Growth trajectory and neurodevelopmental outcome in infants with congenital diaphragmatic hernia

Abstract

PurposeThe purpose of this study was to evaluate the impact of impaired growth on short-term neurodevelopmental (ND) outcomes in CDH survivors. MethodsBetween 9/2005–12/2014, 84 of 215 (39%) CDH survivors underwent ND assessment at 12months of age using the BSID-III. ResultsMean cognitive, language, and motor scores were 92.6±13.5, 87.1±11.6, and 87.0±14.4, respectively (normal 100±15). 51% of patients scored 1 SD below the population mean in at least one domain, and 13% scored 2 SD below the population mean.Group-based trajectory analysis identified two trajectory groups (‘high’ and ‘low’) for weight, length, and head circumference (HC) z-scores. (Fig. 1) 74% of the subjects were assigned to the ‘high’ trajectory group for weight, 77% to the ‘high’ height group, and 87% to the ‘high’ HC group, respectively. In multivariate analysis, longer NICU stay (p<0.01) was associated with lower cognitive scores. Motor scores were 11 points higher in the ‘high’ HC group compared to the ‘low’ HC group (p=0.05). Motor scores were lower in patients with longer NICU length of stay (p<0.001). ConclusionsAt 1 year, half of CDH survivors had a mild delay in at least one developmental domain. Low HC trajectory was associated with worse neurodevelopmental outcomes. Type of studyPrognosis Study/Retrospective Study. Level of evidenceLevel II.