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Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease

BACKGROUND: The changes in inspiratory capacity (IC) over time in chronic obstructive pulmonary disease (COPD) patients are unknown. The Understanding Potential Long-term Impacts on Function with Tiotropium (UPLIFT®) trial included IC measurements. METHODS: IC analysis from UPLIFT® (N = 5992) was pe...

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Autores principales: Celli, Bartolome R, Decramer, Marc, Lystig, Theodore, Kesten, Steven, Tashkin, Donald P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443002/
https://www.ncbi.nlm.nih.gov/pubmed/22866681
http://dx.doi.org/10.1186/1465-9921-13-66
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author Celli, Bartolome R
Decramer, Marc
Lystig, Theodore
Kesten, Steven
Tashkin, Donald P
author_facet Celli, Bartolome R
Decramer, Marc
Lystig, Theodore
Kesten, Steven
Tashkin, Donald P
author_sort Celli, Bartolome R
collection PubMed
description BACKGROUND: The changes in inspiratory capacity (IC) over time in chronic obstructive pulmonary disease (COPD) patients are unknown. The Understanding Potential Long-term Impacts on Function with Tiotropium (UPLIFT®) trial included IC measurements. METHODS: IC analysis from UPLIFT® (N = 5992) was performed at 1 and 6 months, and every 6 months through 4 years. Annualized rate of decline in pre- and post-bronchodilator IC and mean differences at each time point were analyzed by mixed-effects models. The relationships between baseline IC and exacerbation rate and mortality were explored using Cox regression analysis. RESULTS: Baseline characteristics: age, 65 years; 75% men; post-bronchodilator forced expiratory volume in 1 second, 1.32 L (48% predicted); pre- and post-bronchodilator IC, 2.03 and 2.33 L. Mean IC rate of decline (mL/year) was 34 ± 2 (1.7% of baseline) and 50 ± 3 (2.1% of baseline) pre- and post-bronchodilator, respectively, without significant between-group differences. Morning pre-bronchodilator (trough) IC improved with tiotropium versus placebo: 124 mL (1 month), 103 mL (1 year), 107 mL (2 years), 98 mL (3 years), and 97 mL (4 years) (all p < 0.001). Post-bronchodilator improvements were similar between treatment groups. Lower baseline IC values were associated with reduced time to first exacerbation. For the lowest quartile (n = 1413) the values in months were 14.3 (11.7–17.0) for tiotropium and 10.3 (8.8–11.7) for controls (p < 0.01). CONCLUSION: IC declines from approximately 34 to 50 mL/year in patients with stage II to IV COPD. Tiotropium treatment does not change the IC decline rate but provides 24-hour improvements in IC sustained over the long term. Trough IC differences suggest that tiotropium provides sustained decrease in end-expiratory lung volume.
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spelling pubmed-34430022012-09-15 Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease Celli, Bartolome R Decramer, Marc Lystig, Theodore Kesten, Steven Tashkin, Donald P Respir Res Research BACKGROUND: The changes in inspiratory capacity (IC) over time in chronic obstructive pulmonary disease (COPD) patients are unknown. The Understanding Potential Long-term Impacts on Function with Tiotropium (UPLIFT®) trial included IC measurements. METHODS: IC analysis from UPLIFT® (N = 5992) was performed at 1 and 6 months, and every 6 months through 4 years. Annualized rate of decline in pre- and post-bronchodilator IC and mean differences at each time point were analyzed by mixed-effects models. The relationships between baseline IC and exacerbation rate and mortality were explored using Cox regression analysis. RESULTS: Baseline characteristics: age, 65 years; 75% men; post-bronchodilator forced expiratory volume in 1 second, 1.32 L (48% predicted); pre- and post-bronchodilator IC, 2.03 and 2.33 L. Mean IC rate of decline (mL/year) was 34 ± 2 (1.7% of baseline) and 50 ± 3 (2.1% of baseline) pre- and post-bronchodilator, respectively, without significant between-group differences. Morning pre-bronchodilator (trough) IC improved with tiotropium versus placebo: 124 mL (1 month), 103 mL (1 year), 107 mL (2 years), 98 mL (3 years), and 97 mL (4 years) (all p < 0.001). Post-bronchodilator improvements were similar between treatment groups. Lower baseline IC values were associated with reduced time to first exacerbation. For the lowest quartile (n = 1413) the values in months were 14.3 (11.7–17.0) for tiotropium and 10.3 (8.8–11.7) for controls (p < 0.01). CONCLUSION: IC declines from approximately 34 to 50 mL/year in patients with stage II to IV COPD. Tiotropium treatment does not change the IC decline rate but provides 24-hour improvements in IC sustained over the long term. Trough IC differences suggest that tiotropium provides sustained decrease in end-expiratory lung volume. BioMed Central 2012 2012-08-06 /pmc/articles/PMC3443002/ /pubmed/22866681 http://dx.doi.org/10.1186/1465-9921-13-66 Text en Copyright ©2012 Celli 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
Celli, Bartolome R
Decramer, Marc
Lystig, Theodore
Kesten, Steven
Tashkin, Donald P
Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title_full Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title_fullStr Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title_full_unstemmed Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title_short Longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
title_sort longitudinal inspiratory capacity changes in chronic obstructive pulmonary disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443002/
https://www.ncbi.nlm.nih.gov/pubmed/22866681
http://dx.doi.org/10.1186/1465-9921-13-66
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