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ATI RN Paediatric Nursing 2023 Exam-6
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School-age child admitted, diagnosed with cystic fibrosis at 3 months of age, has experienced failure to thrive, and has chronic obstructive pulmonary disease.

The child presents with wheezing, rhonchi, paroxysmal cough, and dyspnea.

The parent reports large, frothy foul- smelling stools.

The child has deficient levels of vitamin A, D, E, and K.

Barrel-shaped chest

Clubbing of the fingers bilaterally

Respiratory rate 40/min with wheezing and rhonchi noted bilaterally, dyspnea, and paroxysmal cough

Temperature 38.4° C (101° F)

Heart rate 100/min

Respiratory rate 40/min

Blood pressure 100/57 mm Hg

Sputum culture positive for Pseudomonas aeruginosa

Stool analysis positive for presence of fat and enzymes

Chest x-ray indicates obstructive emphysema

WBC count 20,000/mm3 (5,000 to IO,OOO/mm3)


A nurse is reviewing the child's medical record. Which of the following medications should the nurse expect the provider to prescribe or reconcile from the child's home medication list? Select all that apply


Answer Options

Hint : 🧪Look for medications that support both airway clearance and nutritional absorption in chronic conditions.

Correct Answers:

  • Water-soluble vitamin
  • Dornase alfa


Rationale :

🫁Dornase alfa is a mucolytic agent specifically prescribed for clients with cystic fibrosis to thin and loosen thick pulmonary secretions, thereby improving airway clearance and reducing the risk of infections.

💊Clients with fat-soluble vitamin malabsorption (vitamins A, D, E, K) require water-soluble forms of these vitamins to improve absorption due to pancreatic enzyme deficiency and steatorrhea.

🔬The presence of Pseudomonas aeruginosa and elevated WBC count confirms infection, but acetaminophen is only symptomatic and not a CF-specific treatment, while meperidine is not recommended for children due to the risk of toxic metabolite accumulation.

🩻The child’s symptoms—paroxysmal cough, barrel chest, and clubbing—are classic signs of chronic hypoxia in cystic fibrosis, supporting the need for targeted pulmonary and nutritional therapies.

📌Core Message

Children with cystic fibrosis require airway clearance agents like dornase alfa and water-soluble vitamins to manage mucus build-up and fat-soluble vitamin deficiencies due to malabsorption.

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