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术中局部麻醉以减轻儿童和青少年牙科治疗全身麻醉后的术后疼痛。

Intraoperative local anaesthesia for reduction of postoperative pain following general anaesthesia for dental treatment in children and adolescents.

作者信息

Parekh Susan, Gardener Collette, Ashley Paul F, Walsh Tanya

机构信息

Unit of Paediatric Dentistry, Department of Craniofacial Growth and Development, UCL Eastman Dental Institute, 256 Gray's Inn Road, London, WC1X 8LD, UK.

出版信息

Cochrane Database Syst Rev. 2014 Dec 23;2014(12):CD009742. doi: 10.1002/14651858.CD009742.pub2.

Abstract

BACKGROUND

Whilst carrying out dental procedures under general anaesthesia (GA), practitioners routinely give local anaesthetics (LA) intraoperatively to children. Local anaesthetics are used to help manage postoperative pain and reduce bleeding and the physiological response to procedures. Studies of effectiveness of intraoperative LA to date have reported contradictory results.

OBJECTIVES

To assess the effects of intraoperative local anaesthesia for reducing postoperative pain following general anaesthesia for dental treatment in children and young people aged 17 years or younger.

SEARCH METHODS

We searched the following electronic databases: the Cochrane Oral Health Group Trials Register; the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, 2013, Issue 12), MEDLINE via OVID (1946 to 02 January 2014), EMBASE via OVID (1980 to 02 January 2014) and Web of Science Conference Proceedings (1990 to 02 January 2014). We searched for ongoing trials in the US National Institutes of Health Register, the metaRegister of Controlled Trials (mRCT) and the International Federation of Pharmaceutical Manufacturers & Associations (IFPMA) Clinical Trials Portal. We did not place any restrictions on the language or date of publication when searching the electronic databases.

SELECTION CRITERIA

Randomised controlled trials in which local anaesthetic was given intraoperatively under general anaesthesia for dental treatment of children and young people aged 17 years or younger.

DATA COLLECTION AND ANALYSIS

We used standard methodological procedures expected by The Cochrane Collaboration. We performed data extraction and assessment of risk of bias independently and in duplicate. We contacted authors to clarify omissions in trial reports. In the 'Summary of findings' tables, we elected to report the outcomes pain, distress, postoperative bleeding, and physiological parameters related to the general anaesthetic, as we considered these to be the outcomes of greatest importance to readers of the review.

MAIN RESULTS

We included 14 trials in this review, with 1152 randomised participants. The studies were published between 1990 and 2009 and were conducted in the United Kingdom, Egypt, Saudi Arabia, and the United States. The age of participants ranged from 2 to 40 years. Three studies were at an overall high risk of bias, seven studies were at an unclear risk of bias, and we judged four studies to be at low risk of bias. The clinical heterogeneity of the included studies precluded pooling of studies in terms of method of administration of LA (e.g., intraligamental injection, infiltration injection, or topical delivery) and variation in the use of supplementary analgesics and follow-up time.Of the seven studies where administration of LA was by infiltration injection, six studies (very low-quality body of evidence, 542 participants analysed, 1 study had overall high risk of bias, 4 studies had overall unclear risk of bias, 1 study had overall low risk of bias) measured postoperative pain. The results were equivocal. There was a decrease in bleeding and increase in soft tissue damage in the LA groups, but we did not judge this to be clinically significant.In the 2 studies where administration of LA was by intraligamental injection, there was no difference in mean pain scores, and they did not report any soft tissue damage (very low-quality body of evidence, 115 participants analysed, 1 study had overall high risk of bias, 1 study had overall unclear risk of bias).One 3-armed study (very low-quality body of evidence, 54 participants analysed, overall high risk of bias) compared the effects of intraligamental and infiltration LA injection with no treatment. There was no evidence of a mean difference in pain, distress, or postoperative anxiety among the three groups.Four studies (very low-quality body of evidence, 343 participants analysed, 2 studies had overall low risk of bias, 2 studies had overall unclear risk of bias) evaluated the effects of topical LA compared with no treatment or placebo. One study (overall unclear risk of bias) with a no-treatment comparator reported lower mean pain in the LA group; all other studies reported no difference in mean pain scores. Two studies reported on bleeding (overall unclear risk of bias): One study reported a clinically insignificant increase in bleeding with no treatment; the other reported no difference.None of the studies reported on participant or child satisfaction.

AUTHORS' CONCLUSIONS: In this review, it was difficult to reach firm conclusions as to the benefit of using local anaesthetic for dental treatment under general anaesthesia. The information reported in the included studies was comprehensive and applicable to the review question, but ultimately it was not sufficient to address the objective of the review. We were unable to pool the included studies in a meta-analysis because of substantial variation in outcome measures, interventions, and treatment types. The use of supplementary analgesia further obscured the effect of local anaesthetics.Based on the literature review and the results of this review, we recommend further randomised controlled trials that minimise bias through adequate allocation concealment and blinding of participants and assessors, and assess the effect of intraoperative local anaesthetic on the volume and type of anaesthetic used and on the cardiovascular system in participants receiving supplementary analgesics as well. Researchers should give consideration to the impact of any changes on the health and well-being of the participant and report baseline measures of pain or distress, or both, and preoperative anxiety.

