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Validation of the "FIRST-ROP" Algorithm at a Neonatal Intensive Care Unit Tertiary Center over Three Decades.

Davina A Malek1, Francisco Altamirano2, Celine Chaaya3

  • 1From the Bascom Palmer Eye Institute (D.A.M., C.N., N.A., J.S.L., N.A.Y., H.U.H., A.M.B.), University of Miami, Miami, Florida, USA.

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The FIRST-ROP algorithm safely defers retinopathy of prematurity screening to 34 weeks postmenstrual age in medium-risk infants. This approach reduces infant eye exam visits without missing treatment-warranted cases.

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Area of Science:

  • Ophthalmology
  • Neonatology
  • Pediatric screening

Background:

  • Retinopathy of prematurity (ROP) is a leading cause of childhood blindness.
  • Current ROP screening guidelines involve frequent eye examinations for premature infants.
  • The FIRST-ROP algorithm proposes deferring initial screening to 34 weeks postmenstrual age (PMA).

Purpose of the Study:

  • To validate the efficacy of the FIRST-ROP algorithm in a medium-risk infant cohort.
  • To assess the safety and efficiency of deferring ROP screening to 34 weeks PMA.

Main Methods:

  • Retrospective diagnostic comparison of infants with gestational age ≥27 weeks and birth weight ≥800 g.
  • Comparison of ROP diagnosis and treatment-warranted ROP (TW-ROP) rates between standard screening and the FIRST-ROP algorithm.
  • McNemar test used to compare paired binary detection outcomes.

Main Results:

  • 3,641 infants met inclusion criteria; 17% developed ROP.
  • Median PMA for ROP diagnosis was 35.1 weeks; treatment initiation was 40.0 weeks.
  • FIRST-ROP strategy significantly reduced examinations (estimated 17% fewer visits) without missing TW-ROP cases.

Conclusions:

  • No infants in this medium-risk cohort required treatment before 34 weeks PMA.
  • The FIRST-ROP algorithm is validated, supporting safe deferral of initial ROP screening.
  • Deferring screening to 34 weeks PMA reduces burden while maintaining sensitivity for TW-ROP.