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

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 a...

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Veröffentlicht in:Nature medicine 2021-12, Vol.27 (12), p.2144-2153
Hauptverfasser: Patone, Martina, Handunnetthi, Lahiru, Saatci, Defne, Pan, Jiafeng, Katikireddi, Srinivasa Vittal, Razvi, Saif, Hunt, David, Mei, Xue W., Dixon, Sharon, Zaccardi, Francesco, Khunti, Kamlesh, Watkinson, Peter, Coupland, Carol A. C., Doidge, James, Harrison, David A., Ravanan, Rommel, Sheikh, Aziz, Robertson, Chris, Hippisley-Cox, Julia
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container_end_page 2153
container_issue 12
container_start_page 2144
container_title Nature medicine
container_volume 27
creator Patone, Martina
Handunnetthi, Lahiru
Saatci, Defne
Pan, Jiafeng
Katikireddi, Srinivasa Vittal
Razvi, Saif
Hunt, David
Mei, Xue W.
Dixon, Sharon
Zaccardi, Francesco
Khunti, Kamlesh
Watkinson, Peter
Coupland, Carol A. C.
Doidge, James
Harrison, David A.
Ravanan, Rommel
Sheikh, Aziz
Robertson, Chris
Hippisley-Cox, Julia
description 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–Barré 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–Barré 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–Barré syndrome (IRR, 5.25; 95% CI: 3.00–9.18). Overall, we estimated 38 excess cases of Guillain–Barré 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–Barré syndrome per 10 million ChAdOx1nCoV-19 vaccinations.
doi_str_mv 10.1038/s41591-021-01556-7
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C. ; Doidge, James ; Harrison, David A. ; Ravanan, Rommel ; Sheikh, Aziz ; Robertson, Chris ; Hippisley-Cox, Julia</creator><creatorcontrib>Patone, Martina ; Handunnetthi, Lahiru ; Saatci, Defne ; Pan, Jiafeng ; Katikireddi, Srinivasa Vittal ; Razvi, Saif ; Hunt, David ; Mei, Xue W. ; Dixon, Sharon ; Zaccardi, Francesco ; Khunti, Kamlesh ; Watkinson, Peter ; Coupland, Carol A. C. ; Doidge, James ; Harrison, David A. ; Ravanan, Rommel ; Sheikh, Aziz ; Robertson, Chris ; Hippisley-Cox, Julia</creatorcontrib><description>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–Barré 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–Barré 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–Barré syndrome (IRR, 5.25; 95% CI: 3.00–9.18). Overall, we estimated 38 excess cases of Guillain–Barré 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. 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C.</creatorcontrib><creatorcontrib>Doidge, James</creatorcontrib><creatorcontrib>Harrison, David A.</creatorcontrib><creatorcontrib>Ravanan, Rommel</creatorcontrib><creatorcontrib>Sheikh, Aziz</creatorcontrib><creatorcontrib>Robertson, Chris</creatorcontrib><creatorcontrib>Hippisley-Cox, Julia</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale in Context : Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patone, Martina</au><au>Handunnetthi, Lahiru</au><au>Saatci, Defne</au><au>Pan, Jiafeng</au><au>Katikireddi, Srinivasa Vittal</au><au>Razvi, Saif</au><au>Hunt, David</au><au>Mei, Xue W.</au><au>Dixon, Sharon</au><au>Zaccardi, Francesco</au><au>Khunti, Kamlesh</au><au>Watkinson, Peter</au><au>Coupland, Carol A. C.</au><au>Doidge, James</au><au>Harrison, David A.</au><au>Ravanan, Rommel</au><au>Sheikh, Aziz</au><au>Robertson, Chris</au><au>Hippisley-Cox, Julia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurological complications after first dose of COVID-19 vaccines and SARS-CoV-2 infection</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>27</volume><issue>12</issue><spage>2144</spage><epage>2153</epage><pages>2144-2153</pages><issn>1078-8956</issn><issn>1546-170X</issn><eissn>1546-170X</eissn><abstract>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–Barré 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–Barré 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–Barré syndrome (IRR, 5.25; 95% CI: 3.00–9.18). Overall, we estimated 38 excess cases of Guillain–Barré 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–Barré syndrome per 10 million ChAdOx1nCoV-19 vaccinations.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>34697502</pmid><doi>10.1038/s41591-021-01556-7</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-3674-3100</orcidid><orcidid>https://orcid.org/0000-0003-2307-550X</orcidid><orcidid>https://orcid.org/0000-0001-6593-9092</orcidid><orcidid>https://orcid.org/0000-0003-3324-9024</orcidid><orcidid>https://orcid.org/0000-0003-4230-0207</orcidid><orcidid>https://orcid.org/0000-0002-6279-4884</orcidid><orcidid>https://orcid.org/0000-0001-7022-3056</orcidid><orcidid>https://orcid.org/0000-0002-2479-7283</orcidid><orcidid>https://orcid.org/0000-0002-8242-3722</orcidid><oa>free_for_read</oa></addata></record>
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subjects 631/378
692/617/375
Adolescent
Adult
Aged
Aged, 80 and over
Bell Palsy - epidemiology
Bell Palsy - virology
Bell's palsy
Biomedical and Life Sciences
Biomedicine
BNT162 Vaccine - adverse effects
BNT162 Vaccine - immunology
Cancer Research
ChAdOx1 nCoV-19 - adverse effects
ChAdOx1 nCoV-19 - immunology
Confidence intervals
Coronaviruses
COVID-19
COVID-19 - diagnosis
COVID-19 - immunology
COVID-19 - pathology
COVID-19 vaccines
Diagnosis
England - epidemiology
Female
Guillain-Barre syndrome
Guillain-Barre Syndrome - epidemiology
Guillain-Barre Syndrome - virology
Hemorrhage
Hemorrhagic Stroke - epidemiology
Hemorrhagic Stroke - virology
Hospitalization - statistics & numerical data
Humans
Immunization
Infections
Infectious Diseases
Male
Metabolic Diseases
Middle Aged
Molecular Medicine
Nervous System Diseases - epidemiology
Nervous System Diseases - virology
Neurological complications
Neurosciences
Paralysis
Patient outcomes
Public health
Risk
Risk factors
SARS-CoV-2 - immunology
Scotland - epidemiology
Severe acute respiratory syndrome coronavirus 2
Stroke
Vaccines
Young Adult
title Neurological complications after first dose of COVID-19 vaccines and SARS-CoV-2 infection
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