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Characteristics of viral pneumonia in the COVID-19 era: an update
Influenza virus, rhinovirus, and adenovirus frequently cause viral pneumonia, an important cause of morbidity and mortality especially in the extreme ages of life. During the last two decades, three outbreaks of coronavirus-associated pneumonia, namely Severe Acute Respiratory Syndrome, Middle-East...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006879/ https://www.ncbi.nlm.nih.gov/pubmed/33782861 http://dx.doi.org/10.1007/s15010-021-01603-y |
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author | Pagliano, P. Sellitto, C. Conti, V. Ascione, T. Esposito, Silvano |
author_facet | Pagliano, P. Sellitto, C. Conti, V. Ascione, T. Esposito, Silvano |
author_sort | Pagliano, P. |
collection | PubMed |
description | Influenza virus, rhinovirus, and adenovirus frequently cause viral pneumonia, an important cause of morbidity and mortality especially in the extreme ages of life. During the last two decades, three outbreaks of coronavirus-associated pneumonia, namely Severe Acute Respiratory Syndrome, Middle-East Respiratory Syndrome, and the ongoing Coronavirus Infectious Disease—2019 (COVID-19) were reported. The rate of diagnosis of viral pneumonia is increasingly approaching 60% among children identified as having community-acquired pneumonia (CAP). Clinical presentation ranges from mild to severe pneumonitis complicated by respiratory failure in severe cases. The most vulnerable patients, the elderly and those living with cancer, report a relevant mortality rate. No clinical characteristics can be useful to conclusively distinguish the different etiology of viral pneumonia. However, accessory symptoms, such as anosmia or ageusia together with respiratory symptoms suggest COVID-19. An etiologic-based treatment of viral pneumonia is possible in a small percentage of cases only. Neuraminidase inhibitors have been proven to reduce the need for ventilatory support and mortality rate while only a few data support the large-scale use of other antivirals. A low-middle dose of dexamethasone and heparin seems to be effective in COVID-19 patients, but data regarding their possible efficacy in viral pneumonia caused by other viruses are conflicting. In conclusion, viral pneumonia is a relevant cause of CAP, whose interest is increasing due to the current COVID-19 outbreak. To set up a therapeutic approach is difficult because of the low number of active molecules and the conflicting data bearing supportive treatments such as steroids. |
format | Online Article Text |
id | pubmed-8006879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80068792021-03-30 Characteristics of viral pneumonia in the COVID-19 era: an update Pagliano, P. Sellitto, C. Conti, V. Ascione, T. Esposito, Silvano Infection Review Influenza virus, rhinovirus, and adenovirus frequently cause viral pneumonia, an important cause of morbidity and mortality especially in the extreme ages of life. During the last two decades, three outbreaks of coronavirus-associated pneumonia, namely Severe Acute Respiratory Syndrome, Middle-East Respiratory Syndrome, and the ongoing Coronavirus Infectious Disease—2019 (COVID-19) were reported. The rate of diagnosis of viral pneumonia is increasingly approaching 60% among children identified as having community-acquired pneumonia (CAP). Clinical presentation ranges from mild to severe pneumonitis complicated by respiratory failure in severe cases. The most vulnerable patients, the elderly and those living with cancer, report a relevant mortality rate. No clinical characteristics can be useful to conclusively distinguish the different etiology of viral pneumonia. However, accessory symptoms, such as anosmia or ageusia together with respiratory symptoms suggest COVID-19. An etiologic-based treatment of viral pneumonia is possible in a small percentage of cases only. Neuraminidase inhibitors have been proven to reduce the need for ventilatory support and mortality rate while only a few data support the large-scale use of other antivirals. A low-middle dose of dexamethasone and heparin seems to be effective in COVID-19 patients, but data regarding their possible efficacy in viral pneumonia caused by other viruses are conflicting. In conclusion, viral pneumonia is a relevant cause of CAP, whose interest is increasing due to the current COVID-19 outbreak. To set up a therapeutic approach is difficult because of the low number of active molecules and the conflicting data bearing supportive treatments such as steroids. Springer Berlin Heidelberg 2021-03-29 2021 /pmc/articles/PMC8006879/ /pubmed/33782861 http://dx.doi.org/10.1007/s15010-021-01603-y Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Pagliano, P. Sellitto, C. Conti, V. Ascione, T. Esposito, Silvano Characteristics of viral pneumonia in the COVID-19 era: an update |
title | Characteristics of viral pneumonia in the COVID-19 era: an update |
title_full | Characteristics of viral pneumonia in the COVID-19 era: an update |
title_fullStr | Characteristics of viral pneumonia in the COVID-19 era: an update |
title_full_unstemmed | Characteristics of viral pneumonia in the COVID-19 era: an update |
title_short | Characteristics of viral pneumonia in the COVID-19 era: an update |
title_sort | characteristics of viral pneumonia in the covid-19 era: an update |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006879/ https://www.ncbi.nlm.nih.gov/pubmed/33782861 http://dx.doi.org/10.1007/s15010-021-01603-y |
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