摘要

背景

在全身麻醉(GA)下进行牙科手术时,从业者通常会在术中给儿童使用局部麻醉剂(LA)。局部麻醉剂用于帮助控制术后疼痛、减少出血以及减轻手术引起的生理反应。迄今为止,关于术中使用局部麻醉剂效果的研究报告结果相互矛盾。

目的

评估术中局部麻醉对17岁及以下儿童和青少年牙科治疗全身麻醉后减轻术后疼痛的效果。

检索方法

我们检索了以下电子数据库:Cochrane口腔健康组试验注册库;Cochrane对照试验中央注册库(CENTRAL)(Cochrane图书馆,2013年第12期),通过OVID检索的MEDLINE(1946年至2014年1月2日),通过OVID检索的EMBASE(1980年至2014年1月2日)以及科学网会议论文集(1990年至2014年1月2日)。我们在美国国立卫生研究院注册库、对照试验元注册库(mRCT)和国际制药商协会联合会(IFPMA)临床试验门户中检索正在进行的试验。在检索电子数据库时,我们未对语言或出版日期设置任何限制。

选择标准

随机对照试验,其中在全身麻醉下对17岁及以下儿童和青少年进行牙科治疗时术中给予局部麻醉剂。

数据收集与分析

我们采用了Cochrane协作网期望的标准方法程序。我们独立且重复地进行数据提取和偏倚风险评估。我们联系作者以澄清试验报告中的遗漏之处。在“结果总结”表中,我们选择报告疼痛、痛苦、术后出血以及与全身麻醉相关的生理参数等结果,因为我们认为这些是对本综述读者最重要的结果。

主要结果

我们在本综述中纳入了14项试验,有1152名随机参与者。这些研究发表于1990年至2009年之间,在英国、埃及、沙特阿拉伯和美国进行。参与者年龄范围为2至40岁。三项研究总体偏倚风险高,七项研究偏倚风险不明确,我们判定四项研究偏倚风险低。纳入研究的临床异质性使得无法根据局部麻醉剂的给药方法(例如韧带内注射、浸润注射或局部给药)以及辅助镇痛药使用的差异和随访时间对研究进行合并。

在七项通过浸润注射给予局部麻醉剂的研究中,六项研究(证据质量极低,分析了542名参与者,1项研究总体偏倚风险高,4项研究总体偏倚风险不明确,1项研究总体偏倚风险低)测量了术后疼痛。结果不明确。局部麻醉剂组出血减少,软组织损伤增加,但我们认为这在临床上不具有显著意义。

在两项通过韧带内注射给予局部麻醉剂的研究中,平均疼痛评分无差异,且未报告任何软组织损伤(证据质量极低,分析了115名参与者,1项研究总体偏倚风险高,1项研究总体偏倚风险不明确)。

一项三臂研究(证据质量极低,分析了54名参与者,总体偏倚风险高)比较了韧带内和浸润局部麻醉剂注射与不治疗的效果。三组之间在疼痛、痛苦或术后焦虑方面没有平均差异的证据。

四项研究(证据质量极低,分析了343名参与者,2项研究总体偏倚风险低,2项研究总体偏倚风险不明确)评估了局部麻醉剂与不治疗或安慰剂相比的效果。一项有不治疗对照的研究(总体偏倚风险不明确)报告局部麻醉剂组平均疼痛较低;所有其他研究报告平均疼痛评分无差异。两项研究报告了出血情况(总体偏倚风险不明确):一项研究报告不治疗时出血有临床意义的增加;另一项报告无差异。

没有研究报告参与者或儿童的满意度。

作者结论

在本综述中,很难就全身麻醉下牙科治疗使用局部麻醉剂的益处得出确凿结论。纳入研究报告的信息全面且适用于本综述问题,但最终不足以实现本综述的目标。由于结局测量、干预措施和治疗类型存在很大差异,我们无法将纳入研究进行荟萃分析。辅助镇痛药的使用进一步掩盖了局部麻醉剂的效果。

基于文献综述和本综述结果,我们建议进一步开展随机对照试验,通过充分的分配隐藏和对参与者及评估者进行盲法来尽量减少偏倚,并评估术中局部麻醉剂对使用的麻醉剂的量和类型以及对接受辅助镇痛药的参与者心血管系统的影响。研究人员应考虑任何变化对参与者健康和福祉的影响,并报告疼痛或痛苦或两者的基线测量值以及术前焦虑情况。

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