Nisa Shams Ul, Saggu Tajinder Kaur
Department of Oral Medicine and Radiology, Bharati Vidyapeeth Dental College and Hospital, Pune, Maharashtra, India.
Department of Oral and Maxillofacial Pathology, Dasmesh Institute of Research and Dental Sciences, Faridkot, Punjab, India.
Indian J Dent. 2016 Jan-Mar;7(1):23-7. doi: 10.4103/0975-962X.179373.
To investigate the efficacy of 0.1% tacrolimus with Colgate Oraguard-B paste for the treatment of patients with oral lichen planus (OLP).
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.
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.
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.
Topical tacrolimus ointment 0.1% in Oraguard-B paste is an effective treatment for different types of OLP.
探讨0.1%他克莫司与高露洁Oraguard - B牙膏联合用于治疗口腔扁平苔藓(OLP)患者的疗效。
150例有症状的OLP患者参与本研究,这些患者经临床和组织病理学确诊为OLP。在本研究中,为患者提供0.1%他克莫司软膏与高露洁Oraguard - B牙膏作为研究用药。要求患者每天在病损部位使用该药物3次,直至病损消退。每15天召回患者评估药物反应。治疗持续时间为3个月至4个月,随访2年6个月。
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、匹配样本或对单个样本的重复测量,以评估它们的总体平均秩是否不同(即它是一种配对差异检验)。在我们的研究中,比较了视觉模拟量表(VAS)的治疗前后值,并计算了均值、标准差和P值。
150例患者中,71例(47.33%)患者经局部他克莫司治疗后病损完全消退。65例(43.33%)患者病损明显消退,即病损大小减小。14例(9.33%)患者根据VAS记录症状缓解(烧灼感和病损大小减轻)。
0.1%他克莫司软膏与Oraguard - B牙膏联合局部应用是治疗不同类型OLP的有效方法。