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Published online before print November 14, 2008, 10.1183/09031936.00043108
Eur Respir J 2009; 33:305-311
Copyright ©ERS Journals Ltd 2009
doi: 10.1183/09031936.00043108

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Acquisition and eradication of P. aeruginosa in young children with cystic fibrosis

T. A. Douglas1,2, S. Brennan2, S. Gard2, L. Berry2, C. Gangell2, S. M. Stick1,2, B. S. Clements1 and P. D. Sly1,2

1 Dept of Respiratory Medicine, Princess Margaret Hospital, and 2 Division of Clinical Sciences, Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, Perth, Australia.

CORRESPONDENCE: P. D. Sly, Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia Perth, Western Australia 6008. Fax: 61 894897706. E-mail: peters{at}ichr.uwa.edu.au

Keywords: Bronchoalveolar lavage, children, cystic fibrosis, eradication, microbiological surveillance, Pseudomonas aeruginosa

Received: March 19, 2008
Accepted October 12, 2008

When do infants and young children with cystic fibrosis acquire infection with Pseudomonas aeruginosa? Can this be eradicated when first detected?

Children <6 yrs of age participated in an annual bronchoalveolar lavage (BAL)-based microbiological surveillance programme in Perth, Australia. When P. aeruginosa was detected, an eradication programme using combination treatment with i.v., oral and nebulised antibiotics was undertaken. Repeat BAL was performed 3 months following treatment, to assess eradication success.

P. aeruginosa was detected in 33 (28.4%) children; median (range) age at detection was 30.5 (3.3–71.4) months. P. aeruginosa was mucoid at detection in six (18.2%) out of 33 patients and associated with respiratory symptoms in 16 (48.5%) out of 33 children. In total, 26 children underwent eradication therapy, with P. aeruginosa eradicated in 20 (77%) out of 26 following one eradication cycle and in three (total 88%) additional children following a second cycle. Eradication was associated with a significant decrease in neutrophil elastase and interleukin-1β in BAL fluid 12 months post eradication.

Eradication of Pseudomonas aeruginosa infection is achievable in young children with cystic fibrosis for up to 5 yrs using combination i.v., oral and nebulised antibiotic therapy and is associated with reduced pulmonary inflammation 12 months post eradication.




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