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ERS School Course Cystic Fibrosis

A. Bush, S. Elborn, I. Götz
Breathe 2005 1: 321-331; DOI: 10.1183/18106838.0104.321
A. Bush
Professor of Paediatric Respirology, Imperial School of Medicine at National Heart and Lung Institute and Honorary Consultant, Paediatric Chest Physician, Dept of Paediatric Respiratory, Medicine, Royal Brompton Hospital, Sydney Street, London, SW3 6NP, UK. Fax: 44 2073518763, E-mail:
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  • For correspondence: a.bush@rbh.nthames.nhs.uk
S. Elborn
Adult Cystic Fibrosis Unit, Belfast City Hospital, Lisburn Road, Belfast, BT9 7A, Ireland. E-mail:
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  • For correspondence: stuart.elborn@bch.n-i.nhs.uk
I. Götz
University Children's Hospital, AKH, Währinger Gürtel 18–20, 1090 Vienna, Austria. Fax: 43 1404003194 E-mail:
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Abstract

Educational aims

  • To identify patients with advanced and rapidly progressive lung disease.

  • To discuss how to best optimise standard therapies.

  • To understand the different approaches appropriate to patients who have and have not decided that lung transplantation is an option.

  • To detail innovative strategies which may be worth attempting if conventional means failure.

Summary More than 90% of CF patients will eventually die of advanced lung disease, despite everything that has been attempted. This article will discuss strategies that can be adopted when a patient is doing badly.

  • ©ERS 2005

Breathe articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.

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ERS School Course Cystic Fibrosis
A. Bush, S. Elborn, I. Götz
Breathe Jun 2005, 1 (4) 321-331; DOI: 10.1183/18106838.0104.321

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ERS School Course Cystic Fibrosis
A. Bush, S. Elborn, I. Götz
Breathe Jun 2005, 1 (4) 321-331; DOI: 10.1183/18106838.0104.321
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