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Inhaled therapy in cystic fibrosis: agents, devices and regimens

Penny Agent, Helen Parrott
Breathe 2015 11: 110-118; DOI: 10.1183/20734735.021014
Penny Agent
Royal Brompton and Harefield NHS Foundation Trust, London, UK
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  • For correspondence: p.agent@rbht.nhs.uk
Helen Parrott
Royal Brompton and Harefield NHS Foundation Trust, London, UK
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Article Information

vol. 11 no. 2 110-118
DOI 
https://doi.org/10.1183/20734735.021014

Published By 
European Respiratory Society
Print ISSN 
1810-6838
Online ISSN 
2073-4735
History 
  • Published online June 3, 2015.

Copyright & Usage 
©ERS 2015 Breathe articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.

Author Information

  1. Penny Agent⇑ and
  2. Helen Parrott
  1. Royal Brompton and Harefield NHS Foundation Trust, London, UK
  1. Penny Agent, Director of Rehabilitation and Therapies, Royal Brompton Hospital, Sydney Street, London, SW3 6NP, UK. E-mail: p.agent{at}rbht.nhs.uk
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Vol 11 Issue 2 Table of Contents
Breathe: 11 (2)
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Inhaled therapy in cystic fibrosis: agents, devices and regimens
Penny Agent, Helen Parrott
Breathe Jun 2015, 11 (2) 110-118; DOI: 10.1183/20734735.021014

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Inhaled therapy in cystic fibrosis: agents, devices and regimens
Penny Agent, Helen Parrott
Breathe Jun 2015, 11 (2) 110-118; DOI: 10.1183/20734735.021014
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  • Article
    • Abstract
    • Nebuliser devices
    • Inhaled antibiotics
    • Other inhaled therapies
    • Delivery optimisation
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    • Conclusion
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  • CF and non-CF bronchiectasis
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