4.8 Article

Neurological complications after first dose of COVID-19 vaccines and SARS-CoV-2 infection

Journal

NATURE MEDICINE
Volume 27, Issue 12, Pages 2144-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41591-021-01556-7

Keywords

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Funding

  1. National Institute for Health Research (NIHR) Biomedical Research Centre, Oxford
  2. John Fell Oxford University Press Research Fund
  3. Cancer Research UK (CR-UK) [C5255/A18085]
  4. Cancer Research UK Oxford Centre
  5. Oxford Wellcome Institutional Strategic Support Fund [204826/Z/16/Z]
  6. UK Research and Innovation [MC_PC_20029]
  7. National Institute for Health Research (NIHR) Applied Research Collaboration East Midlands
  8. NIHR Lifestyle BRC
  9. NRS Senior Clinical Fellowship [SCAF/15/02]
  10. UK Medical Research Council [MC_UU_00022/2]
  11. Scottish Government Chief Scientist Office [SPHSU17]
  12. NIHR-funded clinical lectureship [CL-2019-13-001]
  13. Office For National Statistics

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Emerging reports of rare neurological complications associated with COVID-19 infection and vaccinations are leading to concerns in regulatory, clinical, and public health sectors. A self-controlled case series study in England showed an increased risk of rare neurological complications following COVID-19 vaccination and infection. The study highlighted a higher risk of Guillain-Barre syndrome after ChAdOx1nCoV-19 vaccination.
Emerging reports of rare neurological complications associated with COVID-19 infection and vaccinations are leading to regulatory, clinical and public health concerns. We undertook a self-controlled case series study to investigate hospital admissions from neurological complications in the 28 days after a first dose of ChAdOx1nCoV-19 (n = 20,417,752) or BNT162b2 (n = 12,134,782), and after a SARS-CoV-2-positive test (n = 2,005,280). There was an increased risk of Guillain-Barre syndrome (incidence rate ratio (IRR), 2.90; 95% confidence interval (CI): 2.15-3.92 at 15-21 days after vaccination) and Bell's palsy (IRR, 1.29; 95% CI: 1.08-1.56 at 15-21 days) with ChAdOx1nCoV-19. There was an increased risk of hemorrhagic stroke (IRR, 1.38; 95% CI: 1.12-1.71 at 15-21 days) with BNT162b2. An independent Scottish cohort provided further support for the association between ChAdOx1nCoV and Guillain-Barre syndrome (IRR, 2.32; 95% CI: 1.08-5.02 at 1-28 days). There was a substantially higher risk of all neurological outcomes in the 28 days after a positive SARS-CoV-2 test including Guillain-Barre syndrome (IRR, 5.25; 95% CI: 3.00-9.18). Overall, we estimated 38 excess cases of Guillain-Barre syndrome per 10 million people receiving ChAdOx1nCoV-19 and 145 excess cases per 10 million people after a positive SARS-CoV-2 test. In summary, although we find an increased risk of neurological complications in those who received COVID-19 vaccines, the risk of these complications is greater following a positive SARS-CoV-2 test. A self-controlled case series analysis of nearly 32 million people in England shows an increased risk of rare neurological complications in those who received COVID-19 vaccines and following SARS-CoV-2 infection. The results highlight 38 excess cases of Guillain-Barre syndrome per 10 million ChAdOx1nCoV-19 vaccinations.

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