FP-I3ID (Instituto de Investigação, Inovação e Desenvolvimento da UFP)/HE-UFP (Hospital-Escola da UFP).
Department of Ophthalmology, Hospital de Braga, Braga, Portugal.
Eur J Ophthalmol. 2022 Jul;32(4):2034-2040. doi: 10.1177/11206721211035634. Epub 2021 Aug 2.
Compare the performance of different amblyopia screening tests.
Based on exploratory factor analyses (EFA) of different screening tests performed in 3295 children, we created models of screening strategies in a matrix with: uncorrected visual acuity (UCVA), Plusoptix measurements (PO), Randot Stereo-test (SR), and Cover-Test (CT). Receiver Operating Characteristic (ROC) curves and confusion matrix were used to compare performance of different model's algorithm to predict new diagnosis of amblyopia. Estimated screening costs per screened and treated child were compared.
Regression analyses revealed that, although all models predicted amblyopia (all < 0.001), only models including PO or UCVA had higher prediction capacity ( > 0.4) and better discriminating ROC curves (AUC > 0.95; < 0.001). For 96% sensitivity, UCVA + PO was the most cost-effective model, since the estimated average screening costs per treated child, almost doubled and tripled if using PO or UCVA alone, respectively, versus using both exams. When UCVA + PO is not possible to implement, adding SR to either UCVA or PO resulted in cost-savings of 28% and 18%, respectively.
In a previous unscreened population, aged 3-4 years, screening programs using either UCVA or PO alone, should reconsider doing both tests simultaneously, since, for a high level of sensitivity, using simultaneously UCVA + PO is more cost-effective, per screened, and treated amblyopia. Concerns relating higher time-consuming exams for the combination of UCVA + PO should be surpassed, since costs per treated child drop considerably. When children benefit from good primary-care routine examinations since birth, no benefit was found for using CT in a screening setting. SR showed little benefit.
比较不同弱视筛查测试的性能。
基于对 3295 名儿童进行的不同筛查测试的探索性因素分析(EFA),我们在矩阵中创建了筛查策略模型:未矫正视力(UCVA)、Plusoptix 测量(PO)、Randot 立体测试(SR)和遮盖试验(CT)。使用受试者工作特征(ROC)曲线和混淆矩阵比较不同模型算法预测新诊断弱视的性能。比较了每个筛查和治疗儿童的估计筛查成本。
回归分析表明,虽然所有模型都预测了弱视(均<0.001),但只有包含 PO 或 UCVA 的模型具有更高的预测能力(>0.4)和更好的 ROC 曲线(AUC>0.95;<0.001)。对于 96%的敏感性,UCVA+PO 是最具成本效益的模型,因为治疗儿童的估计平均筛查成本,如果单独使用 PO 或 UCVA,几乎翻了一番和三倍,而如果同时使用这两种检查则翻了一番和三倍。如果不可能同时实施 UCVA+PO,可以将 SR 添加到 UCVA 或 PO 中,分别节省 28%和 18%的成本。
在之前未经筛查的 3-4 岁人群中,单独使用 UCVA 或 PO 的筛查计划应重新考虑同时进行两项检查,因为为了达到高敏感性,同时使用 UCVA+PO 每筛查和治疗的弱视儿童更具成本效益。应该克服对同时进行 UCVA+PO 检查的更高耗时检查的担忧,因为每个治疗儿童的成本会大大降低。当儿童从出生起就受益于良好的初级保健常规检查时,在筛查环境中使用 CT 没有发现任何好处。SR 显示出很少的好处。