Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Article
  • Published:

Should amplitude-integrated electroencephalography be used to identify infants suitable for hypothermic neuroprotection?

Abstract

Objective:

Amplitude-integrated electroencephalography (aEEG) has been used adjunctively to identify infants suitable for hypothermic neuroprotection following severe intrapartum asphyxia. To determine whether an early aEEG predicts short-term adverse outcome in infants with significant hypoxic–ischemic encephalopathy (HIE) evaluated for hypothermic neuroprotection.

Study Design:

The aEEG recordings were obtained within 6 h of birth in infants 36 weeks' gestational age during evaluation for possible selective head or whole-body cooling. Recordings were subsequently re-evaluated for both background pattern and voltage abnormalities by a certified reader masked to clinical history and brain-oriented interventions. All infants with moderate or severe HIE evaluated for hypothermic neuroprotection also underwent magnetic resonance imaging (MRI) of the brain at a median postnatal age of 7 days. The predictive value using the aEEG for determining short-term dichotomous outcomes, defined as early death related to HIE, or a characteristic pattern of abnormalities consistent with hypoxic–ischemic injury on the MRI brain scans was assessed.

Result:

Fifty-four infants with moderate or severe HIE were evaluated with aEEG for hypothermic neuroprotection; 34 infants received selective head cooling, 12 infants underwent total body cooling and 8 infants were not cooled. Outcome data, available for 46 of the 54 infants, revealed a poor correlation between the early aEEG and short-term adverse outcomes, with a sensitivity of 54.8% and negative predictive value (NPV) of only 44%.

Conclusion:

Because of the poor NPV of an early aEEG for a short-term adverse outcome, its use as an ‘additional selection criterion’ for hypothermic neuroprotection may not be appropriate.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Volpe JJ . Hypoxic–ischemic encephalopathy: clinical aspects In: Volpe JJ (ed). Neurology of the Newborn. W.B. Saunders: Philadelphia, 1994, pp 314–369.

    Google Scholar 

  2. Gunn AJ, Gunn TR, Gunning MI, Williams CE, Gluckman PD . Neuroprotection with prolonged head cooling started before postischemic seizures in fetal sheep. Pediatrics 1998; 102: 1098–1106.

    Article  CAS  Google Scholar 

  3. Gluckman PD, Wyatt JS, Azzopardi D, Ballard R, Edwards AD, Ferriero DM et al. Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial. Lancet 2005; 365: 663–670.

    Article  Google Scholar 

  4. Rutherford M, Pennock J, Schwieso J, Cowan F, Dubowitz L . Hypoxic–ischaemic encephalopathy: early and late magnetic resonance imaging findings in relation to outcome. Arch Dis Child Fetal Neonatal Ed 1996; 75: F145–F151.

    Article  CAS  Google Scholar 

  5. Rutherford MA, Pennock JM, Counsell SJ, Mercuri E, Cowan FM, Dubowitz LM 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.

    Article  CAS  Google Scholar 

  6. Sarnat HB, Sarnat MS . Neonatal encephalopathy following fetal distress: a clinical and electroencephalographic study. Arch Neurol 1976; 33: 696–705.

    Article  CAS  Google Scholar 

  7. Shankaran S, Laptook AR, Ehrenkranz RA, Tyson JE, McDonald SA, Donovan EF et al. Whole-body hypothermia for neonates with hypoxic–ischemic encephalopathy. N Engl J Med 2005; 353: 1574–1584.

    Article  CAS  Google Scholar 

  8. de Vries LS, Hellstrom-Westas L . Role of cerebral function monitoring in the newborn. Arch Dis Child Fetal Neonatal Ed 2005; 90 (3): F201–F207.

    Article  CAS  Google Scholar 

  9. al Naqeeb N, Edwards AD, Cowan FM, Azzopardi D . Assessment of neonatal encephalopathy by amplitude-integrated electroencephalography. Pediatrics 1999; 103: 1263–1271.

    Article  CAS  Google Scholar 

  10. Ter Horst HJ, Sommer C, Bergman KA, Fock JM, van Weerden TW, Bos AF et al. Prognostic significance of amplitude-integrated EEG during the first 72 h after birth in severely asphyxiated neonates. Pediatr Res 2004; 55: 1026–1033.

    Article  Google Scholar 

  11. van Rooij LG, Toet MC, Osredkar D, van Huffelen AC, Groenendaal F, de Vries LS . Recovery of amplitude integrated electroencephalographic background patterns within 24 h of perinatal asphyxia. Arch Dis Child Fetal Neonatal Ed 2005; 90 (3): F245–F251.

    Article  CAS  Google Scholar 

  12. Toet MC, Hellström-Westas L, Groenendaal F, Eken P, de Vries LS . Amplitude integrated EEG 3 and 6 h after birth in full term neonates with hypoxic–ischaemic encephalopathy. Arch Dis Child Fetal Neonatal Ed 1999; 81: F19–F23.

    Article  CAS  Google Scholar 

  13. Westgate JA, Gunn AJ, Gunn TR . Antecedents of neonatal encephalopathy with fetal acidaemia at term. Br J Obstet Gynaecol 1999; 106: 774–782.

    Article  CAS  Google Scholar 

  14. Battin MR, Dezoete JA, Gunn TR, Gluckman PD, Gunn AJ . Neurodevelopmental outcome of infants treated with head cooling and mild hypothermia after perinatal asphyxia. Pediatrics 2001; 107: 480–484.

    Article  CAS  Google Scholar 

  15. Wyatt JS, Gluckman PD, Liu PY, Azzopardi D, Ballard R, Edwards AD et al. Determinants of outcomes after head cooling for neonatal encephalopathy. Pediatrics 2007; 119 (5): 912–921.

    Article  Google Scholar 

  16. Geddes R, Vannucci RC, Vannucci SJ . Delayed cerebral atrophy following moderate hypoxia-ischemia in the immature rat. Dev Neurosci 2001; 23: 180–185.

    Article  CAS  Google Scholar 

  17. 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: 351–357.

    Article  Google Scholar 

  18. Rutherford MA, Azzopardi D, Whitelaw A, Cowan F, Renowden S, Edwards AD et al. Mild hypothermia and the distribution of cerebral lesions in neonates with hypoxic–ischemic encephalopathy. Pediatrics 2005; 116 (4): 1001–1006.

    Article  Google Scholar 

  19. Robertson CM, Finer NN, Grace MG . School performance of survivors of neonatal encephalopathy associated with birth asphyxia at term. J Pediatr 1989; 114: 753–760.

    Article  CAS  Google Scholar 

  20. Miller SP, Latal B, Clark H, Clark H, Barnwell A, Glidden D et al. Clinical signs predict 30-month neurodevelopmental outcome after neonatal encephalopathy. Am J Obstet Gynecol 2004; 190: 93–99.

    Article  Google Scholar 

  21. Shankaran S, Woldt E, Koepke T, Bedard MP, Nandayal R . Acute neonatal morbidity and long-term central nervous system sequelae of perinatal asphyxia in term infants. Early Hum Dev 1991; 25: 135–148.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S Sarkar.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sarkar, S., Barks, J. & Donn, S. Should amplitude-integrated electroencephalography be used to identify infants suitable for hypothermic neuroprotection?. J Perinatol 28, 117–122 (2008). https://doi.org/10.1038/sj.jp.7211882

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.jp.7211882

Keywords

This article is cited by

Search

Quick links