Bromfenac 0.09% for the treatment of macular edema secondary to noninfectious uveitis
| dc.contributor.author | S.Saade, Joanna S. | |
| dc.contributor.author | Istambouli, Rachid | |
| dc.contributor.author | Abdulaal, Marwan R. | |
| dc.contributor.author | Antonios, Rafic S. | |
| dc.contributor.author | Hamam, Rola N. | |
| dc.contributor.department | Ophthalmology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T12:08:50Z | |
| dc.date.available | 2025-01-24T12:08:50Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | PURPOSE: The topical nonsteroidal anti-inflammatory drug bromfenac 0.09% has a potential benefit in uveitic macular edema (UME) with a safe side effect profile. The aim of the study is to assess the efficacy of bromfenac sodium solution in the treatment of UME. METHODS: The charts of 10 patients with macular edema due to noninfectious uveitis treated with bromfenac 0.09% were reviewed retrospectively. The main outcomes studied were the best-corrected visual acuity (BCVA) and the central retinal thickness (CRT) compared 4 months before bromfenac initiation, at the time of its initiation, and 4 months later. RESULTS: Twelve eyes of 10 patients were included. BCVA and CRT were unchanged 4 months befoew bromfenac compared to the time of bromfenac initiation (P = 1.0 and P = 0.2, respectively). There were a significant improvement in BCVA after 4 months of bromfenac treatment (P = 0.043) and a significant decrease in CRT (P = 0.002). Subretinal fluid resolved completely in 8/9 eyes, and 4/9 eyes had a complete resolution of cystoid macular edema at 4 months. CONCLUSION: Bromfenac may be a useful addition to the treatment of UME. © 2021 Middle East African Journal of Ophthalmology | Published by Wolters Kluwer - Medknow. | |
| dc.identifier.doi | https://doi.org/10.4103/meajo.meajo_134_21 | |
| dc.identifier.eid | 2-s2.0-85116408916 | |
| dc.identifier.pmid | 34759667 | |
| dc.identifier.uri | http://hdl.handle.net/10938/31931 | |
| dc.language.iso | en | |
| dc.publisher | Wolters Kluwer Medknow Publications | |
| dc.relation.ispartof | Middle East African Journal of Ophthalmology | |
| dc.source | Scopus | |
| dc.subject | Bromfenac | |
| dc.subject | Macular edema | |
| dc.subject | Nonsteroidal anti-inflammatory drugs | |
| dc.subject | Ocular inflammation | |
| dc.subject | Uveitis | |
| dc.subject | Benzophenones | |
| dc.subject | Bromobenzenes | |
| dc.subject | Humans | |
| dc.subject | Retrospective studies | |
| dc.subject | Tomography, optical coherence | |
| dc.subject | Visual acuity | |
| dc.subject | Acetazolamide | |
| dc.subject | Indometacin | |
| dc.subject | Infliximab | |
| dc.subject | Ketorolac | |
| dc.subject | Benzophenone derivative | |
| dc.subject | Bromobenzene | |
| dc.subject | Adult | |
| dc.subject | Article | |
| dc.subject | Best corrected visual acuity | |
| dc.subject | Case report | |
| dc.subject | Central retinal thickness | |
| dc.subject | Clinical article | |
| dc.subject | Cohort analysis | |
| dc.subject | Continuous infusion | |
| dc.subject | Controlled study | |
| dc.subject | Drug efficacy | |
| dc.subject | Female | |
| dc.subject | Human | |
| dc.subject | Macular thickness | |
| dc.subject | Male | |
| dc.subject | Medical record review | |
| dc.subject | Middle aged | |
| dc.subject | Optical coherence tomography | |
| dc.subject | Retina macula cystoid edema | |
| dc.subject | Retrospective study | |
| dc.subject | Spondylarthritis | |
| dc.subject | Subretinal fluid | |
| dc.subject | Treatment duration | |
| dc.subject | Treatment indication | |
| dc.subject | Treatment outcome | |
| dc.subject | Complication | |
| dc.title | Bromfenac 0.09% for the treatment of macular edema secondary to noninfectious uveitis | |
| dc.type | Article |
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