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231225s2020 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2020.108614
|2 doi
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|a pubmed25n1057.xml
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|a (PII)S1521-6616(20)30774-9
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|a DE-627
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|a eng
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|a Keddie, S
|e verfasserin
|4 aut
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|a Laboratory biomarkers associated with COVID-19 severity and management
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|c 2020
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 04.12.2020
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|a Date Revised 21.12.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Crown Copyright © 2020. Published by Elsevier Inc. All rights reserved.
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|a The heterogeneous disease course of COVID-19 is unpredictable, ranging from mild self-limiting symptoms to cytokine storms, acute respiratory distress syndrome (ARDS), multi-organ failure and death. Identification of high-risk cases will enable appropriate intervention and escalation. This study investigates the routine laboratory tests and cytokines implicated in COVID-19 for their potential application as biomarkers of disease severity, respiratory failure and need of higher-level care. From analysis of 203 samples, CRP, IL-6, IL-10 and LDH were most strongly correlated with the WHO ordinal scale of illness severity, the fraction of inspired oxygen delivery, radiological evidence of ARDS and level of respiratory support (p ≤ 0.001). IL-6 levels of ≥3.27 pg/ml provide a sensitivity of 0.87 and specificity of 0.64 for a requirement of ventilation, and a CRP of ≥37 mg/l of 0.91 and 0.66. Reliable stratification of high-risk cases has significant implications on patient triage, resource management and potentially the initiation of novel therapies in severe patients
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Biomarkers
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|a COVID-19
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|a CRP
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|a Cytokines
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|a IL-10
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|a IL-6
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|a Intensive care
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|a LDH
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|a Biomarkers
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|a IL10 protein, human
|2 NLM
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|a IL6 protein, human
|2 NLM
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|a Interleukin-6
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|a Interleukin-10
|2 NLM
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|a 130068-27-8
|2 NLM
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|a C-Reactive Protein
|2 NLM
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|a 9007-41-4
|2 NLM
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|a L-Lactate Dehydrogenase
|2 NLM
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|a EC 1.1.1.27
|2 NLM
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|a Ziff, O
|e verfasserin
|4 aut
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|a Chou, M K L
|e verfasserin
|4 aut
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|a Taylor, R L
|e verfasserin
|4 aut
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|a Heslegrave, A
|e verfasserin
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|a Garr, E
|e verfasserin
|4 aut
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|a Lakdawala, N
|e verfasserin
|4 aut
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|a Church, A
|e verfasserin
|4 aut
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|a Ludwig, D
|e verfasserin
|4 aut
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|a Manson, J
|e verfasserin
|4 aut
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|a Scully, M
|e verfasserin
|4 aut
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|a Nastouli, E
|e verfasserin
|4 aut
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|a Chapman, M D
|e verfasserin
|4 aut
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|a Hart, M
|e verfasserin
|4 aut
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|a Lunn, M P
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 221(2020) vom: 01. Dez., Seite 108614
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnas
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|g volume:221
|g year:2020
|g day:01
|g month:12
|g pages:108614
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|u http://dx.doi.org/10.1016/j.clim.2020.108614
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