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EEG maturation and stability of cerebral oxygen extraction in very low birth weight infants

Abstract

Objective:

Fractional cerebral tissue oxygen extraction (FTOE) can be continuously monitored by simultaneous near-infrared spectroscopy (NIRS) and pulse oximetry. The objective of this study is to test the hypothesis that in very low birth weight (VLBW) infants, the more mature EEG activity is, the less variable FTOE is.

Study Design:

A prospective study was conducted on VLBW infants (<1500 g and 34 weeks gestation) without significant brain injury. Simultaneous continuous two-channel electroencephalography (EEG), NIRS and pulse oximetry were recorded. Absolute and relative powers of EEG in the delta, theta, alpha, beta and total frequency bands have been calculated. FTOE variability was calculated on two scales: short scales (3 to 20 s) and long scales (20 to 150 s). FTOE variability was examined against changes in relative spectral power of different EEG bands.

Result:

We evaluated 67 studies performed on 46 VLBW infants. Average study duration was 21.3±5.5 h. Relative power of delta band positively correlated with FTOE short- and long-scale variability (r=0.45, P<0.001; r=0.44, P<0.001, respectively). Relative power of alpha bands negatively correlated with FTOE short- and long-scale variability (r=−0.38, P=0.002; r=−0.42, P<0.001, respectively). These correlations continued to be significant when controlling for sex, small for gestational age, postmenstrual age, being on respiratory support, hemoglobin concentration, systemic oxygen saturation and transcutaneous carbon dioxide tension.

Conclusion:

Increased maturation of EEG activity is associated with decreased variability in cerebral oxygen extraction. The implications of increased variability in FTOE on brain injury in premature infants need further exploration.

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References

  1. El Dib M, Massaro AN, Aly H . Electroencephalography, amplitude-integrated electroencephalography and neurodevelopmental outcome in premature infants. In: Figueredo B, Meléndezc F (eds). Neuroscience Research Advances. Nova Science Publishers, Inc.: New York, NY, USA, 2010, pp 109–134.

    Google Scholar 

  2. Scher MS, Sun M, Steppe DA, Guthrie RD, Sclabassi RJ . Comparisons of EEG spectral and correlation measures between healthy term and preterm infants. Pediatr Neurol 1994; 10 (2): 104–108.

    Article  CAS  Google Scholar 

  3. Victor S, Appleton RE, Beirne M, Marson AG, Weindling AM . Spectral analysis of electroencephalography in premature newborn infants: normal ranges. Pediatr Res 2005; 57 (3): 336–341.

    Article  Google Scholar 

  4. Niemarkt HJ, Jennekens W, Pasman JW, Katgert T, van Pul C, Gavilanes AW et al. Maturational changes in automated EEG spectral power analysis in preterm infants. Pediatr Res 2011; 70 (5): 529–534.

    Article  Google Scholar 

  5. Bell AH, McClure BG, McCullagh PJ, McClelland RJ . Variation in power spectral analysis of the EEG with gestational age. J Clin Neurophysiol 1991; 8 (3): 312–319.

    Article  CAS  Google Scholar 

  6. Wolfberg AJ, du Plessis AJ . Near-infrared spectroscopy in the fetus and neonate. Clin Perinatol 2006; 33 (3): 707–728.

    Article  Google Scholar 

  7. Wolf M, Greisen G . Advances in near-infrared spectroscopy to study the brain of the preterm and term neonate. Clin Perinatol 2009; 36 (4): 807–834.

    Article  Google Scholar 

  8. Rais-Bahrami K, Rivera O, Short B . Validation of a noninvasive neonatal optical cerebral oximeter in veno-venous ECMO patients with a cephalad catheter. J Perinatol 2006; 26 (10): 628–635.

    Article  CAS  Google Scholar 

  9. O'Leary H, Gregas MC, Limperopoulos C, Zaretskaya I, Bassan H, Soul JS et al. Elevated cerebral pressure passivity is associated with prematurity-related intracranial hemorrhage. Pediatrics 2009; 124 (1): 302–309.

    Article  Google Scholar 

  10. Soul JS, Hammer PE, Tsuji M, Saul JP, Bassan H, Limperopoulos C et al. Fluctuating pressure-passivity is common in the cerebral circulation of sick premature infants. Pediatr Res 2007; 61 (4): 467–473.

    Article  Google Scholar 

  11. Tsuji M, Saul JP, du Plessis A, Eichenwald E, Sobh J, Crocker R et al. Cerebral intravascular oxygenation correlates with mean arterial pressure in critically ill premature infants. Pediatrics 2000; 106 (4): 625–632.

