Clinical Features of Vaccine-Induced Immune Thrombocytopenia and Thrombosis

Quick Takes

  • Following the ChAdOx1 nCoV-19 vaccine, VITT occurs across a wide age range (18-79 years) and nearly even between men and women.
  • VITT has a very high risk of mortality, up to 22% of patients in this large cohort study.
  • Predictors of mortality among patients with VITT include low platelet counts and the presence of intracranial hemorrhage.

Study Questions:

What are the clinical features of and prognostic criteria for vaccine-induced immune thrombocytopenia and thrombosis (VITT)?

Methods:

The authors conducted a prospective cohort study of patients with suspected VITT who presented to hospitals in the United Kingdom (UK) between March 22–June 6, 2021. Cases were defined as definite or probable based on prespecified criteria. Multivariable logistic regression analysis was used to investigate the association between clinical variables and mortality.

Results:

Among 294 patients who were evaluated, the authors identified 170 definite and 50 probable cases of VITT. All patients had received the first dose of ChAdOx1 nCoV-19 (AstraZeneca) vaccine between 5–48 days previously (median, 14 days). Age ranges were from 1–79 years (median, 48 years) with no sex preponderance and no identifiable medical risk factors. Overall mortality was 22% with odds of death that increased by 2.7 (95% confidence interval [CI], 1.4-5.2) among patients with cerebral venous sinus thrombosis. Odds of death increased by a factor of 1.7 (95% CI, 1.3-2.3) for every 50% decline in platelet count and by a factor of 1.2 (95% CI, 1.0-1.3) for every increase of 10,000 fibrinogen-equivalent units in the baseline D-dimer level. Finally, mortality odds were increased by a factor of 1.7 (95% CI, 1.1-2.5) for every 50% decrease in baseline fibrinogen level. Multivariable analysis identified that baseline platelet count and the presence of intracranial hemorrhage were independently associated with death. The observed mortality was 73% among patients with platelet counts below 30,000 per cubic millimeter and intracranial hemorrhage.

Conclusions:

The authors concluded that VITT has a high mortality rate, especially among patients with a low platelet count and intracranial hemorrhage.

Perspective:

Since late March 2021, the UK had experienced one of the largest cohorts of VITT following the AstraZeneca COVID-19 vaccine. This, the largest cohort reported to date, highlights the high mortality risk among patients with COVID-19, especially among those with low platelet count and intracranial hemorrhage complicating cerebral sinus vein thrombosis. It is notable that all cases occurred after the first dose of the AstraZeneca COVID-19 vaccine and that the median age was 48 (range 18-79) without a sex difference. How that differs from the Johnson & Johnson COVID-19 vaccine remains to be seen in larger cohort studies.

Clinical Topics: Anticoagulation Management, COVID-19 Hub, Prevention, Vascular Medicine

Keywords: Anticoagulants, Coronavirus, COVID-19, Fibrinogen, Intracranial Hemorrhages, Platelet Count, Primary Prevention, Purpura, Thrombocytopenic, Idiopathic, Risk Factors, Sex Characteristics, Sinus Thrombosis, Intracranial, Thrombocytopenia, Thrombosis, Vaccination, Vascular Diseases


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