221 Relationship between growth, nutritional status and pulmonary function in children and adolescents with Cystic Fibrosis
| Autor: | P. Savopoulou, E. Kirvasilis, E. Hatziagorou, Pinelopi Anagnostopoulou, J. Kioumis, John Tsanakas |
|---|---|
| Rok vydání: | 2006 |
| Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty Vital capacity Pediatrics business.industry Nutritional status medicine.disease Cystic fibrosis Pulmonary function testing FEV1/FVC ratio Malnutrition Pulmonology Internal medicine Pediatrics Perinatology and Child Health Cohort medicine Pediatrics Perinatology and Child Health business |
| Zdroj: | Journal of Cystic Fibrosis. 5:S52 |
| ISSN: | 1569-1993 |
| DOI: | 10.1016/s1569-1993(06)80203-1 |
| Popis: | Background; Nutritional status and lung function are associated with survival in Cystic Fibrosis (CF). Aim; To determine the relationship among growth, nutritional status and pulmonary function in children and adolescents with CE Methods; A cohort of 48 children aged 6 to 10 was followed every 4 months over a 13-year period at Thessaloniki CF center. Weight-for age, (WFA), height-forage (HFA), percent ideal body weight (%IBW) and pulmonary function test (PFT) results were recorded. Results; The prevalence of abnormal weight for height ( |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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