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Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study

INTRODUCTION: Manifestations of sepsis are sensitive but are poorly specific of infection. Our aim was to assess the value of daily measurements of C-reactive protein (CRP), temperature and white cell count (WCC) in the early identification of intensive care unit (ICU)-acquired infections. METHODS:...

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Autores principales: Póvoa, Pedro, Coelho, Luís, Almeida, Eduardo, Fernandes, Antero, Mealha, Rui, Moreira, Pedro, Sabino, Henrique
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550913/
https://www.ncbi.nlm.nih.gov/pubmed/16635270
http://dx.doi.org/10.1186/cc4892
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author Póvoa, Pedro
Coelho, Luís
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
author_facet Póvoa, Pedro
Coelho, Luís
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
author_sort Póvoa, Pedro
collection PubMed
description INTRODUCTION: Manifestations of sepsis are sensitive but are poorly specific of infection. Our aim was to assess the value of daily measurements of C-reactive protein (CRP), temperature and white cell count (WCC) in the early identification of intensive care unit (ICU)-acquired infections. METHODS: We undertook a prospective observational cohort study (14 month). All patients admitted for ≥72 hours (n = 181) were divided into an infected (n = 35) and a noninfected group (n = 28). Infected patients had a documented ICU-acquired infection and were not receiving antibiotics for at least 5 days before diagnosis. Noninfected patients never received antibiotics and were discharged alive. The progression of CRP, temperature and WCC from day -5 to day 0 (day of infection diagnosis or of ICU discharge) was analyzed. Patients were divided into four patterns of CRP course according to a cutoff value for infection diagnosis of 8.7 mg/dl: pattern A, day 0 CRP >8.7 mg/dl and, in the previous days, at least once below the cutoff; pattern B, CRP always >8.7 mg/dl; pattern C, day 0 CRP ≤8.7 mg/dl and, in the previous days, at least once above the cutoff; and pattern D, CRP always ≤8.7 mg/dl. RESULTS: CRP and the temperature time-course showed a significant increase in infected patients, whereas in noninfected it remained almost unchanged (P < 0.001 and P < 0.001, respectively). The area under the curve for the maximum daily CRP variation in infection prediction was 0.86 (95% confidence interval: 0.752–0.933). A maximum daily CRP variation >4.1 mg/dl was a good marker of infection prediction (sensitivity 92.1%, specificity 71.4%), and in combination with a CRP concentration >8.7 mg/dl the discriminative power increased even further (sensitivity 92.1%, specificity 82.1%). Infection was diagnosed in 92% and 90% of patients with patterns A and B, respectively, and in only two patients with patterns C and D (P < 0.001). CONCLUSION: Daily CRP monitoring and the recognition of the CRP pattern could be useful in the prediction of ICU-acquired infections. Patients presenting maximum daily CRP variation >4.1 mg/dl plus a CRP level >8.7 mg/dl had an 88% risk of infection.
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spelling pubmed-15509132006-08-22 Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study Póvoa, Pedro Coelho, Luís Almeida, Eduardo Fernandes, Antero Mealha, Rui Moreira, Pedro Sabino, Henrique Crit Care Research INTRODUCTION: Manifestations of sepsis are sensitive but are poorly specific of infection. Our aim was to assess the value of daily measurements of C-reactive protein (CRP), temperature and white cell count (WCC) in the early identification of intensive care unit (ICU)-acquired infections. METHODS: We undertook a prospective observational cohort study (14 month). All patients admitted for ≥72 hours (n = 181) were divided into an infected (n = 35) and a noninfected group (n = 28). Infected patients had a documented ICU-acquired infection and were not receiving antibiotics for at least 5 days before diagnosis. Noninfected patients never received antibiotics and were discharged alive. The progression of CRP, temperature and WCC from day -5 to day 0 (day of infection diagnosis or of ICU discharge) was analyzed. Patients were divided into four patterns of CRP course according to a cutoff value for infection diagnosis of 8.7 mg/dl: pattern A, day 0 CRP >8.7 mg/dl and, in the previous days, at least once below the cutoff; pattern B, CRP always >8.7 mg/dl; pattern C, day 0 CRP ≤8.7 mg/dl and, in the previous days, at least once above the cutoff; and pattern D, CRP always ≤8.7 mg/dl. RESULTS: CRP and the temperature time-course showed a significant increase in infected patients, whereas in noninfected it remained almost unchanged (P < 0.001 and P < 0.001, respectively). The area under the curve for the maximum daily CRP variation in infection prediction was 0.86 (95% confidence interval: 0.752–0.933). A maximum daily CRP variation >4.1 mg/dl was a good marker of infection prediction (sensitivity 92.1%, specificity 71.4%), and in combination with a CRP concentration >8.7 mg/dl the discriminative power increased even further (sensitivity 92.1%, specificity 82.1%). Infection was diagnosed in 92% and 90% of patients with patterns A and B, respectively, and in only two patients with patterns C and D (P < 0.001). CONCLUSION: Daily CRP monitoring and the recognition of the CRP pattern could be useful in the prediction of ICU-acquired infections. Patients presenting maximum daily CRP variation >4.1 mg/dl plus a CRP level >8.7 mg/dl had an 88% risk of infection. BioMed Central 2006 2006-04-24 /pmc/articles/PMC1550913/ /pubmed/16635270 http://dx.doi.org/10.1186/cc4892 Text en Copyright © 2006 Póvoa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Póvoa, Pedro
Coelho, Luís
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title_full Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title_fullStr Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title_full_unstemmed Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title_short Early identification of intensive care unit-acquired infections with daily monitoring of C-reactive protein: a prospective observational study
title_sort early identification of intensive care unit-acquired infections with daily monitoring of c-reactive protein: a prospective observational study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550913/
https://www.ncbi.nlm.nih.gov/pubmed/16635270
http://dx.doi.org/10.1186/cc4892
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