2020
DOI: 10.1016/j.survophthal.2019.12.003
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Current management of uveitis-associated ocular hypertension and glaucoma

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Cited by 29 publications
(16 citation statements)
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“…Uveitic glaucoma is defined as the type of glaucoma that manifests as glaucomatous optic nerve head damage and/or visual field defect due to elevated IOP associated with increased resistance to aqueous outflow following inflammation [ 22 ]. Uveitis was diagnosed based on clinical examination, and its type was classified according to the criteria of the International Uveitis Study group [ 23 ].…”
Section: Methodsmentioning
confidence: 99%
“…Uveitic glaucoma is defined as the type of glaucoma that manifests as glaucomatous optic nerve head damage and/or visual field defect due to elevated IOP associated with increased resistance to aqueous outflow following inflammation [ 22 ]. Uveitis was diagnosed based on clinical examination, and its type was classified according to the criteria of the International Uveitis Study group [ 23 ].…”
Section: Methodsmentioning
confidence: 99%
“…The equivalent logarithm of the minimum angle of resolution (logMAR) was calculated and used for analysis [ 15 ]. Complications included posterior synechiae, cataract, band keratopathy, uveitic ocular hypertension (uveitic OHT, defined as intraocular pressure > 21 mmHg without optic disk or visual field changes), steroid-induced ocular hypertension (SIOHT, defined as IOP increase > 5 mmHg due to glucocorticoid use in the eye) [ 16 ], uveitic glaucoma (UG, defined as repeated IOP measurements > 21 mmHg with optic disk changes and/or visual field changes), and cystoid macular edema (CME). Ocular surgery was classified according to the indication.…”
Section: Methodsmentioning
confidence: 99%
“…These deficits could be abrogated by a week of systemic immunosuppressant therapy with fingolimod, a sphingosine-1phosphate receptor agonist, a drug that is used in relapsingremitting multiple sclerosis disease, thus offering another therapeutic approach to combat optic nerve damage due to pigment accumulation in the ANC of the eye that prevents AQH drainage and results in OHT. Mycophenolate, sustained release corticosteroids (Borkar et al, 2017), other pharmacological agents, trabeculectomy and AQH drainage shunts (Kwon et al, 2017), along with new generation biologics (Thomas et al, 2019) provide much hope for patients who succumb to non-infectious posterior uveitis, and uveitis-associated OHT/glaucoma (Kesav et al, 2020).…”
Section: Various Forms Of Glaucomamentioning
confidence: 99%