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Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients

OBJECTIVES: To summarise and discuss current knowledge about SARS-CoV-2-associated infectious/immune-mediated central nervous system (CNS)-disease. METHOD: Literature review. RESULTS: Altogether 28 articles were found, which reported 48 patients with SARS-CoV-2-associated infectious/immune-mediated ...

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Autores principales: Finsterer, Josef, Scorza, Fulvio A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166526/
https://www.ncbi.nlm.nih.gov/pubmed/34275539
http://dx.doi.org/10.1016/j.jocn.2021.05.065
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author Finsterer, Josef
Scorza, Fulvio A.
author_facet Finsterer, Josef
Scorza, Fulvio A.
author_sort Finsterer, Josef
collection PubMed
description OBJECTIVES: To summarise and discuss current knowledge about SARS-CoV-2-associated infectious/immune-mediated central nervous system (CNS)-disease. METHOD: Literature review. RESULTS: Altogether 28 articles were found, which reported 48 patients with SARS-CoV-2-associated infectious/immune-mediated CNS-disease. Age ranged from 22 to 79y. There was male preponderance. There were 14 patients with infectious CNS-disease (meningitis (n = 1), encephalitis (n = 5), meningo-encephalitis (n = 5), myelitis (n = 3)), and 34 patients with parainfectious CNS-disease (encephalopathy (n = 18), autoimmune encephalitis (n = 11), acute, disseminated, encephalo-myelitis (n = 3), acute, haemorrhagic, necrotizing encephalopathy (n = 2)). The cerebrospinal fluid (CSF) was tested for SARS-CoV-2 in 40 patients and was positive for the virus in 4 patients with infectious CNS-disease but was negative for the virus in all patients with parainfectious CNS-disease. Immune-modulating treatment may be more effective than virostatics/antibiotics for SARS-CoV-2-associated infectious/parainfectious, non-vascular, non-hypoxic CNS-disease. In patients with autoimmune encephalitis plasmapheresis may be beneficial. Twenty-two patients recovered, 2 did not, and 6 patients died. CONCLUSIONS: SARS-CoV-2 can cause infectious/immune-mediated CNS-disease. The CSF is positive for virus-RNA in only few patients with infectious CNS-disease but negative for virus-RNA in immune-mediated CNS-disease, suggesting an immune-mediated pathophysiological mechanism. The outcome of SARS-CoV-2-associated infectious/immune-mediated CNS-disease is favourable in the majority of cases but can be fatal in single cases.
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spelling pubmed-81665262021-06-01 Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients Finsterer, Josef Scorza, Fulvio A. J Clin Neurosci Short Communication OBJECTIVES: To summarise and discuss current knowledge about SARS-CoV-2-associated infectious/immune-mediated central nervous system (CNS)-disease. METHOD: Literature review. RESULTS: Altogether 28 articles were found, which reported 48 patients with SARS-CoV-2-associated infectious/immune-mediated CNS-disease. Age ranged from 22 to 79y. There was male preponderance. There were 14 patients with infectious CNS-disease (meningitis (n = 1), encephalitis (n = 5), meningo-encephalitis (n = 5), myelitis (n = 3)), and 34 patients with parainfectious CNS-disease (encephalopathy (n = 18), autoimmune encephalitis (n = 11), acute, disseminated, encephalo-myelitis (n = 3), acute, haemorrhagic, necrotizing encephalopathy (n = 2)). The cerebrospinal fluid (CSF) was tested for SARS-CoV-2 in 40 patients and was positive for the virus in 4 patients with infectious CNS-disease but was negative for the virus in all patients with parainfectious CNS-disease. Immune-modulating treatment may be more effective than virostatics/antibiotics for SARS-CoV-2-associated infectious/parainfectious, non-vascular, non-hypoxic CNS-disease. In patients with autoimmune encephalitis plasmapheresis may be beneficial. Twenty-two patients recovered, 2 did not, and 6 patients died. CONCLUSIONS: SARS-CoV-2 can cause infectious/immune-mediated CNS-disease. The CSF is positive for virus-RNA in only few patients with infectious CNS-disease but negative for virus-RNA in immune-mediated CNS-disease, suggesting an immune-mediated pathophysiological mechanism. The outcome of SARS-CoV-2-associated infectious/immune-mediated CNS-disease is favourable in the majority of cases but can be fatal in single cases. Elsevier Ltd. 2021-08 2021-06-01 /pmc/articles/PMC8166526/ /pubmed/34275539 http://dx.doi.org/10.1016/j.jocn.2021.05.065 Text en © 2021 Elsevier Ltd. All rights reserved. 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 Short Communication
Finsterer, Josef
Scorza, Fulvio A.
Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title_full Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title_fullStr Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title_full_unstemmed Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title_short Infectious and immune-mediated central nervous system disease in 48 COVID-19 patients
title_sort infectious and immune-mediated central nervous system disease in 48 covid-19 patients
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166526/
https://www.ncbi.nlm.nih.gov/pubmed/34275539
http://dx.doi.org/10.1016/j.jocn.2021.05.065
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