Department of Periodontics, S.C.B Dental College and Hospital, Cuttack, Odisha, India.
Department of Prosthodontics and Crown and Bridge, S.C.B Dental College and Hospital, Cuttack, Odisha, India.
Indian J Dent Res. 2021 Apr-Jun;32(2):192-198. doi: 10.4103/ijdr.IJDR_943_20.
Oral Lichen planus (OLP) is a chronic, debilitating, immune-mediated disease whose management is considered a challenge in medical science.
To quantitatively evaluate the effect of administration of enteral hydroxychloroquine (HCQS) as a monotherapy for six months on the extent and severity of erosive OLP using reticular score, erythema score and ulcerative score (REU score), and to subjectively evaluate the success of HCQS as a therapeutic drug for OLP-e using Tel Aviv-San Francisco Scale, visual analogue scale (VAS) and severity of burning sensation (BURN score).
Prospective clinical trial.
A total of 45 subjects received 200 mg of HCQS bid for six months. REU, VAS, BURN scores and Tel Aviv-San Francisco Scale readings were taken at the beginning of the study (baseline) and three- and six-month intervals post administration of enteral HCQS. Subjects were examined for any adverse drug outcomes for one year after the cessation of enteric HCQS therapy. Data were analysed with SPSS version 25.
There was a stark reduction in REU, VAS and BURN scores during the study period, with a statistically significant reduction (P < 0.05) seen at three- and six-month time intervals as compared to baseline. Further, the mean of change in R, E and U scores showed a statistically significant difference, with the highest reduction seen at baseline to six-month time interval. The Tel Aviv-San Francisco Scale showed 70%-100% remission in disease in more than 70% of subjects.
Enteral HCQS can be considered a viable treatment option for the enigma that is erosive OLP.
口腔扁平苔藓(OLP)是一种慢性、使人虚弱的、免疫介导的疾病,其管理被认为是医学科学的一项挑战。
定量评估口服羟氯喹(HCQS)单药治疗 6 个月对糜烂性 OLP 网状评分、红斑评分和溃疡评分(REU 评分)的严重程度和严重程度的影响,并使用特拉维夫-旧金山量表、视觉模拟量表(VAS)和烧灼感严重程度(BURN 评分)主观评估 HCQS 作为 OLP-e 的治疗药物的疗效。
前瞻性临床试验。
共 45 名患者接受 200mg HCQS 每日两次治疗 6 个月。REU、VAS、BURN 评分和特拉维夫-旧金山量表读数在研究开始时(基线)和口服 HCQS 给药后 3 个月和 6 个月进行。在停止肠内 HCQS 治疗后 1 年内,对患者进行任何不良药物结局的检查。数据使用 SPSS 版本 25 进行分析。
在研究期间,REU、VAS 和 BURN 评分明显降低,与基线相比,在 3 个月和 6 个月的时间间隔内有统计学显著降低(P<0.05)。此外,R、E 和 U 评分的平均变化显示出统计学上的显著差异,在基线至 6 个月的时间间隔内降幅最大。特拉维夫-旧金山量表显示,超过 70%的患者疾病缓解率为 70%-100%。
口服 HCQS 可被视为糜烂性 OLP 这一难题的可行治疗选择。