Department of Ophthalmology, Rigshospitalet-Glostrup, Glostrup, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
JAMA Ophthalmol. 2021 Jan 1;139(1):33-40. doi: 10.1001/jamaophthalmol.2020.4854.
Red reflex testing is a simple and inexpensive method implemented in many countries as an important part of infant screening for ocular pathologies.
To review the literature on the diagnostic accuracy of the red reflex test in infant screening for ocular pathologies and to perform meta-analyses to provide summary estimates.
The following literature databases were searched for English-language, peer-reviewed literature, published until April 19, 2020: Cochrane Central, PubMed/MEDLINE, Embase, Web of Science Core Collection, BIOSIS Previews, Current Contents Connect, Data Citation Index, Derwent Innovations Index, KCI-Korean Journal Database, Russian Science Citation Index, SciELO Citation Index, CINAHL (Cumulative Index to Nursing and Allied Health Literature), and ClinicalTrials.gov.
Eligibility criteria were defined according to population (studies of consecutively screened infants), exposure (red reflex or Brückner test as the index test), comparator (any ophthalmological examination), and study type (any study with diagnostic test accuracy data).
The Preferred Reporting Items for Systematic Reviews and Meta-Analysis of Diagnostic Test Accuracy Studies (PRISMA-DTA) guidelines were followed. Data were extracted independently by 2 authors. For summary estimates of diagnostic test accuracy, the hierarchical summary receiver operating characteristics curve was used. Prevalence of ocular pathologies was introduced for a prevalence meta-analysis, which was then used in calculations of diagnostic accuracy of the red reflex test when applied in infant screening.
True-positive, false-positive, true-negative, and false-negative findings; sensitivity; specificity; and positive and negative predictive values.
In this meta-analysis, 8713 unique infants from 5 unique studies were eligible for qualitative and quantitative review. All studies used the red reflex test without pupillary dilation and were compared with a reference test performed with pupillary dilation. For any ocular pathology, an estimated sensitivity of 7.5% (95% CI, 7.4%-7.5%) and specificity of 97.5% (95% CI, 97.5%-97.5%) was found. Focusing on ocular pathologies that required a medical or surgical intervention, sensitivity improved to 17.5% (95% CI, 0.8%-84.8%) and specificity remained high at 97.6% (95% CI, 87.7%-99.6%).
These findings suggest that an abnormal red reflex finding most likely reflects an underlying ocular pathology. However, a normal red reflex finding during screening does not exclude ocular disease.
红反射测试是一种简单且廉价的方法,在许多国家被用作婴儿眼部疾病筛查的重要组成部分。
综述红反射测试在婴儿眼部疾病筛查中的诊断准确性的文献,并进行荟萃分析以提供汇总估计值。
检索了以下英文同行评审文献数据库,截至 2020 年 4 月 19 日发表的文献:Cochrane 中央、PubMed/MEDLINE、Embase、Web of Science 核心合集、BIOSIS 预览、当前内容连接、数据引文索引、德温特创新索引、KCI-韩国期刊数据库、俄罗斯科学引文索引、SciELO 引文索引、CINAHL(护理与联合健康文献累积索引)和 ClinicalTrials.gov。
根据人群(连续筛查婴儿的研究)、暴露(红反射或 Brückner 测试作为指标测试)、比较(任何眼科检查)和研究类型(具有诊断测试准确性数据的任何研究)来定义纳入标准。
遵循了诊断测试准确性研究的系统评价和荟萃分析的首选报告项目(PRISMA-DTA)指南。两名作者独立提取数据。对于诊断测试准确性的汇总估计,使用分层汇总接收者操作特征曲线。引入眼部疾病的患病率进行患病率荟萃分析,然后将其用于计算红反射测试在婴儿筛查中的应用时的诊断准确性。
真阳性、假阳性、真阴性和假阴性结果;敏感性;特异性;阳性和阴性预测值。
在这项荟萃分析中,5 项独特研究中的 8713 名独特婴儿符合定性和定量审查的条件。所有研究均使用未散瞳的红反射测试,并与散瞳后的参考测试进行比较。对于任何眼部疾病,估计的敏感性为 7.5%(95%CI,7.4%-7.5%),特异性为 97.5%(95%CI,97.5%-97.5%)。将重点放在需要医疗或手术干预的眼部疾病上,敏感性提高到 17.5%(95%CI,0.8%-84.8%),特异性仍保持在 97.6%(95%CI,87.7%-99.6%)。
这些发现表明,异常的红反射结果很可能反映了潜在的眼部疾病。然而,在筛查期间出现正常的红反射结果并不能排除眼部疾病。