Department of Oral Diagnostic Sciences, Faculty of Dentistry, King AbdulAziz University, Jeddah, Saudi Arabia.
Division of Oral Medicine, Department of Diagnostic Sciences, Tufts School of Dental Medicine, Boston, MA, USA.
Oral Dis. 2023 Mar;29(2):343-368. doi: 10.1111/odi.13817. Epub 2021 Mar 12.
OBJECTIVES: To determine the effectiveness of systemic pharmacotherapeutic interventions compared to placebo in burning mouth syndrome (BMS) randomized controlled trials (RCTs) based on the core outcome domains recommended by the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT). METHODS: A systematic literature review of RCTs, concerning systemic pharmacotherapeutic interventions for BMS, published from January 1994 through October 2019, and meta-analysis was performed. RESULTS: Fourteen RCTs (n = 734 participants) were included. Of those, nine were eligible for the quantitative assessment due to the availability/homogeneity of data for at least one of the IMMPACT domains. Pain intensity was the only domain reported in all RCTs. Weighted mean changes in pain intensity, based on visual analogue scale (ΔVAS), were reported in three RCTs at 6 ± 2 weeks and only one RCT at 10+ weeks follow-ups. Quantitative assessment, based on ΔVAS, yielded very low evidence for the effectiveness of alpha-lipoic acid and clonazepam, low evidence for effectiveness of trazodone and melatonin, and moderate evidence for herbal compounds. CONCLUSIONS: Based on the RCTs studied, variable levels of evidence exist that suggest that select pharmacological interventions are associated with improved symptoms. However, the underreporting of IMMPACT domains in BMS RCTs restricts the multidimensional assessment of systemic interventions outcomes. Standardized outcome measures need to be applied to future RCTs to improve understanding of intervention outcomes.
目的:根据临床试验方法、测量和疼痛评估倡议(IMMPACT)推荐的核心结局领域,确定与安慰剂相比,全身性药物治疗干预对灼口综合征(BMS)随机对照试验(RCT)的疗效。
方法:对 1994 年 1 月至 2019 年 10 月期间发表的关于 BMS 全身性药物治疗干预的 RCT 进行系统文献回顾和荟萃分析。
结果:纳入了 14 项 RCT(n=734 名参与者)。其中,由于至少有一个 IMMPACT 领域的数据可用/具有同质性,有 9 项 RCT 可进行定量评估。所有 RCT 均报告了疼痛强度这一结局。在 3 项 RCT 中报告了基于视觉模拟量表(ΔVAS)的疼痛强度的加权平均变化,在 6±2 周时,只有 1 项 RCT 在 10 周随访时报告了这一变化。基于ΔVAS 的定量评估表明,α-硫辛酸和氯硝西泮的有效性具有极低证据,曲唑酮和褪黑素的有效性具有低证据,草药化合物的有效性具有中等证据。
结论:根据研究的 RCT,有不同程度的证据表明某些药物治疗干预与症状改善相关。然而,BMS RCT 中 IMMPACT 领域的报告不足限制了全身性干预结局的多维评估。需要在未来的 RCT 中应用标准化的结局测量方法,以提高对干预结局的理解。
Cochrane Database Syst Rev. 2022-2-1
Cochrane Database Syst Rev. 2005-1-25
J Oral Pathol Med. 2011-11-18
J Oral Rehabil. 2020-10-6
Cochrane Database Syst Rev. 2024-7-22