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Guillain-Barré syndrome following SARS-CoV-2 vaccination in the UK: a prospective surveillance study

Authors :
Peter M Fernandes
Louise Wiblin
Tom Solomon
Jonathan Evans
Benedict D Michael
Bart C Jacobs
Daniel Whittam
Harry Tucker
Emma Tallantyre
David P Breen
Neshika Samarasekera
Kathryn Knight
Martin Zeidler
Julia Stowe
Sonja E Leonhard
Victoria Harris
Helen McDonald
Kathryn Brennan
Eva Maria Hodel
Ralph Gregory
Katy Murray
Simon Shields
Andreas C Themistocleous
Stephen Sawcer
CLARE GALTON
Orla Tuohy
Stephan Hinze
Jacob Roelofs
James Holt
Julian Furby
Bhagteshwar Singh
Lucy Hogg
Scott Ramsay
Shue Jun Cheng
Andrew McHattie
Arina A Tamborska
Taylor Watson-Fargie
Caroline Morrice
Christopher M Allen
Gionathan Amante
Ana Carrilho Romeiro
Ginette Crossingham
Jon Evison
Alifa Isaacs-Itua
Mireia Moragas Garrido
Shelby Ramsamy
Pyae Phyo San
Robyn Terry
Source :
BMJ Neurology Open, Vol 4, Iss 2 (2022)
Publication Year :
2022
Publisher :
BMJ Publishing Group, 2022.

Abstract

Objective To investigate features of Guillain-Barré syndrome (GBS) following SARS-CoV-2 vaccines and evaluate for a causal link between the two.Methods We captured cases of GBS after SARS-CoV-2 vaccination through a national, open-access, online surveillance system. For each case, the certainty of GBS was graded using the Brighton criteria, and the relationship to the vaccine was examined using modified WHO Causality Assessment criteria. We compared age distribution of cases with that of prepandemic GBS cases and clinical features with the International GBS Outcome Study (IGOS).Results Between 1 January and 30 June 2021, we received 67 reports of GBS following the ChAdOx1 vaccine (65 first doses) and three reports following the BNT162b2 vaccine (all first doses). The causal association with the vaccine was classified as probable for 56 (80%, all ChAdOx1), possible for 12 (17%, 10 ChAdOx1) and unlikely for two (3%, 1 ChAdOx1). A greater proportion of cases occurred in the 50–59 age group in comparison with prepandemic GBS. Most common clinical variants were sensorimotor GBS (n=55; 79%) and facial diplegia with paraesthesias (n=10; 14%). 10% (n=7/69) of patients reported an antecedent infection, compared with 77% (n=502/652) of the IGOS cohort (p

Details

Language :
English
ISSN :
26326140
Volume :
4
Issue :
2
Database :
Directory of Open Access Journals
Journal :
BMJ Neurology Open
Publication Type :
Academic Journal
Accession number :
edsdoj.520eb838f5a64a8a9e594d4a133f5181
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjno-2022-000309