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. 2017:2017:3765253.
doi: 10.1155/2017/3765253. Epub 2017 Jun 27.

Effect of Topical Nepafenac on Central Foveal Thickness following Panretinal Photocoagulation in Diabetic Patients

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Effect of Topical Nepafenac on Central Foveal Thickness following Panretinal Photocoagulation in Diabetic Patients

Nahla B Abu Hussein et al. J Ophthalmol. 2017.

Abstract

Purpose: To evaluate effectiveness of topical nepafenac in reducing macular edema following panretinal photocoagulation (PRP).

Design: Prospective randomized double-blinded controlled study.

Methods: Sixty eyes of 60 patients having proliferative or severe nonproliferative diabetic retinopathy had PRP. Patients were then divided into two groups: nepafenac group (30 eyes) receiving 1% topical nepafenac eye drops for 6 months and control group (30 eyes) receiving carboxymethylcellulose eye drops for 6 months. Best-corrected visual acuity (BCVA) and macular optical coherence tomography were followed up at 1, 2, 4, and 6 months after PRP.

Results: BCVA was significantly better in nepafenac group than in control group at all follow-ups (P < 0.01). At 6 months post-PRP, logMAR BCVA was 0.11 ± 0.04 (equivalent to 20/26 Snellen acuity) in the nepafenac group and 0.18 ± 0.08 (equivalent to 20/30 Snellen acuity) in the control group (P < 0.01). Central foveal thickness (CFT) increased in both groups from the first month after PRP. Increase in CFT was higher in control group than in nepafenac group throughout follow-up, but the difference became statistically significant only after 4 months. No significant ocular adverse events were reported with topical nepafenac.

Conclusion: Topical nepafenac can minimize macular edema and stabilize visual acuity following PRP for diabetic patients.

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Figures

Figure 1
Figure 1
Best-corrected visual acuity (BCVA) at baseline and during follow-ups in nepafenac and control groups.
Figure 2
Figure 2
Central foveal thickness (CFT) at baseline and during follow-ups in nepafenac and control groups.

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