Comparison of the PlusoptiX A16 and vision screener V100.

Frontiers in ophthalmology Pub Date : 2024-09-26 eCollection Date: 2024-01-01 DOI:10.3389/fopht.2024.1414417
Jorge Jorge, Paulo Fernandes
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Abstract

Clinical relevance: This study compares a novel photoscreening device with a previously validated one in a school-age population. It highlights a tendency of the new device to underestimate myopic spherical equivalent and overestimate hyperopic cases.

Purpose: To compare the PlusoptiX A16 and Vision Screener V100 photoscreeners in a study population of school-age children.

Methods: One hundred and thirty-three children, with a mean age of 6.4 ± 0.5 years, were evaluated using both the PlusoptiX A16 and Vision Screener V100 photoscreeners. The measurements were taken in random order in a room with diminished ambient lighting.

Results: The mean refractive error values for the M component were 0.27 ± 0.67D (PlusoptiX A16) and 0.21 ± 0.58D (Vision Screener V100). For the J0 component, means were 0.16 ± 0.38D (PlusoptiX A16) and 0.06 ± 0.33D (Vision Screener V100) and for theJ45 component the means were 0.03 ± 0.17D (PlusoptiX A16) and 0.06 ± 0.22D (Vision Screener V100). When compared both instruments, statistically significant differences were observed for the M (p=0.017) and J0 (p=0.004) components. The agreement rates between PlusoptiX A16 and Vision Screener V100 across different refractive components were 80.5% for sphere, 82.0% for cylinder, and 40.6% for axis when considering a range of ±0.75 D for sphere and cylinder and ±25.0 degrees for cylinder axis. Simultaneously considering all three conditions, the overall agreement was 73.7%.

Conclusion: The Vision Screener V100, while generally aligning well with PlusoptiX A16, tends to underestimate myopic spherical equivalent, overestimate hyperopic cases, and underestimate J0 astigmatism.

PlusoptiX A16 与视力筛查仪 V100 的比较。
临床意义:本研究比较了一种新型光筛设备和以前在学龄儿童中验证过的光筛设备。目的:在学龄儿童中比较 PlusoptiX A16 和 Vision Screener V100 光筛仪:方法:使用 PlusoptiX A16 和 Vision Screener V100 光筛仪对 133 名平均年龄为 6.4 ± 0.5 岁的儿童进行了评估。测量在环境光线较暗的房间内随机进行:M分量的屈光不正平均值为0.27 ± 0.67D(PlusoptiX A16)和0.21 ± 0.58D(Vision Screener V100)。J0 分量的平均值为 0.16 ± 0.38D(PlusoptiX A16)和 0.06 ± 0.33D(Vision Screener V100),J45 分量的平均值为 0.03 ± 0.17D(PlusoptiX A16)和 0.06 ± 0.22D(Vision Screener V100)。比较两种仪器,M(p=0.017)和 J0(p=0.004)分量的差异具有统计学意义。当球面和柱面的屈光度范围为±0.75 D,柱面轴的屈光度范围为±25.0度时,PlusoptiX A16和Vision Screener V100在不同屈光成分上的一致率分别为球面80.5%、柱面82.0%和轴面40.6%。同时考虑所有三个条件时,总体一致性为 73.7%:视力筛查仪 V100 与 PlusoptiX A16 大致吻合,但往往会低估近视球面等效度数,高估远视度数,低估 J0 散光度数。
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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