Early continuous video electroencephalography was used to detect seizures in term infants at high risk of hypoxic ischemic encephalopathy (HIE) in a study at University College Cork, and St Vincent’s University Hospital, Dublin, Ireland. The predictive value of high-risk markers, the so-called “3-strikes“ (Apgar score of <5 at 5 min, pH <7.00, and need for intubation) for EEG seizures, abnormal background EEG activity, and Sarnat grade, based on clinical behavior at 24 hours, was examined. Electrographic seizures occurred in 11 (22%) of 49 infants suitable for analysis. Encephalopathy scored by Sarnat grades was severe in 6 infants, moderate in 18, and mild in 25. EEG background abnormalities were severe in 4, moderate in 16, and mild or moderate in 25. Positive predictive values for neonatal seizures based on the 3-strikes were 18% for an Apgar score of <5 at 5 min, 16% for a pH <7.00, and 21% for a need for intubation. A positive predictive value of 25% and a negative value of 77% were obtained for the 3 strikes combined. Base deficit (< -15 mEq/L) or lactate (> 10 mmol/L) values substituted for pH in the 3-strikes model did not improve its predictive value. Apgar score <5, nucleated red cells, and base deficit showed some association with Sarnat grade. The 5 min Apgar was significantly associated with both Sarnat grade and EEG grade. The risk of HIE after perinatal asphyxia may be predicted by Sarnat scores at 24 hours of age, but the neonatal EEG soon after delivery offers an early indication of seizures and neurologic outcome. Metabolic acidosis, in particular lactic acidosis may identify infants at risk of HIE but does not predict the occurrence of seizures or grade of encephalopathy. 
COMMENT. Early monitoring of continuous EEG recordings was the best indicator of risk of neonatal seizures and severity of encephalopathy following perinatal asphyxia in the above study. Previous EEG studies used intermittent recordings that overlooked the occurrence of subclinical seizures. The model described by Shah PS et al  offers an additional prognostic indicator within 4 hours of birth, of value in selection of cases for trials of neuroprotective therapies. The potential of therapies such as selective head cooling with systemic hypothermia has emphasized the importance of accurate and early prediction of outcome of neonatal encephalopathy in the first 6 hours of life. 
Bedside EEG measures in encephalopathic infants are found to correlate with severity of cerebral injury defined by MRI in a study using 2-channel bedside amplitude-integrated EEG, at Royal Children’s Hospital, Melbourne, Australia.  A minimum amplitude of <4 mcV gives a specificity of 75%, and a minimum of 6 mcV has a greater sensitivity, allowing the bedside monitor to be used as a screening test for diagnosis and treatment. The amplitude-integrated EEG is useful as a prognostic indicator up to 3 days after admission of an asphyxiated infant to the NICU, even during anticonvulsant therapy. In 40 term-born HI encephalopathic infants, the lower the EEG amplitude, the greater the degree of MRI abnormality.