In addition to aggressive monitoring of disease course and the use of novel strategies for respiratory and antimicrobial therapies, marked attention to the maintenance of excellent growth and nutrition has played a key role in improving long-term outcomes of children with cystic fibrosis (CF). CF centers play particular attention to changes in growth measurements as useful markers of nutrition and disease activity, leading to earlier and more rigorous evaluations and interventions. As such, the optimal care of young children with CF is highly dependent on the use of standardized growth charts. In this study, Zhang et al analyzed data from 2587 children followed in the Cystic Fibrosis Foundation Patient Data Registry in order to compare differences in the classification of growth status of young children with CF as assessed by the World Health Organization (WHO) and Centers for Disease Control (CDC) growth percentiles. Currently, WHO standards often are followed up to 23.9 months, followed by the use of CDC references. Among several findings, this study reports that using weight status measures (weight-for-length and body mass index) at 24 months, 26% of children who were classified as normal growth using WHO references were underweight using CDC references. These findings are important to ensure greater understanding of the potential impact of changing growth standards on the interpretation of individual growth status, the impact on clinical practice, and to allow accurate comparisons between CF centers. These findings further set the stage to explore relationships between early nutritional interventions and long-term growth and pulmonary outcomes.Article page 1089▶ In addition to aggressive monitoring of disease course and the use of novel strategies for respiratory and antimicrobial therapies, marked attention to the maintenance of excellent growth and nutrition has played a key role in improving long-term outcomes of children with cystic fibrosis (CF). CF centers play particular attention to changes in growth measurements as useful markers of nutrition and disease activity, leading to earlier and more rigorous evaluations and interventions. As such, the optimal care of young children with CF is highly dependent on the use of standardized growth charts. In this study, Zhang et al analyzed data from 2587 children followed in the Cystic Fibrosis Foundation Patient Data Registry in order to compare differences in the classification of growth status of young children with CF as assessed by the World Health Organization (WHO) and Centers for Disease Control (CDC) growth percentiles. Currently, WHO standards often are followed up to 23.9 months, followed by the use of CDC references. Among several findings, this study reports that using weight status measures (weight-for-length and body mass index) at 24 months, 26% of children who were classified as normal growth using WHO references were underweight using CDC references. These findings are important to ensure greater understanding of the potential impact of changing growth standards on the interpretation of individual growth status, the impact on clinical practice, and to allow accurate comparisons between CF centers. These findings further set the stage to explore relationships between early nutritional interventions and long-term growth and pulmonary outcomes. Article page 1089▶ Comparing the Use of Centers for Disease Control and Prevention and World Health Organization Growth Charts in Children with Cystic Fibrosis through 2 Years of AgeThe Journal of PediatricsVol. 167Issue 5PreviewTo examine differences between use of World Health Organization (WHO) and Centers for Disease Control and Prevention (CDC) growth reference in children with cystic fibrosis (CF) up to 2 years of age. Full-Text PDF
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