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Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival
BACKGROUND: The clinical value of inflammatory biomarkers is still questionable. AIM OF THE WORK: The aim of this study is to compare the clinical informative value of procalcitonin (PCT) and C-reactive protein (CRP) plasma concentration in the early detection of sepsis, as well as relating these bi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258970/ https://www.ncbi.nlm.nih.gov/pubmed/25886324 http://dx.doi.org/10.4103/0259-1162.143115 |
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author | Hegazy, M. A. Omar, Amr Salah Samir, N. Moharram, A. Weber, S. Radwan, W. A. |
author_facet | Hegazy, M. A. Omar, Amr Salah Samir, N. Moharram, A. Weber, S. Radwan, W. A. |
author_sort | Hegazy, M. A. |
collection | PubMed |
description | BACKGROUND: The clinical value of inflammatory biomarkers is still questionable. AIM OF THE WORK: The aim of this study is to compare the clinical informative value of procalcitonin (PCT) and C-reactive protein (CRP) plasma concentration in the early detection of sepsis, as well as relating these biomarkers to other scoring systems. PATIENTS AND METHODS: A total of 138 patients were enrolled in our study. All were subjected to PCT, CRP, and sequential organ failure assessment (SOFA) scores daily for 7 days (starting from admission day). Blood samples were collected before starting antibiotics, with 28 days follow-up and patients were assigned to three groups: Group I: SOFA 2-7, Group II: SOFA 8-10, and Group III: SOFA ≥11. RESULTS: Underlying clinical diagnosis revealed pneumonia in 72 patients, urinary tract infections in eight, bloodstream infection in four, and other infections in 23, while infection could not be traced in 25 patients. The mean PCT was 3 ng/ml (95% confidence interval [CI]: 1-4), 12 ng/ml (95% CI: 9.1-14), and 19 ng/ml (95% CI: 16.3-22.3) in Groups I, II, and III, respectively, with a statistically significant difference in the mean PCT level among the three groups (P < 0.0001). On the other hand, CRP mean level did not significantly differentiate between the groups (147.1 mg/L in Group II, which was even higher than the level of Group III, 138.4 mg/L). CONCLUSION: PCT seems to do better than CRP in predicting the SOFA groups, giving its patronage display over a wide spectrum of insults. |
format | Online Article Text |
id | pubmed-4258970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42589702014-12-08 Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival Hegazy, M. A. Omar, Amr Salah Samir, N. Moharram, A. Weber, S. Radwan, W. A. Anesth Essays Res Original Article BACKGROUND: The clinical value of inflammatory biomarkers is still questionable. AIM OF THE WORK: The aim of this study is to compare the clinical informative value of procalcitonin (PCT) and C-reactive protein (CRP) plasma concentration in the early detection of sepsis, as well as relating these biomarkers to other scoring systems. PATIENTS AND METHODS: A total of 138 patients were enrolled in our study. All were subjected to PCT, CRP, and sequential organ failure assessment (SOFA) scores daily for 7 days (starting from admission day). Blood samples were collected before starting antibiotics, with 28 days follow-up and patients were assigned to three groups: Group I: SOFA 2-7, Group II: SOFA 8-10, and Group III: SOFA ≥11. RESULTS: Underlying clinical diagnosis revealed pneumonia in 72 patients, urinary tract infections in eight, bloodstream infection in four, and other infections in 23, while infection could not be traced in 25 patients. The mean PCT was 3 ng/ml (95% confidence interval [CI]: 1-4), 12 ng/ml (95% CI: 9.1-14), and 19 ng/ml (95% CI: 16.3-22.3) in Groups I, II, and III, respectively, with a statistically significant difference in the mean PCT level among the three groups (P < 0.0001). On the other hand, CRP mean level did not significantly differentiate between the groups (147.1 mg/L in Group II, which was even higher than the level of Group III, 138.4 mg/L). CONCLUSION: PCT seems to do better than CRP in predicting the SOFA groups, giving its patronage display over a wide spectrum of insults. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4258970/ /pubmed/25886324 http://dx.doi.org/10.4103/0259-1162.143115 Text en Copyright: © Anesthesia: Essays and Researches 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hegazy, M. A. Omar, Amr Salah Samir, N. Moharram, A. Weber, S. Radwan, W. A. Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title | Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title_full | Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title_fullStr | Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title_full_unstemmed | Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title_short | Amalgamation of procalcitonin, C-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
title_sort | amalgamation of procalcitonin, c-reactive protein, and sequential organ failure scoring system in predicting sepsis survival |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258970/ https://www.ncbi.nlm.nih.gov/pubmed/25886324 http://dx.doi.org/10.4103/0259-1162.143115 |
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