Evidence map›Paper›PMID 40264969›Full record

Observational studyInternational journal of chronic obstructive pulmonary disease2025

Characteristics of Patients Initiated on Budesonide/Glycopyrronium Bromide/Formoterol Fumarate Single Inhaler Triple Therapy for the Treatment of Chronic Obstructive Pulmonary Disease: A Population-Based Observational Study.

Gaétan Deslee, Caroline Fabry-Vendrand, Elsa Salmi, Nolwenn Poccardi, Adrien Coriat, Idir Ghout, Caroline Eteve-Pitsaer, Nicola J Adderley, Henri Leleu

Abstract readObservational Study
In one paragraph

Observational study in International journal of chronic obstructive pulmonary disease, 2025. 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

9 authors.

Gaétan DesleeService de Pneumologie, INSERM UMRS-1250, Centre Hospitalier Universitaire de Reims, Université Reims, Champagne-Ardenne, France.ORCID 0000-0002-4919-5916
Caroline Fabry-VendrandAstraZeneca, Courbevoie, France.ORCID 0000-0001-8786-7843
Elsa SalmiAstraZeneca, Courbevoie, France.
Nolwenn PoccardiAstraZeneca, Courbevoie, France.
Adrien CoriatCegedim Group, Boulogne-Billancourt, France.
Idir GhoutCegedim Group, Boulogne-Billancourt, France.
Caroline Eteve-PitsaerCegedim Group, Boulogne-Billancourt, France.
Nicola J AdderleyDepartment of Applied Health Sciences, University of Birmingham, Edgbaston, Birmingham, UK.ORCID 0000-0003-0543-3254
Henri LeleuPublic Health Expertise, Paris, Île-de-France, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Budesonide/glycopyrronium bromide/formoterol fumarate (BUD/GLY/FOR) single inhaler triple therapy became available to prescribe to patients with severe chronic obstructive pulmonary disease (COPD) in France in 2021. The characteristics of patients prescribed BUD/GLY/FOR triple therapy and guideline adherence have not been previously described in France. Objective: To describe the characteristics of COPD patients initiated on BUD/GLY/FOR triple therapy, assess adherence to COPD management guidelines, and explore any differences by prescribing physician. Materials and Methods: A cross-sectional study using data from The Health Improvement Network (THIN Results: A total of 263 patients initiating BUD/GLY/FOR triple therapy were included. Mean (SD) age was 68.8 (11.8) years; 53.6% were male. Mean (SD) COPD duration was 6.4 (5.5) years. Comorbidities were common, with slightly more cardiometabolic and mental health conditions recorded in the GP-initiated group, and more comorbid respiratory conditions recorded in the pulmonologist-initiated group. About 77.2% (n=203) of patients had at least one moderate or severe exacerbation in the 12 months before initiation. About 86.3% had a previous record of dual (n=117, 44.5%) or triple (n=110, 41.8%) therapy. About 68.8% had been initiated on BUD/GLY/FOR triple therapy in line with SPLF guidelines (62.4% and 72.4% in the GP- and pulmonologist-initiated groups, respectively); among those with a record of COPD severity, 75.2% were initiated in line with HAS guidelines (69.2% and 76.3% in the GP- and pulmonologist-initiated groups, respectively). Conclusion: The majority of COPD patients are prescribed BUD/GLY/FOR triple therapy in accordance with current treatment guidelines, irrespective of whether the therapy is prescribed by a general practitioner or a pulmonologist.

Indexed as

Adrenergic beta-2 Receptor AgonistsBronchodilator AgentsBudesonideBudesonide, Formoterol Fumarate Drug CombinationFormoterol FumarateGlycopyrrolateMuscarinic AntagonistsPractice Patterns, Physicians'Pulmonary Disease, Chronic ObstructiveAdministration, InhalationAgedCross-Sectional StudiesDatabases, FactualDrug CombinationsFemaleFranceAdrenergic beta-2 Receptor AgonistsBronchodilator AgentsBudesonideBudesonide, Formoterol Fumarate Drug CombinationDrug CombinationsFormoterol FumarateGlycopyrrolateMuscarinic Antagonistsbudesonide/glycopyrronium bromide/formoterol fumaratechronic obstructive pulmonary diseasemanagementtriple therapy

Identifiers

PMID40264969
PMCPMC12013627

What OpenQuestion holds

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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.