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Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial

BACKGROUND: Symptom severity is the largest factor in determining subjective health in COPD. Symptoms (eg, chronic cough, dyspnea) are associated with decreased health-related quality of life (HRQoL). We evaluated the impact of arformoterol on HRQoL in COPD patients, measured by St George’s Respirat...

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Autores principales: Donohue, James F, Bollu, Vamsi K, Stull, Donald E, Nelson, Lauren M, Williams, Valerie SL, Stensland, Michael D, Hanania, Nicola A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804733/
https://www.ncbi.nlm.nih.gov/pubmed/29440887
http://dx.doi.org/10.2147/COPD.S141729
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author Donohue, James F
Bollu, Vamsi K
Stull, Donald E
Nelson, Lauren M
Williams, Valerie SL
Stensland, Michael D
Hanania, Nicola A
author_facet Donohue, James F
Bollu, Vamsi K
Stull, Donald E
Nelson, Lauren M
Williams, Valerie SL
Stensland, Michael D
Hanania, Nicola A
author_sort Donohue, James F
collection PubMed
description BACKGROUND: Symptom severity is the largest factor in determining subjective health in COPD. Symptoms (eg, chronic cough, dyspnea) are associated with decreased health-related quality of life (HRQoL). We evaluated the impact of arformoterol on HRQoL in COPD patients, measured by St George’s Respiratory Questionnaire (SGRQ). Post hoc growth mixture model (GMM) analysis examined symptom response profiles. METHODS: We examined data from a randomized, double-blind, parallel-group, 12-month safety trial of twice-daily nebulized arformoterol 15 µg (n=420) versus placebo (n=421). COPD severity was assessed by Global Initiative for Chronic Obstructive Lung Disease (GOLD) status. GMM analysis identified previously unknown patient subgroups and examined the heterogeneity in response to SGRQ Symptoms scores. RESULTS: SGRQ Total score improved by 4.24 points with arformoterol and 2.02 points with placebo (P=0.006). Significantly greater improvements occurred for arformoterol versus placebo in SGRQ Symptoms (6.34 vs 4.25, P=0.031) and Impacts (3.91 vs 0.97, P=0.001) scores, but not in Activity score (3.57 vs 1.75, P=0.057). GMM identified responders and nonresponders based on the SGRQ Symptoms score. End-of-study mean difference in SGRQ Symptoms scores between these latent classes was 20.7 points (P<0.001; 95% confidence interval: 17.6–23.9). Compared with nonresponders, responders were more likely current smokers (55.52% vs 44.02%, P=0.0021) and had more severe COPD (forced expiratory volume in 1 second [FEV(1)]: 1.16 vs 1.23 L, P=0.0419), more exacerbations (0.96 vs 0.69, P=0.0018), and worse mean SGRQ Total (59.81 vs 40.57, P<0.0001), Clinical COPD Questionnaire (3.29 vs 2.05, P<0.0001), and Modified Medical Research Council Dyspnea Scale (3.13 vs 2.75, P<0.0001) scores. Arformoterol-receiving responders exhibited significantly greater improvements in FEV(1) (0.09 vs 0.008, P=0.03) and fewer hospitalizations (0.13 vs 0.24, P=0.02) than those receiving placebo. CONCLUSION: In this study, arformoterol treatment significantly improved HRQoL reflected by SGRQ. For the analysis performed on these data, arformoterol may be particularly effective in improving lung function and reducing hospitalizations among patients who are unable to quit smoking or present with more severe symptoms.
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spelling pubmed-58047332018-02-13 Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial Donohue, James F Bollu, Vamsi K Stull, Donald E Nelson, Lauren M Williams, Valerie SL Stensland, Michael D Hanania, Nicola A Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Symptom severity is the largest factor in determining subjective health in COPD. Symptoms (eg, chronic cough, dyspnea) are associated with decreased health-related quality of life (HRQoL). We evaluated the impact of arformoterol on HRQoL in COPD patients, measured by St George’s Respiratory Questionnaire (SGRQ). Post hoc growth mixture model (GMM) analysis examined symptom response profiles. METHODS: We examined data from a randomized, double-blind, parallel-group, 12-month safety trial of twice-daily nebulized arformoterol 15 µg (n=420) versus placebo (n=421). COPD severity was assessed by Global Initiative for Chronic Obstructive Lung Disease (GOLD) status. GMM analysis identified previously unknown patient subgroups and examined the heterogeneity in response to SGRQ Symptoms scores. RESULTS: SGRQ Total score improved by 4.24 points with arformoterol and 2.02 points with placebo (P=0.006). Significantly greater improvements occurred for arformoterol versus placebo in SGRQ Symptoms (6.34 vs 4.25, P=0.031) and Impacts (3.91 vs 0.97, P=0.001) scores, but not in Activity score (3.57 vs 1.75, P=0.057). GMM identified responders and nonresponders based on the SGRQ Symptoms score. End-of-study mean difference in SGRQ Symptoms scores between these latent classes was 20.7 points (P<0.001; 95% confidence interval: 17.6–23.9). Compared with nonresponders, responders were more likely current smokers (55.52% vs 44.02%, P=0.0021) and had more severe COPD (forced expiratory volume in 1 second [FEV(1)]: 1.16 vs 1.23 L, P=0.0419), more exacerbations (0.96 vs 0.69, P=0.0018), and worse mean SGRQ Total (59.81 vs 40.57, P<0.0001), Clinical COPD Questionnaire (3.29 vs 2.05, P<0.0001), and Modified Medical Research Council Dyspnea Scale (3.13 vs 2.75, P<0.0001) scores. Arformoterol-receiving responders exhibited significantly greater improvements in FEV(1) (0.09 vs 0.008, P=0.03) and fewer hospitalizations (0.13 vs 0.24, P=0.02) than those receiving placebo. CONCLUSION: In this study, arformoterol treatment significantly improved HRQoL reflected by SGRQ. For the analysis performed on these data, arformoterol may be particularly effective in improving lung function and reducing hospitalizations among patients who are unable to quit smoking or present with more severe symptoms. Dove Medical Press 2018-02-05 /pmc/articles/PMC5804733/ /pubmed/29440887 http://dx.doi.org/10.2147/COPD.S141729 Text en © 2018 Donohue 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
Donohue, James F
Bollu, Vamsi K
Stull, Donald E
Nelson, Lauren M
Williams, Valerie SL
Stensland, Michael D
Hanania, Nicola A
Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title_full Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title_fullStr Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title_full_unstemmed Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title_short Long-term health-related quality-of-life and symptom response profiles with arformoterol in COPD: results from a 52-week trial
title_sort long-term health-related quality-of-life and symptom response profiles with arformoterol in copd: results from a 52-week trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804733/
https://www.ncbi.nlm.nih.gov/pubmed/29440887
http://dx.doi.org/10.2147/COPD.S141729
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