How can the findings of the EMAX trial on long-acting bronchodilation in chronic obstructive pulmonary disease be applied in the primary care setting?

Author:

Kerwin Edward M1ORCID,Jones Paul W2,Bjermer Leif H3,Maltais François4,Boucot Isabelle H2,Naya Ian P2,Lipson David A56ORCID,Compton Chris2,Tombs Lee7,Vogelmeier Claus F8

Affiliation:

1. Clinical Trials Department, Altitude Clinical Consulting and Clinical Research Institute of Southern Oregon, Medford, OR, USA

2. GSK, Brentford, UK

3. Department of Clinical Sciences, Respiratory Medicine and Allergology, Lund University, Lund, Sweden

4. Centre de Pneumologie, Institut Universitaire de Cardiologie et de Pneumologie de Québec, Université Laval, Québec, QC, Canada

5. Respiratory Clinical Sciences, GSK, Collegeville, PA, USA

6. Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

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

8. Department of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-Universität Marburg, Marburg, Germany

Abstract

This review addresses outstanding questions regarding initial pharmacological management of chronic obstructive pulmonary disease (COPD). Optimizing initial treatment improves clinical outcomes in symptomatic patients, including those with low exacerbation risk. Long-acting muscarinic antagonist/long-acting β2-agonist (LAMA/LABA) dual therapy improves lung function versus LAMA or LABA monotherapy, although other treatment benefits have been less consistently observed. The benefits of dual bronchodilation in symptomatic patients with COPD at low exacerbation risk, and its duration of efficacy and cost effectiveness in this population, are not yet fully established. Questions remain on the impact of baseline symptom severity, prior treatment, degree of reversibility to bronchodilators, and smoking status on responses to dual bronchodilator treatment. Using evidence from EMAX (NCT03034915), a 6-month trial comparing the LAMA/LABA combination umeclidinium/vilanterol with umeclidinium and salmeterol monotherapy in symptomatic patients with COPD at low exacerbation risk who were inhaled corticosteroid-naïve, we describe how these findings can be applied in primary care.

Funder

GSK

Publisher

SAGE Publications

Subject

Pulmonary and Respiratory Medicine

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