Myth: Cerebral palsy cannot be predicted by neonatal brain imaging
Introduction
The aim of this review is to refute the myth that cerebral palsy (CP) cannot be predicted by neonatal brain imaging in neonates when combining sequential cranial ultrasonography (cUS) for a sufficient length of time with conventional magnetic resonance imaging (MRI) at term-equivalent age (TEA) in the preterm infant and when using first week MRI including diffusion-weighted imaging (DWI) in the term infant.
Section snippets
The preterm infant
Preterm birth is still increasing. The rate of neurodevelopmental impairment in survivors remains high and recent data have failed to show an improvement in neurodevelopmental outcome in infants with a gestational age (GA) of ≤25 weeks.1, 2 Others have reported a significant decrease in the rates of CP, severe cognitive impairments, and overall neurodevelopmental impairment, but these studies include infants with a GA >25 weeks and are hospital- rather than population-based studies.3, 4, 5
The term infant
Newer techniques, such as evoked potentials, amplitude-integrated electroencephalography (aEEG), and neuroimaging have been used to predict outcome, in particular the development of CP, in term neonates with hypoxic-ischaemic encephalopathy. These techniques were used to assess the severity of the hypoxic-ischaemic insult, to evaluate the effects of neonatal intensive care, and to identify patients who might benefit from interventions such as physical therapy.53, 54
Although electrophysiology
Acknowledgements
The authors would like to thank Frances Cowan for her helpful comments when reading the manuscript and the enthusiasm and patience of magnetic resonance technicians.
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