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A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression

Since the outbreak of the COVID-19 pandemic, much has been learned regarding its clinical course, prognostic inflammatory markers, disease complications, and mechanical ventilation strategy. Clinically, three stages have been identified based on viral infection, pulmonary involvement with inflammati...

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Autores principales: Polak, Samuel B., Van Gool, Inge C., Cohen, Danielle, von der Thüsen, Jan H., van Paassen, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: United States & Canadian Academy of Pathology. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306927/
https://www.ncbi.nlm.nih.gov/pubmed/32572155
http://dx.doi.org/10.1038/s41379-020-0603-3
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author Polak, Samuel B.
Van Gool, Inge C.
Cohen, Danielle
von der Thüsen, Jan H.
van Paassen, Judith
author_facet Polak, Samuel B.
Van Gool, Inge C.
Cohen, Danielle
von der Thüsen, Jan H.
van Paassen, Judith
author_sort Polak, Samuel B.
collection PubMed
description Since the outbreak of the COVID-19 pandemic, much has been learned regarding its clinical course, prognostic inflammatory markers, disease complications, and mechanical ventilation strategy. Clinically, three stages have been identified based on viral infection, pulmonary involvement with inflammation, and fibrosis. Moreover, low and high elastance phenotypes can be distinguished in mechanically ventilated patients, based on lung mechanics, ventilation-to-perfusion ratio, and CT scans; these two phenotypes have presumed differences in their underlying pathophysiology. Although essential for therapeutic guidance, the pathophysiology of COVID-19 is poorly understood. Here, we systematically reviewed published case reports and case series in order to increase our understanding of COVID-19 pathophysiology by constructing a timeline and correlating histopathological findings with clinical stages of COVID-19. Using PRISMA-IPD guidelines, 42 articles reporting 198 individual cases were included in our analysis. In lung samples (n = 131 cases), we identified three main histological patterns: epithelial (n = 110, 85%), with reactive epithelial changes and DAD; vascular (n = 76, 59%) with microvascular damage, (micro)thrombi, and acute fibrinous and organizing pneumonia; and fibrotic (n = 28, 22%) with interstitial fibrosis. The epithelial and vascular patterns can present in all stages of symptomatic COVID-19, whereas the fibrotic pattern presents starting at ~3 weeks. Moreover, patients can present with more than one pattern, either simultaneously or consecutively. These findings are consistent with knowledge regarding clinical patterns of viral infection, development of hyperinflammation and hypercoagulability, and fibrosis. Close collaboration among medical staff is necessary in order to translate this knowledge and classification of pathophysiological mechanisms into clinical stages of disease in individual patients. Moreover, further research, including histopathological studies, is warranted in order to develop reliable, clinically relevant biomarkers by correlating these pathological findings with laboratory results and radiological findings, thus, increasing our understanding of COVID-19 and facilitating the move to precision medicine for treating patients.
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spelling pubmed-73069272020-06-22 A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression Polak, Samuel B. Van Gool, Inge C. Cohen, Danielle von der Thüsen, Jan H. van Paassen, Judith Mod Pathol Review Article Since the outbreak of the COVID-19 pandemic, much has been learned regarding its clinical course, prognostic inflammatory markers, disease complications, and mechanical ventilation strategy. Clinically, three stages have been identified based on viral infection, pulmonary involvement with inflammation, and fibrosis. Moreover, low and high elastance phenotypes can be distinguished in mechanically ventilated patients, based on lung mechanics, ventilation-to-perfusion ratio, and CT scans; these two phenotypes have presumed differences in their underlying pathophysiology. Although essential for therapeutic guidance, the pathophysiology of COVID-19 is poorly understood. Here, we systematically reviewed published case reports and case series in order to increase our understanding of COVID-19 pathophysiology by constructing a timeline and correlating histopathological findings with clinical stages of COVID-19. Using PRISMA-IPD guidelines, 42 articles reporting 198 individual cases were included in our analysis. In lung samples (n = 131 cases), we identified three main histological patterns: epithelial (n = 110, 85%), with reactive epithelial changes and DAD; vascular (n = 76, 59%) with microvascular damage, (micro)thrombi, and acute fibrinous and organizing pneumonia; and fibrotic (n = 28, 22%) with interstitial fibrosis. The epithelial and vascular patterns can present in all stages of symptomatic COVID-19, whereas the fibrotic pattern presents starting at ~3 weeks. Moreover, patients can present with more than one pattern, either simultaneously or consecutively. These findings are consistent with knowledge regarding clinical patterns of viral infection, development of hyperinflammation and hypercoagulability, and fibrosis. Close collaboration among medical staff is necessary in order to translate this knowledge and classification of pathophysiological mechanisms into clinical stages of disease in individual patients. Moreover, further research, including histopathological studies, is warranted in order to develop reliable, clinically relevant biomarkers by correlating these pathological findings with laboratory results and radiological findings, thus, increasing our understanding of COVID-19 and facilitating the move to precision medicine for treating patients. United States & Canadian Academy of Pathology. 2020-11 2023-01-05 /pmc/articles/PMC7306927/ /pubmed/32572155 http://dx.doi.org/10.1038/s41379-020-0603-3 Text en © 2020 United States & Canadian Academy of Pathology. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review Article
Polak, Samuel B.
Van Gool, Inge C.
Cohen, Danielle
von der Thüsen, Jan H.
van Paassen, Judith
A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title_full A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title_fullStr A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title_full_unstemmed A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title_short A systematic review of pathological findings in COVID-19: a pathophysiological timeline and possible mechanisms of disease progression
title_sort systematic review of pathological findings in covid-19: a pathophysiological timeline and possible mechanisms of disease progression
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306927/
https://www.ncbi.nlm.nih.gov/pubmed/32572155
http://dx.doi.org/10.1038/s41379-020-0603-3
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