Evidence map›Paper›PMID 40817178›Full record

ArticleJournal of ophthalmic inflammation and infection2025

Efficacy and safety of fluocinolone acetonide intravitreal implant (0.2 µg/day) in patients with post-surgical inflammation associated with macular edema: a case series study.

Maria Madeira, Ana Cabugueira, Helena Urbano, Miguel Cordeiro, Marta Guedes

Abstract read
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Article in Journal of ophthalmic inflammation and infection, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maria MadeiraOphthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal. mfmadeira@ulslo.min-saude.pt.
Ana CabugueiraOphthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal.
Helena UrbanoOphthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal.
Miguel CordeiroOphthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal.
Marta GuedesOphthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPostoperative cystoid macular edema (PCME) is a primary cause of reduced vision following both cataract and/or vitreoretinal surgery, which may spontaneously resolve. This study aimed to evaluate the effectiveness and safety of the fluocinolone acetonide intravitreal (FAc) implant (0.2 µg/day) in patients with refractory PCME.

methodsRetrospective, non-interventional, and single center study conducted on patients with PCME treated with 0.2 µg/day FAc implant. All the patients received previous treatment with topical corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), triancinolone injection and dexamethasone implant. The primary end-points were the mean change in best-corrected-visual-acuity (BCVA) and the proportion of patients gaining ≥ 15 letters from baseline to the last follow-up visit. The secondary endpoints included the mean CRT reduction and the mean intraocular pressure (IOP) during the 36 months study period.

resultsEight eyes from 8 patients were included in the study. Median (95% Confidence-interval) BCVA was significantly improved from 60.0 (50.05-69.95) letters at baseline to 80.15 (77.25-85.00) letters at month-36, p = 0.043. At the last follow-up visit, 5 (62.5%) eyes gained ≥ 15 letters, without any eye experiencing a loss of BCVA compared to baseline. There was significant CRT reduction from baseline (median: 497.5 μm; 95%CI: 380.0-596.0 μm) to month-36 (Median: 252.0 μm; 95%CI: 242.0-268.0 μm); p = 0.012. Regarding safety, IOP remained stable from baseline (median: 14.5mmHg; 95%Confidence-interval: 12.0-23.0 mmHg) to the last follow-up visit (median: 13.5mmHg; 95% Confidence-interval: 9.0-19.0 mm Hg); p = 0.123.

conclusionsThe FAc implant significantly improved both visual and anatomic outcomes, and was effective in preventing recurrences, while maintaining a reasonable safety profile, in PCME refractory to intravitreal triancinolone and dexamethasone.

Indexed as

Fluocinolone acetonide intravitreal implantILUVIENInflammationIntraocular inflammationIntraocular pressurePostoperative cystoid macular edema

Identifiers

PMID40817178
PMCPMC12356776

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.