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LPN Nursing · Respiratory Disorders in Children · Practice question

A nurse is assisting with the care of a 15-year-old adolescent who has Streptococcus pneumonia. The nurse is collecting data on the adolescent 24 hr later. How should the nurse interpret the findings? For each finding, click to specify whether the finding is unrelated to the admitting diagnosis, an indication of potential improvement, or an indication of potential worsening condition.

History and Physical

Cystic fibrosis

Blood-streaked sputum

Foul-smelling, fatty stools

Productive cough, crackles throughout lung fields

Vital Signs

0900:

Tympanic temperature 37.7° C (99.9° F)

Heart rate 130/min

Respiratory rate 36/min

Blood pressure 110/65 mm Hg

Oxygen saturation 92% on 2 L oxygen via nasal cannula

1300:

Tympanic temperature 37.5° C (99.5° F)

Heart rate 130/min

Respiratory rate 32/min

Blood pressure 100/60 mm Hg

Oxygen saturation 95% on 2 L oxygen via nasal cannula

Diagnostic Results

Chest x-ray shows infiltrate and an increased anteroposterior diameter

WBC count 22,000/mm³ (5,000 to 10,000/mm³)

Answer & explanation

Correct:

This adolescent has both cystic fibrosis and Streptococcus pneumoniae pneumonia. Interpreting the 24-hour follow-up findings requires distinguishing between changes related to the pneumonia, changes related solely to cystic fibrosis, and trends suggesting improvement or worsening. A WBC count of 17,000/mm³ is a decrease from the admission value of 22,000/mm³, though still mildly elevated; this trend toward normal indicates potential improvement in the infectious process. Hemoptysis of 300 mL is a significant new finding representing a large volume of blood-streaked sputum; this indicates potential worsening, as major hemoptysis is a serious complication of both cystic fibrosis and pneumonia. A respiratory rate of 32 per minute is a decrease from the admission rate of 36 per minute, suggesting the respiratory effort is lessening and pointing toward potential improvement. Steatorrhea — fatty, foul-smelling stools — is a hallmark manifestation of cystic fibrosis resulting from pancreatic enzyme insufficiency; it is unrelated to the pneumonia diagnosis. Oxygen saturation of 95% on 1 L oxygen (down from 2 L) demonstrates that the patient is maintaining the same saturation with less supplemental oxygen, indicating potential improvement in oxygenation. Barrel chest is a chronic structural change associated with air trapping in cystic fibrosis and is unrelated to the pneumonia diagnosis being monitored.

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