pressure (MDP) and a significant (P<0.01) increase in the median compliance and the median age a djusted bladder capacity (AABC). Eleven out of 32 patients remained inconti nent under this dosage (A). Their median MDP, their median compliance and t heir median AABC remained nearly unchanged. Seven out of 11 incontinent pat ients under dosage (A) were treated efficiently with the higher dosages (B) . Their median necessary dosage escalation to achieve treatment success was 0.7 mg/kg bodyweight per day (range 0.5 to 0.9 mg/kg bodyweight per day). Their median MDP was significantly (P < 0.05) decreased and their median co mpliance and median AABC were significantly (P<0.05) increased. Four out of 11 patients remained incontinent and showed only little improvement in uro dynamic data. Two out of 11 patients with the dosage escalation (B) showed side effects at a dosage of 0.9 mg/kg bodyweight per day. Conclusions: The intravesical application of oxybutynin was a well tolerate d and efficacious therapy. The topical oxybutynin therapy dosage (A) was ef ficient in 66% of our selected patients, the escalating dosage titration (B ) could increase the efficiency to 87%.