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About:
Tocilizumab for the treatment of severe coronavirus disease 2019
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
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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
Tocilizumab for the treatment of severe coronavirus disease 2019
Creator
Alsoub, Hussam
Omrani, Ali
Abdalla, Shiema
Correspondence, Ali
Omrani,
Aboukamar, Mohamed
Abukhattab, |
Alattar, Rand
Almaslamani, Muna
Daghfal, Joanne
Ibrahim, B
Khatib, Mohamed
Shaar, Shahd
Shukri, Kinda
Tawheeda, |
source
Medline; PMC
abstract
Tocilizumab, an interleukin‐6 inhibitor, may ameliorate the inflammatory manifestations associated with severe coronavirus disease 2019 (COVID‐19) and thus improve clinical outcomes. This was a retrospective review of patients with laboratory‐confirmed severe COVID‐19 who received tocilizumab and completed 14 days of follow up. Twenty‐five patients were included, median age was 58 years (interquartile range, 50‐63) and the majority were males (92%). Co‐morbidities included diabetes mellitus (48%), chronic kidney disease (16%), and cardiovascular disease (12%). Fever (92%), cough (84%), and dyspnea (72%) were the commonest presenting symptoms. All patients received at least two concomitant investigational antiviral agents. Median oral temperature was on day 1, 3, and 7 was 38.0°C, 37.3°C (P = .043), and 37.0°C (P = .064), respectively. Corresponding median C‐reactive protein was 193 and 7.9 mg/L (P < .0001) and <6 mg/L (P = .0001). Radiological improvement was noted in 44% of patients by day 7% and 68% by day 14. Nine patients (36%) were discharged alive from intensive care unit and three (12%) died. The proportion of patients on invasive ventilation declined from (84%) at the time of tocilizumab initiation to 60% on day 7 (P = .031) and 28% on day 14 (P = .001). The majority (92%) of patients experienced at least one adverse event. However, it is not possible to ascertain which adverse events were directly related to tocilizumab therapy. In patients with severe COVID‐19, tocilizumab was associated with dramatic decline in inflammatory markers, radiological improvement and reduced ventilatory support requirements. Given the study's limitations, the results require assessment in adequately powered randomized controlled trials.
has issue date
2020-05-10
(
xsd:dateTime
)
bibo:doi
10.1002/jmv.25964
bibo:pmid
32369191
has license
no-cc
sha1sum (hex)
59231a3b62cd4d351a59dc9b837fb085a14d4029
schema:url
https://doi.org/10.1002/jmv.25964
resource representing a document's title
Tocilizumab for the treatment of severe coronavirus disease 2019
has PubMed Central identifier
PMC7267594
has PubMed identifier
32369191
schema:publication
J Med Virol
resource representing a document's body
covid:59231a3b62cd4d351a59dc9b837fb085a14d4029#body_text
is
schema:about
of
named entity 'presenting'
named entity 'alive'
named entity 'dyspnea'
named entity 'The'
named entity 'median age'
named entity 'coronavirus disease 2019'
named entity 'majority'
named entity 'tocilizumab'
named entity 'day'
named entity 'proportion'
named entity 'investigational'
named entity 'chronic kidney disease'
named entity 'Radiological'
named entity 'patients'
named entity 'tocilizumab'
named entity 'interleukin-6'
named entity 'retrospective review'
named entity 'Fever'
named entity 'tocilizumab'
named entity 'Tocilizumab'
named entity 'adverse event'
named entity 'COVID'
named entity 'clinical outcomes'
named entity 'control arm'
named entity 'critically ill'
named entity 'COVID'
named entity 'adverse events'
named entity 'immune response'
named entity 'histopathological examination'
named entity 'Italy'
named entity 'COVID'
named entity 'tocilizumab'
named entity 'infection'
named entity 'Candida'
named entity 'giant cell arteritis'
named entity 'juvenile idiopathic arthritis'
named entity 'tocilizumab'
named entity 'COVID'
named entity 'co-morbidities'
named entity 'ICU'
named entity 'IL-6'
named entity 'tocilizumab'
named entity 'cytokine interleukin-6'
named entity 'Qatar'
named entity 'therapeutic interventions'
named entity 'serum'
named entity 'hydroxychloroquine'
named entity 'severe pneumonia'
named entity 'COVID'
named entity 'oral Herpes'
named entity 'COVID-19'
named entity 'adverse events'
named entity 'invasive ventilation'
named entity 'inflammatory'
named entity 'rheumatoid arthritis'
named entity 'lung tissue'
named entity 'pneumonia'
named entity 'tocilizumab'
named entity 'ICU'
named entity 'ICU'
named entity 'tocilizumab'
named entity 'tocilizumab'
named entity 'clinical characteristics'
named entity 'tocilizumab'
named entity 'hypoxia'
named entity 'all-cause mortality'
named entity 'tocilizumab'
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