Evidence map›Paper›PMID 34347255›Full record

ArticleAdvances in therapy2021

Efficacy and Safety of Umeclidinium/Vilanterol in Current and Former Smokers with COPD: A Prespecified Analysis of The EMAX Trial.

Leif H Bjermer, Isabelle H Boucot, Claus F Vogelmeier, François Maltais, Paul W Jones, Lee Tombs, Chris Compton, David A Lipson, Edward M Kerwin

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  3. Review
  4. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 4 countries.

Leif H BjermerRespiratory Medicine and Allergology, Skane University Hospital, Lund University, 221 85, Lund, Sweden. leif.bjermer@med.lu.se.ORCID 0000-0002-3441-8099
Isabelle H BoucotGSK, Brentford, Middlesex, UK.ORCID 0000-0003-0410-4969
Claus F VogelmeierDepartment 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), Marburg, Germany.ORCID 0000-0002-9798-2527
François MaltaisCentre de Pneumologie, Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval, Québec, QC, Canada.ORCID 0000-0002-6809-4651
Paul W JonesGSK, Brentford, Middlesex, UK.ORCID 0000-0001-6087-9182
Lee TombsPrecise Approach Ltd, Contingent Worker on Assignment at GSK, Stockley Park West, Uxbridge, Middlesex, UK.
Chris ComptonGSK, Brentford, Middlesex, UK.
David A LipsonRespiratory Clinical Sciences, GSK, Collegeville, PA, USA.ORCID 0000-0001-6732-4593
Edward M KerwinAltitude Clinical Consulting and Clinical Research Institute of Southern Oregon, Medford, OR, USA.ORCID 0000-0002-1697-9036
Clinical Research Institute · USGlaxoSmithKline (United States) · USInstitut universitaire de cardiologie et de pneumologie de Québec · CALund University · SEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSmoking may reduce the efficacy of inhaled corticosteroids (ICS) in patients with chronic obstructive pulmonary disease (COPD), but its impact on bronchodilator efficacy is unclear. This analysis of the EMAX trial explored efficacy and safety of dual- versus mono-bronchodilator therapy in current or former smokers with COPD.

methodsThe 24-week EMAX trial evaluated lung function, symptoms, health status, exacerbations, clinically important deterioration, and safety with umeclidinium/vilanterol, umeclidinium, and salmeterol in symptomatic patients at low exacerbation risk who were not receiving ICS. Current and former smoker subgroups were defined by smoking status at screening.

resultsThe analysis included 1203 (50%) current smokers and 1221 (50%) former smokers. Both subgroups demonstrated greater improvements from baseline in trough FEV

conclusionsIn current and former smokers, umeclidinium/vilanterol provided greater improvements in lung function and symptoms versus umeclidinium and salmeterol, supporting consideration of dual-bronchodilator therapy in symptomatic patients with COPD regardless of their smoking status.

Indexed as

Pulmonary Disease, Chronic ObstructiveSmokersAdministration, InhalationBenzyl AlcoholsBronchodilator AgentsChlorobenzenesDouble-Blind MethodDrug CombinationsForced Expiratory VolumeHumansQuinuclidinesTreatment OutcomeBenzyl AlcoholsBronchodilator AgentsChlorobenzenesDrug CombinationsGSK573719QuinuclidinesvilanterolCOPDLABALAMAMaintenance treatmentSalmeterolSmokerSmokingUmeclidiniumUmeclidinium/vilanterol

Identifiers

PMID34347255
PMCPMC8408076
OpenAlexW3187202922

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.