Retrospective comparison between growth and retinopathy of prematurity model versus WINROP model

Ana C Almeida1, Teresa Sandinha2, Rita Azevedo3

  • 1Department of Ophthalmology, Hospital Beatriz Angelo, Loures, Portugal; Neonatal Intensive Care Unit, Hospital São Francisco Xavier - Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal; CEDOC, NOVA Medical School - Universidade Nova de Lisboa, Lisbon, Portugal; Department of Ophthalmology, Hospital da Luz, Lisbon, Portugal.

Insights

The Weight and Insulin-like Growth Factor-1 in Neonatal Retinopathy (WINROP) and Growth and Retinopathy of Prematurity (G-ROP) models showed similar sensitivity for detecting type 1 retinopathy of prematurity. Both models achieved 100% sensitivity for infants with gestational age <30 weeks.

Area of Science:

  • Neonatology
  • Ophthalmology
  • Pediatric Growth

Background:

  • Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
  • Accurate and timely detection of ROP is crucial for effective treatment and prevention of vision loss.
  • The Weight and Insulin-like Growth Factor-1 in Neonatal Retinopathy (WINROP) and Growth and Retinopathy of Prematurity (G-ROP) models are used for ROP screening.

Purpose of the Study:

  • To compare the diagnostic performance of the WINROP and G-ROP models in a Portuguese cohort.
  • To evaluate the sensitivity and specificity of both models for identifying type 1 ROP.
  • To assess model performance specifically in preterm infants with gestational age (GA) less than 30 weeks.

Main Methods:

  • Retrospective review of clinical records of infants screened for ROP between April 2012 and May 2019.
  • Analysis of sensitivity and specificity for type 1 ROP using both WINROP and G-ROP algorithms.
  • Subgroup analysis for infants with GA <30 weeks.

Main Results:

  • Of 375 infants, 313 were analyzed with G-ROP and 311 with WINROP.
  • G-ROP identified type 1 ROP in 22 infants (sensitivity 90.91%).
  • WINROP identified 23 infants requiring treatment (sensitivity 86.96%).
  • Both models achieved 100% sensitivity for type 1 ROP in infants with GA <30 weeks.

Conclusions:

  • The WINROP and G-ROP models demonstrated comparable sensitivities for detecting type 1 ROP.
  • Both models are user-friendly and effective screening tools.
  • For infants with GA <30 weeks, both models successfully identified all cases of type 1 ROP.
Abstract