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Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department

BACKGROUND: Deciding whether to transfer patients with sepsis from the emergency department (ED) to intensive care units (ICUs) is challenging. We hypothesised that the new biomarker plasma calprotectin (p-calprotectin) could be used to aid the selection of patients for intensive care transfer, sinc...

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Autores principales: Parke, Åsa, Unge, Christian, Yu, David, Sundén-Cullberg, Jonas, Strålin, Kristoffer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922172/
https://www.ncbi.nlm.nih.gov/pubmed/36774492
http://dx.doi.org/10.1186/s12873-023-00785-y
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author Parke, Åsa
Unge, Christian
Yu, David
Sundén-Cullberg, Jonas
Strålin, Kristoffer
author_facet Parke, Åsa
Unge, Christian
Yu, David
Sundén-Cullberg, Jonas
Strålin, Kristoffer
author_sort Parke, Åsa
collection PubMed
description BACKGROUND: Deciding whether to transfer patients with sepsis from the emergency department (ED) to intensive care units (ICUs) is challenging. We hypothesised that the new biomarker plasma calprotectin (p-calprotectin) could be used to aid the selection of patients for intensive care transfer, since it has been shown to be a promising tool for the determination of sepsis severity in critical care. METHODS: This prospective study was performed on consecutive sepsis alert patients in the ED of Karolinska University Hospital Huddinge. The sepsis alert mandates clinical assessment and decisions regarding treatment, disposition, and level of care by physicians from the ED, the Department of Infectious Diseases, and the ICU. Blood sample analysis for C-reactive protein, procalcitonin, neutrophils, and lymphocytes was routinely performed. P-calprotectin was analysed from frozen plasma samples, using a specific turbidimetric assay. RESULTS: Three-hundred fifty-one patients who triggered the sepsis alert were available for the study. Among 319 patients who were considered to have an infection, 66 patients (26%) were immediately transferred to the ICU or high-dependency unit (HDU), and 253 patients (74%) were transferred to ordinary wards. Median p-calprotectin was 2.2 mg/L (IQR 1.2–3.9 mg/L) for all patients with infection, it was 3.3 (IQR 1.6–5.2) for those transferred to ICU/HDU and 2.1 (IQR 1.1–3.5) for those transferred to ward units (p = 0.0001). Receiver operating characteristic curve analysis for transfer to the ICU/HDU showed superiority for p-calprotectin compared with procalcitonin and neutrophil–lymphocyte ratio, regarding both all sepsis alert cases and the patients with infection (p < 0.001 for all comparisons). The best p-calprotectin cut-off, 4.0 mg/L, showed a sensitivity of 42.5% and specificity of 83% for transfer to the ICU/HDU among patients with infection. CONCLUSIONS: In sepsis alert patients, p-calprotectin was significantly elevated in patients who were subject to immediate ICU/HDU transfer after assessment by a multidisciplinary team. P-calprotectin was superior to traditional biomarkers in predicting the need for transfer to the ICU/HDU.
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spelling pubmed-99221722023-02-13 Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department Parke, Åsa Unge, Christian Yu, David Sundén-Cullberg, Jonas Strålin, Kristoffer BMC Emerg Med Research BACKGROUND: Deciding whether to transfer patients with sepsis from the emergency department (ED) to intensive care units (ICUs) is challenging. We hypothesised that the new biomarker plasma calprotectin (p-calprotectin) could be used to aid the selection of patients for intensive care transfer, since it has been shown to be a promising tool for the determination of sepsis severity in critical care. METHODS: This prospective study was performed on consecutive sepsis alert patients in the ED of Karolinska University Hospital Huddinge. The sepsis alert mandates clinical assessment and decisions regarding treatment, disposition, and level of care by physicians from the ED, the Department of Infectious Diseases, and the ICU. Blood sample analysis for C-reactive protein, procalcitonin, neutrophils, and lymphocytes was routinely performed. P-calprotectin was analysed from frozen plasma samples, using a specific turbidimetric assay. RESULTS: Three-hundred fifty-one patients who triggered the sepsis alert were available for the study. Among 319 patients who were considered to have an infection, 66 patients (26%) were immediately transferred to the ICU or high-dependency unit (HDU), and 253 patients (74%) were transferred to ordinary wards. Median p-calprotectin was 2.2 mg/L (IQR 1.2–3.9 mg/L) for all patients with infection, it was 3.3 (IQR 1.6–5.2) for those transferred to ICU/HDU and 2.1 (IQR 1.1–3.5) for those transferred to ward units (p = 0.0001). Receiver operating characteristic curve analysis for transfer to the ICU/HDU showed superiority for p-calprotectin compared with procalcitonin and neutrophil–lymphocyte ratio, regarding both all sepsis alert cases and the patients with infection (p < 0.001 for all comparisons). The best p-calprotectin cut-off, 4.0 mg/L, showed a sensitivity of 42.5% and specificity of 83% for transfer to the ICU/HDU among patients with infection. CONCLUSIONS: In sepsis alert patients, p-calprotectin was significantly elevated in patients who were subject to immediate ICU/HDU transfer after assessment by a multidisciplinary team. P-calprotectin was superior to traditional biomarkers in predicting the need for transfer to the ICU/HDU. BioMed Central 2023-02-11 /pmc/articles/PMC9922172/ /pubmed/36774492 http://dx.doi.org/10.1186/s12873-023-00785-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Parke, Åsa
Unge, Christian
Yu, David
Sundén-Cullberg, Jonas
Strålin, Kristoffer
Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title_full Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title_fullStr Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title_full_unstemmed Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title_short Plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
title_sort plasma calprotectin as an indicator of need of transfer to intensive care in patients with suspected sepsis at the emergency department
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922172/
https://www.ncbi.nlm.nih.gov/pubmed/36774492
http://dx.doi.org/10.1186/s12873-023-00785-y
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