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Pulmonary Infection in Cystic Fibrosis: The Australian Approach

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Part of the book series: Respiratory Pharmacology and Pharmacotherapy ((RPP))

Abstract

Death in patients with cystic fibrosis is almost always the result of failure to control the progressive lung infection so characteristic of the disease. Consequently this aspect of management has received predominant attention in CF centres in Australia but the importance of maintenance of optimal nutrition, control of gastrointestinal symptoms, prevention of salt depletion and psychosocial support of patients and families are integral aspects of optimal management.

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References

  1. Button BM, Heine RG, Catto-Smith AG, Phelan PD, Olinsky A. Effect of postural draining chest physiotherapy on gastro-oesophageal reflux in infants with cystic fibrosis. Am J Respir Crit Care Med 1995; 151: A738.

    Google Scholar 

  2. Armstrong DS, Grimwood K, Carzino R, Carlin J, Olinsky A, Phelan PD. Bacterial colonisation of the lungs in infants with cystic fibrosis diagnosed by newborn screening. Am Rev Respir Dis 1993; 147: A463.

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  3. Ramsey BW, Wentz KR, Smith AL, Richardson M, Williams-Warren J, Hedges DL et al. Predictive value of oropharyngeal cultures for identifying lower airway bacteria in cystic fibrosis populations. Am Rev Respir Dis 1991; 144: 331–7.

    Article  PubMed  CAS  Google Scholar 

  4. Allan JA, Phelan PD. Cystic fibrosis. The ability to survive disability. Med J Aust 1980; I: 600–2.

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  5. Kerem E, Corey M, Gold R, Levison H. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonisation with Pseudomonas aeruginoso. J Pediatr 1990; 116: 714–9.

    Article  PubMed  CAS  Google Scholar 

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© 1996 Birkhäuser Verlag Basel/Switzerland

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Phelan, P.D. (1996). Pulmonary Infection in Cystic Fibrosis: The Australian Approach. In: Bauernfeind, A., Marks, M.I., Strandvik, B. (eds) Cystic Fibrosis Pulmonary Infections: Lessons from Around the World. Respiratory Pharmacology and Pharmacotherapy. Birkhäuser Basel. https://doi.org/10.1007/978-3-0348-7359-8_11

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  • DOI: https://doi.org/10.1007/978-3-0348-7359-8_11

  • Publisher Name: Birkhäuser Basel

  • Print ISBN: 978-3-0348-7361-1

  • Online ISBN: 978-3-0348-7359-8

  • eBook Packages: Springer Book Archive

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