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About:
The Combined Use of Tocilizumab and Hemoadsorption in a Patient with SARS-COV-2-19-Associated Pneumonia: A Case Report
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
The Combined Use of Tocilizumab and Hemoadsorption in a Patient with SARS-COV-2-19-Associated Pneumonia: A Case Report
Creator
Berlot, Giorgio
Amato, Paola
Bianco, Francesco
Chiella, Fabrizio
Gerini, Ugo
Piva, Marco
Randino, Anna
Roman Pognuz, Erik
Tomasini, Ariella
Tomietto, Paola
Trenti, Tommaso
Di Maso, Vittorio
Fata, Cristina
source
Medline; PMC
abstract
The SARS-COV-2-19-associated respiratory involvement is caused by the massive release of inflammatory cytokines ultimately leading to interstitial pneumonia and acute respiratory distress syndrome (ARDS). In the absence of an effective antiviral treatment, a reasonable causal approach could be constituted by the neutralization of these substances. The authors describe the clinical course of a patient with SARS-COV-2-19 interstitial pneumonia treated with the combination of an anti-interleukin 6 (IL-6) agent (tocilizumab) and hemoadsorption (HA). This combination was used to abate the surge of inflammatory mediators leading to the lung damage. Blood levels of IL-6 and C-reactive protein (CRP) were measured before the initiation of the treatment and in the following 3 days. At the end of the treatment, the values of IL-6 and CRP decreased from 1,040 to 415 pg/mL and from 229 to 59 mg/L, respectively. The gas exchanges and the chest imaging rapidly improved, and the patient was extubated 10 days later. The combination of tocilizumab and HA could be valuable in the treatment of SARS-COV-2-19-associated pneumonia and ARDS that are caused by the release of inflammatory mediators.
has issue date
2020-07-21
(
xsd:dateTime
)
bibo:doi
10.1159/000509738
bibo:pmid
32694244
has license
no-cc
sha1sum (hex)
0eb926f409d2bfd123718cd23812e4bccc622b3e
schema:url
https://doi.org/10.1159/000509738
resource representing a document's title
The Combined Use of Tocilizumab and Hemoadsorption in a Patient with SARS-COV-2-19-Associated Pneumonia: A Case Report
has PubMed Central identifier
PMC7445375
has PubMed identifier
32694244
schema:publication
Nephron Clin Pract
resource representing a document's body
covid:0eb926f409d2bfd123718cd23812e4bccc622b3e#body_text
is
schema:about
of
named entity 'SARS-COV-2'
named entity 'antiviral treatment'
named entity 'neutralization'
named entity 'SARS-COV-2'
named entity 'authors'
named entity 'Tocilizumab'
named entity 'RAPIDLY'
named entity 'LUNG'
named entity 'TREATMENT'
named entity 'COMBINATION'
named entity 'IMPROVED'
named entity 'PROTEIN '
named entity 'DAYS'
named entity '2-19'
named entity 'PATIENT'
named entity 'USED'
named entity 'ARDS'
named entity 'INFLAMMATORY MEDIATORS'
named entity 'C-reactive protein'
named entity 'reasonable'
named entity 'constituted'
named entity 'inflammatory mediators'
named entity 'exchanges'
named entity 'Case'
named entity 'chest imaging'
named entity 'SARS-COV-2'
named entity 'IL-6'
named entity 'inflammatory cytokines'
named entity 'C-reactive protein'
named entity 'IL-6'
named entity 'interstitial pneumonia'
named entity 'Blood levels'
named entity 'Tocilizumab'
named entity 'normal range'
named entity 'extracorporeal membrane oxygenation'
named entity 'C-reactive protein'
named entity 'tocilizumab'
named entity 'interstitial pneumonia'
named entity 'IL-6'
named entity 'blood oxygenation'
named entity 'rheumatoid arthritis'
named entity 'ICU'
named entity 'interstitial pneumonia'
named entity 'pneumonia'
named entity 'procalcitonin'
named entity 'endothelial'
named entity 'acute-phase reactant'
named entity 'systemic inflammation'
named entity 'tocilizumab'
named entity 'molecular weight'
named entity 'inflammatory'
named entity 'chimeric antibody'
named entity 'inflammation'
named entity 'bronchoalveolar lavage'
named entity 'free of symptoms'
named entity 'receptor'
named entity 'coronavirus disease'
named entity 'CytoSorbents'
named entity 'immune response'
named entity 'septic shock'
named entity 'anticoagulation'
named entity 'ARDS'
named entity 'tocilizumab'
named entity 'CRP'
named entity 'antiviral agents'
named entity 'hepatomegaly'
named entity 'ARDS'
named entity 'clinical investigations'
named entity 'interleukin'
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