Abstract
Cystic fibrosis is a genetic disease characterized by chronic lung infection, often with Pseudomonas aeruginosa, requiring repeated antibiotic treatment for pulmonary exacerbations. In the era of cystic fibrosis transmembrane conductance regulator modulator therapy, we assessed susceptibility to antipseudomonal antibiotics in modulator-eligible and modulator-ineligible children over 3 years and found that P. aeruginosa isolates largely remained susceptible to standard parenteral but not oral antimicrobial agents.
| Original language | English |
|---|---|
| Pages (from-to) | e77-e80 |
| Journal | Pediatric Infectious Disease Journal |
| Volume | 44 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1 Mar 2025 |
Keywords
- antibiotic susceptibility
- cystic fibrosis
- Pseudomonas aeruginosa
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