Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?

Bibliographic Details
Main Author: Jukemura, Elisa Maria [UNIFESP]
Publication Date: 2007
Other Authors: Burattini, Marcelo Nascimento [UNIFESP], Pereira, Carlos Alberto Pires [UNIFESP], Braga, Alfésio L.f., Medeiros, Eduardo Alexandrino Servolo de [UNIFESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNIFESP
Download full: http://dx.doi.org/10.1590/S1413-86702007000400010
http://repositorio.unifesp.br/handle/11600/3833
Summary: Potent antimicrobial agents have been developed as a response to the development of antibiotic-resistant bacteria, which especially affect patients with prolonged hospitalization in Intensive Care Units (ICU) and who had been previously treated with antimicrobials, especially third-generation cephalosporins.This study was to determine how changes in the empirical treatment of infections in ICU patients affect the incidence of Gram-negative bacteria species and their susceptibility to antimicrobials, and examine the impact of these changes on nosocomial infections. A prospective interventional study was performed in a university hospital during two periods: 1) First period (September 1999 to February 2000); and 2) Second period (August 2000 to December 2000); empirical treatment was changed from ceftriaxone and/or ceftazidime in the first period to piperacillin/tazobactam in the second. ICU epidemiological and infection control rates, as well as bacterial isolates from upper airways were analyzed. Ceftazidime consumption dropped from 34.83 to 0.85 DDD/1000 patients per day (p=0.004). Piperacillin/tazobactam was originally not available; its consumption reached 157.07 DDD/1000 patients per day in the second period (p=0.0002). Eighty-seven patients and 66 patients were evaluated for upper airway colonization in the first and second periods, respectively. There was a significant decrease in the incidence of K. pneumoniae (p=0.004) and P. mirabilis (p=0.036), restoration of K. pneumoniae susceptibility to cephalosporins (p<0.0001) and reduction of ventilator-associated pneumonia rates (p<0.0001). However, there was an increase in P. aeruginosa incidence (p=0.005) and increases in ceftazidime (p=0.003) and meropenem (p<0.0001) susceptibilities. Changing antimicrobial selective pressure on multi-resistant Gram-negative bacteria helps control ventilator-associated pneumonia and decreases antimicrobial resistance.
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spelling Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?Ventilator associated pneumoniamulti-resistant bacteriainfection controlPotent antimicrobial agents have been developed as a response to the development of antibiotic-resistant bacteria, which especially affect patients with prolonged hospitalization in Intensive Care Units (ICU) and who had been previously treated with antimicrobials, especially third-generation cephalosporins.This study was to determine how changes in the empirical treatment of infections in ICU patients affect the incidence of Gram-negative bacteria species and their susceptibility to antimicrobials, and examine the impact of these changes on nosocomial infections. A prospective interventional study was performed in a university hospital during two periods: 1) First period (September 1999 to February 2000); and 2) Second period (August 2000 to December 2000); empirical treatment was changed from ceftriaxone and/or ceftazidime in the first period to piperacillin/tazobactam in the second. ICU epidemiological and infection control rates, as well as bacterial isolates from upper airways were analyzed. Ceftazidime consumption dropped from 34.83 to 0.85 DDD/1000 patients per day (p=0.004). Piperacillin/tazobactam was originally not available; its consumption reached 157.07 DDD/1000 patients per day in the second period (p=0.0002). Eighty-seven patients and 66 patients were evaluated for upper airway colonization in the first and second periods, respectively. There was a significant decrease in the incidence of K. pneumoniae (p=0.004) and P. mirabilis (p=0.036), restoration of K. pneumoniae susceptibility to cephalosporins (p<0.0001) and reduction of ventilator-associated pneumonia rates (p<0.0001). However, there was an increase in P. aeruginosa incidence (p=0.005) and increases in ceftazidime (p=0.003) and meropenem (p<0.0001) susceptibilities. Changing antimicrobial selective pressure on multi-resistant Gram-negative bacteria helps control ventilator-associated pneumonia and decreases antimicrobial resistance.Federal University of São Paulo School of Medicine Internal Medicine DepartmentCatholic University of Santos Collective Health Pos-graduation ProgramUNIFESP, EPM, Internal Medicine DepartmentSciELOBrazilian Society of Infectious DiseasesUniversidade Federal de São Paulo (UNIFESP)Catholic University of Santos Collective Health Pos-graduation ProgramJukemura, Elisa Maria [UNIFESP]Burattini, Marcelo Nascimento [UNIFESP]Pereira, Carlos Alberto Pires [UNIFESP]Braga, Alfésio L.f.Medeiros, Eduardo Alexandrino Servolo de [UNIFESP]2015-06-14T13:37:01Z2015-06-14T13:37:01Z2007-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion418-422application/pdfhttp://dx.doi.org/10.1590/S1413-86702007000400010Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 11, n. 4, p. 418-422, 2007.10.1590/S1413-86702007000400010S1413-86702007000400010.pdf1413-8670S1413-86702007000400010http://repositorio.unifesp.br/handle/11600/3833WOS:000254388600010engBrazilian Journal of Infectious Diseasesinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T23:59:08Zoai:repositorio.unifesp.br/:11600/3833Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T23:59:08Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
title Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
spellingShingle Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
Jukemura, Elisa Maria [UNIFESP]
Ventilator associated pneumonia
multi-resistant bacteria
infection control
title_short Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
title_full Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
title_fullStr Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
title_full_unstemmed Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
title_sort Control of multi-resistant bacteria and ventilator-associated pneumonia: is it possible with changes in antibiotics?
