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雷莫司琼与雷莫司琼联合咪达唑仑预防儿童术后恶心呕吐的效果比较:一项双盲、随机临床试验。

Comparison of the antiemetic effect of ramosetron and combined ramosetron and midazolam in children: a double-blind, randomised clinical trial.

机构信息

Department of Anesthesiology and Pain Medicine, Seoul National University College of Medicine, Seoul, Korea.

出版信息

Eur J Anaesthesiol. 2012 Apr;29(4):192-6. doi: 10.1097/EJA.0b013e32834fc1fb.

Abstract

CONTEXT

Postoperative nausea and vomiting remains a clinically important problem after strabismus surgery in children.

OBJECTIVE

To study the benefit of adding midazolam to ramosetron on the incidence of postoperative nausea, retching or vomiting and on the incidence of postoperative agitation.

DESIGN

A randomised, double-blind comparison.

SETTING

The operating theatre suite and day care unit of Seoul National University Hospital. The study period was January to December 2010.

PATIENTS

In total, 405 paediatric patients (aged 4-12 years) undergoing strabismus surgery were enrolled and randomly assigned to one of two groups, ramosetron or ramosetron with midazolam.

INTERVENTION

Patients received either ramosetron 6 μg kg or ramosetron 6 μg kg and midazolam 0.1 mg kg prior to induction of anaesthesia.

MAIN OUTCOME MEASURES

The incidences of nausea, retching or vomiting in the first 48 h after surgery, and the incidence of emergence agitation in the post-anaesthetic care unit.

RESULT

The incidences of nausea, retching or vomiting during the first and second 24-h periods after surgery were similar in the two groups. There was a small, clinically insignificant reduction in delirium scores in the ramosetron with midazolam group.

CONCLUSION

Adding midazolam to ramosetron had no advantages over ramosetron alone in reducing the incidence of postoperative nausea and vomiting in children undergoing strabismus surgery.

摘要

背景

斜视手术后,患儿仍存在术后恶心和呕吐这一重要的临床问题。

目的

研究在雷莫司琼中添加咪达唑仑对斜视手术后恶心、呕吐或干呕的发生率和术后激越的发生率的影响。

设计

随机、双盲对照研究。

地点

首尔国立大学医院的手术室和日间护理病房。研究期间为 2010 年 1 月至 12 月。

患者

共有 405 名(年龄 4-12 岁)接受斜视手术的小儿患者入组,并随机分为雷莫司琼组或雷莫司琼联合咪达唑仑组。

干预

患者在麻醉诱导前分别接受雷莫司琼 6μg/kg 或雷莫司琼 6μg/kg 联合咪达唑仑 0.1mg/kg。

主要观察指标

术后 48 小时内恶心、呕吐或干呕的发生率,以及麻醉后护理单元的激越发生率。

结果

两组患者在术后第 1 天和第 2 天的恶心、呕吐或干呕发生率相似。咪达唑仑联合雷莫司琼组的谵妄评分略有降低,但无统计学意义。

结论

在斜视手术患儿中,与单独使用雷莫司琼相比,在降低术后恶心和呕吐发生率方面,雷莫司琼联合咪达唑仑并无优势。

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