Retinopathy of prematurity: optimal timing of the initial check and progression after discharge

Wen-Hsien Lin1, Shu-Jen Chen, Fenq-Lin Lee

  • 1Department of Pediatrics, Chutung Veterans Hospital, Chutung, Taiwan.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|July 9, 2003
PubMed

Insights

Early screening for retinopathy of prematurity (ROP) is crucial. A dual approach using postnatal age or postconceptional age can optimize initial ROP detection in premature infants after discharge.

Area of Science:

  • Ophthalmology
  • Neonatology
  • Perinatal Medicine

Background:

  • Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
  • Timely detection of threshold ROP is critical for preventing severe visual outcomes.
  • Outpatient department (OPD) follow-up after discharge plays a vital role in managing ROP progression.

Purpose of the Study:

  • To determine the optimal timing for initial ROP screening in preterm infants.
  • To evaluate ROP progression during OPD follow-up after hospital discharge.
  • To analyze the relationship between ROP severity, timing, and infant characteristics like birth weight and gestational age.

Main Methods:

  • Retrospective chart review of 224 preterm infants (gestational age < 35 weeks or birth weight ≤ 2000 g).
  • Analysis of ROP stages, time course, and detection timing relative to birth weight and gestational age.
  • Categorization of infants based on ROP stage at discharge and OPD follow-up results.

Main Results:

  • 31.7% of infants with stage III ROP and 27.8% with threshold ROP were detected post-discharge.
  • For extremely low birth weight infants (BW ≤ 1000 g), ROP was first detected around 7 weeks postnatal age (PNA) and 35-36 weeks postconceptional age (PCA).
  • The dual criteria of 4 weeks PNA or 33 weeks PCA (whichever is later) emerged as optimal for initial screening.

Conclusions:

  • A significant proportion of threshold ROP cases are identified after discharge, underscoring the importance of continued follow-up.
  • ROP detection timing varies with birth weight, but postconceptional age remains relatively consistent.
  • Implementing a dual screening criterion (4 weeks PNA or 33 weeks PCA) can enhance early detection of ROP in high-risk premature infants.