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1998 
To the Editor. I recently had a telephone conversation with the guardian of Heather, a 5-year-old patient of ours with cystic fibrosis. Her airway is colonized with Staphylococcus aureus and Pseudomonas aeruginosa, and she also has a history of failure to thrive and poor oral intake. She has an older sister with cystic fibrosis. I was interested in her response to an aggressive outpatient medication regimen prescribed by my partner, that included oral …
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