Cerebral function monitoring: a new scoring system for the evaluation of brain maturation in neonates.

OBJECTIVE Cerebral function monitoring (CFM), using compressed single-channel amplitude-integrated electroencephalogram recorded from 2 biparietal electrodes, has been shown previously to be a simple bedside tool for monitoring neonatal central nervous system (CNS) status. As the pattern of the CFM changes with gestational age, the technique can be used to assess brain maturation in premature infants. We have developed a new scoring system for the interpretation of neonatal CFM recordings. The objective of this study was to evaluate CFM tracings at increasing gestational and postnatal ages to develop a scoring system to quantify CFM pattern changes. METHODS Term and preterm neonates were studied with CFM at 12 to 24 hours of life, 48 to 72 hours of life, and then weekly or biweekly until hospital discharge. Each study comprised 8 to 24 hours of continuous CFM recording. CFM recordings were evaluated using the scoring system for record continuity, presence of cyclic changes in electrical activity, degree of voltage amplitude depression, and bandwidth. Each variable was scored for each recording. All variables were summed to yield a total score (minimum 0, maximum 13). Total scores were correlated with gestational and postconceptional ages. RESULTS Thirty infants were studied with gestational ages at birth that ranged from 24 to 39 weeks and birth weights that varied between 450 and 3850 g. A total of 146 CFM tracings were analyzed. With advancing gestational and postconceptional age, scores for each variable as well as total scores progressively increased with CNS maturation. The highest scores were attained at 35 to 36 weeks' postconceptional age, which corresponded to previously reported subjective observations performed by visual description of CFM patterns. Of the 4 component variables that we analyzed, the most sensitive indicators of CNS maturity were 1) the presence of a cycling pattern, 2) the continuity of the record pattern, and 3) the CFM recording bandwidth. CONCLUSIONS Our proposed scoring system may be a valuable tool to quantify changes during CFM more objectively, reflecting variations in CNS activity in newborn infants and allowing for better statistical comparisons between amplitude-integrated electroencephalogram tracings from different patients as well as from the same patient at different points of time.

[1]  D. Maynard,et al.  Device for continuous monitoring of cerebral activity in resuscitated patients. , 1969, British medical journal.

[2]  E. Mercuri,et al.  Prognostic value of continuous electroencephalographic recording in full term infants with hypoxic ischaemic encephalopathy , 1994, Archives of disease in childhood. Fetal and neonatal edition.

[3]  B Guyer,et al.  Annual summary of vital statistics--1998. , 1999, Pediatrics.

[4]  G. Virzì,et al.  [The importance of using the cerebral function monitor (CFM) in the neurological prognosis of neonates in intensive care]. , 1998, La Pediatria medica e chirurgica : Medical and surgical pediatrics.

[5]  Tape-recorded EEG and the cerebral function monitor: amplitude-integrated, time-compressed EEG. , 1994, Journal of perinatal medicine.

[6]  I. Rosén,et al.  Predictive value of early continuous amplitude integrated EEG recordings on outcome after severe birth asphyxia in full term infants. , 1995, Archives of disease in childhood. Fetal and neonatal edition.

[7]  S. Kuhle,et al.  Evaluation of the Cerebral Function Monitor as a tool for neurophysiological surveillance in neonatal intensive care patients , 2001, Child’s Nervous System.

[8]  D. Altman,et al.  Calculating correlation coefficients with repeated observations: Part 2—correlation between subjects , 1995, BMJ.

[9]  L. D. de Vries,et al.  Amplitude integrated EEG 3 and 6 hours after birth in full term neonates with hypoxic–ischaemic encephalopathy , 1999, Archives of disease in childhood. Fetal and neonatal edition.

[10]  Linda S de Vries,et al.  Comparison between simultaneously recorded amplitude integrated electroencephalogram (cerebral function monitor) and standard electroencephalogram in neonates. , 2002, Pediatrics.

[11]  J. Volpe Neurology of the Newborn , 1959, Major problems in clinical pediatrics.

[12]  E. Stenninger,et al.  Monitoring of early postnatal glucose homeostasis and cerebral function in newborn infants of diabetic mothers. A pilot study. , 2001, Early human development.

[13]  I. Rosén,et al.  Lidocaine for Treatment of Severe Seizures in Newborn Infants , 1988, Acta paediatrica Scandinavica.

[14]  L. Skov,et al.  Cerebroelectrical depression following surfactant treatment in preterm neonates. , 1992, Pediatrics.

[15]  I Rosén,et al.  Cerebral function monitoring during the first week of life in extremely small low birthweight (ESLBW) infants. , 1991, Neuropediatrics.

[16]  N. Tejani,et al.  CEREBRAL FUNCTION MONITOR IN THE NEONATE. II: BIRTH ASPHYXIA , 1984, Developmental medicine and child neurology.

[17]  E. Thornberg,et al.  Normal Pattern of the Cerebral Function Monitor Trace in Term and Preterm Neonates , 1990, Acta paediatrica Scandinavica.

[18]  Changes in Electrocortical Brain Activity during Exchange Transfusions in Newborn Infants , 2000, Neonatology.

[19]  E. Thornberg,et al.  Cerebral function monitoring: a method of predicting outcome in term neonates after severe perinatal asphyxia , 1994, Acta paediatrica.

[20]  M. Levene,et al.  Evaluation of the Cerebro Trac 2500 for monitoring of cerebral function in the neonatal intensive care. , 1994, Neuropediatrics.

[21]  L. Hellström-Westas Comparison between tape‐recorded and amplitude‐integrated EEG monitoring in sick newborn infants , 1992, Acta paediatrica.

[22]  I Rosén,et al.  Silent Seizures in Sick Infants in Early Life , 1985, Acta paediatrica Scandinavica.

[23]  A. Prusa,et al.  Sleep-wake cycles in preterm infants below 30 weeks of gestational age. Preliminary results of a prospective amplitude-integrated EEG study. , 2001, Wiener klinische Wochenschrift.

[24]  V. Denenberg,et al.  State organization in neonates: developmental inconsistency indicates risk for developmental dysfunction. , 1981, Neuropediatrics.

[25]  D. Altman,et al.  Statistics notes: Calculating correlation coefficients with repeated observations: Part 1—correlation within subjects , 1995 .

[26]  A. David Edwards,et al.  Assessment of Neonatal Encephalopathy by Amplitude-integrated Electroencephalography , 1999, Pediatrics.

[27]  L. Dubowitz,et al.  Reversible changes in cerebral activity associated with acidosis in preterm neonates , 1994, Acta paediatrica.

[28]  N. Tejani,et al.  CEREBRAL FUNCTION MONITOR IN THE NEONATE, I: NORMAL PATTERNS , 1984, Developmental medicine and child neurology.

[29]  D. Maynard,et al.  Cerebral Function Monitor Studies in Neonates , 1984, Clinical EEG.