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Application of an Amplitude-integrated EEG Monitor (Cerebral Function Monitor) to Neonates
Published on: September 6, 2017
Sleep-wake cycles in preterm infants below 30 weeks of gestational age. Preliminary results of a prospective
S Kuhle1, K Klebermass, M Olischar
1Department of Neonatology and Paediatric Intensive Care, University Children's Hospital Vienna, Austria.
Insights
Early sleep-wake cycles in preterm infants, detected via amplitude-integrated electroencephalography (aEEG), indicate central nervous system integrity. These cycles may predict long-term neurological outcomes in premature babies.
Area of Science:
- Neonatal neurology
- Neurodevelopmental pediatrics
- Brain function monitoring
Background:
- Sleep-wake cycles in newborns signify central nervous system maturity.
- Early detection of sleep-wake cycles in preterm infants (as early as 27 weeks gestation) using spectral EEG and polygraphy suggests potential for predicting neurological outcomes.
- Limited research exists on sleep-wake cycles and their long-term significance in very preterm infants.
Purpose of the Study:
- To prospectively investigate the maturational changes in electroencephalography (EEG) activity and sleep-wake cycles in preterm infants under 30 weeks gestational age.
- To utilize the Cerebral Function Monitor (CFM), an amplitude-integrated EEG, for assessing brain function in this vulnerable population.
- To present preliminary findings on the emergence of sleep-wake cycles in very preterm infants.
Main Methods:
- Prospective study design.
- Utilized the Cerebral Function Monitor (CFM), a form of amplitude-integrated EEG.
- Included a reference group of 38 preterm infants without neurological complications (mean gestational age 27 weeks).
Main Results:
- Cyclical variations in EEG background activity, indicative of early sleep-wake cycles, were observed at a mean gestational age of 28 weeks and a median postnatal age of 6 days in the reference group.
- Preliminary data from an ongoing study on 100 enrolled infants are presented.
- These findings suggest early emergence of sleep-wake patterns in preterm infants.
Conclusions:
- The observed cyclical EEG variations may represent thalamo-cortical and neo-cortical pattern generator switches, indicating central nervous system integrity.
- Amplitude-integrated EEG (aEEG) shows promise as a non-invasive tool for assessing brain function in preterm infants.
- Early detection of sleep-wake cycles could have positive predictive value for long-term neurological outcomes.
Abstract:
In the newborn, presence of sleep-wake cycles indicates integrity and maturity of the central nervous system. By spectral EEG analysis and polygraphic recordings subtle variations of EEG background activity and behavioural patterns corresponding to early sleep-wake cycles have been found in preterm infants as young as 27 weeks of gestation. The emergence of sleep-wake cycles at early gestational ages may have a positive predictive value for long-term neurological outcome. Sleep-wake cycles and their significance for later outcome have not been studied in very preterm infants so far. Accordingly, we prospectively investigated maturational changes of EEG activity and sleep-wake cycles in preterm infants below 30 weeks of gestational age using the Cerebral Function Monitor, an amplitude-integrated EEG. We present preliminary data on the emergence of sleep-wake cycles in preterm infants from this ongoing study. Of 100 infants enrolled during a 1-year period, 38 infants without neurological complications were included in the reference group. In this group (mean gestational age 27 weeks), we observed cyclical variations of EEG background activity resembling early sleep-wake cycles at a mean gestational age of 28 weeks and a median postnatal age of 6 days. It is hypothesised that these cyclical variations of EEG background activity may represent switches between thalamo-cortical and neo-cortical pattern generators and indicate integrity of central nervous system function. Amplitude-integrated EEG may thus serve as a useful noninvasive test for brain function in preterm infants.
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