257 Improving nutrition for pediatric cystic fibrosis patients
نویسندگان
چکیده
منابع مشابه
Consensus report on nutrition for pediatric patients with cystic fibrosis.
Laura K. Bachrach, M.D. Robert J. Beall, Ph.D. Preston W. Campbell, III, M.D. Susan C. Casey, B.S., R.D. Mitchell B. Cohen, M.D. Mary Corey, Ph.D. W. Hobart Davies, Ph.D. Judy A. Fulton, R.D. Richard J. Grand, M.D. John E. Grunow, M.D. Dana S. Hardin, M.D. Lesles Hendeles, Pharm.D. James E. Heubi, M.D. Van S. Hubbard, M.D. Hui-Chuan Kai, Ph.D. Sheila Innis, Ph.D. Elisabeth Luder, Ph.D., R.D. Ka...
متن کاملImproving screening for cystic fibrosis-related diabetes at a pediatric cystic fibrosis program.
OBJECTIVE Despite guidelines recommending an annual oral glucose tolerance test (OGTT) for all patients with cystic fibrosis (CF) aged ≥ 10 years, screening rates for cystic fibrosis-related diabetes (CFRD) remained low at our center. The aim of this project was to implement an outpatient system to provide effective, evidence-based screening for CFRD at a pediatric CF program. METHODS Develop...
متن کاملNutrition in cystic fibrosis.
Cystic fibrosis (CF) is mostly recognized for its pulmonary morbidity, but the earliest manifestations of the disease are related to its gastrointestinal and nutritional derangements. Destruction of acinar pancreatic tissue, pancreatic ductular obstruction, and lack of enzymatic activity lead to malabsorption (particularly of fats), diarrhea, and failure to thrive. A minority of CF patients car...
متن کاملNutrition in cystic fibrosis.
A L T E R E D E N E R G Y E X P E N D I T U R E A N D N U T R I E N T METABOLISM . Increased energy expenditure. . Protein turnover and metabolism . . Abnormalities of essential fat ty acid metabolism . . N U T R I T I O N A L C A R E I N CF . N U T R I T I O N A L E V A L U A T I O N . . N U T R I T I O N A L C A R E . F U T U R E DIRECTIONS . . REFERENCES . . 51 52 55 55 56 57 57 59 60 61 61 ...
متن کاملImproving nutritional status in a pediatric cystic fibrosis center.
BACKGROUND The nutritional status of patients with cystic fibrosis (CF) is strongly associated with pulmonary function, respiratory status and survival. Malnutrition could result from a discrepancy between energy needs and food intake while malabsorption results from pancreatic insufficiency which occurs in 85% of people with CF. METHODS A quality improvement (QI) project was designed to impr...
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ژورنال
عنوان ژورنال: Journal of Cystic Fibrosis
سال: 2012
ISSN: 1569-1993
DOI: 10.1016/s1569-1993(12)60426-3