Master Cystic Fibrosis Assessment with Picmonic for Nursing RN

Thickened mucus and decreased functioning of cilia allows mucus to stay in the lungs, creating an environment for infection. Infections are typically caused by organisms, such as Staphylococcus aureus and Pseudomonas, which are chronic in nature. Antibiotic resistance may develop in these patients.

Inflammation and mucus buildup in the bronchioles (bronchiolitis) initially occurs in patients with CF. Bronchiolitis, if chronic, will eventually lead to permanent widening of the airway, known as bronchiectasis.

Mucus secreted in the pancreas is also abnormally thick, causing the exocrine ducts to become plugged. Insufficient production of pancreatic enzymes prevents adequate absorption of nutrients such as fat, protein, and fat-soluble vitamins. Patients with CF may also develop CF-related diabetes, due to destruction of insulin-producing islet cells in the pancreas. For this reason, it is important to closely monitor blood glucose levels to prevent dangerous complications related to hyperglycemia.

Malabsorption of fat will cause a patient’s stool to become bulky and foul-smelling. The stool will also float due to its increased lipid content.

Inability to absorb fat-soluble vitamins, such as vitamin D, can lead to osteoporosis and osteopenia if left untreated.

Patients with CF cannot absorb sodium chloride from their sweat as it passes through the sweat glands. As a result, these patients excrete four times the normal amount of sodium chloride in their sweat.

One of the first signs of CF in infants is meconium ileus. Meconium, an infant’s first stool, becomes thickened in the intestines and can become stuck. When this happens, the bowel becomes obstructed, and the meconium is unable to pass.

Inadequate absorption of nutrients due to insufficient production of pancreatic enzymes can lead to delayed growth and poor weight gain in children.