E. Martin et al., DIAGNOSTIC AND PROGNOSTIC VALUE OF CEREBRAL P-31 MAGNETIC-RESONANCE SPECTROSCOPY IN NEONATES WITH PERINATAL ASPHYXIA, Pediatric research, 40(5), 1996, pp. 749-758
The impact of depressed neonatal cerebral oxidative phosphorylation fo
r diagnosing the severity of perinatal asphyxia was estimated by corre
lating the concentrations of phosphocreatine (PCr) and ATP as determin
ed by magnetic resonance spectroscopy with the degree of hypoxic-ische
mic encephalopathy (HIE) in 23 asphyxiated term neonates. Ten healthy
age-matched neonates served as controls. In patients, the mean concent
rations +/-SD of PCr and ATP were 0.99 +/- 0.46 mmol/L (1.6 +/- 0.2 mm
ol/L) and 0.99 +/- 0.35 mmol/L (1.7 +/- 0.2 mmol/L), respectively (nor
mal values in parentheses), [PCr] and [ATP] correlated significantly w
ith the severity of HIE (r = 0.85 and 0.9, respec tively, p < 0.001),
indicating that the neonatal encephalopathy is the clinical manifestat
ion of a marred brain energy metabolism. Neurodevelopmental outcome wa
s evaluated in 21 children at 3, 9, and 18 mo. Seven infants had multi
ple impairments, five were moderately handicapped, five had only mild
symptoms, and four were normal. There was a significant correlation be
tween the cerebral concentrations of PCr or ATP at birth and outcome (
r = 0.8, p < 0.001) and between the degree of neonatal neurologic depr
ession and outcome (r = 0.7). More important, the outcome of neonates
with moderate HIE could better be predicted with information from quan
titative P-31 magnetic resonance spectroscopy than from neurologic exa
minations. In general, the accuracy of outcome predictability could si
gnificantly be increased by adding results from P-31 magnetic resonanc
e spectroscopy to the neonatal neurologic score, but not vice versa. N
o correlation with outcome was found for other perinatal risk factors,
including Apgar score.