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Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients

OBJECTIVES: Effective treatments for the critically ill patient with novel coronavirus disease 2019 are desperately needed. Given the role of cytokine release syndrome in the pathogenesis of coronavirus disease 2019-associated respiratory distress, therapies aimed at mitigating cytokine release, suc...

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Autores principales: Sirimaturos, Michael, Gotur, Deepa B., Patel, Samir J., Dreucean, Diane, Jakowenko, Nicholas, Cooper, Megan H., Brahmbhatt, Nishal, Graviss, Edward A., Nguyen, Duc T., Pingali, Sai Ravi, Lin, Jiejian, Musick, William L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531754/
https://www.ncbi.nlm.nih.gov/pubmed/33063035
http://dx.doi.org/10.1097/CCE.0000000000000232
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author Sirimaturos, Michael
Gotur, Deepa B.
Patel, Samir J.
Dreucean, Diane
Jakowenko, Nicholas
Cooper, Megan H.
Brahmbhatt, Nishal
Graviss, Edward A.
Nguyen, Duc T.
Pingali, Sai Ravi
Lin, Jiejian
Musick, William L.
author_facet Sirimaturos, Michael
Gotur, Deepa B.
Patel, Samir J.
Dreucean, Diane
Jakowenko, Nicholas
Cooper, Megan H.
Brahmbhatt, Nishal
Graviss, Edward A.
Nguyen, Duc T.
Pingali, Sai Ravi
Lin, Jiejian
Musick, William L.
author_sort Sirimaturos, Michael
collection PubMed
description OBJECTIVES: Effective treatments for the critically ill patient with novel coronavirus disease 2019 are desperately needed. Given the role of cytokine release syndrome in the pathogenesis of coronavirus disease 2019-associated respiratory distress, therapies aimed at mitigating cytokine release, such as the interleukin-6 receptor-inhibiting monoclonal antibody tocilizumab, represent potential treatment strategies. Therefore, we examined the outcomes of critically ill coronavirus disease 2019 patients treated with tocilizumab and factors associated with clinical improvement. DESIGN: A retrospective cohort analysis of 21-day outcomes for consecutive mechanically ventilated patients treated with tocilizumab from March 24, 2020, to May 4, 2020. SETTING: Nine ICUs at six hospitals within a hospital system in Houston, Texas, United States. PATIENTS: The first 62 coronavirus disease 2019 patients on invasive mechanical ventilation who were treated with tocilizumab, which was considered for all patients with severe disease. INTERVENTIONS: Tocilizumab was administered either at a weight-based dose of 4–8 mg/kg or at a flat dose of 400 mg, with repeat administration in some patients at the physician’s discretion. MEASUREMENTS AND MAIN RESULTS: The primary outcomes were mortality and clinical improvement, defined as extubation. By day 21 post-tocilizumab, clinical improvement occurred in 36 patients (58%) and 13 patients (21%) died. In both univariable and multivariable analyses, age less than 60 years was associated with clinical improvement. Transient transaminitis was the most common adverse reaction, occurring in 25 patients (40%). CONCLUSIONS: Based on clinical outcomes and mortality rates seen in previous reports of mechanically ventilated patients, tocilizumab, as part of the management strategy for severe coronavirus disease 2019, represents a promising option. These findings support the need for evaluation of tocilizumab in a randomized controlled trial.
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spelling pubmed-75317542020-10-14 Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients Sirimaturos, Michael Gotur, Deepa B. Patel, Samir J. Dreucean, Diane Jakowenko, Nicholas Cooper, Megan H. Brahmbhatt, Nishal Graviss, Edward A. Nguyen, Duc T. Pingali, Sai Ravi Lin, Jiejian Musick, William L. Crit Care Explor Observational Study OBJECTIVES: Effective treatments for the critically ill patient with novel coronavirus disease 2019 are desperately needed. Given the role of cytokine release syndrome in the pathogenesis of coronavirus disease 2019-associated respiratory distress, therapies aimed at mitigating cytokine release, such as the interleukin-6 receptor-inhibiting monoclonal antibody tocilizumab, represent potential treatment strategies. Therefore, we examined the outcomes of critically ill coronavirus disease 2019 patients treated with tocilizumab and factors associated with clinical improvement. DESIGN: A retrospective cohort analysis of 21-day outcomes for consecutive mechanically ventilated patients treated with tocilizumab from March 24, 2020, to May 4, 2020. SETTING: Nine ICUs at six hospitals within a hospital system in Houston, Texas, United States. PATIENTS: The first 62 coronavirus disease 2019 patients on invasive mechanical ventilation who were treated with tocilizumab, which was considered for all patients with severe disease. INTERVENTIONS: Tocilizumab was administered either at a weight-based dose of 4–8 mg/kg or at a flat dose of 400 mg, with repeat administration in some patients at the physician’s discretion. MEASUREMENTS AND MAIN RESULTS: The primary outcomes were mortality and clinical improvement, defined as extubation. By day 21 post-tocilizumab, clinical improvement occurred in 36 patients (58%) and 13 patients (21%) died. In both univariable and multivariable analyses, age less than 60 years was associated with clinical improvement. Transient transaminitis was the most common adverse reaction, occurring in 25 patients (40%). CONCLUSIONS: Based on clinical outcomes and mortality rates seen in previous reports of mechanically ventilated patients, tocilizumab, as part of the management strategy for severe coronavirus disease 2019, represents a promising option. These findings support the need for evaluation of tocilizumab in a randomized controlled trial. Lippincott Williams & Wilkins 2020-10-01 /pmc/articles/PMC7531754/ /pubmed/33063035 http://dx.doi.org/10.1097/CCE.0000000000000232 Text en Copyright © 2020 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Observational Study
Sirimaturos, Michael
Gotur, Deepa B.
Patel, Samir J.
Dreucean, Diane
Jakowenko, Nicholas
Cooper, Megan H.
Brahmbhatt, Nishal
Graviss, Edward A.
Nguyen, Duc T.
Pingali, Sai Ravi
Lin, Jiejian
Musick, William L.
Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title_full Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title_fullStr Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title_full_unstemmed Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title_short Clinical Outcomes Following Tocilizumab Administration in Mechanically Ventilated Coronavirus Disease 2019 Patients
title_sort clinical outcomes following tocilizumab administration in mechanically ventilated coronavirus disease 2019 patients
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7531754/
https://www.ncbi.nlm.nih.gov/pubmed/33063035
http://dx.doi.org/10.1097/CCE.0000000000000232
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