Validation of a Published Model to Reduce Burden of Retinopathy of Prematurity Screening

Jaron Pruett1, Kelly Ruland2, Sean Donahue3

  • 1From the Vanderbilt University School of Medicine (J.P.) Nashville, Tennessee, USA.

PubMed

Insights

Infants born after 27 weeks' gestational age with birthweights over 750 g who show no retinopathy of prematurity (ROP) by 37 weeks do not develop treatable ROP. Continued screening is unnecessary for these infants.

Area of Science:

  • Neonatology
  • Ophthalmology
  • Pediatrics

Background:

  • Retinopathy of prematurity (ROP) is a leading cause of blindness in premature infants.
  • The E-ROP study suggested discontinuing ROP screening at 37 weeks for infants born at or after 27 weeks' gestational age with birthweights over 750 g if no ROP is present.
  • This study aimed to validate these findings in a larger, multi-center cohort.

Purpose of the Study:

  • To replicate and validate the E-ROP study's findings on the cessation of retinopathy of prematurity screening.
  • To determine if infants meeting specific gestational age and birthweight criteria who have no ROP at 37 weeks develop treatable disease later.

Main Methods:

  • Retrospective cohort study of 6729 infants screened for ROP.
  • Chart review at 6 medical centers from February 2004 to April 2022.
  • Evaluation of gestational age, birthweight, and ROP status at 37 weeks to identify "missed" cases.

Main Results:

  • 298 (4.43%) of screened infants required treatment for ROP.
  • Ten infants developed ROP after 37 weeks' gestational age.
  • Only one infant >750 g birthweight and >27 weeks' gestational age developed ROP after 37 weeks, and it was detected at the first post-37-week examination.

Conclusions:

  • Findings support the E-ROP study's conclusion: infants >750 g birthweight and >27 weeks' gestational age without ROP at 37 weeks do not develop treatable ROP.
  • Termination of ROP screening at 37 weeks is supported for infants meeting these criteria.
  • This validation in a larger cohort strengthens the evidence for refining ROP screening protocols.
Abstract