Author: McMullen, Phillip; Pytel, Peter; Snyder, Alexis; Smith, Heather; Vickery, Jasmine; Brainer, James; Guzy, Robert; Wu, David; Schoettler, Nathan; Adegunsoye, Ayodeji; Sperling, Anne; Hart, John; Alpert, Lindsay; Chang, Anthony; Gurbuxani, Sandeep; Krausz, Thomas; Husain, Aliya N; Mueller, Jeffrey
Title: A series of COVIDâ€19 autopsies with clinical and pathologic comparisons to both seasonal and pandemic influenza Cord-id: egjbk5dg Document date: 2021_5_7
ID: egjbk5dg
Snippet: Autopsies of patients who have died from COVIDâ€19 have been crucial in delineating patterns of injury associated with SARSâ€CoVâ€2 infection. Despite their utility, comprehensive autopsy studies are somewhat lacking relative to the global burden of disease, and very few comprehensive studies contextualize the findings to other fatal viral infections. We developed a novel autopsy protocol in order to perform postmortem examinations on victims of COVIDâ€19 and herein describe detailed clinica
Document: Autopsies of patients who have died from COVIDâ€19 have been crucial in delineating patterns of injury associated with SARSâ€CoVâ€2 infection. Despite their utility, comprehensive autopsy studies are somewhat lacking relative to the global burden of disease, and very few comprehensive studies contextualize the findings to other fatal viral infections. We developed a novel autopsy protocol in order to perform postmortem examinations on victims of COVIDâ€19 and herein describe detailed clinical information, gross findings, and histologic features observed in the first 16 complete COVIDâ€19 autopsies. We also critically evaluated the role of ancillary studies used to establish a diagnosis of COVIDâ€19 at autopsy, including immunohistochemistry (IHC), in situ hybridization (ISH), and electron microscopy (EM). IHC and ISH targeting SARSâ€CoVâ€2 were comparable in terms of the location and number of infected cells in lung tissue; however, nonspecific staining of bacteria was seen occasionally with IHC. EM was unrevealing in blindly sampled tissues. We then compared the clinical and histologic features present in this series to six archival cases of fatal seasonal influenza and six archival cases of pandemic influenza from the fourth wave of the ‘Spanish Flu’ in the winter of 1920. In addition to routine histology, the inflammatory infiltrates in the lungs of COVIDâ€19 and seasonal influenza victims were compared using quantitative IHC. Our results demonstrate that the clinical and histologic features of COVIDâ€19 are similar to those seen in fatal cases of influenza, and the two diseases tend to overlap histologically. There was no significant difference in the composition of the inflammatory infiltrate in COVIDâ€19 and influenza at sites of acute lung injury at the time of autopsy. Our study underscores the relatively nonspecific clinical features and pathologic changes shared between severe cases of COVIDâ€19 and influenza, while also providing important caveats to ancillary methods of viral detection.
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