دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: Guillain-Barré syndrome following SARS-CoV-2 vaccination in the UK: a prospective surveillance study.
المؤلفون: Tamborska AA; National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK., Singh B; National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.; Tropical and Infectious Diseases Unit, Royal Liverpool University Hospital, Liverpool, UK., Leonhard SE; Department of Neurology, Erasmus MC, Rotterdam, the Netherlands., Hodel EM; National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK., Stowe J; UK Health Security Agency, London, UK., Watson-Fargie T; Institute of Neurological Sciences, Queen Elizabeth University Hospital, Glasgow, UK., Fernandes PM; Department of Clinical Neurosciences, Royal Infirmary of Edinburgh, Edinburgh, UK., Themistocleous AC; Nuffield Department of Clinical Neurociences, University of Oxford, Oxford, UK., Roelofs J; Neurosciences Centre, Royal Victoria Infirmary, Newcastle upon Tyne, UK., Brennan K; Institute of Neurological Sciences, Queen Elizabeth University Hospital, Glasgow, UK., Morrice C; GAIN (Guillain-Barré & Associated Inflammatory Neuropathies) Charity, Sleaford, UK., Michael BD; National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK., Jacobs BC; Department of Neurology and Immunology, Erasmus MC, Rotterdam, The Netherlands., McDonald H; NIHR Health Protection Research Unit in Vaccines and Immunisation, London School of Hygiene & Tropical Medicine, London, UK., Solomon T; National Institute for Health Research Health Protection Research Unit for Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.; Department of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK.
مؤلفون مشاركون: UK Covid Vaccine GBS Study Group
المصدر: BMJ neurology open [BMJ Neurol Open] 2022 Jul 12; Vol. 4 (2), pp. e000309. Date of Electronic Publication: 2022 Jul 12 (Print Publication: 2022).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 101775450 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-6140 (Electronic) Linking ISSN: 26326140 NLM ISO Abbreviation: BMJ Neurol Open Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: London : British Medical Association, [2019]-
مستخلص: 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.
Competing Interests: Competing interests: TS was chair/cochair of the UK Research and Innovation/National Institute for Health Research COVID-19 Rapid Response and Rolling Funding Initiatives, was an Advisor to the UK COVID-19 Therapeutics Advisory Panel and is a member of the UK Medicines and Healthcare Products Regulatory Agency COVID-19 Vaccines Benefit Risk Expert Working Group. BCJ is a chair of Steering Committee of IGOS. HM is an invited expert for the Commission on Human Medicines COVID-19 Vaccines Safety Surveillance Methodologies Expert Working Group. The remaining authors have no relevant conflict of interest to declare.
(© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.)
References: Ann Neurol. 2021 Aug;90(2):315-318. (PMID: 34114269)
Lancet Infect Dis. 2001 Aug;1(1):29-37. (PMID: 11871407)
JAMA. 2021 Oct 12;326(14):1390-1399. (PMID: 34477808)
Egypt J Neurol Psychiatr Neurosurg. 2021;57(1):55. (PMID: 33967575)
BMC Med Res Methodol. 2014 Dec 19;14:135. (PMID: 25524443)
Brain. 2022 Feb 18;:. (PMID: 35180300)
Vaccine. 2021 Apr 15;39(16):2187-2189. (PMID: 33757668)
Haematologica. 2017 Apr;102(4):e140-e143. (PMID: 27927770)
JAMA Neurol. 2021 Nov 1;78(11):1409-1411. (PMID: 34468703)
J Neurol. 2012 Jun;259(6):1181-90. (PMID: 22143612)
NPJ Vaccines. 2019 Sep 24;4:39. (PMID: 31583123)
J Neurol Neurosurg Psychiatry. 2022 Mar;93(3):341-342. (PMID: 34261746)
CNS Drugs. 2020 Jan;34(1):1-8. (PMID: 31576507)
Ann Neurol. 2021 Aug;90(2):312-314. (PMID: 34114256)
Neuroepidemiology. 2009;32(2):150-63. (PMID: 19088488)
Vaccine. 2011 Jan 10;29(3):599-612. (PMID: 20600491)
Nat Med. 2021 Dec;27(12):2144-2153. (PMID: 34697502)
Neurology. 1998 Oct;51(4):1110-5. (PMID: 9781538)
Lancet. 2021 Mar 27;397(10280):1214-1228. (PMID: 33647239)
Brain. 2021 Mar 3;144(2):357-360. (PMID: 33313690)
Muscle Nerve. 2022 Feb;65(2):233-237. (PMID: 34786740)
Influenza Other Respir Viruses. 2017 Sep;11(5):372-393. (PMID: 28745014)
Mayo Clin Proc. 2017 May;92(5):838-850. (PMID: 28473042)
Neurology. 2010 May 25;74(21):1680-6. (PMID: 20427754)
Nat Rev Neurol. 2019 Nov;15(11):671-683. (PMID: 31541214)
Brain. 2021 Mar 3;144(2):682-693. (PMID: 33313649)
Vaccine. 2017 Mar 23;35(13):1729-1732. (PMID: 28245941)
J Neurol Neurosurg Psychiatry. 2021 Nov;92(11):1144-1151. (PMID: 34362855)
N Engl J Med. 2021 Jun 10;384(23):2202-2211. (PMID: 33861525)
Drug Saf. 2006;29(5):385-96. (PMID: 16689555)
Brain. 2018 Oct 1;141(10):2866-2877. (PMID: 30247567)
MMWR Morb Mortal Wkly Rep. 2021 Aug 13;70(32):1094-1099. (PMID: 34383735)
Lancet. 1978 Oct 7;2(8093):750-3. (PMID: 80682)
Clin Immunol. 2021 Sep;230:108818. (PMID: 34358692)
QJM. 2021 Nov 13;114(9):648-653. (PMID: 33471128)
Muscle Nerve. 2020 Oct;62(4):485-491. (PMID: 32678460)
Ann Neurol. 1998 Nov;44(5):780-8. (PMID: 9818934)
Front Psychiatry. 2020 Nov 12;11:577427. (PMID: 33304283)
Lancet Neurol. 2020 Sep;19(9):767-783. (PMID: 32622375)
Nat Rev Neurol. 2021 May;17(5):285-296. (PMID: 33649531)
معلومات مُعتمدة: MR/V033441/1 United Kingdom MRC_ Medical Research Council
فهرسة مساهمة: Investigator: CM Allen; G Amante; DP Breen; K Brennan; AC Romeiro; SJ Cheng; G Crossingham; J Evans; J Evison; PM Fernandes; J Furby; C Galton; R Gregory; V Harris; S Hinze; L Hogg; J Holt; A Isaacs-Itua; K Knight; A McHattie; MM Garrido; K Murray; S Ramsamy; S Ramsay; J Roelofs; N Samarasekera; PP San; S Sawcer; S Shields; E Tallantyre; R Terry; AC Themistocleous; H Tucker; O Tuohy; T Watson-Fargie; D Whittam; L Wiblin; M Zeidler
Keywords: COVID-19; clinical neurology; guillain-barre syndrome
تواريخ الأحداث: Date Created: 20220720 Latest Revision: 20230517
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC9277028
DOI: 10.1136/bmjno-2022-000309
PMID: 35856053
قاعدة البيانات: MEDLINE
الوصف
تدمد:2632-6140
DOI:10.1136/bmjno-2022-000309