The morphine sparing effects of diclofenac sodium following abdominal surgery

Anaesthesia. 1987 Sep;42(9):1005-8. doi: 10.1111/j.1365-2044.1987.tb05377.x.


A randomised, double-blind placebo controlled study was undertaken to assess the analgesic efficacy of diclofenac. Following major abdominal surgery and 12 hours later, patients received either placebo or diclofenac 75 mg intramuscularly and their cumulative morphine requirements administered by a patient-controlled system over 24 hours were compared. Pain scores were also measured. Arterial blood gases and coagulation studies were assessed pre- and postoperatively. Morphine consumption was significantly greater in the placebo group (59.5 compared to 38.5 mg, p less than 0.01). Pain scores were significantly lower in the diclofenac group at 4 hours, but not thereafter. Arterial carbon dioxide was significantly increased in the control groups. There was no significant change in platelet count within each group, but a significant difference between the groups (p less than 0.05).

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen / surgery
  • Adolescent
  • Adult
  • Aged
  • Carbon Dioxide / blood
  • Diclofenac / therapeutic use*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Morphine / administration & dosage*
  • Pain Measurement
  • Pain, Postoperative / drug therapy*
  • Platelet Count
  • Random Allocation


  • Carbon Dioxide
  • Diclofenac
  • Morphine