Efficacy of Topical Nepafenac 0.3% in the Management of Postoperative Cystoid Macular Edema
- PMID: 33192068
- PMCID: PMC7654537
- DOI: 10.2147/TCRM.S271184
Efficacy of Topical Nepafenac 0.3% in the Management of Postoperative Cystoid Macular Edema
Abstract
Purpose: To assess the effect of twice-daily nepafenac ophthalmic suspension 0.3% on postoperative cystoid-macular-edema (CME).
Patients and methods: In this prospective, clinic-based, non-randomized case-series, 21 patients (21 eyes) were enrolled with either acute or chronic postoperative CME after cataract extraction. Patients were treated with twice-daily nepafenac 0.3% drops, and followed for at least a 4-month period. Best-corrected visual acuity (BCVA) and spectral-domain optical coherence tomography (SD-OCT)-derived central retinal thickness (CRT) were measured.
Results: From 21 patients, eight presented with acute postoperative CME and 13 with chronic CME. Mean follow-up was 4.82±1.24 months. No adverse events were reported during the study. Baseline BCVA was 0.49±0.36 logMAR and improved to 0.36±0.42 logMAR at the last follow-up visit (P<0.005). CRT decreased from 450.40±90.74 μm at baseline to 354.60±81.49 μm (P<0.05), following treatment.
Conclusion: Our outcomes strongly suggest that administrating nepafenac 0.3% drops on a twice-daily regimen could be a promising alternative for the management of postoperative CME. Additional studies are necessary to further validate our results.
Keywords: cataract operation; nepafenac; postoperative macular edema; topical use; treatment.
© 2020 Giarmoukakis et al.
Conflict of interest statement
Miltiadis K Tsilimbaris reports grants, personal fees from Novartis Hellas, personal fees from Bayer Hellas, grants, personal fees from Allergan Hellas, grants from Alcon Hellas, outside the submitted work. The authors report no other potential conflicts of interest for this work.
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