Impact of multiple births on retinopathy of prematurity in preterm infants

Szy Yann Chan1, Chung Ting Pan2, Feng Liu1

  • 1Department of Ophthalmology, Peking University Third Hospital, Beijing Key Laboratory of Restoration of Damaged Ocular Nerve, Peking University Third Hospital, Beijing, China.

Eye (London, England)
|February 6, 2026
PubMed

Insights

Infants born from multiple births have a higher risk and severity of retinopathy of prematurity (ROP). This independent association suggests tailored screening strategies may be needed for these vulnerable preterm infants.

Area of Science:

  • Neonatalogy
  • Ophthalmology
  • Perinatal Medicine

Background:

  • Multiple births are increasing due to assisted reproductive technologies.
  • Retinopathy of prematurity (ROP) is a significant concern in preterm infants.
  • Understanding risks independent of gestational age and birth weight is crucial.

Purpose of the Study:

  • To investigate the independent impact of multiple birth status on ROP incidence and severity.
  • To clarify ROP risks in preterm infants from multiple gestations.
  • To inform potential adjustments in ROP screening protocols.

Main Methods:

  • Retrospective observational study of 4392 preterm infants screened for ROP (2010-2023).
  • Inclusion criteria: gestational age ≤ 32 weeks, birth weight ≤ 2000g, or clinical instability.
  • Multivariable logistic regression analyzed ROP predictors, including multiple birth status, gestational age, and birth weight.

Main Results:

  • 17.8% of infants were diagnosed with ROP; 37.4% were from multiple births.
  • Multiple birth status independently predicted higher ROP incidence (OR=1.51).
  • Lower birth weight and multiple birth status significantly predicted increased ROP severity.

Conclusions:

  • Multiple birth status is independently associated with increased ROP risk and severity.
  • Findings suggest a need for further validation and exploration of tailored screening for multiple-gestation infants.
  • Potential implications for optimizing ROP surveillance in high-risk neonatal populations.
Abstract

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