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Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia

RATIONALE: Empirical antimicrobial therapy (EAT) for Acinetobacter infections may not be appropriate as it tends to be multidrug-resistant. This study evaluated the relationship between appropriate EAT and the outcomes of Intensive Care Unit (ICU) patients with Acinetobacter bacteremia. METHODS: Thi...

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Autores principales: Al-Dorzi, Hasan M., Asiri, Abdulaziz M., Shimemri, Abdullah, Tamim, Hani M., Al Johani, Sameera M., Al Dabbagh, Tarek, Arabi, Yaseen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652291/
https://www.ncbi.nlm.nih.gov/pubmed/26664563
http://dx.doi.org/10.4103/1817-1737.164302
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author Al-Dorzi, Hasan M.
Asiri, Abdulaziz M.
Shimemri, Abdullah
Tamim, Hani M.
Al Johani, Sameera M.
Al Dabbagh, Tarek
Arabi, Yaseen M.
author_facet Al-Dorzi, Hasan M.
Asiri, Abdulaziz M.
Shimemri, Abdullah
Tamim, Hani M.
Al Johani, Sameera M.
Al Dabbagh, Tarek
Arabi, Yaseen M.
author_sort Al-Dorzi, Hasan M.
collection PubMed
description RATIONALE: Empirical antimicrobial therapy (EAT) for Acinetobacter infections may not be appropriate as it tends to be multidrug-resistant. This study evaluated the relationship between appropriate EAT and the outcomes of Intensive Care Unit (ICU) patients with Acinetobacter bacteremia. METHODS: This is a retrospective study of patients admitted to a medical-surgical ICU (2005-2010) and developed Acinetobacter bacteremia during the stay. Patients were categorized according to EAT appropriateness, defined as administration of at least one antimicrobial agent to which the Acinetobacter was susceptible before susceptibility results were known. The relation between EAT appropriateness and outcomes was evaluated. RESULTS: Sixty patients developed Acinetobacter bacteremia in the 6-year period (age = 50 ± 19 years; 62% males; Acute Physiology and Chronic Health Evaluation II score = 28 ± 9; 98.3% with central lines; 67% in shock and 59% mechanically ventilated) on average on day 23 of ICU and day 38 of hospital stay. All isolates were resistant to at least three of the tested antimicrobials. Appropriate EAT was administered to 60% of patients, mostly as intravenous colistin. Appropriate EAT was associated with lower ICU mortality risk (odds ratio: 0.15; 95% confidence interval: 0.03-0.96) on multivariate analysis. CONCLUSIONS: In this 6-year cohort, Acinetobacter bacteremia was related to multidrug-resistant strains. Appropriate EAT was associated with decreased ICU mortality risk.
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spelling pubmed-46522912015-12-09 Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia Al-Dorzi, Hasan M. Asiri, Abdulaziz M. Shimemri, Abdullah Tamim, Hani M. Al Johani, Sameera M. Al Dabbagh, Tarek Arabi, Yaseen M. Ann Thorac Med Original Article RATIONALE: Empirical antimicrobial therapy (EAT) for Acinetobacter infections may not be appropriate as it tends to be multidrug-resistant. This study evaluated the relationship between appropriate EAT and the outcomes of Intensive Care Unit (ICU) patients with Acinetobacter bacteremia. METHODS: This is a retrospective study of patients admitted to a medical-surgical ICU (2005-2010) and developed Acinetobacter bacteremia during the stay. Patients were categorized according to EAT appropriateness, defined as administration of at least one antimicrobial agent to which the Acinetobacter was susceptible before susceptibility results were known. The relation between EAT appropriateness and outcomes was evaluated. RESULTS: Sixty patients developed Acinetobacter bacteremia in the 6-year period (age = 50 ± 19 years; 62% males; Acute Physiology and Chronic Health Evaluation II score = 28 ± 9; 98.3% with central lines; 67% in shock and 59% mechanically ventilated) on average on day 23 of ICU and day 38 of hospital stay. All isolates were resistant to at least three of the tested antimicrobials. Appropriate EAT was administered to 60% of patients, mostly as intravenous colistin. Appropriate EAT was associated with lower ICU mortality risk (odds ratio: 0.15; 95% confidence interval: 0.03-0.96) on multivariate analysis. CONCLUSIONS: In this 6-year cohort, Acinetobacter bacteremia was related to multidrug-resistant strains. Appropriate EAT was associated with decreased ICU mortality risk. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4652291/ /pubmed/26664563 http://dx.doi.org/10.4103/1817-1737.164302 Text en Copyright: © 2015 Annals of Thoracic Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Al-Dorzi, Hasan M.
Asiri, Abdulaziz M.
Shimemri, Abdullah
Tamim, Hani M.
Al Johani, Sameera M.
Al Dabbagh, Tarek
Arabi, Yaseen M.
Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title_full Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title_fullStr Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title_full_unstemmed Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title_short Impact of empirical antimicrobial therapy on the outcome of critically ill patients with Acinetobacter bacteremia
title_sort impact of empirical antimicrobial therapy on the outcome of critically ill patients with acinetobacter bacteremia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652291/
https://www.ncbi.nlm.nih.gov/pubmed/26664563
http://dx.doi.org/10.4103/1817-1737.164302
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