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肉毒杆菌毒素治疗颞下颌关节紊乱病的疗效:系统评价和荟萃分析。

The effectiveness of botulinum toxin for temporomandibular disorders: A systematic review and meta-analysis.

机构信息

Department of Dental Technology, COAMS, King Khalid University, Abha, Saudi Arabia.

Department of Basic Medical Sciences, COAMS, King Khalid University, Abha, Saudi Arabia.

出版信息

PLoS One. 2024 Mar 14;19(3):e0300157. doi: 10.1371/journal.pone.0300157. eCollection 2024.

Abstract

OBJECTIVE

The current body of research on utilizing botulinum toxin (BTX) to manage temporomandibular disorders (TMDs) has not yet yielded definitive conclusions. The primary objective of this study was to determine the effectiveness of BTX in pain reduction for TMDs compared to placebo and other treatments. The secondary outcomes evaluated were adverse events, maximum mouth opening, bruxism events, and maximum occlusal force.

MATERIALS AND METHODS

A literature search was performed on PubMed, Dimension Publication, Scopus, and Google Scholar. The RoB 2 tool was used for quality assessment. The mean differences in pain scores were estimated to measure the effect of BTX on pain reduction. For adverse events, the risk ratio for the incidence of side effects was calculated.

RESULTS

Two hundred and sixty non-duplicate articles were identified; however, only 14 RCTS were included in this review. The total study population included 395 patients. The overall risk of bias showed a low to moderate quality of evidence. Results from 6 studies were reported only narratively; four studies were used for meta-analysis on pain reduction, and five were used for meta-analysis on adverse events. The control used in the meta-analysis was placebo injections. Results of the meta-analysis for pain reduction were statistically insignificant for the BTX group with mean differences at MD = -1.71 (95% CI, -2.87 to -0.5) at one month, -1.53 (95% CI, -2.80 to -0.27) at three months, and -1.33 (95% CI, -2.74 to 0.77) at six months. This showed that BTX treatment was not significantly better than placebo for a reduction in pain scores at 1, 3, and 6 months. Regarding safety, the placebo group showed a relative risk of 1.34 (95%CI, 0.48-6.78) and 1.17 (95%CI, 0.54-3.88) at 1 and 3 months respectively. However, the risks were not statistically significant. There was also no difference in the effectiveness of BTX compared to placebo and other treatments for maximum mouth opening, bruxism events, and maximum occlusal force.

CONCLUSION

BTX was not associated with better outcomes in terms of pain reduction, adverse events, maximum mouth opening, bruxism events, and maximum occlusal force. More high-quality RCTs are needed to better understand this topic.

摘要

目的

目前关于利用肉毒毒素 (BTX) 治疗颞下颌关节紊乱 (TMD) 的研究结果尚未得出明确结论。本研究的主要目的是确定 BTX 在减轻 TMD 疼痛方面与安慰剂和其他治疗方法相比的有效性。次要结局评估包括不良事件、最大张口度、磨牙事件和最大咬合力。

材料和方法

在 PubMed、Dimension Publication、Scopus 和 Google Scholar 上进行文献检索。使用 RoB 2 工具进行质量评估。估计疼痛评分的平均差异以衡量 BTX 对疼痛减轻的影响。对于不良事件,计算副作用发生率的风险比。

结果

确定了 260 篇非重复文章,但本综述仅纳入了 14 项 RCT。总研究人群包括 395 名患者。总体偏倚风险显示证据质量为低到中度。6 项研究的结果仅进行了叙述性报告;4 项研究用于疼痛减轻的荟萃分析,5 项研究用于不良事件的荟萃分析。荟萃分析中使用的对照为安慰剂注射。BTX 组在一个月时 MD = -1.71(95%CI,-2.87 至-0.5)、三个月时 MD = -1.53(95%CI,-2.80 至-0.27)和六个月时 MD = -1.33(95%CI,-2.74 至 0.77)时的疼痛缓解结果无统计学意义。这表明 BTX 治疗在 1、3 和 6 个月时的疼痛评分减轻方面并不明显优于安慰剂。关于安全性,安慰剂组在 1 个月和 3 个月时的相对风险分别为 1.34(95%CI,0.48-6.78)和 1.17(95%CI,0.54-3.88)。然而,风险无统计学意义。BTX 与安慰剂和其他治疗方法在最大张口度、磨牙事件和最大咬合力方面的疗效也无差异。需要更多高质量的 RCT 来更好地了解这一主题。

结论

BTX 在减轻疼痛、不良事件、最大张口度、磨牙事件和最大咬合力方面与更好的结局无关。需要更多高质量的 RCT 来更好地了解这一主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c565/10939295/a9b2eb6f757d/pone.0300157.g001.jpg

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