Swiss Eye Institute and Clinic for Vitreoretinal Diseases, Berner Augenklinik, Bern, Switzerland.
Department of Ophthalmology, Bern University Hospital, Bern, Switzerland.
J Ocul Pharmacol Ther. 2024 Jul-Aug;40(6):361-369. doi: 10.1089/jop.2023.0105. Epub 2023 Dec 20.
To assess the impact of switching to, or adding, an intravitreal dexamethasone implant (Dex; Ozurdex) in anti-vascular endothelial growth factor (VEGF) therapy on disease stability and treatment intervals in eyes with neovascular age-related macular degeneration (nAMD) and persistent disease activity and high treatment demand. This retrospective noncomparative multicenter longitudinal case series included pseudophakic eyes with nAMD and persistent retinal fluid despite regular anti-VEGF therapy (ranibizumab or aflibercept) that received at least 1 intravitreal Dex implant. Visual acuity, central retinal thickness (CRT), and intraocular pressure were recorded before, and after, the addition of Dex to anti-VEGF therapy. Sixteen eyes of 16 patients met the inclusion criteria of persistent fluid despite anti-VEGF therapy, under treatment intervals of ≤7 weeks in 14 instances. Patients were 80.9 ± 7.4 years old and had received 25.5 ± 17.4 anti-VEGF injections before Dex over a period of 36.4 ± 21.9 months before switching. The treatment interval increased from 5.5 ± 3.2 weeks between the last anti-VEGF and first Dex injection to 11.7 ± 7.3 weeks thereafter ( = 0.022). CRT remained stable (385.3 ± 152.1, 383.9 ± 129.7, and 458.3 ± 155.2 μm before switching as well as 12 and 24 months after switching = 0.78 and = 0.36, respectively). An insignificant mean short-term early increase in visual acuity was not sustained over time. The addition of Dex resulted in a relevant and sustained increase in treatment intervals, whereas CRT and visual acuity remained stable in these difficult-to-treat eyes. It may be discussed whether inflammation or other steroid-responsive factors play a significant role in cases of nAMD with nonsatisfactory responses to anti-VEGF.
评估在接受抗血管内皮生长因子 (VEGF) 治疗的新生血管性年龄相关性黄斑变性 (nAMD) 且疾病持续活动且治疗需求较高的患者中,转换或添加玻璃体内地塞米松植入物 (Dex; Ozurdex) 对疾病稳定性和治疗间隔的影响。本回顾性非对照多中心纵向病例系列纳入了患有 nAMD 且尽管接受了雷珠单抗或阿柏西普等常规抗 VEGF 治疗后仍存在持续性视网膜液的非白内障眼,并至少接受了 1 次玻璃体内 Dex 植入。在添加 Dex 进行抗 VEGF 治疗前后,记录视力、中心视网膜厚度 (CRT) 和眼内压。16 例患者的 16 只眼符合持续存在视网膜液但仍需接受抗 VEGF 治疗的纳入标准,其中 14 例的治疗间隔小于等于 7 周。患者的年龄为 80.9±7.4 岁,在转换前已接受 Dex 治疗,期间共接受了 25.5±17.4 次抗 VEGF 注射,历时 36.4±21.9 个月。治疗间隔从最后一次抗 VEGF 注射到第一次 Dex 注射之间的 5.5±3.2 周增加到此后的 11.7±7.3 周 ( = 0.022)。CRT 在转换前后均保持稳定(分别为 385.3±152.1、383.9±129.7 和 458.3±155.2μm, = 0.78 和 = 0.36)。视力在短期内出现了短暂的、轻微的、无统计学意义的早期增高,但未持续。在这些治疗困难的眼中,添加 Dex 可显著增加治疗间隔,同时 CRT 和视力保持稳定。可能需要讨论在对抗 VEGF 反应不理想的 nAMD 病例中,炎症或其他对类固醇有反应的因素是否起重要作用。