Pseudomonas aeruginosa in Cystic Fibrosis Patients With G551D-CFTR Treated With Ivacaftor
2014; Oxford University Press; Volume: 60; Issue: 5 Linguagem: Inglês
10.1093/cid/ciu944
ISSN1537-6591
AutoresSonya L. Heltshe, Nicole Mayer-Hamblett, Jane L. Burns, Umer Khan, Arthur Baines, Bonnie W. Ramsey, Steven M. Rowe,
Tópico(s)Respiratory viral infections research
ResumoBackground. Ivacaftor improves outcomes in cystic fibrosis (CF) patients with the G551D mutation; however, effects on respiratory microbiology are largely unknown. This study examines changes in CF respiratory pathogens with ivacaftor and correlates them with baseline characteristics and clinical response.
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