Early real-world outcomes of intravitreal aflibercept 8 mg in treatment-Naïve neovascular AMD: AI-assisted fluid volume analysis.

IF 1.9 Q2 OPHTHALMOLOGY
Jennifer Cattaneo, Eva C De Oliveira Figueiredo, Andrea Montesel, Sandra Vermeirsch, Chiara M Eandi
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引用次数: 0

Abstract

Background: This study was conducted as a retrospective, exploratory analysis to assess early anatomical and functional effects of intravitreal aflibercept 8 mg in neovascular age-related macular degeneration (nAMD) in a small cohort of patients.

Methods: This retrospective study was conducted at the Jules Gonin Eye Hospital in Lausanne, Switzerland, and included treatment-naïve patients with nAMD. Patients received a minimum of two intravitreal injections (IVT) of aflibercept 8 mg over a 3-month period. Key outcomes assessed were changes in best-corrected visual acuity (BCVA), central subfield thickness (CST), mean retinal thickness (RT), total fluid (TF) volume which was calculated as the sum of intraretinal fluid (IRF), subretinal fluid (SRF) and pigment epithelial detachment (PED) volumes. These parameters were evaluated at baseline, month 1, and month 3 using the RetinAI Discovery® platform, an artificial intelligence-based analysis system.

Results: 10 eyes of 10 patients were enrolled. Mean age was 77.7 ± 12.5 years. Comparative analysis between baseline, month 1, and month 3 revealed statistically significant reduction in CST, RT and TF volume, indicating a positive early response to treatment. One adverse event of intraocular inflammation (IOI) occurred in one patient (10%) after the second IVT injection. Treatment was subsequently interrupted, and IOI resolved with topical corticosteroids therapy.

Conclusion: Intravitreal aflibercept 8 mg demonstrated early anatomical and functional improvements in nAMD treatment-naïve patients after the first 3-months. The use of the AI-based analysis allowed for detailed and automated assessment of retinal changes, providing valuable insights into early treatment effects. Given the retrospective design and small cohort, further studies are warranted to assess long-term outcomes and the potential predictive value of early changes on long-term visual prognosis and safety.

Clinical trial number: Not applicable.

研究背景这项研究是一项回顾性探索分析,目的是评估8毫克玻璃体内阿弗利百普治疗新生血管性年龄相关性黄斑变性(nAMD)的早期解剖和功能效果:这项回顾性研究在瑞士洛桑的儒勒-戈宁眼科医院进行,研究对象包括未接受过治疗的nAMD患者。患者在3个月内至少接受了两次阿弗利百普8毫克的玻璃体内注射(IVT)。评估的主要结果包括最佳矫正视力(BCVA)、中央子场厚度(CST)、平均视网膜厚度(RT)、总积液量(TF)的变化,总积液量是视网膜内积液量(IRF)、视网膜下积液量(SRF)和色素上皮脱落量(PED)的总和。这些参数分别在基线、第1个月和第3个月使用基于人工智能的分析系统RetinAI Discovery®平台进行评估:结果:10 名患者的 10 只眼睛入选。平均年龄为 77.7 ± 12.5 岁。基线、第1个月和第3个月之间的比较分析显示,CST、RT和TF的体积均有统计学意义的显著减少,表明治疗的早期反应良好。一名患者(10%)在第二次注射 IVT 后出现了眼内炎症(IOI)的不良反应。随后治疗中断,局部皮质类固醇治疗后,眼内炎缓解:结论:8 毫克玻璃体内阿弗利贝赛(aflibercept 8 mg)在头 3 个月后对 nAMD 治疗无效的患者显示出早期的解剖和功能改善。使用基于人工智能的分析方法可以对视网膜变化进行详细的自动评估,为了解早期治疗效果提供了宝贵的信息。鉴于该研究采用回顾性设计,队列规模较小,因此有必要开展进一步研究,以评估长期疗效以及早期变化对长期视觉预后和安全性的潜在预测价值:临床试验编号:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
4.30%
发文量
81
审稿时长
19 weeks
期刊介绍: International Journal of Retina and Vitreous focuses on the ophthalmic subspecialty of vitreoretinal disorders. The journal presents original articles on new approaches to diagnosis, outcomes of clinical trials, innovations in pharmacological therapy and surgical techniques, as well as basic science advances that impact clinical practice. Topical areas include, but are not limited to: -Imaging of the retina, choroid and vitreous -Innovations in optical coherence tomography (OCT) -Small-gauge vitrectomy, retinal detachment, chromovitrectomy -Electroretinography (ERG), microperimetry, other functional tests -Intraocular tumors -Retinal pharmacotherapy & drug delivery -Diabetic retinopathy & other vascular diseases -Age-related macular degeneration (AMD) & other macular entities
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