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Improving Tolerance and Compliance with Topical Immunomodulators Using Micro-Emulsion Lipid Layer Artificial Tears

机译:使用微乳液脂质层人工泪液改善潜在免疫调节剂的耐受性和遵守性

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Purpose: To investigate the efficacy of a micro-emulsion (ME) lipid layer artificial tear in improving tolerance of immunomodulator eye drops for the treatment of dry eye disease. Patients and Methods: A total of 33 patients with previously diagnosed dry eye disease were given the micro-emulsion lipid layer artificial tear in conjunction with either lifitegrast or cyclosporine. Patients were queried on their tolerance of the regimen by reporting VAS scores before starting the adjunctive eye drop, immediately after starting, and 2– 3 weeks later. Tolerance was statistically compared over time and with respect to previous medication compliance, timing of the adjunctive eye drop, age, gender, and ethnicity. Results: Across all patients, the VAS pre-treatment score (6.8 ± 0.6) was significantly higher than both the VAS 1-day post ME lipid tear instillation time point (3.0 ± 0.7) (post hoc Bonferroni, p 0.001) and the VAS 2– 3-week post instillation time point (1.7 ± 0.7) (post hoc Bonferroni, p 0.001), with the mean VAS score improving over time (post hoc Bonferroni, p 0.028). Average VAS scores did not vary with respect to specific medical therapy or the timing of instillation of this artificial tear. Both the “at-risk” and “conversion” groups independently had significant improvements at both 1-day and 2– 3-week time points compared to baseline. Conclusion: The micro-emulsion lipid layer artificial tear was effective as an adjunctive eye drop to improve tolerance of lifitegrast and cyclosporine for patients with dry eye disease who were at risk of failing or had previously failed immunomodulatory therapy.
机译:目的:探讨微乳液(ME)脂质层人工撕裂在改善免疫调节剂眼药水中治疗干眼症的耐受性的疗效。患者和方法:将33例患有先前诊断的干眼症患者进行了微乳液脂质层人造撕裂,与寿命拉伸或环孢菌素一起结合。通过在开始辅助眼药水之前,在开始之前,在开始之前,患者询问患者对方案的耐受性,并在开始后立即,2-3周后。随着时间的推移,耐受性和关于先前的药物遵守,辅助眼药滴,年龄,性别和种族的时间,耐受性差异。结果:遍布所有患者,VAS预处理评分(6.8±0.6)明显高于VAS 1日发布的血液撕裂时间点(3.0±0.7)(HOC Bonferroni,P <0.001)和VAS 2- 3周灌输时间点(1.7±0.7)(后HOC Bonferroni,P <0.001),随着时间的推移,平均VAS评分改善(HOC Bonferroni,P <0.028)。对于特定的医疗治疗或这种人造撕裂的滴注时,平均VAS分数并没有变化。与基线相比,“有风险”和“转换”群体在1天和2-3周的时间点中独立改善。结论:微乳液脂质层人工撕裂是有效的,作为改善患有失败或先前未发生免疫调节治疗失败的干眼症患者的升降眼球耐受性和环孢菌素的耐受性。

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