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Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic

Deaths during the 1918–19 influenza pandemic have been attributed to a hypervirulent influenza strain. Hence, preparations for the next pandemic focus almost exclusively on vaccine prevention and antiviral treatment for infections with a novel influenza strain. However, we hypothesize that infection...

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Detalles Bibliográficos
Autores principales: Brundage, John F., Shanks, G. Dennis
Formato: Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600384/
https://www.ncbi.nlm.nih.gov/pubmed/18680641
http://dx.doi.org/10.3201/eid1408.071313
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author Brundage, John F.
Shanks, G. Dennis
author_facet Brundage, John F.
Shanks, G. Dennis
author_sort Brundage, John F.
collection PubMed
description Deaths during the 1918–19 influenza pandemic have been attributed to a hypervirulent influenza strain. Hence, preparations for the next pandemic focus almost exclusively on vaccine prevention and antiviral treatment for infections with a novel influenza strain. However, we hypothesize that infections with the pandemic strain generally caused self-limited (rarely fatal) illnesses that enabled colonizing strains of bacteria to produce highly lethal pneumonias. This sequential-infection hypothesis is consistent with characteristics of the 1918–19 pandemic, contemporaneous expert opinion, and current knowledge regarding the pathophysiologic effects of influenza viruses and their interactions with respiratory bacteria. This hypothesis suggests opportunities for prevention and treatment during the next pandemic (e.g., with bacterial vaccines and antimicrobial drugs), particularly if a pandemic strain–specific vaccine is unavailable or inaccessible to isolated, crowded, or medically underserved populations.
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spelling pubmed-26003842009-01-13 Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic Brundage, John F. Shanks, G. Dennis Emerg Infect Dis Historical Review Deaths during the 1918–19 influenza pandemic have been attributed to a hypervirulent influenza strain. Hence, preparations for the next pandemic focus almost exclusively on vaccine prevention and antiviral treatment for infections with a novel influenza strain. However, we hypothesize that infections with the pandemic strain generally caused self-limited (rarely fatal) illnesses that enabled colonizing strains of bacteria to produce highly lethal pneumonias. This sequential-infection hypothesis is consistent with characteristics of the 1918–19 pandemic, contemporaneous expert opinion, and current knowledge regarding the pathophysiologic effects of influenza viruses and their interactions with respiratory bacteria. This hypothesis suggests opportunities for prevention and treatment during the next pandemic (e.g., with bacterial vaccines and antimicrobial drugs), particularly if a pandemic strain–specific vaccine is unavailable or inaccessible to isolated, crowded, or medically underserved populations. Centers for Disease Control and Prevention 2008-08 /pmc/articles/PMC2600384/ /pubmed/18680641 http://dx.doi.org/10.3201/eid1408.071313 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Historical Review
Brundage, John F.
Shanks, G. Dennis
Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title_full Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title_fullStr Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title_full_unstemmed Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title_short Deaths from Bacterial Pneumonia during 1918–19 Influenza Pandemic
title_sort deaths from bacterial pneumonia during 1918–19 influenza pandemic
topic Historical Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600384/
https://www.ncbi.nlm.nih.gov/pubmed/18680641
http://dx.doi.org/10.3201/eid1408.071313
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