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Association of cerebral venous thrombosis with recent COVID-19 vaccination: case-crossover study using ascertainment through neuroimaging in Scotland.
McKeigue, Paul M; Burgul, Raj; Bishop, Jen; Robertson, Chris; McMenamin, Jim; O'Leary, Maureen; McAllister, David A; Colhoun, Helen M.
  • McKeigue PM; Usher Institute, College of Medicine and Veterinary Medicine, University of Edinburgh, Teviot Place, Edinburgh, EH8 9AG, Scotland, UK.
  • Burgul R; Public Health Scotland, Meridian Court, 5 Cadogan Street, Glasgow, G2 6QE, Scotland, UK.
  • Bishop J; Forth Valley Royal Hospital, Larbert, FK5 4WR, Scotland, UK.
  • Robertson C; Public Health Scotland, Meridian Court, 5 Cadogan Street, Glasgow, G2 6QE, Scotland, UK.
  • McMenamin J; Public Health Scotland, Meridian Court, 5 Cadogan Street, Glasgow, G2 6QE, Scotland, UK.
  • O'Leary M; Department of Mathematics and Statistics, University of Strathclyde, 16 Richmond Street, Glasgow, G1 1XQ, Scotland, UK.
  • McAllister DA; Public Health Scotland, Meridian Court, 5 Cadogan Street, Glasgow, G2 6QE, Scotland, UK.
  • Colhoun HM; Public Health Scotland, Meridian Court, 5 Cadogan Street, Glasgow, G2 6QE, Scotland, UK.
BMC Infect Dis ; 21(1): 1275, 2021 Dec 20.
Article in English | MEDLINE | ID: covidwho-1635338
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT

BACKGROUND:

To investigate the association of primary acute cerebral venous thrombosis (CVT) with COVID-19 vaccination through complete ascertainment of all diagnosed CVT in the population of Scotland.

METHODS:

Case-crossover study comparing cases of CVT recently exposed to vaccination (1-14 days after vaccination) with cases less recently exposed. Cases in Scotland from 1 December 2020 were ascertained through neuroimaging studies up to 17 May 2021 and diagnostic coding of hospital discharges up to 28 April 2021, linked to national vaccination records. The main outcome measure was primary acute CVT.

RESULTS:

Of 50 primary acute CVT cases, 29 were ascertained only from neuroimaging studies, 2 were ascertained only from hospital discharges, and 19 were ascertained from both sources. Of these 50 cases, 14 had received the Astra-Zeneca ChAdOx1 vaccine and 3 the Pfizer BNT162b2 vaccine. The incidence of CVT per million doses in the first 14 days after vaccination was 2.2 (95% credible interval 0.9 to 4.1) for ChAdOx1 and 1 (95% credible interval 0.1 to 2.9) for BNT162b2. The rate ratio for CVT associated with exposure to ChAdOx1 in the first 14 days compared with exposure 15-84 days after vaccination was 3.2 (95% credible interval 1.1 to 9.5).

CONCLUSIONS:

These findings support a causal association between CVT and the AstraZeneca vaccine. The absolute risk of post-vaccination CVT in this population-wide study in Scotland was lower than has been reported for populations in Scandinavia and Germany; the explanation for this is not clear.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Venous Thrombosis / COVID-19 Type of study: Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Humans Country/Region as subject: Europa Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06960-5

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Venous Thrombosis / COVID-19 Type of study: Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Humans Country/Region as subject: Europa Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06960-5