Rhenis Nursing Rhenis Nursing
ATI RN Paediatric nursing 2023 Exam-7
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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 At D, E, and K.

Barrel-shaped chest

Clubbing of the fingers bilaterally

Respiratory rate 40/min with wheezing and rhonchi noted bilaterally

dyspnea

paroxysmal cough

Temperature 38.4° C (101.1° 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 207000/mm3 (5,000 to 10,000/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 : 🧬Think about the consequences of enzyme deficiency and thick mucus in this condition.

Correct Answers:

  • Water-soluble vitamins
  • Dornase alfa
  • Pancreatic lipase


Rationale :

🧪Cystic fibrosis impairs the absorption of fat-soluble vitamins (A, D, E, K) due to pancreatic insufficiency, so water-soluble forms of these vitamins are required to enhance absorption.

🌬️Dornase alfa is a mucolytic agent that reduces the viscosity of pulmonary secretions, improving airway clearance and respiratory function in children with chronic obstructive pulmonary disease caused by CF.

🍽️Pancreatic lipase is essential for children with CF who have pancreatic enzyme deficiency. Supplementation with enzymes helps with the digestion of fats and proteins, improving nutrient absorption and weight gain.

🧴Medications like acetaminophen and meperidine are not specific to CF management and do not address the underlying disease complications like malabsorption or thickened mucus.


📌core message

Children with cystic fibrosis often require vitamin supplementation, mucolytics, and pancreatic enzymes to manage malabsorption and pulmonary complications.

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