AI Article Synopsis

  • - The study focused on prenatal ventriculomegaly (VM) and its classification into mild, moderate, or severe, assessing its impact on neurodevelopmental outcomes based on various factors like VM progression and associated anomalies.
  • - Researchers followed 73 pregnancies diagnosed with VM through regular ultrasounds, collecting data on demographics, VM type, and developmental status, with an average follow-up of 14.6 months.
  • - Results showed that while 62.5% of patients had normal developmental status, those with mild VM fared better than those with severe VM; significant relationships were found between neurodevelopmental outcomes and VM progression, as well as the presence of other cranial abnormalities.

Article Abstract

Objective: Prenatal ventriculomegaly (VM) is classified as mild, moderate, or severe on the basis of the diameter of the atrium. Neurodevelopmental status in prenatal VM is associated with various factors such as the course of VM, VM type, progression, and associated anomalies. In this study, the authors aimed to evaluate neurodevelopmental outcome in patients with prenatal VM and to detect possible associated risk factors.

Methods: In this study, 73 pregnancies with VM who were referred to Children's Medical Center, Tehran, Iran, between 2019 and 2021 were prospectively followed. They were followed up every 2-4 weeks with ultrasonography (US) before delivery and were then observed for an average time of 14.6 months. The authors collected demographic and ultrasound information, associated abnormalities, pregnancy outcomes, and developmental status according to Centers for Disease Control criteria.

Results: The mean gestational age at the time of diagnosis was 28.1 weeks, and 46.6% of fetuses were female. According to the first US, 46.6% had mild, 21.9% had moderate, and 31.5% had severe VM. Serial US scans showed that VM had regressed in 20.5% of patients, remained stable in 35.6%, and progressed in 43.8%. Other cranial abnormalities were detected in 38.4% of fetuses. During follow-up, 62.5% of cases had normal developmental status, 26.6% had mild delay, and 10.9% had severe neurodevelopmental delay. Pregnancy was terminated in 9 (12.3%) cases. Normal neurodevelopment was reported in 75.8% of patients with mild VM versus 50% of those with severe VM (p = 0.19). Neurodevelopmental status was normal in 72.5% of cases without other cranial abnormalities (p = 0.018) and in 86.7% of cases with regression of VM (p = 0.028).

Conclusions: Despite analysis of different factors in prenatal VM, only progression of VM and associated cranial abnormalities had significant relationships with neurodevelopmental prognosis.

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Source
http://dx.doi.org/10.3171/2023.2.PEDS22522DOI Listing

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