Evidence map›Paper›PMID 34858023›Full record

ArticleInternational journal of chronic obstructive pulmonary disease

Comparison of Risk of Pneumonia Caused by Fluticasone Propionate versus Budesonide in Chronic Obstructive Pulmonary Disease: A Nationwide Retrospective Cohort Study.

Jae-Hwa Choi, Keun-Bae Jeong, You Hyun Park, Iseul Yu, Seok Jeong Lee, Myoung Kyu Lee, Sang-Ha Kim, Won-Yeon Lee, Suk Joong Yong, Ji-Ho Lee

Open access · goldAbstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Eosinophil count and treatment response in COPD patients.Lung India : official organ of Indian Chest Society · 2025
    Article
  3. Article
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 at 1 institution in 1 country.

Jae-Hwa Choi *Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Keun-Bae Jeong *Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID 0000-0002-1453-7621
You Hyun ParkDepartment of Biostatistics, Yonsei University, Seoul, Korea.ORCID 0000-0002-3248-9993
Iseul YuDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Seok Jeong LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Myoung Kyu LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID 0000-0002-2450-4882
Sang-Ha KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID 0000-0002-1763-5366
Won-Yeon LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID 0000-0002-5461-6770
Suk Joong YongDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Ji-Ho LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.ORCID 0000-0001-8744-156X
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInhaled corticosteroids (ICSs) play an important role in lowering the risk of acute exacerbation of chronic obstructive pulmonary disease (COPD). However, ICSs are known to increase the risk of pneumonia. Moreover, previous studies have shown that the incidence rate of pneumonia varies depending on the type of ICS. In this study, the risk of pneumonia according to the type of ICS was investigated in a population-based cohort.

methodsA retrospective cohort study was conducted using claims data of the entire population from the Korean National Health Insurance Service. Patients who were newly diagnosed with COPD and prescribed fluticasone propionate or budesonide were enrolled as study subjects. Cumulative doses of ICSs were classified into categorical variables to analyze the risk of pneumonia within identical ICS doses.

resultsA total of 47,473 subjects were identified and allocated as 14,518 fluticasone propionate and 14,518 budesonide users through 1:1 propensity score matching. Fluticasone propionate users were more likely to develop pneumonia than budesonide users (14.22% vs 10.66%, p<0.0001). The incidence rate per 100,000 person-years was 2,914.77 for fluticasone propionate users and 2,102.90 for budesonide users. The hazard ratio (HR) of pneumonia in fluticasone propionate compared to budesonide was 1.34 (95% CI 1.26-1.43, p<0.0001). The risk of pneumonia for fluticasone propionate compared to budesonide increased with higher ICS cumulative doses: 1.06 (0.93-1.21), 1.41 (1.19-1.66), 1.41 (1.23-1.63), and 1.49 (1.33-1.66) from the lowest to highest quartiles, respectively.

conclusionICS types and doses need to be carefully considered during treatment with ICSs in patients with COPD.

Indexed as

PneumoniaPulmonary Disease, Chronic ObstructiveAdministration, InhalationAdrenal Cortex HormonesAndrostadienesBronchodilator AgentsBudesonideFluticasoneHumansRetrospective StudiesAdrenal Cortex HormonesAndrostadienesBronchodilator AgentsBudesonideFluticasonebudesonidechronic obstructive pulmonary diseasefluticasone propionateinhaled corticosteroidpneumonia

Identifiers

PMID34858023
PMCPMC8629914
OpenAlexW3214936758

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.