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C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department

INTRODUCTION: C-reactive protein (CRP) is a real-time and low-cost biomarker to distinguish febrile bacterial infections from non-bacterial febrile illnesses. We hypothesised that measuring the velocity of the biomarker instead of its absolute serum concentration could enhance its ability to differe...

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Autores principales: Paran, Yael, Yablecovitch, Doron, Choshen, Guy, Zeitlin, Ina, Rogowski, Ori, Ben-Ami, Ronen, Katzir, Michal, Saranga, Hila, Rosenzweig, Tovit, Justo, Dan, Orbach, Yaffa, Halpern, Pinhas, Berliner, Shlomo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689495/
https://www.ncbi.nlm.nih.gov/pubmed/19351421
http://dx.doi.org/10.1186/cc7775
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author Paran, Yael
Yablecovitch, Doron
Choshen, Guy
Zeitlin, Ina
Rogowski, Ori
Ben-Ami, Ronen
Katzir, Michal
Saranga, Hila
Rosenzweig, Tovit
Justo, Dan
Orbach, Yaffa
Halpern, Pinhas
Berliner, Shlomo
author_facet Paran, Yael
Yablecovitch, Doron
Choshen, Guy
Zeitlin, Ina
Rogowski, Ori
Ben-Ami, Ronen
Katzir, Michal
Saranga, Hila
Rosenzweig, Tovit
Justo, Dan
Orbach, Yaffa
Halpern, Pinhas
Berliner, Shlomo
author_sort Paran, Yael
collection PubMed
description INTRODUCTION: C-reactive protein (CRP) is a real-time and low-cost biomarker to distinguish febrile bacterial infections from non-bacterial febrile illnesses. We hypothesised that measuring the velocity of the biomarker instead of its absolute serum concentration could enhance its ability to differentiate between these two conditions. METHODS: We prospectively recruited adult patients (age ≥ 18 years) who presented to the emergency department with fever. We recorded their data regarding the onset of fever and accompanying symptoms. CRP measurements were obtained upon admission. CRP velocity (CRPv) was defined as the ratio between CRP on admission and the number of hours since the onset of fever. Patients were diagnosed by clinical symptoms, blood cultures and imaging studies, and the diagnoses were confirmed by an infectious disease specialist. The efficacy of CRPv as a diagnostic marker was evaluated by using receiver operator curves (ROC). Excluded were patients who did not know the time fever started with certainty, patients with malignancy, patients with HIV infection and patients who had been using antibiotics upon presentation. RESULTS: Of 178 eligible patients, 108 (60.7%) had febrile bacterial infections (mean CRP: 63.77 mg/L, mean CRPv: 3.61 mg/L/hour) and 70 (39.3%) had non-bacterial febrile illnesses (mean CRP: 23.2 mg/L, mean CRPv: 0.41 mg/L/hour). The area under the curve for CRP and CRPv were 0.783 (95% confidence interval (CI) = 0.717 to 0.850) and 0.871 (95% CI = 0.817 to 0.924), respectively. In a 122-patient subgroup with a CRP level of less than 100 mg/L, the area under the curve increased from 0.689 (95% CI = 0.0595 to 0.782) to 0.842 (95% CI = 0.77 to 0.914) by using the CRPv measurements. CONCLUSIONS: CRPv improved differentiation between febrile bacterial infections and non-bacterial febrile illnesses compared with CRP alone, and could identify individuals who need prompt therapeutic intervention.
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spelling pubmed-26894952009-06-02 C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department Paran, Yael Yablecovitch, Doron Choshen, Guy Zeitlin, Ina Rogowski, Ori Ben-Ami, Ronen Katzir, Michal Saranga, Hila Rosenzweig, Tovit Justo, Dan Orbach, Yaffa Halpern, Pinhas Berliner, Shlomo Crit Care Research INTRODUCTION: C-reactive protein (CRP) is a real-time and low-cost biomarker to distinguish febrile bacterial infections from non-bacterial febrile illnesses. We hypothesised that measuring the velocity of the biomarker instead of its absolute serum concentration could enhance its ability to differentiate between these two conditions. METHODS: We prospectively recruited adult patients (age ≥ 18 years) who presented to the emergency department with fever. We recorded their data regarding the onset of fever and accompanying symptoms. CRP measurements were obtained upon admission. CRP velocity (CRPv) was defined as the ratio between CRP on admission and the number of hours since the onset of fever. Patients were diagnosed by clinical symptoms, blood cultures and imaging studies, and the diagnoses were confirmed by an infectious disease specialist. The efficacy of CRPv as a diagnostic marker was evaluated by using receiver operator curves (ROC). Excluded were patients who did not know the time fever started with certainty, patients with malignancy, patients with HIV infection and patients who had been using antibiotics upon presentation. RESULTS: Of 178 eligible patients, 108 (60.7%) had febrile bacterial infections (mean CRP: 63.77 mg/L, mean CRPv: 3.61 mg/L/hour) and 70 (39.3%) had non-bacterial febrile illnesses (mean CRP: 23.2 mg/L, mean CRPv: 0.41 mg/L/hour). The area under the curve for CRP and CRPv were 0.783 (95% confidence interval (CI) = 0.717 to 0.850) and 0.871 (95% CI = 0.817 to 0.924), respectively. In a 122-patient subgroup with a CRP level of less than 100 mg/L, the area under the curve increased from 0.689 (95% CI = 0.0595 to 0.782) to 0.842 (95% CI = 0.77 to 0.914) by using the CRPv measurements. CONCLUSIONS: CRPv improved differentiation between febrile bacterial infections and non-bacterial febrile illnesses compared with CRP alone, and could identify individuals who need prompt therapeutic intervention. BioMed Central 2009 2009-04-08 /pmc/articles/PMC2689495/ /pubmed/19351421 http://dx.doi.org/10.1186/cc7775 Text en Copyright © 2009 Paran 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
Paran, Yael
Yablecovitch, Doron
Choshen, Guy
Zeitlin, Ina
Rogowski, Ori
Ben-Ami, Ronen
Katzir, Michal
Saranga, Hila
Rosenzweig, Tovit
Justo, Dan
Orbach, Yaffa
Halpern, Pinhas
Berliner, Shlomo
C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title_full C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title_fullStr C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title_full_unstemmed C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title_short C-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
title_sort c-reactive protein velocity to distinguish febrile bacterial infections from non-bacterial febrile illnesses in the emergency department
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689495/
https://www.ncbi.nlm.nih.gov/pubmed/19351421
http://dx.doi.org/10.1186/cc7775
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