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Prenatal ventriculomegaly: natural course, survival, and neurodevelopmental status
Insights
Most cases of mild or moderate prenatal ventriculomegaly showed stable or regressed courses with near-normal neurodevelopmental outcomes. Further prospective studies are needed to confirm these findings for prenatal ventriculomegaly prognosis.
Area of Science:
- Neuroscience
- Pediatric Neurosurgery
- Prenatal Medicine
Background:
- Prenatal ventriculomegaly, classified by atrial diameter, necessitates understanding its natural course and neurodevelopmental impact.
- Mild and moderate ventriculomegaly are common prenatal conditions requiring careful monitoring.
Purpose of the Study:
- To retrospectively analyze the natural course, associated abnormalities, survival rates, and neurodevelopmental outcomes of mild and moderate prenatal ventriculomegaly.
- To evaluate the progression and regression patterns of ventriculomegaly in utero.
Main Methods:
- Retrospective study of 122 pregnancies with mild/moderate ventriculomegaly from 2010-2018.
- Collected demographic, ultrasonographic, outcome, and neurodevelopmental data (CDC criteria) via parental interviews at least one year post-birth.
Main Results:
- Ventriculomegaly regressed in 5%, remained stable in 67%, and progressed in 12% of cases.
- Associated abnormalities were noted in 29.7% (mild) and 16.2% (moderate) cases, with corpus callosum agenesis being most frequent.
- Normal neurodevelopmental status was observed in 69.8% of evaluated children.
Conclusions:
- Mild and moderate prenatal ventriculomegaly often exhibit stable or regressed courses with favorable neurodevelopmental outcomes.
- Despite data limitations, the study suggests a generally positive prognosis for mild/moderate cases.
- Larger prospective studies are recommended for definitive conclusions on prenatal ventriculomegaly prognosis.
Objective:
Prenatal ventriculomegaly is classified as mild, moderate, or severe based on the atrium diameter. The natural course and intrauterine progression of mild and moderate ventriculomegaly associated with the neurodevelopmental status of these children has been widely reported.
Methods:
One hundred twenty-two pregnancies with mild and moderate ventriculomegaly referred to the pediatric neurosurgery clinic of Children's Medical Center between 2010 and 2018 were retrospectively studied. The authors collected demographic and first and sequential ultrasonographic information, associated abnormalities, information about pregnancy outcomes, and the latest developmental status of these children according to Centers for Disease Control and Prevention criteria by calling parents at least 1 year after birth.
Results:
The mean gestational age at the time of diagnosis was 29.1 weeks, and 53% of fetuses were female. The width of the atrium was registered precisely in 106 cases, in which 61% had mild and 39% had moderate ventriculomegaly. Information on serial ultrasound scans was collected in 84 cases in which ventriculomegaly regressed in 5, remained stable in 67, and progressed in 12 patients. Fourteen cases (29.7%) in the mild ventriculomegaly group and 6 cases (16.2%) in the moderate group had associated abnormalities, with corpus callosum agenesis as the most frequent abnormality. The survival rate was 80% in mild and 89.4% in moderate ventriculomegaly. Considering survival to live birth and progression of the ventriculomegaly, the survival rate was 100% in regressed, 97% in stable, and 41.6% in progressed ventricular width groups (p < 0.001). Neurodevelopmental status was evaluated in 73 cases and found to be normal in 69.8% of the cases; 16.4% of children had mild delay, and 5.4% and 8.2% of cases were diagnosed with moderate and severe delays, respectively.
Conclusions:
In spite of a high rate of missed data in our retrospective study, most patients with mild or moderate ventriculomegaly had a stable or regressed course. Most cases had near-normal developmental status. Prospective studies with a larger sample size and detailed developmental evaluation tests are needed to answer the questions related to the natural course, survival, and prognosis of prenatal ventriculomegaly.
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