早产儿视网膜病变+病变的演变:ROPtool定量分析。

David K Wallace, Sharon F Freedman, Zheen Zhao
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摘要

目的:激光治疗早产儿视网膜病变(ROP)的主要适应症是合并病变或小动脉、小静脉异常扩张、扭曲。ROPtool是一个追踪视网膜血管并测量其宽度和弯曲度的计算机程序。我们的目的是通过将ROPtool应用于RetCam图像来深入了解plus疾病的演变,这些图像来自在ROP筛查期间拍摄了一系列照片的婴儿的眼睛。方法:作为另一项研究的一部分,收集了62名婴儿眼睛的连续图像。采用ROPtool对7例合并疾病患儿单眼59张图像进行分析。计算每幅图像中最弯曲血管的平均弯曲度和最扩张血管的平均宽度。结果:挠度由第一次检查时的平均7.72个单位增加到最大挠度检查时的24.44个单位,平均6.2周内增加217%。两只眼睛的扭曲度比第一次检查时增加了500%以上。血管宽度从第一次检查时的平均8.60单位增加到血管宽度最大时的11.03单位,在平均5.1周的时间内增加了28%。结论:ROPtool可以测量个体眼视网膜血管扩张和弯曲随时间的变化。随着疾病的发展,扭曲度的变化有时非常大,而血管宽度的变化往往更微妙。随着时间的推移,疾病的量化可能有助于提高我们对其机制的理解,并监测疾病进展或对治疗的反应。
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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Evolution of plus disease in retinopathy of prematurity: quantification by ROPtool.

Purpose: The primary indication for laser treatment in retinopathy of prematurity (ROP) is plus disease, or abnormal dilation and tortuosity of arterioles and venules. ROPtool is a computer program that traces retinal blood vessels and measures their width and tortuosity. Our purpose was to gain insight into the evolution of plus disease by applying ROPtool to RetCam images from eyes of infants who had serial photographs taken during their ROP screening period.

Methods: Serial images were collected from eyes of 62 infants screened for ROP as part of another study. Fifty-nine images of one eye of 7 infants who developed plus disease were selected and analyzed by ROPtool. The average tortuosity of the most tortuous blood vessel and the average width of the most dilated vessel in each quadrant were calculated for each image.

Results: Tortuosity increased from an average of 7.72 units at the first examination to 24.44 units at the examination with maximum tortuosity, or an increase of 217% over a mean time period of 6.2 weeks. Two eyes had an increase in tortuosity of more than 500% from the first examination. Vessel width increased from an average of 8.60 units at the first examination to 11.03 units at the examination with maximum blood vessel width, or an increase of 28% over a mean time period of 5.1 weeks.

Conclusions: ROPtool can measure changes in retinal vascular dilation and tortuosity in individual eyes over time. As plus disease develops, changes in tortuosity are sometimes very large, whereas changes in vessel width tend to be more subtle. Quantification of plus disease over time may help to improve our understanding of its mechanism and to monitor disease progression or response to treatment.

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