Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia

Detalhes bibliográficos
Autor(a) principal: Seligman, Renato
Data de Publicação: 2006
Outros Autores: Meisner, Michael, Lisboa, Thiago Costa, Hertz, Felipe Teixeira, Filippin, Tania B., Fachel, Jandyra Maria Guimarães, Teixeira, Paulo Jose Zimermann
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/21613
Resumo: Introduction This study sought to assess the prognostic value of the kinetics of procalcitonin (PCT), C-reactive protein (CRP) and clinical scores (clinical pulmonary infection score (CPIS), Sequential Organ Failure Assessment (SOFA)) in the outcome of ventilator-associated pneumonia (VAP) at an early time point, when adequacy of antimicrobial treatment is evaluated. Methods This prospective observational cohort study was conducted in a teaching hospital. The subjects were 75 patients consecutively admitted to the intensive care unit from October 2003 to August 2005 who developed VAP. Patients were followed for 28 days after the diagnosis, when they were considered survivors. Patients who died before the 28th day were non-survivors. There were no interventions. Results PCT, CRP and SOFA score were determined on day 0 and day 4. Variables included in the univariable logistic regression model for survival were age, Acute Physiology and Chronic Health Evaluation (APACHE) II score, decreasing ΔSOFA, decreasing ΔPCT and decreasing ΔCRP. Survival was directly related to decreasing ΔPCT with odds ratio (OR) = 5.67 (95% confidence interval 1.78 to 18.03), decreasing ΔCRP with OR = 3.78 (1.24 to 11.50), decreasing ΔSOFA with OR = 3.08 (1.02 to 9.26) and APACHE II score with OR = 0.92 (0.86 to 0.99). In a multivariable logistic regression model for survival, only decreasing ΔPCT with OR = 4.43 (1.08 to 18.18) and decreasing ΔCRP with OR = 7.40 (1.58 to 34.73) remained significant. Decreasing ΔCPIS was not related to survival (p = 0.59). There was a trend to correlate adequacy to survival. Fifty percent of the 20 patients treated with inadequate antibiotics and 65.5% of the 55 patients on adequate antibiotics survived (p = 0.29). Conclusion Measurement of PCT and CRP at onset and on the fourth day of treatment can predict survival of VAP patients. A decrease in either one of these marker values predicts survival.
id UFRGS-2_ffe3ac498b6bd116c7b1764dbcd7443a
oai_identifier_str oai:www.lume.ufrgs.br:10183/21613
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Seligman, RenatoMeisner, MichaelLisboa, Thiago CostaHertz, Felipe TeixeiraFilippin, Tania B.Fachel, Jandyra Maria GuimarãesTeixeira, Paulo Jose Zimermann2010-05-06T04:16:23Z20061364-8535http://hdl.handle.net/10183/21613000574032Introduction This study sought to assess the prognostic value of the kinetics of procalcitonin (PCT), C-reactive protein (CRP) and clinical scores (clinical pulmonary infection score (CPIS), Sequential Organ Failure Assessment (SOFA)) in the outcome of ventilator-associated pneumonia (VAP) at an early time point, when adequacy of antimicrobial treatment is evaluated. Methods This prospective observational cohort study was conducted in a teaching hospital. The subjects were 75 patients consecutively admitted to the intensive care unit from October 2003 to August 2005 who developed VAP. Patients were followed for 28 days after the diagnosis, when they were considered survivors. Patients who died before the 28th day were non-survivors. There were no interventions. Results PCT, CRP and SOFA score were determined on day 0 and day 4. Variables included in the univariable logistic regression model for survival were age, Acute Physiology and Chronic Health Evaluation (APACHE) II score, decreasing ΔSOFA, decreasing ΔPCT and decreasing ΔCRP. Survival was directly related to decreasing ΔPCT with odds ratio (OR) = 5.67 (95% confidence interval 1.78 to 18.03), decreasing ΔCRP with OR = 3.78 (1.24 to 11.50), decreasing ΔSOFA with OR = 3.08 (1.02 to 9.26) and APACHE II score with OR = 0.92 (0.86 to 0.99). In a multivariable logistic regression model for survival, only decreasing ΔPCT with OR = 4.43 (1.08 to 18.18) and decreasing ΔCRP with OR = 7.40 (1.58 to 34.73) remained significant. Decreasing ΔCPIS was not related to survival (p = 0.59). There was a trend to correlate adequacy to survival. Fifty percent of the 20 patients treated with inadequate antibiotics and 65.5% of the 55 patients on adequate antibiotics survived (p = 0.29). Conclusion Measurement of PCT and CRP at onset and on the fourth day of treatment can predict survival of VAP patients. A decrease in either one of these marker values predicts survival.application/pdfengCritical care. London. Vol. 10, no. 5 (Sept. 2006), p. 1-9Estatística aplicadaProteina C-reativaPneumoniaDecreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumoniaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000574032.pdf000574032.pdfTexto completo (inglês)application/pdf255899http://www.lume.ufrgs.br/bitstream/10183/21613/1/000574032.pdf3e30964bd4a88a12d119d0d82a433a24MD51TEXT000574032.pdf.txt000574032.pdf.txtExtracted Texttext/plain40510http://www.lume.ufrgs.br/bitstream/10183/21613/2/000574032.pdf.txtb97df4fec8a21495d8d2106746ae402dMD52THUMBNAIL000574032.pdf.jpg000574032.pdf.jpgGenerated Thumbnailimage/jpeg2112http://www.lume.ufrgs.br/bitstream/10183/21613/3/000574032.pdf.jpge2707ee156510dff4d1873c537e30f7dMD5310183/216132023-10-27 03:30:08.410845oai:www.lume.ufrgs.br:10183/21613Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-10-27T06:30:08Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
title Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
spellingShingle Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
Seligman, Renato
Estatística aplicada
Proteina C-reativa
Pneumonia
title_short Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
title_full Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
title_fullStr Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
title_full_unstemmed Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
title_sort Decreases in procalcitonin and C-reactive protein are strong predictors of survival in ventilator-associated pneumonia
author Seligman, Renato
author_facet Seligman, Renato
Meisner, Michael
Lisboa, Thiago Costa
Hertz, Felipe Teixeira
Filippin, Tania B.
