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COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update
BACKGROUND: We previously summarized outcomes for 46 cladribine tablets (CladT)-treated patients with multiple sclerosis (MS) and confirmed or suspected COVID-19, as reported to the Merck KGaA Global Patient Safety Database. This report updates on these findings, to 15 January 2021, for a total of 2...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997846/ https://www.ncbi.nlm.nih.gov/pubmed/33813097 http://dx.doi.org/10.1016/j.msard.2021.102929 |
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author | Jack, Dominic Damian, Doris Nolting, Axel Galazka, Andrew |
author_facet | Jack, Dominic Damian, Doris Nolting, Axel Galazka, Andrew |
author_sort | Jack, Dominic |
collection | PubMed |
description | BACKGROUND: We previously summarized outcomes for 46 cladribine tablets (CladT)-treated patients with multiple sclerosis (MS) and confirmed or suspected COVID-19, as reported to the Merck KGaA Global Patient Safety Database. This report updates on these findings, to 15 January 2021, for a total of 272 reported cases of COVID-19 among CladT recipients. METHODS: Case definitions: confirmed (COVID-19 diagnostic test was positive); suspected (no confirmatory test performed/reported). Cases fulfilling the criteria of hospitalized, medically significant, or fatal were designated as serious and outcomes were classified per usual pharmacovigilance practice. RESULTS: The evaluable cohort comprised 261 patients (confirmed COVID-19, n=160; suspected, n=101); an additional 11 patients had symptoms compatible with COVID-19 but were not evaluated further given their negative diagnostic tests. Median time to onset of COVID-19 from the most recent preceding CladT treatment course was 162 days (n=139). Outcomes were: recovered/recovering, n=133 (51%); not recovered/not resolved, n=19 (7%); died, n=1 (0.4%); and not reported/missing/pending, n=108 (41%). Of the total cohort, 40 (15%) experienced serious COVID-19. CONCLUSION: Our results suggest that CladT-treated patients with MS are generally not at greater risk of serious disease and/or a severe outcome with COVID-19 compared with the general population and other patients with MS who acquired COVID-19. |
format | Online Article Text |
id | pubmed-7997846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Author(s). Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79978462021-03-29 COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update Jack, Dominic Damian, Doris Nolting, Axel Galazka, Andrew Mult Scler Relat Disord Original Article BACKGROUND: We previously summarized outcomes for 46 cladribine tablets (CladT)-treated patients with multiple sclerosis (MS) and confirmed or suspected COVID-19, as reported to the Merck KGaA Global Patient Safety Database. This report updates on these findings, to 15 January 2021, for a total of 272 reported cases of COVID-19 among CladT recipients. METHODS: Case definitions: confirmed (COVID-19 diagnostic test was positive); suspected (no confirmatory test performed/reported). Cases fulfilling the criteria of hospitalized, medically significant, or fatal were designated as serious and outcomes were classified per usual pharmacovigilance practice. RESULTS: The evaluable cohort comprised 261 patients (confirmed COVID-19, n=160; suspected, n=101); an additional 11 patients had symptoms compatible with COVID-19 but were not evaluated further given their negative diagnostic tests. Median time to onset of COVID-19 from the most recent preceding CladT treatment course was 162 days (n=139). Outcomes were: recovered/recovering, n=133 (51%); not recovered/not resolved, n=19 (7%); died, n=1 (0.4%); and not reported/missing/pending, n=108 (41%). Of the total cohort, 40 (15%) experienced serious COVID-19. CONCLUSION: Our results suggest that CladT-treated patients with MS are generally not at greater risk of serious disease and/or a severe outcome with COVID-19 compared with the general population and other patients with MS who acquired COVID-19. The Author(s). Published by Elsevier B.V. 2021-06 2021-03-27 /pmc/articles/PMC7997846/ /pubmed/33813097 http://dx.doi.org/10.1016/j.msard.2021.102929 Text en © 2021 The Authors 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 | Original Article Jack, Dominic Damian, Doris Nolting, Axel Galazka, Andrew COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title | COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title_full | COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title_fullStr | COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title_full_unstemmed | COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title_short | COVID-19 in patients with multiple sclerosis treated with cladribine tablets: An update |
title_sort | covid-19 in patients with multiple sclerosis treated with cladribine tablets: an update |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997846/ https://www.ncbi.nlm.nih.gov/pubmed/33813097 http://dx.doi.org/10.1016/j.msard.2021.102929 |
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