Topical Cyclosporine a (0.05%) Treatment in Dry Eye Patients: a Comparison Study of Sjogren's Syndrome Versus Non-sjogren's Syndrome

Abstract

Purpose To evaluate the clinical effect of topical cyclosporine A (CsA) (0.05%) on dry eye patients with Sjogren's syndrome (SS) and non-Sjogren's syndrome (NSS). Method This retrospective comparative study includes the dry eye (DE) patients who were treated with topical CsA. DE patients were divided into two groups as follows: DE with Sjogren's syndrome (DE-SS) and DE with Non-Sjogren's syndrome (DE-NSS). Dry eye parameters were recorded at baseline and each visit. Results Schirmer's test 1 scores were 2.7 +/- 0.5 mm at baseline and 3.5 +/- 0.7 mm at 12th month in DE-SS, 2.9 +/- 0.7 mm at baseline and 9.5 +/- 0.7 mm in DE-NSS groups at 12th month. Mean ST score was higher in DE-NSS group than DE-SS group at sixth and 12th months of the treatment (both p = 0.001). Tear break-up time score showed a significant improvement in DE-NSS group, and it was lower in DE-NSS group than DE-SS group group at sixth and 12th months of the treatment (p = 0.044 and 0.027, respectively). Mean OSDI score was lower in DE-NSS group than DE-SS group at sixth and 12th months of the treatment (p = 0.030 and 0.032, respectively). Conclusion Topical CsA seems to be more effective in the treatment of the DE-NSS.