Approaches to the treatment of initial Pseudomonas aeruginosa infection in children who have cystic fibrosis.

Abstract:

:Pseudomonas aeruginosa remains an important cause of pulmonary disease in patients who have cystic fibrosis. The development of antimicrobial therapy directed against this organism has resulted in the preservation of lung function and improved longevity. Efficacy has been demonstrated with agents administered via parenteral, inhaled, and oral routes. The optimal antibiotic regimen remains unclear. There is an active effort to use randomized, controlled clinical trials to rigorously test effective antibiotic for the eradication of P aeruginosa in young children or at least to delay the establishment of chronic infection.

journal_name

Clin Chest Med

authors

Lahiri T

doi

10.1016/j.ccm.2007.02.003

subject

Has Abstract

pub_date

2007-06-01 00:00:00

pages

307-18

issue

2

eissn

0272-5231

issn

1557-8216

pii

S0272-5231(07)00017-2

journal_volume

28

pub_type

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