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Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course

BACKGROUND: The aim of the present study was to evaluate the C-reactive protein level, the body temperature and the white cell count in patients after prescription of antibiotics in order to describe the clinical resolution of severe community-acquired pneumonia. METHODS: A cohort of 53 consecutive...

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Autores principales: Coelho, Luís, Póvoa, Pedro, Almeida, Eduardo, Fernandes, Antero, Mealha, Rui, Moreira, Pedro, Sabino, Henrique
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206486/
https://www.ncbi.nlm.nih.gov/pubmed/17723153
http://dx.doi.org/10.1186/cc6105
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author Coelho, Luís
Póvoa, Pedro
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
author_facet Coelho, Luís
Póvoa, Pedro
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
author_sort Coelho, Luís
collection PubMed
description BACKGROUND: The aim of the present study was to evaluate the C-reactive protein level, the body temperature and the white cell count in patients after prescription of antibiotics in order to describe the clinical resolution of severe community-acquired pneumonia. METHODS: A cohort of 53 consecutive patients with severe community-acquired pneumonia was studied. The C-reactive protein levels, body temperature and white cell count were monitored daily. RESULTS: By day 3 a C-reactive protein level 0.5 times the initial level was a marker of poor outcome (sensitivity, 0.91; specificity, 0.59). Patients were divided according to their C-reactive protein patterns of response to antibiotics, into fast response, slow response, nonresponse, and biphasic response. About 96% of patients with a C-reactive protein pattern of fast response and 74% of patients with a slow response pattern survived, whereas those patients with the patterns of nonresponse and of biphasic response had a mortality rate of 100% and 33%, respectively (P < 0.001). On day 3 of antibiotic therapy, a decrease in C-reactive protein levels by 0.31 or more from the previous day's level was a marker of good prognosis (sensitivity, 0.75; specificity, 0.85). CONCLUSION: Daily C-reactive protein measurement after antibiotic prescription is useful in identification, as early as day 3, of severe community-acquired pneumonia patients with poor outcome. The identification of the C-reactive protein pattern of response to antibiotic therapy was useful in the recognition of the individual clinical course, either improving or worsening, as well as the rate of improvement, in patients with severe community-acquired pneumonia.
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spelling pubmed-22064862008-01-19 Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course Coelho, Luís Póvoa, Pedro Almeida, Eduardo Fernandes, Antero Mealha, Rui Moreira, Pedro Sabino, Henrique Crit Care Research BACKGROUND: The aim of the present study was to evaluate the C-reactive protein level, the body temperature and the white cell count in patients after prescription of antibiotics in order to describe the clinical resolution of severe community-acquired pneumonia. METHODS: A cohort of 53 consecutive patients with severe community-acquired pneumonia was studied. The C-reactive protein levels, body temperature and white cell count were monitored daily. RESULTS: By day 3 a C-reactive protein level 0.5 times the initial level was a marker of poor outcome (sensitivity, 0.91; specificity, 0.59). Patients were divided according to their C-reactive protein patterns of response to antibiotics, into fast response, slow response, nonresponse, and biphasic response. About 96% of patients with a C-reactive protein pattern of fast response and 74% of patients with a slow response pattern survived, whereas those patients with the patterns of nonresponse and of biphasic response had a mortality rate of 100% and 33%, respectively (P < 0.001). On day 3 of antibiotic therapy, a decrease in C-reactive protein levels by 0.31 or more from the previous day's level was a marker of good prognosis (sensitivity, 0.75; specificity, 0.85). CONCLUSION: Daily C-reactive protein measurement after antibiotic prescription is useful in identification, as early as day 3, of severe community-acquired pneumonia patients with poor outcome. The identification of the C-reactive protein pattern of response to antibiotic therapy was useful in the recognition of the individual clinical course, either improving or worsening, as well as the rate of improvement, in patients with severe community-acquired pneumonia. BioMed Central 2007 2007-08-28 /pmc/articles/PMC2206486/ /pubmed/17723153 http://dx.doi.org/10.1186/cc6105 Text en Copyright © 2007 Coelho 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
Coelho, Luís
Póvoa, Pedro
Almeida, Eduardo
Fernandes, Antero
Mealha, Rui
Moreira, Pedro
Sabino, Henrique
Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title_full Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title_fullStr Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title_full_unstemmed Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title_short Usefulness of C-reactive protein in monitoring the severe community-acquired pneumonia clinical course
title_sort usefulness of c-reactive protein in monitoring the severe community-acquired pneumonia clinical course
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206486/
https://www.ncbi.nlm.nih.gov/pubmed/17723153
http://dx.doi.org/10.1186/cc6105
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