Evidence map›Paper›PMID 41782097›Full record

Observational studyBMC pulmonary medicine2026

Outcomes of beta-blocker use in people living with chronic obstructive pulmonary disease and a co-existent beta-blocker indicated cardiovascular disease. Insights from a global federated network.

Mert Kaşkal, Tommaso Bucci, Dennis Wat, Dilip Nazareth, Gregory Y H Lip, Freddy Frost

Abstract readObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

6 authors.

Mert KaşkalLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.
Tommaso BucciLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.
Dennis WatLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.
Dilip NazarethLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.
Gregory Y H LipLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK. gregory.lip@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-7566-1626
Freddy FrostLiverpool Centre for Cardiovascular Sciences, University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBeta-blockers (BBs) are a cornerstone of the management of cardiovascular diseases (CVD) such as heart failure with reduced ejection fraction (HFrEF), acute myocardial infarction (AMI), and atrial fibrillation (AF). Their use in patients with co-existing chronic obstructive pulmonary disease (COPD) remains controversial due to concerns about potential bronchoconstriction and respiratory side effects. This study aimed to assess the safety and effectiveness of BBs in patients with COPD and co-existing cardiovascular conditions using real-world data.

methodsWe conducted a retrospective, propensity score-matched analysis using the TriNetX global federated research network. Patients with a diagnosis of both COPD and CVD (HFrEF, AMI, or AF) between January 2010 and January 2023 were included. Outcomes assessed over a one-year follow-up included all-cause mortality (primary outcome), emergency admissions (EA), and acute exacerbations of COPD (AECOPD). Subgroup analyses were conducted based on cardiovascular indication, BB selectivity, sex, and age group.

resultsA total of 394,476 patients were included; 241,837 were BB users and 152,639 were non-users. After propensity score matching (n = 103,249 per group), there was no significant difference in mortality (HR: 0.98, 95% CI: 0.94-1.02). BB use was associated with an increased risk of EA (HR: 1.30, 95% CI: 1.22-1.40) and a modest increase in AECOPD (HR: 1.03, 95% CI: 1.02-1.04). Findings were consistent across subgroups.

conclusionIn people with COPD and a cardiac indication for BB use, the use of BBs was not associated with mortality benefit but was associated with a modest increased risk of AECOPD and a pronounced risk of increased EA. CLINICAL

trial registrationNot applicable. This study is not a clinical trial; therefore, no trial registry, registration number, or registration date is required.

Indexed as

Adrenergic beta-AntagonistsCardiovascular DiseasesPulmonary Disease, Chronic ObstructiveAgedAged, 80 and overAtrial FibrillationFemaleHeart FailureHumansMaleMiddle AgedMyocardial InfarctionPropensity ScoreRetrospective StudiesTreatment OutcomeAdrenergic beta-AntagonistsBeta-blockersCardiovascular diseaseChronic obstructive pulmonary disease

Identifiers

PMID41782097
PMCPMC13067551

What Socratic 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 Socratic graph.