Study objective: Ketoprofen exerts its clinical effect by inhibition o
f prostaglandin synthesis, but also acts as an NMDA-receptor antagonis
t by means of the kynurenic acid. Based on ketoprofen's supposed centr
al mechanism of analgesia, we expected a preemptive effect, which was
assessed by the present study. Methods: In a prospective, randomised,
double-blind investigation of 48 patients undergoing gynaecological pr
ocedures (la parotomy, pelvioscopy), the first group received ketoprof
en 2 mg/kg body weight i.v. 20 min before the beginning of surgery and
placebo i.v. at the end of surgery. In the second group, placebo was
administered first and ketoprofen al the end of surgery. Premedication
and anaesthesia were standardised by protocol. The postoperative anal
gesic patient-controlled analgesia consumption by was also standardise
d (piritramide). Efficacy was assessed by visual analogue scale (VAS)
and total requirement of analgesics within the first 24 postoperative
hours. The time to the first request for postoperative analgesics was
also recorded. Safety was assessed by continous monitoring of vital pa
rameters such as respiratory rate, heart rate, blood pressure, and oxy
gen saturation. The incidence and severity of adverse events was docum
ented. Results: There were no significant differences between the grou
ps in demographic data or type or duration of surgery. The time to the
first request for analgesic,VAS pain intensity, and analgesic consump
tion in the first 24 h post-surgery were not significantly different b
etween the groups (t-test). Conclusion: Ketoprofen is an effective pos
toperative analgesic in combination with an opioid, but has no pre-emp
tive effect according to the results of this study.