Neurodevelopmental Outcomes at 18-24 Months of Corrected Age in Very Low Birth Weight Infants with Late-onset Sepsis

J Korean Med Sci. 2021 Sep 6;36(35):e205. doi: 10.3346/jkms.2021.36.e205.

Abstract

Background: Preterm infants are prone to sepsis owing to their immature innate immunity and prolonged hospitalization. We aimed to evaluate the association between late-onset sepsis (LOS) during hospitalization and neurodevelopmental delay at 18-24 months of corrected age in very low birth weight infants (VLBWIs), and to ascertain this association when adjusted for perinatal risk factors.

Methods: This is a population-based study of VLBWIs born at 23-32 weeks of gestation between January 2014 and December 2017 who were enrolled in the Korean Neonatal Network. Bayley scales of infant development were evaluated at 18-24 months of corrected age in 2,098 infants. To test for LOS as a risk factor for neurodevelopmental delay, multiple logistic regression was used and adjusted for parental education status and clinical variables.

Results: Blood culture positive LOS was identified in 419 (20.0%) infants. Cognitive and motor delays were found in 392 (18.7%) and 347 (16.5%) infants, respectively. When multivariate analysis was performed, LOS had a significant association with cognitive delay (odds ratio, 1.48; 95% confidence interval, 1.02-2.16), but no association with motor delay in VLBWIs. Both delays were significantly more frequent in cases of intraventricular hemorrhage (IVH) ≥ grade 3, periventricular leukomalacia (PVL), and intrauterine growth restriction (IUGR) and duration of mechanical ventilation. Male sex and necrotizing enterocolitis ≥ grade 2 had an effect on motor delay, whereas paternal college graduation affected cognitive delay.

Conclusion: In VLBWIs with LOS, there is a heightened risk of cognitive delays at 18-24 months of corrected age. Brain injury, such as severe IVH and PVL, duration of mechanical ventilation, and IUGR, were also associated with cognitive and motor delays.

Keywords: Developmental Delay; Late-onset Sepsis; Very Low Birth Weight Infant.

MeSH terms

  • Cerebral Hemorrhage / diagnosis
  • Cerebral Hemorrhage / pathology
  • Cognitive Dysfunction / pathology
  • Enterocolitis, Necrotizing / pathology
  • Female
  • Fetal Growth Retardation / pathology
  • Gestational Age
  • Humans
  • Infant
  • Infant, Premature / growth & development
  • Infant, Very Low Birth Weight
  • Late Onset Disorders
  • Male
  • Neurodevelopmental Disorders / pathology*
  • Sepsis / pathology*
  • Severity of Illness Index