BMJ Neurology Open (Jul 2022)
Guillain-Barré syndrome following SARS-CoV-2 vaccination in the UK: a prospective surveillance study
- ,
- 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
Affiliations
- assistant clinical professor and deputy director of Global Health
- Peter M Fernandes
- College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, UK
- Louise Wiblin
- Neurology, South Tees Hospitals NHS Foundation Trust, Middlesbrough, UK
- Tom Solomon
- 11 NIHR Health Protection Research Unit, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool, UK
- Jonathan Evans
- Bristol Medical School, Bristol Population Health Science Institute, University of Bristol, Bristol, UK
- Benedict D Michael
- Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK
- Bart C Jacobs
- 6 Neurology and Immunology, Erasmus MC, Rotterdam, The Netherlands
- Daniel Whittam
- Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK
- Harry Tucker
- 1 Department of Neurology, Lancashire Teaching Hospitals NHS Foundation Trust, Preston, UK
- Emma Tallantyre
- Division of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff, UK
- David P Breen
- 8 Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK
- Neshika Samarasekera
- Division of Clinical Neurosciences, NHS Lothian, Edinburgh, UK
- Kathryn Knight
- Core Medical Trainee, NHS Fife, Kirkaldy, UK
- Martin Zeidler
- 3Victoria Hospital, Kirkcaldy, UK
- Julia Stowe
- senior epidemiologist
- Sonja E Leonhard
- 1 Neurology, Erasmus MC, Rotterdam, The Netherlands
- Victoria Harris
- Foundation for Innovative New Diagnostics, Geneva, Switzerland
- Helen McDonald
- 4 London School of Hygiene and Tropical Medicine, London, UK
- Kathryn Brennan
- Neurology, NHS Glasgow and Clyde South Glasgow University Hospitals NHS Trust, Glasgow, UK
- Eva Maria Hodel
- 3LSTM, United Kingdom
- Ralph Gregory
- chair, services and standards committee
- Katy Murray
- Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh, UK
- Simon Shields
- Norfolk & Norwich University Hospital; Merck Serono Ltd
- Andreas C Themistocleous
- 1Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, Oxfordshire, UK
- Stephen Sawcer
- Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK
- CLARE GALTON
- Registrar
- Orla Tuohy
- Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK
- Stephan Hinze
- 2 Great Western Hospital, Swindon
- Jacob Roelofs
- 1Princess Alexandra Hospital
- James Holt
- 1Department of Neurology, The Walton Centre Foundation Trust
- Julian Furby
- Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK
- Bhagteshwar Singh
- University of Liverpool, Liverpool, UK
- Lucy Hogg
- 4 NHS Fife, Kirkcaldy, UK
- Scott Ramsay
- consultant physician and geriatrician, lead clinician for stroke
- Shue Jun Cheng
- 2South Tees Hospitals NHS Foundation Trust
- Andrew McHattie
- St Georges Hospital
- Arina A Tamborska
- National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK
- Taylor Watson-Fargie
- Institute of Neurological Sciences, Queen Elizabeth University Hospital, Glasgow, UK
- Caroline Morrice
- GAIN (Guillain-Barré & Associated Inflammatory Neuropathies) Charity, Sleaford, UK
- 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
- DOI
- https://doi.org/10.1136/bmjno-2022-000309
- Journal volume & issue
-
Vol. 4,
no. 2
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<0.00001). Facial weakness (63% (n=44/70) vs 36% (n=220/620); p<0.00001) and sensory dysfunction (93% (n=63/68) vs 69% (n=408/588); p=0.00005) were more common but disease severity and outcomes were similar to the IGOS study.Interpretation Most reports of GBS followed the first dose of ChAdOx1 vaccine. While our study cannot confirm or refute causation, this observation, together with the absence of alternative aetiologies, different than expected age distribution and the presence of unusual clinical features support a causal link. Clinicians and surveillance bodies should remain vigilant to the possibility of this very rare adverse event and its atypical variants.