Evaluation of the infant at risk for neurodevelopmental disability

Citation
Cd. Molteno et al., Evaluation of the infant at risk for neurodevelopmental disability, S AFR MED J, 89(10), 1999, pp. 1084-1087
Citations number
19
Categorie Soggetti
General & Internal Medicine
Journal title
SOUTH AFRICAN MEDICAL JOURNAL
ISSN journal
02569574 → ACNP
Volume
89
Issue
10
Year of publication
1999
Pages
1084 - 1087
Database
ISI
SICI code
0256-9574(199910)89:10<1084:EOTIAR>2.0.ZU;2-G
Abstract
Background. Infants with neurodevelopmental abnormality need to start thera py early, and because of this they should be detected as soon as possible. Currently, no widely accepted method of early evaluation exists. Objectives. To assess and compare, in terms of predicting neurodevelopmenta l outcome at 1 year of age: (i) a perinatal risk rating (PRR); (ii) the Dub owitz Neurological Assessment (DNA); and (iii) the Infant Neuromotor Assess ment (INA). Design and setting. A prospective neurodevelopmental followup study on grad uates from the Groote Schuur Hospital (GSH) neonatal intensive care unit (N ICU). Subjects. A cohort of 130 consecutive NICU graduates were selected accordin g to high-risk criteria. Outcome measures. Each infant was examined at term gestational age on the D NA before discharge, and a PRR was allocated. Study infants were seen again at 18 weeks of age when an INA was done, and at 1 year of age a Griffiths Developmental Assessment and full neurological examination was carried out. Results. All of the 130 infants assessed at term were seen at 18 weeks. The reafter 5 were lost to follow-up and 2 died. The outcome for the remaining 123 is known. Conclusions. Prediction of a normal outcome at 1 year of age was 96% on the DNA and 98% for the PRR, but for an abnormal outcome they predicted only 5 6% and 42%, respectively. The INA done at 18 weeks predicted a normal outco me at 1 year in 99% of cases if 3 or less abnormal signs were present and a n abnormal outcome in 82% of cases with 4 or more abnormal signs. Based on these findings a protocol for follow-up of these high-risk infants is sugge sted.