Evidence map›Paper›PMID 41868726›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2026

Evaluating Arrhythmia Risk in Patients with Chronic Obstructive Pulmonary Disease Treated with Aclidinium/Formoterol Fumarate and Other Inhaled Bronchodilators: A Post-Authorization Safety Study.

Cristina Rebordosa, Jaume Aguado, Jennifer Bartsch, Nuria Saigi-Morgui, Anne-Elie Carsin, Raquel Garcia-Esteban, Elena Ignatova, Daniel Freedman, Susana Perez-Gutthann, Elena Rivero-Ferrer

Abstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 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

10 authors.

Cristina RebordosaRTI Health Solutions, Barcelona, Spain.ORCID 0000-0002-8064-5997
Jaume AguadoRTI Health Solutions, Barcelona, Spain.ORCID 0000-0002-9575-0212
Jennifer BartschRTI Health Solutions, Research Triangle Park, NC, USA.ORCID 0000-0003-1506-5715
Nuria Saigi-MorguiRTI Health Solutions, Barcelona, Spain.ORCID 0000-0003-2503-1818
Anne-Elie CarsinRTI Health Solutions, Barcelona, Spain.ORCID 0000-0003-3981-977X
Raquel Garcia-EstebanRTI Health Solutions, Barcelona, Spain.ORCID 0000-0002-0911-1220
Elena IgnatovaCovis Pharma Gmbh, a Wholly-Owned Subsidiary of Azurity Pharmaceuticals, Inc., Woburn, MA, USA.ORCID 0009-0007-9855-4261
Daniel FreedmanCovis Pharma Gmbh, a Wholly-Owned Subsidiary of Azurity Pharmaceuticals, Inc., Woburn, MA, USA.
Susana Perez-GutthannRTI Health Solutions, Barcelona, Spain.ORCID 0000-0001-5798-3691
Elena Rivero-FerrerRTI Health Solutions, Barcelona, Spain.ORCID 0000-0001-5093-2445

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: A post-authorization safety study program examined the cardiovascular safety of the long-acting muscarinic antagonist (LAMA) aclidinium bromide monotherapy and the LAMA/long-acting β Patients and Methods: This population-based cohort study included adults with chronic obstructive pulmonary disease (COPD) initiating COPD medications in the UK Clinical Practice Research Datalink Aurum database (Jan 2015-Mar 2021). CA, AF, and SVA incidence rate ratios (IRR) were estimated using Poisson regression models for continuous current users initiating aclidinium and aclidinium/formoterol versus LABA, and during the first episode of current single use for aclidinium versus LAMA and aclidinium/formoterol versus LAMA/LABA, adjusting for clinically relevant covariables. Results: The study included a total of 248,148 initiators. For CA and AF, respectively, adjusted IRRs (95% confidence intervals [CIs]) ranged from 0.98 (0.69-1.41) for LAMA/LABA to 2.08 (1.36-3.18) for aclidinium/formoterol and from 0.83 (0.55-1.24) for LAMA/LABA to 1.85 (1.15-3.00) for aclidinium/formoterol versus current LABA use. For current single use (first episode), adjusted IRRs (95% CIs) for CA and AF were 1.46 (0.93-2.29) and 1.57 (0.94-2.62) for aclidinium versus other LAMAs, and 2.15 (1.33-3.49) and 1.79 (0.96-3.33) for aclidinium/formoterol versus LAMA/LABA, respectively. There were few SVA events. Conclusion: CA and AF risks were increased for most study medications compared with LABA. Increased risks of CA and AF for several medications relative to LABA, LAMA, or LAMA/LABA may be driven by differences in baseline characteristics (eg, COPD severity).

Indexed as

Adrenergic beta-2 Receptor AgonistsArrhythmias, CardiacBronchodilator AgentsFormoterol FumarateMuscarinic AntagonistsPulmonary Disease, Chronic ObstructiveTropanesAdministration, InhalationAgedFemaleHumansMaleMiddle AgedProduct Surveillance, PostmarketingRisk AssessmentRisk Factorsaclidinium bromideAdrenergic beta-2 Receptor AgonistsBronchodilator AgentsFormoterol FumarateMuscarinic AntagonistsTropanesaclidiniumarrhythmiaLABALAMAUnited Kingdom

Identifiers

PMID41868726
PMCPMC13003635

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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 OpenQuestion graph.