Until when can the initial screening for Retinopathy of Prematurity (ROP) be done for a preterm baby?

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Last updated: December 29, 2025View editorial policy

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Timing of Initial ROP Screening in Preterm Infants

Initial ROP screening should be performed at 31 weeks postmenstrual age (PMA) OR 4 weeks chronological age, whichever is later. 1

Screening Initiation Based on Gestational Age at Birth

The timing of the first examination depends on how premature the infant was:

  • Infants born ≤26 6/7 weeks gestation: Screen at 31 weeks PMA 2
  • Infants born ≥27 weeks gestation: Screen at 4 weeks chronological age 2
  • Use whichever timing comes later to ensure adequate retinal development for meaningful examination 1, 3

Who Needs Screening

Screen all infants meeting these criteria: 1, 2

  • Gestational age ≤30 6/7 weeks (regardless of birth weight) 2
  • Birth weight ≤1250 grams (regardless of gestational age) 2
  • Some centers extend screening to infants with birth weight ≤1500 grams 2

Special populations requiring screening even if 29-37 weeks gestation: 1

  • Infants with chronic lung disease of infancy (CLDI) 1
  • Infants who were NOT medically stable (required supplemental oxygen) 1

Do NOT screen: 1

  • Infants >37 weeks gestation at birth 1
  • Infants 29-37 weeks who had a medically stable course without oxygen requirement 1

Evidence Supporting This Timing

The 31-week/4-week guideline is strongly evidence-based. In the landmark CRYO-ROP and LIGHT-ROP studies analyzing 4,460 infants, 99% of infants did not develop retinal conditions indicating risk of poor outcome before 31 weeks PMA or 4 weeks chronological age 3.

More recent data from extremely preterm infants (<27 weeks gestation) confirms this safety margin: no infants required laser therapy prior to 32 weeks PMA, and none had severe ROP detected before 31 weeks PMA 4. This validates that screening at 31 weeks PMA is appropriately timed even for the most vulnerable infants 4.

Common Pitfall to Avoid

Do not delay screening beyond these timeframes. While earlier screening (before 31 weeks PMA) has not proven necessary 4, delaying the initial examination risks missing rapidly progressive disease. Approximately 8% of premature infants overall require treatment, rising to 25% of those born <750 grams 5. In extremely low birth weight infants, 13% may have threshold ROP by their first examination if screening is delayed 6.

Follow-Up Examination Frequency

After the initial screening 1, 5:

  • If ROP is present in Zone I or Zone II: Repeat examinations every 1-2 weeks 1, 5
  • If no ROP or minimal disease: Follow ophthalmologist's recommendations, typically every 1-2 weeks until resolution 5
  • More frequent examinations may be needed if disease is rapidly progressing 5

When Screening Can Be Discontinued

Stop screening when any of these criteria are met: 1, 7

  • Complete retinal vascularization 1
  • ROP regressing with vessels passed into Zone III on at least two sequential examinations 1, 7
  • Infant reaches 45 weeks PMA without developing prethreshold ROP or worse 3

Critical Coordination for High-Risk Infants

For infants with chronic lung disease being discharged home with unresolved ROP, careful coordination of follow-up ophthalmology appointments is crucial 1. Missing appointments in infants with Zone I or Zone II disease can lead to missed treatment opportunities and preventable vision loss 1, 7.

References

Guideline

Timing of First ROP Screening Examination in Newborns

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Retinopathy of prematurity: Recommendations for screening.

Paediatrics & child health, 2010

Research

Do extremely preterm infants need retinopathy of prematurity screening earlier than 31 weeks postmenstrual age?

Journal of perinatology : official journal of the California Perinatal Association, 2021

Research

Retinopathy of prematurity.

Advances in pediatrics, 2006

Guideline

Treatment and Management of Retinopathy of Prematurity

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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