Ugurbas Silay Canturk, Alpay Atilla, Tutar Huseyin, Sagdik Haci Murat, Ugurbas Suat Hayri
Zonguldak Karaelmas University, Department of Ophthalmology, Kozlu, Zonguldak, Turkey.
J AAPOS. 2011 Oct;15(5):476-9. doi: 10.1016/j.jaapos.2011.05.023.
Intellectual disability (ID) is a major public health issue, affecting more than 1% of children worldwide. Pediatric vision screening using standard eye charts may be challenging for children with ID, who may benefit from a quick noninvasive vision screening tool. This study evaluated the accuracy of plusoptiX S04 (Plusoptix Gmbh, Nuremberg, Germany) in detecting amblyopia risk factors in children with ID.
Children diagnosed with ID according to age-appropriate psychological tests were examined consecutively. Vision screening was performed using the plusoptiX S04 prior to complete ophthalmological examination, including cycloplegic refraction. Pass/refer screening results was compared with findings of ophthalmological examination. Amblyogenic risk factors were defined according to American Association for Pediatric Ophthalmology and Strabismus referral criteria.
A total of 182 infants and children were examined. Only 3% of children were uncooperative for screening. Ophthalmological examination detected amblyogenic risk factors in 32% of patients. The sensitivity of plusoptiX S04 was 95% (95% CI, 85.6%-98.9%), and specificity was 50% (95% CI, 40.8%-59.1%). The positive predictive value was 47% (95% CI, 37.7%-56.4%) and the negative predictive value was 95.4% (95% CI, 87.1%-99.1%).
High sensitivity and negative predictive values suggest that the plusoptiX S04 will detect most children with ID who have amblyogenic risk factors, but one-half of all children referred will have no risk factors.
智力残疾(ID)是一个重大的公共卫生问题,影响着全球超过1%的儿童。对于患有ID的儿童,使用标准视力表进行儿科视力筛查可能具有挑战性,他们可能会从快速、无创的视力筛查工具中受益。本研究评估了plusoptiX S04(德国纽伦堡Plusoptix有限公司)在检测ID儿童弱视危险因素方面的准确性。
根据适合年龄的心理测试诊断为ID的儿童接受连续检查。在包括散瞳验光在内的全面眼科检查之前,使用plusoptiX S04进行视力筛查。将通过/转诊筛查结果与眼科检查结果进行比较。根据美国小儿眼科与斜视协会的转诊标准定义致弱视危险因素。
共检查了182名婴幼儿和儿童。只有3%的儿童不配合筛查。眼科检查在32%的患者中检测到致弱视危险因素。plusoptiX S04的敏感性为95%(95%CI,85.6%-98.9%),特异性为50%(95%CI,40.8%-59.1%)。阳性预测值为47%(95%CI,37.7%-56.4%),阴性预测值为95.4%(95%CI,87.1%-99.1%)。
高敏感性和阴性预测值表明,plusoptiX S04将检测出大多数患有致弱视危险因素的ID儿童,但所有被转诊的儿童中有一半没有危险因素。