首页> 外文期刊>European journal of ophthalmology >Evaluation of the effect of topical tacrolimus 0.03 versus cyclosporine 0.05 in the treatment of dry eye secondary to Sjogren syndrome
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Evaluation of the effect of topical tacrolimus 0.03 versus cyclosporine 0.05 in the treatment of dry eye secondary to Sjogren syndrome

机译:外用他克莫司 0.03 与环孢素 0.05 治疗继发于干燥综合征的干眼症的效果评估

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Purpose: To compare the effect of topical application of tacrolimus 0.03 eyedrops versus cyclosporine 0.05 in Sjogren syndrome subjects with severe dry eyes. Design: A prospective single-blinded simply randomized controlled study. Methodology: 60 Sjogren patients were randomized into Group A: 30 patients were instructed to put tacrolimus 0.03 eyedrops in one eye for 6 months and placebo eyedrops in the other eye, (N = 30, 44.9 +/- 12.58 years). Group B: 30 patients were instructed to put cyclosporine 0.05 eyedrops in one eye for 6 months and placebo eyedrops in the other eye (N = 30, 49.4 +/- 12.92 years). Main outcome measures: Patients were evaluated at day 0, 90, and 180 for Ocular Surface Disease Index Questionnaire (OSDI), frequency of use of artificial tears, average fluorescein tear break up time (TBUT), ocular surface staining scores, Schirmer I test, meibum quality, and expressibility scores. Results: Upon comparing both eyedrops, the mean value of OSDI decrease was 38.25 +/- 18.29 versus 31.69 +/- 18.57 (p-value 0.09), SICCA score decrease was 2.97 +/- 1.92 versus 2.27 +/- 2.02 (p-value 0.124) the decrease in artificial tear substitute use was 3.90 +/- 2.22 versus 3.63 +/- 1.92 (p-value 0.616), increase in Schirmer I values were 4.10 +/- 4.21 and 4.26 +/- 2.00 (p-value 0.590) in eyes treated with tacrolimus and cyclosporine respectively. Neither of them affected meibum quality or expressibility scores. Conclusion: Both tacrolimus and cyclosporine significantly improved patient symptoms, frequency of artificial tears use and ocular surface staining compared to placebo-controlled eyes. However, no significant difference regarding the efficacy of both eyedrops at the end of 6 months treatment of severe dry eyes of Sjogren syndrome patients.
机译:目的:比较局部应用0.03%他克莫司滴眼液与0.05%环孢素对严重干眼症干燥综合征受试者的效果。设计:一项前瞻性单盲简单随机对照研究。方法:60 例干燥患者被随机分为 A 组:30 例患者被指示在一只眼睛中滴入 0.03% 他克莫司滴眼液,持续 6 个月,在另一只眼睛中滴入安慰剂滴眼液,(N = 30,44.9 +/- 12.58 年)。B 组:30 名患者被指示在一只眼睛中滴入 0.05% 环孢菌素滴眼液,持续 6 个月,在另一只眼睛中滴入安慰剂滴眼液(N = 30,49.4 +/- 12.92 年)。主要结局指标: 在第 0、90 和 180 天评估患者的眼表疾病指数问卷 (OSDI)、人工泪液使用频率、平均荧光素泪液破裂时间 (TBUT)、眼表染色评分、Schirmer I 检验、睑板质量和表达性评分。结果:比较两种滴眼液后,OSDI 降低的平均值为 38.25 +/- 18.29% 和 31.69 +/- 18.57%(p 值 0.09),SICCA 评分降低 2.97 +/- 1.92 和 2.27 +/- 2.02(p 值 0.124),人工泪液替代品使用的减少为 3.90 +/- 2.22 对 3.63 +/- 1.92(p 值 0.616),Schirmer I 值分别增加 4.10 +/- 4.21 和 4.26 +/- 2.00(p 值 0.590)。它们均不影响睑板质量或表达性评分。结论:与安慰剂对照组相比,他克莫司和环孢素均能显著改善患者症状、人工泪液使用频率和眼表染色。然而,在干燥综合征患者严重干眼症 6 个月结束时,两种滴眼液的疗效没有显着差异。

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