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Optimising inhaled mannitol for cystic fibrosis in an adult population

ABSTRACT: There has been remarkable progress in the treatment of cystic fibrosis (CF) patients over the past 20 years. However, limitations of standard therapies have highlighted the need for a convenient alternative treatment to effectively target the pathophysiologic basis of CF-related disease by...

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Autores principales: Flume, Patrick A., Aitken, Moira L., Bilton, Diana, Agent, Penny, Charlton, Brett, Forster, Emma, Fox, Howard G., Hebestreit, Helge, Kolbe, John, Zuckerman, Jonathan B, Button, Brenda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487380/
https://www.ncbi.nlm.nih.gov/pubmed/26306102
http://dx.doi.org/10.1183/20734735.021414
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author Flume, Patrick A.
Aitken, Moira L.
Bilton, Diana
Agent, Penny
Charlton, Brett
Forster, Emma
Fox, Howard G.
Hebestreit, Helge
Kolbe, John
Zuckerman, Jonathan B
Button, Brenda M.
author_facet Flume, Patrick A.
Aitken, Moira L.
Bilton, Diana
Agent, Penny
Charlton, Brett
Forster, Emma
Fox, Howard G.
Hebestreit, Helge
Kolbe, John
Zuckerman, Jonathan B
Button, Brenda M.
author_sort Flume, Patrick A.
collection PubMed
description ABSTRACT: There has been remarkable progress in the treatment of cystic fibrosis (CF) patients over the past 20 years. However, limitations of standard therapies have highlighted the need for a convenient alternative treatment to effectively target the pathophysiologic basis of CF-related disease by improving mucociliary clearance of airway secretions and consequently improve lung function and reduce respiratory exacerbations. Mannitol is an osmotic agent available as a dry powder, dispensed in a convenient disposable inhaler device for the treatment of adult patients with CF. Inhalation of mannitol as a dry powder is thought to change the viscoelastic properties of airway secretions, increase the hydration of the airway surface liquid and contribute to increased mucociliary and cough clearance of retained secretions. In two large phase 3 studies [1, 2], long-term use of inhaled mannitol resulted in a significant and clinically meaningful improvement in lung function relative to control in adult CF subjects and had an acceptable safety profile. Clinical experience with inhaled mannitol confirms that it is safe and effective. A minority of patients are unable to tolerate the medication. However, through training in proper inhaler technique and setting clear expectations regarding therapeutic effects, both the tolerance and adherence necessary for long term efficacy can be positively influenced. EDUCATIONAL AIMS: To discuss the importance of airway clearance treatments in the management of cystic fibrosis. To describe the clinical data that supports the use of mannitol in adult patients with cystic fibrosis. To highlight the role of mannitol tolerance testing in screening for hyperresponsiveness. To provide practical considerations for patient education in use of mannitol inhaler. KEY POINTS: Inhaled mannitol is a safe and effective option in adult patients with cystic fibrosis. Mannitol tolerance testing effectively screens for hyperresponsiveness prior to initiation of therapy. Physiotherapists and respiratory therapists play an integral role in the introduction and maintenance of dry powder inhalation therapy. Patient training and follow-up is important for optimising longer term adherence.
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spelling pubmed-44873802015-08-24 Optimising inhaled mannitol for cystic fibrosis in an adult population Flume, Patrick A. Aitken, Moira L. Bilton, Diana Agent, Penny Charlton, Brett Forster, Emma Fox, Howard G. Hebestreit, Helge Kolbe, John Zuckerman, Jonathan B Button, Brenda M. Breathe (Sheff) Reviews ABSTRACT: There has been remarkable progress in the treatment of cystic fibrosis (CF) patients over the past 20 years. However, limitations of standard therapies have highlighted the need for a convenient alternative treatment to effectively target the pathophysiologic basis of CF-related disease by improving mucociliary clearance of airway secretions and consequently improve lung function and reduce respiratory exacerbations. Mannitol is an osmotic agent available as a dry powder, dispensed in a convenient disposable inhaler device for the treatment of adult patients with CF. Inhalation of mannitol as a dry powder is thought to change the viscoelastic properties of airway secretions, increase the hydration of the airway surface liquid and contribute to increased mucociliary and cough clearance of retained secretions. In two large phase 3 studies [1, 2], long-term use of inhaled mannitol resulted in a significant and clinically meaningful improvement in lung function relative to control in adult CF subjects and had an acceptable safety profile. Clinical experience with inhaled mannitol confirms that it is safe and effective. A minority of patients are unable to tolerate the medication. However, through training in proper inhaler technique and setting clear expectations regarding therapeutic effects, both the tolerance and adherence necessary for long term efficacy can be positively influenced. EDUCATIONAL AIMS: To discuss the importance of airway clearance treatments in the management of cystic fibrosis. To describe the clinical data that supports the use of mannitol in adult patients with cystic fibrosis. To highlight the role of mannitol tolerance testing in screening for hyperresponsiveness. To provide practical considerations for patient education in use of mannitol inhaler. KEY POINTS: Inhaled mannitol is a safe and effective option in adult patients with cystic fibrosis. Mannitol tolerance testing effectively screens for hyperresponsiveness prior to initiation of therapy. Physiotherapists and respiratory therapists play an integral role in the introduction and maintenance of dry powder inhalation therapy. Patient training and follow-up is important for optimising longer term adherence. European Respiratory Society 2015-03 /pmc/articles/PMC4487380/ /pubmed/26306102 http://dx.doi.org/10.1183/20734735.021414 Text en ©ERS 2015 http://creativecommons.org/licenses/by-nc/4.0/ Breathe articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0 (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Reviews
Flume, Patrick A.
Aitken, Moira L.
Bilton, Diana
Agent, Penny
Charlton, Brett
Forster, Emma
Fox, Howard G.
Hebestreit, Helge
Kolbe, John
Zuckerman, Jonathan B
Button, Brenda M.
Optimising inhaled mannitol for cystic fibrosis in an adult population
title Optimising inhaled mannitol for cystic fibrosis in an adult population
title_full Optimising inhaled mannitol for cystic fibrosis in an adult population
title_fullStr Optimising inhaled mannitol for cystic fibrosis in an adult population
title_full_unstemmed Optimising inhaled mannitol for cystic fibrosis in an adult population
title_short Optimising inhaled mannitol for cystic fibrosis in an adult population
title_sort optimising inhaled mannitol for cystic fibrosis in an adult population
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487380/
https://www.ncbi.nlm.nih.gov/pubmed/26306102
http://dx.doi.org/10.1183/20734735.021414
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