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Direct OPTOS Nerve Size Determination of Prevalent Optic Nerve Hypoplasia in Alaska

机译:直接optos神经大小测定阿拉斯加普遍视神经发育不全的测定

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Background: Optic nerve hypoplasia (ONH), one of the most common causes of pediatric blindness in developed countries, has been difficult to directly quantify. We sought to measure optic nerve size in Alaskan pediatric patients with optic nerve hypoplasia using ultra-widefield fundus imaging. Methods: Adult and pediatric patients underwent conventional ultra widefield fundus imaging (OPTOS, Dunfermline, Scotland) with manual image processing to determine optic nerve size validated against refractive error and nystagmus and compared to optical spectral domain tomography. De-identified cases were then compared relative to visual acuity and birth prevalence. Results: In Alaska’s only pediatric ophthalmology outreach clinic, 108 cases of ONH less than 20 years old were clinically identified with 80 having ultra-widefield analysis. Median horizontal optic nerve diameter for 135 normals was 1.70 (95% C.I. 1.49, 2.14) whereas in patients clinically diagnosed with optic nerve hypoplasia was 1.23 (95% C.I 0.38, 1.45). Visual acuity (20/y) was related to horizontal optic nerve diameter (x) by y = 187 xsup-4.1/sup. Horizontal nerve diameter h could be estimated from vertical nerve diameter v by h = 0.73 v + 0.3 even in nystagmus patients. From 108 with ONH, 6 had threshold retinopathy of prematurity, 12 profound nystagmus, 32 legally blind, 6 with septo-optic dysplasia, and 5 with fetal alcohol syndrome. ONH is very prevalent in Alaska occurring at least 8– 10 per 10,000 births. Conclusion: Compared to vertical diameter, horizontal diameter was more distinctive of optic nerve hypoplasia and more perturbed by nystagmus. Both were independent of refractive error. When hand-held, spectral domain OCT is not convenient, ultra-widefield fundus analysis is recommended for direct estimation of optic nerve size in children and adults. Optic nerve hypoplasia is prevalent in Alaskan children.
机译:背景:视神经发育不全(ONH)是发达国家儿科失明的最常见原因之一,一直难以直接量化。我们试图测量阿拉斯加小儿科患者的视神经大小,使用超宽泛的底部成像进行视神经发育不全。方法:成人和儿科患者经过传统的超宽FIVEICUS底座成像(OPTOS,Dunfermline,Scotland),具有手动图像处理,以确定针对屈光误差和眼球菌验证的视神经尺寸,并与光谱域断层扫描进行比较。然后将去鉴定的病例相对于视力和出生患病率进行比较。结果:在阿拉斯加唯一的儿科眼科外展诊所,少于20岁的108例临床上鉴定了80个具有超界面分析。 135个法线的中间横向视神经直径为1.70(95%C.I. 1.49,2.14),而临床诊断为视神经发育不全的患者为1.23(95%C.i 0.38,1.45)。视力(20 / y)与横距视神经直径(x)y = 187 x -4.1 有关。卧式神经直径H可以通过H = 0.73 V + 0.3估计H = 0.73 V + 0.3,即使在眼球菌患者中也是如此。从108次,6例,6例过早的阈值视网膜病变,12个深刻的眼球菌,32种合法盲,6例,6种带散发光发育不全性,5例,胎儿酒精综合征。 ONH在阿拉斯加非常普遍,每10,000名诞生至少8-10。结论:与垂直直径相比,水平直径更为独特的视神经发育不全,并且由眼球菌的扰动越多。两者都与屈光误差无关。当手持式时,光谱域10月不方便,建议超宽泛的基底分析进行直接估计儿童和成人的视神经大小。视神经发育不全在阿拉斯加儿童普遍存在。

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