Management of Exocrine Pancreatic Insufficiency in Children.
Senthilkumar SankararamanTeresa SchindlerThomas J SferraPublished in: Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition (2020)
The diagnosis of exocrine pancreatic insufficiency (EPI) can be difficult, as symptoms may be nonspecific. A delayed diagnosis of EPI can negatively impact health through poor weight gain, impaired growth, and malabsorption of nutrients. Because of active growth and development, children are more vulnerable to the consequences of untreated EPI. Pancreatic enzyme replacement therapy is the cornerstone of management and offers both symptomatic relief and improvement in clinical outcomes. Additionally, a high-energy diet with unrestricted fat and supplementation with fat-soluble vitamins is often required to optimize growth and prevent nutrition deficiencies. Cystic fibrosis (CF) is the most common condition in children that causes EPI, and improvement in nutrition management is associated with improved pulmonary function and increased survival. Currently, the management of other conditions leading to EPI in children is not well studied, and inferences from the CF literature are often necessary in caring for these patients.
Keyphrases
- cystic fibrosis
- young adults
- weight gain
- replacement therapy
- physical activity
- systematic review
- adipose tissue
- public health
- body mass index
- end stage renal disease
- healthcare
- mental health
- pseudomonas aeruginosa
- newly diagnosed
- weight loss
- ejection fraction
- chronic kidney disease
- fatty acid
- peritoneal dialysis
- heavy metals
- climate change
- sleep quality