在具有持续疾病活动和高治疗需求的新生血管性老年黄斑变性中,将静脉内地塞米松作为抗血管内皮生长因子疗法的辅助疗法。

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY Journal of Ocular Pharmacology and Therapeutics Pub Date : 2024-07-01 Epub Date: 2023-12-20 DOI:10.1089/jop.2023.0105
Marlena Pietzuch, Irmela Mantel, Aude Ambresin, Christoph Tappeiner, Dana Nagyova, Guy Donati, Isabel B Pfister, Christin Schild, Justus G Garweg
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引用次数: 0

摘要

目的:评估在抗血管内皮生长因子(VEGF)治疗中改用或添加玻璃体内地塞米松植入剂(Dex;Ozurdex®)对患有新生血管性年龄相关性黄斑变性(nAMD)、疾病活动持续且治疗需求高的患者的疾病稳定性和治疗间隔的影响。方法:该回顾性非比较性多中心纵向病例系列纳入了接受过至少一次玻璃体内 Dex 植入的 nAMD 假性视网膜眼,这些假性视网膜眼在接受常规抗血管内皮生长因子治疗(雷尼珠单抗或阿弗利贝赛普)后仍有持续的视网膜积液。在抗血管内皮生长因子疗法中添加 Dex 之前和之后,均记录了视力、视网膜中央厚度 (CRT) 和眼压。结果:16名患者的16只眼睛符合抗血管内皮生长因子治疗后仍持续积液的纳入标准,其中14人的治疗间隔≤7周。患者年龄为(80.9 ± 7.4)岁,在改用 Dex 之前已接受了 25.5 ± 17.4 次抗血管内皮生长因子注射,间隔时间为(36.4 ± 21.9)个月。治疗间隔从最后一次注射抗血管内皮生长因子和第一次注射 Dex 之间的 5.5 ± 3.2 周延长至之后的 11.7 ± 7.3 周(P = 0.022)。CRT 保持稳定(切换前为 385.3 ± 152.1、383.9 ± 129.7 和 458.3 ± 155.2 μm,切换后分别为 12 个月和 24 个月;P = 0.78 和 P = 0.36)。早期视力的平均短期增长并不显著,但随着时间的推移并不持久。结论:在这些难以治疗的眼睛中,添加地塞米松可使治疗间隔显著而持续地延长,而CRT和视力则保持稳定。在抗血管内皮生长因子反应不理想的 nAMD 病例中,炎症或其他类固醇反应因素是否起着重要作用,这一点值得讨论。
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Intravitreal Dexamethasone as a Rescue for Anti-Vascular Endothelial Growth Factor Therapy in Neovascular Age-Related Macular Degeneration with Persistent Disease Activity and High Treatment Demand.

Purpose: 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. Methods: 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. Results: 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 (P = 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; P = 0.78 and P = 0.36, respectively). An insignificant mean short-term early increase in visual acuity was not sustained over time. Conclusions: 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.

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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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