A nurse is explaining the role of the CFTR protein in cystic fibrosis to a client. Which function of the CFTR protein should the nurse highlight?
"The CFTR protein regulates blood sugar levels in the body."
"CFTR facilitates the transport of oxygen in the bloodstream."
"The CFTR protein controls the movement of chloride ions and water across cell membranes."
"CFTR is responsible for the production of digestive enzymes in the pancreas."
The Correct Answer is C
A) Incorrect. The CFTR protein does not regulate blood sugar levels.
B) Incorrect. CFTR does not play a role in oxygen transport in the bloodstream.
C) Correct. The primary function of the CFTR protein is to regulate chloride ion and water movement across cell membranes, which is disrupted in individuals with CF.
D) Incorrect. The production of digestive enzymes in the pancreas is not a direct function of the CFTR protein.
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Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
A) Incorrect. While coughing is important, huff coughing is a more effective and less strenuous airway clearance technique for CF patients.
B) Incorrect. Controlled breathing exercises may help with relaxation but are not the primary airway clearance technique.
C) Correct. Huff coughing is a technique where the client takes a deep breath and forcefully exhales in short bursts, helping to move mucus from the airways.
D) Incorrect. Vigorous exercise is beneficial for CF patients but should not replace specific airway clearance techniques.
Correct Answer is A
Explanation
A) Correct. CF is primarily caused by mutations in a single gene, the CFTR gene, and it can be inherited from one parent, resulting in a carrier state, or from both parents for the disease to manifest.
B) Incorrect. While genetic factors are the primary cause of CF, environmental factors can exacerbate symptoms but are not the root cause.
C) Incorrect. CF is not an X-linked genetic disorder; it follows an autosomal recessive pattern of inheritance.
D) Incorrect. CF is not caused by exposure to respiratory pathogens during infancy; it is primarily a genetic disorder.
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