Maternal infection, fetal inflammatory response, and brain damage in very low birth weight infants. Developmental

A Leviton1, N Paneth, M L Reuss

  • 1Children's Hospital, Boston, Massachusetts, USA.

Pediatric Research
|December 14, 1999
PubMed

Insights

Maternal and fetal infections increase the risk of echolucent images (EL) in very low birth weight newborns. These findings highlight the importance of infection markers in predicting neurological outcomes for vulnerable infants.

Area of Science:

  • Neonatal neurology
  • Perinatal infection
  • Neurodevelopmental outcomes

Background:

  • Echolucent images (EL) of cerebral white matter in very low birth weight (VLBW) newborns are linked to motor and cognitive deficits.
  • Understanding factors contributing to EL is crucial for early intervention and improved neurodevelopmental outcomes.

Purpose of the Study:

  • To investigate the association between maternal and feto-placental infection markers and the risk of early and late EL in VLBW infants.
  • To determine if the timing of membrane rupture influences the impact of infection markers on EL development.

Main Methods:

  • A multi-center cohort study of 1078 VLBW infants (<1500g) was conducted.
  • Maternal infection was assessed via fever, leukocytosis, and antibiotic use. Feto-placental inflammation was indicated by fetal vasculitis and membrane inflammation.
  • Analyses were stratified based on the interval between membrane rupture and delivery (within 1 hour vs. longer).

Main Results:

  • Fetal vasculitis significantly increased the risk of both early and late EL.
  • The association between fetal vasculitis and early EL was observed only in infants born after a longer interval post-membrane rupture with membrane inflammation.
  • Maternal antibiotic use was linked to late EL specifically in infants born within 1 hour of membrane rupture.

Conclusions:

  • Maternal infection indicators and fetal inflammatory responses are independently associated with EL in VLBW infants.
  • These associations are particularly strong for late-onset EL.
  • The timing of delivery relative to membrane rupture modifies the impact of infection markers on EL development.