Subscribe to RSS
DOI: 10.1055/s-2007-986686
Relationship between Electroencephalography and Magnetic Resonance Imaging Findings after Hypoxic-Ischemic Encephalopathy at Term
Publication History
Publication Date:
14 September 2007 (online)

ABSTRACT
Hypoxic-ischemic encephalopathy (HIE) is a major cause of neonatal morbidity and mortality. Electroencephalography (EEG) and brain magnetic resonance imaging (MRI) are frequently performed in these infants, but the prognostic value of the combined use of EEG and MRI needs additional exploration. The purpose of this study was to investigate, in neonates with HIE, the role of early EEG and conventional MRI in the prediction of infants at risk for persistent encephalopathy at 18 months of age. Thirty-four term infants with HIE were enrolled in this prospective study. EEG was recorded within the first 72 hours after birth and a brain MRI scan was done between 1 and 4 weeks of age. Denver Developmental Screening Test II was performed at 6, 12, and 18 months of age. Three infants (9%) had mild HIE, 21 infants (62%) had moderate HIE, and 10 infants (29%) had severe HIE. The EEG background was normal, moderately, severely, and extremely discontinuous in eight (24%), three (9%), sixteen (47%), and seven (20%) neonates, respectively. EEG background activities correlated significantly with HIE severity (p = 0.0001). MRI findings significantly correlated with EEG background (p = 0.001). Normal MRI scans and minimal basal ganglia lesions were always associated with normal EEG background. Patients with severe basal ganglia and thalamic lesions in MRI (n = 2) had extreme discontinuous EEG background. For the prediction of poor outcomes, abnormal EEG background activity had a sensitivity (Sn) = 100%, a specificity (Sp) = 100%, positive predictive value (PPV) = 100%, and negative predictive value (NPV) = 100%, whereas values of abnormal MRI scans were Sn of 100%, Sp = 43%, PPV = 82%, and NPV=100%. EEG background activity is the best element to predict abnormal outcomes. Severe basal ganglia and thalamic injuries on MRI scans are associated with poor outcomes. Otherwise, MRI does not contribute to the prediction of outcomes at 18 months of age.
KEYWORDS
Electroencephalography - magnetic resonance imaging - encephalopathy - Denver Developmental Screening Test II - asphyxia
REFERENCES
- 1 World Health organization .Child Health and Development: Health of the Newborn. Geneva; WHO 1991
-
2 Volpe J.
Hypoxic ischemic encephalopathy . In: Volpe J Neurology of the Newborn. Philadelphia; WB Saunders 2001: 217-331 - 3 Biagioni E, Mercuri E, Rutherford M et al.. Combined use of electroencephalogram and magnetic resonance imaging in full-term neonates with acute encephalopathy. Pediatrics. 2001; 107 461-468
- 4 Toet M C, van der Meij W, de Vries L S et al.. Comparison between simultaneously recorded amplitude integrated electroencephalogram (cerebral function monitor) and standard electroencephalogram in neonates. Pediatrics. 2002; 109 772-779
- 5 Shalak L F, Laptook A R, Velaphi S C et al.. Amplitude-integrated electroencephalography coupled with an early neurologic examination enhances prediction of term infants at risk for persistent encephalopathy. Pediatrics. 2003; 111 351-357
- 6 Rutherford M A, Pennock J M, Counsell S J et al.. Abnormal magnetic resonance signal in the internal capsule predicts poor neurodevelopmental outcome in infants with hypoxic-ischemic encephalopathy. Pediatrics. 1998; 102 323-328
- 7 Jyoti R, O'Neil R. Predicting outcome in term neonates with hypoxic-ischaemic encephalopathy using simplified MR criteria. Pediatr Radiol. 2006; 36 38-42
- 8 Rutherford M A, Ward P, Malamatentiou C. Advanced MR techniques in the term-born neonate with perinatal brain injury. Semin Fetal Neonatal Med. 2005; 10 445-460
- 9 Rutherford M, Pennock J, Schwieso J et al.. Hypoxic-ischaemic encephalopathy: Early and late magnetic resonance imaging findings in relation to outcome. Arch Dis Child Fetal Neonatal Ed. 1996; 75 F145-F151
