Patient‐reported daily functioning after SARSCoV‐2 vaccinations in autoimmune neuromuscular diseases

Author:

van Dam Koos P. J.1ORCID,Wieske Luuk12,Stalman Eileen W.1,Kummer Laura Y. L.13,van der Kooi Anneke J.1,Raaphorst Joost1,van de Beek Diederik1ORCID,Verschuuren Jan J. G. M.4ORCID,Ruiter Annabel M.4,Brusse Esther5,van Doorn Pieter A.5,Baars Adája E.5ORCID,van der Pol W. Ludo6,Goedee H. Stephan6,ten Brinke Anja6,van Ham S. Marieke37,Rispens Theo3,Kuijpers Taco W.8,Eftimov Filip1,

Affiliation:

1. Department of Neurology and Neurophysiology, Amsterdam Neuroscience, Amsterdam UMC, location AMC University of Amsterdam Amsterdam the Netherlands

2. Department of Clinical Neurophysiology St. Antonius Hospital Nieuwegein the Netherlands

3. Sanquin Research and Landsteiner Laboratory, Department of Immunopathology Amsterdam UMC Amsterdam the Netherlands

4. Department of Neurology Leiden University Medical Center Leiden the Netherlands

5. Department of Neurology Erasmus MC University Medical Center Rotterdam the Netherlands

6. Department of Neurology and Neurosurgery Brain Center UMC Utrecht Utrecht the Netherlands

7. Swammerdam Institute for Life Sciences University of Amsterdam Amsterdam the Netherlands

8. Department of Pediatric Immunology, Rheumatology, and Infectious Disease, Amsterdam UMC, location AMC University of Amsterdam Amsterdam the Netherlands

Abstract

AbstractBackground and purposeThere are concerns for safety regarding SARS‐CoV‐2 vaccines for patients with autoimmune neuromuscular disease. We compared daily functioning using disease‐specific patient‐reported outcome measures (PROMs) before and after SARS‐CoV‐2 vaccinations.MethodsIn this substudy of a prospective observational cohort study (Target‐to‐B!), patients with myasthenia gravis (MG), chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy (MMN), and idiopathic inflammatory myopathy (IIM) vaccinated against SARS‐CoV‐2 were included. Surveys of daily functioning (Myasthenia Gravis Activities of Daily Living, Inflammatory Rasch‐Built Overall Disability Scale, Multifocal Motor Neuropathy Rasch‐Built Overall Disability Scale, and Health Assessment Questionnaire–Disability Index) were sent before first vaccination and every 60 days thereafter for up to 12 months. Regression models were constructed to assess differences in PROM scores related to vaccination, compared to scores unrelated to vaccination. We also assessed the proportion of patients with deterioration of at least the minimal clinically important difference (MCID) between before first vaccination and 60 days thereafter.ResultsWe included 325 patients (median age = 59 years, interquartile range = 47–67, 156 [48%] female sex), of whom 137 (42%) had MG, 79 (24%) had CIDP, 43 (13%) had MMN, and 66 (20%) had IIM. PROM scores related to vaccination did not differ from scores unrelated to vaccination. In paired PROMs, MCID for deterioration was observed in three of 49 (6%) MG patients, of whom none reported a treatment change. In CIDP, MCID for deterioration was observed in eight of 29 patients (28%), of whom two of eight (25%) reported a treatment change.ConclusionsSARS‐CoV‐2 vaccination had no effect on daily functioning in patients with autoimmune neuromuscular diseases, confirming its safety in these patients.

Funder

ZonMw

Publisher

Wiley

Reference37 articles.

1. Covid-19 Vaccine Effectiveness in New York State

2. Risk and course of COVID-19 in immunosuppressed patients with myasthenia gravis

3. Perspective of patients with autoimmune diseases on COVID-19 vaccination

4. Disease activity in patients with immune‐mediated inflammatory diseases after SARS‐CoV‐2 vaccinations;Dam KPJ;J Autoimmun,2023

5. SARS‐CoV‐2 vaccination safety in Guillain‐Barré syndrome, chronic inflammatory demyelinating polyneuropathy, and multifocal motor neuropathy;Baars AE;Neurology,2022

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