Severe Thrombocytopenia, Thrombosis and Anti-PF4 Antibody after Pfizer-BioNTech COVID-19 mRNA Vaccine Booster-Is It Vaccine-Induced Immune Thrombotic Thrombocytopenia?
Victor W T LingBingwen Eugene FanSoon Lee LauXiu Hue LeeChuen Wen TanShir Ying LeePublished in: Vaccines (2022)
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a serious and life-threatening complication occurring after adenovirus-vector COVID-19 vaccines, and is rarely reported after other vaccine types. Herein, we report a case of possible VITT after the Pfizer-BioNTech mRNA vaccine booster, who presented with extensive lower limb deep vein thrombosis, severe thrombocytopenia, markedly elevated D-dimer and positive anti-PF4 antibody occurring 2 weeks post-vaccination, concurrent with a lupus anticoagulant. A complete recovery was made after intravenous immunoglobulin, prednisolone and anticoagulation with the oral direct Xa inhibitor rivaroxaban. The presenting features of VITT may overlap with those of antiphospholipid syndrome associated with anti-PF4 and immune thrombocytopenia. We discuss the diagnostic considerations in VITT and highlight the challenges of performing VITT confirmatory assays in non-specialized settings. The set of five diagnostic criteria for VITT is a useful tool for guiding initial management, but may potentially include patients without VITT. The bleeding risks of severe thrombocytopenia in the face of thrombosis, requiring anticoagulant therapy, present a clinical challenge, but early recognition and management can potentially lead to favorable outcomes.
Keyphrases
- atrial fibrillation
- venous thromboembolism
- lower limb
- coronavirus disease
- sars cov
- end stage renal disease
- pulmonary embolism
- early onset
- high glucose
- ejection fraction
- chronic kidney disease
- newly diagnosed
- systemic lupus erythematosus
- prognostic factors
- stem cells
- palliative care
- case report
- peritoneal dialysis
- binding protein
- skeletal muscle
- rheumatoid arthritis
- oxidative stress
- high dose
- radiation therapy
- bone marrow
- metabolic syndrome
- high throughput
- endothelial cells
- patient reported