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The goal of this study was to identify clinical features associated with abnormal infant pulmonary function tests (iPFTs), specifically functional residual capacity (FRC), in infants with cystic fibrosis (CF) diagnosed… Click to show full abstract
The goal of this study was to identify clinical features associated with abnormal infant pulmonary function tests (iPFTs), specifically functional residual capacity (FRC), in infants with cystic fibrosis (CF) diagnosed via newborn screen (NBS). We hypothesized that poor nutritional status in the first 6–12 months would be associated with increased FRC at 12‐24 months.
Keywords:
hyperinflation associated;
cystic fibrosis;
respiratory rate;
increased respiratory;
associated increased
Journal Title: Pediatric Pulmonology
Year Published: 2021
Link to full text (if available)
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Journal Title: Pediatric Pulmonology
Year Published: 2021
Link to full text (if available)
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recommendations!