Impact of baseline COPD symptom severity on the benefit from dual


Journal

Therapeutic advances in respiratory disease
ISSN: 1753-4666
Titre abrégé: Ther Adv Respir Dis
Pays: England
ID NLM: 101316317

Informations de publication

Date de publication:
Historique:
entrez: 10 11 2020
pubmed: 11 11 2020
medline: 16 9 2021
Statut: ppublish

Résumé

Symptom relief is a key treatment goal in patients with chronic obstructive pulmonary disease (COPD). However, there are limited data available on the response to bronchodilator therapy in patients at low risk of exacerbations with different levels of symptom severity. This study compared treatment responses in patients with a range of symptom severities as indicated by baseline COPD assessment test (CAT) scores. The 24-week EMAX trial evaluated the benefits of umeclidinium/vilanterol Of the intent-to-treat population ( Patients with symptomatic COPD benefit similarly from dual bronchodilator treatment with umeclidinium/vilanterol. Fractional polynomial analyses demonstrated the greatest treatment differences favouring dual therapy in patients with a CAT score <20, although benefits were seen up to scores of 30. This suggests that dual bronchodilation may be considered as initial therapy for patients across a broad range of symptom severities, not only those with severe symptoms (CAT ⩾20).

Identifiants

pubmed: 33167780
doi: 10.1177/1753466620968500
pmc: PMC7659027
doi:

Substances chimiques

Adrenergic beta-2 Receptor Agonists 0
Benzyl Alcohols 0
Bronchodilator Agents 0
Chlorobenzenes 0
Drug Combinations 0
GSK573719 0
Muscarinic Antagonists 0
Quinuclidines 0
vilanterol 028LZY775B
Salmeterol Xinafoate 6EW8Q962A5

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1753466620968500

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Auteurs

Claus F Vogelmeier (CF)

Department of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-Universität Marburg, Germany.
Member of the German Centre for Lung Research (DZL), Baldingerstraße, Marburg 35043, Germany.

Edward M Kerwin (EM)

Clinical Research Institute of Southern Oregon, Medford, OR, USA.

Leif H Bjermer (LH)

Respiratory Medicine and Allergology, Lund University, Lund, Sweden.

Lee Tombs (L)

Precise Approach Ltd, Contingent Worker on Assignment at GSK, Stockley Park West, Uxbridge, Middlesex, UK.

Paul W Jones (PW)

GSK, Brentford, Middlesex, UK.

Isabelle H Boucot (IH)

GSK, Brentford, Middlesex, UK.

Ian P Naya (IP)

GSK, Brentford, Middlesex, UK.
RAMAX Ltd., Bramhall, Cheshire, UK.

David A Lipson (DA)

Respiratory Clinical Sciences, GSK, Collegeville, PA, USA.
Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Chris Compton (C)

GSK, Brentford, Middlesex, UK.

Neil Barnes (N)

GSK, Brentford, Middlesex, UK.

François Maltais (F)

Centre de Pneumologie, Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval, Québec, Québec, Canada.

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Classifications MeSH