Rebecca Hughes1, Wai-Yan Poon1, A Simon Harvey2. 1. Department of Neurology, The Royal Children's Hospital, Melbourne, Australia. 2. Department of Neurology, The Royal Children's Hospital, Melbourne, Australia Department of Paediatrics, The University of Melbourne, Melbourne, Australia.
Abstract
AIM: The assessment of staring episodes in children with autism spectrum disorder (ASD) is difficult due to the range of diagnostic possibilities, the increased frequency of epileptiform activity on electroencephalogram (EEG), and the inability of normal EEG to exclude seizures. We reviewed the diagnostic use of routine EEG in this setting. METHOD: The routine EEG database of the Royal Children's Hospital, Melbourne was searched for recordings during 2005-2010 in children with ASD below 16 years of age who were referred for staring. EEG reports and recordings were reviewed and epileptiform activity was characterised. RESULTS: Ninety-two EEGs in children with ASD were requested for episodes of staring. No child had absence or focal dyscognitive seizures confirmed on EEG. Findings were normal or showed non-epileptiform abnormalities in 80 children. Interictal epileptiform abnormalities were recorded in 12 children, but were judged potentially significant in only three. Seven children had epileptiform activity typical of benign focal epilepsy of childhood, such discharges seen not uncommonly in developmentally normal and delayed children without seizures. INTERPRETATION: Given the difficulties of performing EEG in children with ASD, the low yield of positive diagnostic findings and the high frequency of insignificant abnormalities, we suggest that EEG should be undertaken judiciously when evaluating children with ASD and staring episodes. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
AIM: The assessment of staring episodes in children with autism spectrum disorder (ASD) is difficult due to the range of diagnostic possibilities, the increased frequency of epileptiform activity on electroencephalogram (EEG), and the inability of normal EEG to exclude seizures. We reviewed the diagnostic use of routine EEG in this setting. METHOD: The routine EEG database of the Royal Children's Hospital, Melbourne was searched for recordings during 2005-2010 in children with ASD below 16 years of age who were referred for staring. EEG reports and recordings were reviewed and epileptiform activity was characterised. RESULTS: Ninety-two EEGs in children with ASD were requested for episodes of staring. No child had absence or focal dyscognitive seizures confirmed on EEG. Findings were normal or showed non-epileptiform abnormalities in 80 children. Interictal epileptiform abnormalities were recorded in 12 children, but were judged potentially significant in only three. Seven children had epileptiform activity typical of benign focal epilepsy of childhood, such discharges seen not uncommonly in developmentally normal and delayed children without seizures. INTERPRETATION: Given the difficulties of performing EEG in children with ASD, the low yield of positive diagnostic findings and the high frequency of insignificant abnormalities, we suggest that EEG should be undertaken judiciously when evaluating children with ASD and staring episodes. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.