Amplitude Integrated Electroencephalogram as a Prognostic Tool in Neonates with Hypoxic-Ischemic Encephalopathy: A Systematic Review

Ruth Del Río, Carlos Ochoa, Ana Alarcon, Juan Arnáez, Dorotea Blanco, Alfredo García-Alix, Ruth Del Río, Carlos Ochoa, Ana Alarcon, Juan Arnáez, Dorotea Blanco, Alfredo García-Alix

Abstract

Introduction: Perinatal management and prognostic value of clinical evaluation and diagnostic tools have changed with the generalization of therapeutic hypothermia (TH) in infants with hypoxic-ischemic encephalopathy (HIE).

Aim: to ascertain the prognostic value of amplitude integrated electroencephalogram (aEEG) in neonates with HIE considering hours of life and treatment with TH.

Methods: A systematic review was performed. Inclusion criteria were studies including data of neonates with HIE, treated or not with TH, monitored with aEEG and with neurodevelopmental follow-up of at least 12 months. The period of bibliographic search was until February 2016. No language restrictions were initially applied. Consulted databases were MEDLINE, Scopus, CINHAL and the Spanish language databases GuiaSalud and Bravo. Article selection was performed by two independent reviewers. Quality for each individual paper selected was evaluated using QUADAS-2. Review Manager (RevMan) version 5.3 software was used. Forest plots were constructed to graphically show sensitivity and specificity for all included studies, separating patients treated or not with hypothermia. Summary statistics were estimated using bivariate models and random effects approaches with the R package MADA from summary ROC curves. Meta-regression was used to estimate heterogeneity and trends.

Results: from the 403 articles initially identified, 17 were finally included and critically reviewed. In infants not treated with hypothermia the maximum reliability of an abnormal aEEG background to predict death or moderate/severe disability was at 36 hours of life, when a positive post-test probability of 97.90% was achieved (95%CI 88.40 to 99.40%). Positive likelihood ratio (+LR) at these hours of life was 26.60 (95%CI 4.40 to 94.90) and negative likelihood ratio (-LR) was 0.23 (95%CI 0.10 to 0.44). A high predictive value was already present at 6 hours of life in this group of patients, with a positive post-test probability of 88.20% (95%CI 79.80 to 93%) and a +LR of 4.34 (95%CI 2.31 to 7.73). In patients treated with TH the maximum predictive reliability was achieved at 72 hours of life (post-test probability of 95.70%, 95%CI 84.40 to 98.50%). +LR at this age was 24.30 (95%CI 5.89 to 71.30) and-LR was 0.40 (95%CI 0.25 to 0.57). Predictive value of aEEG at 6 hours of life was low in these patients (59.10%, 95%CI 55.70 to 63%).

Conclusion: This study confirms that aEEG´s background activity, as recorded during the first 72 hours after birth, has a strong predictive value in infants with HIE treated or not with TH. Predictive values of traces throughout the following 72 hours are a helpful guide when considering and counselling parents about the foreseeable long-term neurological outcome.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1. Search and section process flowchart.
Fig 1. Search and section process flowchart.
Fig 2. Forest plot for all included…
Fig 2. Forest plot for all included studies, considering hours of life and treatment or not with hypothermia.
Fig 3. QUADAS 2 assessment of included…
Fig 3. QUADAS 2 assessment of included papers.
Fig 4. ROC curves for different hours…
Fig 4. ROC curves for different hours of life.
Fig 5. Likelihood ratios and post-test probability…
Fig 5. Likelihood ratios and post-test probability of abnormal aEEG and adverse neurological outcome, patients not treated with hypothermia according to hours of life.
Fig 6. Likelihood ratios and post-test probability…
Fig 6. Likelihood ratios and post-test probability of abnormal aEEG and adverse neurological outcome, patients treated with hypothermia according to hours of life.

