Tocilizumab shortens time on mechanical ventilation and length of hospital stay in patients with severe COVID‐19: a retrospective cohort study

among patients with COVID‐19 who require treatment in intensive care for acute respiratory distress syndrome (ARDS), mortality rates have been reported between 16 – 78% (1). In patients who are discharged alive, an increased risk of sequelae from COVID‐19 is anticipated (2). The hyperinflammatory re...

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Published inJournal of Internal Medicine Vol. 289; no. 3; pp. 434 - 436
Main Authors Eimer, J., Vesterbacka, J., Svensson, A.‐K., Stojanovic, B., Wagrell, C., Sönnerborg, A., Nowak, P.
Format Journal Article Web Resource
LanguageEnglish
Published England John Wiley & Sons, Inc 01.03.2021
Blackwell Publishing Ltd
John Wiley and Sons Inc
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Summary:among patients with COVID‐19 who require treatment in intensive care for acute respiratory distress syndrome (ARDS), mortality rates have been reported between 16 – 78% (1). In patients who are discharged alive, an increased risk of sequelae from COVID‐19 is anticipated (2). The hyperinflammatory response induced by SARS‐CoV‐2 is pivotal in the pathogenesis of COVID‐19 and is accompanied by an upregulated expression of interleukin 6 (IL‐6) that correlates with disease severity (3). Tocilizumab, a monoclonal antibody against the IL‐6 receptor originally licensed for the use in rheumatoid arthritis, is also approved for treatment of chimeric antigen receptor T cell–related cytokine release syndromes and secondary hemophagocytic syndromes that share important features with the hyperinflammatory phase in COVID‐19. Several small studies from China and Europe have reported promising results of the treatment with tocilizumab in patients with COVID‐19, preventing the need for admission to an intensive care unit and improving clinical outcomes (4,5). We aimed to evaluate the impact of treatment with tocilizumab compared to routine care on important clinical outcomes in critically ill patients admitted to an intensive care unit with ARDS due to COVID‐19.
Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:0954-6820
1365-2796
1365-2796
DOI:10.1111/joim.13162