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抗血管内皮生长因子治疗对伴或不伴视网膜色素上皮脱离的新生血管性年龄相关性黄斑变性的影响:一项真实世界研究

Impact of Anti-Vascular Endothelial Growth Factor Treatment on Neovascular Age-Related Macular Degeneration with and without Retinal Pigment Epithelial Detachment: A Real-World Study.

作者信息

Kuo Yu-Wei, Lee Cheng-Yung, Hsieh Yi-Ting, Yang Chung-May, Ho Tzyy-Chang, Lai Tso-Ting, Yang Chang-Hao

机构信息

Department of Ophthalmology, National Taiwan University Hospital, Taipei City 100225, Taiwan.

Department of Ophthalmology, Sijhih Cathay General Hospital, New Taipei City 221037, Taiwan.

出版信息

J Pers Med. 2024 Sep 28;14(10):1041. doi: 10.3390/jpm14101041.

DOI:10.3390/jpm14101041
PMID:39452548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11508268/
Abstract

BACKGROUND/OBJECTIVES: This study evaluates the impact of anti-vascular endothelial growth factor (anti-VEGF) treatment on neovascular age-related macular degeneration (nAMD) with and without pigment epithelial detachment (PED) over a one-year period.

METHODS

Conducted at a tertiary referral center in Taiwan, this retrospective analysis included 88 eyes treated with intravitreal aflibercept injections. Patients were categorized into four groups based on the presence or absence of PED at baseline and 12 months post-treatment.

RESULTS

Significant reductions in central macular thickness (CMT) and PED height were observed, although no statistical difference was found in best-corrected visual acuity (BCVA). The presence or type of PED did not negatively impact visual outcomes. Among nAMD patients with persistent PED throughout the first year of anti-VEGF treatment, linear regression analysis showed that mixed-type PED revealed poor final BCVA compared to those with serous PED. The analysis also identified older age and poorer initial BCVA as predictors of less favorable visual outcomes.

CONCLUSIONS

This study highlights the effectiveness of anti-VEGF therapy in real-world settings and offers insights into factors influencing visual outcomes for nAMD patients with PED.

摘要

背景/目的:本研究评估了抗血管内皮生长因子(anti-VEGF)治疗在一年时间内对伴有和不伴有色素上皮脱离(PED) 的新生血管性年龄相关性黄斑变性(nAMD)的影响。

方法

本回顾性分析在台湾的一家三级转诊中心进行,纳入了88只接受玻璃体内阿柏西普注射治疗的眼睛。根据基线和治疗后12个月时是否存在PED,将患者分为四组。

结果

观察到黄斑中心厚度(CMT)和PED高度显著降低,尽管最佳矫正视力(BCVA)没有统计学差异。PED的存在或类型对视力结果没有负面影响。在抗VEGF治疗的第一年中持续存在PED的nAMD患者中,线性回归分析显示,与浆液性PED患者相比,混合型PED患者的最终BCVA较差。分析还确定年龄较大和初始BCVA较差是视力结果较差的预测因素。

结论

本研究强调了抗VEGF治疗在实际临床中的有效性,并为影响伴有PED的nAMD患者视力结果的因素提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de91/11508268/587f9445a1e5/jpm-14-01041-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de91/11508268/587f9445a1e5/jpm-14-01041-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de91/11508268/587f9445a1e5/jpm-14-01041-g001.jpg

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本文引用的文献

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BMC Ophthalmol. 2024 Sep 3;24(1):393. doi: 10.1186/s12886-024-03663-8.
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Impact of Anti-VEGF Treatment and Patient Characteristics on Vision Outcomes in Neovascular Age-related Macular Degeneration: Up to 6-Year Analysis of the AAO IRIS® Registry.抗血管内皮生长因子(VEGF)治疗及患者特征对新生血管性年龄相关性黄斑变性视力预后的影响:美国眼科学会(AAO)虹膜(IRIS®)注册研究长达6年的分析
Ophthalmol Sci. 2023 Oct 31;4(2):100421. doi: 10.1016/j.xops.2023.100421. eCollection 2024 Mar-Apr.
3
Comparative efficacy of aflibercept and ranibizumab in the treatment of age-related macular degeneration with retinal pigment epithelial detachment: a systematic review and network meta-analysis.
比较阿柏西普和雷珠单抗治疗伴有视网膜色素上皮脱离的年龄相关性黄斑变性的疗效:系统评价和网络荟萃分析。
BMC Ophthalmol. 2023 Nov 21;23(1):473. doi: 10.1186/s12886-023-03214-7.
4
Clinical Characteristics of Eyes with Neovascular Age-Related Macular Degeneration and Retinal Pigment Epithelium Tears.新生血管性年龄相关性黄斑变性合并视网膜色素上皮撕裂眼的临床特征
J Clin Med. 2023 Aug 24;12(17):5496. doi: 10.3390/jcm12175496.
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Second eyes to develop neovascular age-related macular degeneration have fewer symptoms and better one-year visual outcomes.继发眼中新生血管性年龄相关性黄斑变性的症状较少,一年后的视力预后较好。
BMC Ophthalmol. 2023 Jul 7;23(1):303. doi: 10.1186/s12886-023-03021-0.
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Faricimab in neovascular AMD: first report of real-world outcomes in an independent retina clinic.法西单抗治疗新生血管性年龄相关性黄斑变性:独立视网膜诊所真实世界结局的首次报告。
Eye (Lond). 2023 Oct;37(15):3282-3289. doi: 10.1038/s41433-023-02505-z. Epub 2023 Mar 23.
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Sci Rep. 2023 Jan 2;13(1):68. doi: 10.1038/s41598-022-27078-x.
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Ophthalmol Ther. 2023 Apr;12(2):827-837. doi: 10.1007/s40123-022-00618-4. Epub 2022 Dec 20.