References

    1. Smith J, Wells l, Dodd K.The continuing fall in incidence of hypoxic-ischaemic encephalopathy in term infants. BJOG 2000; 107(4): 461–6.
    1. García-Alix A, Martinez Biarge M. Neonatal hypoxic-ischemic encephalopathy: Incidence and prevalence in the first decade of the 21st century. An Pediatr (Barc) 2009; 71: 319–26.
    1. Tagin MA, Woolcott CG, Vincer MJ, Whyte RK, Stinson DA. Hypothermia for neonatal hypoxic ischemic encephalopathy: an updated systematic review and meta-analysis. Arch Pediatr Adolesc Med 2012; 166(6): 558–66. 10.1001/archpediatrics.2011.1772
    1. Blanco D, García-Alix A, Valverde E, Tenorio V, Vento M, Cabañas F. Neuroprotection with hypothermia in the newborn with hypoxic-ischaemic encephalopathy. Standard guidelines for its clinical application. An Pediatr (Barc) 2011; 75: 341.e1–20.
    1. Therapeutic hypothermia with intracorporeal temperature monitoring for hypoxic perinatal brain injury. National Institute for Health and Clinical Excellence. .
    1. Chalak L, Kaiser J. Neonatal Guideline Hypoxic-Ischemic Encephalopathy (HIE). Available in: .
    1. Hypothermia for newborns with hypoxic ischemic encephalopathy. Fetus and Newborn Committee Canadian Paediatric Society. Paediatr Child Health 2012; 17: 41–43.
    1. Hellström-Westas L, de Vries L, Rosen I. An atlas of amplitude integrated EEGs in the newborn. 1st edition London: Parthenon Publishing; 2003.
    1. Hellstrom-Westas L. Comparison between tape-recorded and amplitude-integrated EEG monitoring in sick newborn infants. Acta Paediatr 1992; 81(10): 812–9.
    1. Toet MC, van der Meij W, de Vries LS, Uiterwaal CS, van Huffelen KC. Comparison between simultaneously recorded amplitude integrated electroencephalogram (cerebral function monitor) and standard electroencephalogram in neonates. Pediatrics 2002; 109(5): 772–9.
    1. Shah DK, Mackay MT, Lavery S, Watson S, Harvey AS, Zempel J, et al. Accuracy of bedside electroencephalographic monitoring in comparison with simultaneous continuous conventional electroencephalography for seizure detection in term infants. Pediatrics 2008; 121(6): 1146–54. 10.1542/peds.2007-1839
    1. Al Naqeeb N, Edwards AD, Cowan FM, Azzopardi D. Assessment of neonatal encephalopathy by amplitude integrated electroencephalography. Pediatrics 1999; 103: 1263–71.
    1. Hellstrom Westas L, Rosen I, de Vries LS, Greisen G. Amplitude integrated EEG: Classification and interpretation in preterm and term infants. Neoreviews 2006; 7: e76–87.
    1. Hellström-Westas. Monitoring brain function with aEEG in term asphyxiated infants before and during cooling. Acta Paediatr 2013; 102(7):678–9. 10.1111/apa.12287
    1. Toet MC, Hellström-Westas L, Groenendaal F, Eken P, de Vries LS. Amplitude integrated EEG 3 and 6 hours after birth in full term neonates with hypoxic-ischaemic encephalopathy. Arch Dis Child Fetal Neonatal Ed. 1999; 81(1): F19–23.
    1. Shalak LF, Laptook AR, Velaphi SC, Perlman JM. Amplitude-integrated electroencephalography coupled with an early neurologic examination enhances prediction of term infants at risk for persistent encephalopathy. Pediatrics 2003; 111(2): 351–7.
    1. Thoresen M, Hellström-Westas L, Liu X, de Vries LS. Effect of hypothermia on amplitude-integrated electroencephalogram in infants with asphyxia. Pediatrics 2010; 126(1): e131–9. 10.1542/peds.2009-2938
    1. Spitzmiller RE, Phillips T, Meinzen-Derr J, Hoath SB. Amplitude-integrated EEG is useful in predicting neurodevelopmental outcome in full-term infants with hypoxic-ischemic encephalopathy: a meta-analysis. J ChildNeurol 2007; 22(9): 1069–78.
    1. Grupo de trabajo de la Guía de Práctica Clínica sobre Encefalopatía Hipóxico-Isquémica Perinatal en el Recién Nacido. Guía de Práctica Clínica sobre Encefalopatía Hipóxico-Isquémica Perinatal en el Recién Nacido. Ministerio de Sanidad, Servicios Sociales e Igualdad. Agència de Qualitat i AvaluacióSanitàries de Catalunya (AQuAS); 2015. Guías de PrácticaClínica en el SNS.
    1. Whiting PF, Rutjes AW, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, et al. QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med 2011; 155 (8): 529–36. 10.7326/0003-4819-155-8-201110180-00009
    1. Eken P, Toet MC, Groenendaal F, de Vries LS. Predictive value of early neuroimaging, pulsed Doppler and neurophysiology in full term infants with hypoxic-ischaemic encephalopathy. Arch Dis Child Fetal Neonatal Ed. 1995; 73(2): F75–80.
    1. Reitsma J, Glas A, Rutjes A, Scholten R, Bossuyt P, Zwinderman A. Bivariate analysis of sensitivity and specificity produces informative summary measures in diagnostic reviews. Journal of Clinical Epidemiology 2005; 58: 982–990. 10.1016/j.jclinepi.2005.02.022
