The prognostic value of amplitude-integrated electroencephalography in neonates with hypoxic-ischemic encephalopathy

• Main Authors: Vasiljević Brankica, Maglajlić-Đukić Svjetlana, Gojnić Miroslava
• Format: Article
• Language: English
• Published: Military Health Department, Ministry of Defance, Serbia 2012-01-01
• Series: Vojnosanitetski Pregled
• Subjects: elektroencephalography; intensive care units, neonatal; hypoxia-ishemia, brain; infant, premature; infant, newborn; prognosis
• Online Access: http://www.doiserbia.nb.rs/img/doi/0042-8450/2012/0042-84501206492V.pdf

Background/Aim. Diagnosis of perinatal hypoxic-ischemic encephalopathy (HIE) and early prediction neurological outcome is important and difficult. The aim of this study was to determine the prognostic value of amplitude integrated electroencephalography (aEEG) for abnormal neurodevelopment outcome in a neonate with HIE. Methods. A total of 90 neonates > 32 gestational age (GA) with HIE were enrolled prospectively. All neonates with HIE were categorized into three grades according to the Sarnat and Sarnat clinical scoring system (mild HIE, moderate HIE and severe HIE). aEEG traces were recorded with a cerebral function monitor (CFM) during the first 72 h of life. The neurodevelopment outcome was assessed at 12 months of age of corrected gestational age. Results. The pattern of aEEG correlated with the severity of HIE (p < 0.0001) and subsequent neurodevelopment outcome (p < 0.001). We found that aEEG background patterns exhibited superior prediction of abnormal outcomes at 12 months of age (sensitivity of 91.7% and specificity of 94.3%, positive predictive value of 78.6% and negative predictive value of 98.1%) when compared to aEEG seizure (sensitivity of 94% and specificity of 48%, positive predictive value of 57% and a negative predictive value of 92%). Electroclinical dissociation seizure was detected in 28% of the neonates with HIE. Conclusions. Our results confirm that aEEG is simple and accurate bedside diagnostic method for assessing extension of hypoxic-ischemic brain damage and early identification of neonates with perinatal HIE who are at high risk of neurodevelopmental impairment.