Evidence map›Paper›PMID 41277954›Full record

ArticleFrontiers in microbiology2025

Impact of COVID-19 therapeutics on the development of post-infectious lung fibrosis.

Yong Jun Choi, Ji Eun Nam, Chul Hwan Park, Ji Ye Jung, Eun Hye Lee, Hye Jung Park, Chi Young Kim, Jae Hwa Cho, Min Kwang Byun

Abstract read
In one paragraph

Article in Frontiers in microbiology, 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.

Yong Jun Choi *Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Ji Eun Nam *Department of Radiology and the Research Institute of Radiological Science, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Chul Hwan ParkDepartment of Radiology and the Research Institute of Radiological Science, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Ji Ye JungDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eun Hye LeeDivision of Pulmonology, Allergy and Critical Care Medicine, Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, Republic of Korea.
Hye Jung ParkDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Chi Young KimDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jae Hwa ChoDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min Kwang ByunDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Post-COVID-19 pulmonary fibrosis (PCPF) is a significant long-term complication in survivors of COVID-19. In this study, we aimed to identify clinical risk factors for PCPF and evaluate the impact of COVID-19-related therapies. Methods: We retrospectively studied hospitalized adults with confirmed COVID-19 across three hospitals in South Korea from 2020 to 2022. Inclusion required chest computed tomography (CT) imaging both before and after COVID-19 infection. PCPF was defined as fibrotic changes seen on follow-up CT performed at least one month after recovery. Results: Among 5,720 hospitalized adults with COVID-19, 688 met the inclusion criteria, and 87 (12.6%) developed PCPF based on follow-up CT. In the multivariate logistic regression, pre-existing renal disease (adjusted odds ratio [aOR] 3.287; 95% confidential interval [CI]: 1.260-8.580; Conclusion: PCPF remains a relevant sequela in COVID-19 survivors. Remdesivir and baricitinib use were associated with a reduced and increased risk of PCPF, respectively. Although adjusted for multiple confounders, residual indication bias of each treatment cannot be completely excluded. Therefore, prospective studies are needed to validate these associations.

Indexed as

baricitinibcomputed tomographyCOVID-19 pandemicpost-COVID-19 pulmonary fibrosisremdesivirSARS-CoV-2 infection

Identifiers

PMID41277954
PMCPMC12631368

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.