    Article  CAS  Google Scholar 

  12. Balegar KK, Stark MJ, Briggs N, Andersen CC . Early cerebral oxygen extraction and the risk of death or sonographic brain injury in very preterm infants. J Pediatr 2014; 164 3 (475–480): e471.

    Google Scholar 

  13. Alderliesten T, Lemmers PM, Smarius JJ, van de Vosse RE, Baerts W, van Bel F . Cerebral oxygenation, extraction, and autoregulation in very preterm infants who develop peri-intraventricular hemorrhage. J Pediatr 2013; 162 (4): 698–704, e692.

    Article  Google Scholar 

  14. Roche-Labarbe N, Fenoglio A, Radhakrishnan H, Kocienski-Filip M, Carp SA, Dubb J et al. Somatosensory evoked changes in cerebral oxygen consumption measured non-invasively in premature neonates. Neuroimage 2014; 85: 279–286.

    Article  Google Scholar 

  15. Roche-Labarbe N, Wallois F, Ponchel E, Kongolo G, Grebe R . Coupled oxygenation oscillation measured by NIRS and intermittent cerebral activation on EEG in premature infants. Neuroimage 2007; 36 (3): 718–727.

    Article  CAS  Google Scholar 

  16. Victor S, Appleton RE, Beirne M, Marson AG, Weindling AM . Effect of carbon dioxide on background cerebral electrical activity and fractional oxygen extraction in very low birth weight infants just after birth. Pediatr Res 2005; 58 (3): 579–585.

    Article  Google Scholar 

  17. Victor S, Marson AG, Appleton RE, Beirne M, Weindling AM . Relationship between blood pressure, cerebral electrical activity, cerebral fractional oxygen extraction, and peripheral blood flow in very low birth weight newborn infants. Pediatr Res 2006; 59 (2): 314–319.

    Article  Google Scholar 

  18. Fenton TR, Kim JH . A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants. BMC Pediatr 2013; 13: 59.

    Article  Google Scholar 

  19. Naulaers G, Meyns B, Miserez M, Leunens V, Van Huffel S, Casaer P et al. Use of tissue oxygenation index and fractional tissue oxygen extraction as non-invasive parameters for cerebral oxygenation: a validation study in piglets. Neonatology 2007; 92 (2): 120–126.

    Article  CAS  Google Scholar 

  20. Govindan RB, Massaro AN, Al-Shargabi T, Andescavage NN, Chang T, Glass P et al. Detrended fluctuation analysis of non-stationary cardiac beat-to-beat interval of sick infants. EPL (Europhys Lett) 2014; 108 (4): 40005.

    Article  Google Scholar 

  21. Schumacher EM, Larsson PG, Sinding-Larsen C, Aronsen R, Lindeman R, Skjeldal OH et al. Automated spectral EEG analyses of premature infants during the first three days of life correlated with developmental outcomes at 24 months. Neonatology 2013; 103 (3): 205–212.

    Article  CAS  Google Scholar 

  22. ter Horst HJ, Verhagen EA, Keating P, Bos AF . The relationship between electrocerebral activity and cerebral fractional tissue oxygen extraction in preterm infants. Pediatr Res 2011; 70 (4): 384–388.

    Article  CAS  Google Scholar 

  23. Yanowitz TD, Potter DM, Bowen A, Baker RW, Roberts JM . Variability in cerebral oxygen delivery is reduced in premature neonates exposed to chorioamnionitis. Pediatr Res 2006; 59 (2): 299–304.

    Article  CAS  Google Scholar 

  24. Roberton NR . Effect of acute hypoxia on blood pressure and electroencephalogram of newborn babies. Arch Dis Child 1969; 44 (238): 719–725.

    Article  CAS  Google Scholar 

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Acknowledgements

We acknowledge Dr Khalid Alyami, Dr Saleh Alqahtani and Dr Ahmad Ibrahim for their contribution in the data collection. This study was approved by the University Institutional Review Board (IRB). Informed consents were obtained from parents before enrollment.

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Correspondence to M El-Dib.

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El-Dib, M., Govindan, R., Aly, S. et al. EEG maturation and stability of cerebral oxygen extraction in very low birth weight infants. J Perinatol 36, 311–316 (2016). https://doi.org/10.1038/jp.2015.200

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  • DOI: https://doi.org/10.1038/jp.2015.200

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