This double-blind study enrolled 120 female patients who were scheduled for gynecologic surgery under general anesthesia. Patients were randomly allocated to one of three groups (n =40 for each group). The concentration of naloxone and morphine respectively was 0 μg/mL and 1 mg/mL in group 1, 0.1 μg/mL and 1 mg/mL in group 2 (1:10,000), and 1 μg/mL and 1 mg/mL in group 3 (1:1000). Morphine consumption, verbal rating score of wound pain at rest and with exertion, and morphine-related side effects were investigated at 1, 2, 4 and 24 hours postoperatively.
A total of 112 patients completed the study (37 in group 1, 36 in group 2, 39 in group 3). The in-cidence of nausea during the postoperative 4–24 hours was significantly lower in group 3 than in group 1 (23.1 % vs. 56.8 % , p <0.05). Furthermore, the overall incidence of severe nausea was significantly lower in group 3 than in group 1 (2.6 % vs. 24.3 % , p <0.05) as was the rescue antiemetic requirements (5.1 % vs. 24.3 % , p <0.05). However, there were no significant differences between groups 2 and 1. The pain scores (at rest and with exertion) and 24-hour morphine consumption were not significantly different among the three groups.
The antiemetic efficacy of ultralow-dose naloxone combined with PCA morphine is limited by a cut-off ratio of naloxone to morphine of 1:10,000.