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COPD phenotypes: differences in survival
BACKGROUND: The aim of the study was to analyze the characteristics and survival of a group of patients with COPD according to their clinical phenotype. PATIENTS AND METHODS: The study population was selected from patients undergoing scheduled spirometry between January 1, 2011 and June 30, 2011 at...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055897/ https://www.ncbi.nlm.nih.gov/pubmed/30050297 http://dx.doi.org/10.2147/COPD.S166163 |
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author | Hernández Vázquez, Julio Ali García, Ismael Jiménez-García, Rodrigo Álvaro Meca, Alejandro López de Andrés, Ana Matesanz Ruiz, Carmen Buendía García, María Jesús de Miguel Díez, Javier |
author_facet | Hernández Vázquez, Julio Ali García, Ismael Jiménez-García, Rodrigo Álvaro Meca, Alejandro López de Andrés, Ana Matesanz Ruiz, Carmen Buendía García, María Jesús de Miguel Díez, Javier |
author_sort | Hernández Vázquez, Julio |
collection | PubMed |
description | BACKGROUND: The aim of the study was to analyze the characteristics and survival of a group of patients with COPD according to their clinical phenotype. PATIENTS AND METHODS: The study population was selected from patients undergoing scheduled spirometry between January 1, 2011 and June 30, 2011 at the respiratory function laboratory of a teaching hospital and comprised those with a previous and confirmed diagnosis of COPD and forced expiratory volume in the first second (FEV(1)) of <70%. The patients selected were classified into 4 groups: positive bronchodilator response, non-exacerbator, exacerbator with emphysema, and exacerbator with chronic bronchitis. Patients were followed up until April 2017. RESULTS: We recruited 273 patients, of whom 89% were men. The distribution by phenotype was as follows: non-exacerbator, 47.2%; positive bronchodilator response, 25.8%; exacerbator with chronic bronchitis, 13.8%; and exacerbator with emphysema, 13.0%. A total of 90 patients died during follow-up (32.9%). Taking patients with a positive bronchodilator response as the reference category, the risk factors that were independently associated with death were older age (HR, 1.06; 95% CI, 1.03–1.09), lower FEV(1) (HR, 0.98; 95% CI, 0.96–0.99), and exacerbator with chronic bronchitis phenotype (HR, 3.28; 95% CI, 1.53–7.03). CONCLUSION: Classification of COPD patients by phenotype makes it possible to identify subgroups with different prognoses. Thus, mortality was greater in exacerbators with chronic bronchitis and lower in those with a positive bronchodilator response. |
format | Online Article Text |
id | pubmed-6055897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60558972018-07-26 COPD phenotypes: differences in survival Hernández Vázquez, Julio Ali García, Ismael Jiménez-García, Rodrigo Álvaro Meca, Alejandro López de Andrés, Ana Matesanz Ruiz, Carmen Buendía García, María Jesús de Miguel Díez, Javier Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: The aim of the study was to analyze the characteristics and survival of a group of patients with COPD according to their clinical phenotype. PATIENTS AND METHODS: The study population was selected from patients undergoing scheduled spirometry between January 1, 2011 and June 30, 2011 at the respiratory function laboratory of a teaching hospital and comprised those with a previous and confirmed diagnosis of COPD and forced expiratory volume in the first second (FEV(1)) of <70%. The patients selected were classified into 4 groups: positive bronchodilator response, non-exacerbator, exacerbator with emphysema, and exacerbator with chronic bronchitis. Patients were followed up until April 2017. RESULTS: We recruited 273 patients, of whom 89% were men. The distribution by phenotype was as follows: non-exacerbator, 47.2%; positive bronchodilator response, 25.8%; exacerbator with chronic bronchitis, 13.8%; and exacerbator with emphysema, 13.0%. A total of 90 patients died during follow-up (32.9%). Taking patients with a positive bronchodilator response as the reference category, the risk factors that were independently associated with death were older age (HR, 1.06; 95% CI, 1.03–1.09), lower FEV(1) (HR, 0.98; 95% CI, 0.96–0.99), and exacerbator with chronic bronchitis phenotype (HR, 3.28; 95% CI, 1.53–7.03). CONCLUSION: Classification of COPD patients by phenotype makes it possible to identify subgroups with different prognoses. Thus, mortality was greater in exacerbators with chronic bronchitis and lower in those with a positive bronchodilator response. Dove Medical Press 2018-07-20 /pmc/articles/PMC6055897/ /pubmed/30050297 http://dx.doi.org/10.2147/COPD.S166163 Text en © 2018 Hernández Vázquez et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Hernández Vázquez, Julio Ali García, Ismael Jiménez-García, Rodrigo Álvaro Meca, Alejandro López de Andrés, Ana Matesanz Ruiz, Carmen Buendía García, María Jesús de Miguel Díez, Javier COPD phenotypes: differences in survival |
title | COPD phenotypes: differences in survival |
title_full | COPD phenotypes: differences in survival |
title_fullStr | COPD phenotypes: differences in survival |
title_full_unstemmed | COPD phenotypes: differences in survival |
title_short | COPD phenotypes: differences in survival |
title_sort | copd phenotypes: differences in survival |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055897/ https://www.ncbi.nlm.nih.gov/pubmed/30050297 http://dx.doi.org/10.2147/COPD.S166163 |
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