The clinical efficacy of artificial saliva using four point ordinal scale and visual analogue scale in patients of sjogrens syndrome with xerostomia

S. Samreen, B. Salim, H. Nasim
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Abstract

Objective: To evaluate the efficacy of artificial saliva for relief of xerostomia in patients with Sjogrens syndrome. Place/duration of study: This is a quasi-experimental trial of 6 months’ duration from 1st October 2019 till 30th march 2020 conducted at Fauji Foundation Hospital, Rawalpindi. Patients and methods: We enrolled 50 patients with xerostomia due to Sjogrens syndrome. The clinical efficacy of Xerostomia was evaluated by means of a patient reported score on a 10-point visual analog scale (VAS) and assessment of the oral tissue condition by means of a 4-point ordinal scale at 0, 2, 4 and 6 weeks. Mean ± standard deviation of quantitative variables was calculated and level of significance was determined using paired-t-test. An improvement in xerostomia was measured by comparing patient reported VAS and a physician recorded 4-point ordinal score at baseline, 2nd, 4th and 6th week. Results: All of the patients were female with a mean age (years ± SD) of 48.48 ± 10.8.Four-point ordinal score at screening visit was 25.30 ± 5.21(mean ± SD) whereas patient VAS was 57.92 ± 12.03 (mean ± SD). The mean change in both four-point ordinal score and patients VAS was statistically significant at 2 weeks, 4 weeks and 6 weeks (p value 0.000 in each). It was well tolerated in most of the patients (only 7 patients discontinued ;5 due to mucositis ,1 due to respiratory tract infection and one had mouth bleed due to dental issues). Conclusions: Artificial saliva is a safe and efficacious option for patients with xerostomia.
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采用四点顺序量表和视觉模拟量表观察人工唾液在斜视综合征合并口干症患者中的临床疗效
目的:评价人工唾液对干燥综合征患者口干症的治疗效果。研究地点/时间:这是一项为期6个月的准实验试验,从2019年10月1日至2020年3月30日,在拉瓦尔品第Fauji基金会医院进行。患者和方法:我们招募了50例由收缩综合征引起的口干症患者。在0、2、4和6周时,采用患者报告的10分视觉模拟量表(VAS)评分和4分有序量表评估口腔组织状况来评估口干症的临床疗效。计算定量变量的均数±标准差,采用配对t检验确定显著性水平。通过比较患者报告的VAS和医生在基线、第2、第4和第6周记录的4分顺序评分来衡量口干症的改善。结果:所有患者均为女性,平均年龄(years±SD)为48.48±10.8岁。筛查时4分顺序评分为25.30±5.21(平均±SD),患者VAS评分为57.92±12.03(平均±SD)。在2周、4周和6周时,四分序评分和患者VAS的平均变化均有统计学意义(p值均为0.000)。大多数患者耐受性良好(仅7例停药,5例因黏膜炎,1例因呼吸道感染,1例因牙齿问题导致口出血)。结论:人工唾液是治疗口干症的一种安全有效的方法。
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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