Effects of short- and long-acting beta-agonists on asthma exacerbations: a prospective cohort.


Journal

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
ISSN: 1534-4436
Titre abrégé: Ann Allergy Asthma Immunol
Pays: United States
ID NLM: 9503580

Informations de publication

Date de publication:
03 2020
Historique:
received: 17 09 2019
revised: 13 11 2019
accepted: 08 12 2019
pubmed: 22 12 2019
medline: 12 5 2020
entrez: 22 12 2019
Statut: ppublish

Résumé

In asthma, short- and long-acting β-agonists (SABAs and LABAs) should be used together with inhaled corticosteroids (ICS), and regular use is inappropriate. To assess the relationship between patterns of use of therapy and asthma exacerbations (AEx). Patients with asthma (6-40 years) were enrolled in France and the United Kingdom. Prescribing data, computer-assisted telephone interviews (CATIs), and text messages assessed medication use and AEx over a maximum period of 24 months. Generalized linear mixed models provided AEx risks associated with therapy. Among the 908 patients (median age: 20.0 years, 46.6% women, 24.5% children) answering a total of 4248 CATIs over 486 (±235) days, regular (ie, daily) use was more frequent for single LABAs and fixed dose combinations (FDCs) than for single ICS (75.6%, 70.1%, and 65.4% of investigated periods of use, respectively). Regular (ie, daily or almost daily) SABA use was observed for 21.1% of periods of use. Altogether, 265 patients (29.2%) experienced 1 or more AEx. The ORs for AEx risk related to regular vs no use of FDCs, single ICS, and single LABAs were 0.98 (95% CI = [0.73-1.33]), 0.90 (95% CI = [0.61-1.33]), and 1.29 (95% CI = [0.76-2.17]), respectively, after adjustment for cotherapy, sociodemographic, and disease characteristics. The OR was 2.09 (95% CI = [1.36-3.21]) in regular SABA users. Inhaled corticosteroids and FDCs were often used intermittently, whereas SABAs and LABAs could be used regularly, and exacerbations were frequent. Compared with non-users, the risk of exacerbation increased moderately under regular use of single LABAs, whereas it doubled, significantly, in regular SABA users, likely in relationship with poor overall asthma control.

Sections du résumé

BACKGROUND
In asthma, short- and long-acting β-agonists (SABAs and LABAs) should be used together with inhaled corticosteroids (ICS), and regular use is inappropriate.
OBJECTIVE
To assess the relationship between patterns of use of therapy and asthma exacerbations (AEx).
METHODS
Patients with asthma (6-40 years) were enrolled in France and the United Kingdom. Prescribing data, computer-assisted telephone interviews (CATIs), and text messages assessed medication use and AEx over a maximum period of 24 months. Generalized linear mixed models provided AEx risks associated with therapy.
RESULTS
Among the 908 patients (median age: 20.0 years, 46.6% women, 24.5% children) answering a total of 4248 CATIs over 486 (±235) days, regular (ie, daily) use was more frequent for single LABAs and fixed dose combinations (FDCs) than for single ICS (75.6%, 70.1%, and 65.4% of investigated periods of use, respectively). Regular (ie, daily or almost daily) SABA use was observed for 21.1% of periods of use. Altogether, 265 patients (29.2%) experienced 1 or more AEx. The ORs for AEx risk related to regular vs no use of FDCs, single ICS, and single LABAs were 0.98 (95% CI = [0.73-1.33]), 0.90 (95% CI = [0.61-1.33]), and 1.29 (95% CI = [0.76-2.17]), respectively, after adjustment for cotherapy, sociodemographic, and disease characteristics. The OR was 2.09 (95% CI = [1.36-3.21]) in regular SABA users.
CONCLUSION
Inhaled corticosteroids and FDCs were often used intermittently, whereas SABAs and LABAs could be used regularly, and exacerbations were frequent. Compared with non-users, the risk of exacerbation increased moderately under regular use of single LABAs, whereas it doubled, significantly, in regular SABA users, likely in relationship with poor overall asthma control.

Identifiants

pubmed: 31862434
pii: S1081-1206(19)31490-5
doi: 10.1016/j.anai.2019.12.012
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Adrenergic beta-Agonists 0
Anti-Asthmatic Agents 0
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

254-260

Informations de copyright

Copyright © 2019 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Eric Van Ganse (E)

Lyon Pharmaco-Epidemiology Unit, Health Services and Performance Research (HESPER), Claude Bernard Lyon 1 University, Lyon, France; Respiratory Medicine, Croix-Rousse University Hospital, Lyon, France; PELyon, Lyon, France. Electronic address: eric.van-ganse@univ-lyon1.fr.

Nathalie Texier (N)

Kappa Santé, Paris, France.

Alexandra L Dima (AL)

Amsterdam School of Communication Research ASCoR, University of Amsterdam, the Netherlands.

Manon Belhassen (M)

Lyon Pharmaco-Epidemiology Unit, Health Services and Performance Research (HESPER), Claude Bernard Lyon 1 University, Lyon, France; PELyon, Lyon, France.

Laurent Laforest (L)

Lyon Pharmaco-Epidemiology Unit, Health Services and Performance Research (HESPER), Claude Bernard Lyon 1 University, Lyon, France.

Sandrine Herbage (S)

Lyon Pharmaco-Epidemiology Unit, Health Services and Performance Research (HESPER), Claude Bernard Lyon 1 University, Lyon, France.

Stéphane Schuck (S)

Kappa Santé, Paris, France.

Gimena Hernandez (G)

IMIM-Hospital del Mar Medical, Research Institute, Barcelona, Spain.

Olatz Garin (O)

IMIM-Hospital del Mar Medical, Research Institute, Barcelona, Spain.

Montse Ferrer (M)

IMIM-Hospital del Mar Medical, Research Institute, Barcelona, Spain.

Marijn de Bruin (M)

Amsterdam School of Communication Research ASCoR, University of Amsterdam, the Netherlands; University of Aberdeen, Scotland.

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Classifications MeSH