首页> 外文期刊>American Journal of Ophthalmology: The International Journal of Ophthalmology >Mechanism of retinal pigment epithelium tear formation following intravitreal anti-vascular endothelial growth factor therapy revealed by spectral-domain optical coherence tomography
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Mechanism of retinal pigment epithelium tear formation following intravitreal anti-vascular endothelial growth factor therapy revealed by spectral-domain optical coherence tomography

机译:光谱域光学相干断层扫描揭示玻璃体内抗血管内皮生长因子治疗后视网膜色素上皮撕裂形成的机制

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Purpose To demonstrate the mechanism by which retinal pigment epithelium (RPE) tears occur in eyes with neovascular age-related macular degeneration (AMD) treated with intravitreal anti-vascular endothelial growth factor (VEGF) agents using spectral-domain optical coherence tomography (OCT). Design Retrospective observational case series. Methods OCT images of 8 eyes that developed RPE tears following the administration of intravitreal anti-VEGF agents for neovascular AMD were evaluated. Pretear and posttear images were compared in order to elucidate the mechanism by which RPE tears occur in this setting. Results In all eyes, pretear images revealed a vascularized pigment epithelial detachment (PED) containing hyperreflective material consistent with choroidal neovascularization (CNV). This CNV was adherent to the undersurface of the RPE and created contractile folds in the RPE contour. In 6 eyes, contractile neovascular tissue spanned the PED, causing outward bowing of the Bruch membrane and a peaked appearance to the overlying RPE monolayer. RPE tears occurred after the first anti-VEGF injection in 6 of 8 eyes. The posttear OCT images showed a discontinuity in the RPE with the CNV adherent to the retracted RPE. In all eyes, the RPE ruptured along a segment of bare RPE not in contact with the CNV or Bruch membrane. Conclusions Eyes with vascularized PEDs secondary to AMD may show specific OCT findings that increase the risk for RPE tear following intravitreal anti-VEGF injection. Rapid involution and contraction of neovascular tissue adherent to the undersurface of the RPE may impart a substantial contractile force that tears this already-strained tissue layer.
机译:目的通过光谱域光学相干断层扫描(OCT)证实玻璃体内抗血管内皮生长因子(VEGF)药物治疗的新生血管性年龄相关性黄斑变性(AMD)眼中视网膜色素上皮(RPE)撕裂的发生机理。设计回顾性观察病例系列。方法对8只眼的OCT图像进行评估,这些眼在使用玻璃体内抗VEGF药物治疗新生血管性AMD后出现RPE眼泪。比较了前后眼的图像,以阐明在这种情况下RPE眼泪发生的机制。结果在所有眼睛中,眼前图像均显示血管化色素上皮脱离(PED),其中包含与脉络膜新血管形成(CNV)相符的高反射材料。该CNV附着在RPE的下表面,并在RPE轮廓上产生收缩褶皱。在6只眼中,收缩的新生血管组织跨过PED,导致Bruch膜向外弯曲,并在上方的RPE单层上出现峰顶。 8眼中有6眼首次注射抗VEGF后发生RPE眼泪。后撕裂OCT图像显示RPE中的不连续性,CNV附着在缩回的RPE上。在所有的眼睛中,RPE沿未与CNV或Bruch膜接触的裸露RPE的一部分破裂。结论玻璃体腔注射抗VEGF后,继发于AMD的具有血管化PED的眼睛可能显示出特定的OCT结果,从而增加RPE撕裂的风险。粘附在RPE底面上的新血管组织的快速向内收缩和收缩可能会产生相当大的收缩力,从而撕裂该已经应变的组织层。

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