Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nutritional deterioration enables prompt intervention and correction. The aims of this project were to define the nutritional status of CF patients in Iran and New Zealand, compare and contrast the McDonald Nutritional Risk Screening (NRS) tool with the Australasian Guidelines for Nutrition in Cystic Fibrosis, and validate these results with each patient’s evaluation by their CF clinical team. Methods: Children with CF (2 - 18 years) were assessed during routine outpatient visits over one year. Anthropometric measurements were obtained. Both tools were applied and the results compared to their clinical evaluation (as gold standard) with c...
Objective: \ud \ud To investigate measures aimed at defining the nutritional status of cystic fibros...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...
Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nut...
ABSTRACT Objective: To evaluate the nutritional profile of the population assisted at a reference ...
Introduction: Cystic Fibrosis (CF) is an autosomal recessive disorder with serious pulmonary and nut...
ABSTRACT Objective: To evaluate the nutritional profile of the population assisted at a reference ...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
BACKGROUND: Malnutrition is both a feature and major cause of morbidity in cystic fibrosis (CF). The...
BACKGROUND: Malnutrition is both a feature and major cause of morbidity in cystic fibrosis (CF). The...
The importance of nutritional intervention for children with cystic fibrosis (CF) is well recognised...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
BACKGROUND: Optimal nutrition for children with cystic fibrosis (CF) improves prognosis and survival...
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: \ud \ud To investigate measures aimed at defining the nutritional status of cystic fibros...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...
Aims: Patients with Cystic Fibrosis (CF) have increased risk of malnutrition. Early detection of nut...
ABSTRACT Objective: To evaluate the nutritional profile of the population assisted at a reference ...
Introduction: Cystic Fibrosis (CF) is an autosomal recessive disorder with serious pulmonary and nut...
ABSTRACT Objective: To evaluate the nutritional profile of the population assisted at a reference ...
Background: Poor clinical outcomes in cystic fibrosis are often associated with undernutrition. Nutr...
BACKGROUND: Malnutrition is both a feature and major cause of morbidity in cystic fibrosis (CF). The...
BACKGROUND: Malnutrition is both a feature and major cause of morbidity in cystic fibrosis (CF). The...
The importance of nutritional intervention for children with cystic fibrosis (CF) is well recognised...
Objective: To investigate measures aimed at defining the nutritional status of cystic fibrosis (CF) ...
BACKGROUND: Optimal nutrition for children with cystic fibrosis (CF) improves prognosis and survival...
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: \ud \ud To investigate measures aimed at defining the nutritional status of cystic fibros...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...
BACKGROUND: Malnutrition is both a frequent feature and a comorbidity of cystic fibrosis (CF), with ...