Objective: \ud \ud To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) populations, this study compared standard anthropometric measurements and total body potassium (TBK) as indicators of malnutrition. Methods: Height, weight, and TBK measurements of 226 children with CF from Royal Children's Hospital, Brisbane, Australia, were analyzed. Z scores for height for age, weight for age, and weight for height were analyzed by means of the National Centre for Health Statistics reference. TBK was measured by means of whole body counting and compared with predicted TBK for age. Two criteria were evaluated with respect to malnutrition: (1) a z score < -2.0 and (2) a TBK for age <80% of predicted. \ud \ud Results:...
AbstractBackgroundFor the past decade, percentage of ideal body weight (%IBW) was recommended by Eur...
Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nut...
Background—In 2005, the Cystic Fibrosis Foundation (CFF) revised the nutrition classification guidel...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
BACKGROUND: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
AbstractBackground: Assessment of nutritional status in children with cystic fibrosis (CF) is clinic...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
Background: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
AbstractBackgroundFor the past decade, percentage of ideal body weight (%IBW) was recommended by Eur...
Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nut...
Background—In 2005, the Cystic Fibrosis Foundation (CFF) revised the nutrition classification guidel...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
BACKGROUND: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
AbstractBackground: Assessment of nutritional status in children with cystic fibrosis (CF) is clinic...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
Background: Many children with cystic fibrosis grow poorly and are malnourished. This study was unde...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
To further evaluate the nature of malnutrition, define at-risk groups, and confirm the efficacy of n...
AbstractBackgroundFor the past decade, percentage of ideal body weight (%IBW) was recommended by Eur...
Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nut...
Background—In 2005, the Cystic Fibrosis Foundation (CFF) revised the nutrition classification guidel...