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Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia
Guillain–Barré syndrome (GBS) is an adverse event of special interest (AESI) for surveillance systems monitoring adverse events following immunisation (AEFI) with COVID-19 vaccines. Emerging data support a temporal association between GBS and adenovirus-vector COVID-19 vaccines. We present a case se...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637534/ https://www.ncbi.nlm.nih.gov/pubmed/36357291 http://dx.doi.org/10.1016/j.vaccine.2022.10.084 |
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author | Osowicki, Joshua Morgan, Hannah J. Harris, Adele Clothier, Hazel J. Buttery, Jim P. Kiers, Lynette Crawford, Nigel W. |
author_facet | Osowicki, Joshua Morgan, Hannah J. Harris, Adele Clothier, Hazel J. Buttery, Jim P. Kiers, Lynette Crawford, Nigel W. |
author_sort | Osowicki, Joshua |
collection | PubMed |
description | Guillain–Barré syndrome (GBS) is an adverse event of special interest (AESI) for surveillance systems monitoring adverse events following immunisation (AEFI) with COVID-19 vaccines. Emerging data support a temporal association between GBS and adenovirus-vector COVID-19 vaccines. We present a case series of GBS reports submitted between February and November 2021 to our enhanced spontaneous surveillance system (SAEFVIC) in Victoria, Australia, following vaccination with either the adenovirus-vector vaccine Vaxzevria ChadOx1-S (AstraZeneca) or an mRNA vaccine (Comirnaty BNT162b2 [Pfizer-BioNTech] or Spikevax mRNA-1273 [Moderna]). For each report, Brighton Collaboration case definitions were used to describe diagnostic certainty. Severity was graded using the GBS Disability Score. The observed incidence of GBS following immunisation against COVID-19 was compared to expected background ICD10-AM G61.0 coded hospitalisations. There were 41 total cases of GBS reported to SAEFVIC following Vaxzevria (n = 38), Comirnaty (n = 3), or Spikevax (n = 0) vaccines. The observed GBS incidence rate exceeded the expected background rate for Vaxzevria only, with 1.85 reports per 100,000 doses following dose 1, higher than the expected rate of 0.39 hospital admissions per 100,000 adults within 42 days of vaccination. Of 38 GBS reports following Vaxzevria, the median age at vaccination was 66 years and median onset of symptoms was 14 days following immunisation. There was one death. Four cases initially categorised as GBS were later reclassified as acute-onset chronic inflammatory demyelinating polyneuropathy. Fatigue was the predominant persisting symptom reported at follow up. Additional global studies are required to characterise risk factors, clinical variability, and to provide precision and generalizability regarding AEFI risks such as GBS associated with different vaccine platforms, which will help inform communication of the potential benefits and risks of COVID19 vaccination. |
format | Online Article Text |
id | pubmed-9637534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96375342022-11-07 Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia Osowicki, Joshua Morgan, Hannah J. Harris, Adele Clothier, Hazel J. Buttery, Jim P. Kiers, Lynette Crawford, Nigel W. Vaccine Article Guillain–Barré syndrome (GBS) is an adverse event of special interest (AESI) for surveillance systems monitoring adverse events following immunisation (AEFI) with COVID-19 vaccines. Emerging data support a temporal association between GBS and adenovirus-vector COVID-19 vaccines. We present a case series of GBS reports submitted between February and November 2021 to our enhanced spontaneous surveillance system (SAEFVIC) in Victoria, Australia, following vaccination with either the adenovirus-vector vaccine Vaxzevria ChadOx1-S (AstraZeneca) or an mRNA vaccine (Comirnaty BNT162b2 [Pfizer-BioNTech] or Spikevax mRNA-1273 [Moderna]). For each report, Brighton Collaboration case definitions were used to describe diagnostic certainty. Severity was graded using the GBS Disability Score. The observed incidence of GBS following immunisation against COVID-19 was compared to expected background ICD10-AM G61.0 coded hospitalisations. There were 41 total cases of GBS reported to SAEFVIC following Vaxzevria (n = 38), Comirnaty (n = 3), or Spikevax (n = 0) vaccines. The observed GBS incidence rate exceeded the expected background rate for Vaxzevria only, with 1.85 reports per 100,000 doses following dose 1, higher than the expected rate of 0.39 hospital admissions per 100,000 adults within 42 days of vaccination. Of 38 GBS reports following Vaxzevria, the median age at vaccination was 66 years and median onset of symptoms was 14 days following immunisation. There was one death. Four cases initially categorised as GBS were later reclassified as acute-onset chronic inflammatory demyelinating polyneuropathy. Fatigue was the predominant persisting symptom reported at follow up. Additional global studies are required to characterise risk factors, clinical variability, and to provide precision and generalizability regarding AEFI risks such as GBS associated with different vaccine platforms, which will help inform communication of the potential benefits and risks of COVID19 vaccination. Elsevier Ltd. 2022-12-12 2022-11-07 /pmc/articles/PMC9637534/ /pubmed/36357291 http://dx.doi.org/10.1016/j.vaccine.2022.10.084 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Osowicki, Joshua Morgan, Hannah J. Harris, Adele Clothier, Hazel J. Buttery, Jim P. Kiers, Lynette Crawford, Nigel W. Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title | Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title_full | Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title_fullStr | Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title_full_unstemmed | Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title_short | Guillain-Barré syndrome temporally associated with COVID-19 vaccines in Victoria, Australia |
title_sort | guillain-barré syndrome temporally associated with covid-19 vaccines in victoria, australia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637534/ https://www.ncbi.nlm.nih.gov/pubmed/36357291 http://dx.doi.org/10.1016/j.vaccine.2022.10.084 |
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