Cystic Fibrosis Project Quiz
Quiz
•
Health Sciences
•
University
•
Easy
Trinitee Green
Used 1+ times
FREE Resource
8 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What causes cystic fibrosis?
bacterial infection
positive sweat test
a mutation in the CFTR gene
autoimmune response
Answer explanation
Cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of thick mucus in various organs. This genetic defect is the primary cause of the disease, unlike bacterial infections or autoimmune responses.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Cystic fibrosis primarily affects which organs?
Lungs and digestive system
Heart and Blood vessels
Spleen and Renal
Brain and spinal cord.
Answer explanation
Cystic fibrosis primarily affects the lungs and digestive system, leading to thick mucus production that obstructs airflow and impairs digestion. This makes 'Lungs and digestive system' the correct choice.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following is a common respiratory symptom of CF?
Dry throat with no cough.
Wheezing with no mucus production.
Chest pain without mucus
Persistent coughing with mucus.
Answer explanation
Cystic fibrosis (CF) commonly leads to persistent coughing with mucus due to thickened secretions in the lungs. This symptom is a hallmark of CF, unlike the other options which do not typically occur in this condition.
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What digestive issue is common in CF patients?
Malabsorption of nutrients
Constipation without mucus buildup
Overproduction of bile.
Excess insulin secretion.
Answer explanation
Cystic fibrosis (CF) leads to thick mucus that obstructs pancreatic enzymes, causing malabsorption of nutrients. This is a common digestive issue in CF patients, making the correct answer 'Malabsorption of nutrients'.
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which therapy helps clear mucus from the lungs in CF?
Nebulizers only
Exercise
Chest physiotherapy
Antibiotics.
Answer explanation
Chest physiotherapy is specifically designed to help clear mucus from the lungs in cystic fibrosis (CF) patients. It involves techniques that aid in loosening and expelling mucus, improving lung function.
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why are CF patients at increased risk for lung infections?
Reduced blood flow to the lungs
Thick mucus traps bacteria in the lungs
Constant coughing
Too much chest physiotherapy
Answer explanation
CF patients have thick mucus in their lungs, which traps bacteria and makes it difficult to clear infections. This leads to an increased risk of lung infections, making the choice 'Thick mucus traps bacteria in the lungs' correct.
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What kind of medications are used to help CF patients digest food?
Pancreatic enzyme replacement therapy medications.
Antibiotics for lung infections
Insulin for blood sugar control
Antacids for stomach acid reduction
Answer explanation
Pancreatic enzyme replacement therapy medications are essential for CF patients as they help in digesting food properly, compensating for the lack of natural enzymes due to pancreatic dysfunction.
8.
MULTIPLE CHOICE QUESTION
45 sec • 1 pt
Why is a high-calorie diet recommended for CF patients?
It's not recommended, they're fine.
To reduce mucus production.
To strengthen lung function.
They need extra energy due to malabsorption and increased metabolic demands.
Answer explanation
A high-calorie diet is essential for CF patients because they experience malabsorption of nutrients and have increased metabolic demands, requiring extra energy to maintain their health and support lung function.
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