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Review
. 2012 Jun;105 Suppl 2(Suppl 2):S19-24.
doi: 10.1258/jrsm.2012.12s004.

Inhaled antibiotics in cystic fibrosis: what's new?

Simon Langton Hewer  1
Affiliations
Review

Inhaled antibiotics in cystic fibrosis: what's new?

Simon Langton Hewer. J R Soc Med. 2012 Jun.
No abstract available

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Figures

Figure 1
Figure 1
Altera nebulizer for administration of AZLI
Figure 2
Figure 2
Podhaler for inhalation of Tobramycin Inhalation Powder
Figure 3
Figure 3
UK cystic fibrosis population. Proportion of a) males and b) females of each 3-yr cohort surviving until 2003. ▪: 1968–1970; ○: 1971–1973; ▴: 1974–1976; □: 1977–1979; ♦: 1980–1982; ◊: 1983–1985; ▵: 1986–1988; •: 1989–1991; ▿: 1992–1994
See this image and copyright information in PMC

References

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    1. Ranganathan SC, Dezateux C, Bush A, et al. Airway function in infants newly diagnosed with cystic fibrosis. Lancet 2001;358:1964–5 - PubMed
    1. Emerson J, Rosenfeld M, McNamara S, Ramsey B, Gibson RL Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatric Pulmonology 2002;34:91–100 - PubMed
    1. Cystic Fibrosis Foundation. 2009. Patient Registry Annual Report.
    1. Kosorok MR, Zeng L, West SE, et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatric Pulmonology 2001;32:277–87 - PubMed

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