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Preoperative analgesics for additional pain relief in children and adolescents having dental treatment.

机译:术前镇痛药可进一步减轻牙科治疗的儿童和青少年的疼痛。

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摘要

BACKGROUND: Fear of dental pain is a major barrier to treatment for children who need dental care. The use of preoperative analgesics has the potential to reduce postoperative discomfort and intraoperative pain. We reviewed the available evidence to determine whether further research is warranted and to inform the development of prescribing guidelines. This is an update of a Cochrane review published in 2012. OBJECTIVES: To assess the effects of preoperative analgesics for intraoperative or postoperative pain relief (or both) in children and adolescents undergoing dental treatment without general anaesthesia or sedation. SEARCH METHODS: We searched the following electronic databases: Cochrane Oral Health's Trials Register (to 5 January 2016), the Cochrane Central Register of Controlled Trials (CENTRAL) (the Cochrane Library 2015, Issue 12), MEDLINE via OVID (1946 to 5 January 2016), EMBASE via OVID (1980 to 5 January 2016), LILACS via BIREME (1982 to 5 January 2016) and the ISI Web of Science (1945 to 5 January 2016). We searched ClinicalTrials.gov and the World Health Organization (WHO) International Clinical Trials Registry Platform for ongoing trials to 5 January 2016. There were no restrictions regarding language or date of publication in the searches of the electronic databases. We handsearched several specialist journals dating from 2000 to 2011.We checked the reference lists of all eligible trials for additional studies. We contacted specialists in the field for any unpublished data. SELECTION CRITERIA: Randomised controlled clinical trials of analgesics given before dental treatment versus placebo or no analgesics in children and adolescents up to 17 years of age. We excluded children and adolescents having dental treatment under sedation (including nitrous oxide/oxygen) or general anaesthesia. DATA COLLECTION AND ANALYSIS: Two review authors assessed titles and abstracts of the articles obtained from the searches for eligibility, undertook data extraction and assessed the risk of bias in the included studies. We assessed the quality of the evidence using GRADE criteria. MAIN RESULTS: We included five trials in the review, with 190 participants in total. We did not identify any new studies for inclusion from the updated search in January 2016.Three trials were related to dental treatment, i.e. restorative and extraction treatments; two trials related to orthodontic treatment. We did not judge any of the included trials to be at low risk of bias.Three of the included trials compared paracetamol with placebo, only two of which provided data for analysis (presence or absence of parent-reported postoperative pain behaviour). Meta-analysis of the two trials gave arisk ratio (RR) for postoperative pain of 0.81 (95% confidence interval (CI) 0.53 to 1.22; two trials, 100 participants; P = 0.31), which showed no evidence of a benefit in taking paracetamol preoperatively (52% reporting pain in the placebo group versus 42% in the paracetamol group). One of these trials