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正畸治疗期间缓解疼痛的药物干预措施。

Pharmacological interventions for pain relief during orthodontic treatment.

作者信息

Monk Aoife B, Harrison Jayne E, Worthington Helen V, Teague Annabel

机构信息

Orthodontic Department, Liverpool University Dental Hospital, Pembroke Place, Liverpool, UK, L3 5PS.

出版信息

Cochrane Database Syst Rev. 2017 Nov 28;11(11):CD003976. doi: 10.1002/14651858.CD003976.pub2.

Abstract

BACKGROUND

Pain is a common side effect of orthodontic treatment. It increases in proportion to the amount of force applied to the teeth, and the type of orthodontic appliance used can affect the intensity of the pain. Pain during orthodontic treatment has been shown to be the most common reason for people wanting to discontinue treatment, and has been ranked as the worst aspect of treatment. Although pharmacological methods of pain relief have been investigated, there remains some uncertainty among orthodontists about which painkillers are most suitable and whether pre-emptive analgesia is beneficial. We conducted this Cochrane Review to assess and summarize the international evidence relating to the effectiveness of analgesics for preventing this unwanted side effect associated with orthodontic treatment.

OBJECTIVES

The objectives of this review are to determine:- the effectiveness of drug interventions for pain relief during orthodontic treatment; and- whether there is a difference in the analgesic effect provided by different types, forms and doses of analgesia taken during orthodontic treatment.

SEARCH METHODS

Cochrane Oral Health's Information Specialist searched the following databases: the Cochrane Oral Health Trials Register (to 19 June 2017), the Cochrane Central Register of Controlled Trials (CENTRAL;the Cochrane Library 2016, Issue 7), MEDLINE Ovid (1946 to 19 June 2017), Embase Ovid (1980 to 19 June 2017) and CINAHL EBSCO (Cumulative Index to Nursing and Allied Health Literature; 1937 to 19 June 2017). The US National Institutes of Health Ongoing Trials Register (ClinicalTrials.gov) and the World Health Organization International Clinical Trials Registry Platform were searched on the 19 June 2017 for ongoing studies. We placed no restrictions on language or date of publication when searching the electronic databases.

SELECTION CRITERIA

We included randomized controlled trials (RCTs) relating to pain control during orthodontic treatment. Pain could be measured on a visual analogue scale (VAS), numerical rating scale (NRS) or categorical scale.

DATA COLLECTION AND ANALYSIS

Two review authors independently screened the search results, agreed the studies to be included and extracted information from the included studies regarding methods, participants, interventions, outcomes, harms and results. We planned to resolve any discrepancies or disagreements through discussion. We used the Cochrane 'Risk of bias' tool to assess the risk of bias in the studies.

MAIN RESULTS

We identified 32 relevant RCTs, which included 3110 participants aged 9 to 34 years, 2348 of whom we were able to include in our analyses. Seventeen of the studies had more than two arms. We were able to use data from 12 trials in meta-analyses that compared analgesics versus control (no treatment or a placebo); nine that compared non-steroidal anti-inflammatories (NSAIDs) versus paracetamol; and two that compared pre-emptive versus post-treatment ibuprofen for pain control following orthodontic treatment. One study provided data for the comparison of NSAIDs versus local anaesthetic.We found moderate-quality evidence that analgesics effectively reduced pain following orthodontic treatment when compared to no treatment or a placebo at 2 hours (mean difference (MD) -11.66 mm on a 0 to 100 mm VAS, 95% confidence interval (CI) -16.15 to -7.17; 10 studies, 685 participants), 6 hours (MD -24.27 mm on a VAS, 95% CI -31.44 to -17.11; 9 studies, 535 participants) and 24 hours (MD -21.19 mm on a VAS, 95% CI -28.31 to -14.06; 12 studies, 1012 participants).We did not find any evidence of a difference in efficacy between NSAID and paracetamol at 2, 6 or 24 hours (at 24 hours: MD -0.51, 95% CI -8.93 to 7.92; 9 studies, 734 participants; low-quality evidence).Very low-quality evidence suggested pre-emptive ibuprofen gave better pain relief at 2 hours than ibuprofen taken post treatment (MD -11.30, 95% CI -16.27 to -6.33; one study, 41 participants), however, the difference was no longer significant at 6 or 24 hours.A single study of 48 participants compared topical NSAIDs versus local anaesthetic and showed no evidence of a difference in the effectiveness of the interventions (very low-quality evidence).Use of rescue analgesia was poorly reported. The very low-quality evidence did not show evidence of a difference between participants taking ibuprofen and participants taking paracetamol (relative risk (RR) 1.5, 95% CI 0.6 to 3.6). Nor did we find evidence of a difference between groups in likelihood of requiring rescue analgesia when ibuprofen was taken pre-emptively compared to after treatment (RR 0.8, 95% CI 0.3 to 1.9).Adverse effects were identified in one study, with one participant developing a rash that required treatment with antihistamines. This was provisionally diagnosed as a hypersensitivity to paracetamol.

