• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

抗血管内皮生长因子治疗新生血管性年龄相关性黄斑变性后视网膜色素上皮撕裂。

Retinal Pigment Epithelium Tears after Anti-Vascular Endothelial Growth Factor Therapy for Neovascular Age-Related Macular Degeneration.

机构信息

Department of Ophthalmology, HanGil Eye Hospital, Incheon, Republic of Korea.

Department of Ophthalmology, Catholic Kwandong University College of Medicine, Incheon, Republic of Korea.

出版信息

Ophthalmologica. 2022;245(1):1-9. doi: 10.1159/000514991. Epub 2021 Feb 4.

DOI:10.1159/000514991
PMID:33540419
Abstract

PURPOSE

The aim of this study was to assess the visual prognostic factors of retinal pigment epithelium (RPE) tears and describe their clinical features.

METHODS

The medical records of treatment-naive neovascular age-related macular degeneration patients who received intravitreal anti-vascular endothelial growth factor (VEGF) injections were retrospectively reviewed.

RESULTS

The incidence of RPE tears was 1.36% (10 out of 733 eyes). The type of anti-VEGF agent administered did not affect the incidence (p = 0.985). The median best-corrected visual acuity (BCVA) of 10 patients decreased after an RPE tear (0.4-0.6 logarithm of the minimum angle of resolution [logMAR]); however, subsequent injections restored the BCVA to a level similar to that before the RPE tear (0.4 logMAR, p = 0.436). Central macular thickness improved significantly during the study (794.4-491.9 μm, p = 0.013). The final BCVA was positively correlated with the BCVA before and immediately after the RPE tear (p = 0.025 and 0.002, respectively) and was weakly correlated with foveal involvement of the RPE tear (p = 0.061).

CONCLUSION

The incidence of RPE tears did not differ according to the type of anti-VEGF agent. The final BCVA was proportional to the BCVA before and after RPE tears. Continuous treatment with anti-VEGF after the occurrence of RPE tears can benefit the final visual acuity and macular anatomy.

摘要

目的

本研究旨在评估视网膜色素上皮(RPE)撕裂的视觉预后因素,并描述其临床特征。

方法

回顾性分析接受玻璃体内抗血管内皮生长因子(VEGF)注射治疗的未经治疗的新生血管性年龄相关性黄斑变性患者的病历。

结果

RPE 撕裂的发生率为 1.36%(733 只眼中有 10 只)。给予的抗 VEGF 药物类型不影响发生率(p=0.985)。10 例患者的最佳矫正视力(BCVA)中位数在 RPE 撕裂后下降(0.4-0.6 最小角分辨率对数[logMAR]);然而,随后的注射将 BCVA 恢复到 RPE 撕裂前的水平(0.4 logMAR,p=0.436)。研究期间中央黄斑厚度显著改善(794.4-491.9μm,p=0.013)。最终 BCVA 与 RPE 撕裂前和立即后的 BCVA 呈正相关(p=0.025 和 0.002),与 RPE 撕裂的中心凹受累呈弱相关(p=0.061)。

结论

RPE 撕裂的发生率与抗 VEGF 药物的类型无关。最终的 BCVA 与 RPE 撕裂前后的 BCVA 成正比。RPE 撕裂发生后持续进行抗 VEGF 治疗有助于提高最终视力和黄斑解剖结构。

