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Paediatr Respir Rev ; 16 Suppl 1: 19-21, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26410283

ABSTRACT

Pulmonary exacerbations and malabsorption in children with cystic fibrosis (CF) can lead to faltering growth and poor weight gain. Children with a higher BMI (body mass index) show a slower decline in lung function. Our specialist CF centre has experienced a death following gastrostomy insertion in a young CF child, despite maximal medical intervention, which has made us reflect on our practice and the urgency with which we discuss the option for a gastrostomy to improve nutrition.


Subject(s)
Cystic Fibrosis/therapy , Enteral Nutrition , Gastrostomy/methods , Nutritional Status , Body Height/physiology , Body Weight/physiology , Child , Fatal Outcome , Female , Gastrostomy/adverse effects , Humans , Time Factors , Tomography, X-Ray Computed
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