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Initial antimicrobial management of sepsis
Sepsis is a common consequence of infection, associated with a mortality rate > 25%. Although community-acquired sepsis is more common, hospital-acquired infection is more lethal. The most common site of infection is the lung, followed by abdominal infection, catheter-associated blood steam infec...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390082/ https://www.ncbi.nlm.nih.gov/pubmed/34446092 http://dx.doi.org/10.1186/s13054-021-03736-w |
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author | Niederman, Michael S. Baron, Rebecca M. Bouadma, Lila Calandra, Thierry Daneman, Nick DeWaele, Jan Kollef, Marin H. Lipman, Jeffrey Nair, Girish B. |
author_facet | Niederman, Michael S. Baron, Rebecca M. Bouadma, Lila Calandra, Thierry Daneman, Nick DeWaele, Jan Kollef, Marin H. Lipman, Jeffrey Nair, Girish B. |
author_sort | Niederman, Michael S. |
collection | PubMed |
description | Sepsis is a common consequence of infection, associated with a mortality rate > 25%. Although community-acquired sepsis is more common, hospital-acquired infection is more lethal. The most common site of infection is the lung, followed by abdominal infection, catheter-associated blood steam infection and urinary tract infection. Gram-negative sepsis is more common than gram-positive infection, but sepsis can also be due to fungal and viral pathogens. To reduce mortality, it is necessary to give immediate, empiric, broad-spectrum therapy to those with severe sepsis and/or shock, but this approach can drive antimicrobial overuse and resistance and should be accompanied by a commitment to de-escalation and antimicrobial stewardship. Biomarkers such a procalcitonin can provide decision support for antibiotic use, and may identify patients with a low likelihood of infection, and in some settings, can guide duration of antibiotic therapy. Sepsis can involve drug-resistant pathogens, and this often necessitates consideration of newer antimicrobial agents. |
format | Online Article Text |
id | pubmed-8390082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83900822021-08-27 Initial antimicrobial management of sepsis Niederman, Michael S. Baron, Rebecca M. Bouadma, Lila Calandra, Thierry Daneman, Nick DeWaele, Jan Kollef, Marin H. Lipman, Jeffrey Nair, Girish B. Crit Care Review Sepsis is a common consequence of infection, associated with a mortality rate > 25%. Although community-acquired sepsis is more common, hospital-acquired infection is more lethal. The most common site of infection is the lung, followed by abdominal infection, catheter-associated blood steam infection and urinary tract infection. Gram-negative sepsis is more common than gram-positive infection, but sepsis can also be due to fungal and viral pathogens. To reduce mortality, it is necessary to give immediate, empiric, broad-spectrum therapy to those with severe sepsis and/or shock, but this approach can drive antimicrobial overuse and resistance and should be accompanied by a commitment to de-escalation and antimicrobial stewardship. Biomarkers such a procalcitonin can provide decision support for antibiotic use, and may identify patients with a low likelihood of infection, and in some settings, can guide duration of antibiotic therapy. Sepsis can involve drug-resistant pathogens, and this often necessitates consideration of newer antimicrobial agents. BioMed Central 2021-08-26 /pmc/articles/PMC8390082/ /pubmed/34446092 http://dx.doi.org/10.1186/s13054-021-03736-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Niederman, Michael S. Baron, Rebecca M. Bouadma, Lila Calandra, Thierry Daneman, Nick DeWaele, Jan Kollef, Marin H. Lipman, Jeffrey Nair, Girish B. Initial antimicrobial management of sepsis |
title | Initial antimicrobial management of sepsis |
title_full | Initial antimicrobial management of sepsis |
title_fullStr | Initial antimicrobial management of sepsis |
title_full_unstemmed | Initial antimicrobial management of sepsis |
title_short | Initial antimicrobial management of sepsis |
title_sort | initial antimicrobial management of sepsis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390082/ https://www.ncbi.nlm.nih.gov/pubmed/34446092 http://dx.doi.org/10.1186/s13054-021-03736-w |
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