27 August 2021
Study compares risks of thrombocytopenia and thromboembolic events following ChAdOx1 nCov-19 (Oxford-AstraZeneca), BNT162b2 mRNA (Pfizer-BioNTech) vaccination, and SARS-CoV-2 (Covid-19) infection
- Study shows increased risk of thrombocytopenia and venous thromboembolism with ChAdOx1 nCoV-19, and increased risk of arterial thromboembolism following BNT162b2 mRNA
- Risks of these adverse events were however much higher following SARS-CoV-2 infection
- Study authors fully independent from Oxford vaccine developers
Researchers from the University of Oxford have today announced the results of a study into thrombocytopenia (a condition with low platelet counts) and thromboembolic events (blood clots) following vaccination for Covid-19, some of the same events which have led to restricted use of the Oxford-AstraZeneca vaccine in a number of countries.
Writing in the British Medical Journal (BMJ), they detail the findings from over 29 million people vaccinated with first doses of either the ChAdOx1 nCov-19 ‘Oxford-AstraZeneca’ vaccine or the BNT162b2 mRNA ‘Pfizer-BioNTech’ vaccine. They conclude that with both of these vaccines, for short time intervals following the first dose, there are increased risks of some haematological and vascular adverse events leading to hospitalisation or death.
Julia Hippisley-Cox, Professor of Clinical Epidemiology and General Practice at the University of Oxford, lead author of the paper, said:
‘People should be aware of these increased risks after Covid-19 vaccination and seek medical attention promptly if they develop symptoms, but also be aware that the risks are considerably higher and over longer periods of time if they become infected with SARS-CoV-2’.
The authors further note that the risk of these adverse events is substantially higher and for a longer period of time, following infection from the SARS-CoV-2 ‘coronavirus’ than after either vaccine.
All of the coronavirus vaccines currently in use have been tested in randomized clinical trials, which are unlikely to be large enough to detect very rare adverse events. When rare events are uncovered, then regulators perform a risk-benefit analysis of the medicine; to compare the risks of the adverse events if vaccinated versus the benefits of avoidance of the disease – in this case, Covid-19.
In this paper, the team of authors from the University of Oxford, University of Leicester, Guys and St Thomas’ NHS Foundation Trust, the Intensive Care National Audit & Research Centre, the London School of Hygiene and Tropical Medicine, the University of Cambridge, the University of Edinburgh and the University of Nottingham, compared rates of adverse events after vaccination with Pfizer-BioNTech and Oxford-AstraZeneca vaccines with rates of the same events after a positive SARS-CoV-2 test result.
For this, they used routinely collected electronic health records to evaluate the short-term risks (within 28 days) of hospital admission with thrombocytopenia, venous thromboembolism (VTE) and arterial thromboembolism (ATE), using data collected from across England between December 1, 2020 and April 24, 2021. Other outcomes studied were cerebral venous sinus thrombosis (CVST), ischemic stroke, myocardial infarction and other rare arterial thrombotic events.
Prof. Hippisley-Cox added: ‘This research is important as many other studies, while useful, have been limited by small numbers and potential biases. Electronic healthcare records, which contain detailed recording of vaccinations, infections, outcomes and confounders, have provided us with a rich source of data with which to perform a robust evaluation of these vaccines, and compare to risks associated with Covid-19 infection.’
The authors detail the following limitations to their study:
- restricting the analysis to first vaccine dose only
- a short vaccination exposure window
- the lack of formal adjudication of routinely acquired outcomes, and the potential for misclassification of outcomes or exposures
- admissions where patients were still in hospital by the study end date being excluded.
However, they believe that any bias, if present, is likely to not change with respect to each vaccine and so the comparisons between vaccines are unlikely to be affected.
Aziz Sheikh, Professor of Primary Care Research & Development and Director of the Usher Institute at The University of Edinburgh and a co-author of the paper, said:
‘This enormous study, using data on over 29 million vaccinated people, has shown that there is a very small risk of clotting and other blood disorders following first dose Covid-19 vaccination. Though serious, the risk of these same outcomes is much higher following SARS-CoV-2 infection.
‘On balance, this analysis therefore clearly underscores the importance of getting vaccinated to reduce the risk of these clotting and bleeding outcomes in individuals, and because of the substantial public health benefit that Covid-19 vaccinations offer.’
Notes to editors:
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About the study:
This study was funded by Health Data Research (HDR UK) and Office for National Statistics (ONS) Data and Connectivity National Core Study funding.
This research is part of the Data and Connectivity National Core Study, led by Health Data Research UK in partnership with the Office for National Statistics and funded by UK Research and Innovation (grant ref MC_PC_20029)
The researchers report an increased risk of thrombocytopenia, VTE, and other rare arterial
thrombotic events in short periods of time following a first dose of ChAdOx1nCoV-19, and of ATE and ischemic stroke following a first dose of BNT162b2.
They also found an increased risk of cerebral venous sinus thrombosis (CVST) following a first dose of both vaccines, although the number of cases was very small and further confirmation is needed. The risks of these adverse outcomes following vaccination were all much lower than those associated with a SARS-CoV-2 infection.
For example, the researchers estimate that out of ten million people vaccinated with a first dose of ChAdOx1nCoV-19 107 extra people will be hospitalised or die from thrombocytopaenia in the 8 to 28 days following vaccination, compared with 934 extra people in ten million after a positive test for SARS-CoV-2 infection.
For venous thromboembolism the figures are 66 extra events for ten million people vaccinated with ChAdOx1nCoV-19 and 12614 extra events for ten million with a positive test. For ischaemic stroke, the figures are an estimated 143 extra events per ten million people vaccinated with BNT162b2 mRNA compared with 1699 extra events per ten million people with a positive test for SARS-CoV-2 infection.
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