4.5 Article

A Case Report of Thrombotic Thrombocytopenia After ChAdOx1 nCov-19 Vaccination and Heparin Use During Hemodialysis

Journal

JOURNAL OF KOREAN MEDICAL SCIENCE
Volume 37, Issue 10, Pages -

Publisher

KOREAN ACAD MEDICAL SCIENCES
DOI: 10.3346/jkms.2022.37.e75

Keywords

Anti-Platelet Factor 4 Antibody; ChAdOx1 COVID-19 Vaccine; Heparin; Thrombotic Thrombocytopenia

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Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a rare but life-threatening complication that mimics heparin-induced thrombocytopenia (HIT). This study reports a case of a patient receiving hemodialysis with heparin and developing thrombotic thrombocytopenia after vaccination. Treatment with anticoagulation and IVIG resolved the symptoms.
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a rare but life-threatening complication. VITT strongly mimics heparin-induced thrombocytopenia (HIT) and shares clinical features. Heparin is commonly used to prevent coagulation during hemodialysis. Therefore, nephrologists might encounter patients needing dialysis with a history of heparin exposure who developed thrombotic thrombocytopenia after vaccination. A 70-year-old male presented with acute kidney injury and altered mental status due to lithium intoxication. He needed consecutive hemodialysis using heparin. Deep vein thrombosis of left lower extremity and accompanying severe thrombocytopenia of 15,000/mu L on 24 days after vaccination and at the same time, nine days after heparin use. Anti-platelet factor 4 antibody test was positive. Anticoagulation with apixaban and intravenous immunoglobulin (IVIG) infusion resolved swelling of his left calf and thrombocytopenia. There were no definitive diagnostic tools capable of differentiating between VITT and HIT in this patient. Although VITT and HIT share treatment with IVIG and non-heparin anticoagulation, distinguishing between VITT and HIT will make it possible to establish a follow-up vaccination plan in a person who has had a thrombocytopenic thrombotic event. Further research is needed to develop the tools to make a clear distinction between the clinical syndromes.

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