3.8 Article

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

Journal

BMJ NEUROLOGY OPEN
Volume 4, Issue 2, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjno-2022-000309

Keywords

clinical neurology; guillain-barre syndrome; COVID-19

Funding

  1. UK NIHR [ACF-2020-07-003]
  2. NIHR Health Protection Research Unit in Emerging and Zoonotic Infections [NIHR200907]
  3. NIHR Global Health Research Group on Brain Infections [17/63/110]
  4. UK Medical Research Council [MR/V03]
  5. NIHR Health Protection Research Unit in Vaccines and Immunisation
  6. National Institutes of Health Research (NIHR) [17/63/110] Funding Source: National Institutes of Health Research (NIHR)

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This study investigated the features of Guillain-Barre syndrome (GBS) following SARS-CoV-2 vaccines and evaluated the causal link between the two. The study found that most GBS cases occurred after the first dose of the ChAdOx1 vaccine and had different age distribution and unusual clinical features, supporting a causal link.
Objective To investigate features of Guillain-Barre 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.

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