    1. Hellström-Westas L, Rosén I, Svenningsen NW. 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(1): F34–8.
    1. Thornberg E, Ekström-Jodal B. Cerebral function monitoring: a method of predicting outcome in term neonates after severe perinatal asphyxia. Acta Paediatr 1994; 83(6): 596–601.
    1. Ter Horst HJ, Sommer C, Bergman KA, Fock JM, van Weerden T W, Bos AF. Prognostic significance of amplitude-integrated EEG during the first 72 hours after birth in severely asphyxiated neonates. Pediatr Res 2004; 55(6): 1026–33. 10.1203/01.pdr.0000127019.52562.8c
    1. van Rooij LG, Toet MC, Osredkar D, van Huffelen AC, Groenendaal F, de Vries LS. Recovery of amplitude integrated electroencephalographic background patterns within 24 hours of perinatal asphyxia. Arch Dis Child Fetal Neonatal Ed.2005; 90(3): F245–51. 10.1136/adc.2004.064964
    1. Shany E, Goldstein E, Khvatskin S, Friger MD, Heiman N, Goldstein M, et al. Predictive value of amplitude-integrated electroencephalography pattern and voltage in asphyxiated term infants. Pediatric Neurol 2006; 35(5): 335–42.
    1. Ancora G, Soffritti S, Lodi R, Tonon C, Grandi S, Locatelli C, et al. A combined a-EEG and MR spectroscopy study in term newborns with hypoxic-ischemic encephalopathy. Brain Dev 2010; 32(10): 835–42. 10.1016/j.braindev.2009.11.008
    1. Hallberg B, Grossmann K, Bartocci M, Blennow M. The prognostic value of early aEEG in asphyxiated infants undergoing systemic hypothermia treatment. Acta Paediatr 2010; 99(4): 531–6. 10.1111/j.1651-2227.2009.01653.x
    1. Ancora G, Maranella E, Grandi S, Sbravati F, Coccolini E, Savini S, et al. Early predictors of short term neurodevelopmental outcome in asphyxiated cooled infants. A combined brain amplitude integrated electroencephalography and near infrared spectroscopy study. Brain Dev 2013; 35(1):26–31. 10.1016/j.braindev.2011.09.008
    1. Shankaran S, Pappas A, McDonald SA, Laptook AR, Bara R, Ehrenkranz RA, et al. Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Predictive value of an early amplitude integrated electroencephalogram and neurologic examination. Pediatrics 2011; 128(1): e112–20. 10.1542/peds.2010-2036
    1. Gucuyener K, Beken S, Ergenekon E, Soysal S, Hirfanoglu I, Turan O, et al. Use of amplitude-integrated electroencephalography (aEEG) and near infrared spectroscopy findings in neonates with asphyxia during selective head cooling. Brain Dev 2012; 34(4): 280–6. 10.1016/j.braindev.2011.06.005
    1. Csekő AJ, Bangó M, Lakatos P, Kárdási J, Pusztai L, Szabó M. Accuracy of amplitude-integrated electroencephalography in the prediction of neurodevelopmental outcome in asphyxiated infants receiving hypothermia treatment. Acta Paediatr 2013; 102(7): 707–11. 10.1111/apa.12226
    1. Azzopardi D; TOBY study group. Predictive value of the amplitude integrated EEG in infants with hypoxic ischaemic encephalopathy: data from a randomised trial of therapeutic hypothermia. ArchDisChild Fetal Neonatal Ed. 2014; 99(1): F80–2.
    1. Sarnat HB, Sarnat MS. Neonatal encephalopathy following fetal distress. A clinical and electroencephalographic study. Arch Neurol 1976; 33(10): 696–705.
    1. van Laerhoven H, de Haan TR, Offringa M, Post B, van der Lee JH. Prognostic tests in term neonates with hypoxic-ischemic encephalopathy: a systematic review. Pediatrics 2013; 131: 88–98. 10.1542/peds.2012-1297
    1. Thoresen M. Supportive care during neuroprotective hypothermia in the term newborn: adverse effects and their prevention. Clin Perinatol 2008; 35(4): 749–63. 10.1016/j.clp.2008.07.018
    1. Horan M, Azzopardi D, Edwards AD, Firmin RK, Field D. Lack of influence of mild hypothermia on amplitude integrated-electroencephalography in neonates receiving extracorporeal membrane oxygenation. Early Hum Dev 2007; 83(2): 69–75. 10.1016/j.earlhumdev.2006.05.004
    1. Róka A, Melinda KT, Vásárhelyi B, Machay T, Azzopardi D, Szabó M. Elevated morphine concentrations in neonates treated with morphine and prolonged hypothermia for hypoxic ischemic encephalopathy. Pediatrics 2008; 12(4) 844–9.
    1. Gunn AJ, Wyatt JS, Whitelaw A, Barks J, Azzopardi D, Ballard R et al. Therapeutic hypothermia changes the prognostic value of clinical evaluation of neonatalencephalopathy. J Pediatr 2008; 152(1):55–8, 10.1016/j.jpeds.2007.06.003
    1. Shankaran S, Laptook AR, Tyson JE, Ehrenkranz RA, Bann CM, Das A, et al. Evolution of encephalopathy during whole body hypothermia for neonatal hypoxic-ischemic encephalopathy. J Pediatr 2012; 160(4): 567–572. 10.1016/j.jpeds.2011.09.018
    1. Rutherford M, Malamateniou C, McGuinness A, Allsop J, Biarge MM, Counsell S. Magnetic resonance imaging in hypoxic-ischaemic encephalopathy. Early Hum Dev 2010; 86(6): 351–60. 10.1016/j.earlhumdev.2010.05.014

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