Recurrent Late-Onset Sepsis in Extremely Low Birth Weight Infants Is Associated with Motor Deficits in Early School

Alexander Humberg1, Mats Ingmar Fortmann1, Juliane Spiegler2

  • 1Department of Pediatrics, University Hospital of Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.

Neonatology
|November 3, 2022
PubMed

Insights

Extremely low birth weight infants surviving recurrent late-onset sepsis (LOS) face higher risks of adverse motor development. This study highlights the motor development impact of sepsis in high-risk preterm infants.

Area of Science:

  • Neonatal neurology
  • Pediatric infectious diseases
  • Developmental pediatrics

Background:

  • Sepsis is a known risk factor for brain injury in preterm infants.
  • Extremely low birth weight infants (ELBWI) are particularly vulnerable to sepsis.
  • Recurrent late-onset sepsis (LOS) may significantly impact long-term neurodevelopmental outcomes in ELBWI.

Purpose of the Study:

  • To investigate the association between recurrent LOS and long-term neurodevelopmental outcomes in ELBWI.
  • To evaluate the impact of sepsis episodes on motor, cognitive, and behavioral development at 5-6 years of age.

Main Methods:

  • A large multicenter observational study included ELBWI born at ≤28 6/7 weeks gestation.
  • Neurodevelopment, behavior, and motor skills were assessed by blinded investigators at 5-6 years.
  • Univariate and logistic regression analyses were used to evaluate the impact of recurrent LOS.

Main Results:

  • Recurrent sepsis was significantly associated with adverse motor development (pB = 0.012).
  • Infants with recurrent LOS had 1.7 times higher odds of critical motor testing results compared to those with one LOS.
  • No significant impact of recurrent LOS was found on intelligence quotient or behavioral difficulties.

Conclusions:

  • Recurrent sepsis in preterm infants is linked to poorer long-term motor development.
  • While recurrent infections correlate with adverse motor outcomes, other preterm-related complications may also contribute to neurodevelopmental differences.
Abstract

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