Abstract | PURPOSE: MATERIALS AND METHODS:
Dry eye and treatment outcomes were assessed by Schirmer I test, tear BUT, lissamine green conjunctival staining, fluorescein corneal staining, and HLA-DR expression on conjunctival cells. Patients received either loteprednol-etabonate 0.5% twice daily for 14 days tapered to once daily for 14 days, and then twice weekly for 28 days (n = 10), or NaCl 0.9%. RESULTS: A significant decrease of ocular surface inflammation and improvement of symptoms was recorded in the study group compared with controls at days 14 and 56. Change from baseline in HLA-DR expression in CD45+ conjunctival cells was significantly higher in treated patients at day 14. Intraocular pressure and best corrected visual acuity were preserved in all treated eyes. CONCLUSIONS:
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Authors | Stefano Barabino, Elisa Montaldo, Maria Cristina Mingari, Cosimo Mazzotta, Sebastiano Giuffrida, Maurizio Rolando |
Journal | European journal of ophthalmology
(Eur J Ophthalmol)
Vol. 32
Issue 4
Pg. 2452-2458
(Jul 2022)
ISSN: 1724-6016 [Electronic] United States |
PMID | 34585595
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- HLA-DR Antigens
- Ophthalmic Solutions
- Loteprednol Etabonate
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Topics |
- Dry Eye Syndromes
(diagnosis, drug therapy)
- HLA-DR Antigens
(genetics)
- Humans
- Inflammation
- Loteprednol Etabonate
(therapeutic use)
- Ophthalmic Solutions
(therapeutic use)
- Pilot Projects
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