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Multiple sclerosis, rituximab, and COVID‐19
We conducted a retrospective cohort study in Kaiser Permanente Southern California from 1 January 2020 to 30 September 2020. We found that rituximab‐treated persons with multiple sclerosis (pwMS, n = 1895) were more likely be hospitalized (n = 8, 33.3%), but not die (n = 0) from COVID‐19, compared t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045943/ https://www.ncbi.nlm.nih.gov/pubmed/33783140 http://dx.doi.org/10.1002/acn3.51342 |
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author | Langer‐Gould, Annette Smith, Jessica B. Li, Bonnie H. |
author_facet | Langer‐Gould, Annette Smith, Jessica B. Li, Bonnie H. |
author_sort | Langer‐Gould, Annette |
collection | PubMed |
description | We conducted a retrospective cohort study in Kaiser Permanente Southern California from 1 January 2020 to 30 September 2020. We found that rituximab‐treated persons with multiple sclerosis (pwMS, n = 1895) were more likely be hospitalized (n = 8, 33.3%), but not die (n = 0) from COVID‐19, compared to the 4.81 million non‐MS population (5.8% and 1.4%, respectively). Time in months (adjusted OR = 0.32, 95% CI = 0.15–0.69, p = 0.0033) and receiving 1000 mg compared to lower doses at last infusion (adjusted OR = 6.28, 95% CI = 1.38–28.5, p = 0.0173) were independent predictors of COVID‐19 severity. Rituximab‐treated pwMS should be counseled to take extra precautions in the 5 months following each infusion. Using extended dosing intervals and lower doses could be considered. |
format | Online Article Text |
id | pubmed-8045943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80459432021-04-16 Multiple sclerosis, rituximab, and COVID‐19 Langer‐Gould, Annette Smith, Jessica B. Li, Bonnie H. Ann Clin Transl Neurol Brief Communications We conducted a retrospective cohort study in Kaiser Permanente Southern California from 1 January 2020 to 30 September 2020. We found that rituximab‐treated persons with multiple sclerosis (pwMS, n = 1895) were more likely be hospitalized (n = 8, 33.3%), but not die (n = 0) from COVID‐19, compared to the 4.81 million non‐MS population (5.8% and 1.4%, respectively). Time in months (adjusted OR = 0.32, 95% CI = 0.15–0.69, p = 0.0033) and receiving 1000 mg compared to lower doses at last infusion (adjusted OR = 6.28, 95% CI = 1.38–28.5, p = 0.0173) were independent predictors of COVID‐19 severity. Rituximab‐treated pwMS should be counseled to take extra precautions in the 5 months following each infusion. Using extended dosing intervals and lower doses could be considered. John Wiley and Sons Inc. 2021-03-30 /pmc/articles/PMC8045943/ /pubmed/33783140 http://dx.doi.org/10.1002/acn3.51342 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Communications Langer‐Gould, Annette Smith, Jessica B. Li, Bonnie H. Multiple sclerosis, rituximab, and COVID‐19 |
title | Multiple sclerosis, rituximab, and COVID‐19 |
title_full | Multiple sclerosis, rituximab, and COVID‐19 |
title_fullStr | Multiple sclerosis, rituximab, and COVID‐19 |
title_full_unstemmed | Multiple sclerosis, rituximab, and COVID‐19 |
title_short | Multiple sclerosis, rituximab, and COVID‐19 |
title_sort | multiple sclerosis, rituximab, and covid‐19 |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045943/ https://www.ncbi.nlm.nih.gov/pubmed/33783140 http://dx.doi.org/10.1002/acn3.51342 |
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