Cerebral Ultrasound at Term-Equivalent Age: Correlations with Neuro-Motor Outcomes at 12–24 Months Corrected Age

<b>Background/Objectives:</b> Our research aimed to assess if correlations could be found between items evaluated at the cerebral ultrasound performed at term-equivalent age (TEA) and neuro-motor outcomes evaluated at 12 and 24 months of corrected age in a group of preterm infants. <b>Methods:</b> The following were assessed: the Levine Index, the diagonals of the lateral ventricles, the size of the ventricular midbody, the sinocortical distance, the width of the basal ganglia, the cortical depth at the level of the cingular sulcus and the maturation of the gyral folding. The neurologic evaluation was performed at 12 and 24 months of corrected age, according to the Amiel Tison neurologic examination, and the items from the calendar of motor acquisitions were used as outcome measures of the study-gross and fine motor subsets. The comparisons between the different groups were performed using the FANOVA test, with a statistically significant association for a <i>p</i> < 0.05. <b>Results:</b> The abnormal gross motor acquisitions at 12 months were significantly associated with an increased size of the ventricular midbody (<i>p</i> < 0.009) and a significantly decreased diameter of the basal ganglia (<i>p</i> < 0.011) on the TEA cerebral ultrasound. At 24 months, a significant association was found with increased size of the ventricular midbody (>10.33 mm) (<i>p</i> < 0.001), a decreased diameter of the basal ganglia (<12.9 mm) (<i>p</i> < 0.016), a decreased cortical depth (<i>p</i> < 0.021) and an immature gyral maturation pattern (<i>p</i> < 0.001). In the case of severely abnormal fine motor outcomes, at 12 months, there were statistically significant associations with an increased size of the ventricular midbody (<i>p</i> < 0.001) and an immature gyral folding pattern (<i>p</i> < 0.0180); at 24 months, significant associations were noted with the size of ventricular midbody (<i>p</i> < 0.001), a decreased diameter of the basal ganglia (<i>p</i> < 0.016), a decreased cortical depth (<i>p</i> < 0.021) and an immature gyration folding (<i>p</i> < 0.001). <b>Conclusions:</b> The abnormal gross and fine motor outcome in former premature infants at 12-24 months corrected age is significantly associated with abnormal findings in the head ultrasound examination performed at TEA reflecting both white matter (increased midbody distance) and grey matter (decreased diameter of the basal ganglia, decreased cortical depth and an immature gyration pattern) involvement.

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Journal
Children
Published
2024-12-28
DOI
https://doi.org/10.3390/children12010030
Citations
4
Primary Topic
Neonatal and fetal brain pathology
Type
article
Field-Weighted Citation Impact
4.44
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article

Cerebral Ultrasound at Term-Equivalent Age: Correlations with Neuro-Motor Outcomes at 12–24 Months Corrected Age

Andreea Ioana Necula, Bogdan Florin Gonț, Vlad Dima, Al Jashi Isam et al.
4 citations
Children
Neonatal and fetal brain pathology
4.44
article

Cerebral Ultrasound at Term-Equivalent Age: Correlations with Neuro-Motor Outcomes at 12–24 Months Corrected Age

Andreea Ioana Necula, Bogdan Florin Gonț, Vlad Dima, Al Jashi Isam, Claudia Mehedințu, Alexandra Floriana Nemeș, Lidia Rusu, Loredana Mitran, Roxana Stoiciu, Alexandra Arghirescu, Alina Fieraru, Larisa Nicoleta Andrășoaie, Adrian Ioan Toma
article en
4 citations

Abstract

<b>Background/Objectives:</b> Our research aimed to assess if correlations could be found between items evaluated at the cerebral ultrasound performed at term-equivalent age (TEA) and neuro-motor outcomes evaluated at 12 and 24 months of corrected age in a group of preterm infants. <b>Methods:</b> The following were assessed: the Levine Index, the diagonals of the lateral ventricles, the size of the ventricular midbody, the sinocortical distance, the width of the basal ganglia, the cortical depth at the level of the cingular sulcus and the maturation of the gyral folding. The neurologic evaluation was performed at 12 and 24 months of corrected age, according to the Amiel Tison neurologic examination, and the items from the calendar of motor acquisitions were used as outcome measures of the study-gross and fine motor subsets. The comparisons between the different groups were performed using the FANOVA test, with a statistically significant association for a <i>p</i> < 0.05. <b>Results:</b> The abnormal gross motor acquisitions at 12 months were significantly associated with an increased size of the ventricular midbody (<i>p</i> < 0.009) and a significantly decreased diameter of the basal ganglia (<i>p</i> < 0.011) on the TEA cerebral ultrasound. At 24 months, a significant association was found with increased size of the ventricular midbody (>10.33 mm) (<i>p</i> < 0.001), a decreased diameter of the basal ganglia (<12.9 mm) (<i>p</i> < 0.016), a decreased cortical depth (<i>p</i> < 0.021) and an immature gyral maturation pattern (<i>p</i> < 0.001). In the case of severely abnormal fine motor outcomes, at 12 months, there were statistically significant associations with an increased size of the ventricular midbody (<i>p</i> < 0.001) and an immature gyral folding pattern (<i>p</i> < 0.0180); at 24 months, significant associations were noted with the size of ventricular midbody (<i>p</i> < 0.001), a decreased diameter of the basal ganglia (<i>p</i> < 0.016), a decreased cortical depth (<i>p</i> < 0.021) and an immature gyration folding (<i>p</i> < 0.001). <b>Conclusions:</b> The abnormal gross and fine motor outcome in former premature infants at 12-24 months corrected age is significantly associated with abnormal findings in the head ultrasound examination performed at TEA reflecting both white matter (increased midbody distance) and grey matter (decreased diameter of the basal ganglia, decreased cortical depth and an immature gyration pattern) involvement.

ChildrenVol. 12(1)
Titu Maiorescu University (RO), Carol Davila University of Medicine and Pharmacy (RO), Clinical Emergency Hospital Bucharest (RO)
Openalex Percentile: Top 6%
Neonatal and fetal brain pathology
4.44
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