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Salmeterol/fluticasone combination in the treatment of COPD

Clinical trials of a combination therapy of an inhaled corticosteroid, fluticasone propionate (FP), with a long-acting β(2)-agonist, salmeterol (Sal), have demonstrated a greater improvement in lung function and in quality of life measures after the combination compared with either component of alon...

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Detalles Bibliográficos
Autor principal: Chung, K F
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2707153/
https://www.ncbi.nlm.nih.gov/pubmed/18046860
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author Chung, K F
author_facet Chung, K F
author_sort Chung, K F
collection PubMed
description Clinical trials of a combination therapy of an inhaled corticosteroid, fluticasone propionate (FP), with a long-acting β(2)-agonist, salmeterol (Sal), have demonstrated a greater improvement in lung function and in quality of life measures after the combination compared with either component of alone. In a subanalysis of the data of the TRISTAN study, Sal/FP reduced exacerbation rates in COPD patients with a baseline FEV(1)<50% of predicted. A combination therapy of budesonide and formoterol improved quality of life and FEV(1), and reduced exacerbations better than either component alone. In studies of FP or of Sal/FP in COPD, there was a reduction in all-cause mortality by 25% relative to placebo. Sal/FP has anti-inflammatory effects in COPD airways. FP inhibits markers of systemic inflammation, and it is not known whether Sal/FP has an advantage over FP alone. While long-acting β(2)-agonists such as Sal can be recommended for treatment of moderate COPD, addition of inhaled steroid therapy such as FP should be considered in more severe disease.
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spelling pubmed-27071532009-07-27 Salmeterol/fluticasone combination in the treatment of COPD Chung, K F Int J Chron Obstruct Pulmon Dis Review Clinical trials of a combination therapy of an inhaled corticosteroid, fluticasone propionate (FP), with a long-acting β(2)-agonist, salmeterol (Sal), have demonstrated a greater improvement in lung function and in quality of life measures after the combination compared with either component of alone. In a subanalysis of the data of the TRISTAN study, Sal/FP reduced exacerbation rates in COPD patients with a baseline FEV(1)<50% of predicted. A combination therapy of budesonide and formoterol improved quality of life and FEV(1), and reduced exacerbations better than either component alone. In studies of FP or of Sal/FP in COPD, there was a reduction in all-cause mortality by 25% relative to placebo. Sal/FP has anti-inflammatory effects in COPD airways. FP inhibits markers of systemic inflammation, and it is not known whether Sal/FP has an advantage over FP alone. While long-acting β(2)-agonists such as Sal can be recommended for treatment of moderate COPD, addition of inhaled steroid therapy such as FP should be considered in more severe disease. Dove Medical Press 2006-09 2006-09 /pmc/articles/PMC2707153/ /pubmed/18046860 Text en © 2006 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Chung, K F
Salmeterol/fluticasone combination in the treatment of COPD
title Salmeterol/fluticasone combination in the treatment of COPD
title_full Salmeterol/fluticasone combination in the treatment of COPD
title_fullStr Salmeterol/fluticasone combination in the treatment of COPD
title_full_unstemmed Salmeterol/fluticasone combination in the treatment of COPD
title_short Salmeterol/fluticasone combination in the treatment of COPD
title_sort salmeterol/fluticasone combination in the treatment of copd
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2707153/
https://www.ncbi.nlm.nih.gov/pubmed/18046860
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