To estimate the efficacy of 0.1% tacrolimus with Colgate Oraguard-B paste for the treatment of patients with symptomatic oral lichen planus.

Shams Ul Nisa, Tajinder Kaur Saggu
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引用次数: 4

Abstract

Aim and objectives: To investigate the efficacy of 0.1% tacrolimus with Colgate Oraguard-B paste for the treatment of patients with oral lichen planus (OLP).

Materials and methods: One hundred and fifty patients with symptomatic OLP participated in the study, who had clinically and histopathologically proven OLP. In this study, patients were provided with 0.1% tacrolimus ointment with Colgate Oraguard-B paste as the study medication. Patients were asked to use the medication over the areas three times a day until resolution of the lesion. Patients were recalled to assess the drug response every 15 days. The duration of treatment ranged from 3 months to 4 months, with follow-up of 2 years and 6 months.

Statistical analysis: The Wilcoxon signed-rank test was performed, which is a nonparametric statistical hypothesis test for comparing two related samples, matched samples or repeated measurements on a single sample to assess whether their population mean ranks differ (i.e., it is a paired difference test). In our study, the pre- and post-Visual Analogue Scale (VAS) values were compared and the mean, standard deviation and P values were calculated.

Results: Of 150 patients, 71 (47.33%) patients had complete resolution of the lesion to the topical tacrolimus therapy. Sixty-five (43.33%) patients had marked resolution of their lesions, i.e., the size of the lesion was decreased. Fourteen (9.33%) patients had remission of lesion (reduction in burning sensation and size of lesion) in symptoms as recorded by the VAS.

Conclusion: Topical tacrolimus ointment 0.1% in Oraguard-B paste is an effective treatment for different types of OLP.

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目的评价0.1%他克莫司联合高露洁oraguerb膏剂治疗有症状性口腔扁平苔藓的疗效。
目的:探讨0.1%他克莫司与高露洁orguard - b膏剂联合治疗口腔扁平苔藓(OLP)的疗效。材料与方法:150例经临床及组织病理学证实的有症状的OLP患者参与研究。本研究给予患者0.1%他克莫司软膏和高露洁orguard - b膏剂作为研究药物。患者被要求每天在这些区域使用三次药物,直到病变消退。每15天召回患者评估一次药物反应。治疗时间3 ~ 4个月,随访2年6个月。统计分析:采用Wilcoxon符号秩检验,这是一种非参数统计假设检验,用于比较两个相关样本、匹配样本或在单个样本上重复测量,以评估其总体平均秩是否不同(即配对差异检验)。在我们的研究中,比较了视觉模拟量表(VAS)前后的数值,并计算了平均值、标准差和P值。结果:150例患者中,71例(47.33%)患者经局部他克莫司治疗后病变完全消退。65例(43.33%)患者的病变明显消退,即病变大小减小。14例(9.33%)患者在VAS记录的症状中病变缓解(烧灼感和病变大小减轻)。结论:0.1%他克莫司软膏在Oraguard-B糊剂中外用是治疗不同类型OLP的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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