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Risk of thrombosis with thrombocytopenia syndrome after COVID-19 vaccination prior to the recognition of vaccine-induced thrombocytopenia and thrombosis: A self-controlled case series study in England.
Higgins, Hannah; Andrews, Nick; Stowe, Julia; Amirthalingam, Gayatri; Ramsay, Mary; Bahra, Gurpreet; Hackett, Anthony; Breen, Karen A; Desborough, Michael; Khan, Dalia; Leary, Heather; Sweeney, Connor; Hutchinson, Elizabeth; Shapiro, Susan E; Lees, Charlotte; Dhanapal, Jay; MacCallum, Peter K; Burke, Shoshana; McDonald, Vickie; Entwistle, Ngai Mun Aiman; Booth, Stephen; Atchison, Christina J; Hunt, Beverley J.
  • Higgins H; Health Protection Division UK Health Security Agency London UK.
  • Andrews N; Immunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
  • Stowe J; Immunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
  • Amirthalingam G; Immunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
  • Ramsay M; Immunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
  • Bahra G; Centre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
  • Hackett A; Centre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
  • Breen KA; Centre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
  • Desborough M; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Khan D; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Leary H; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Sweeney C; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Hutchinson E; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Shapiro SE; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Lees C; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Dhanapal J; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • MacCallum PK; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Burke S; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • McDonald V; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Entwistle NMA; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Booth S; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
  • Atchison CJ; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Hunt BJ; Oxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Res Pract Thromb Haemost ; 6(3): e12698, 2022 Mar.
Article in English | MEDLINE | ID: covidwho-1797756
ABSTRACT

Background:

Several studies have found increased risks of thrombosis with thrombocytopenia syndrome (TTS) following the ChAdOx1 vaccination. However, case ascertainment is often incomplete in large electronic health record (EHR)-based studies.

Objectives:

To assess for an association between clinically validated TTS and COVID-19 vaccination.

Methods:

We used the self-controlled case series method to assess the risks of clinically validated acute TTS after a first COVID-19 vaccine dose (BNT162b2 or ChAdOx1) or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Case ascertainment was performed uninformed of vaccination status via a retrospective clinical review of hospital EHR systems, including active ascertainment of thrombocytopenia.

Results:

One hundred seventy individuals were admitted to the hospital for a TTS event at the study sites between January 1 and March 31, 2021. A significant increased risk (relative incidence [RI], 5.67; 95% confidence interval [CI], 1.02-31.38) of TTS 4 to 27 days after ChAdOx1 was observed in the youngest age group (18- to 39-year-olds). No other period had a significant increase, although for ChAdOx1 for all ages combined the RI was >1 in the 4- to 27- and 28- to 41-day periods (RI, 1.52; 95% CI, 0.88-2.63; and (RI, 1.70; 95% CI, 0.73-3.8, respectively). There was no significant increased risk of TTS after BNT162b2 in any period. Increased risks of TTS following a positive SARS-CoV-2 test occurred across all age groups and exposure periods.

Conclusions:

We demonstrate an increased risk of TTS in the 4 to 27 days following COVID-19 vaccination, particularly for ChAdOx1. These risks were lower than following SARS-CoV-2 infection. An alternative vaccine may be preferable in younger age groups in whom the risk of postvaccine TTS is greatest.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: Res Pract Thromb Haemost Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: Res Pract Thromb Haemost Year: 2022 Document Type: Article