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1.
J Refract Surg ; 33(12): 834-839, 2017 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-29227512

RESUMO

PURPOSE: This study compared the efficacy and safety of suberoylanilide hydroxamic acid (SAHA) and mitomycin C (MMC) up to 4 months in the prevention of corneal haze induced by photorefractive keratectomy (PRK) in rabbits in vivo. METHODS: Corneal haze in rabbits was produced with -9.00 diopter PRK. A single application of SAHA (25 µM) or MMC (0.02%) was applied topically immediately after PRK. Effects of the two drugs were analyzed by slit-lamp microscope, specular microscope, TUNEL assay, and immunofluorescence. RESULTS: Single topical adjunct use of SAHA (25 µM) or MMC (0.02%) after PRK attenuated more than 95% corneal haze and myofibroblast formation (P < .001). SAHA did not reduce keratocyte density, cause keratocyte apoptosis, or increase immune cell infiltration compared to MMC (P < .01 or .001). Furthermore, SAHA dosing did not compromise corneal endothelial phenotype, density, or function in rabbit eyes, whereas MMC application did (P < .01 or .001). CONCLUSIONS: SAHA and MMC significantly decreased corneal haze after PRK in rabbits in vivo. SAHA exhibited significantly reduced short- and long-term damage to the corneal endothelium compared to MMC in rabbits. SAHA is an effective and potentially safer alternative to MMC for the prevention of corneal haze after PRK. Clinical trials are warranted. [J Refract Surg. 2017;33(12):834-839.].


Assuntos
Alquilantes/uso terapêutico , Opacidade da Córnea/prevenção & controle , Modelos Animais de Doenças , Inibidores de Histona Desacetilases/uso terapêutico , Ácidos Hidroxâmicos/uso terapêutico , Mitomicina/uso terapêutico , Ceratectomia Fotorrefrativa/efeitos adversos , Alquilantes/efeitos adversos , Animais , Apoptose , Córnea/cirurgia , Opacidade da Córnea/etiologia , Técnica Indireta de Fluorescência para Anticorpo , Inibidores de Histona Desacetilases/efeitos adversos , Ácidos Hidroxâmicos/efeitos adversos , Marcação In Situ das Extremidades Cortadas , Mitomicina/efeitos adversos , Coelhos , Lâmpada de Fenda , Resultado do Tratamento , Vorinostat
2.
Arch Ophthalmol ; 127(1): 45-9, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19139337

RESUMO

OBJECTIVE: To assess optical coherence tomography in differentiating optic disc edema (ODE) due to papilledema and other optic neuropathies from optic nerve head drusen (ONHD). METHODS: Optical coherence tomographic images from 60 subjects (20 with ODE, 20 with ONHD, and 20 control subjects) were assessed qualitatively and quantitatively. Qualitative criteria for ODE included an elevated optic nerve head with smooth internal contour and subretinal hyporeflective space (SHYPS) with recumbent "lazy V" pattern. Optic nerve head drusen displayed a "lumpy-bumpy" internal optic nerve contour and a rapid decline in SHYPS thickness. Quantitative comparisons included retinal nerve fiber layer and SHYPS thickness. RESULTS: Optical coherence tomography differentiated ODE from ONHD qualitatively (sensitivity, 63%; specificity, 63%) and quantitatively (sensitivity, 80%; specificity, 90%). Respective differences in mean retinal nerve fiber layer thickness between ODE and ONHD were significant (P < .002) superiorly (206.8 vs 121.7 microm), nasally (176.3 vs 78.6 microm), inferiorly (247.2 vs 153.8 microm), and temporally (180.0 vs 85.5 microm). Respective differences in mean SHYPS thickness between ODE and ONHD were significant (P < .001) at radii of 0.75 mm (512.1 vs 274.4 microm), 1.5 mm (291.4 vs 103.0 microm), and 2.0 mm (145.5 vs 60.7 microm). CONCLUSION: Optical coherence tomography can differentiate ODE from ONHD, particularly when the nasal retinal nerve fiber layer and SHYPS thickness at the 2.0-mm radius are greater than 86 microm and 127 microm, respectively.


Assuntos
Drusas do Disco Óptico/diagnóstico , Papiledema/diagnóstico , Tomografia de Coerência Óptica/métodos , Diagnóstico Diferencial , Reações Falso-Positivas , Humanos , Fibras Nervosas/patologia , Valor Preditivo dos Testes , Curva ROC , Células Ganglionares da Retina/patologia , Sensibilidade e Especificidade
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