Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept-source optical coherence

Sandra Rezar-Dreindl1, Katharina Eibenberger1, Reinhard Told1

  • 1Department of Ophthalmology and Optometry, Medical University of Vienna, Vienna, Austria.

Acta Ophthalmologica
|August 5, 2020
PubMed

Insights

Children with a history of retinopathy of prematurity (ROP) show microvascular changes, including a smaller foveal avascular zone (FAZ), indicating disturbed retinal development. Swept-source optical coherence tomography angiography (SS-OCTA) revealed these anomalies.

Area of Science:

  • Ophthalmology
  • Pediatric Medicine
  • Medical Imaging

Background:

  • Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
  • Understanding the long-term microvascular consequences of ROP is crucial for pediatric eye care.

Purpose of the Study:

  • To investigate microvascular changes in children with a history of ROP using advanced imaging techniques.
  • To compare these changes with a control group of full-term children.

Main Methods:

  • A cross-sectional study involving 15 children (30 eyes) with a history of ROP and 22 age-matched full-term children (28 eyes).
  • Swept-source optical coherence tomography angiography (SS-OCTA) was used to evaluate the foveal avascular zone (FAZ), vessel density (VD), and choroidal vascular flow area (VFA).
  • Correlations were assessed with central retinal thickness (CRT), visual acuity (VA), birth weight (BW), gestational age (GA), and ROP severity.

Main Results:

  • Children with ROP history exhibited a significantly higher central retinal thickness (CRT).
  • A smaller mean FAZ area and perimeter were observed in the ROP group, with an oval shape noted.
  • No significant differences in choroidal vascular flow area (VFA) or vessel density (VD) were found between groups.

Conclusions:

  • SS-OCTA imaging demonstrates significant microvascular anomalies in children with a history of ROP.
  • These findings suggest disturbances in the early morphological development of the central retina in ROP survivors.
Abstract

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