Duke University Department of Ophthalmology, Durham, North Carolina; Massachusetts Eye and Ear Infirmary, Boston, Massachusetts.
Indiana University Department of Ophthalmology, Indianapolis, Indiana.
J AAPOS. 2020 Apr;24(2):89.e1-89.e7. doi: 10.1016/j.jaapos.2020.01.010. Epub 2020 Mar 27.
The presence of plus disease is important in determining when to treat retinopathy of prematurity (ROP), but the diagnosis of plus disease is subjective. Semiautomated computer programs (eg, ROPtool) can objectively measure retinal vascular characteristics in retinal images, but are limited by image quality. The purpose of this study was to evaluate whether ROPtool can accurately identify pre-plus and plus disease in narrow-field images of varying qualities using a new methodology that combines quadrant-level data from multiple images of a single retina.
This was a cross-sectional study of previously collected narrow-field retinal images of infants screened for ROP. Using one imaging session per infant, we evaluated the ability of ROPtool to analyze images using our new methodology and the accuracy of ROPtool indices (tortuosity index [TI], maximum tortuosity [T], dilation index [DI], maximum dilation [D], sum of adjusted indices [SAI], and tortuosity-weighted plus [TWP]) to identify pre-plus and plus disease in images compared to clinical examination findings.
Of 198 eyes (from 99 infants) imaged, 769/792 quadrants (98%) were analyzable. Overall, 98% of eyes had 3-4 analyzable quadrants. For plus disease, area under the curves (AUCs) of receiver operating characteristic curves were: TWP (0.98) > TI (0.97) = T (0.97) > SAI (0.96) > DI (0.88) > D (0.84). For pre-plus or plus disease, AUCs were: TWP (0.95) > TI (0.94) = T (0.94) = SAI (0.94) > DI (0.86) > D (0.83).
Using a novel methodology combining quadrant-level data, ROPtool can analyze narrow-field images of varying quality to identify pre-plus and plus disease with high accuracy.
在决定何时治疗早产儿视网膜病变(ROP)时,出现“+”病是很重要的,但“+”病的诊断是主观的。半自动计算机程序(例如,ROPtool)可以客观地测量视网膜图像中的视网膜血管特征,但受到图像质量的限制。本研究的目的是评估 ROPtool 是否可以使用一种新的方法,该方法结合了单个视网膜的多个图像的象限级数据,准确识别不同质量的窄视野图像中的“pre-plus”和“+”病。
这是一项回顾性研究,研究对象为接受 ROP 筛查的婴儿的窄视野视网膜图像。每例婴儿使用一个成像期,我们评估了 ROPtool 使用我们新方法进行图像分析的能力,以及 ROPtool 指数(扭曲指数[TI]、最大扭曲[T]、扩张指数[DI]、最大扩张[D]、调整后指数总和[SAI]和扭曲加权+[TWP])在与临床检查结果比较时识别“pre-plus”和“+”病的准确性。
在 198 只眼(来自 99 名婴儿)的成像中,769/792 个象限(98%)可分析。总体而言,98%的眼睛有 3-4 个可分析象限。对于“+”病,受试者工作特征曲线的曲线下面积(AUC)为:TWP(0.98)>TI(0.97)=T(0.97)>SAI(0.96)>DI(0.88)>D(0.84)。对于“pre-plus”或“+”病,AUC 为:TWP(0.95)>TI(0.94)=T(0.94)=SAI(0.94)>DI(0.86)>D(0.83)。
使用一种新的方法,结合象限级数据,ROPtool 可以分析不同质量的窄视野图像,以高精度识别“pre-plus”和“+”病。