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Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus

INTRODUCTION: Infections in status epilepticus (SE) patients result in severe morbidity making early diagnosis crucial. As SE may lead to inflammatory reaction, the value of acute phase proteins and white blood cells (WBC) for diagnosis of infections during SE may be important. We examined the relia...

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Autores principales: Sutter, Raoul, Tschudin-Sutter, Sarah, Grize, Leticia, Widmer, Andreas F, Marsch, Stephan, Rüegg, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388641/
https://www.ncbi.nlm.nih.gov/pubmed/22099124
http://dx.doi.org/10.1186/cc10555
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author Sutter, Raoul
Tschudin-Sutter, Sarah
Grize, Leticia
Widmer, Andreas F
Marsch, Stephan
Rüegg, Stephan
author_facet Sutter, Raoul
Tschudin-Sutter, Sarah
Grize, Leticia
Widmer, Andreas F
Marsch, Stephan
Rüegg, Stephan
author_sort Sutter, Raoul
collection PubMed
description INTRODUCTION: Infections in status epilepticus (SE) patients result in severe morbidity making early diagnosis crucial. As SE may lead to inflammatory reaction, the value of acute phase proteins and white blood cells (WBC) for diagnosis of infections during SE may be important. We examined the reliability of C-reactive protein (CRP), procalcitonin (PCT), and WBC for diagnosis of infections during SE. METHODS: All consecutive SE patients treated in the ICU from 2005 to 2009 were included. Clinical and microbiological records, and measurements of CRP and WBC during SE were analyzed. Subgroup analysis was performed for additional PCT measurements in the first 48 hours of SE. RESULTS: A total of 22.5% of 160 consecutive SE patients had infections during SE. Single levels of CRP and WBC had no association with the presence of infections. Their linear changes over the first three days after SE onset were significantly associated with the presence of infections (P = 0.0012 for CRP, P = 0.0137 for WBC). Levels of PCT were available for 31 patients and did not differ significantly in patients with and without infections. Sensitivity of PCT and CRP was high (94% and 83%) and the negative predictive value of CRP increased over the first three days to 97%. Specificity was low, without improvement for different cut-offs. CONCLUSIONS: Single levels of CRP and WBC are not reliable for diagnosis of infections during SE, while their linear changes over time significantly correlate with the presence of infections. In addition, low levels of CRP and PCT rule out hospital-acquired infections in SE patients.
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spelling pubmed-33886412012-07-04 Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus Sutter, Raoul Tschudin-Sutter, Sarah Grize, Leticia Widmer, Andreas F Marsch, Stephan Rüegg, Stephan Crit Care Research INTRODUCTION: Infections in status epilepticus (SE) patients result in severe morbidity making early diagnosis crucial. As SE may lead to inflammatory reaction, the value of acute phase proteins and white blood cells (WBC) for diagnosis of infections during SE may be important. We examined the reliability of C-reactive protein (CRP), procalcitonin (PCT), and WBC for diagnosis of infections during SE. METHODS: All consecutive SE patients treated in the ICU from 2005 to 2009 were included. Clinical and microbiological records, and measurements of CRP and WBC during SE were analyzed. Subgroup analysis was performed for additional PCT measurements in the first 48 hours of SE. RESULTS: A total of 22.5% of 160 consecutive SE patients had infections during SE. Single levels of CRP and WBC had no association with the presence of infections. Their linear changes over the first three days after SE onset were significantly associated with the presence of infections (P = 0.0012 for CRP, P = 0.0137 for WBC). Levels of PCT were available for 31 patients and did not differ significantly in patients with and without infections. Sensitivity of PCT and CRP was high (94% and 83%) and the negative predictive value of CRP increased over the first three days to 97%. Specificity was low, without improvement for different cut-offs. CONCLUSIONS: Single levels of CRP and WBC are not reliable for diagnosis of infections during SE, while their linear changes over time significantly correlate with the presence of infections. In addition, low levels of CRP and PCT rule out hospital-acquired infections in SE patients. BioMed Central 2011 2011-11-18 /pmc/articles/PMC3388641/ /pubmed/22099124 http://dx.doi.org/10.1186/cc10555 Text en Copyright ©2011 Sutter 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
Sutter, Raoul
Tschudin-Sutter, Sarah
Grize, Leticia
Widmer, Andreas F
Marsch, Stephan
Rüegg, Stephan
Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title_full Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title_fullStr Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title_full_unstemmed Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title_short Acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
title_sort acute phase proteins and white blood cell levels for prediction of infectious complications in status epilepticus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388641/
https://www.ncbi.nlm.nih.gov/pubmed/22099124
http://dx.doi.org/10.1186/cc10555
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