Neurological Events Reported after COVID‐19 Vaccines: An Analysis of Vaccine Adverse Event Reporting System
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- Jennifer A. Frontera
- Department of Neurology New York University Grossman School of Medicine New York NY
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- Arina A. Tamborska
- Institute of Infection Veterinary and Ecological Sciences, University of Liverpool Liverpool UK
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- Mohamed F. Doheim
- Department of Medicine Alexandria University Alexandria Egypt
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- David Garcia‐Azorin
- Department of Neurology Hospital Clínico Universitario de Valladolid Valladolid Spain
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- Hasim Gezegen
- Faculty of Medicine Department of Neurology, Istanbul University Istanbul Turkey
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- Alla Guekht
- Moscow Research and Clinical Center for Neuropsychiatry Moscow Russia
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- Abdul Hanif Khan Yusof Khan
- Department of Neurology Faculty of Medicine and Health Sciences, Universiti Putra Malaysia Serdang Malaysia
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- Michele Santacatterina
- Department of Population Health New York University New York NY
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- James Sejvar
- Division of High‐Consequence Pathogens and Pathology National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention Atlanta GA
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- Kiran T. Thakur
- Department of Neurology Columbia University Irving Medical Center/New York Presbyterian Hospital New York NY
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- Erica Westenberg
- Department of Neurology Center for Global Health, Klinikum rechts der Isar, Technical University of Munich Munich Germany
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- Andrea S. Winkler
- Department of Neurology Center for Global Health, Klinikum rechts der Isar, Technical University of Munich Munich Germany
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- Ettore Beghi
- Department of Neuroscience Istituto di Ricerche Farmacologiche Mario Negri IRCCS Milan Italy
書誌事項
- 公開日
- 2022-03-23
- 権利情報
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- http://onlinelibrary.wiley.com/termsAndConditions#vor
- DOI
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- 10.1002/ana.26339
- 公開者
- Wiley
この論文をさがす
説明
<jats:sec><jats:title>Objective</jats:title><jats:p>To identify the rates of neurological events following administration of mRNA (Pfizer, Moderna) or adenovirus vector (Janssen) vaccines in the U.S.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used publicly available data from the U.S. Vaccine Adverse Event Reporting System (VAERS) collected between January 1, 2021 and June 14, 2021. All free text symptoms that were reported within 42 days of vaccine administration were manually reviewed and grouped into 36 individual neurological diagnostic categories. Post‐vaccination neurological event rates were compared between vaccine types and to age‐matched baseline incidence rates in the U.S. and rates of neurological events following COVID.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Of 306,907,697 COVID vaccine doses administered during the study timeframe, 314,610 (0.1%) people reported any adverse event and 105,214 (0.03%) reported neurological adverse events in a median of 1 day (IQR0‐3) from inoculation. Guillain‐Barre Syndrome (GBS), and cerebral venous thrombosis (CVT) occurred in fewer than 1 per 1,000,000 doses. Significantly more neurological adverse events were reported following Janssen (Ad26.COV2.S) vaccination compared to either Pfizer‐BioNtech (BNT162b2) or Moderna (mRNA‐1,273; 0.15% vs 0.03% vs 0.03% of doses, respectively, <jats:italic>p</jats:italic> < 0.0001). The observed‐to‐expected ratios for GBS, CVT and seizure following Janssen vaccination were ≥1.5‐fold higher than background rates. However, the rate of neurological events after acute SARS‐CoV‐2 infection was up to 617‐fold higher than after COVID vaccination.</jats:p></jats:sec><jats:sec><jats:title>Interpretation</jats:title><jats:p>Reports of serious neurological events following COVID vaccination are rare. GBS, CVT and seizure may occur at higher than background rates following Janssen vaccination. Despite this, rates of neurological complications following acute SARS‐CoV‐2 infection are up to 617‐fold higher than after COVID vaccination. ANN NEUROL 2022;91:756–771</jats:p></jats:sec>
収録刊行物
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- Annals of Neurology
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Annals of Neurology 91 (6), 756-771, 2022-03-23
Wiley
