Neurodevelopmental outcome in isolated mild fetal ventriculomegaly: systematic review and meta-analysis

G Pagani1, B Thilaganathan, F Prefumo

  • 1Maternal-Fetal Medicine Unit, Department of Obstetrics and Gynaecology, Spedali Civili and University of Brescia, Brescia, Italy; Fetal Medicine Unit, Division of Developmental Sciences, St George's University of London, London, UK.

Insights

Mild fetal ventriculomegaly (10-15 mm) has a 7.9% rate of neurodevelopmental delay. Prenatal imaging has a 7.4% false-negative rate for associated abnormalities, highlighting the need for further research.

Area of Science:

  • Perinatology
  • Developmental Neuroscience
  • Medical Imaging

Background:

  • Fetal ventriculomegaly, particularly when mild and isolated, is associated with potential neurodevelopmental concerns.
  • Accurate assessment of associated abnormalities and long-term outcomes is crucial for informed clinical management.

Purpose of the Study:

  • To systematically review and meta-analyze the literature on isolated mild fetal ventriculomegaly (10-15 mm).
  • To determine the prevalence of neurodevelopmental delay in these cases.
  • To evaluate the false-negative rate of prenatal imaging for detecting associated abnormalities.

Main Methods:

  • Systematic literature search of scientific databases for studies on neurodevelopmental outcome in isolated ventriculomegaly.
  • Inclusion criteria: assessment of neurodevelopmental outcome, karyotype check, and mild ventriculomegaly (10-15 mm atrial width).
  • Exclusion criteria: absence of karyotype, bilateral ventriculomegaly, or pre/postnatal abnormalities.

Main Results:

  • Included 20 studies with 699 cases of isolated mild fetal ventriculomegaly.
  • Overall prevalence of neurodevelopmental delay was 7.9% (95% CI, 4.7-11.1%).
  • Postnatal imaging in 9 studies revealed a 7.4% (95% CI, 3.1-11.8%) prevalence of previously undiagnosed findings.

Conclusions:

  • The false-negative rate of prenatal imaging for associated abnormalities in isolated mild fetal ventriculomegaly (≤ 15 mm) is 7.4%.
  • The incidence of neurodevelopmental delay in truly isolated mild ventriculomegaly (≤ 15 mm) is 7.9%, similar to the general population.
  • Further large prospective studies are needed to assess childhood disability prevalence rather than subtle neurodevelopmental delays.
Abstract