Abstract

Background. Hypoxic-ischemic encepha-lopathy (HIE) is a leading cause of dis-ability in full-term newborns. Long-term consequences of HIE, even when treated by hypothermia, are not easily predictable. Aims. To assess the potential role of elec-troencephalography and neuroimaging parameters as early predictors of neurode-velopmental outcome in HIE newborns treated with hypothermia.Methods. We retrospectively evaluated 13 HIE patients treated with hypothermia in January 2012-September 2014. We re-viewed their amplitude-integrated electro-encephalography (a-EEG) at 6, 12 and 24 hours (h), cranial ultrasonography (US) at 12, 72 h and >7 days of life (DOL) and brain magnetic resonance (MRI) performed at 7-28 DOL, according to validated scores. aEEG, US and MRI patterns were correlat-ed to neurodevelopmental outcome at 18-24 months, considered as negative if one of the following was present: Mental Devel-opment Index (MDI)<85, motor, visual or hearing impairment.Results. The severity of a-EEG, US and MRI alterations at each time point was not different according to the outcome. MDI was negatively correlated with aEEG score at 12h (R= -0.571, p=0.04) and with US score at 72h (R= -0.630, p=0.02). A positive correlation was found between aEEG score at 6h and US score at >7DOL(R=0.690, p=0.013). US alterations of the cortical matter at 72h were directly corre-lated with a-EEG score at 12h (R = 0.606, p=0.028) and 24h (R=0.605, p=0.029). Conclusions. Early instrumental evalua-tions, in particular aEEG and US, seem to predict neurodevelopmental outcome at 18-24 months in HIE newborns treated with hypothermia.&nbsp

Highlights

  • Hypoxic-ischemic encephalopathy (HIE), following neonatal asphyxia, is a leading cause of neurological disability in newborns: [1] it can result in serious consequences such as death, cerebral palsy, epilepsy, cognitive, behavioural and developmental deficits. [2,3] Brain damage is an evolutionary process characterized by an acute stage of neuronal necrosis followed by a phase of reperfusion injury characterized by neural apoptosis

  • We reviewed their amplitude-integrated electroencephalography (a-EEG) at 6, 12 and 24 hours (h), cranial ultrasonography (US) at 12, 72 h and >7 days of life (DOL) and brain magnetic resonance (MRI) performed at 7-28 DOL, according to validated scores. aEEG, US and magnetic resonance imaging (MRI) patterns were correlated to neurodevelopmental outcome at 1824 months, considered as negative if one of the following was present: Mental Development Index (MDI)

  • This study aimed to analyse the presence of early anomalies detected by a-EEG, cranial US and brain MRI, in neonates undergoing therapeutic hypothermia for HIE, and to assess their potential prognostic value with respect to neurodevelopmental outcomes at 18 -24 months

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Summary

Introduction

Hypoxic-ischemic encephalopathy (HIE), following neonatal asphyxia, is a leading cause of neurological disability in newborns: [1] it can result in serious consequences such as death, cerebral palsy, epilepsy, cognitive, behavioural and developmental deficits. [2,3] Brain damage is an evolutionary process characterized by an acute stage of neuronal necrosis followed by a phase of reperfusion injury characterized by neural apoptosis. [3] the aim of this study was to assess the potential role of amplitude-integrated electroencephalography (a-EEG) background patterns, cranial ultrasonography (US) and cerebral magnetic resonance imaging (MRI) findings as early predictors of neurodevelopmental outcome at 18 -24 months in neonates undergoing therapeutic hypothermia for HIE. We retrospectively evaluated 13 HIE patients treated with hypothermia in January 2012-September 2014 We reviewed their amplitude-integrated electroencephalography (a-EEG) at 6, 12 and 24 hours (h), cranial ultrasonography (US) at 12, 72 h and >7 days of life (DOL) and brain magnetic resonance (MRI) performed at 7-28 DOL, according to validated scores. In particular aEEG and US, seem to predict neurodevelopmental outcome at 18-24 months in HIE newborns treated with hypothermia.

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