author Jukemura, Elisa Maria [UNIFESP]
author_facet Jukemura, Elisa Maria [UNIFESP]
Burattini, Marcelo Nascimento [UNIFESP]
Pereira, Carlos Alberto Pires [UNIFESP]
Braga, Alfésio L.f.
Medeiros, Eduardo Alexandrino Servolo de [UNIFESP]
author_role author
author2 Burattini, Marcelo Nascimento [UNIFESP]
Pereira, Carlos Alberto Pires [UNIFESP]
Braga, Alfésio L.f.
Medeiros, Eduardo Alexandrino Servolo de [UNIFESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Catholic University of Santos Collective Health Pos-graduation Program
dc.contributor.author.fl_str_mv Jukemura, Elisa Maria [UNIFESP]
Burattini, Marcelo Nascimento [UNIFESP]
Pereira, Carlos Alberto Pires [UNIFESP]
Braga, Alfésio L.f.
Medeiros, Eduardo Alexandrino Servolo de [UNIFESP]
dc.subject.por.fl_str_mv Ventilator associated pneumonia
multi-resistant bacteria
infection control
topic Ventilator associated pneumonia
multi-resistant bacteria
infection control
description Potent antimicrobial agents have been developed as a response to the development of antibiotic-resistant bacteria, which especially affect patients with prolonged hospitalization in Intensive Care Units (ICU) and who had been previously treated with antimicrobials, especially third-generation cephalosporins.This study was to determine how changes in the empirical treatment of infections in ICU patients affect the incidence of Gram-negative bacteria species and their susceptibility to antimicrobials, and examine the impact of these changes on nosocomial infections. A prospective interventional study was performed in a university hospital during two periods: 1) First period (September 1999 to February 2000); and 2) Second period (August 2000 to December 2000); empirical treatment was changed from ceftriaxone and/or ceftazidime in the first period to piperacillin/tazobactam in the second. ICU epidemiological and infection control rates, as well as bacterial isolates from upper airways were analyzed. Ceftazidime consumption dropped from 34.83 to 0.85 DDD/1000 patients per day (p=0.004). Piperacillin/tazobactam was originally not available; its consumption reached 157.07 DDD/1000 patients per day in the second period (p=0.0002). Eighty-seven patients and 66 patients were evaluated for upper airway colonization in the first and second periods, respectively. There was a significant decrease in the incidence of K. pneumoniae (p=0.004) and P. mirabilis (p=0.036), restoration of K. pneumoniae susceptibility to cephalosporins (p<0.0001) and reduction of ventilator-associated pneumonia rates (p<0.0001). However, there was an increase in P. aeruginosa incidence (p=0.005) and increases in ceftazidime (p=0.003) and meropenem (p<0.0001) susceptibilities. Changing antimicrobial selective pressure on multi-resistant Gram-negative bacteria helps control ventilator-associated pneumonia and decreases antimicrobial resistance.
publishDate 2007
dc.date.none.fl_str_mv 2007-08-01
2015-06-14T13:37:01Z
2015-06-14T13:37:01Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S1413-86702007000400010
Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 11, n. 4, p. 418-422, 2007.
10.1590/S1413-86702007000400010
S1413-86702007000400010.pdf
1413-8670
S1413-86702007000400010
http://repositorio.unifesp.br/handle/11600/3833
WOS:000254388600010
url http://dx.doi.org/10.1590/S1413-86702007000400010
http://repositorio.unifesp.br/handle/11600/3833
identifier_str_mv Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 11, n. 4, p. 418-422, 2007.
10.1590/S1413-86702007000400010
S1413-86702007000400010.pdf
1413-8670
S1413-86702007000400010
WOS:000254388600010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brazilian Journal of Infectious Diseases
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 418-422
application/pdf
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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