Eradication ofPseudomonas aeruginosain an adult patient with cystic fibrosis

Author:

Hayes Don1,Feola David J.2,Murphy Brian S.3,Kuhn Robert J.2,Davis George A.4

Affiliation:

1. Departments of Pediatrics and Internal Medicine, College of Medicine

2. Department of Pharmacy Practice and Science, College of Pharmacy

3. Department of Internal Medicine, College of Medicine

4. Therapeutic Drug Monitoring/Internal Medicine, Chandler Medical Center, and Associate Adjunct Professor, College of Pharmacy, University of Kentucky, Lexington

Publisher

Oxford University Press (OUP)

Subject

Health Policy,Pharmacology

Reference22 articles.

1. Cystic Fibrosis Foundation. Patient registry 2008 annual data report. www.cff.org/UploadedFiles/research/ClinicalResearch/2008-Patient-Registry-Report.pdf (accessed 2010 Nov 3).

2. Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis;Henry;Pediatr Pulmonol.,1992

3. Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study;Treggiari;Contemp Clin Trials.,2009

4. Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial;Ratjen;Thorax.,2010

5. Novel approach to the eradication of Pseudomonas aeruginosa in an infant with CF after outpatient treatment failure;Hayes;Pediatr Pulmonol.,2008

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