4.1 Article

Influence of 0.002% Omidenepag Isopropyl on Intraocular Pressure and the Cornea in Normal Tension Glaucoma

Journal

JOURNAL OF GLAUCOMA
Volume 32, Issue 4, Pages 245-251

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/IJG.0000000000002167

Keywords

central corneal thickness; coefficient of variation; corneal erosion; normal tension glaucoma; Omidenepag isopropyl

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Analyzing the efficacy and safety of 0.002% omidenepag Isopropyl (OMDI) eye drops in glaucoma patients, it was found that the drops significantly reduced intraocular pressure but also caused transient changes in refraction and corneal endothelial cells, an increase in central corneal thickness, and corneal erosion.
Precis:Although Omidenepag isopropyl drops elicited stable intraocular pressure reductions in NTG patients, transient changes in refraction and corneal endothelial cells, significant increase of central corneal thickness, and corneal erosion should be considered. Purpose:To analyze the efficacy and safety of 0.002% omidenepag Isopropyl (OMDI) eye drops in patients with normal tension glaucoma (NTG). Methods:Medical records for 62 eyes treated with OMDI for >= 6 months were analyzed. Intraocular pressure (IOP), refraction, keratometry, central corneal thickness (CCT), endothelial cell count, coefficient of variation of endothelial cell area (CV), corneal erosion, and central retinal thickness were compared at baseline and 1, 3, and 6 months. Results:IOP significantly decreased from 13.4 +/- 3.8 to 11.9 +/- 3.0, 11.7 +/- 2.9, and 12.2 +/- 3.3 mm Hg at each follow-up (P<0.001). Endothelial cell count did not change, but CV transiently increased from 12.6 to 17.0 at 1 month, CCT increased from 531.5 to 538.4 mu m, myopia changed from -1.5 to -1.9 D, and keratometry changed from 44.5 to 44.7 D. CV, myopia, and keratometry recovered to baseline at 6 months; however, CCT remained high. Significant corneal erosion was observed at 6 months. Central retinal thickness changes were not observed. There were improvements in prostaglandin-associated skin pigmentation (86.7%), eyelash elongation (40.0%), and deepening of the upper eyelid sulcus and ptosis (similar to 30%) at 3 months after exchange to OMDI. Adverse reactions were corneal erosion (27.4%), corneal thickening (21.0%), conjunctival hyperemia (11.3%), photophobia (5.7%), blurred vision (5.7%), and anterior chamber cells (4.8%). Conclusions:OMDI eye drops elicited significant and stable IOP reductions after 6 months in NTG patients with low IOP. However, transient myopic and corneal endothelial cell changes, development of corneal thickening, and corneal erosion should be considered when using OMDI.

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