Pseudomonas aeruginosa in cystic fibrosis patients with c.1652G›A (G551D)-CFTR treated with ivacaftor-Changes in microbiological parameters

Author:

Millar B. C.12,McCaughan J.3,Rendall J. C.4,Downey D. G.45,Moore J. E.1245

Affiliation:

1. Northern Ireland Public Health Laboratory; Department of Bacteriology; Belfast City Hospital; Belfast UK

2. School of Biomedical Sciences; Ulster University; Coleraine UK

3. Department of Medical Microbiology; Belfast Health & Social Care Trust (BHSCT), Kelvin Building; Royal Group of Hospitals; Belfast UK

4. Northern Ireland Regional Adult Cystic Fibrosis Centre, Level 8; Belfast City Hospital; Belfast UK

5. Centre for Experimental Medicine; Queen's University; Belfast UK

Funder

Vertex Pharmaceuticals

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference8 articles.

1. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation;Ramsey;N Engl J Med,2011

2. Development, clinical utility, and place of ivacaftor in the treatment of cystic fibrosis;O'Reilly;Drug Des Devel Ther,2013

3. Relative Resistance Index (RRI)-a scoring system for antibiotic resistance in Pseudomonas aeruginosa;Ewing;Br J Biomed Sci,2017

4. Ivacaftor in cystic fibrosis adults: Czech experience with six years of follow-up;Fila;Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub,2016

5. Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftor;Heltshe;Clin Infect Dis,2015

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