• Anaesth Intensive Care · Aug 1998

    Randomized Controlled Trial Clinical Trial

    Lack of efficacy of propofol in the treatment of early postoperative nausea and vomiting.

    • I Harper, E Della-Marta, H Owen, J Plummer, and A Ilsley.
    • Department of Anaesthesia, Flinders Medical Centre, Bedford Park, South Australia.
    • Anaesth Intensive Care. 1998 Aug 1;26(4):366-70.

    AbstractThe anti-nauseant efficacy of low-dose propofol was investigated in a blinded, randomized trial. Patients who complained of nausea and/or vomiting following laparoscopic gynaecological surgery and who requested antiemetic were randomly assigned to receive placebo, propofol 3 mg, propofol 9 mg or propofol 27 mg by intravenous injection. Nausea, vomiting and sedation were recorded by a blinded observer for 90 minutes following administration of the test drug, prior to discharge, and 24 hours following surgery. Rescue antiemetic (droperidol 1.0 mg i.v.) was available from 10 minutes after administration of test drug. Propofol failed to reduce nausea scores and did not reduce the incidence of vomiting. Numbers of patients receiving rescue antiemetic were similar in the four treatment groups. In the first 10 minutes following test drug administration, sedation scores were increased by propofol in a dose-related manner. We conclude that, in the dose range studied, propofol is ineffective for the treatment of nausea and vomiting occurring soon after laparoscopic gynaecological surgery.

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