Evidence map›Paper›PMID 41809863›Full record

ArticleERJ open research2026

Acute effects of low-dose bisoprolol on lung function and blood pressure in COPD patients.

Thomas F Bradbury, Allison Martin, Robert J Hancox, Catherina L Chang, Richard Beasley, Jeremy P Wrobel, Vanessa M McDonald, Claudia C Dobler, Ian A Yang, Claude S Farah and 7 more

Abstract read
In one paragraph

Article in ERJ open research, 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

17 authors.

Thomas F BradburyRespiratory Group, The George Institute for Global Health, Barangaroo, Australia.
Allison MartinRespiratory Group, The George Institute for Global Health, Barangaroo, Australia.
Robert J HancoxPreventive and Social Medicine, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0002-3922-7144
Catherina L ChangRespiratory Medicine, Waikato Hospital, Hamilton, New Zealand.ORCID https://orcid.org/0000-0002-8390-670X
Richard BeasleyAsthma Programme, Medical Research Institute of New Zealand, Wellington, New Zealand.ORCID https://orcid.org/0000-0003-0337-406X
Jeremy P WrobelRespiratory Medicine, Fiona Stanley Hospital, Murdoch, Australia.
Vanessa M McDonaldSchool of Nursing and Midwifery, The University of Newcastle, Newcastle, Australia.
Claudia C DoblerRespiratory and Sleep Medicine, Liverpool Hospital, Liverpool, Australia.
Ian A YangDepartment of Thoracic Medicine, The Prince Charles Hospital, Chermside, Australia.
Claude S FarahRespiratory/Thoracic Medicine, Concord Repatriation General Hospital, Concord, Australia.ORCID https://orcid.org/0000-0003-2489-227X
Belinda CochraneRespiratory and Sleep Medicine, Campbelltown Hospital, Campbelltown, Australia.
Graham S HillisDepartment of Cardiology, Royal Perth Hospital, Perth, Australia.ORCID https://orcid.org/0000-0003-2417-4673
Caroline Polak ScowcroftConsumer Representative, Canberra, Australia.
Ashutosh AggarwalDepartment of Pulmonary Medicine, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Channa RanasinhaFaculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
Shane GalgeyRespiratory Group, The George Institute for Global Health, Barangaroo, Australia.
Christine R JenkinsRespiratory Group, The George Institute for Global Health, Barangaroo, Australia.ORCID https://orcid.org/0000-0003-2717-5647

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objective: Recent observational data suggest that cardioselective β-blockers like bisoprolol are safe and beneficial for patients with COPD. However, the acute effects of bisoprolol on lung and cardiovascular function in these patients is unclear, a gap that this study aimed to address. Methods: This was a subanalysis of pre-randomisation screening visit data from the ongoing Preventing Adverse Cardiac Events (PACE) in COPD randomised controlled trial. If all other eligibility criteria were met, participants were orally administered an unblinded 1.25 mg tablet of bisoprolol. Post-bronchodilator spirometry, heart rate and blood pressure were monitored at 0, 30 (cardiovascular parameters only), 60 and 120 min. For this subanalysis, respiratory intolerance was defined as a decrease in forced expiratory volume in 1 s (FEV Results: Of 359 consented participants, 292 conducted the test-dose procedure. 13 (4.5%) were respiratory intolerant and six (2.1%) were cardiovascular intolerant at 1 or 2 h. No participant was intolerant for both. There was no significant difference in FEV Conclusion: The administration of 1.25 mg bisoprolol was acutely well tolerated in >95% of COPD patients.

Identifiers

PMID41809863
PMCPMC12969693

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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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.