Evidence map›Paper›PMID 31907054›Full record

Trial reportRespiratory research2020

Risk factors for exacerbations and pneumonia in patients with chronic obstructive pulmonary disease: a pooled analysis.

Benjamin F Hartley, Neil C Barnes, Sally Lettis, Chris H Compton, Alberto Papi, Paul Jones

5 registry-linked trialsOpen access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Respiratory research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
3.4field-weighted citation impact, top 6% 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.

NCT00115492 phase4completednot on this map

A Randomized, Double-Blind, Parallel Group, 52-Week Study to Compare the Effect of Fluticasone Propionate/Salmeterol Diskus Combination Product 250/50mcg BID With Salmeterol Diskus 50mcg BID on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorGlaxoSmithKlineRan2004 to 2007Enrolled797ConditionsPulmonary Disease, Chronic ObstructiveArmsFluticasone Propionate/Salmeterol Combination Product, Salmeterol
NCT00144911 phase4completednot on this map

A Randomized, Double-Blind, Parallel Group, 52-Week Study to Compare the Effect of Fluticasone Propionate/Salmeterol DISKUS® Inhaler Combination Product 250/50mcg Twice Daily With Salmeterol DISKUS® Inhaler 50mcg Twice Daily on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

TypeinterventionalSponsorGlaxoSmithKlineRan2004 to 2006Enrolled740ConditionsPulmonary Disease, Chronic ObstructiveArmsSalmeterol, Fluticasone Propionate/Salmeterol Combination Product
NCT00268216 phase3completednot on this map

A Multicentre, Randomised, Double-blind, Parallel Group, Placebo-controlled Study to Investigate the Long-term Effects of Salmeterol/Fluticasone Propionate (Seretide tm) 50/500mcg BD, Salmeterol 50mcg BD and Fluticasone Propionate 500mcg BD, All Delivered Via the Diskus tm/Accuhaler tm Inhaler, on Mortality and Morbidity of Subjects With Chronic Obstructive Pulmonary Disease (COPD) Over 3 Years of Treatment

TypeinterventionalSponsorGlaxoSmithKlineRan2000 to 2005Enrolled6,228ConditionsPulmonary Disease, Chronic ObstructiveArmsSalmeterol 50mcg/ Fluticasone Propionate 500mcg
NCT01009463 phase3completednot on this map

HZC102871: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

TypeinterventionalSponsorGlaxoSmithKlineRan2009 to 2011Enrolled1,626ConditionsPulmonary Disease, Chronic ObstructiveArmsFF/GW642444 Inhalation Powder, GW642444 Inhalation Powder
NCT01017952 phase3completednot on this map

HZC102970: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

TypeinterventionalSponsorGlaxoSmithKlineRan2009 to 2011Enrolled1,635ConditionsPulmonary Disease, Chronic ObstructiveArmsFF/GW642444 Inhalation Powder, GW642444 Inhalation Powder
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Clinical Concepts for Triple Therapy Use in Patients with COPD: A Delphi Consensus.International journal of chronic obstructive pulmonary disease · 2023
    Article
  12. Article
  13. Observational
  14. Review
  15. Article
  16. Dual Bronchodilator in the Era of Triple Therapy.International journal of chronic obstructive pulmonary disease · 2020
    Review
  17. Benefit/Risk Profile of Single-Inhaler Triple Therapy in COPD.International journal of chronic obstructive pulmonary disease
    Review
  18. Article
  19. Article
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

6 authors at 3 institutions in 2 countries.

Benjamin F HartleyVeramed Ltd, Twickenham, UK.
Neil C BarnesGlaxoSmithKline plc, Brentford, UK.
Sally LettisGlaxoSmithKline plc, Uxbridge, UK. sally.x.lettis@gsk.com.ORCID http://orcid.org/0000-0002-2238-8144
Chris H ComptonGlaxoSmithKline plc, Brentford, UK.
Alberto PapiUniversity of Ferrara, Ferrara, Italy.
Paul JonesGlaxoSmithKline plc, Brentford, UK.
GlaxoSmithKline (United Kingdom) · GBSt George's, University of London · GBUniversity of Ferrara · IT

Funding

GlaxoSmithKline plc 207941
6 · The paper itself

Abstract

backgroundPatients with chronic obstructive pulmonary disease (COPD) are at risk of exacerbations and pneumonia; how the risk factors interact is unclear.

methodsThis post-hoc, pooled analysis included studies of COPD patients treated with inhaled corticosteroid (ICS)/long-acting β

resultsFive studies contributed: NCT01009463, NCT01017952, NCT00144911, NCT00115492, and NCT00268216. Low body mass index (BMI), exacerbation history, worsening lung function (Global Initiative for Chronic Obstructive Lung Disease [GOLD] stage), and ICS treatment were identified as factors increasing pneumonia risk. BMI was the only pneumonia risk factor influenced by ICS treatment, with ICS further increasing risk for those with BMI <25 kg/m

conclusionsThe probability of an exacerbation was considerably higher than for pneumonia. ICS reduced exacerbations but did not influence the effect of risks associated with prior exacerbation history, GOLD stage, or female sex. The only identified risk factor for ICS-induced pneumonia was BMI <25 kg/m

Indexed as

Administration, InhalationAdrenergic beta-2 Receptor AgonistsAgedDrug Therapy, CombinationFemaleGlucocorticoidsHumansIncidenceMaleMiddle AgedPneumoniaPulmonary Disease, Chronic ObstructiveRisk FactorsUnited KingdomAdrenergic beta-2 Receptor AgonistsGlucocorticoidsChronic obstructive pulmonary diseaseExacerbationMeta-analysisPneumonia

Identifiers

PMID31907054
PMCPMC6945447
OpenAlexW3003546074

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.