Early Anatomical Injury Patterns Predict Epilepsy in Head Cooled Neonates With Hypoxic-Ischemic Encephalopathy.
Early Anatomical Injury Patterns Predict Epilepsy in Head Cooled Neonates With Hypoxic-Ischemic Encephalopathy.
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DOI:
10.1016/j.pediatrneurol.2015.04.009
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发表时间:
2015-08
影响因子:
3.8
通讯作者:
Venkatesan C
中科院分区:
文献类型:
--
作者:
Jung DE;Ritacco DG;Nordli DR;Koh S;Venkatesan C
To determine whether early anatomical injury patterns in MRI correlate with the development of post-neonatal epilepsy in infants treated with selective head cooling for hypoxic ischemic encephalopathy. A retrospective study of infants ≥35 weeks’ gestation born between 2008 and 2013 and followed for at least one year at Northwestern University. All had brain MRI at day 4–5 and EEGs during rewarming and at 3 to 6 months of age. Outcome was favorable for our cohort of 73 with mean follow-up of 41 (± 7) months. The majority (66%) survived with no seizure recurrence, while 13 (18%) developed post neonatal epilepsy including 8, who had infantile spasms. Twelve infants (16%) died. The most common MRI pattern was diffuse brain injury involving both cortical and subcortical gray matter (26/73, 35%) followed by cortical and subcortical white matter injury (18/73, 25%), and normal MRI (16/73, 22%). In 13 infants (18%), the brainstem was involved in addition to cortical and subcortical gray matter; 9 died and all 4 surviving infants developed infantile spams. All 18 infants with cortical and subcortical white matter injury survived and none developed post neonatal epilepsy. Risk of post neonatal epilepsy was associated with injury involving subcortical regions (basal ganglia, thalamus ± brainstem) (12/39 vs 1/34, p<0.003). Brainstem injury was highly predictive of infantile spams while cortical injury alone predicted low risk for short term post neonatal epilepsy. Location of anatomical injury on MRI can be an early predictive factor for development of infantile spams and inform prognostic decisions in newborns treated with selective head cooling for hypoxic ischemic encephalopathy.