Dahlmann-Noor A H, Vrotsou K, Kostakis V, Brown J, Heath J, Iron A, McGill S, Vivian A J
Eye Treatment Centre, West Suffolk Hospital NHS Trust, Hardwick Lane, Bury St Edmunds IP33 2QZ, UK.
Br J Ophthalmol. 2009 Mar;93(3):342-5. doi: 10.1136/bjo.2008.138115. Epub 2008 Nov 19.
BACKGROUND/AIMS: To evaluate a new autorefractor, the Plusoptix Vision Screener (PVS), as a screening tool to detect risk factors for amblyopia by comparing it with gold-standard orthoptic vision screening in children.
Community-based screening study including 288 children age 4-7 years who were screened with the PVS and by orthoptic assessment (distance acuity, cover test, extraocular movements, 20 PD prism test, Lang stereotest). Follow-up comprehensive eye examination of screening-positive children included manual cycloplegic retinoscopy.
Testability was high for both methods. Orthoptic screening identified 36 children with reduced vision and/or factors associated with amblyopia (referral rate 12.5%). The PVS identified 16 children with potential vision problems (referral rate 5.6%), indicating only moderate sensitivity (44%; 95% CI 27.9 to 61.9%), but high specificity (100%; 95% CI 98.5 to 100%) to detect factors associated with amblyopia. The PVS underestimated visually significant refractive errors.
Use of the PVS as single screening test in young children may miss a significant number of children with amblyopia or amblyogenic risk factors.
背景/目的:通过将新型自动验光仪Plusoptix视力筛查仪(PVS)与儿童弱视金标准眼科视力筛查进行比较,评估其作为检测弱视危险因素的筛查工具的效果。
基于社区的筛查研究,纳入288名4至7岁儿童,分别使用PVS和眼科评估(远视力、遮盖试验、眼外肌运动、20棱镜度棱镜试验、Lang立体视试验)进行筛查。对筛查阳性儿童的后续综合眼科检查包括手动睫状肌麻痹视网膜检影。
两种方法的可测试性都很高。眼科筛查发现36名视力下降和/或有弱视相关因素的儿童(转诊率12.5%)。PVS发现16名有潜在视力问题的儿童(转诊率5.6%),表明其检测弱视相关因素的敏感性仅为中等(44%;95%可信区间27.9至61.9%),但特异性较高(100%;95%可信区间98.5至100%)。PVS低估了具有明显视觉意义的屈光不正。
将PVS作为幼儿的单一筛查测试可能会遗漏大量患有弱视或弱视危险因素的儿童。