was at unclear risk of bias, and the other was at high risk. The quality of the evidence is low. One study did not have any adverse events; the other two trials did not mention adverse events.Four of the included trials compared ibuprofen with placebo. Three of these trials provided useable data. One trial reported no statistical difference in postoperative pain experienced by the ibuprofen group and the control group for children undergoing dental treatment. We pooled the data from the other two trials, which included participants who were having orthodontic separator replacement without a general anaesthetic, to determine the effect of preoperative ibuprofen on the severity of postoperative pain. There was a statistically significant mean difference in severity of postoperative pain of -13.44 (95% CI -23.01 to -3.88; two trials, 85 participants; P = 0.006) on a visual analogue scale (0 to 100), which indicated a probable benefit for preoperative ibuprofen before this orthodontic procedure. However, both trials were at high risk of bias. The quality of the evidence is low. Only one of the trials reported adverse events (one participant from the ibuprofen group and one from the placebo group reporting a lip or cheek biting injury). AUTHORS' CONCLUSIONS: From the available evidence, we cannot determine whether or not preoperative analgesics are of benefit in paediatric dentistry for procedures under local anaesthetic. There is probably a benefit in using preoperative analgesics prior to orthodontic separator placement. The quality of the evidence is low. Further randomised clinical trials should be completed with appropriate sample sizes and well defined outcome measures.
机译:背景:担心牙齿疼痛是需要牙齿护理的儿童治疗的主要障碍。术前使用镇痛药有可能减轻术后不适和术中疼痛。我们审查了可用的证据,以确定是否需要进行进一步的研究,并为制定指导原则提供依据。这是对2012年发表的Cochrane综述的更新。目的:评估术前镇痛药对未接受全身麻醉或镇静作用的牙科治疗的儿童和青少年的术中或术后疼痛缓解(或两者)的影响。搜索方法:我们搜索了以下电子数据库:Cochrane口腔健康试验注册簿(至2016年1月5日),Cochrane对照试验中央注册簿(CENTRAL)(Cochrane图书馆2015年第12期),MEDLINE通过OVID(1946年1月5日至1月5日) 2016年),通过OVID的EMBASE(1980年至2016年1月5日),通过BIREME的LILACS(1982年至2016年1月5日)和ISI Web of Science(1945年至2016年1月5日)。我们搜索了ClinicalTrials.gov和世界卫生组织(WHO)国际临床试验注册平台,以进行截至2016年1月5日的试验。在电子数据库的搜索中,语言或出版日期没有限制。我们手动搜索了2000年至2011年的几本专业期刊,并检查了所有符合条件的试验的参考文献清单以进行其他研究。我们联系了该领域的专家以获取任何未发布的数据。选择标准:在17岁以下的儿童和青少年中,在牙科治疗之前与安慰剂或不使用镇痛药之间进行的镇痛药随机对照临床试验。我们排除了在镇静(包括一氧化二氮/氧气)或全身麻醉下接受牙科治疗的儿童和青少年。数据收集与分析:两位评价作者评估了从检索资格中获得的文章的标题和摘要,进行了数据提取,并评估了纳入研究的偏倚风险。我们使用GRADE标准评估了证据的质量。主要结果:我们纳入了五项试验,共有190名参与者。我们没有在2016年1月的更新搜索中发现任何要纳入的新研究。三项试验与牙齿治疗有关,即修复和拔牙治疗;两项与正畸治疗有关的试验。我们没有判断任何纳入的试验有低偏倚风险。纳入的三项试验将扑热息痛与安慰剂进行了比较,其中只有两项提供了分析数据(是否存在父母报告的术后疼痛行为)。两项试验的荟萃分析得出术后疼痛的风险比(RR)为0.81(95%置信区间(CI)为0.53至1.22;两项试验,100名参与者; P = 0.31),没有证据表明服用该药有益处术前对乙酰氨基酚(安慰剂组有52%的人报告疼痛,而对乙酰氨基酚组为42%)。这些试验中的一项处于不清楚的偏倚风险中,另一项处于高风险中。证据质量很差。一项研究没有任何不良事件。其他两项试验未提及不良事件。其中包括的四项试验将布洛芬与安慰剂进行了比较。其中三项试验提供了有用的数据。一项试验表明,布洛芬组和对照组在接受牙科治疗的儿童中,术后疼痛无统计学差异。我们汇总了其他两项试验的数据,其中包括在没有全身麻醉的情况下进行正畸分离器置换的参与者,以确定术前布洛芬对术后疼痛严重程度的影响。在视觉模拟量表(0至100)上,术后疼痛严重程度的统计学平均差异为-13.44(95%CI -23.01至-3.88;两项试验,85名参与者; P = 0.006),表明可能正畸手术前对布洛芬的治疗有益。但是,这两个试验都有偏见的高风险。证据质量很差。只有一项试验报告了不良事件(布洛芬组的一名参与者和安慰剂组的一名参与者报告嘴唇或脸颊咬伤)。作者的结论:根据现有证据,我们无法确定术前使用镇痛药对局部麻醉下的儿科牙科是否有益。在放置正畸分离器之前使用术前镇痛药可能会有好处。证据质量很差。进一步的随机临床试验应以适当的样本量和明确的结局指标完成。

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