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Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population
Blood eosinophils are a potentially useful biomarker for guiding inhaled corticosteroid (ICS) treatment decisions in COPD. We investigated whether existing blood eosinophil counts predict benefit from initiation of ICS compared to bronchodilator therapy. We used routinely collected data from UK prim...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819252/ https://www.ncbi.nlm.nih.gov/pubmed/35141324 http://dx.doi.org/10.1183/23120541.00606-2021 |
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author | Ashdown, Helen F. Smith, Margaret McFadden, Emily Pavord, Ian D. Butler, Chris C. Bafadhel, Mona |
author_facet | Ashdown, Helen F. Smith, Margaret McFadden, Emily Pavord, Ian D. Butler, Chris C. Bafadhel, Mona |
author_sort | Ashdown, Helen F. |
collection | PubMed |
description | Blood eosinophils are a potentially useful biomarker for guiding inhaled corticosteroid (ICS) treatment decisions in COPD. We investigated whether existing blood eosinophil counts predict benefit from initiation of ICS compared to bronchodilator therapy. We used routinely collected data from UK primary care in the Clinical Practice Research Datalink. Participants were aged ≥40 years with COPD, were ICS-naïve and starting a new inhaled maintenance medication (intervention group: ICS; comparator group: long-acting bronchodilator, non-ICS). Primary outcome was time to first exacerbation, compared between ICS and non-ICS groups, stratified by blood eosinophils (“high” ≥150 cells·µL(−1) and “low” <150 cells·µL(−1)). Out of 9475 eligible patients, 53.9% initiated ICS and 46.1% non-ICS treatment with no difference in eosinophils between treatment groups (p=0.71). Exacerbation risk was higher in patients prescribed ICS than those prescribed non-ICS treatment, but with a lower risk in those with high eosinophils (hazard ratio (HR) 1.04, 95% CI 0.98–1.10) than low eosinophils (HR 1.19, 95% CI 1.09–1.31) (p-value for interaction 0.01). Risk of pneumonia hospitalisation with ICS was greatest in those with low eosinophils (HR 1.26, 95% CI 1.05–1.50; p-value for interaction 0.04). Results were similar whether the most recent blood eosinophil count or the mean of blood eosinophil counts was used. In a primary care population, the most recent blood eosinophil count could be used to guide initiation of ICS in COPD patients. We suggest that ICS should be considered in those with higher eosinophils and avoided in those with lower eosinophils (<150 cells·µL(−1)). |
format | Online Article Text |
id | pubmed-8819252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88192522022-02-08 Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population Ashdown, Helen F. Smith, Margaret McFadden, Emily Pavord, Ian D. Butler, Chris C. Bafadhel, Mona ERJ Open Res Original Research Article Blood eosinophils are a potentially useful biomarker for guiding inhaled corticosteroid (ICS) treatment decisions in COPD. We investigated whether existing blood eosinophil counts predict benefit from initiation of ICS compared to bronchodilator therapy. We used routinely collected data from UK primary care in the Clinical Practice Research Datalink. Participants were aged ≥40 years with COPD, were ICS-naïve and starting a new inhaled maintenance medication (intervention group: ICS; comparator group: long-acting bronchodilator, non-ICS). Primary outcome was time to first exacerbation, compared between ICS and non-ICS groups, stratified by blood eosinophils (“high” ≥150 cells·µL(−1) and “low” <150 cells·µL(−1)). Out of 9475 eligible patients, 53.9% initiated ICS and 46.1% non-ICS treatment with no difference in eosinophils between treatment groups (p=0.71). Exacerbation risk was higher in patients prescribed ICS than those prescribed non-ICS treatment, but with a lower risk in those with high eosinophils (hazard ratio (HR) 1.04, 95% CI 0.98–1.10) than low eosinophils (HR 1.19, 95% CI 1.09–1.31) (p-value for interaction 0.01). Risk of pneumonia hospitalisation with ICS was greatest in those with low eosinophils (HR 1.26, 95% CI 1.05–1.50; p-value for interaction 0.04). Results were similar whether the most recent blood eosinophil count or the mean of blood eosinophil counts was used. In a primary care population, the most recent blood eosinophil count could be used to guide initiation of ICS in COPD patients. We suggest that ICS should be considered in those with higher eosinophils and avoided in those with lower eosinophils (<150 cells·µL(−1)). European Respiratory Society 2021-02-07 /pmc/articles/PMC8819252/ /pubmed/35141324 http://dx.doi.org/10.1183/23120541.00606-2021 Text en Copyright ©The authors 2022 https://creativecommons.org/licenses/by/4.0/This version is distributed under the terms of the Creative Commons Attribution Licence 4.0. |
spellingShingle | Original Research Article Ashdown, Helen F. Smith, Margaret McFadden, Emily Pavord, Ian D. Butler, Chris C. Bafadhel, Mona Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title | Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title_full | Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title_fullStr | Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title_full_unstemmed | Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title_short | Blood eosinophils to guide inhaled maintenance therapy in a primary care COPD population |
title_sort | blood eosinophils to guide inhaled maintenance therapy in a primary care copd population |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819252/ https://www.ncbi.nlm.nih.gov/pubmed/35141324 http://dx.doi.org/10.1183/23120541.00606-2021 |
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