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Influenza A(H1N1)pdm09-related pneumonia and other complications
Influenza A(H1N1)pdm09 virus infection was associated with significant morbidity, mainly among children and young adults. The majority of patients had self-limited mild-to-moderate uncomplicated disease. However, some patients developed severe illness and some died. In addition to respiratory compli...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier España, S.L.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130364/ https://www.ncbi.nlm.nih.gov/pubmed/23116792 http://dx.doi.org/10.1016/S0213-005X(12)70104-0 |
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author | Viasus, Diego Oteo Revuelta, José A. Martínez-Montauti, Joaquín Carratalà, Jordi |
author_facet | Viasus, Diego Oteo Revuelta, José A. Martínez-Montauti, Joaquín Carratalà, Jordi |
author_sort | Viasus, Diego |
collection | PubMed |
description | Influenza A(H1N1)pdm09 virus infection was associated with significant morbidity, mainly among children and young adults. The majority of patients had self-limited mild-to-moderate uncomplicated disease. However, some patients developed severe illness and some died. In addition to respiratory complications, several complications due to direct and indirect effects on other body systems were associated with influenza A(H1N1)pdm09 virus infection. The main complications reported in hospitalized adults with influenza A(H1N1)pdm09 were pneumonia (primary influenza pneumonia and concomitant/secondary bacterial pneumonia), exacerbations of chronic pulmonary diseases (mainly chronic obstructive pulmonary disease and asthma), the need for intensive unit care admission (including mechanical ventilation, acute respiratory distress syndrome and septic shock), nosocomial infections and acute cardiac events. In experimentally infected animals, the level of pulmonary replication of the influenza A(H1N1)pdm09 virus was higher than that of seasonal influenza viruses. Pathological studies in autopsy specimens indicated that the influenza A(H1N1)pdm09 virus mainly targeted the lower respiratory tract, resulting in diffuse alveolar damage (edema, hyaline membranes, inflammation, and fibrosis), manifested clinically by severe acute respiratory distress syndrome with refractory hypoxemia. Influenza A(H1N1)pdm09-related pneumonia and other complications were associated with increased morbidity and mortality among hospitalized patients. |
format | Online Article Text |
id | pubmed-7130364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier España, S.L. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71303642020-04-08 Influenza A(H1N1)pdm09-related pneumonia and other complications Viasus, Diego Oteo Revuelta, José A. Martínez-Montauti, Joaquín Carratalà, Jordi Enferm Infecc Microbiol Clin Article Influenza A(H1N1)pdm09 virus infection was associated with significant morbidity, mainly among children and young adults. The majority of patients had self-limited mild-to-moderate uncomplicated disease. However, some patients developed severe illness and some died. In addition to respiratory complications, several complications due to direct and indirect effects on other body systems were associated with influenza A(H1N1)pdm09 virus infection. The main complications reported in hospitalized adults with influenza A(H1N1)pdm09 were pneumonia (primary influenza pneumonia and concomitant/secondary bacterial pneumonia), exacerbations of chronic pulmonary diseases (mainly chronic obstructive pulmonary disease and asthma), the need for intensive unit care admission (including mechanical ventilation, acute respiratory distress syndrome and septic shock), nosocomial infections and acute cardiac events. In experimentally infected animals, the level of pulmonary replication of the influenza A(H1N1)pdm09 virus was higher than that of seasonal influenza viruses. Pathological studies in autopsy specimens indicated that the influenza A(H1N1)pdm09 virus mainly targeted the lower respiratory tract, resulting in diffuse alveolar damage (edema, hyaline membranes, inflammation, and fibrosis), manifested clinically by severe acute respiratory distress syndrome with refractory hypoxemia. Influenza A(H1N1)pdm09-related pneumonia and other complications were associated with increased morbidity and mortality among hospitalized patients. Elsevier España, S.L. 2012-10 2012-10-29 /pmc/articles/PMC7130364/ /pubmed/23116792 http://dx.doi.org/10.1016/S0213-005X(12)70104-0 Text en Copyright © 2012 Elsevier España, S.L. 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 | Article Viasus, Diego Oteo Revuelta, José A. Martínez-Montauti, Joaquín Carratalà, Jordi Influenza A(H1N1)pdm09-related pneumonia and other complications |
title | Influenza A(H1N1)pdm09-related pneumonia and other complications |
title_full | Influenza A(H1N1)pdm09-related pneumonia and other complications |
title_fullStr | Influenza A(H1N1)pdm09-related pneumonia and other complications |
title_full_unstemmed | Influenza A(H1N1)pdm09-related pneumonia and other complications |
title_short | Influenza A(H1N1)pdm09-related pneumonia and other complications |
title_sort | influenza a(h1n1)pdm09-related pneumonia and other complications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130364/ https://www.ncbi.nlm.nih.gov/pubmed/23116792 http://dx.doi.org/10.1016/S0213-005X(12)70104-0 |
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