SPATIAL PATTERN OF RETINAL PIGMENT EPITHELIUM TEAR DEVELOPMENT AND PROGRESSION AFTER ANTIVASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY FOR NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.

Q3 Medicine
Takuma Fukui, Keijiro Ishikawa, Satomi Shiose, Kumiko Kano, Kenichiro Mori, Shoji Notomi, Koh-Hei Sonoda
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Abstract

Purpose: The aim of this study was to demonstrate the spatial pattern of retinal pigment epithelium (RPE) tear development and progression after antivascular endothelial growth factor therapy for neovascular age-related macular degeneration.

Methods: We retrospectively reviewed six eyes with neovascular age-related macular degeneration that showed RPE tears after administration of intravitreal antivascular endothelial growth factor agents and were followed up for 12 months. The patterns of RPE tear development and progression were evaluated by analyzing positional relationships among the locations of the choroidal neovascularization membrane and pigment epithelial detachment (PED) area at baseline and the tear area using spectral-domain optical coherence tomography, color photography, fluorescein angiography, and fundus autofluorescence images.

Results: Pretear OCT images revealed fibrovascular PED in all eyes, one of which showed complications of hemorrhagic PED after treatment. In five eyes, RPE tears developed at the PED edge located on the opposite side of the choroidal neovascularization membrane. In the eye showing hemorrhagic PED, the RPE tear developed along the wide area of the PED edge. The torn RPE monolayer contracted toward the side of the choroidal neovascularization membrane in all eyes, and RPE loss involved the fovea in five eyes that showed significantly worse visual acuity (VA) after 12 months in comparison with the baseline value before the tear (logMAR VA; 0.3 vs. 1.29; P < 0.02).

Conclusion: The location of choroidal neovascularization membrane in PED determines the spatial pattern of RPE tear development and progression and helps to predict the visual outcome after RPE tears.

抗血管内皮生长因子治疗新生血管性老年黄斑变性后视网膜色素上皮撕裂发展和恶化的空间模式。
目的:展示抗血管内皮生长因子(VEGF)治疗新生血管性年龄相关性黄斑变性(nAMD)后视网膜色素上皮(RPE)撕裂发生和发展的空间模式:我们回顾性研究了六只患有 nAMD 的眼睛,这些眼睛在使用玻璃体内抗血管内皮生长因子药物后出现了 RPE 泪液,并随访了 12 个月。通过光谱域光学相干断层扫描(SD-OCT)、彩色照片、荧光素血管造影和眼底自动荧光成像,分析基线时脉络膜新生血管膜(CNVM)和色素上皮脱落(PED)区域与泪液区域的位置关系,评估 RPE 泪液发展和进展的模式:结果:所有眼球撕裂前的 OCT 图像均显示出纤维血管性 PED,其中一只眼球在治疗后出现出血性 PED 并发症。有五只眼睛在位于 CNVM 另一侧的 PED 边缘出现了 RPE 泪点。在出现出血性 PED 的那只眼睛中,RPE 撕裂是沿着 PED 边缘的宽区域形成的。所有眼球中撕裂的 RPE 单层都向 CNVM 一侧收缩,5 只眼球的 RPE 缺失涉及眼窝,与撕裂前的基线值相比,12 个月后视力(VA)明显下降(logMAR VA; 0.3 vs. 1.29; P < 0.02):PED中CNVM的位置决定了RPE撕裂发展和进展的空间模式,有助于预测RPE撕裂后的视力结果。
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
Retinal Cases and Brief Reports
Retinal Cases and Brief Reports Medicine-Ophthalmology
CiteScore
2.10
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发文量
342
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