The Impact of Poor Fat Absorption in Cystic Fibrosis on Stool Appearance
How does poor absorption of fat in the digestive system change the appearance of stool in cystic fibrosis?
a) Stool becomes greasy and foul-smelling
b) Stool becomes hard and dry
c) Stool becomes black and tarry
d) Stool becomes watery and pale
Final answer: Cystic fibrosis impairs the absorption of nutrients, particularly fats, in the digestive system. When the digestive system cannot absorb fats properly, resulting in a condition called steatorrhea, the stool typically becomes greasy and foul-smelling.
Answer:
When fat absorption is impaired in individuals with cystic fibrosis, the appearance of stool changes. Stool becomes greasy and foul-smelling.
Cystic fibrosis is a genetic disease that affects various organs in the body, including the digestive system. One of the consequences of cystic fibrosis is poor absorption of nutrients, particularly fats. This impaired fat absorption leads to a condition known as steatorrhea.
Steatorrhea is characterized by the excretion of large amounts of lipids in the stool. This results in stool that is greasy and foul-smelling. The greasy texture and unpleasant odor of the stool are directly linked to the inability of the digestive system to properly absorb fats.
Individuals with cystic fibrosis may also experience other symptoms related to poor fat absorption, such as diarrhea, nausea, and stomach cramps. These symptoms can further impact the quality of life and overall health of individuals with cystic fibrosis.
It is important for healthcare providers to monitor and manage fat absorption issues in individuals with cystic fibrosis to optimize their nutritional status and overall well-being.