Eye Research Center of the Mashhad University of Medical Sciences, Khatam-al-Anbia Eye Hospital, Mashhad, Iran.
Br J Ophthalmol. 2012 Jan;96(1):83-6. doi: 10.1136/bjo.2010.190405. Epub 2011 Apr 21.
To evaluate the accuracy and applicability of Plusoptix photoscreener in screening pre-verbal children at risk of amblyopia.
In this cross-sectional population-based study 996 children aged 6-36 months were screened with the Plusoptix. The children underwent complete examinations that included a manual cycloplegic retinoscopy, slit lamp examination, cover test, the Hirschberg test and an assessment of fixation pattern. In addition, the prevalence of amblyogenic risk factors was estimated, the Plusopix measurements were compared with cycloplegic retinoscopy, and the referral criteria were modified to improve the accuracy of the device.
Amblyogenic hyperopia >+3.50 D, myopia >-3.00 D, astigmatism >1.50 D in the orthogonal meridian or >1.00 D in the oblique meridian, or anisometropia >1.50 D was detected in 4.7%, 0.0%, 12.3% and 0.5% of the samples, respectively. The average difference between retinoscopy and photorefraction for spherical equivalence was -0.16 ± 1.0 D (p<0.05). Testability was 98.1% for the Plusoptix. The Plusoptix vision screener referred 47.8% of these children for sensitivity, specificity, positive predictive value and false-negative rates of 100%, 38.7%, 19% and 100%, respectively. These same measurements with the modified referral criteria (hyperopia ≥ 2.00 D in children under 12 months and astigmatism ≥ 1.25 D) were 93.6%, 51.2%, 21.7% and 98.2%.
The Plusoptix is a useful objective screening instrument, but still has low specificity for detecting amblyopia risk factors in the paediatric population.
评估 Plusoptix 照片筛选仪在筛查有弱视风险的言语前儿童中的准确性和适用性。
在这项横断面基于人群的研究中,使用 Plusoptix 对 996 名 6-36 月龄的儿童进行了筛查。这些儿童接受了全面的检查,包括手动睫状肌麻痹检影验光、裂隙灯检查、遮盖试验、Hirschberg 试验和固视模式评估。此外,还估计了弱视危险因素的患病率,比较了 Plusopix 测量值与睫状肌麻痹检影验光的结果,并修改了转诊标准以提高设备的准确性。
远视>+3.50 D、近视>-3.00 D、正交子午线散光>1.50 D 或斜子午线散光>1.00 D,或屈光参差>1.50 D 的患儿分别占 4.7%、0.0%、12.3%和 0.5%。检影验光和光折射验光的平均球镜等效差异为-0.16±1.0 D(p<0.05)。Plusoptix 的可测试性为 98.1%。Plusoptix 视力筛选仪将 47.8%的儿童转诊,其灵敏度、特异性、阳性预测值和假阴性率分别为 100%、38.7%、19%和 100%。对于修改后的转诊标准(12 个月以下儿童远视≥2.00 D,散光≥1.25 D),这些测量值的敏感性、特异性、阳性预测值和假阴性率分别为 93.6%、51.2%、21.7%和 98.2%。
Plusoptix 是一种有用的客观筛选工具,但在检测儿科人群的弱视危险因素方面特异性仍然较低。