dc.contributor.author |
Zena-Huancas, P. |
|
dc.contributor.author |
Leon-Jimenez, F. |
|
dc.contributor.author |
Bryce-Alberti, M. |
|
dc.contributor.author |
Portmann Baracco, Arianna Sibila |
|
dc.date.accessioned |
2021-12-12T20:24:53Z |
|
dc.date.available |
2021-12-12T20:24:53Z |
|
dc.date.issued |
2021 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12866/10191 |
|
dc.description.abstract |
Based on the pathophysiological characterization of COVID-19, initial studies suggested the use of tocilizumab (TCZ), a recombinant humanized monoclonal antibody of the immunoglobulin G1 class, for management of the cytokine storm witnessed in severe cases. Thus, we decided to present a case series of 18 patients with severe COVID-19 treated with TCZ at our hospital. Our results coincide with the fact that the routine use of TCZ in severe COVID-19 is not robustly supported. We believe that the efficacy and safety of this drug and other related molecules should be validated in large randomized clinical trials |
en_US |
dc.language.iso |
eng |
|
dc.publisher |
Wolters Kluwer Health |
|
dc.relation.ispartofseries |
Lung India |
|
dc.rights |
info:eu-repo/semantics/restrictedAccess |
|
dc.rights.uri |
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es |
|
dc.subject |
adult |
en_US |
dc.subject |
Article |
en_US |
dc.subject |
C reactive protein |
en_US |
dc.subject |
clinical article |
en_US |
dc.subject |
clinical decision making |
en_US |
dc.subject |
clinical feature |
en_US |
dc.subject |
clinical trial |
en_US |
dc.subject |
coronavirus disease 2019 |
en_US |
dc.subject |
COVID-19 |
en_US |
dc.subject |
disease severity |
en_US |
dc.subject |
drug efficacy |
en_US |
dc.subject |
drug safety |
en_US |
dc.subject |
evidence based practice |
en_US |
dc.subject |
female |
en_US |
dc.subject |
high flow nasal cannula therapy |
en_US |
dc.subject |
human |
en_US |
dc.subject |
life threat |
en_US |
dc.subject |
lung embolism |
en_US |
dc.subject |
male |
en_US |
dc.subject |
middle aged |
en_US |
dc.subject |
mortality rate |
en_US |
dc.subject |
outcome assessment |
en_US |
dc.subject |
pneumopericardium |
en_US |
dc.subject |
randomized controlled trial (topic) |
en_US |
dc.subject |
single drug dose |
en_US |
dc.subject |
tocilizumab |
en_US |
dc.subject |
treatment |
en_US |
dc.title |
Tocilizumab in COVID-19: Enthusiasm vs. evidence |
en_US |
dc.type |
info:eu-repo/semantics/article |
|
dc.identifier.doi |
https://doi.org/10.4103/lungindia.lungindia_766_20 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.02.07 |
|
dc.relation.issn |
0974-598X |
|