Pragmatic criteria to define chronic pseudomonas aeruginosa infection among adults with cystic fibrosis

Author:

Hoo Zhe HuiORCID,Coates Elizabeth,Maguire Chin,Cantrill Hannah,Shafi Nadia,Nash Edward F.,McGowan Angela,Bourke Stephen J.,Flight William G.,Daniels Thomas V.,Nightingale Julia A.,Allenby Mark I.,Curley Rachael,Wildman Martin J.

Funder

Research Trainees Coordinating Centre

Programme Grants for Applied Research

Publisher

Springer Science and Business Media LLC

Subject

Infectious Diseases,Microbiology (medical),General Medicine

Reference22 articles.

1. Salsgiver EL, Fink AK, Knapp EA, LiPuma JJ, Olivier KN, Marshall BC, Saiman L (2016) Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis. Chest 149:390–400. https://doi.org/10.1378/chest.15-0676

2. Lee TW, Brownlee KG, Conway SP, Denton M, Littlewood JM (2003) Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros 2:29–34. https://doi.org/10.1016/S1569-1993(02)00141-8

3. Mogayzel PJ Jr, Naureckas ET, Robinson KA, Brady C, Guill M, Lahiri T, Lubsch L, Matsui J, Oermann CM, Ratjen F, Rosenfeld M, Simon RH, Hazle L, Sabadosa K, Marshall BC, Cystic Fibrosis Foundation Pulmonary Clinical Practice Guidelines Committee (2014) Cystic Fibrosis Foundation pulmonary guideline. Pharmacologic approaches to prevention and eradication of initial Pseudomonas aeruginosa infection. Ann Am Thorac Soc 11:1640–1650. https://doi.org/10.1513/AnnalsATS.201404-166OC

4. Mogayzel PJ Jr, Naureckas ET, Robinson KA, Mueller G, Hadjiliadis D, Hoag JB, Lubsch L, Hazle L, Sabadosa K, Marshall B, Pulmonary Clinical Practice Guidelines Committee (2013) Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health. Am J Respir Crit Care Med 187:680–689. https://doi.org/10.1164/rccm.201207-1160OE

5. da Silva Filho LV, Tateno AF, Martins KM, Azzuz Chernishev AC, Garcia Dde O, Haug M, Meisner C, Rodrigues JC, Döring G (2007) The combination of PCR and serology increases the diagnosis of Pseudomonas aeruginosa colonization/infection in cystic fibrosis. Pediatr Pulmonol 42:938–944. https://doi.org/10.1002/ppul.20686

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