Purpose:To evaluate the effects of dexamethasone implant for macular edema secondary to central retinal vein occlusion in patients younger than 50 years.Methods:Patients with no previous treatment, macular edema with central foveal thickness >250 m and best-corrected visual acuity between 1.30 LogMAR and 0.30 LogMAR were prospectively recruited for a 12-month follow-up study. After baseline dexamethasone implant, re-treatment was performed starting from the fourth month if a best-corrected visual acuity deterioration with central foveal thickness >250 m occurred after an initial improvement. The primary outcome was the change in the best-corrected visual acuity. Secondary outcomes included the proportion of eyes gaining at least 3 Early Treatment Diabetic Retinopathy Study lines, the change in the central foveal thickness, and the number of treatments.Results:Mean best-corrected visual acuity changed significantly from 0.60 0.38 LogMAR at baseline to 0.43 +/- 0.48 at the 12-month examination (P = 0.03). Eight of 16 eyes (50%) gained 3 Early Treatment Diabetic Retinopathy Study lines. Mean central foveal thickness improved significantly from 705 +/- 202 m at baseline to 408 +/- 196 m at 12-month visit (P < 0.001). The patients received a mean of 1.8 +/- 0.9 implants with 8/16 eyes and 3/16 receiving 1 and 2 implants, respectively.Conclusion:This present investigation indicates that dexamethasone implant can provide a 3-line improvement in half of the patients younger than 50 years and affected by macular edema secondary to central retinal vein occlusion.

DEXAMETHASONE IMPLANT FOR MACULAR EDEMA SECONDARY TO CENTRAL RETINAL VEIN OCCLUSION IN PATIENTS YOUNGER THAN 50 YEARS

Parodi MB;BANDELLO , FRANCESCO
2015-01-01

Abstract

Purpose:To evaluate the effects of dexamethasone implant for macular edema secondary to central retinal vein occlusion in patients younger than 50 years.Methods:Patients with no previous treatment, macular edema with central foveal thickness >250 m and best-corrected visual acuity between 1.30 LogMAR and 0.30 LogMAR were prospectively recruited for a 12-month follow-up study. After baseline dexamethasone implant, re-treatment was performed starting from the fourth month if a best-corrected visual acuity deterioration with central foveal thickness >250 m occurred after an initial improvement. The primary outcome was the change in the best-corrected visual acuity. Secondary outcomes included the proportion of eyes gaining at least 3 Early Treatment Diabetic Retinopathy Study lines, the change in the central foveal thickness, and the number of treatments.Results:Mean best-corrected visual acuity changed significantly from 0.60 0.38 LogMAR at baseline to 0.43 +/- 0.48 at the 12-month examination (P = 0.03). Eight of 16 eyes (50%) gained 3 Early Treatment Diabetic Retinopathy Study lines. Mean central foveal thickness improved significantly from 705 +/- 202 m at baseline to 408 +/- 196 m at 12-month visit (P < 0.001). The patients received a mean of 1.8 +/- 0.9 implants with 8/16 eyes and 3/16 receiving 1 and 2 implants, respectively.Conclusion:This present investigation indicates that dexamethasone implant can provide a 3-line improvement in half of the patients younger than 50 years and affected by macular edema secondary to central retinal vein occlusion.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/18013
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