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416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era

BACKGROUND: Rituximab (RTX), a widely used anti-CD20 monoclonal antibody, has been suggested as a risk factor for poor outcomes of coronavirus disease 2019 (COVID-19). However, it remains largely unknown whether COVID-19 outcomes remain worse in patients receiving RTX compared to those not being tre...

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Autores principales: Lee, Chan Mi, Kang, Chang Kyung, Jo, Hyeon Jae, Choe, Pyoeng Gyun, Kim, Nam Joong, Park, Wan Beom, Oh, Myoung-don
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678911/
http://dx.doi.org/10.1093/ofid/ofad500.486
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author Lee, Chan Mi
Kang, Chang Kyung
Jo, Hyeon Jae
Choe, Pyoeng Gyun
Kim, Nam Joong
Park, Wan Beom
Oh, Myoung-don
author_facet Lee, Chan Mi
Kang, Chang Kyung
Jo, Hyeon Jae
Choe, Pyoeng Gyun
Kim, Nam Joong
Park, Wan Beom
Oh, Myoung-don
author_sort Lee, Chan Mi
collection PubMed
description BACKGROUND: Rituximab (RTX), a widely used anti-CD20 monoclonal antibody, has been suggested as a risk factor for poor outcomes of coronavirus disease 2019 (COVID-19). However, it remains largely unknown whether COVID-19 outcomes remain worse in patients receiving RTX compared to those not being treated with RTX during the Omicron-dominant period, when patient fatality has significantly decreased compared to the Delta-dominant period. Therefore, we aimed to investigate the outcomes of COVID-19 patients receiving RTX during the Omicron-dominant period. METHODS: Among all laboratory-confirmed COVID-19 patients who were admitted to Seoul National University Hospital from February 2022 to January 2023, those who had received RTX before diagnosis of COVID-19 were included in the RTX group, while those who had the same underlying diseases but had not received RTX were included in the non-RTX group. The COVID-19-related outcomes were compared between the RTX and non-RTX groups. Multivariate logistic regression analyses were used to identify factors associated with severe to critical COVID-19 and COVID-19-related mortality. RESULTS: The proportion of severe to critical COVID-19 and COVID-19-related mortality were significantly higher in the RTX group than in the non-RTX group (41.9% vs. 28.3%, P = 0.030; 11.8% vs. 2.8%, P = 0.005). RTX therapy (adjusted odds ratio [aOR] 2.21, 95% confidence interval [CI] 1.21–4.04, P = 0.010) and chronic kidney disease (aOR 3.28, 95% CI 1.56–6.91, P = 0.002) were independent risk factors for severe to critical COVID-19, whereas being effectively vaccinated (aOR 0.47, 95% CI 0.25–0.85, P = 0.013) was a protective factor. In addition, only RTX therapy was independently associated with COVID-19-related mortality (aOR 4.03, 95% CI 1.17–13.86, P = 0.027). [Figure: see text] [Figure: see text] CONCLUSION: RTX therapy was associated with poor clinical outcomes of COVID-19, even in the Omicron-dominant period. This suggests that RTX should be used with caution even during the Omicron-dominant period. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106789112023-11-27 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era Lee, Chan Mi Kang, Chang Kyung Jo, Hyeon Jae Choe, Pyoeng Gyun Kim, Nam Joong Park, Wan Beom Oh, Myoung-don Open Forum Infect Dis Abstract BACKGROUND: Rituximab (RTX), a widely used anti-CD20 monoclonal antibody, has been suggested as a risk factor for poor outcomes of coronavirus disease 2019 (COVID-19). However, it remains largely unknown whether COVID-19 outcomes remain worse in patients receiving RTX compared to those not being treated with RTX during the Omicron-dominant period, when patient fatality has significantly decreased compared to the Delta-dominant period. Therefore, we aimed to investigate the outcomes of COVID-19 patients receiving RTX during the Omicron-dominant period. METHODS: Among all laboratory-confirmed COVID-19 patients who were admitted to Seoul National University Hospital from February 2022 to January 2023, those who had received RTX before diagnosis of COVID-19 were included in the RTX group, while those who had the same underlying diseases but had not received RTX were included in the non-RTX group. The COVID-19-related outcomes were compared between the RTX and non-RTX groups. Multivariate logistic regression analyses were used to identify factors associated with severe to critical COVID-19 and COVID-19-related mortality. RESULTS: The proportion of severe to critical COVID-19 and COVID-19-related mortality were significantly higher in the RTX group than in the non-RTX group (41.9% vs. 28.3%, P = 0.030; 11.8% vs. 2.8%, P = 0.005). RTX therapy (adjusted odds ratio [aOR] 2.21, 95% confidence interval [CI] 1.21–4.04, P = 0.010) and chronic kidney disease (aOR 3.28, 95% CI 1.56–6.91, P = 0.002) were independent risk factors for severe to critical COVID-19, whereas being effectively vaccinated (aOR 0.47, 95% CI 0.25–0.85, P = 0.013) was a protective factor. In addition, only RTX therapy was independently associated with COVID-19-related mortality (aOR 4.03, 95% CI 1.17–13.86, P = 0.027). [Figure: see text] [Figure: see text] CONCLUSION: RTX therapy was associated with poor clinical outcomes of COVID-19, even in the Omicron-dominant period. This suggests that RTX should be used with caution even during the Omicron-dominant period. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678911/ http://dx.doi.org/10.1093/ofid/ofad500.486 Text en © The Author(s) 2023. 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 Abstract
Lee, Chan Mi
Kang, Chang Kyung
Jo, Hyeon Jae
Choe, Pyoeng Gyun
Kim, Nam Joong
Park, Wan Beom
Oh, Myoung-don
416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title_full 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title_fullStr 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title_full_unstemmed 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title_short 416. Poor clinical outcomes of COVID-19 patients receiving rituximab during the Omicron era
title_sort 416. poor clinical outcomes of covid-19 patients receiving rituximab during the omicron era
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678911/
http://dx.doi.org/10.1093/ofid/ofad500.486
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