Sujet(s)
Cardiomégalie/congénital , Érythème infectieux/congénital , Érythème infectieux/complications , Maladies foetales/virologie , Cirrhose du foie/congénital , Anémie/complications , Cardiomégalie/complications , Issue fatale , Femelle , Hémosidérose/complications , Hémosidérose/anatomopathologie , Hépatomégalie , Humains , Nouveau-né , Cirrhose du foie/complications , Cirrhose du foie/anatomopathologie , GrossesseRÉSUMÉ
We examined events that precede a diagnosis of developmental delay by comparing 16 very low birth weight premature infants whose condition was diagnosed as developmental delay at 18 months corrected age with 16 matched developmentally normal infants. All infants were observed with their mothers during maternal visits to the nursery and during home visits 1, 3, 6, and 9 months after discharge. The mothers' reactions to their infants were rated at these times. All the children were followed up at a neonatal clinic, and detailed clinic records were used to document the time when a physician first suspected a delay and when this delay was first mentioned to the mother. The results indicate that parents had usually been told of their child's handicap by the time the child was 6 to 9 months old; yet mothers of the delayed children changed the interaction with their children as early as 1 month after discharge from hospital. These mothers initially touched, smiled at, and talked to their developmentally delayed infants significantly more often, but by 9 months they did so much less often than mothers of nondelayed children. The degree of change in mothers' behavior was related to their psychosocial background, with better-adjusted mothers showing the most change. We conclude that mothers' statements about their infants are usually valid and that physicians may share their potential concerns about infants more freely.