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鼻腔内芬太尼与安慰剂在儿童排尿性膀胱尿道造影导管插入术疼痛中的比较。

Intranasal fentanyl versus placebo for pain in children during catheterization for voiding cystourethrography.

机构信息

Division of Pediatric Emergency Medicine, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.

出版信息

Pediatr Radiol. 2010 Jul;40(7):1236-40. doi: 10.1007/s00247-009-1521-1. Epub 2010 Feb 24.

Abstract

BACKGROUND

Voiding cystourethrogram (VCUG) is a common procedure at pediatric tertiary care centres that can be painful as it involves a urinary catheter. Currently there are no widely utilized protocols for non-topical medications to decrease pain that children feel during catheterization.

OBJECTIVE

To determine if intranasal (IN) fentanyl is effective at decreasing pain that children feel during catheterization of VCUG when compared with sterile water.

MATERIALS AND METHODS

We performed a double-blind randomized controlled trial, using IN fentanyl (2 microg/kg) compared to placebo (sterile water,) in children 4-8 years of age scheduled for elective VCUG in one urban pediatric tertiary center.

RESULTS

Using the Face Pain Score-Revised, children receiving IN fentanyl scored 2.58 (1.93-3.25 95% CI) while those receiving sterile water scored 2.86 (2.20-3.51 95% CI) showing no statistically significant difference. There were no adverse events.

CONCLUSIONS

Although we were unable to show a statistically significant difference between our study and control groups, we believe that this may be due to technique (positioning, delivery device) and timing of administration of IN fentanyl as well as multi-factorial causes of distress during VCUG. Future studies investigating alternative delivery techniques of IN fentanyl for analgesia during VCUG may yield more promising results.

摘要

背景

排尿性膀胱尿道造影(VCUG)是儿科三级保健中心的常见程序,由于涉及导尿管,因此可能会引起疼痛。目前,尚无广泛使用的非局部药物方案来减轻儿童在导尿过程中的疼痛。

目的

确定与无菌水相比,鼻内(IN)芬太尼是否可有效减轻接受 VCUG 导管插入术的儿童的疼痛。

材料和方法

我们在一家城市儿科三级中心进行了一项双盲随机对照试验,比较了 IN 芬太尼(2μg/kg)与安慰剂(无菌水)在 4-8 岁接受选择性 VCUG 的儿童中的作用。

结果

使用面部疼痛评分修订版,接受 IN 芬太尼的儿童得分为 2.58(95%CI 2.20-3.51),而接受无菌水的儿童得分为 2.86(95%CI 2.20-3.51),无统计学差异。没有不良事件。

结论

尽管我们无法显示研究组和对照组之间存在统计学差异,但我们认为这可能是由于 IN 芬太尼的技术(定位、给药装置)和给药时间以及 VCUG 期间多因素引起的痛苦所致。未来研究调查 IN 芬太尼在 VCUG 期间镇痛的替代给药技术可能会产生更有希望的结果。

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