Seizures in preterm infants with germinal-matrix-intraventricular hemorrhage (GM-IVH): a retrospective monocentric

Stephanie C Schüssler1, Anna Paul1, Undine Niederreiter1

  • 1Department of Pediatrics and Adolescent Medicine, Pediatric Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany.

Insights

Seizures in preterm infants with germinal-matrix-intraventricular hemorrhage (GM-IVH) are linked to lower gestational age and pneumonia. Further research is needed to confirm these findings on seizure development and outcomes.

Area of Science:

  • Neonatal neurology
  • Pediatric neurology
  • Perinatal medicine

Background:

  • Germinal-matrix-intraventricular hemorrhage (GM-IVH) is a significant cause of seizures in premature infants.
  • Understanding risk factors and neurodevelopmental outcomes is crucial for this vulnerable population.

Purpose of the Study:

  • To identify risk factors associated with seizures in preterm infants diagnosed with GM-IVH (grades 2-4).
  • To evaluate the neurodevelopmental outcomes of preterm infants experiencing seizures secondary to GM-IVH.

Main Methods:

  • A retrospective study analyzed data from 2011-2019, including preterm infants with GM-IVH grades 2-4.
  • Seizures were confirmed by clinical signs and EEG; neurodevelopment was assessed using the Bayley Scales of Infant Development II (BSID-II) at two years.
  • Infants with seizures were compared to those without seizures and a broader cohort of preterm infants (<1500g).

Main Results:

  • Seizures occurred in 52.9% of the 34 preterm infants with GM-IVH.
  • Lower gestational age (28.1 vs. 30 weeks) and pneumonia were significantly associated with seizures (p=0.04 and p=0.003, respectively).
  • Infants with seizures showed significantly lower BSID-II Mental scores (86.3 ± 18.3 vs. 104.9 ± 8.5, p=0.03), though immaturity was a confounding factor.

Conclusions:

  • Seizures in preterm infants with GM-IVH are associated with lower gestational age and pneumonia.
  • Infections and inflammation are potential contributors to seizure development.
  • Larger studies employing continuous EEG monitoring are recommended to validate these findings and clarify outcome determinants.
Abstract