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342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia
BACKGROUND: Guidelines recommend use of tocilizumab (TCZ), an inhibitor of pro-inflammatory IL-6 signaling, for hospitalized patients with progressive severe or critical Coronavirus disease 2019 (COVID-19). The incidence of infectious complications following the use of TCZ for COVID-19 has not been...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690531/ http://dx.doi.org/10.1093/ofid/ofab466.543 |
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author | Warner, Adam Abbas, Mujahed Avner, Benjamin S Flynn, Thomas E Walroth, Todd A Jagger, Brett W |
author_facet | Warner, Adam Abbas, Mujahed Avner, Benjamin S Flynn, Thomas E Walroth, Todd A Jagger, Brett W |
author_sort | Warner, Adam |
collection | PubMed |
description | BACKGROUND: Guidelines recommend use of tocilizumab (TCZ), an inhibitor of pro-inflammatory IL-6 signaling, for hospitalized patients with progressive severe or critical Coronavirus disease 2019 (COVID-19). The incidence of infectious complications following the use of TCZ for COVID-19 has not been well-described. METHODS: We conducted a retrospective, observational matched cohort study of severely ill, hospitalized adult patients with confirmed COVID-19 who were treated with TCZ between 2/24/2021 and 6/1/2021. The intervention group, comprised of patients who received a single dose of TCZ, was matched based on c-reactive protein (CRP) and fraction of inspired oxygen (FiO(2)) with a control group who did not receive TCZ, and were hospitalized between 10/12/2020 and 3/6/2021. The primary outcome of the study was diagnosis of a bacterial or fungal infection after day 3 of the index hospitalization. Secondary outcomes included all-cause mortality during the study period and length of stay. RESULTS: 75 patients who received TCZ were identified during the study period, and matched 1:1 with 75 control patients. Baseline CRP and FiO(2) were similar between groups, while the median age in the TCZ group was younger (61 versus 71 years), reflecting the epidemiology of the outbreak during the TCZ and control study periods. 15 bacterial and fungal infections were identified in the TCZ group (20.0%) and 4 (5.3%) infections in the control group (p = 0.012). The majority of infections in both groups were bacterial, with a disproportionate number of bloodstream infections in the TCZ group [7 (9.3%) vs 2(2.6%); p = 0.166]. 28 patients (37.3%) died in the TCZ group compared to 39 (52.0%) in the matched control (p = 0.068). Median time to discharge was similar between TCZ and control patients (11 versus 12 days; 95% CI -2,2). CONCLUSION: Secondary infections in adult patients with severe and critical COVID-19 were more common in patients who had received TCZ. Prospective studies are needed to confirm and further describe this association. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-8690531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86905312022-01-05 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia Warner, Adam Abbas, Mujahed Avner, Benjamin S Flynn, Thomas E Walroth, Todd A Jagger, Brett W Open Forum Infect Dis Poster Abstracts BACKGROUND: Guidelines recommend use of tocilizumab (TCZ), an inhibitor of pro-inflammatory IL-6 signaling, for hospitalized patients with progressive severe or critical Coronavirus disease 2019 (COVID-19). The incidence of infectious complications following the use of TCZ for COVID-19 has not been well-described. METHODS: We conducted a retrospective, observational matched cohort study of severely ill, hospitalized adult patients with confirmed COVID-19 who were treated with TCZ between 2/24/2021 and 6/1/2021. The intervention group, comprised of patients who received a single dose of TCZ, was matched based on c-reactive protein (CRP) and fraction of inspired oxygen (FiO(2)) with a control group who did not receive TCZ, and were hospitalized between 10/12/2020 and 3/6/2021. The primary outcome of the study was diagnosis of a bacterial or fungal infection after day 3 of the index hospitalization. Secondary outcomes included all-cause mortality during the study period and length of stay. RESULTS: 75 patients who received TCZ were identified during the study period, and matched 1:1 with 75 control patients. Baseline CRP and FiO(2) were similar between groups, while the median age in the TCZ group was younger (61 versus 71 years), reflecting the epidemiology of the outbreak during the TCZ and control study periods. 15 bacterial and fungal infections were identified in the TCZ group (20.0%) and 4 (5.3%) infections in the control group (p = 0.012). The majority of infections in both groups were bacterial, with a disproportionate number of bloodstream infections in the TCZ group [7 (9.3%) vs 2(2.6%); p = 0.166]. 28 patients (37.3%) died in the TCZ group compared to 39 (52.0%) in the matched control (p = 0.068). Median time to discharge was similar between TCZ and control patients (11 versus 12 days; 95% CI -2,2). CONCLUSION: Secondary infections in adult patients with severe and critical COVID-19 were more common in patients who had received TCZ. Prospective studies are needed to confirm and further describe this association. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2021-12-04 /pmc/articles/PMC8690531/ http://dx.doi.org/10.1093/ofid/ofab466.543 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Abstracts Warner, Adam Abbas, Mujahed Avner, Benjamin S Flynn, Thomas E Walroth, Todd A Jagger, Brett W 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title | 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title_full | 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title_fullStr | 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title_full_unstemmed | 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title_short | 342. Secondary Infections following Tocilizumab for Treatment of COVID-19 Pneumonia |
title_sort | 342. secondary infections following tocilizumab for treatment of covid-19 pneumonia |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690531/ http://dx.doi.org/10.1093/ofid/ofab466.543 |
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