Chapter 33: Medical Nutrition Therapy for Pulmonary Disease Flashcards
cilia
“Hair-like” structures that move the superficial liquid lining layer from deep within the lungs toward the pharynx to enter the gastrointestinal tract, thereby playing an important role as a lung defense mechanism by clearing bacteria and other foreign bodies
surfactant
Secreted by alveolar cells. A compound synthesized from proteins and phospholipids that maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung
tachypnea
Rapid breathing
dyspnea
Shortness of breath
pulmonary function tests
Used to diagnose or monitor the status of lung disease; they are designed to measure the ability of the respiratory system to exchange O2 and CO2
pulse oximetry
A pulmonary function test. A small device called a pulse oximeter, which uses light waves to measure the O2 saturation of arterial blood, is placed on the end of the finger. Normal for a young, healthy person is 95% to 99%
spirometry
A common pulmonary function test. This involves breathing into a spirometer that gives information on lung volume and the rate at which air can be inhaled or exhaled
cystic fibrosis (CF)
A life-threatening autosomal recessive inherited disorder. CF is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) protein, a complex chloride channel and regulatory protein found in all exocrine tissue. Most of the clinical manifestations are related to the thick, viscous secretions. Lung disease and malnutrition are predominant consequences of the disease
bronchioectasis
A chronic condition of dilation of the bronchi that develops as a result of recurrent long infections
clubbing
Physical sign characterized by bulbous enlargement of the ends of one or more fingers or toes
pancreatic insufficiency (PI)
The pancreas fails to make adequate enzymes to digest food in the small intestine, is the most common gastrointestinal complication of CF
steatorrhea
Characterized by foul smelling, bulky, oily stools and failure to thrive or poor weight gain
cystic fibrosis related diabetes (CFRD)
Most common comorbidity in the CF population. CFRD is associated with poor growth, clinical and nutritional deterioration, and early death. The use of hemoglobin A1C is not recommended for screening because it has low sensitivity in CFRD
kyphosis
An increased curvature of the upper back
pancreatic enzyme replacement therapy (PERT)
An important component of the management of CF patients to adequately absorb carbohydrates, protein, and fat
pancreatic acinus
The secretory unit of exocrine pancreas, where pancreatic juice is produced
acinar destruction
Results in impaired secretion of pancreatic juice, which results in loose, oily, frequent stools and malabsorption
elastase
Protein-digesting enzyme secreted by the pancreas and involved in hydrolysis of peptide bonds
distal intestinal obstruction syndrome (DIOS)
The blockage of intestines resulting from stool and intussusceptions (obstructions)
asthma
A chronic disorder that affects the airways and is characterized by bronchial hyper-reactivity, reversible airflow obstruction, and airway remodeling. Asthmatic symptoms include periodic episodes of chest tightness, breathlessness, and wheezing