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Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD

INTRODUCTION: Vaccination against the coronavirus disease 2019 (COVID-19) is recommended for patients with multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD), and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). However, vaccine safety in these patients t...

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Autores principales: Kim, Sohyeon, Seok, Hung Youl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924883/
https://www.ncbi.nlm.nih.gov/pubmed/36781562
http://dx.doi.org/10.1007/s10072-023-06676-1
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author Kim, Sohyeon
Seok, Hung Youl
author_facet Kim, Sohyeon
Seok, Hung Youl
author_sort Kim, Sohyeon
collection PubMed
description INTRODUCTION: Vaccination against the coronavirus disease 2019 (COVID-19) is recommended for patients with multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD), and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). However, vaccine safety in these patients taking immunotherapeutic agents is unclear as they were not included in the vaccine trials. OBJECTIVES: To evaluate the safety of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD. METHODS: We reviewed the medical records of MS, NMOSD, and MOGAD patients at the Keimyung University Dongsan Hospital. Information regarding vaccination schedules and adverse events was collected. RESULTS: A total of 56 patients (19, 22, and 15 patients with MS, NMOSD, and MOGAD, respectively) with a median age of 48.18 ± 15.72 years (range, 16–81 years) were included. Of them, 42 (75.0%) were female. In total, 76.8% (43/56) of all patients were vaccinated, and the vaccination rate was the highest for NMOSD patients (81.8%) and the lowest for MS patients (68.4%). All vaccinated patients were administered mRNA vaccines at least once in single or multiple vaccination doses. Only 3 of 43 (7.0%) vaccinated patients experienced clinical relapse following vaccination. Facial sensory changes with a brainstem lesion developed in an MS patient taking dimethyl fumarate, while myelitis occurred in a MOGAD patient receiving azathioprine maintenance therapy. The first episode of optic neuritis occurred in a patient who was later diagnosed with MOGAD. CONCLUSIONS: Our study demonstrated a favorable safety profile with no serious adverse events associated with COVID-19 vaccines in patients with MS, NMOSD, and MOGAD.
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spelling pubmed-99248832023-02-14 Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD Kim, Sohyeon Seok, Hung Youl Neurol Sci Covid-19 INTRODUCTION: Vaccination against the coronavirus disease 2019 (COVID-19) is recommended for patients with multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD), and myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). However, vaccine safety in these patients taking immunotherapeutic agents is unclear as they were not included in the vaccine trials. OBJECTIVES: To evaluate the safety of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD. METHODS: We reviewed the medical records of MS, NMOSD, and MOGAD patients at the Keimyung University Dongsan Hospital. Information regarding vaccination schedules and adverse events was collected. RESULTS: A total of 56 patients (19, 22, and 15 patients with MS, NMOSD, and MOGAD, respectively) with a median age of 48.18 ± 15.72 years (range, 16–81 years) were included. Of them, 42 (75.0%) were female. In total, 76.8% (43/56) of all patients were vaccinated, and the vaccination rate was the highest for NMOSD patients (81.8%) and the lowest for MS patients (68.4%). All vaccinated patients were administered mRNA vaccines at least once in single or multiple vaccination doses. Only 3 of 43 (7.0%) vaccinated patients experienced clinical relapse following vaccination. Facial sensory changes with a brainstem lesion developed in an MS patient taking dimethyl fumarate, while myelitis occurred in a MOGAD patient receiving azathioprine maintenance therapy. The first episode of optic neuritis occurred in a patient who was later diagnosed with MOGAD. CONCLUSIONS: Our study demonstrated a favorable safety profile with no serious adverse events associated with COVID-19 vaccines in patients with MS, NMOSD, and MOGAD. Springer International Publishing 2023-02-13 2023 /pmc/articles/PMC9924883/ /pubmed/36781562 http://dx.doi.org/10.1007/s10072-023-06676-1 Text en © Fondazione Società Italiana di Neurologia 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Covid-19
Kim, Sohyeon
Seok, Hung Youl
Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title_full Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title_fullStr Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title_full_unstemmed Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title_short Evaluation of the safety profile of COVID-19 vaccines in patients with MS, NMOSD, and MOGAD
title_sort evaluation of the safety profile of covid-19 vaccines in patients with ms, nmosd, and mogad
topic Covid-19
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924883/
https://www.ncbi.nlm.nih.gov/pubmed/36781562
http://dx.doi.org/10.1007/s10072-023-06676-1
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