Fachel, Jandyra Maria Guimarães
Teixeira, Paulo Jose Zimermann
author_role author
author2 Meisner, Michael
Lisboa, Thiago Costa
Hertz, Felipe Teixeira
Filippin, Tania B.
Fachel, Jandyra Maria Guimarães
Teixeira, Paulo Jose Zimermann
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Seligman, Renato
Meisner, Michael
Lisboa, Thiago Costa
Hertz, Felipe Teixeira
Filippin, Tania B.
Fachel, Jandyra Maria Guimarães
Teixeira, Paulo Jose Zimermann
dc.subject.por.fl_str_mv Estatística aplicada
Proteina C-reativa
Pneumonia
topic Estatística aplicada
Proteina C-reativa
Pneumonia
description Introduction This study sought to assess the prognostic value of the kinetics of procalcitonin (PCT), C-reactive protein (CRP) and clinical scores (clinical pulmonary infection score (CPIS), Sequential Organ Failure Assessment (SOFA)) in the outcome of ventilator-associated pneumonia (VAP) at an early time point, when adequacy of antimicrobial treatment is evaluated. Methods This prospective observational cohort study was conducted in a teaching hospital. The subjects were 75 patients consecutively admitted to the intensive care unit from October 2003 to August 2005 who developed VAP. Patients were followed for 28 days after the diagnosis, when they were considered survivors. Patients who died before the 28th day were non-survivors. There were no interventions. Results PCT, CRP and SOFA score were determined on day 0 and day 4. Variables included in the univariable logistic regression model for survival were age, Acute Physiology and Chronic Health Evaluation (APACHE) II score, decreasing ΔSOFA, decreasing ΔPCT and decreasing ΔCRP. Survival was directly related to decreasing ΔPCT with odds ratio (OR) = 5.67 (95% confidence interval 1.78 to 18.03), decreasing ΔCRP with OR = 3.78 (1.24 to 11.50), decreasing ΔSOFA with OR = 3.08 (1.02 to 9.26) and APACHE II score with OR = 0.92 (0.86 to 0.99). In a multivariable logistic regression model for survival, only decreasing ΔPCT with OR = 4.43 (1.08 to 18.18) and decreasing ΔCRP with OR = 7.40 (1.58 to 34.73) remained significant. Decreasing ΔCPIS was not related to survival (p = 0.59). There was a trend to correlate adequacy to survival. Fifty percent of the 20 patients treated with inadequate antibiotics and 65.5% of the 55 patients on adequate antibiotics survived (p = 0.29). Conclusion Measurement of PCT and CRP at onset and on the fourth day of treatment can predict survival of VAP patients. A decrease in either one of these marker values predicts survival.
publishDate 2006
dc.date.issued.fl_str_mv 2006
dc.date.accessioned.fl_str_mv 2010-05-06T04:16:23Z
dc.type.driver.fl_str_mv Estrangeiro
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://hdl.handle.net/10183/21613
dc.identifier.issn.pt_BR.fl_str_mv 1364-8535
dc.identifier.nrb.pt_BR.fl_str_mv 000574032
identifier_str_mv 1364-8535
000574032
url http://hdl.handle.net/10183/21613
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Critical care. London. Vol. 10, no. 5 (Sept. 2006), p. 1-9
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/21613/1/000574032.pdf
http://www.lume.ufrgs.br/bitstream/10183/21613/2/000574032.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/21613/3/000574032.pdf.jpg
bitstream.checksum.fl_str_mv 3e30964bd4a88a12d119d0d82a433a24
b97df4fec8a21495d8d2106746ae402d
e2707ee156510dff4d1873c537e30f7d
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1815447408821141504