Evidence map›Paper›PMID 35475292›Full record

ArticleResearch and practice in thrombosis and haemostasis2022

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.

Hannah Higgins, Nick Andrews, Julia Stowe, Gayatri Amirthalingam, Mary Ramsay, Gurpreet Bahra, Anthony Hackett, Karen A Breen, Michael Desborough, Dalia Khan and 13 more

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 8 institutions in 2 countries.

Hannah HigginsHealth Protection Division UK Health Security Agency London UK.ORCID https://orcid.org/0000-0001-9115-0992
Nick AndrewsImmunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
Julia StoweImmunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
Gayatri AmirthalingamImmunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
Mary RamsayImmunisation and Vaccine Preventable Diseases Division UK Health Security Agency London UK.
Gurpreet BahraCentre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
Anthony HackettCentre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
Karen A BreenCentre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.
Michael DesboroughOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.ORCID https://orcid.org/0000-0002-1951-5616
Dalia KhanOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Heather LearyOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Connor SweeneyOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Elizabeth HutchinsonOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Susan E ShapiroOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Charlotte LeesOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Jay DhanapalOxford University Hospitals NHS Foundation Trust Oxford NIHR Biomedical Research Centre Oxford UK.
Peter K MacCallumWolfson Institute of Population Health Queen Mary University of London London UK.
Shoshana BurkeBarts Health NHS Trust London UK.
Vickie McDonaldBarts Health NHS Trust London UK.
Ngai Mun Aiman EntwistleBarts Health NHS Trust London UK.
Stephen BoothDepartment of Haematology Royal Berkshire Hospital NHS Foundation Trust London UK.ORCID https://orcid.org/0000-0003-2687-0234
Christina J AtchisonPatient Experience Research Centre School of Public Health Imperial College London London UK.ORCID https://orcid.org/0000-0001-8304-7389
Beverley J HuntCentre for Thrombosis and Haemostasis St Thomas' Hospital Guy's and Saint Thomas' NHS Foundation Trust London UK.ORCID https://orcid.org/0000-0002-4709-0774
University of Oxford · GBSt Thomas' Hospital · GBUK Health Security Agency · GBBarts Health NHS Trust · GBHealth Protection Agency · MVNIHR Imperial Biomedical Research Centre · GBQueen Mary University of London · GBRoyal Berkshire Hospital · GB

Funding

Medical Research Council MR/T024054/1
6 · The paper itself

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.

Indexed as

COVID‐19COVID‐19 vaccinesSARS‐CoV‐2thrombocytopeniathrombosis

Identifiers

PMID35475292
PMCPMC9020167
OpenAlexW4224257080

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.