Pulmonary Disease Flashcards
Small air sacs at the terminal end of the
bronchioles
alveoli
alveoli are surrounded by a network of _________ and are responsible for _______
capillaries
exchange of gases from air to blood
respiratory muscles
diaphragm
intercostal
Impact of Malnutrition on Respiratory Function
- Decreased respiratory muscle mass, _____, & endurance
- Reductions in vital ______
- Decreased ________ drive
- Decreased ______ leading to decreased lung compliance
- ______________ leading to pulmonary edema
strength
capacity
ventilatory
surfactant
Hypoalbuminemia
Decreased_____ function and ability to fight infection
Diminished oxygen carrying _____ of blood
Low levels of Phos, Ca, Mg, & K+ compromise respiratory ______ function at the cellular level
Prolonged intubation
immune
capacity
muscle
Cystic Fibrosis (CF) is an Autosomal-recessive inherited disorder
Dysfunction of the _______ glands=> impaired transport of ______ across cell membranes
Multisystem disorder
Results in=>production of abnormally ________ that obstruct ______
exocrine
chloride & Na
thick secretions
glands & ducts
~_______ children & adults in the U.S. have CF
About _____ new cases of CF are diagnosed each year
More common in ______
Survival rates are improving
40,000
1,000
Caucasians
Pulmonary Manifestations of CF
- Mucous is thick and accumulates in the _____
- Chronic ____ and ____
- Frequent respiratory infections: _________
- Permanent lung damage
lungs
cough and dyspnea
pneumonia, bronchitis
Pancreatic Manifestations of CF
- ____% of CF patients have pancreatic insufficiency
- Plugs of thick mucous reduce the quantity of digestive enzymes & _______ released from the pancreas
resulting in maldigestion & malabsorption of nutrients
(especially fat)
CF-related diabetes mellitus
90%
bicarbonate
Excessive fat content in stool causes diarrhea is called ?
Signs & symptoms:
________ stools, oily film in toilet water, foul odor
Weight loss despite adequate intake
Steatorrhea
Pale, greasy
Diagnosis of Steatorrhea
Fecal Fat Test
____ hr stool collection
Consume a ____ g fat diet
Normally ____ g fat in stool per day
>____ g/day=> malabsorption
72
100 g
2-6 g
7 g
Clinical Manifestations of CF
______ stasis & obstruction
__________ obstruction
Sweat glands=>Lose excessive amounts of _______ in sweat
Biliary
Intestinal
Na & Cl
Diagnosis of CF
Prenatal screening for those with a family history
Neonatal screening
Definitive diagnosis=>Genetic analysis and a positive chloride sweat test
Pancreatic insufficiency:
Fecal fat test: >7 g/day
Fecal elastase-1 test: _____ mcg/g of stool
<100
fecal elastase-1 is one sample and tests for enzyme
Medical Treatment
- Chest physiotherapy
- Mucolytics, bronchodilators
- Antibiotics
- Corticosteroids
- Pancreatic insufficiency=> __________
- Cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies (e.g., ivacaftor)
- Lung transplant
pancreatic enzyme replacement therapy (PERT)
Nutritional Concerns for CF
- High risk for _________
- Inadequate growth is common
Decreased _____ intake
- Dyspnea, coughing
- GI distress
- Anorexia
- Impaired taste
- Emotional burden
___________
Increased _________ needs
malnutrition
oral
Malabsorption
nutritional
for CF patients, perform nutritional assessment including diet history, nutrition focused physical exam, anthropometrics, meds, and biochemical tests, such as _______________
fecal fat, fat soluble vitamin levels, and electrolytes
weight goals
newborn to 24 months old ___________
2-20 year old ______________
adult females ________
adult males _________
≥50th percentile weight for length
50 - 85 percentile for BMI
BMI 22-27
BMI 23-27
CF energy needs vary widely from ______ to _____ % of estimated energy needs for the healthy population of similar age, sex, and size
must individualize
120-150%
protein requirements for CF
increased needs of 1.5 g/kg
- due to inflammation, infections, corticosteroids, and malabsorption
CF patients should consume _____ of total kcal from fat.
fat has _________,
provides _____,
increases _______,
and lowers ____ production
also need __________
35-40%
high caloric density
EFA
palatability
CO2
treat fat malabsorption with pancreatic enzyme replacements (NOT NOT NOT 40 g low fat diet)
CF patients should take a MVI with minerals
If pancreatic insufficiency=> high risk for fat-soluble vitamin deficiencies=> supplementation of fat-soluble vitamins required in a __________ (this is in ___________)
Increased ____ requirements=> typical diet should provide adequate amount but ______ may need supplementation
Increased risk for ____ deficiency
water-soluble form
addition to the MVIM
Na
infants
zinc
MNT for CF
___________________ diet
Pancreatic insufficiency=> treat with
_______________
High kcal, high protein, moderate fat
pancreatic enzymes
Infants:
Breastfed
- ____________
Formula-fed
- Standard formula
- ______________ if needed
Human milk fortifier added to expressed milk
Higher kcal formulas
Pancreatic Enzyme Replacement Therapy (PERT)
Contain __________________
Examples:_______________
lipase
protease
amylase
Creon
Pancreaze
Viocase
Pancreatic Enzyme Replacement Therapy (PERT) Given _____ with __________
Individually dosed based on individual’s ___________
Infants/small children=> open capsule and mix the microspheres with an ________, easy to swallow food=> _______
orally with all meals & snacks
fat intake or weight
acidic
applesauce
Enteral Nutrition Support for CF
- Supplemental tube feeding may be required to meet nutritional needs
- Cyclic feeding given at ______
- Use a calorically dense, high protein formula
- Most common enteral access route is a ___________
night
percutaneous endoscopic gastrostomy (PEG) tube
Enteral Nutrition Support for Pancreatic insufficiency:
______________ formula
No evidence-based guidelines for ______ administration with enteral feeding tubes
Option: Provide pancreatic enzymes _________ of the feeding and then ______ through the feeding
Hydrolyzed, semi-elemental
PERT
orally at the beginning
halfway
Chronic Obstructive Pulmonary Disease (COPD) is characterized by slow, progressive __________ that is worse with ________
More ____ is required to expire air and emptying of the lungs is _____
Diseases: ________________
Primary symptom=> _____
Primary cause is ___________
obstruction of the airways
expiration
force
slowed
chronic bronchitis & emphysema
dyspnea
cigarette smoking
~_____ million Americans have COPD
More common in ______ than other racial and ethnic groups
_____ leading cause of death among adults in the U.S.
12.5
Whites
6th
Chronic Bronchitis is the Inflammation of the bronchi caused by inspired irritants
Characterized by ____________ and chronic ____________that continues for at least _____ months of the
year for at least____ consecutive years
hypersecretion of mucus
productive cough
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