AUTHORS' CONCLUSIONS: Analgesics are more effective at reducing pain following orthodontic treatment than placebo or no treatment. Low-quality evidence did not show a difference in effectiveness between systemic NSAIDs compared with paracetamol, or topical NSAIDs compared with local anaesthetic. More high-quality research is needed to investigate these comparisons, and to evaluate pre-emptive versus post-treatment administration of analgesics.

摘要

背景

疼痛是正畸治疗常见的副作用。疼痛程度与施加于牙齿的力量大小成正比,且所使用的正畸矫治器类型会影响疼痛强度。正畸治疗期间的疼痛已被证明是人们想要中断治疗的最常见原因,并且被列为治疗中最糟糕的方面。尽管已经对缓解疼痛的药理学方法进行了研究,但正畸医生对于哪种止痛药最合适以及预防性镇痛是否有益仍存在一些不确定性。我们进行了这项Cochrane系统评价,以评估和总结有关镇痛药预防正畸治疗相关不良副作用有效性的国际证据。

目的

本系统评价的目的是确定:- 药物干预在正畸治疗期间缓解疼痛的有效性;- 正畸治疗期间服用的不同类型、剂型和剂量的镇痛药在镇痛效果上是否存在差异。

检索方法

Cochrane口腔健康信息专家检索了以下数据库:Cochrane口腔健康试验注册库(截至2017年6月19日)、Cochrane对照试验中央注册库(CENTRAL;Cochrane图书馆2016年第7期)、MEDLINE Ovid(1946年至2017年6月19日)、Embase Ovid(1980年至2017年6月19日)和CINAHL EBSCO(护理及相关健康文献累积索引;1937年至2017年6月19日)。2017年6月19日检索了美国国立卫生研究院正在进行的试验注册库(ClinicalTrials.gov)和世界卫生组织国际临床试验注册平台,以查找正在进行的研究。检索电子数据库时,我们未对语言或出版日期设限。

选择标准

我们纳入了与正畸治疗期间疼痛控制相关的随机对照试验(RCT)。疼痛可通过视觉模拟量表(VAS)、数字评定量表(NRS)或分类量表进行测量。

数据收集与分析

两位综述作者独立筛选检索结果,商定纳入的研究,并从纳入研究中提取有关方法、参与者、干预措施、结局、危害和结果的信息。我们计划通过讨论解决任何差异或分歧。我们使用Cochrane“偏倚风险”工具评估研究中的偏倚风险。

主要结果

我们识别出32项相关RCT,其中包括3110名年龄在9至34岁之间的参与者,我们能够将其中2348名纳入分析。17项研究有两个以上的组。我们能够在荟萃分析中使用12项试验的数据,这些试验比较了镇痛药与对照(无治疗或安慰剂);9项比较了非甾体抗炎药(NSAIDs)与对乙酰氨基酚;2项比较了正畸治疗后预防性使用布洛芬与治疗后使用布洛芬对疼痛的控制情况。一项研究提供了NSAIDs与局部麻醉剂比较的数据。我们发现中等质量的证据表明,与无治疗或安慰剂相比,镇痛药在正畸治疗后2小时(在0至100mm的VAS上平均差(MD)为-11.66mm,95%置信区间(CI)为-16.15至-7.17;10项研究,685名参与者)、6小时(VAS上MD为-24.27mm,95%CI为-31.44至-17.11;9项研究,535名参与者)和24小时(VAS上MD为-21.19mm,95%CI为-28.31至-14.06;12项研究,1012名参与者)能有效减轻疼痛。我们未发现NSAIDs和对乙酰氨基酚在2、

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