Evidence map›Paper›PMID 41262358›Full record

ArticleOpen forum infectious diseases2025

Clinical, Radiographic, and Physiological Correlates of Post-COVID-19 Dyspnea in Military Health System Beneficiaries: Results From the Chronic Impairment With Pulmonary Symptoms (ChIPS) Sub-study.

S Michael Goertzen, David A Lindholm, Robert J Walter, Nikhil A Huprikar, Anuradha Ganesan, Stephanie A Richard, Katrin Mende, Travis E Harrell, P Gabriel Peterson, Mark Simons and 5 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 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

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

1 citing paper in PubMed.

  1. 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

15 authors.

S Michael GoertzenDepartment of Medicine, Brooke Army Medical Center, JBSA Fort Sam Houston, Texas, United States.
David A LindholmDepartment of Medicine, Brooke Army Medical Center, JBSA Fort Sam Houston, Texas, United States.
Robert J WalterDepartment of Medicine, Brooke Army Medical Center, JBSA Fort Sam Houston, Texas, United States.
Nikhil A HuprikarDepartment of Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, United States.
Anuradha GanesanDepartment of Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, United States.
Stephanie A RichardInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
Katrin MendeDepartment of Medicine, Brooke Army Medical Center, JBSA Fort Sam Houston, Texas, United States.
Travis E HarrellDepartment of Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, United States.
P Gabriel PetersonDepartment of Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, United States.
Mark SimonsInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
David R TribbleInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
Brian K AganInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
Timothy H BurgessInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
Simon D PollettInfectious Disease Clinical Research Program, Department of Preventive Medicine & Biostatistics, Uniformed Services University, Bethesda, Maryland, United States.
Michael J MorrisDepartment of Medicine, Brooke Army Medical Center, JBSA Fort Sam Houston, Texas, United States.ORCID https://orcid.org/0000-0003-4903-4343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dyspnea has been described in up to 10-30% of patients post-SARS-CoV-2 infection. The underlying pathology for these persistent symptoms remains poorly understood. This study aimed to characterize changes in cardiopulmonary anatomical structure and physiology that may explain ongoing dyspnea after COVID-19. Methods: Participants had a history of symptomatic COVID-19, were between 18 and 65 years of age, and without significant pre-existing cardiopulmonary disease. Each participant underwent prospective chest high resolution computed tomography (HRCT), transthoracic echocardiography (TTE), electrocardiogram (ECG), pulmonary function testing (PFT) with lung volumes and diffusing capacity for carbon monoxide (DLCO), impulse oscillometry (IOS), and a six-minute walk test (6MWT) with Borg dyspnea scoring. Results: Among 115 enrolled participants, 39 had persistent dyspnea. The mean forced expiratory volume at 1 s/forced vital capacity (FEV Conclusions: This study demonstrated a difference in 6MWT distance and Borg scores between those with and without persistent dyspnea. There were no clear PFT, cardiac test, or HRCT findings that explained these persistent symptoms. Overall, this study demonstrates both subjective and objective differences between those with ongoing dyspnea following COVID-19 that are not explained by standard investigations typically ordered in clinical care for chronic dyspnea. These findings underscore the importance of further research into the etiology of post-COVID-19 dyspnea, including other investigations which may detect more subtle alterations in pulmonary physiology.

Indexed as

dyspnealong COVIDphysiologyradiology

Identifiers

PMID41262358
PMCPMC12625653

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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.