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ABSTRACT: Objective
The aim of the study is to test the hypothesis of a positive relationship between initial dose of pancreatic enzyme replacement therapy (PERT) in infants with cystic fibrosis (CF) and optimal weight gain over the first 2 years of life.Methods
Using the CF Foundation Patient Registry, we identified 502 children born in 2010 and used multivariable models to compare as our primary analysis their 2-year changes in weight-for-age z score (WAZ) and as our secondary analysis weight-for-length percentile (W/L%) by initial PERT dose. We focused on initial dose without reference to subsequent changes in treatment to avoid confounding by indication (severity).Results
Initial PERT dose demonstrated a linear relationship to change in WAZ and W/L% at age 2 years. An ini
SUBMITTER: Schechter MS
PROVIDER: S-EPMC6155359 | biostudies-literature | 2018 Oct
REPOSITORIES: biostudies-literature