Evidence map›Paper›PMID 26559138›Full record

SynthesisBMC pulmonary medicine2015

Mortality and drug therapy in patients with chronic obstructive pulmonary disease: a network meta-analysis.

David A Scott, Bethan Woods, Juliette C Thompson, James F Clark, Neil Hawkins, Mike Chambers, Bartolome R Celli, Peter Calverley

Open access · goldAbstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in BMC pulmonary medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Prescription is not enough: the importance of adherence to pharmacological treatment of COPD.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2022
    Article
  3. Review
  4. Article
  5. Review
  6. Review
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

8 authors at 3 institutions in 2 countries.

David A ScottICON Health Economics and Epidemiology, Seacourt Tower, West Way, Oxford, OX2 0JJ, UK. david.scott@iconplc.com.
Bethan WoodsICON Health Economics and Epidemiology, Seacourt Tower, West Way, Oxford, OX2 0JJ, UK. beth.woods@york.ac.uk.
Juliette C ThompsonICON Health Economics and Epidemiology, Seacourt Tower, West Way, Oxford, OX2 0JJ, UK. juliette.thompson@iconplc.com.
James F ClarkICON Health Economics and Epidemiology, Seacourt Tower, West Way, Oxford, OX2 0JJ, UK. james.clark-wright@pharmagenesis.com.
Neil HawkinsICON Health Economics and Epidemiology, Seacourt Tower, West Way, Oxford, OX2 0JJ, UK. neil.hawkins@iconplc.com.
Mike ChambersGlaxoSmithKline, Brentford, UK. mgchambers@ntlworld.com.
Bartolome R CelliBrigham and Women's Hospital, Harvard University, Boston, MA, USA. bcelli@copdnet.org.
Peter CalverleyInstitute of Aging and Chronic Disease, University of Liverpool, Liverpool, UK. pmacal@liverpool.ac.uk.
GlaxoSmithKline (United Kingdom) · GBHarvard University · USUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing evidence suggests pharmacological treatments may impact on overall survival in Chronic Obstructive Pulmonary Disease (COPD) patients. Individual clinical trials are rarely powered to detect mortality differences between treatments and may not include all treatment options relevant to healthcare decision makers.

methodsA systematic review was conducted to identify RCTs of COPD treatments reporting mortality; evidence was synthesised using network meta-analysis (NMA). The analysis included 40 RCTs; a quantitative indirect comparison between 14 treatments using data from 55,220 patients was conducted.

resultsThe analysis reported two treatments reducing all-cause mortality; salmeterol/fluticasone propionate combination (SFC) was associated with a reduction in mortality versus placebo in the fixed effects (HR 0.79; 95 % Crl 0.67, 0.94) but not the random effects model (0.79; 0.56, 1.09). Indacaterol was associated with a reduction in mortality versus placebo in fixed (0.28; 0.08 to 0.85) and random effects (0.29; 0.08, 0.89) models. Mean estimates and credible intervals for hazard ratios for indacaterol versus placebo are based on a small number of events; estimates may change when the results of future studies are included. These results were maintained across a variety of assumptions and provide evidence that SFC and indacaterol may lead to improved survival in COPD patients.

conclusionResults of an NMA of COPD treatments suggest that SFC and indacaterol may reduce mortality. Further research is warranted to strengthen this conclusion.

Indexed as

AlbuterolAminopyridinesBeclomethasoneBenzamidesBenzyl AlcoholsBronchodilator AgentsBudesonideChlorobenzenesCyclopropanesFluticasone-Salmeterol Drug CombinationFormoterol FumarateGlucocorticoidsHumansIndansIpratropiumProportional Hazards ModelsAlbuterolAminopyridinesBeclomethasoneBenzamidesBenzyl AlcoholsBronchodilator AgentsBudesonideChlorobenzenesCyclopropanesFluticasone-Salmeterol Drug CombinationFormoterol FumarateGlucocorticoidsindacaterolIndansIpratropiumQuinolonesRoflumilastTheophyllineTiotropium BromideTriamcinolonevilanterol

Identifiers

PMID26559138
PMCPMC4642642
OpenAlexW2176327587

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.