Functional outcome at school age of neonatal post-hemorrhagic ventricular dilatation

Janyte C Holwerda1, Koenraad N J A Van Braeckel1, Elise Roze1

  • 1Department of Pediatrics, Division of Neonatology, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Hanzeplein 1, PO Box 30.001, 9700 RB Groningen, The Netherlands.

Insights

Children with post-hemorrhagic ventricular dilatation (PHVD) experience deficits in intelligence, attention, and visual perception at school age. Surgical intervention in PHVD cases was linked to lower IQ scores.

Area of Science:

  • Pediatrics
  • Neonatology
  • Neurodevelopmental Disorders

Background:

  • Functional outcomes for preterm children with post-hemorrhagic ventricular dilatation (PHVD) are not well-established.
  • PHVD is a serious complication in preterm infants, potentially impacting long-term development.

Purpose of the Study:

  • To assess the school-age functional outcomes of children with PHVD.
  • To identify specific PHVD characteristics associated with increased risk for developmental deficits.

Main Methods:

  • A single-center case-control study included preterm children with PHVD and matched controls.
  • Standardized tests assessed intelligence, attention, memory, executive function, perception, motor skills, and behavior at school age.
  • Outcomes were compared between the PHVD group and controls, with subgroup analysis for surgical intervention.

Main Results:

  • Children with PHVD showed significantly lower total and verbal IQ scores compared to controls.
  • The PHVD group performed worse on tests of visual perception and attention, with a trend toward attention deficits.
  • Within the PHVD group, those who underwent surgical intervention had significantly lower total IQ scores.

Conclusions:

  • Preterm children with PHVD exhibit impaired intelligence, attention, and visual perception at school age.
  • Surgical intervention for PHVD is associated with poorer intellectual outcomes.
  • Further research is needed to understand the long-term neurodevelopmental trajectory and management of PHVD.
Abstract

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