Systematic Review Finds Higher Risk of Thromboembolic Events Following First Dose of ChAdOx1-S Vaccine
India: One of the COVID-19 vaccinations namely ChAdOx1-S is found to be associated with cerebral venous sinus thrombosis (CVS), and peripheral venous thrombosis (PVT) by 2-3 folds.
Research published in the Indian Journal of Community Medicine showcases the increased risk of certain events such as CVS, PVT, and thrombocytopenia by 2-3 times at the first dose of the ChAdOx1-S vaccine. However, for secondary outcomes like any venous, arterial thromboembolic, and hemorrhagic events, heart attack, or coronary artery disease (CAD), no significant link was found, or the evidence was low to very low.
ChAdOx1-S (AstraZeneca COVID-19 vaccine AZD1222, Vaxzevria™, SII COVISHIELD™) is an adenoviral vector vaccine administered in two doses, with a recommended interval of 4 to 12 weeks between doses. In early 2021, cases of venous thrombosis with thrombocytopenia were reported within 3 to 4 weeks after receiving the ChAdOx1-S vaccine.
Numerous case reports and case studies have been published mentioning CVS thrombosis, deep vein thrombosis, and pulmonary embolism but none of the studies reported any epidemiological measure of the strength of association between ChAdOx1-S vaccination and the incidence of thromboembolic, thrombocytopenic, and hemorrhagic events.
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