We used a double-blind design to study urodynamic changes induced by m
u-agonists (fentanyl, morphine), a partial mu-agonist antagonist (bupr
enorphine), a putative CL-antagonist, K-agonist (nalbuphine), and keto
profen, an injectable nonsteroidal antiinflammatory drug. Men (20-55 y
r old) were randomly assigned to receive one of the following IV befor
e anesthesia for endoscopic extraction of a ureteral stone: 10 mg of m
orphine, 0.3 mg of buprenorphine, 0.35 mg of fentanyl, 20 mg of nalbup
hine, 100 mg of ketoprofen, or 10 mt of 0.9% sodium chloride. The urod
ynamic study consisted of cystometry followed by urethral pressure pro
file. Measurements were taken before the TV infusion of drugs and 15 m
in thereafter. Statistical comparisons were performed by using analysi
s of variance with repeated measurements (P < 0.05). Ketoprofen and sa
line did not induce any urodynamic changes. Opioids altered bladder se
nsations, and the residual volume after voiding increased, except afte
r morphine. Detrusor contraction decreased only after the administrati
on of fentanyl and buprenorphine. Some patients could not micturate af
ter receiving morphine, fentanyl, and buprenorphine. Compliance and ur
ethral pressures did not change with any drug. This study suggests tha
t ketoprofen and nalbuphine are useful analgesics in terms of their ur
odynamics. Implications: We compared the urodynamic effects of opioids
and ketoprofen used as analgesics in surgical patients. In contrast t
o ketoprofen, opioids altered urodynamics. The opioid nalbuphine had n
o effect on detrusor contraction. This study suggests that ketoprofen
and nalbuphine are useful analgesics in terms of their urodynamics.