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Evaluating the novel application of cyclosporine 0.1% in ocular surface disease.

TitleEvaluating the novel application of cyclosporine 0.1% in ocular surface disease.
Publication TypeJournal Article
Year of Publication2018
AuthorsBoboridis, K. G., & Konstas A. G. P.
JournalExpert Opin Pharmacother
Volume19
Issue9
Pagination1027-1039
Date Published2018 Jun
ISSN1744-7666
KeywordsConjunctivitis, Cyclosporine, Dry Eye Syndromes, Humans, Keratitis, Ophthalmic Solutions, Quality of Life, Severity of Illness Index, Tears, Treatment Outcome
Abstract

INTRODUCTION: Ocular surface disease (OSD) is a highly prevalent symptomatic condition caused by dry eye disease (DED), intrinsic, environmental, or iatrogenic causes. It affects patient's visual function and quality of life. Its pathophysiology is centered on tear hyperosmolarity, inflammation, and epithelial damage. Current management is suboptimal and includes artificial tear supplementation and short-term use of topical steroids in severe cases. The recent approval of cyclosporine 0.1% has transformed management strategies of severe DED and moderate-to-severe OSD. Areas covered: This review summarizes existing information on the efficacy, safety, and tolerability of the new cyclosporine 0.1% formulation. Expert opinion: Topical cyclosporine A 0.1% represents a promising, novel medication for the management of DED, Meibomian gland dysfunction, and inflammatory OSD. It is primarily beneficial for those patients requiring topical immunomodulatory therapy. This topical formulation also has the potential to meaningfully improve the management of moderate-to-severe glaucoma therapy-related OSD. Currently there is limited published clinical data concerning the efficacy of topical cyclosporine. There are, however, theoretical advantages when comparing this cyclosporine formulation with other established commercial preparations. Future research is needed to delineate the precise role and value of this medication.

DOI10.1080/14656566.2018.1479742
Alternate JournalExpert Opin Pharmacother
PubMed ID29847195

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