Single-Examination Risk Prediction of Severe Retinopathy of Prematurity

Author:

Coyner Aaron S.12,Chen Jimmy S.1,Singh Praveer34,Schelonka Robert L.5,Jordan Brian K.5,McEvoy Cindy T.5,Anderson Jamie E.1,Chan R.V. Paul6,Sonmez Kemal2,Erdogmus Deniz7,Chiang Michael F.8,Kalpathy-Cramer Jayashree34,Campbell J. Peter1

Affiliation:

1. Departments of Ophthalmology

2. Medical Informatics and Clinical Epidemiology

3. Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Harvard University, Boston, Massachusetts

4. Center for Clinical Data Science, Massachusetts General Hospital and Brigham and Women’s Hospital, Boston, Massachusetts

5. Pediatrics, Oregon Health & Science University, Portland, Oregon

6. Department of Ophthalmology and Visual Sciences, University of Illinois Chicago, Chicago, Illinois

7. Department of Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts

8. National Eye Institute, National Institutes of Health, Bethesda, Maryland

Abstract

BACKGROUND AND OBJECTIVES Retinopathy of prematurity (ROP) is a leading cause of childhood blindness. Screening and treatment reduces this risk, but requires multiple examinations of infants, most of whom will not develop severe disease. Previous work has suggested that artificial intelligence may be able to detect incident severe disease (treatment-requiring retinopathy of prematurity [TR-ROP]) before clinical diagnosis. We aimed to build a risk model that combined artificial intelligence with clinical demographics to reduce the number of examinations without missing cases of TR-ROP. METHODS Infants undergoing routine ROP screening examinations (1579 total eyes, 190 with TR-ROP) were recruited from 8 North American study centers. A vascular severity score (VSS) was derived from retinal fundus images obtained at 32 to 33 weeks’ postmenstrual age. Seven ElasticNet logistic regression models were trained on all combinations of birth weight, gestational age, and VSS. The area under the precision-recall curve was used to identify the highest-performing model. RESULTS The gestational age + VSS model had the highest performance (mean ± SD area under the precision-recall curve: 0.35 ± 0.11). On 2 different test data sets (n = 444 and n = 132), sensitivity was 100% (positive predictive value: 28.1% and 22.6%) and specificity was 48.9% and 80.8% (negative predictive value: 100.0%). CONCLUSIONS Using a single examination, this model identified all infants who developed TR-ROP, on average, >1 month before diagnosis with moderate to high specificity. This approach could lead to earlier identification of incident severe ROP, reducing late diagnosis and treatment while simultaneously reducing the number of ROP examinations and unnecessary physiologic stress for low-risk infants.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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