Nutritional management of the infant with cystic fibrosis.
نویسندگان
چکیده
منابع مشابه
PERSONAL PRACTICE Nutritional management of cystic fibrosis
Nutritional support in cystic fibrosis has achieved a new importance. First, nutritional intervention is associated with better growthl and improvement or stabilisation of pulmonary function.23 Second, malnutrition has many adverse effects on pulmonary function including decreased ventilatory drive, impaired pulmonary muscle function, decreased exercise tolerance, and altered pulmonary immune r...
متن کاملCystic fibrosis: nutritional consequences and management.
Life expectancy for patients with Cystic Fibrosis (CF) has steadily improved during the last three decades, and death in childhood is now uncommon. Nutrition is a critical component of the management of CF, and nutritional status is directly associated with both pulmonary status and survival. Expert dietetic care is necessary, and attention must be given to ensuring an adequate energy intake in...
متن کاملThe Effect of Nutritional Consultation on the Level of Malnutrition and Growth Indices in Children with Cystic Fibrosis
Background: Malnutrition is one of the most common disorders among children with Cystic Fibrosis (CF). The present study aimed to investigate the effect of nutritional consultation on the type and severity of malnutrition in children with CF. Materials and Methods: This quasi-experimental stud...
متن کاملNutritional Assesment in Cystic Fibrosis Patients( Iran and Newzeland)
Introduction: Patients with Cystic Fibrosis 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 MacDonald Nutritional Screening tool with the Australasian guidelines for Nutrition in Cyst...
متن کاملPresentation of an infant with nutritional deficiency dermatitis as the initial manifestation of cystic fibrosis.
INTRODUCTION Cystic fibrosis (CF) is a multisystemic autosomal recessive disease most frequently recognized by characteristic respiratory and/or digestive manifestations. Exceptionally rare, as is the case with the infant we are presenting, the initial sign of the disease can be nutritional deficiency dermatitis (NDD). CASE OUTLINE A three-month-old male infant of young and healthy non-consan...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1995
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.72.5.452