Evidence map›Paper›PMID 41294093›Full record

Trial reportJournal of the American Heart Association2025

Aspirin Dosing for Secondary Prevention of Atherosclerotic Cardiovascular Disease in Chronic Obstructive Pulmonary Disease and Asthma: Insights From ADAPTABLE.

Christopher L Mosher, Amanda Stebbins, Courtney E Lamberton, Lisa M Wruck, Adrian F Hernandez, Catherine P Benziger, Jeffrey Whittle, Kamal Gupta, Russell L Rothman, Sunil Kripalani and 4 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Christopher L MosherDivision of Pulmonary, Allergy, and Critical Care Medicine Duke University School of Medicine Durham NC.ORCID 0000-0002-8463-1947
Amanda StebbinsDuke Clinical Research Institute Durham NC.ORCID 0000-0002-0808-9025
Courtney E LambertonDivision of Pulmonary, Allergy, and Critical Care Medicine Duke University School of Medicine Durham NC.
Lisa M WruckDuke Clinical Research Institute Durham NC.ORCID 0000-0003-1732-9067
Adrian F HernandezDuke Clinical Research Institute Durham NC.ORCID 0000-0003-3387-9616
Catherine P BenzigerHeart and Vascular Center Essentia Health Duluth MN.ORCID 0000-0002-8992-6197
Jeffrey WhittleDivision of Medicine Clement J. Zablocki Veterans Affairs Medical Center Milwaukee WI.ORCID 0000-0002-9544-838X
Kamal GuptaDepartment of Cardiovascular Medicine University of Kansas Medical Center Kansas City KS.ORCID 0000-0002-2440-9033
Russell L RothmanCenter for Clinical Quality and Implementation Research Vanderbilt University Medical Center Nashville TN.ORCID 0000-0002-1506-3990
Sunil KripalaniCenter for Clinical Quality and Implementation Research Vanderbilt University Medical Center Nashville TN.ORCID 0000-0002-4214-7129
Ken M KunisakiPulmonary Section, Minneapolis VA Health Care System Minneapolis MN.ORCID 0000-0001-8644-2827
Ashraf FawzyDivision of Pulmonary and Critical Care Johns Hopkins University School of Medicine Baltimore MD.ORCID 0000-0002-6089-366X
Mark T DransfieldDivision of Pulmonary, Allergy, and Critical Care University of Alabama at Birmingham Birmingham AL.ORCID 0000-0002-9207-1820
W Schuyler JonesDuke Clinical Research Institute Durham NC.ORCID 0000-0002-7288-9596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuidelines recommend aspirin (75-100 mg daily) for the secondary prevention of atherosclerotic cardiovascular disease (ASCVD). However, it is unknown if people with a history of ASCVD and chronic obstructive pulmonary disease (COPD) or asthma, which are independent risk factors for ASCVD, would benefit from higher dose aspirin.

methodsWe evaluated the effectiveness and safety of 2 aspirin doses among individuals with and without COPD/asthma in the ADAPTABLE (Aspirin Dosing: A Patient-Centric Trial Assessing Benefits and Long-Term Effectiveness) trial. The ADAPTABLE study was an open-label, randomized clinical trial that assigned people with ASCVD to aspirin 81 or 325 mg. We performed a secondary analysis of data from the ADAPTABLE study to investigate the difference in clinical effectiveness and safety among people with and without COPD or asthma randomized to aspirin 325 versus 81 mg. We assessed if history of COPD/asthma modified the association between aspirin dose and outcomes.

resultsAmong the 14 662 participants, 2778 had a history of COPD or asthma and 11 884 had no history of COPD or asthma. We observed no significant interaction between aspirin dose and history of COPD/asthma in our adjusted primary composite outcome (adjusted hazard ratio [aHR], 1.15 [95% CI, 0.92-1.43];

conclusionsAmong people with ASCVD and COPD/asthma, there were no significant differences in ASCVD outcomes based on aspirin dosing except stroke. Further evaluation of stroke prevention in this population is warranted.

Indexed as

AspirinAsthmaAtherosclerosisPlatelet Aggregation InhibitorsPulmonary Disease, Chronic ObstructiveSecondary PreventionAgedDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedTreatment OutcomeAspirinPlatelet Aggregation Inhibitorsaspirinasthmaatherosclerotic cardiovascular diseaseCOPDsecondary prevention

Identifiers

PMID41294093
PMCPMC12748523

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.