Classification Criteria For Multiple Evanescent White Dot Syndrome.
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 33845025.
- Also identified by DOI 10.1016/j.ajo.2021.03.050 and PMC identifier 8594763.
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Abstract
The purpose of this study was to determine classification criteria for multiple evanescent white dot syndrome (MEWDS). Machine learning of cases with MEWDS and 8 other posterior uveitides. Cases of posterior uveitides were collected in an informatics-designed preliminary database, and a final database was constructed of cases achieving supermajority agreement on diagnosis using formal consensus techniques. Cases were split into a training set and a validation set. Machine learning using multinomial logistic regression was used in the training set to determine a parsimonious set of criteria that minimized the misclassification rate among the infectious posterior, or panuveitides. The resulting criteria were evaluated in the validation set. A total of 1,068 cases of posterior uveitides, including 51 cases of MEWDS, were evaluated by machine learning. Key criteria for MEWDS included: 1) multifocal gray-white chorioretinal spots with foveal granularity; 2) characteristic imaging on fluorescein angiography ("wreath-like" hyperfluorescent lesions) and/or optical coherence tomography (hyper-reflective lesions extending from retinal pigment epithelium through ellipsoid zone into the retinal outer nuclear layer); and 3) absent to mild anterior chamber and vitreous inflammation. Overall accuracy for posterior uveitides was 93.9% in the training set and 98.0% (95% confidence interval: 94.3-99.3) in the validation set. Misclassification rates for MEWDS were 7% in the training set and 0% in the validation set. The criteria for MEWDS had a low misclassification rate and appeared to perform sufficiently well for use in clinical and translational research.
Medical subject headings
- Fluorescein Angiography
- Multimodal Imaging
- Retinal Pigment Epithelium
- Tomography, Optical Coherence
- White Dot Syndromes