Madeira Maria, Cabugueira Ana, Urbano Helena, Cordeiro Miguel, Guedes Marta
Ophthalmology Department, West Lisbon Local Health Unit (Unidade de Saúde Local de Lisboa Ocidental), Rua da Junqueira, 126, Lisbon, 1349-019, Portugal.
J Ophthalmic Inflamm Infect. 2025 Aug 16;15(1):61. doi: 10.1186/s12348-025-00503-8.
Postoperative 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.
Retrospective, 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.
Eight 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.
The 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.
术后黄斑囊样水肿(PCME)是白内障和/或玻璃体视网膜手术后视力下降的主要原因,其可能会自发消退。本研究旨在评估玻璃体内注射醋酸氟轻松(FAc)植入物(0.2μg/天)治疗难治性PCME患者的有效性和安全性。
对接受0.2μg/天FAc植入物治疗的PCME患者进行回顾性、非干预性单中心研究。所有患者此前均接受过局部皮质类固醇、非甾体抗炎药(NSAIDs)、曲安奈德注射和地塞米松植入物治疗。主要终点为最佳矫正视力(BCVA)的平均变化以及从基线到最后一次随访时视力提高≥15行的患者比例。次要终点包括在36个月研究期间中央视网膜厚度(CRT)的平均降低和平均眼压(IOP)。
8例患者的8只眼纳入研究。BCVA中位数(95%置信区间)从基线时的60.0(50.05 - 69.95)行显著提高至36个月时的80.15(77.25 - 85.00)行,p = 0.043。在最后一次随访时,5只眼(62.5%)视力提高≥15行,与基线相比无眼出现BCVA下降。从基线(中位数:497.5μm;95%CI:380.0 - 596.0μm)到36个月时(中位数:252.0μm;95%CI:242.0 - 268.0μm)CRT显著降低;p = 0.012。关于安全性,眼压从基线(中位数:14.5mmHg;95%置信区间:12.0 - 23.0mmHg)到最后一次随访时保持稳定(中位数:13.5mmHg;95%置信区间:9.0 - 19.0mmHg);p = 0.123。
对于玻璃体内注射曲安奈德和地塞米松难治的PCME,FAc植入物显著改善了视力和解剖学结果,有效预防了复发,同时保持了合理的安全性。