减少与正畸分离相关的疼痛的干预措施的有效性:系统回顾和荟萃分析。

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE European journal of orthodontics Pub Date : 2024-01-01 DOI:10.1093/ejo/cjad078
Lama Mohammad Saffouh Al-Hanbali, Ahmad Sharafeddin Burhan, Mohammad Younis Hajeer, Kinda Sultan, Fehmieh Rafik Nawaya
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引用次数: 0

摘要

背景介绍疼痛是一种不愉快的体验,也是一种恼人的感觉。为了控制正畸分离过程中的疼痛,人们使用了不同的药物和非药物方法:本系统综述和荟萃分析旨在严格评估药物和非药物方法在减轻正畸分离引起的疼痛方面的有效性证据:使用以下数据库进行了电子检索:PubMed®(Medline)、Scopus®、EMBASE®、Web of ScienceTM、Google ScholarTM、ProQuest 和 Cochrane Central Register of controlled trials (CENTRAL),搜索 2012 年 1 月至 2023 年 4 月间发表的研究:仅纳入随机对照试验(RCT),每个试验组包括接受弹性分离器和一种药物或非药物干预以减轻分离阶段疼痛的患者:采用 Cochrane 的偏倚风险工具(RoB2 工具)。数据收集与分析:采用 Cochrane 的偏倚风险工具(RoB2 工具),并采用建议评估、发展与评价分级法(GRADE)评估证据的强度:本系统综述共纳入 31 项研究(RCT)。结果:本系统综述共纳入 31 项研究(RCT),其中 19 项适合定量综合,并使用 VAS 进行疼痛评估。元分析表明,低强度激光疗法(LLLT)是一种有效的分隔器置入后疼痛缓解方法,6 小时后的标准平均差值为 13.79 毫米(95% 置信区间(CI):-15.64,-11.94),24 小时后的标准平均差值为 23.34 毫米(95% 置信区间(CI):-25.91,-20.77)。LLLT 在分口使用时也很有效,6 小时后的标准平均差值为 8.9 毫米(95% CI:-12.86,-3.33),24 小时后的标准平均差值为 17.15 毫米(95% CI:-30.12,-4.17)。与安慰剂组相比,布洛芬在 6 小时和 24 小时内均有止痛效果。标准平均差分别为 14.37 毫米(95% CI:-20.54,-8.19)和 20.46 毫米(95% CI:-27.79,-13.13)。布洛芬和对乙酰氨基酚在疼痛控制方面没有差异。萘普生在6小时后的疼痛感觉视觉模拟量表评分较低,标准平均差异为7.03毫米(95% CI:-12.67,-1.40):结论:在分牙的第一天,使用激光照射可减轻分牙引起的疼痛;从6小时到24小时结束,疼痛减轻的程度有所增加。与安慰剂相比,镇痛剂可减轻疼痛;从 6 小时到 24 小时结束,疼痛减轻程度有所增加。与安慰剂相比,萘普生凝胶能有效减轻疼痛;这方面的证据强度为中等。与安慰剂相比,萘普生凝胶可有效减轻疼痛,但效果不如口服非甾体抗炎药。不过,这方面的证据属于中等水平:本系统综述在第一阶段进行时已在 PROSPERO 注册(CRD42022335553)。
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The effectiveness of interventions in reducing pain related to orthodontic separation: a systematic review and meta-analysis.

Background: Pain is an unpleasant experience and annoying sensation. To control this pain during orthodontic separation, different pharmacological and non-pharmacological methods have been used.

Objective: This systematic review and meta-analysis aimed to critically assess the evidence of the effectiveness of pharmacological and non-pharmacological methods in reducing pain induced by orthodontic separation.

Search strategy: An electronic search was conducted using the following databases: PubMed® (Medline), Scopus®, EMBASE®, Web of ScienceTM, Google ScholarTM, ProQuest, and Cochrane Central Register of controlled trials (CENTRAL) searching for the studies published between January 2012 and April 2023.

Selection criteria: Only randomized controlled trials (RCTs) were included, each experimental group included patients who received elastomeric separators and one kind of pharmacological or non-pharmacological interventions for pain reduction during the separation stage.

Data collection and analysis: Cochrane's risk of bias tool (RoB2 tool) was applied. The Grading of Recommendations Assessment, Development, and Evaluation [GRADE] approach was used to evaluate the strength of the evidence.

Results: Thirty-one studies (RCTs) were included in this systematic review. Nineteen of them were appropriate for quantitative synthesis and used VAS for pain assessment. Meta-analysis showed that low-level laser therapy (LLLT) was an effective approach for pain relief after separators placement with standard mean difference of 13.79 mm (95% confidence interval (CI): -15.64, -11.94) at 6 h and 23.34 mm at 24 h (95% CI: -25.91, -20.77). LLLT was also effective when applied in split-mouth and the standard mean difference was 8.9 mm at 6 h (95% CI: -12.86, -3.33) and 17.15 mm at 24 h (95% CI: -30.12, -4.17). Ibuprofen had a pain control effect at 6 h and at 24 h compared with the placebo group. The standard mean difference was 14.37 mm (95% CI: -20.54, -8.19) and 20.46 mm (95% CI: -27.79, -13.13), respectively. There was no difference in pain control between ibuprofen and acetaminophen. Naproxen had lower visual analog scale scores in pain perception at 6 h and the standard mean difference was 7.03 mm (95% CI: -12.67, -1.40).

Conclusions: The application of LLLT decreased the pain induced by the separation during the first day of teeth separation; the pain reduction showed an increase from 6 h to the end of the 24 h. However, the evidence is weak to moderate. The analgesics reduced the pain compared to placebo; this pain reduction had shown an increase from 6 h to the end of the 24 h. The strength of the evidence is moderate. Naproxen gel effectively reduced the pain compared to placebo; the evidence in this regard is moderate. Naproxen gel effectively reduced the pain compared to placebo, but it was less effective than the oral intake of non-steroidal anti-inflammatory drugs. However, the evidence in this regard is moderate.

Registration: This systematic review was registered with PROSPERO (CRD42022335553) during the first stages of its conduction.

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来源期刊
European journal of orthodontics
European journal of orthodontics 医学-牙科与口腔外科
CiteScore
5.50
自引率
7.70%
发文量
71
审稿时长
4-8 weeks
期刊介绍: The European Journal of Orthodontics publishes papers of excellence on all aspects of orthodontics including craniofacial development and growth. The emphasis of the journal is on full research papers. Succinct and carefully prepared papers are favoured in terms of impact as well as readability.
期刊最新文献
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