child health Flashcards
Cystic Fibrosis
CF is an inherited autosomal
recessive mutation of ion channels that alters chloride and water transport
in exocrine (mucus-producing) glands.
The child must inherit two copies of the gene (one from each parent) to have CF.
Mobilizing secretions:
Administering
bronchodilators before performing airway
clearance therapies (CPT, PEP) helps mobilize
secretions.
Malnutrition:
Provide a high-calorie, high-
protein diet and supplemental fat-soluble vitamins (A, D, E, K) to meet increased nutrient
requirements.
Notify HCP for complications:
Decreased
activity and decreased appetite are subtle signs
of respiratory infection. Abdominal pain and
distension are signs of intestinal obstruction.
Pancreatic enzyme replacement therapy (PERT):
Administer PERT within 30 minutes of eating to improve absorption of fats, proteins,
and carbohydrates.
Psychosocial support:
Encourage participation
in physical activities like sports as tolerated and connect the client and family with
community resources like support groups.