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How to treat VAP due to MDR pathogens in ICU patients
BACKGROUND: The increasing occurrence of multidrug resistant (MDR) bacteria arises at a time when there is a lack of antibiotics active against these pathogens and few new antimicrobials are in the pipelines of the pharmaceutical industry. Treatment of ventilator-associated pneumonia (VAP) caused es...
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/PMC4289192/ https://www.ncbi.nlm.nih.gov/pubmed/25430700 http://dx.doi.org/10.1186/1471-2334-14-135 |
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author | Garnacho-Montero, José Corcia-Palomo, Yael Amaya-Villar, Rosario Martin-Villen, Luis |
author_facet | Garnacho-Montero, José Corcia-Palomo, Yael Amaya-Villar, Rosario Martin-Villen, Luis |
author_sort | Garnacho-Montero, José |
collection | PubMed |
description | BACKGROUND: The increasing occurrence of multidrug resistant (MDR) bacteria arises at a time when there is a lack of antibiotics active against these pathogens and few new antimicrobials are in the pipelines of the pharmaceutical industry. Treatment of ventilator-associated pneumonia (VAP) caused especially by MDR Gram-negative bacilli (GNB) represents a real challenge due to the dearth of treatment options. METHODS: We searched the medical literature relevant about management of ventilator-associated pneumonia caused by multi-drug resistant pathogens including GNB and methicillin-resistant S. aureus. RESULTS: Empirical therapy should be prescribed based on the local pattern of susceptibilities. Colistin and tigecycline are in many cases the unique options for the treatment of many episodes of VAP caused by MDR-GNB. Tigecyline (not licensed for treatment of pneumonia) should be used with an initial bolus of 200 mg followed by 100 mg every 12 h. The need for a loading dose and the administration of high doses of colistin (9 million IU/day in two or three doses) is currently accepted. Vancomycin has been considered the treatment of choice for pneumonia due to MRSA although linezolid may provide higher rate of clinical cure for MRSA VAP with a good safety profile. The initial antibiotic treatment must be reassessed and simplify in accordance of culture results. CONCLUSIONS: Empirical treatment of VAP due to MDR pathogens should be based on knowledge of local ecology. A strategy combining early high doses of effective agents with subsequent simplification in the light of microbiologic information is recommended. |
format | Online Article Text |
id | pubmed-4289192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42891922015-01-11 How to treat VAP due to MDR pathogens in ICU patients Garnacho-Montero, José Corcia-Palomo, Yael Amaya-Villar, Rosario Martin-Villen, Luis BMC Infect Dis Review BACKGROUND: The increasing occurrence of multidrug resistant (MDR) bacteria arises at a time when there is a lack of antibiotics active against these pathogens and few new antimicrobials are in the pipelines of the pharmaceutical industry. Treatment of ventilator-associated pneumonia (VAP) caused especially by MDR Gram-negative bacilli (GNB) represents a real challenge due to the dearth of treatment options. METHODS: We searched the medical literature relevant about management of ventilator-associated pneumonia caused by multi-drug resistant pathogens including GNB and methicillin-resistant S. aureus. RESULTS: Empirical therapy should be prescribed based on the local pattern of susceptibilities. Colistin and tigecycline are in many cases the unique options for the treatment of many episodes of VAP caused by MDR-GNB. Tigecyline (not licensed for treatment of pneumonia) should be used with an initial bolus of 200 mg followed by 100 mg every 12 h. The need for a loading dose and the administration of high doses of colistin (9 million IU/day in two or three doses) is currently accepted. Vancomycin has been considered the treatment of choice for pneumonia due to MRSA although linezolid may provide higher rate of clinical cure for MRSA VAP with a good safety profile. The initial antibiotic treatment must be reassessed and simplify in accordance of culture results. CONCLUSIONS: Empirical treatment of VAP due to MDR pathogens should be based on knowledge of local ecology. A strategy combining early high doses of effective agents with subsequent simplification in the light of microbiologic information is recommended. BioMed Central 2014-11-28 /pmc/articles/PMC4289192/ /pubmed/25430700 http://dx.doi.org/10.1186/1471-2334-14-135 Text en © Garnacho-Montero et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed 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 Garnacho-Montero, José Corcia-Palomo, Yael Amaya-Villar, Rosario Martin-Villen, Luis How to treat VAP due to MDR pathogens in ICU patients |
title | How to treat VAP due to MDR pathogens in ICU patients |
title_full | How to treat VAP due to MDR pathogens in ICU patients |
title_fullStr | How to treat VAP due to MDR pathogens in ICU patients |
title_full_unstemmed | How to treat VAP due to MDR pathogens in ICU patients |
title_short | How to treat VAP due to MDR pathogens in ICU patients |
title_sort | how to treat vap due to mdr pathogens in icu patients |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289192/ https://www.ncbi.nlm.nih.gov/pubmed/25430700 http://dx.doi.org/10.1186/1471-2334-14-135 |
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