Sm. Di Stasi et al., Intravesical electromotive administration of oxybutynin in patients with detrusor hyperreflexia unresponsive to standard anticholinergic regimens, J UROL, 165(2), 2001, pp. 491-498
Purpose: About 15% to 20% of patients with detrusor hyperreflexia do not be
nefit from oral oxybutynin regimens, frequently because of unpleasant side
effects. Several reports indicate that intravesical oxybutynin is effective
in many of these patients but there are some who still fail to respond.
Materials and Methods: A select group of 10 adults with detrusor hyperrefle
xia unresponsive to standard oral and intravesical oxybutynin regimens were
treated at weekly intervals with 5 mg. oxybutynin orally, or 5 mg. oxybuty
nin in 100 ml. intravesically for 60 minutes of passive diffusion and for 3
0 minutes with 5 mA.. electrical current. Each treatment (plus oral placebo
and 2 intravesical controls) was associated with an 8-hour, full urodynami
c monitoring session, and periodic blood and bladder content sampling.
Results: There was no significant objective improvement with oral or intrav
esical passive diffusion oxybutynin. Conversely there was significant impro
vement in 5 of 6 objective urodynamic measurements with intravesical electr
omotive oxybutynin. Plasma profiles were a single peak and decay following
oral oxybutynin and 2 distinct peaks with intravesical passive diffusion an
d electromotive oxybutynin. Area under the curve for intravesical passive d
iffusion were 709 ng. per 8 hours versus oral 1,485 (p <0.05) versus intrav
esical electromotive 2,781 (p <0.001). Bladder content samples confirmed ox
ybutynin absorption. Oral oxybutynin caused anticholinergic side effects in
7 of 10 patients. There were no side effects with intravesical passive dif
fusion or electromotive administrations.
Conclusions: Accelerated intravesical administration results in greater bio
availability and increased objective benefits without side effects in previ
ously unresponsive patients compared with oral and intravesical passive dif
fusion oxybutynin administration.