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Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy
The WHO defines different COVID-19 disease stages in which the pathophysiological mechanisms differ. We evaluated the characteristics of these COVID-19 disease stages. Forty-four PCR-confirmed COVID-19 patients were included in a prospective minimal invasive autopsy cohort. Patients were classified...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789771/ https://www.ncbi.nlm.nih.gov/pubmed/35079048 http://dx.doi.org/10.1038/s41598-022-05186-y |
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author | D’Onofrio, Valentino Keulen, Lotte Vandendriessche, Annelore Dubois, Jasperina Cartuyvels, Reinoud Vanden Abeele, Marie-Elena Fraussen, Judith Vandormael, Patrick Somers, Veerle Achten, Ruth Dendooven, Amélie Driessen, Ann Augsburg, Lukasz Hellings, Niels Lammens, Martin Vanrusselt, Jan Cox, Janneke |
author_facet | D’Onofrio, Valentino Keulen, Lotte Vandendriessche, Annelore Dubois, Jasperina Cartuyvels, Reinoud Vanden Abeele, Marie-Elena Fraussen, Judith Vandormael, Patrick Somers, Veerle Achten, Ruth Dendooven, Amélie Driessen, Ann Augsburg, Lukasz Hellings, Niels Lammens, Martin Vanrusselt, Jan Cox, Janneke |
author_sort | D’Onofrio, Valentino |
collection | PubMed |
description | The WHO defines different COVID-19 disease stages in which the pathophysiological mechanisms differ. We evaluated the characteristics of these COVID-19 disease stages. Forty-four PCR-confirmed COVID-19 patients were included in a prospective minimal invasive autopsy cohort. Patients were classified into mild-moderate (n = 4), severe-critical (n = 32) and post-acute disease (n = 8) and clinical, radiological, histological, microbiological and immunological data were compared. Classified according to Thoracic Society of America, patients with mild-moderate disease had no typical COVID-19 images on CT-Thorax versus 71.9% with typical images in severe-critical disease and 87.5% in post-acute disease (P < 0.001). Diffuse alveolar damage was absent in mild-moderate disease but present in 93.8% and 87.5% of patients with severe-critical and post-acute COVID-19 respectively (P = 0.002). Other organs with COVID-19 related histopathological changes were liver and heart. Interferon-γ levels were significantly higher in patients with severe-critical COVID-19 (P = 0.046). Anti-SARS CoV-2 IgG was positive in 66%, 40.6% and 87.5% of patients with mild-moderate, severe-critical and post-acute COVID-19 respectively (n.s.). Significant differences in histopathological and immunological characteristics between patients with mild-moderate disease compared to patients with severe-critical disease were found, whereas differences between patients with severe-critical disease and post-acute disease were limited. This emphasizes the need for tailored treatment of COVID-19 patients. |
format | Online Article Text |
id | pubmed-8789771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87897712022-01-27 Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy D’Onofrio, Valentino Keulen, Lotte Vandendriessche, Annelore Dubois, Jasperina Cartuyvels, Reinoud Vanden Abeele, Marie-Elena Fraussen, Judith Vandormael, Patrick Somers, Veerle Achten, Ruth Dendooven, Amélie Driessen, Ann Augsburg, Lukasz Hellings, Niels Lammens, Martin Vanrusselt, Jan Cox, Janneke Sci Rep Article The WHO defines different COVID-19 disease stages in which the pathophysiological mechanisms differ. We evaluated the characteristics of these COVID-19 disease stages. Forty-four PCR-confirmed COVID-19 patients were included in a prospective minimal invasive autopsy cohort. Patients were classified into mild-moderate (n = 4), severe-critical (n = 32) and post-acute disease (n = 8) and clinical, radiological, histological, microbiological and immunological data were compared. Classified according to Thoracic Society of America, patients with mild-moderate disease had no typical COVID-19 images on CT-Thorax versus 71.9% with typical images in severe-critical disease and 87.5% in post-acute disease (P < 0.001). Diffuse alveolar damage was absent in mild-moderate disease but present in 93.8% and 87.5% of patients with severe-critical and post-acute COVID-19 respectively (P = 0.002). Other organs with COVID-19 related histopathological changes were liver and heart. Interferon-γ levels were significantly higher in patients with severe-critical COVID-19 (P = 0.046). Anti-SARS CoV-2 IgG was positive in 66%, 40.6% and 87.5% of patients with mild-moderate, severe-critical and post-acute COVID-19 respectively (n.s.). Significant differences in histopathological and immunological characteristics between patients with mild-moderate disease compared to patients with severe-critical disease were found, whereas differences between patients with severe-critical disease and post-acute disease were limited. This emphasizes the need for tailored treatment of COVID-19 patients. Nature Publishing Group UK 2022-01-25 /pmc/articles/PMC8789771/ /pubmed/35079048 http://dx.doi.org/10.1038/s41598-022-05186-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article D’Onofrio, Valentino Keulen, Lotte Vandendriessche, Annelore Dubois, Jasperina Cartuyvels, Reinoud Vanden Abeele, Marie-Elena Fraussen, Judith Vandormael, Patrick Somers, Veerle Achten, Ruth Dendooven, Amélie Driessen, Ann Augsburg, Lukasz Hellings, Niels Lammens, Martin Vanrusselt, Jan Cox, Janneke Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title | Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title_full | Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title_fullStr | Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title_full_unstemmed | Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title_short | Studying the clinical, radiological, histological, microbiological, and immunological evolution during the different COVID-19 disease stages using minimal invasive autopsy |
title_sort | studying the clinical, radiological, histological, microbiological, and immunological evolution during the different covid-19 disease stages using minimal invasive autopsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789771/ https://www.ncbi.nlm.nih.gov/pubmed/35079048 http://dx.doi.org/10.1038/s41598-022-05186-y |
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