-
10 American Academy of Pediatrics and American College of Obstetricians and Gynaecologists .
Care of the Neonate. Guidelines for Perinatal Care. 5th ed . Gilstrap LC, Oh W Elk Grove Village, IL; American Academy of Pediatrics 2002: 196-197 - 11 Ballard J L, Khoury J C, Wedig K et al.. New Ballard score, expanded to include extremely premature infants. J Pediatr. 1991; 119 417-423
- 12 Sarnat H B, Sarnat M S. Neonatal encephalopathy following fetal distress. A clinical electroencephalographic study. Arch Neurol. 1976; 33 696-705
-
13 Mark S.
Pediatric neurophysiologic evaluation . In: Swaiman KE, Ashwal S Pediatric Neurology-Principles of Practice. St. Louis, MO; Mosby 1999: 142-181 - 14 Biagioni E, Bartalena L, Boldrini A et al.. Constantly discontinuous EEG patterns in full-term neonates with hypoxic-ischemic encephalopathy. Clin Neurophysiol. 1999; 110 1510-1515
- 15 Biagioni E, Boldrini A, Bottone U et al.. Prognostic value of abnormal EEG transients in preterm and full-term neonates. Electroencephalogr Clin Neurophysiol. 1996; 99 1-9
- 16 Barkovich A J, Hajnal B L, Vigneron D et al.. Prediction of neuromotor outcome in perinatal asphyxia: evaluation of MR scoring systems. AJNR Am J Neuroradiol. 1998; 19 143-149
- 17 Frankenburg W K, Dodds J, Archer P et al.. The Denver II: a major revision and restandardization of the Denver Developmental Screening Test. Pediatrics. 1992; 89 91-97
- 18 Azzopardi D, Guarino I, Brayshaw C et al.. Prediction of neurological outcome after birth asphyxia from early continuous two-channel electroencephalography. Early Hum Dev. 1999; 55 113-123
- 19 Hellstrom-Westas L, Rosen I, Svenningsen N W. Predictive value of early continuous amplitude integrated EEG recordings on outcome after severe birth asphyxia in full term infants. Arch Dis Child Fetal Neonatal Ed. 1995; 72 F34-F38
- 20 Al Naqeeb N, Edwards A D, Cowan F M et al.. Assessment of neonatal encephalopathy by amplitude-integrated electroencephalography. Pediatrics. 1999; 103 1263-1271
- 21 Gluckman P D, Wyatt J S, Azzopardi D. Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial. Lancet. 2005; 365 663-670
- 22 Allan W C. The clinical spectrum and prediction of outcome in hypoxic-ischemic encephalopathy. Neoreviews. 2002; 3 e108-e115
- 23 Badawi N, Kurinczuk J J, Keogh J M et al.. Intrapartum risk factors for newborn encephalopathy: the Western Australian case-control study. BMJ. 1998; 317 1554-1558
- 24 Berger R, Garnier Y. Perinatal brain injury. J Perinat Med. 2000; 28 261-285
- 25 Barkovich A J, Westmark K, Partridge C et al.. Perinatal asphyxia: MR findings in the first 10 days. AJNR Am J Neuroradiol. 1995; 16 427-438
- 26 Vexler Z S, Ferriero D M. Molecular and biochemical mechanisms of perinatal brain injury. Semin Neonatol. 2001; 6 99-108
- 27 Black S M, Bedolli M A, Martinez S et al.. Expression of neuronal nitric oxide synthase corresponds to regions of selective vulnerability to hypoxia-ischemia in developing rat brain. Neurobiol Dis. 1995; 2 145-155
- 28 Ment L R, Bada H S, Barnes P et al.. Practice parameter: neuroimaging of the neonate: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2002; 58 1726-1738
Hany AlyM.D.
900 23rd Street
NW Suite # G2092, Washington, DC 20037