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Year in review 2013: critical care - respiratory infections
Infectious complications, particularly in the respiratory tract of critically ill patients, are related to increased mortality. Severe infection is part of a multiple system illness and female patients with severe sepsis have a worse prognosis compared to males. Kallistatin is a protective hormokine...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330923/ https://www.ncbi.nlm.nih.gov/pubmed/25672674 http://dx.doi.org/10.1186/s13054-014-0572-3 |
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author | Nair, Girish B Niederman, Michael S |
author_facet | Nair, Girish B Niederman, Michael S |
author_sort | Nair, Girish B |
collection | PubMed |
description | Infectious complications, particularly in the respiratory tract of critically ill patients, are related to increased mortality. Severe infection is part of a multiple system illness and female patients with severe sepsis have a worse prognosis compared to males. Kallistatin is a protective hormokine released during monocyte activation and low levels in the setting of septic shock can predict adverse outcomes. Presepsin is another biomarker that was recently evaluated and is elevated in patients with severe sepsis patients at risk of dying. The Centers for Disease Control and Prevention has introduced new definitions for identifying patients at risk of ventilator-associated complications (VACs), but several other conditions, such as pulmonary edema and acute respiratory distress syndrome, may cause VACs, and not all patients with VACs may have ventilator-associated pneumonia. New studies have suggested strategies to identify patients at risk for resistant pathogen infection and therapies that optimize efficacy, without the overuse of broad-spectrum therapy in patients with healthcare-associated pneumonia. Innovative strategies using optimized dosing of antimicrobials, maximizing the pharmacokinetic and pharmacodynamic properties of drugs in critically ill patients, and newer routes of drug delivery are being explored to combat drug-resistant pathogens. We summarize the major clinical studies on respiratory infections in critically ill patients published in 2013. |
format | Online Article Text |
id | pubmed-4330923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43309232015-02-18 Year in review 2013: critical care - respiratory infections Nair, Girish B Niederman, Michael S Crit Care Review Infectious complications, particularly in the respiratory tract of critically ill patients, are related to increased mortality. Severe infection is part of a multiple system illness and female patients with severe sepsis have a worse prognosis compared to males. Kallistatin is a protective hormokine released during monocyte activation and low levels in the setting of septic shock can predict adverse outcomes. Presepsin is another biomarker that was recently evaluated and is elevated in patients with severe sepsis patients at risk of dying. The Centers for Disease Control and Prevention has introduced new definitions for identifying patients at risk of ventilator-associated complications (VACs), but several other conditions, such as pulmonary edema and acute respiratory distress syndrome, may cause VACs, and not all patients with VACs may have ventilator-associated pneumonia. New studies have suggested strategies to identify patients at risk for resistant pathogen infection and therapies that optimize efficacy, without the overuse of broad-spectrum therapy in patients with healthcare-associated pneumonia. Innovative strategies using optimized dosing of antimicrobials, maximizing the pharmacokinetic and pharmacodynamic properties of drugs in critically ill patients, and newer routes of drug delivery are being explored to combat drug-resistant pathogens. We summarize the major clinical studies on respiratory infections in critically ill patients published in 2013. BioMed Central 2014-10-29 2014 /pmc/articles/PMC4330923/ /pubmed/25672674 http://dx.doi.org/10.1186/s13054-014-0572-3 Text en © Nair and Niederman; licensee BioMed Central Ltd. 2014 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Nair, Girish B Niederman, Michael S Year in review 2013: critical care - respiratory infections |
title | Year in review 2013: critical care - respiratory infections |
title_full | Year in review 2013: critical care - respiratory infections |
title_fullStr | Year in review 2013: critical care - respiratory infections |
title_full_unstemmed | Year in review 2013: critical care - respiratory infections |
title_short | Year in review 2013: critical care - respiratory infections |
title_sort | year in review 2013: critical care - respiratory infections |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330923/ https://www.ncbi.nlm.nih.gov/pubmed/25672674 http://dx.doi.org/10.1186/s13054-014-0572-3 |
work_keys_str_mv | AT nairgirishb yearinreview2013criticalcarerespiratoryinfections AT niedermanmichaels yearinreview2013criticalcarerespiratoryinfections |