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PERSIST: Physician's Evaluation of Restasis? Satisfaction in Second Trial of topical cyclosporine ophthalmic emulsion 0.05% for dry eye: a retrospective review

机译:PERSIST:医师对安定性的评价?眼局部干燥0.05%环孢素眼用乳剂第二次试验的满意度:回顾性回顾

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Background: Chronic dry eye disease often requires long-term therapy. Tear film alterations in the setting of dry eye may include reduced tear volume as well as an increase in inflammatory cytokines and osmolarity. Topical cyclosporine ophthalmic emulsion 0.05% (Restasis?; Allergan Inc, Irvine, CA) is indicated to increase tear production in patients with dry eye and reduced tear production presumed to be due to ocular inflammation. This study was designed to evaluate the efficacy of a second trial of topical cyclosporine in patients with dry eye who were previously considered treatment failures.Materials and methods: This multicenter (three cornea practices) retrospective chart review evaluated clinical outcomes in patients with dry eye who received a second trial of cyclosporine after a prior treatment failure, defined as prior discontinuation of topical cyclosporine after less than 12 weeks.Results: Thirty-five patients, most of whom were female (71.4%) and Caucasian (62.9%), were identified. Prior discontinuation was most commonly due to burning/stinging (60%). The median duration of second treatment was 10 months (range 1 week to 45 months). Physician education was provided in the second trial in 97.1% of cases. At initiation of the second trial of cyclosporine, 10 (28.6%) patients received courses of topical corticosteroids. Physicians reported on a questionnaire that 80% of patients achieved clinical benefit with a second trial of cyclosporine.Conclusion: A repeat trial with topical cyclosporine can achieve clinical success. Direct patient education via the physician and staff may be key to success. Proper patient education may overcome adherence issues, particularly with respect to the need for long-term treatment of chronic dry eye. This study has the usual limitations associated with a retrospective chart review, and future prospective studies are warranted.
机译:背景:慢性干眼病通常需要长期治疗。干眼症患者眼膜的改变可能包括眼泪量减少以及炎性细胞因子和渗透压的增加。局部用0.05%环孢素眼用乳剂(Restasis?; Allergan Inc,Irvine,CA)显示可增加干眼患者的眼泪产生,并减少眼泪的产生,推测是由于眼部炎症引起的。本研究旨在评估第二次局部环孢素局部治疗在先前被认为治疗失败的干眼患者中的疗效。材料和方法:本多中心(三种角膜实践)回顾性图表回顾评估了干眼患者的临床结局。在先前的治疗失败后接受环孢素的第二次试验,这被定义为在不到12周的时间之前局部停用环孢素。结果:确定了35例患者,其中女性为女性(71.4%)和白种人(62.9%) 。先前停药最常见的原因是燃烧/刺痛(60%)。第二次治疗的中位持续时间为10个月(范围为1周至45个月)。在第二次审判中,有97.1%的病例接受了医师教育。在第二次环孢菌素试验开始时,有10名(28.6%)患者接受了局部皮质类固醇激素疗程。医师在一份调查问卷中报告说,第二次环孢菌素试验使80%的患者获得了临床益处。结论:局部环孢菌素的重复试验可以取得临床成功。通过医师和医护人员进行的直接患者教育可能是成功的关键。适当的患者教育可能会克服依从性问题,尤其是在长期治疗慢性干眼症方面。这项研究具有回顾性图表审查通常存在的局限性,因此有必要进行前瞻性研究。

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