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Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review

Identifying patients at risk of exacerbations and managing them appropriately to reduce this risk represents an important clinical challenge. Numerous treatments have been assessed for the prevention of exacerbations and their efficacy may differ by patient phenotype. Given their centrality in the t...

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Autores principales: Miravitlles, Marc, D’Urzo, Anthony, Singh, Dave, Koblizek, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018159/
https://www.ncbi.nlm.nih.gov/pubmed/27613392
http://dx.doi.org/10.1186/s12931-016-0425-5
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author Miravitlles, Marc
D’Urzo, Anthony
Singh, Dave
Koblizek, Vladimir
author_facet Miravitlles, Marc
D’Urzo, Anthony
Singh, Dave
Koblizek, Vladimir
author_sort Miravitlles, Marc
collection PubMed
description Identifying patients at risk of exacerbations and managing them appropriately to reduce this risk represents an important clinical challenge. Numerous treatments have been assessed for the prevention of exacerbations and their efficacy may differ by patient phenotype. Given their centrality in the treatment of COPD, there is strong rationale for maximizing bronchodilation as an initial strategy to reduce exacerbation risk irrespective of patient phenotype. Therefore, in patients assessed as frequent exacerbators (>1 exacerbation/year) we propose initial bronchodilator treatment with a long-acting muscarinic antagonist (LAMA)/ long-acting β(2)-agonist (LABA). For those patients who continue to experience >1 exacerbation/year despite maximal bronchodilation, we advocate treating according to patient phenotype. Based on currently available data on adding inhaled corticosteroids (ICS) to a LABA, ICS might be added to a LABA/LAMA combination in exacerbating patients who have an asthma-COPD overlap syndrome or high blood eosinophil counts, while in exacerbators with chronic bronchitis, consideration should be given to treating with a phosphodiesterase (PDE)-4 inhibitor (roflumilast) or high-dose mucolytic agents. For those patients who experience frequent bacterial exacerbations and/or bronchiectasis, addition of mucolytic agents or a macrolide antibiotic (e.g. azithromycin) should be considered. In all patients at risk of exacerbations, pulmonary rehabilitation should be included as part of a comprehensive management plan. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0425-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-50181592016-09-11 Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review Miravitlles, Marc D’Urzo, Anthony Singh, Dave Koblizek, Vladimir Respir Res Review Identifying patients at risk of exacerbations and managing them appropriately to reduce this risk represents an important clinical challenge. Numerous treatments have been assessed for the prevention of exacerbations and their efficacy may differ by patient phenotype. Given their centrality in the treatment of COPD, there is strong rationale for maximizing bronchodilation as an initial strategy to reduce exacerbation risk irrespective of patient phenotype. Therefore, in patients assessed as frequent exacerbators (>1 exacerbation/year) we propose initial bronchodilator treatment with a long-acting muscarinic antagonist (LAMA)/ long-acting β(2)-agonist (LABA). For those patients who continue to experience >1 exacerbation/year despite maximal bronchodilation, we advocate treating according to patient phenotype. Based on currently available data on adding inhaled corticosteroids (ICS) to a LABA, ICS might be added to a LABA/LAMA combination in exacerbating patients who have an asthma-COPD overlap syndrome or high blood eosinophil counts, while in exacerbators with chronic bronchitis, consideration should be given to treating with a phosphodiesterase (PDE)-4 inhibitor (roflumilast) or high-dose mucolytic agents. For those patients who experience frequent bacterial exacerbations and/or bronchiectasis, addition of mucolytic agents or a macrolide antibiotic (e.g. azithromycin) should be considered. In all patients at risk of exacerbations, pulmonary rehabilitation should be included as part of a comprehensive management plan. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0425-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-10 2016 /pmc/articles/PMC5018159/ /pubmed/27613392 http://dx.doi.org/10.1186/s12931-016-0425-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Miravitlles, Marc
D’Urzo, Anthony
Singh, Dave
Koblizek, Vladimir
Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title_full Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title_fullStr Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title_full_unstemmed Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title_short Pharmacological strategies to reduce exacerbation risk in COPD: a narrative review
title_sort pharmacological strategies to reduce exacerbation risk in copd: a narrative review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018159/
https://www.ncbi.nlm.nih.gov/pubmed/27613392
http://dx.doi.org/10.1186/s12931-016-0425-5
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