Cranial ultrasonography (cUS) and MRI are the preferred modalities used to image the neonatal brain. Both have their specific contributions and advantages. A neuroimaging study, including sequential cUS and single MRI, was performed in a cohort of very preterm infants (gestational age <32 weeks). The major aims were: to study brain imaging findings and to assess the incidences of brain abnormalities and the relationship between brain abnormalities and perinatal clinical parameters; to compare cUS and MRI findings; to describe imaging findings of the thalami and basal ganglia; and to study the reliability of cUS for detection of (diffuse) white matter injury. Patients & methods: Very preterm infants, born during a 1.5-year period, were eligible if there were no exclusion criteria (i.e., metabolic and genetic disorders, or infections and/or congenital malformations of the CNS). Sequential cUS was performed from admission until discharge and on the day of the MRI following a standardized protocol. MRI (3 Tesla) was performed around or shortly after term equivalent age (TEA). Results: A total of 133 infants were included. The mean number of cUS scans per infant was 8.3 (range: 2–23). MRI was performed in 113 infants at a mean postmenstrual age of 44.7 weeks (range: 40.0–55.9). During admission we found periventricular echodensities and intraventricular hemorrhage in 80 and 30% of infants, respectively – both significantly associated with male gender. The incidence of lenticulo striate vasculopathy (LSV) was 19%. Around TEA, ventricular dilatation and widening of extracerebral spaces were frequent findings. In addition, MRI showed punctate white matter lesions and diffuse excessive high-signal intensity. MRI detected subtle white matter lesions more effectively, whereas cUS was better for the detection of LSV, calcifications and germinolytic and plexus cysts. Diffuse, subtle echogenicity of the basal ganglia and thalami was observed in the majority of infants with normal MRI findings in this area. Focal deep gray matter lesions were only rarely encountered. Conclusions: In very preterm infants, frequent, sequential cUS is an excellent tool to image and follow the brain throughout the neonatal period and detects some lesions and transient changes more effectively than MRI. Single MRI provides invaluable and detailed additional information on the growth and development of, and injury to, the brain. Sequential cUS throughout the neonatal period and a single MRI around TEA are therefore warranted. Bilateral, diffuse and subtle echogenicity in the deep gray matter on cUS probably reflects (normal) maturational processes in the immature brain. With the exception of LSV, focal lesions in the deep gray matter are rare and need to be distinguished from benign phenomena in the deep gray matter. Sequential high-quality cUS during the neonatal period predicts severe white matter injury, but is less predictive of mild-to-moderate white matter injury around TEA.
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