AMD 中的 3 型 MNV:3 年黄斑萎缩发展的基线预测因素。

IF 4.4 Q1 OPHTHALMOLOGY Ophthalmology. Retina Pub Date : 2024-11-18 DOI:10.1016/j.oret.2024.11.011
Riccardo Sacconi, Paolo Forte, Giulia Corradetti, Eliana Costanzo, Vittorio Capuano, Elodie Bousquet, Federico Beretta, Serena Iannuzzi, Maria Sole Polito, Massimo Nicolo', Mariacristina Parravano, Eric Souied, David Sarraf, SriniVas Sadda, Francesco Bandello, Giuseppe Querques
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引用次数: 0

摘要

目的:确定抗血管内皮生长因子疗法(anti-VEGF)治疗继发于新生血管性年龄相关性黄斑变性(nAMD)的3型黄斑新生血管(MNV)3年黄斑萎缩(MA)发展的基线光学相干断层扫描(OCT)预测因素:多中心、回顾性、纵向研究:我们纳入了基线时继发于 nAMD 的 3 型 MNV 患者,他们在 3 年的随访期间接受了抗血管内皮生长因子治疗:患者来自六家视网膜转诊机构:1)意大利米兰的圣拉斐尔大学;2)意大利热那亚的热那亚大学;3)美国洛杉矶的多尼眼科研究所;4)美国洛杉矶的斯坦因眼科研究所;5)法国克里特尔的东巴黎大学;6)意大利罗马的IRCCS Bietti基金会。主要结果指标:多变量分析,以确定抗血管内皮生长因子疗法治疗继发于nAMD的3型MNV患者3年MA发展的基线独立预测因素:我们纳入了 131 名患者的 131 只眼睛(平均年龄为 80±6 岁,81% 为女性)。基线最佳矫正视力为 0.49±0.40 LogMAR,3 年随访结束时显著下降至 0.59±0.43 LogMAR(p结论:黄斑萎缩是接受抗血管内皮生长因子注射治疗的3型MNV的常见并发症。在抗血管内皮生长因子治疗期间,有几种因素可被视为黄斑萎缩发展的基线预测因素。
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Type 3 MNV in AMD: baseline predictors of 3-year macular atrophy development.

Purpose: To identify baseline optical coherence tomography (OCT) predictors of the 3-year macular atrophy (MA) development for type 3 macular neovascularization (MNV) secondary to neovascular age-related macular degeneration (nAMD) treated by anti-VEGF therapy.

Design: Multicenter, retrospective, longitudinal study.

Participants: We included patients with treatment-naïve type 3 MNV secondary to nAMD at baseline, treated with anti-VEGF during a 3-year follow-up.

Methods: Patients were identified from six retinal referral institutions: 1) San Raffaele University, Milan, Italy 2) University of Genova, Genova, Italy; 3) Doheny Eye Institute, Los Angeles, USA; 4) Stein Eye Institute, Los Angeles, USA; 5) University of Paris Est, Creteil, France; 6) IRCCS Bietti Foundation, Rome, Italy. Several baseline predictors of 3-year MA area were analyzed based on structural OCT and demographics.

Main outcome measures: Multivariate analysis in order to identify baseline independent predictors of the 3-year MA development for type 3 MNV secondary to nAMD treated by anti-VEGF therapy.

Results: We included 131 eyes of 131 patients (mean age 80±6-year-old, 81% females). Best-corrected visual acuity was 0.49±0.40 LogMAR at the baseline and significantly decreased to 0.59±0.43 LogMAR at the end of 3-year follow-up (p<0.001). Patients were treated with 11±6 anti-VEGF injections and developed atrophy in 75% of cases (from 18% at the baseline). Eyes that developed 3-year MA were treated with a significantly lower number of injections compared to eyes without MA (9.9±5.5 vs 14.7±7.2 injections, p<0.001). The most relevant independent predictors at baseline of MA area at 3-year follow-up were: area of MA at baseline (p<0.001), AMD phenotype (presence of reticular pseudodrusen) (p=0.017), baseline presence of nascent geographic atrophy (p=0.008), and the baseline presence of subretinal hyper-reflective material (p=0.002).

Conclusions: Macular atrophy development is a frequent complication of type 3 MNV treated with anti-VEGF injections. Several factors could be considered as baseline predictors of atrophy development during the anti-VEGF treatment.

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来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
期刊最新文献
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