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COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort

BACKGROUND: Control in COPD is a dynamic concept that can reflect changes in patients’ clinical status that may have prognostic implications, but there is no information about changes in control status and its long-term consequences. METHODS: We classified 798 patients with COPD from the CHAIN cohor...

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Autores principales: Calle Rubio, Myriam, Rodriguez Hermosa, Juan Luis, de Torres, Juan P., Marín, José María, Martínez-González, Cristina, Fuster, Antonia, Cosío, Borja G., Peces-Barba, Germán, Solanes, Ingrid, Feu-Collado, Nuria, Lopez-Campos, Jose Luis, Casanova, Ciro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863480/
https://www.ncbi.nlm.nih.gov/pubmed/33541356
http://dx.doi.org/10.1186/s12931-021-01633-y
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author Calle Rubio, Myriam
Rodriguez Hermosa, Juan Luis
de Torres, Juan P.
Marín, José María
Martínez-González, Cristina
Fuster, Antonia
Cosío, Borja G.
Peces-Barba, Germán
Solanes, Ingrid
Feu-Collado, Nuria
Lopez-Campos, Jose Luis
Casanova, Ciro
author_facet Calle Rubio, Myriam
Rodriguez Hermosa, Juan Luis
de Torres, Juan P.
Marín, José María
Martínez-González, Cristina
Fuster, Antonia
Cosío, Borja G.
Peces-Barba, Germán
Solanes, Ingrid
Feu-Collado, Nuria
Lopez-Campos, Jose Luis
Casanova, Ciro
author_sort Calle Rubio, Myriam
collection PubMed
description BACKGROUND: Control in COPD is a dynamic concept that can reflect changes in patients’ clinical status that may have prognostic implications, but there is no information about changes in control status and its long-term consequences. METHODS: We classified 798 patients with COPD from the CHAIN cohort as controlled/uncontrolled at baseline and over 5 years. We describe the changes in control status in patients over long-term follow-up and analyze the factors that were associated with longitudinal control patterns and related survival using the Cox hazard analysis. RESULTS: 134 patients (16.8%) were considered persistently controlled, 248 (31.1%) persistently uncontrolled and 416 (52.1%) changed control status during follow-up. The variables significantly associated with persistent control were not requiring triple therapy at baseline and having a better quality of life. Annual changes in outcomes (health status, psychological status, airflow limitation) did not differ in patients, regardless of clinical control status. All-cause mortality was lower in persistently controlled patients (5.5% versus 19.1%, p = 0.001). The hazard ratio for all-cause mortality was 2.274 (95% CI 1.394–3.708; p = 0.001). Regarding pharmacological treatment, triple inhaled therapy was the most common option in persistently uncontrolled patients (72.2%). Patients with persistent disease control more frequently used bronchodilators for monotherapy (53%) at recruitment, although by the end of the follow-up period, 20% had scaled up their treatment, with triple therapy being the most frequent therapeutic pattern. CONCLUSIONS: The evaluation of COPD control status provides relevant prognostic information on survival. There is important variability in clinical control status and only a small proportion of the patients had persistently good control. Changes in the treatment pattern may be relevant in the longitudinal pattern of COPD clinical control. Further studies in other populations should validate our results. Trial registration: Clinical Trials.gov: identifier NCT01122758.
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spelling pubmed-78634802021-02-05 COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort Calle Rubio, Myriam Rodriguez Hermosa, Juan Luis de Torres, Juan P. Marín, José María Martínez-González, Cristina Fuster, Antonia Cosío, Borja G. Peces-Barba, Germán Solanes, Ingrid Feu-Collado, Nuria Lopez-Campos, Jose Luis Casanova, Ciro Respir Res Research BACKGROUND: Control in COPD is a dynamic concept that can reflect changes in patients’ clinical status that may have prognostic implications, but there is no information about changes in control status and its long-term consequences. METHODS: We classified 798 patients with COPD from the CHAIN cohort as controlled/uncontrolled at baseline and over 5 years. We describe the changes in control status in patients over long-term follow-up and analyze the factors that were associated with longitudinal control patterns and related survival using the Cox hazard analysis. RESULTS: 134 patients (16.8%) were considered persistently controlled, 248 (31.1%) persistently uncontrolled and 416 (52.1%) changed control status during follow-up. The variables significantly associated with persistent control were not requiring triple therapy at baseline and having a better quality of life. Annual changes in outcomes (health status, psychological status, airflow limitation) did not differ in patients, regardless of clinical control status. All-cause mortality was lower in persistently controlled patients (5.5% versus 19.1%, p = 0.001). The hazard ratio for all-cause mortality was 2.274 (95% CI 1.394–3.708; p = 0.001). Regarding pharmacological treatment, triple inhaled therapy was the most common option in persistently uncontrolled patients (72.2%). Patients with persistent disease control more frequently used bronchodilators for monotherapy (53%) at recruitment, although by the end of the follow-up period, 20% had scaled up their treatment, with triple therapy being the most frequent therapeutic pattern. CONCLUSIONS: The evaluation of COPD control status provides relevant prognostic information on survival. There is important variability in clinical control status and only a small proportion of the patients had persistently good control. Changes in the treatment pattern may be relevant in the longitudinal pattern of COPD clinical control. Further studies in other populations should validate our results. Trial registration: Clinical Trials.gov: identifier NCT01122758. BioMed Central 2021-02-04 2021 /pmc/articles/PMC7863480/ /pubmed/33541356 http://dx.doi.org/10.1186/s12931-021-01633-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Calle Rubio, Myriam
Rodriguez Hermosa, Juan Luis
de Torres, Juan P.
Marín, José María
Martínez-González, Cristina
Fuster, Antonia
Cosío, Borja G.
Peces-Barba, Germán
Solanes, Ingrid
Feu-Collado, Nuria
Lopez-Campos, Jose Luis
Casanova, Ciro
COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title_full COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title_fullStr COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title_full_unstemmed COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title_short COPD Clinical Control: predictors and long-term follow-up of the CHAIN cohort
title_sort copd clinical control: predictors and long-term follow-up of the chain cohort
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863480/
https://www.ncbi.nlm.nih.gov/pubmed/33541356
http://dx.doi.org/10.1186/s12931-021-01633-y
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