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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 1078-8956</identifier><identifier>ISSN: 1546-170X</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/s41591-021-01556-7</identifier><identifier>PMID: 34697502</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>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</subject><ispartof>Nature medicine, 2021-12, Vol.27 (12), p.2144-2153</ispartof><rights>The Author(s) 2021. corrected publication 2021</rights><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 Nature Publishing Group</rights><rights>The Author(s) 2021. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021, corrected publication 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c744t-8ba8343f3a01f73788dedbc2067ae67e2eb3c9a3d1261dd899e68fa79c7718203</citedby><cites>FETCH-LOGICAL-c744t-8ba8343f3a01f73788dedbc2067ae67e2eb3c9a3d1261dd899e68fa79c7718203</cites><orcidid>0000-0002-3674-3100 ; 0000-0003-2307-550X ; 0000-0001-6593-9092 ; 0000-0003-3324-9024 ; 0000-0003-4230-0207 ; 0000-0002-6279-4884 ; 0000-0001-7022-3056 ; 0000-0002-2479-7283 ; 0000-0002-8242-3722</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41591-021-01556-7$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41591-021-01556-7$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34697502$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patone, Martina</creatorcontrib><creatorcontrib>Handunnetthi, Lahiru</creatorcontrib><creatorcontrib>Saatci, Defne</creatorcontrib><creatorcontrib>Pan, Jiafeng</creatorcontrib><creatorcontrib>Katikireddi, Srinivasa Vittal</creatorcontrib><creatorcontrib>Razvi, Saif</creatorcontrib><creatorcontrib>Hunt, David</creatorcontrib><creatorcontrib>Mei, Xue W.</creatorcontrib><creatorcontrib>Dixon, Sharon</creatorcontrib><creatorcontrib>Zaccardi, Francesco</creatorcontrib><creatorcontrib>Khunti, Kamlesh</creatorcontrib><creatorcontrib>Watkinson, Peter</creatorcontrib><creatorcontrib>Coupland, Carol A. 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><title>Neurological complications after first dose of COVID-19 vaccines and SARS-CoV-2 infection</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><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.</description><subject>631/378</subject><subject>692/617/375</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Bell Palsy - epidemiology</subject><subject>Bell Palsy - virology</subject><subject>Bell's palsy</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>BNT162 Vaccine - adverse effects</subject><subject>BNT162 Vaccine - immunology</subject><subject>Cancer Research</subject><subject>ChAdOx1 nCoV-19 - adverse effects</subject><subject>ChAdOx1 nCoV-19 - immunology</subject><subject>Confidence intervals</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - diagnosis</subject><subject>COVID-19 - immunology</subject><subject>COVID-19 - pathology</subject><subject>COVID-19 vaccines</subject><subject>Diagnosis</subject><subject>England - epidemiology</subject><subject>Female</subject><subject>Guillain-Barre syndrome</subject><subject>Guillain-Barre Syndrome - epidemiology</subject><subject>Guillain-Barre Syndrome - virology</subject><subject>Hemorrhage</subject><subject>Hemorrhagic Stroke - epidemiology</subject><subject>Hemorrhagic Stroke - virology</subject><subject>Hospitalization - statistics & numerical data</subject><subject>Humans</subject><subject>Immunization</subject><subject>Infections</subject><subject>Infectious Diseases</subject><subject>Male</subject><subject>Metabolic Diseases</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Nervous System Diseases - epidemiology</subject><subject>Nervous System Diseases - virology</subject><subject>Neurological complications</subject><subject>Neurosciences</subject><subject>Paralysis</subject><subject>Patient outcomes</subject><subject>Public health</subject><subject>Risk</subject><subject>Risk factors</subject><subject>SARS-CoV-2 - immunology</subject><subject>Scotland - epidemiology</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Stroke</subject><subject>Vaccines</subject><subject>Young