A nurse is educating a client with cystic fibrosis (CF) about the importance of airway clearance techniques. What should the nurse explain as the primary goal of these techniques?
To improve lung capacity
To prevent respiratory infections
To maintain electrolyte balance
To clear mucus and secretions from the airways
The Correct Answer is D
A) Incorrect. While airway clearance techniques can help maintain lung function, their primary goal is not to improve lung capacity.
B) Incorrect. Preventing respiratory infections is an important aspect of CF care, but it is not the primary goal of airway clearance techniques.
C) Incorrect. Maintaining electrolyte balance is important in CF, but it is not the primary goal of airway clearance techniques.
D) Correct. The primary goal of airway clearance techniques in CF is to mobilize and clear mucus and secretions from the airways, improving breathing and reducing the risk of infection.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is D
Explanation
A) Incorrect. Genetic testing is used to confirm CF but does not directly measure chloride ion concentration in sweat.
B) Incorrect. Chest X-rays may be used to assess lung changes in individuals with CF but are not used to measure chloride ion concentration in sweat.
C) Incorrect. Pulmonary function tests assess lung function but do not directly measure chloride ion concentration in sweat.
D) Correct. The sweat chloride test measures the concentration of chloride ions in sweat and is commonly used to confirm CF. Elevated sweat chloride levels are indicative of CF.
Correct Answer is D
Explanation
A) Incorrect. If both parents are carriers, their child's risk of having CF is 25%, not 50%.
B) Incorrect. While the risk is increased, having two carrier parents does not guarantee that a child will have CF.
C) Incorrect. If both parents are carriers, their child can inherit two normal genes (no CF), one normal and one CF gene (carrier status), or two CF genes (CF).
D) Correct. When both parents are carriers, there is a 25% chance that their child will inherit two CF genes and have CF, a 50% chance of being a carrier, and a 25% chance of inheriting two normal genes (no CF).
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