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Comparative risk of cerebral venous sinus thrombosis (CVST) following COVID-19 vaccination or infection: A national cohort study using linked electronic health records.
Ohaeri, Columbus; Thomas, Daniel Rhys; Salmon, Jane; Cottrell, Simon; Lyons, Jane; Akbari, Ashley; Lyons, Ronan A; Torabi, Fatemeh; Davies, Gareth Gi; Williams, Christopher.
  • Ohaeri C; Communicable Disease Surveillance Centre, Public Health Wales, Wales, UK.
  • Thomas DR; Communicable Disease Surveillance Centre, Public Health Wales, Wales, UK.
  • Salmon J; School of Health Sciences, Cardiff Metropolitan University, Wales, UK.
  • Cottrell S; Communicable Disease Surveillance Centre, Public Health Wales, Wales, UK.
  • Lyons J; Vaccine Preventable Disease Programme and Communicable Disease Surveillance Centre, Public Health Wales, Wales, UK.
  • Akbari A; Population Data Science, Faculty of Medicine, Health & Life Science, Swansea University Medical School, Swansea University, Swansea, Wales, UK.
  • Torabi F; Population Data Science, Faculty of Medicine, Health & Life Science, Swansea University Medical School, Swansea University, Swansea, Wales, UK.
  • Davies GG; Population Data Science, Faculty of Medicine, Health & Life Science, Swansea University Medical School, Swansea University, Swansea, Wales, UK.
  • Williams C; Population Data Science, Faculty of Medicine, Health & Life Science, Swansea University Medical School, Swansea University, Swansea, Wales, UK.
Hum Vaccin Immunother ; : 2127572, 2022 Oct 27.
Article in English | MEDLINE | ID: covidwho-2087651
ABSTRACT
To inform the public and policy makers, we investigated and compared the risk of cerebral venous sinus thrombosis (CVST) after SARS-Cov-2 vaccination or infection using a national cohort of 2,643,699 individuals aged 17 y and above, alive, and resident in Wales on 1 January 2020 followed up through multiple linked data sources until 28 March 2021. Exposures were first dose of Oxford-ChAdOx1 or Pfizer-BioNTech vaccine or polymerase chain reaction (PCR)-confirmed SARS-Cov-2 infection. The outcome was an incident record of CVST. Hazard ratios (HR) were calculated using multivariable Cox regression, adjusted for confounders. HR from SARS-Cov-2 infection was compared with that for SARS-Cov-2 vaccination. We identified 910,556 (34.4%) records of first SARS-Cov-2 vaccination and 165,862 (6.3%) of SARS-Cov-2 infection. A total of 1,372 CVST events were recorded during the study period, of which 52 (3.8%) and 48 (3.5%) occurred within 28 d after vaccination and infection, respectively. We observed slight non-significant risk of CVST within 28 d of vaccination [aHR 1.34, 95% CI 0.95-1.90], which remained after stratifying by vaccine [BNT162b2, aHR 1.18 (95% CI 0.63-2.21); ChAdOx1, aHR 1.40 (95% CI 0.95-2.05)]. Three times the number of CVST events is observed within 28 d of a positive SARS-Cov-2 test [aHR 3.02 (95% CI 2.17-4.21)]. The risk of CVST following SARS-Cov-2 infection is 2.3 times that following SARS-Cov-2 vaccine. This is important information both for those designing COVID-19 vaccination programs and for individuals making their own informed decisions on the risk-benefit of vaccination. This record-linkage approach will be useful in monitoring the safety of future vaccine programs.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Hum Vaccin Immunother Year: 2022 Document Type: Article Affiliation country: 21645515.2022.2127572

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Hum Vaccin Immunother Year: 2022 Document Type: Article Affiliation country: 21645515.2022.2127572