Adult</subject><issn>1078-8956</issn><issn>1546-170X</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkltrFDEYhgdRbK3-AS9kQBC9SE0yMzncFJb1tFBc6OqiVyGb-WY2ZTZZk5mi_95st7YdWURCSEie983he7PsOcGnBBfibSxJJQnCNHVSVQzxB9kxqUqGCMffHqY55gIJWbGj7EmMlxjjAlfycXZUlEzyCtPj7PtnGILvfGuN7nLjN9suzXrrXcx100PIGxtin9c-Qu6bfDpfzt4hIvMrbYx1kChX54vJxQJN_RLR3LoGzE7_NHvU6C7Cs5vxJPv64f2X6Sd0Pv84m07OkeFl2SOx0qIoi6bQmDS84ELUUK8MxYxrYBworAojdVETykhdCymBiUZzaTgnguLiJDvb-26H1QZqA64PulPbYDc6_FJeWzXecXatWn-lBKOS4CoZvL4xCP7HALFXGxsNdJ124IeoaCVYWSW2TOjLv9BLPwSXnqfS7TAtMaHkjmp1Byp9iE_nmp2pmjCRfp5iLBOFDlAtOEiX9A4am5ZH_OkBPrUaNtYcFLwZCRLTw8--1UOMara4-H92vhyzr-6xa9Bdv46-G65DMwbpHjTBxxiguS0KwWqXYLVPsEoJVtcJVjyJXtwv563kT2QTUOyBmLZcC-GuBv-w_Q0I8PZr</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Patone, Martina</creator><creator>Handunnetthi, Lahiru</creator><creator>Saatci, Defne</creator><creator>Pan, Jiafeng</creator><creator>Katikireddi, Srinivasa Vittal</creator><creator>Razvi, Saif</creator><creator>Hunt, David</creator><creator>Mei, Xue W.</creator><creator>Dixon, Sharon</creator><creator>Zaccardi, Francesco</creator><creator>Khunti, Kamlesh</creator><creator>Watkinson, Peter</creator><creator>Coupland, Carol A. 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C. ; Doidge, James ; Harrison, David A. ; Ravanan, Rommel ; Sheikh, Aziz ; Robertson, Chris ; Hippisley-Cox, Julia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c744t-8ba8343f3a01f73788dedbc2067ae67e2eb3c9a3d1261dd899e68fa79c7718203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/378</topic><topic>692/617/375</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Bell Palsy - epidemiology</topic><topic>Bell Palsy - virology</topic><topic>Bell's palsy</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>BNT162 Vaccine - adverse effects</topic><topic>BNT162 Vaccine - immunology</topic><topic>Cancer Research</topic><topic>ChAdOx1 nCoV-19 - adverse effects</topic><topic>ChAdOx1 nCoV-19 - immunology</topic><topic>Confidence intervals</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - diagnosis</topic><topic>COVID-19 - immunology</topic><topic>COVID-19 - pathology</topic><topic>COVID-19 vaccines</topic><topic>Diagnosis</topic><topic>England - epidemiology</topic><topic>Female</topic><topic>Guillain-Barre syndrome</topic><topic>Guillain-Barre Syndrome - epidemiology</topic><topic>Guillain-Barre Syndrome - virology</topic><topic>Hemorrhage</topic><topic>Hemorrhagic Stroke - epidemiology</topic><topic>Hemorrhagic Stroke - virology</topic><topic>Hospitalization - statistics & numerical data</topic><topic>Humans</topic><topic>Immunization</topic><topic>Infections</topic><topic>Infectious Diseases</topic><topic>Male</topic><topic>Metabolic Diseases</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Nervous System Diseases - epidemiology</topic><topic>Nervous System Diseases - virology</topic><topic>Neurological complications</topic><topic>Neurosciences</topic><topic>Paralysis</topic><topic>Patient outcomes</topic><topic>Public health</topic><topic>Risk</topic><topic>Risk factors</topic><topic>SARS-CoV-2 - immunology</topic><topic>Scotland - epidemiology</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Stroke</topic><topic>Vaccines</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patone, Martina</creatorcontrib><creatorcontrib>Handunnetthi, Lahiru</creatorcontrib><creatorcontrib>Saatci, Defne</creatorcontrib><creatorcontrib>Pan, Jiafeng</creatorcontrib><creatorcontrib>Katikireddi, Srinivasa Vittal</creatorcontrib><creatorcontrib>Razvi, Saif</creatorcontrib><creatorcontrib>Hunt, David</creatorcontrib><creatorcontrib>Mei, Xue W.</creatorcontrib><creatorcontrib>Dixon, Sharon</creatorcontrib><creatorcontrib>Zaccardi, Francesco</creatorcontrib><creatorcontrib>Khunti, Kamlesh</creatorcontrib><creatorcontrib>Watkinson, Peter</creatorcontrib><creatorcontrib>Coupland, Carol A. 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 & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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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source | MEDLINE; Nature; SpringerLink Journals - AutoHoldings |
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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