The effect of leucocytosis on retinopathy of prematurity

Zhihong Sun1, Lu He1, Congcong Zhao1

  • 1Department of Neonatology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, 33 Longhuwaihuan Road, Zhengzhou, 450018, Henan, China.

Scientific Reports
|November 21, 2023
PubMed

Insights

Postnatal leukocytosis, a sign of inflammation, is linked to severe retinopathy of prematurity (ROP) in preterm infants. Early detection using white blood cell count may improve outcomes for high-risk newborns.

Area of Science:

  • Neonatal Medicine
  • Ophthalmology
  • Pediatric Critical Care

Background:

  • Postnatal leukocytosis indicates inflammation and is associated with various infant health issues.
  • Inflammatory processes are known risk factors for retinopathy of prematurity (ROP) and other visual impairments.

Purpose of the Study:

  • To investigate the association between postnatal leukocytosis and the incidence and severity of ROP in preterm infants.
  • To determine if white blood cell (WBC) count can predict severe ROP in extremely premature neonates.

Main Methods:

  • A cohort study included preterm infants (<28 weeks gestation) admitted between September 2015 and March 2021.
  • Infants were categorized into a leukocytosis group (WBC ≥ 30 × 10^9/L) and a matched control group.
  • Incidence and prognosis of ROP were compared; ROC curves analyzed WBC count correlation with severe ROP.

Main Results:

  • The leukocytosis group exhibited higher incidences of intracranial hemorrhage, leukomalacia, sepsis, and bronchopulmonary dysplasia.
  • Severe ROP incidence and need for ranibizumab injections were significantly higher in infants with leukocytosis.
  • A WBC count cutoff of 19.1 × 10^9/L demonstrated high sensitivity (88.6%) and specificity (77.3%) for detecting severe ROP.

Conclusions:

  • Postnatal leukocytosis is associated with an increased risk of severe ROP in preterm infants.
  • Elevated white blood cell counts may serve as a predictive marker for severe ROP in this vulnerable population.