Tocilizumab reduces the risk of ICU admission and mortality in patients with SARS-CoV-2 infection.
Antibodies, Monoclonal, Humanized
/ therapeutic use
Bed Occupancy
COVID-19
/ immunology
Female
Hospitalization
/ statistics & numerical data
Humans
Intensive Care Units
/ statistics & numerical data
Male
Middle Aged
Respiration, Artificial
/ statistics & numerical data
Retrospective Studies
SARS-CoV-2
COVID-19
intensive care unit
tocilizumab
Journal
Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia
ISSN: 1988-9518
Titre abrégé: Rev Esp Quimioter
Pays: Spain
ID NLM: 9108821
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
pubmed:
9
4
2021
medline:
4
6
2021
entrez:
8
4
2021
Statut:
ppublish
Résumé
In some patients the immune response triggered by SARS-CoV-2 is unbalanced, presenting an acute respiratory distress syndrome which in many cases requires intensive care unit (ICU) admission. The limitation of ICU beds has been one of the major burdens in the management around the world; therefore, clinical strategies to avoid ICU admission are needed. We aimed to describe the influence of tocilizumab on the need of transfer to ICU or death in non-critically ill patients. A retrospective study of 171 patients with SARS-CoV-2 infection that did not qualify as requiring transfer to ICU during the first 24h after admission to a conventional ward, were included. The criteria to receive tocilizumab was radiological impairment, oxygen demand or an increasing of inflammatory parameters, however, the ultimate decision was left to the attending physician judgement. The primary outcome was the need of ICU admission or death whichever came first. A total of 77 patients received tocilizumab and 94 did not. The tocilizumab group had less ICU admissions (10.3% vs. 27.6%, P=0.005) and need of invasive ventilation (0 vs 13.8%, P=0.001). In the multivariable analysis, tocilizumab remained as a protective variable (OR: 0.03, CI 95%: 0.007-0.1, P=0.0001) of ICU admission or death. Tocilizumab in early stages of the inflammatory flare could reduce an important number of ICU admissions and mechanical ventilation. The mortality rate of 10.3% among patients receiving tocilizumab appears to be lower than other reports. This is a non-randomized study and the results should be interpreted with caution.
Identifiants
pubmed: 33829722
doi: 10.37201/req/037.2021
pmc: PMC8179941
pii:
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
tocilizumab
I031V2H011
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
238-244Informations de copyright
©The Author 2021. Published by Sociedad Española de Quimioterapia. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)(https://creativecommons.org/licenses/by-nc/4.0/).
Références
Chest. 2007 Aug;132(2):410-7
pubmed: 17573487
JAMA. 2020 Apr 28;323(16):1574-1581
pubmed: 32250385
Science. 2020 May 1;368(6490):473-474
pubmed: 32303591
JAMA. 2012 Jun 20;307(23):2526-33
pubmed: 22797452
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10970-10975
pubmed: 32350134
J Am Coll Cardiol. 2020 Jun 16;75(23):2950-2973
pubmed: 32311448
JAMA Intern Med. 2020 Jul 1;180(7):934-943
pubmed: 32167524
J Heart Lung Transplant. 2020 May;39(5):405-407
pubmed: 32362390
Lancet Rheumatol. 2020 Jun;2(6):e325-e331
pubmed: 32501454
Int J Antimicrob Agents. 2020 May;55(5):105954
pubmed: 32234467
Nat Commun. 2021 Jan 11;12(1):267
pubmed: 33431879
JAMA. 2020 May 26;323(20):2052-2059
pubmed: 32320003
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Clin Infect Dis. 2021 Jun 15;72(12):e1156-e1157
pubmed: 33201178
Autoimmun Rev. 2020 Jun;19(6):102537
pubmed: 32251717
Lancet Respir Med. 2020 Jun;8(6):544-546
pubmed: 32380023
N Engl J Med. 2020 Jun 11;382(24):2327-2336
pubmed: 32275812
Clin Microbiol Infect. 2021 Feb;27(2):215-227
pubmed: 33161150