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Published on: September 16, 2020
Postnatal weight gain and retinopathy of prematurity
1Divison of Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
Insights
New screening criteria incorporating infant weight gain show promise for improving retinopathy of prematurity (ROP) detection. The G-ROP model may reduce unnecessary eye exams for premature infants, focusing resources on those at highest risk.
Area of Science:
- Neonatal ophthalmology
- Pediatric predictive modeling
Background:
- Current retinopathy of prematurity (ROP) screening relies on birth weight and gestational age, leading to over-screening as few infants require treatment.
- Identifying infants who will develop ROP is crucial for efficient resource allocation and timely intervention.
Purpose of the Study:
- To evaluate the effectiveness of novel screening criteria for retinopathy of prematurity (ROP) that incorporate postnatal weight gain.
- To assess the potential of the G-ROP (Growth for ROP) model to improve the specificity of ROP screening.
Main Methods:
- Development of prediction models using large datasets that include postnatal weight gain measures.
- Validation of the G-ROP modified screening criteria in target populations to assess generalizability.
Main Results:
- Slow postnatal weight gain is a strong predictor of ROP development.
- The G-ROP model, developed on the largest dataset, offers a potentially more robust and precise screening tool.
Conclusions:
- Incorporating weight gain into ROP screening criteria, such as the G-ROP model, can enhance screening precision.
- Further validation studies are essential to confirm the generalizability and clinical utility of the G-ROP criteria before widespread adoption.
Abstract:
Infants meeting retinopathy of prematurity (ROP) screening guidelines based on birth weight and gestational age undergo serial examinations by ophthalmologists for detection and treatment. However, less than 10% require treatment, and less than half develop ROP. Slow postnatal weight gain is highly predictive of ROP, and investigators have incorporated weight gain measures to develop more specific criteria for ROP screening. Such clinical prediction model use involves a large development study, validation studies specific to the target populations, and ongoing impact surveillance, with adjustment as necessary. Of the many weight gain inclusive prediction models intended to improve the precision of ROP screening, the Postnatal Growth and ROP (G-ROP) modified screening criteria were developed using the largest dataset and may provide the most robust model for clinical use. A recently completed G-ROP validation study will evaluate the generalizability of these modified criteria prior to clinical use.
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