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20 November 2024
Publish date: 11 August 2021
A national study involving UCLH has deepened understanding of the symptoms, signs and outcomes of patients with the novel condition vaccine-induced immune thrombocytopenia and thrombosis (VITT), associated with the Oxford/AstraZeneca vaccine.
VITT is a rare condition characterised by a blockage of veins and a marked reduction of platelets, which are an important part of the blood clotting system. VITT was first identified in the UK by UCLH Consultant Haematologist Prof Marie Scully and Dr Will Lester from University Hospitals Birmingham NHS Foundation Trust.
The new research paper, whose lead author is Dr Sue Pavord at Oxford University Hospitals (OUH) NHS Foundation Trust and which is published in the New England Journal of Medicine (NEJM), reports on the first 220 cases of definite and probable VITT in the UK.
The paper is based on cases of VITT presented by 182 consultant haematologists from 96 NHS Trusts, and builds on understanding about the condition outlined in an April 2021 NEJM paper led by Prof Scully which reported on 23 early cases of VITT.
The latest paper also complements a study led by UCLH’s Dr Richard Perry published in the Lancet earlier this month on cases of cerebral venous thrombosis (CVT) when it is caused by VITT. CVT is the commonest and severest manifestation of VITT.
The latest research found that the overall mortality rate of those presenting to hospitals with definite or probable VITT was 23%.
Almost all patients experienced the condition between five and 30 days after their first vaccination. There was no difference in incidence between the sexes, and no prior medical condition was seen more often than expected for the general population.
The chances of death increased significantly the lower the platelet count and the greater the activation of the blood clotting system, increasing to 73% in patients with a very low platelet count and intracranial haemorrhage following blood clots in the brain.
41% of patients had no previous medical diagnoses and 85% were less than 60 years old. Overall incidence in individuals under 50 was estimated to be 1 in 50,000 – consistent with reports from other countries.
Researchers said the optimal treatment was still uncertain, but that treatment approaches were being continually refined in real time. For instance, the introduction of the use of plasma exchange in the most severe cases has led to survival rates that were significantly better than would be predicted based on baseline characteristics.
In addition, the research provides further evidence that non-heparin-based blood thinners should be used to tackle blood clotting in cases of VITT, and that use of intravenous immunoglobin was associated with better outcomes.
Prof Scully, who is also Professor of Haemostasis and Thrombosis at UCL Institute of Cardiovascular Science, said: “As a new condition we are still learning about how best to diagnose and manage VITT, but as time goes on, we have been able to refine our treatment approaches and improve rates of survival and chance of recovery. This continuous learning in real time has been made possible thanks to collaboration between colleagues across the UK.”
Dr Pavord, a Consultant Haematologist at OUH, said: “We have worked relentlessly to understand and manage this new condition, so that the hugely successful vaccine roll out can continue, which is the most viable solution to the global pandemic.”
She added: “It’s important to stress that this kind of reaction to the Oxford-AstraZeneca vaccine is very rare. In those aged under 50, incidence is around one in 50,000 people who have received the vaccine.”
