Evidence map›Paper›PMID 36102236›Full record

ArticleJournal of the American Heart Association2022

Time-Dependent Risk of Cardiovascular Events Following an Exacerbation in Patients With Chronic Obstructive Pulmonary Disease: Post Hoc Analysis From the IMPACT Trial.

Mark T Dransfield, Gerard J Criner, David M G Halpin, MeiLan K Han, Benjamin Hartley, Ravi Kalhan, Peter Lange, David A Lipson, Fernando J Martinez, Dawn Midwinter and 3 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
10.8field-weighted citation impact, top 1% 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.

NCT02164513 phase3completednot on this map

A Phase III, 52 Week, Randomized, Double-blind, 3-arm Parallel Group Study, Comparing the Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination FF/UMEC/VI With the Fixed Dose Dual Combinations of FF/VI and UMEC/VI, All Administered Once-daily in the Morning Via a Dry Powder Inhaler in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorGlaxoSmithKlineRan2014 to 2017Enrolled10,355ConditionsPulmonary Disease, Chronic ObstructiveArmsfluticasone furoate (FF), vilanterol (VI), umeclidinium bromide (UMEC)
NCT07481825 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Impact of Combined cARdio-pUlmonary aSsessment on COPD Clinical Management: the ICARUS Study

TypeinterventionalSponsorUniversity of Bari Aldo MoroRan2026 to 2029Enrolled350ConditionsCOPD (Chronic Obstructive Pulmonary Disease), Cardiovascular DiseaseArmsStructured combined cardio-pulmonary clinical management strategy, Standard Respiratory Management
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 3 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Impact of positive airway pressure for chronic hypercapnic respiratory failure on sleep quality: a systematic review and meta-analysis.European respiratory review : an official journal of the European Respiratory Society · 2025
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
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  10. Third Year in Review, Fourth Year in Preview, and the 2025Journal of the American Heart Association · 2026
    Article
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  15. Article
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  18. GEVResearch (Washington, D.C.) · 2025
    Article
  19. Diagnosis and management of comorbid disease in COPD.Breathe (Sheffield, England) · 2025
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 12 institutions in 3 countries.

Mark T DransfieldLung Health Center University of Alabama at Birmingham Birmingham AL.ORCID 0000-0002-9207-1820
Gerard J CrinerLewis Katz School of Medicine at Temple University Philadelphia PA.
David M G HalpinUniversity of Exeter Medical School University of Exeter Exeter United Kingdom.ORCID 0000-0003-2009-4406
MeiLan K HanUniversity of Michigan Ann Arbor MI.
Benjamin HartleyVeramed Ltd Twickenham United Kingdom.
Ravi KalhanDivision of Pulmonary and Critical Care Medicine Northwestern University Feinberg School of Medicine Chicago IL.ORCID 0000-0003-2443-0876
Peter LangeUniversity of Copenhagen Denmark.ORCID 0000-0003-0401-0081
David A LipsonGSK Collegeville PA.ORCID 0000-0001-6732-4593
Fernando J MartinezNew York-Presbyterian Hospital/Weill Cornell Medical Center New York NY.
Dawn MidwinterGSK Middlesex United Kingdom.
Dave SinghCentre for Respiratory Medicine and Allergy Institute of Inflammation and Repair Manchester Academic Health Science Centre The University of Manchester Manchester University NHS Foundation Hospital Trust Manchester United Kingdom.
Robert WiseJohns Hopkins University School of Medicine Baltimore MD.
Ken M KunisakiMinneapolis Veterans Affairs Health Care System University of Minnesota Twin Cities Medical School Minneapolis MN.ORCID 0000-0001-8644-2827
GlaxoSmithKline (United States) · USHartley McMaster (United Kingdom) · GBJohns Hopkins University · USManchester Academic Health Science Centre · GBNewYork–Presbyterian Hospital · USNorthwestern University · USTemple University · USUniversity of Alabama at Birmingham · USUniversity of Copenhagen · DKUniversity of Exeter · GBUniversity of Michigan · USUniversity of Minnesota · US

Funding

Department of Health
6 · The paper itself

Abstract

Background The association between chronic obstructive pulmonary disease exacerbations and increased cardiovascular event risk has not been adequately studied in a heterogenous population with both low and high cardiovascular risk. Methods and Results This post hoc analysis of the IMPACT (Informing the Pathway of COPD Treatment) trial (N=10 355 symptomatic patients with chronic obstructive pulmonary disease at risk of exacerbations) evaluated time-dependent risk of cardiovascular adverse events of special interest (CVAESI) following exacerbations and impact of exacerbation history, cardiovascular risk factors, and study treatment on this association. Risk (time-to-first) of CVAESI or CVAESI resulting in hospitalization or death was assessed during and 1 to 30, 31 to 90, and 91 to 365 days after resolution of moderate or severe exacerbations. CVAESI risk was compared between the period before and during/after exacerbation. CVAESI risk increased significantly during a moderate (hazard ratio [HR], 2.63 [95% CI, 2.08-3.32]) or severe (HR, 21.84 [95% CI, 17.71-26.93]) exacerbation and remained elevated for 30 days following an exacerbation (moderate: HR, 1.63 [95% CI, 1.28-2.08]; severe: HR, 1.75 [95% CI, 0.99-3.11; nonsignificant]) and decreased over time, returning to baseline by 90 days. Risk of CVAESI resulting in hospitalization or death also increased during an exacerbation (moderate: HR, 2.46 [95% CI, 1.53-3.97]; severe: HR, 41.29 [95% CI, 30.43-56.03]) and decreased in a similar time-dependent pattern. Results were consistent regardless of exacerbation history, cardiovascular risk at screening, or study treatment. Conclusions Overall risk of cardiovascular events was higher during and in the 30 days following chronic obstructive pulmonary disease exacerbations, even among those with low cardiovascular risk, highlighting the need for exacerbation prevention and vigilance for cardiovascular events following exacerbations. Registration URL: https://clinicaltrials.gov/ct2/show/NCT02164513; Unique identifier: NCT02164513.

Indexed as

Cardiovascular DiseasesPulmonary Disease, Chronic ObstructiveDisease ProgressionHospitalizationHumansLungcardiovascular diseasechronic obstructive pulmonary diseaseexacerbationsLAMA/LABAtriple therapy

Identifiers

PMID36102236
PMCPMC9683674
OpenAlexW4295567038

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.