Abstract
Peripheral avascular retina (PAR) predisposes the development of lattice degeneration, atrophic holes, and retinal detachments in individuals with a history of retinopathy of prematurity (ROP). While PAR is commonly observed after vascular endothelial growth factor antagonist therapy for ROP, the prevalence of PAR in spontaneously regressed ROP is unknown. In this study, we evaluate the prevalence of PAR in a cohort of patients with a history of extreme prematurity.
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