相似文献

1
Retinal Pigment Epithelium Tears after Anti-Vascular Endothelial Growth Factor Therapy for Neovascular Age-Related Macular Degeneration.抗血管内皮生长因子治疗新生血管性年龄相关性黄斑变性后视网膜色素上皮撕裂。
Ophthalmologica. 2022;245(1):1-9. doi: 10.1159/000514991. Epub 2021 Feb 4.
2
RETINAL PIGMENT EPITHELIAL TEAR AFTER INTRAVITREAL RANIBIZUMAB TREATMENT FOR NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.玻璃体腔内注射雷珠单抗治疗新生血管性年龄相关性黄斑变性后视网膜色素上皮撕裂
Retina. 2016 Oct;36(10):1851-9. doi: 10.1097/IAE.0000000000001009.
3
RETINAL PIGMENT EPITHELIAL TEAR AND ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY IN EXUDATIVE AGE-RELATED MACULAR DEGENERATION: Clinical Course and Long-Term Prognosis.视网膜色素上皮撕裂与抗血管内皮生长因子疗法治疗渗出性年龄相关性黄斑变性:临床病程与长期预后
Retina. 2016 May;36(5):868-74. doi: 10.1097/IAE.0000000000000823.
4
DOUBLE RETINAL PIGMENT EPITHELIUM TEARS IN NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.新生血管性年龄相关性黄斑变性中的双视网膜色素上皮撕裂
Retina. 2016 Nov;36(11):2197-2204. doi: 10.1097/IAE.0000000000001062.
5
Early and Late Retinal Pigment Epithelium Tears after Anti-Vascular Endothelial Growth Factor Therapy for Neovascular Age-Related Macular Degeneration.抗血管内皮生长因子治疗新生血管性年龄相关性黄斑变性后早期和晚期视网膜色素上皮撕裂。
Ophthalmology. 2018 Feb;125(2):237-244. doi: 10.1016/j.ophtha.2017.08.039. Epub 2017 Oct 6.
6
Long-term visual outcome of pigment epithelial tears in association with anti-VEGF therapy of pigment epithelial detachment in AMD.AMD 中色素上皮脱离的抗 VEGF 治疗相关的色素上皮撕裂的长期视力结果。
Eye (Lond). 2011 Sep;25(9):1181-6. doi: 10.1038/eye.2011.146. Epub 2011 Jun 24.
7
INCIDENCE AND LONG-TERM VISUAL ACUITY OUTCOMES OF RETINAL PIGMENT EPITHELIUM TEARS AFTER INTRAVITREAL ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR TREATMENT OF NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.抗血管内皮生长因子治疗新生血管性年龄相关性黄斑变性后视网膜色素上皮撕裂的发生率和长期视力结局。
Retina. 2019 Apr;39(4):664-669. doi: 10.1097/IAE.0000000000002029.
8
Vascularized retinal pigment epithelial detachment in age-related macular degeneration: treatment and RPE tear incidence.年龄相关性黄斑变性中的血管化视网膜色素上皮脱离:治疗和 RPE 撕裂发生率。
Graefes Arch Clin Exp Ophthalmol. 2012 Sep;250(9):1283-92. doi: 10.1007/s00417-012-1955-2. Epub 2012 Feb 21.
9
Sequential retinal pigment epithelium tears following intravitreal Ranibizumab injections for age-related macular degeneration.玻璃体内注射雷珠单抗治疗年龄相关性黄斑变性后相继发生的视网膜色素上皮撕裂
Eur J Ophthalmol. 2023 May;33(3):NP100-NP104. doi: 10.1177/11206721221093025. Epub 2022 Apr 7.
10
Incidence of retinal pigment epithelial tears after intravitreal ranibizumab injection for neovascular age-related macular degeneration.新生血管性年龄相关性黄斑变性玻璃体内注射雷珠单抗后视网膜色素上皮撕裂的发生率。
Ophthalmology. 2011 Dec;118(12):2447-52. doi: 10.1016/j.ophtha.2011.05.026. Epub 2011 Aug 27.

引用本文的文献

1
Switching to faricimab from the current anti-VEGF therapy: evidence-based expert recommendations.从当前的抗血管内皮生长因子(VEGF)疗法转换为法西单抗:基于证据的专家建议。
BMJ Open Ophthalmol. 2025 Jan 16;10(1):e001967. doi: 10.1136/bmjophth-2024-001967.
2
Short-Term Outcomes of Faricimab Treatment in Aflibercept-Refractory Eyes with Neovascular Age-Related Macular Degeneration.法西单抗治疗阿柏西普难治性新生血管性年龄相关性黄斑变性眼的短期疗效
J Clin Med. 2023 Aug 6;12(15):5145. doi: 10.3390/jcm12155145.
3
Extracellular vesicles as a potential therapeutic for age-related macular degeneration.
细胞外囊泡作为年龄相关性黄斑变性的一种潜在治疗手段。
Neural Regen Res. 2023 Sep;18(9):1876-1880. doi: 10.4103/1673-5374.367835.