Fujii Y, Toyooka H, Tanaka H
Department of Anaesthesiology and Critical Care Medicine, Tokyo Medical and Dental University School of Medicine, Japan.
Can J Anaesth. 1996 Feb;43(2):110-4. doi: 10.1007/BF03011250.
This randomized, placebo-controlled, double-blind study was to evaluate the effects of granisetron, a selective 5-hydroxytryptamine type 3 receptor antagonist, for preventing postoperative nausea and vomiting in 110 patients with (n = 50) and without (n = 60) a history of motion sickness undergoing general anaesthesia for major gynaecological surgery.
The patients received a single dose of either granisetron (40 micrograms.kg-1) or placebo (saline) iv over 2-5 min immediately before induction of anaesthesia. Postoperatively, during the first 24 hr after anaesthesia, the frequencies of nausea and vomiting were recorded.
Except for a positive history of motion sickness, the treatment groups were similar for patient characteristics, types of surgery, anaesthetics administered and opioids given. Postoperatively, the frequency of nausea was 44% and 16% after administration of placebo and granisetron in patients with motion sickness, and was 30% and 7% in patients without it, respectively; the corresponding frequencies of vomiting were 28%, 8%, 13% and 3%. The incidence of adverse events postoperatively were not different among the groups.
These results suggest that preoperative prophylactic administration of granisetron is effective and safe for preventing postoperative nausea and vomiting in patients with motion sickness as well as in patients without it.
本随机、安慰剂对照、双盲研究旨在评估选择性5-羟色胺3型受体拮抗剂格拉司琼对110例行妇科大手术全身麻醉且有晕动病史(n = 50)和无晕动病史(n = 60)患者术后恶心和呕吐的预防效果。
患者在麻醉诱导前2 - 5分钟内静脉注射单剂量格拉司琼(40微克·千克⁻¹)或安慰剂(生理盐水)。术后,在麻醉后的头24小时内记录恶心和呕吐的发生频率。
除晕动病史外,治疗组在患者特征、手术类型、所用麻醉剂和给予的阿片类药物方面相似。术后,有晕动病史的患者服用安慰剂和格拉司琼后恶心发生率分别为44%和16%,无晕动病史的患者分别为30%和7%;相应的呕吐发生率分别为28%、8%、13%和3%。术后不良事件发生率在各组间无差异。
这些结果表明,术前预防性给予格拉司琼对预防有晕动病史和无晕动病史患者的术后恶心和呕吐均有效且安全。