Evidence map›Paper›PMID 40640771›Full record

ArticleBMC pulmonary medicine2025

Reduction in systemic glucocorticoid utilization among COPD patients with type 2 inflammation treated with biologics.

Truong-An A Ho, Stephen Dachert, Anugya Mittal, Gerard J Criner

Abstract read
In one paragraph

Article in BMC pulmonary medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Review
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

4 authors.

Truong-An A HoDepartment of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, PA, Philadelphia, 19140, USA. truong-an.ho@tuhs.temple.edu.
Stephen DachertDepartment of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, PA, Philadelphia, 19140, USA.
Anugya MittalDepartment of Medicine, Temple University Hospital, PA, Philadelphia, USA.
Gerard J CrinerDepartment of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, PA, Philadelphia, 19140, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic glucocorticoids are associated with significant side effects, however, are essential in the treatment of acute exacerbations of chronic obstructive pulmonary disease (COPD). Biologic therapies in COPD with type 2 (T2) inflammation have shown benefit in reducing exacerbations, but their impact on glucocorticoid utilization remains unclear. We aim to examine if use of biologics in COPD patients reduces glucocorticoid burden.

methodsA retrospective review of the electronic medical record (2016-2023) was performed. Patients with COPD that were treated with biologics were included. Data collected included demographics, baseline comorbidities, eosinophil count, pulmonary function testing and dispense reports for glucocorticoids. The primary outcomes were a change in the number of glucocorticoid dispenses and total cumulative systemic glucocorticoid dosage, in the year prior and post initiation of therapy.

results56 patients (mean age 71 ± 8.5) were included in the study. 55% had coronary artery disease, 25% had heart failure, 71% had hypertension, 14% had stroke and 30% had diabetes. Biologics significantly reduced annual glucocorticoid dispenses (3.38 ± 2.58 vs. 2.22 ± 2.33, mean reduction 1.16, 95% CI 0.45-1.87, p = 0.002) and cumulative dosage (1073 ± 831 mg vs. 659 ± 723 mg, mean reduction 413.2 mg, 95% CI 180.8-645.6, p = 0.001). There was no strong association between baseline eosinophil count and glucocorticoid utilization.

conclusionsIn this real-world cohort of COPD patients with T2 inflammation, the addition of biologic therapies was associated with a significant reduction in systemic glucocorticoid usage, both in terms of dispense frequency and overall total dosage of systemic glucocorticoids. This highlights the potential of biologics to reduce glucocorticoid-related adverse effects in COPD patients.

Indexed as

Biological ProductsGlucocorticoidsInflammationPulmonary Disease, Chronic ObstructiveAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesBiological ProductsGlucocorticoidsBiologic therapyCOPDEosinophiliaGlucocorticoid sparingType 2 inflammation

Identifiers

PMID40640771
PMCPMC12243432

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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.