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Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial
BACKGROUND: Data examining the characteristics of patients with frequent exacerbations of chronic obstructive pulmonary disease (COPD) and associated hospitalisations and mortality are scarce. METHODS: Post-hoc analysis of the Prevention Of Exacerbations with Tiotropium in COPD (POET-COPD) trial, ta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833311/ https://www.ncbi.nlm.nih.gov/pubmed/24168767 http://dx.doi.org/10.1186/1465-9921-14-116 |
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author | Beeh, Kai M Glaab, Thomas Stowasser, Susanne Schmidt, Hendrik Fabbri, Leonardo M Rabe, Klaus F Vogelmeier, Claus F |
author_facet | Beeh, Kai M Glaab, Thomas Stowasser, Susanne Schmidt, Hendrik Fabbri, Leonardo M Rabe, Klaus F Vogelmeier, Claus F |
author_sort | Beeh, Kai M |
collection | PubMed |
description | BACKGROUND: Data examining the characteristics of patients with frequent exacerbations of chronic obstructive pulmonary disease (COPD) and associated hospitalisations and mortality are scarce. METHODS: Post-hoc analysis of the Prevention Of Exacerbations with Tiotropium in COPD (POET-COPD) trial, targeting exacerbations as the primary endpoint. Patients were classified as non-, infrequent, and frequent exacerbators (0, 1, or ≥ 2 exacerbations during study treatment), irrespective of study treatment. A multivariate Cox regression model assessed the effect of covariates on time to first exacerbation. RESULTS: In total, 7376 patients were included in the analysis: 63.5% non-exacerbators, 22.9% infrequent, 13.6% frequent exacerbators. Factors significantly associated with exacerbation risk were age, sex, body mass index, COPD duration and severity, smoking history, baseline inhaled corticosteroid use, and preceding antibiotic or systemic corticosteroid courses. Frequent exacerbators had greater severity and duration of COPD, received more pulmonary medication, and ≥ 2 systemic corticosteroid or antibiotic courses in the preceding year, and were more likely to be female and ex-smokers. The small proportion of frequent exacerbators (13.6%) accounted for 56.6% of exacerbation-related hospitalisations, which, overall, were associated with a three-fold increase in mortality. CONCLUSION: The frequent exacerbator phenotype was closely associated with exacerbation-related hospitalisations, and exacerbation-related hospitalisations were associated with poorer survival. TRIAL REGISTRATION: NCT00563381; Study identifier: BI 205.389. |
format | Online Article Text |
id | pubmed-3833311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38333112013-11-20 Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial Beeh, Kai M Glaab, Thomas Stowasser, Susanne Schmidt, Hendrik Fabbri, Leonardo M Rabe, Klaus F Vogelmeier, Claus F Respir Res Research BACKGROUND: Data examining the characteristics of patients with frequent exacerbations of chronic obstructive pulmonary disease (COPD) and associated hospitalisations and mortality are scarce. METHODS: Post-hoc analysis of the Prevention Of Exacerbations with Tiotropium in COPD (POET-COPD) trial, targeting exacerbations as the primary endpoint. Patients were classified as non-, infrequent, and frequent exacerbators (0, 1, or ≥ 2 exacerbations during study treatment), irrespective of study treatment. A multivariate Cox regression model assessed the effect of covariates on time to first exacerbation. RESULTS: In total, 7376 patients were included in the analysis: 63.5% non-exacerbators, 22.9% infrequent, 13.6% frequent exacerbators. Factors significantly associated with exacerbation risk were age, sex, body mass index, COPD duration and severity, smoking history, baseline inhaled corticosteroid use, and preceding antibiotic or systemic corticosteroid courses. Frequent exacerbators had greater severity and duration of COPD, received more pulmonary medication, and ≥ 2 systemic corticosteroid or antibiotic courses in the preceding year, and were more likely to be female and ex-smokers. The small proportion of frequent exacerbators (13.6%) accounted for 56.6% of exacerbation-related hospitalisations, which, overall, were associated with a three-fold increase in mortality. CONCLUSION: The frequent exacerbator phenotype was closely associated with exacerbation-related hospitalisations, and exacerbation-related hospitalisations were associated with poorer survival. TRIAL REGISTRATION: NCT00563381; Study identifier: BI 205.389. BioMed Central 2013 2013-10-29 /pmc/articles/PMC3833311/ /pubmed/24168767 http://dx.doi.org/10.1186/1465-9921-14-116 Text en Copyright © 2013 Beeh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Beeh, Kai M Glaab, Thomas Stowasser, Susanne Schmidt, Hendrik Fabbri, Leonardo M Rabe, Klaus F Vogelmeier, Claus F Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title | Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title_full | Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title_fullStr | Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title_full_unstemmed | Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title_short | Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial |
title_sort | characterisation of exacerbation risk and exacerbator phenotypes in the poet-copd trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833311/ https://www.ncbi.nlm.nih.gov/pubmed/24168767 http://dx.doi.org/10.1186/1465-9921-14-116 |
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