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Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study
BACKGROUND: Various immunomodulatory therapies have been explored to manage the dysregulated immune response seen in severe COVID-19 infection. The objective of this study was to evaluate the efficacy of intravenous immunoglobulin (IVIG) in severe and critical COVID-19 disease. METHODS: This retrosp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825318/ https://www.ncbi.nlm.nih.gov/pubmed/35168081 http://dx.doi.org/10.1016/j.intimp.2022.108615 |
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author | Aggarwal, Ritesh Dewan, Arun Pandey, Ankita Trehan, Nikita Majid, Muhammad Aamir |
author_facet | Aggarwal, Ritesh Dewan, Arun Pandey, Ankita Trehan, Nikita Majid, Muhammad Aamir |
author_sort | Aggarwal, Ritesh |
collection | PubMed |
description | BACKGROUND: Various immunomodulatory therapies have been explored to manage the dysregulated immune response seen in severe COVID-19 infection. The objective of this study was to evaluate the efficacy of intravenous immunoglobulin (IVIG) in severe and critical COVID-19 disease. METHODS: This retrospective study included 535 patients with severe and critical COVID-19 admitted to the intensive care unit (ICU) of a tertiary care hospital, from May 2020 to December 2020. Primary outcome was the percentage of patients requiring mechanical ventilation. Secondary outcomes were a) in-hospital mortality, b) 28-day mortality, c) ICU-length of stay (ICU-LOS), d) days to discontinuation of supplemental oxygen, and e) days to COVID-PCR negativity. Logistic regression and linear regression were performed using the adjusted and unadjusted analyses. RESULTS: We analyzed a total of 535 patients out of which 255 (47.7%) received IVIG along with standard treatment and 280 (52.3%) received only standard treatment. Two groups were similar in terms of COVID-19 severity, APACHE II score, oxygen requirements, and initial management. The requirement of invasive ventilation was significantly less in the IVIG group compared to the Non-IVIG group (32.2% vs 40.4%, p < 0.05). In-hospital mortality, 28-day mortality, and ICU-LOS were also significantly less in the IVIG group (all p < 0.05). Subgroup analysis within the IVIG group showed that early administration of IVIG (≤7 days from ICU admission), old age (≥65 years), and obesity were associated with better outcomes (need for mechanical ventilation and in-hospital mortality) (all p < 0.05). IVIG administration in patients with chronic respiratory disease was associated with a reduced requirement for mechanical ventilation (p < 0.05), but there was an insignificant improvement in mortality. CONCLUSION: High-dose IVIG improves outcomes in severe and critical COVID-19 patients. The study also underscores the importance of timing and patient selection when administering IVIG. |
format | Online Article Text |
id | pubmed-8825318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88253182022-02-09 Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study Aggarwal, Ritesh Dewan, Arun Pandey, Ankita Trehan, Nikita Majid, Muhammad Aamir Int Immunopharmacol Article BACKGROUND: Various immunomodulatory therapies have been explored to manage the dysregulated immune response seen in severe COVID-19 infection. The objective of this study was to evaluate the efficacy of intravenous immunoglobulin (IVIG) in severe and critical COVID-19 disease. METHODS: This retrospective study included 535 patients with severe and critical COVID-19 admitted to the intensive care unit (ICU) of a tertiary care hospital, from May 2020 to December 2020. Primary outcome was the percentage of patients requiring mechanical ventilation. Secondary outcomes were a) in-hospital mortality, b) 28-day mortality, c) ICU-length of stay (ICU-LOS), d) days to discontinuation of supplemental oxygen, and e) days to COVID-PCR negativity. Logistic regression and linear regression were performed using the adjusted and unadjusted analyses. RESULTS: We analyzed a total of 535 patients out of which 255 (47.7%) received IVIG along with standard treatment and 280 (52.3%) received only standard treatment. Two groups were similar in terms of COVID-19 severity, APACHE II score, oxygen requirements, and initial management. The requirement of invasive ventilation was significantly less in the IVIG group compared to the Non-IVIG group (32.2% vs 40.4%, p < 0.05). In-hospital mortality, 28-day mortality, and ICU-LOS were also significantly less in the IVIG group (all p < 0.05). Subgroup analysis within the IVIG group showed that early administration of IVIG (≤7 days from ICU admission), old age (≥65 years), and obesity were associated with better outcomes (need for mechanical ventilation and in-hospital mortality) (all p < 0.05). IVIG administration in patients with chronic respiratory disease was associated with a reduced requirement for mechanical ventilation (p < 0.05), but there was an insignificant improvement in mortality. CONCLUSION: High-dose IVIG improves outcomes in severe and critical COVID-19 patients. The study also underscores the importance of timing and patient selection when administering IVIG. Elsevier B.V. 2022-05 2022-02-09 /pmc/articles/PMC8825318/ /pubmed/35168081 http://dx.doi.org/10.1016/j.intimp.2022.108615 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Aggarwal, Ritesh Dewan, Arun Pandey, Ankita Trehan, Nikita Majid, Muhammad Aamir Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title | Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title_full | Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title_fullStr | Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title_full_unstemmed | Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title_short | Efficacy of high-dose intravenous immunoglobulin in severe and critical COVID-19: A retrospective cohort study |
title_sort | efficacy of high-dose intravenous immunoglobulin in severe and critical covid-19: a retrospective cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825318/ https://www.ncbi.nlm.nih.gov/pubmed/35168081 http://dx.doi.org/10.1016/j.intimp.2022.108615 |
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