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静脉注射单次推注剂量的昂丹司琼预防术后恶心和呕吐。

Single i.v. bolus dose of ondansetron in the prevention of postoperative nausea and emesis.

作者信息

Moens P, Levarlet M, Hendrickx P, De Guchteneere E

机构信息

Cliniques Universitaires de Bruxelles, Hôpital Erasme.

出版信息

Acta Anaesthesiol Belg. 1997;48(4):245-50.

PMID:9526603
Abstract

In this placebo controlled, double blind multicentre study, the efficacy and safety of a single i.v. bolus dose of ondansetron 4 mg were evaluated in the prevention of postoperative nausea and vomiting (PONV), which remains one of the most unpleasant side effects experienced by patients postoperatively. The study population included patients having general anesthesia and undergoing major gynecological or elective abdominal surgery by laparoscopy. Thirty three percent of placebo-treated patients had at least one emetic episode over 24 hrs compared with 21% in the ondansetron group (p = 0.03). Forty two percent of placebo-treated patients experienced nausea in the 24 hours post-recovery period, compared to 27% of patients treated with ondansetron 4 mg (p = 0.01). Several factors appeared to be associated with an increased risk of developing PONV, namely gender (female), type of surgery (gynecological), experience of previous PONV and duration of anesthesia; the use of propofol was not a significant factor. Ondansetron was well tolerated, with no side effect being reported as a significant problem.

摘要

在这项安慰剂对照、双盲多中心研究中,评估了静脉注射4毫克昂丹司琼单次推注剂量预防术后恶心和呕吐(PONV)的有效性和安全性,术后恶心和呕吐仍是患者术后经历的最令人不适的副作用之一。研究人群包括接受全身麻醉并通过腹腔镜进行大型妇科手术或择期腹部手术的患者。24小时内,33%接受安慰剂治疗的患者至少有一次呕吐发作,而昂丹司琼组为21%(p = 0.03)。恢复后24小时内,42%接受安慰剂治疗的患者出现恶心,而接受4毫克昂丹司琼治疗的患者为27%(p = 0.01)。几个因素似乎与发生PONV的风险增加有关,即性别(女性)、手术类型(妇科)、既往PONV经历和麻醉持续时间;丙泊酚的使用不是一个重要因素。昂丹司琼耐受性良好,未报告有副作用是一个重大问题。

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