In one paragraphObservational study in Respiratory research, 2026. 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 itWhat 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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
35 authors.
M Hernandez-ArgudoUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain. mhernandezar@bellvitgehospital.cat.ORCID http://orcid.org/0009-0008-4423-5318 V Vicens-ZygmuntUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-0940-3215 G BermudoUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-2010-7679 G Suarez-CuartinUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0003-2320-6047 S BolivarRadiology Department, UFIP, University Hospital of Bellvitge, Barcelona, Spain.
F ClimentNational Research Network in Respiratory Diseases (CIBERES), Madrid, Spain.
Y GutierrezUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.
S López-MonzoniUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.
X L Perez-FernandezIntensive Care Unit (ICU), University Hospital of Bellvitge, Barcelona, Spain.
M GasaUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-4702-0768 A Robles-PerezRespiratory Department, Consorcio Hospitalario Mataró, Barcelona, Spain.
S BarrilRespiratory Department, Hospital Arnau Vilanova, Lleida, Spain.
R MenendezNational Research Network in Respiratory Diseases (CIBERES), Madrid, Spain.
S SantosUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-5835-1028 M FuentesBiobanc of Bellvitge Biomedical Research Institute (IDIBELL), Barcelona, Spain.
P LuburichNational Research Network in Respiratory Diseases (CIBERES), Madrid, Spain.
M Molina-MolinaUnit of Interstitial Lung Diseases (UFIP), Respiratory Department, Pneumology Research Group Bellvitge Biomedical Research Institute (IDIBELL), Hospital Universitari de Bellvitge, Universitat de Barcelona (UB), Barcelona, Spain.ORCID http://orcid.org/0000-0002-1852-1723 Funding
Instituto de Salud Carlos III PI21/01287
6 · The paper itselfAbstract
introductionChronic interstitial lung changes are potential long-term sequelae of severe COVID-19. This study aims to evaluate the prevalence and type of interstitial changes over time and identify serum biomarkers associated with persistent lung abnormalities.
methodsProspective, multicenter, observational cohort study of patients with severe COVID-19 pneumonia between March 2020 and June 2021. Clinical evaluation, pulmonary function tests (PFTs), and chest high-resolution computed tomography (HRCT) were performed at baseline and up to 24 months. Serum biomarkers were assessed at baseline and at 12 months.
resultsOf the 290 patients enrolled, 247 completed the follow-up. Mild dyspnea (mMRC1) was the most common residual symptom. PFTs showed significant improvement: mean FVC increased from 88.8% to 99.5%, and DLCO from 71.6% to 82%. Among patients with baseline DLCO < 80% (n = 67), only 38.8% achieved normalization. Radiological improvement was observed in all patients, though 32% of the 118 patients assessed at 24 months still had residual changes, primarily mild reticulation, ground glass opacities, and lower lobes traction bronchiectasis. Pulmonary functional improvement correlated with radiological resolution, especially during the first year. Elevated baseline levels of MMP-7 and KL6 were associated with persistent interstitial abnormalities at 12 months.
conclusionSevere COVID-19 survivors exhibit progressive functional and radiological improvement, particularly within the first year. However, a subset of patients shows long-term interstitial changes. Elevated MMP-7 and KL-6 levels may help identify individuals at higher risk for persistent interstitial changes.
Indexed as
COVID-19LungLung Diseases, InterstitialAgedBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedMucin-1Post-Acute COVID-19 SyndromePredictive Value of TestsProspective StudiesRespiratory Function TestsTime FactorsBiomarkersMucin-1Interstitial Lung AbnormalitiesPost-covid interstitial lung diseasePulmonary fibrosis
Identifiers
PMID42021247
PMCPMC13242127
What OpenQuestion holds
Textmetadata
LicenceCC BY-NC-ND
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