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Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2

Tocilizumab is an IL‐6 receptor antagonist with the ability to suppress the cytokine storm in critically ill patients infected with severe acute respiratory syndrome‐coronavirus 2 (SARS‐CoV‐2). We evaluated patients treated with tocilizumab for a SARS‐CoV‐2 infection who were admitted between March...

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Autores principales: Petrak, Russell M., Skorodin, Nathan C., Van Hise, Nicholas W., Fliegelman, Robert M., Pinsky, Jonathan, Didwania, Vishal, Anderson, Michael, Diaz, Melina, Shah, Kairav, Chundi, Vishnu V., Hines, David W., Harting, Brian P., Sidwha, Kamo, Yu, Brian, Brune, Paul, Owaisi, Anjum, Beezhold, David, Kent, Joseph, Vais, Dana, Han, Alice, Gowda, Neethi, Sahgal, Nishi, Silverman, Jan, Stake, Jonathan, Nepomuceno, Jenie, Heddurshetti, Renuka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604239/
https://www.ncbi.nlm.nih.gov/pubmed/32918792
http://dx.doi.org/10.1111/cts.12894
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author Petrak, Russell M.
Skorodin, Nathan C.
Van Hise, Nicholas W.
Fliegelman, Robert M.
Pinsky, Jonathan
Didwania, Vishal
Anderson, Michael
Diaz, Melina
Shah, Kairav
Chundi, Vishnu V.
Hines, David W.
Harting, Brian P.
Sidwha, Kamo
Yu, Brian
Brune, Paul
Owaisi, Anjum
Beezhold, David
Kent, Joseph
Vais, Dana
Han, Alice
Gowda, Neethi
Sahgal, Nishi
Silverman, Jan
Stake, Jonathan
Nepomuceno, Jenie
Heddurshetti, Renuka
author_facet Petrak, Russell M.
Skorodin, Nathan C.
Van Hise, Nicholas W.
Fliegelman, Robert M.
Pinsky, Jonathan
Didwania, Vishal
Anderson, Michael
Diaz, Melina
Shah, Kairav
Chundi, Vishnu V.
Hines, David W.
Harting, Brian P.
Sidwha, Kamo
Yu, Brian
Brune, Paul
Owaisi, Anjum
Beezhold, David
Kent, Joseph
Vais, Dana
Han, Alice
Gowda, Neethi
Sahgal, Nishi
Silverman, Jan
Stake, Jonathan
Nepomuceno, Jenie
Heddurshetti, Renuka
author_sort Petrak, Russell M.
collection PubMed
description Tocilizumab is an IL‐6 receptor antagonist with the ability to suppress the cytokine storm in critically ill patients infected with severe acute respiratory syndrome‐coronavirus 2 (SARS‐CoV‐2). We evaluated patients treated with tocilizumab for a SARS‐CoV‐2 infection who were admitted between March 13, 2020, and April 16, 2020. This was a multicenter study with data collected by chart review both retrospectively and concurrently. Parameters evaluated included age, sex, race, use of mechanical ventilation (MV), usage of steroids and vasopressors, inflammatory markers, and comorbidities. Early dosing was defined as a tocilizumab dose administered prior to or within 1 day of intubation. Late dosing was defined as a dose administered > 1 day after intubation. In the absence of MV, the timing of the dose was related to the patient’s date of admission only. We evaluated 145 patients. The average age was 58.1 years, 64% were men, 68.3% had comorbidities, and 60% received steroid therapy. Disposition of patients was 48.3% discharged and 29.3% died, of which 43.9% were African American. MV was required in 55.9%, of which 34.5% died. Avoidance of MV (P = 0.002) and increased survival (P < 0.001) was statistically associated with early dosing. Tocilizumab therapy was effective at decreasing mortality and should be instituted early in the management of critically ill patients with coronavirus disease 2019) COVID‐19).
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spelling pubmed-86042392021-11-24 Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2 Petrak, Russell M. Skorodin, Nathan C. Van Hise, Nicholas W. Fliegelman, Robert M. Pinsky, Jonathan Didwania, Vishal Anderson, Michael Diaz, Melina Shah, Kairav Chundi, Vishnu V. Hines, David W. Harting, Brian P. Sidwha, Kamo Yu, Brian Brune, Paul Owaisi, Anjum Beezhold, David Kent, Joseph Vais, Dana Han, Alice Gowda, Neethi Sahgal, Nishi Silverman, Jan Stake, Jonathan Nepomuceno, Jenie Heddurshetti, Renuka Clin Transl Sci Research Tocilizumab is an IL‐6 receptor antagonist with the ability to suppress the cytokine storm in critically ill patients infected with severe acute respiratory syndrome‐coronavirus 2 (SARS‐CoV‐2). We evaluated patients treated with tocilizumab for a SARS‐CoV‐2 infection who were admitted between March 13, 2020, and April 16, 2020. This was a multicenter study with data collected by chart review both retrospectively and concurrently. Parameters evaluated included age, sex, race, use of mechanical ventilation (MV), usage of steroids and vasopressors, inflammatory markers, and comorbidities. Early dosing was defined as a tocilizumab dose administered prior to or within 1 day of intubation. Late dosing was defined as a dose administered > 1 day after intubation. In the absence of MV, the timing of the dose was related to the patient’s date of admission only. We evaluated 145 patients. The average age was 58.1 years, 64% were men, 68.3% had comorbidities, and 60% received steroid therapy. Disposition of patients was 48.3% discharged and 29.3% died, of which 43.9% were African American. MV was required in 55.9%, of which 34.5% died. Avoidance of MV (P = 0.002) and increased survival (P < 0.001) was statistically associated with early dosing. Tocilizumab therapy was effective at decreasing mortality and should be instituted early in the management of critically ill patients with coronavirus disease 2019) COVID‐19). John Wiley and Sons Inc. 2021-10-27 2021-11 /pmc/articles/PMC8604239/ /pubmed/32918792 http://dx.doi.org/10.1111/cts.12894 Text en © 2020 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society for Clinical Pharmacology and Therapeutics. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Petrak, Russell M.
Skorodin, Nathan C.
Van Hise, Nicholas W.
Fliegelman, Robert M.
Pinsky, Jonathan
Didwania, Vishal
Anderson, Michael
Diaz, Melina
Shah, Kairav
Chundi, Vishnu V.
Hines, David W.
Harting, Brian P.
Sidwha, Kamo
Yu, Brian
Brune, Paul
Owaisi, Anjum
Beezhold, David
Kent, Joseph
Vais, Dana
Han, Alice
Gowda, Neethi
Sahgal, Nishi
Silverman, Jan
Stake, Jonathan
Nepomuceno, Jenie
Heddurshetti, Renuka
Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title_full Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title_fullStr Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title_full_unstemmed Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title_short Tocilizumab as a Therapeutic Agent for Critically Ill Patients Infected with SARS‐CoV‐2
title_sort tocilizumab as a therapeutic agent for critically ill patients infected with sars‐cov‐2
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604239/
https://www.ncbi.nlm.nih.gov/pubmed/32918792
http://dx.doi.org/10.1111/cts.12894
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