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Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial

BACKGROUND: Exacerbations of chronic obstructive pulmonary disease (COPD) are associated with loss of lung function and poor outcomes for patients. However, there are limited data on the time course of changes in forced expiratory volume in 1 s (FEV(1)) preceding the first reported symptom and after...

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Autores principales: Watz, Henrik, Tetzlaff, Kay, Magnussen, Helgo, Mueller, Achim, Rodriguez-Roisin, Roberto, Wouters, Emiel F. M., Vogelmeier, Claus, Calverley, Peter M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293570/
https://www.ncbi.nlm.nih.gov/pubmed/30545350
http://dx.doi.org/10.1186/s12931-018-0944-3
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author Watz, Henrik
Tetzlaff, Kay
Magnussen, Helgo
Mueller, Achim
Rodriguez-Roisin, Roberto
Wouters, Emiel F. M.
Vogelmeier, Claus
Calverley, Peter M. A.
author_facet Watz, Henrik
Tetzlaff, Kay
Magnussen, Helgo
Mueller, Achim
Rodriguez-Roisin, Roberto
Wouters, Emiel F. M.
Vogelmeier, Claus
Calverley, Peter M. A.
author_sort Watz, Henrik
collection PubMed
description BACKGROUND: Exacerbations of chronic obstructive pulmonary disease (COPD) are associated with loss of lung function and poor outcomes for patients. However, there are limited data on the time course of changes in forced expiratory volume in 1 s (FEV(1)) preceding the first reported symptom and after the start of an exacerbation. METHODS: WISDOM was a multinational, randomized, double-blind, active-controlled, 52-week study in patients with severe-to-very severe COPD. Patients received triple therapy (long-acting muscarinic antagonist and long-acting β(2)-agonist/inhaled corticosteroid [ICS]) for 6 weeks, and were randomized to continue triple therapy or stepwise withdrawal of the ICS (dual bronchodilator group). After suitable training, patients performed daily spirometry at home using a portable, battery-operated spirometer. In the present post hoc analysis, patients who continued to perform daily home spirometry and completed at least one measurement per week for a 56-day period before and after the start of a moderate or severe exacerbation were included. Missing values were imputed by linear interpolation (intermittent), backfilling (beginning) or carry forward (end). Exacerbation onset was the first day of a reported symptom of exacerbation. RESULTS: Eight hundred and eighty-eight patients in the WISDOM study had a moderate/severe exacerbation after the complete ICS withdrawal visit; 360 of them contributed at least one FEV(1) measure per week for the 8 weeks before and after the event and are included in this analysis. Mean daily FEV(1) began to decline from approximately 2 weeks before the onset of symptoms of an exacerbation, dropping from 0.907 L (mean Days − 56 to − 36 before the exacerbation) to 0.860 L on the first day of the exacerbation. After the exacerbation, mean FEV(1) improved but did not return to pre-exacerbation levels (mean Days 36–56 after the exacerbation, 0.875 L). The pattern of FEV(1) changes around exacerbations was similar in the triple therapy and dual bronchodilator groups, and a similar pattern was seen in moderate and severe exacerbations when analysed separately. CONCLUSIONS: Mean lung function starts to decline prior to the first reported symptoms of an exacerbation, and does not recover to pre-exacerbation levels 8 weeks after the event. TRIAL REGISTRATION: WISDOM (ClinicalTrials.gov number, NCT00975195). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0944-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-62935702018-12-18 Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial Watz, Henrik Tetzlaff, Kay Magnussen, Helgo Mueller, Achim Rodriguez-Roisin, Roberto Wouters, Emiel F. M. Vogelmeier, Claus Calverley, Peter M. A. Respir Res Research BACKGROUND: Exacerbations of chronic obstructive pulmonary disease (COPD) are associated with loss of lung function and poor outcomes for patients. However, there are limited data on the time course of changes in forced expiratory volume in 1 s (FEV(1)) preceding the first reported symptom and after the start of an exacerbation. METHODS: WISDOM was a multinational, randomized, double-blind, active-controlled, 52-week study in patients with severe-to-very severe COPD. Patients received triple therapy (long-acting muscarinic antagonist and long-acting β(2)-agonist/inhaled corticosteroid [ICS]) for 6 weeks, and were randomized to continue triple therapy or stepwise withdrawal of the ICS (dual bronchodilator group). After suitable training, patients performed daily spirometry at home using a portable, battery-operated spirometer. In the present post hoc analysis, patients who continued to perform daily home spirometry and completed at least one measurement per week for a 56-day period before and after the start of a moderate or severe exacerbation were included. Missing values were imputed by linear interpolation (intermittent), backfilling (beginning) or carry forward (end). Exacerbation onset was the first day of a reported symptom of exacerbation. RESULTS: Eight hundred and eighty-eight patients in the WISDOM study had a moderate/severe exacerbation after the complete ICS withdrawal visit; 360 of them contributed at least one FEV(1) measure per week for the 8 weeks before and after the event and are included in this analysis. Mean daily FEV(1) began to decline from approximately 2 weeks before the onset of symptoms of an exacerbation, dropping from 0.907 L (mean Days − 56 to − 36 before the exacerbation) to 0.860 L on the first day of the exacerbation. After the exacerbation, mean FEV(1) improved but did not return to pre-exacerbation levels (mean Days 36–56 after the exacerbation, 0.875 L). The pattern of FEV(1) changes around exacerbations was similar in the triple therapy and dual bronchodilator groups, and a similar pattern was seen in moderate and severe exacerbations when analysed separately. CONCLUSIONS: Mean lung function starts to decline prior to the first reported symptoms of an exacerbation, and does not recover to pre-exacerbation levels 8 weeks after the event. TRIAL REGISTRATION: WISDOM (ClinicalTrials.gov number, NCT00975195). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-018-0944-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-13 2018 /pmc/articles/PMC6293570/ /pubmed/30545350 http://dx.doi.org/10.1186/s12931-018-0944-3 Text en © The Author(s). 2018 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 Research
Watz, Henrik
Tetzlaff, Kay
Magnussen, Helgo
Mueller, Achim
Rodriguez-Roisin, Roberto
Wouters, Emiel F. M.
Vogelmeier, Claus
Calverley, Peter M. A.
Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title_full Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title_fullStr Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title_full_unstemmed Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title_short Spirometric changes during exacerbations of COPD: a post hoc analysis of the WISDOM trial
title_sort spirometric changes during exacerbations of copd: a post hoc analysis of the wisdom trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293570/
https://www.ncbi.nlm.nih.gov/pubmed/30545350
http://dx.doi.org/10.1186/s12931-018-0944-3
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