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Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study
(1) Background: Severe COVID-19 outcomes are associated with cytokine release syndrome, characterized by the release of several immune modulators, including Interleukin-6 (IL-6). Tocilizumab (TCZ) is an IL-6 receptor antagonist used to treat rheumatic arthritis. The study aimed to evaluate the effic...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868075/ https://www.ncbi.nlm.nih.gov/pubmed/35203844 http://dx.doi.org/10.3390/antibiotics11020241 |
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author | Hafez, Wael Ziade, Mohamad Azzam Arya, Arun Saleh, Husam Abdelshakor, Mahmoud Fadl Alla, Osman Agrawal, Pragati Ali, Sara Rao, Srinivasa Raghu Gupta, Subrata Abdelli, Ikram Sebastian, Honeymol Ali, Mohamed Gador, Muneir Al Baha, Ziad Abdelrahman, Ahmed |
author_facet | Hafez, Wael Ziade, Mohamad Azzam Arya, Arun Saleh, Husam Abdelshakor, Mahmoud Fadl Alla, Osman Agrawal, Pragati Ali, Sara Rao, Srinivasa Raghu Gupta, Subrata Abdelli, Ikram Sebastian, Honeymol Ali, Mohamed Gador, Muneir Al Baha, Ziad Abdelrahman, Ahmed |
author_sort | Hafez, Wael |
collection | PubMed |
description | (1) Background: Severe COVID-19 outcomes are associated with cytokine release syndrome, characterized by the release of several immune modulators, including Interleukin-6 (IL-6). Tocilizumab (TCZ) is an IL-6 receptor antagonist used to treat rheumatic arthritis. The study aimed to evaluate the efficacy and safety of TCZ against COVID-19. (2) Methods: This was a retrospective study including 49 severe COVID-19 patients who received TCZ therapy in NMC Royal Hospital, UAE. (3) Results: Before Tocilizumab administration, the median temperature was 37.0 (IQR 36.0–39.6), and after day seven, the median reduced to 36.5 (IQR 35.8–37.9), p > 0.001. Thirty (61.2%) patients were admitted to the ICU, of which, eight (16.3%) were on WHO scale 4, sixteen (32.6%) on scale 5, and six (20.0%) on scale 6. TCZ reduced inflammatory markers over time, including CRP, D-Dimer, Ferritin, and Fibrinogen. By the end of week seven, 14 patients died (28.6%) while 35 (71.4%) improved and were discharged. (4) Conclusions: The study showed limited improvements in COVID-19 outcomes with TCZ therapy and highlighted the importance of D-Dimer monitoring for possible risk of thrombosis. Additionally, it could be recommended to upgrade the anti-coagulation dose to therapeutic levels once TCZ therapy is decided upon. |
format | Online Article Text |
id | pubmed-8868075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88680752022-02-25 Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study Hafez, Wael Ziade, Mohamad Azzam Arya, Arun Saleh, Husam Abdelshakor, Mahmoud Fadl Alla, Osman Agrawal, Pragati Ali, Sara Rao, Srinivasa Raghu Gupta, Subrata Abdelli, Ikram Sebastian, Honeymol Ali, Mohamed Gador, Muneir Al Baha, Ziad Abdelrahman, Ahmed Antibiotics (Basel) Article (1) Background: Severe COVID-19 outcomes are associated with cytokine release syndrome, characterized by the release of several immune modulators, including Interleukin-6 (IL-6). Tocilizumab (TCZ) is an IL-6 receptor antagonist used to treat rheumatic arthritis. The study aimed to evaluate the efficacy and safety of TCZ against COVID-19. (2) Methods: This was a retrospective study including 49 severe COVID-19 patients who received TCZ therapy in NMC Royal Hospital, UAE. (3) Results: Before Tocilizumab administration, the median temperature was 37.0 (IQR 36.0–39.6), and after day seven, the median reduced to 36.5 (IQR 35.8–37.9), p > 0.001. Thirty (61.2%) patients were admitted to the ICU, of which, eight (16.3%) were on WHO scale 4, sixteen (32.6%) on scale 5, and six (20.0%) on scale 6. TCZ reduced inflammatory markers over time, including CRP, D-Dimer, Ferritin, and Fibrinogen. By the end of week seven, 14 patients died (28.6%) while 35 (71.4%) improved and were discharged. (4) Conclusions: The study showed limited improvements in COVID-19 outcomes with TCZ therapy and highlighted the importance of D-Dimer monitoring for possible risk of thrombosis. Additionally, it could be recommended to upgrade the anti-coagulation dose to therapeutic levels once TCZ therapy is decided upon. MDPI 2022-02-12 /pmc/articles/PMC8868075/ /pubmed/35203844 http://dx.doi.org/10.3390/antibiotics11020241 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hafez, Wael Ziade, Mohamad Azzam Arya, Arun Saleh, Husam Abdelshakor, Mahmoud Fadl Alla, Osman Agrawal, Pragati Ali, Sara Rao, Srinivasa Raghu Gupta, Subrata Abdelli, Ikram Sebastian, Honeymol Ali, Mohamed Gador, Muneir Al Baha, Ziad Abdelrahman, Ahmed Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title | Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title_full | Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title_fullStr | Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title_full_unstemmed | Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title_short | Treatment Outcomes of Tocilizumab in Critically-Ill COVID-19 Patients, Single-Centre Retrospective Study |
title_sort | treatment outcomes of tocilizumab in critically-ill covid-19 patients, single-centre retrospective study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8868075/ https://www.ncbi.nlm.nih.gov/pubmed/35203844 http://dx.doi.org/10.3390/antibiotics11020241 |
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