Pediatric Vision Laboratory, Retina Foundation of the Southwest , Dallas, Texas.
Heaton Eye Associates , Tyler, Texas.
J Binocul Vis Ocul Motil. 2021 Jan-Mar;71(1):29-34. doi: 10.1080/2576117X.2021.1874776. Epub 2021 Feb 8.
: Age norms and testability for 3-5 year old children have been reported for the PASS III stereotest using a pointing response. We aimed to expand the normative data to children as young as 6 months, assess testability, and evaluate validity use of the PASS III as a preferential-looking test for younger children and children with special needs. : 68 control children, 362 children with eye conditions, and 167 children with special needs were tested with the PASS III. Percent testable was calculated for children with and without special needs, normal tolerance limits were determined, and test validity was assessed. : In controls, mean PASS III stereoacuity improved from 371 arcsec at 12 months to 174 arcsec at 24 months, and 87 arcsec at 36 months. Testability in the 12, 24, and 36 months age groups were 81%, 87%, and 97% respectively and 92% for special needs children. Comparison to previously published norms and testing in a known nil stereoacuity cohort supported PASS III test validity. Compared to gold standard stereoacuity tests, accuracy of the PASS was 89%. : Overall, preferential-looking tests using the PASS III provide a sensitive and specific measure of stereoacuity with high testability for young children and children with special needs.
年龄规范和可测试性为 3-5 岁的儿童已经报道了 PASS III 立体测试使用指点反应。我们旨在扩大规范数据为 6 个月大的儿童,评估可测试性,并评估有效性使用 PASS III 作为年幼儿童和有特殊需要的儿童的优先观察测试。68 名对照儿童、362 名眼部疾病儿童和 167 名特殊需要儿童接受了 PASS III 测试。计算了有和没有特殊需要的儿童的可测试百分比,确定了正常的耐受极限,并评估了测试的有效性。在对照组中,PASS III 立体视力的平均改善从 12 个月时的 371 弧秒提高到 24 个月时的 174 弧秒,36 个月时的 87 弧秒。12、24 和 36 个月年龄组的可测试性分别为 81%、87%和 97%,特殊需要儿童为 92%。与之前发表的规范和在已知的零立体视力队列中的测试相比,支持 PASS III 测试的有效性。与金标准立体视力测试相比,PASS 的准确性为 89%。总体而言,使用 PASS III 的优先观察测试为年幼儿童和有特殊需要的儿童提供了敏感和特异性的立体视力测量,具有较高的可测试性。