Systematic review of ondansetron for the prevention and treatment of postoperative nausea and vomiting in adults.

F Cox
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Abstract

Objectives: To determine the efficacy and safety of ondansetron for the prevention and treatment of postoperative nausea and vomiting (PONV) in adults.

Design: Systematic review of published double-blind randomised controlled trials.

Data sources: Twenty seven trials from 1990 to July 1998 retrieved from a systematic literature search (Medline, Cinahl, Embase, Cochrane Library, reference lists, hand searching of anaesthetic journals, & provided manufacturer information); restricted to English language.

Main outcome measures: Estimation of efficacy (incidence of complete absence of nausea or other outcome measure as defined by the authors) at 24 hours.

Results: Seven double-blind randomised controlled trials with 1,623 patients studied intravenous ondansetron 1 mg, 4 mg, or 8 mg for the treatment of postoperative nausea and vomiting (PONV). Four mg, compared with metoclopramide 10 mg, produced higher patient satisfaction scores and an increased incidence of freedom from nausea at 24 hours. Further studies are required to compare the safety, efficacy and dose response with other anti-emetics at 24 hours. Twenty double-blind randomised controlled trials with 4,364 patients studied intravenous and oral administration of ondansetron 1 mg, 4 mg, and 8 mg for the prevention of postoperative nausea and vomiting. There appears to be no significant difference between droperidol (0.625 mg, 1 mg or 1.25 mg) i.v. and ondansetron 4 mg in efficacy and incidence of side effects. Compared with metoclopramide, ondansetron produced less nausea but the incidence of vomiting was the same at 24 hours.

Conclusions: Further PONV could be prevented with ondansetron 4 mg compared with placebo and metoclopramide 10 mg. Further studies are required to compare ondansetron with other anti-emetics for the treatment of PONV. For prophylaxis of PONV ondansetron 4 mg appears to be equal to low dose droperidol in efficacy and the incidence of side effects, and superior to metoclopramide. Ondansetron should perhaps be limited to second line treatment in view of patient satisfaction, efficacy and cost when compared with droperidol.

昂丹司琼预防和治疗成人术后恶心呕吐的系统评价。
目的:探讨昂丹司琼预防和治疗成人术后恶心呕吐(PONV)的有效性和安全性。设计:对已发表的双盲随机对照试验进行系统评价。数据来源:从系统文献检索(Medline, Cinahl, Embase, Cochrane Library,参考文献列表,手工检索麻醉期刊和提供的制造商信息)中检索1990年至1998年7月的27项试验;仅限于英语。主要结局指标:24小时的疗效评估(恶心完全消失的发生率或作者定义的其他结局指标)。结果:7项双盲随机对照试验纳入1623例患者,研究了静脉注射昂丹司琼1mg、4mg或8mg治疗术后恶心和呕吐(PONV)。与甲氧氯普胺10毫克相比,4毫克的患者满意度评分更高,24小时内不恶心的发生率增加。需要进一步的研究来比较24小时内与其他止吐药的安全性、有效性和剂量反应。20项涉及4364例患者的双盲随机对照试验研究了静脉和口服昂丹司琼1mg、4mg和8mg预防术后恶心和呕吐的效果。静脉注射氟哌啶醇(0.625 mg, 1 mg或1.25 mg)和昂丹司琼(4 mg)在疗效和副作用发生率方面似乎没有显著差异。与甲氧氯普胺相比,昂丹司琼的恶心程度较轻,但24小时呕吐发生率相同。结论:与安慰剂和甲氧氯普胺10 mg相比,昂丹司琼4 mg可以预防进一步的PONV。需要进一步的研究来比较昂丹司琼与其他止吐剂治疗PONV的效果。对于PONV的预防,昂丹司琼4mg在疗效和副作用发生率上与低剂量哌啶醇相当,优于甲氧氯普胺。与氟哌啶醇相比,考虑到患者满意度、疗效和成本,昂丹司琼可能应局限于二线治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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