Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/194309
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dc.contributor.authorTrias-Sabrià, Pere-
dc.contributor.authorDorca Duch, Eduard-
dc.contributor.authorMolina Molina, María-
dc.contributor.authorAso, Samantha-
dc.contributor.authorDíez-Ferrer, Marta-
dc.contributor.authorMarin, Alfredo-
dc.contributor.authorBordas-Martínez, Jaume-
dc.contributor.authorSabater, Joan-
dc.contributor.authorLuburich, Patricio-
dc.contributor.authorDel Río, Belén-
dc.contributor.authorDorca i Sargatal, Jordi-
dc.contributor.authorSantos Perez, Maria De La S.-
dc.contributor.authorSuarez-Cuartin, Guillermo-
dc.date.accessioned2023-02-28T09:58:40Z-
dc.date.available2023-02-28T09:58:40Z-
dc.date.issued2022-01-
dc.identifier.issn2296-858X-
dc.identifier.urihttp://hdl.handle.net/2445/194309-
dc.description.abstractBackground: Patients with coronavirus disease 2019 (COVID-19) can develop severe bilateral pneumonia leading to respiratory failure. Lung histological samples were scarce due to the high risk of contamination during autopsies. We aimed to correlate histological COVID-19 features with radiological findings through lung ultrasound (LU)-guided postmortem core needle biopsies (CNBs) and computerized tomography (CT) scans. Methodology: We performed an observational prospective study, including 30 consecutive patients with severe COVID-19. The thorax was divided into 12 explorations regions to correlate LU and CT-scan features. Histological findings were also related to radiological features through CNBs. Results: Mean age was 62.56 ± 13.27 years old, with 96.7% male patients. Postmortem LU-guided CNBs were performed in 13 patients. Thirty patients were evaluated with both thoracic LU and chest CT scan, representing a total of 279 thoracic regions explored. The most frequent LU finding was B2-lines (49.1%). The most CT-scan finding was ground-glass opacity (GGO, 29%). Pathological CT-scan findings were commonly observed when B2-lines or C-lines were identified through LU (positive predictive value, PPV, 87.1%). Twenty-five postmortem echo-guided histological samples were obtained from 12 patients. Histological samples showed diffuse alveolar damage (DAD) (75%) and chronic interstitial inflammation (25%). The observed DAD was heterogeneous, showing multiple evolving patterns of damage, including exudative (33.3%), fibrotic (33.3%), and organizing (8.3%) phases. In those patients with acute or exudative pattern, two lesions were distinguished: classic hyaline membrane; fibrin "plug" in alveolar space (acute fibrinous organizing pneumonia, AFOP). C-profile was described in 33.3% and presented histological signs of DAD and lung fibrosis. The predominant findings were collagen deposition (50%) and AFOP (50%). B2-lines were identified in 66.7%; the presence of hyaline membrane was the predominant finding (37.5%), then organizing pneumonia (12.5%) and fibrosis (37.5%). No A-lines or B1-lines were observed in these patients. Conclusion: LU B2-lines and C-profile are predominantly identified in patients with severe COVID-19 with respiratory worsening, which correspond to different CT patterns and histological findings of DAD and lung fibrosis.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFrontiers Media-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fmed.2022.820661-
dc.relation.ispartofFrontiers in Medicine, 2022, vol. 9-
dc.relation.urihttps://doi.org/10.3389/fmed.2022.820661-
dc.rightscc-by (c) Trias-Sabrià, Pere et al., 2022-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationCOVID-19-
dc.subject.classificationBiòpsia-
dc.subject.classificationPatologia-
dc.subject.classificationRadiologia-
dc.subject.otherCOVID-19-
dc.subject.otherBiopsy-
dc.subject.otherPathology-
dc.subject.otherRadiology-
dc.titleRadio-histological correlation of lung features in severe COVID19-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec717350-
dc.date.updated2023-02-28T09:58:40Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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