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. 2024 Feb 9;13(4):1012. doi: 10.3390/jcm13041012

Table 1.

A clinical and immunological overview of HIT and VITT.

HIT VITT
Pathophysiology Triggered by antibodies against PF4-heparin complexes [16] Triggered by anti-PF4 specific antibodies, post vaccination [28]
Symptom onset Typically 5–10 days after heparin administration [16] Typically 4–42 days after adenovirus vector-based COVID-19 vaccine administration [28]
Clinical presentation Thrombocytopenia, elevated risk of thrombosis [16] Thrombocytopenia, high frequency of thrombosis at atypical sites like arterial and cerebral venous sinus [65]
Antibody characteristics and persistence Transient anti-PF4/heparin antibodies, median duration of 50–80 days [73,74] Persistent anti-PF4 antibodies, some cases exceeding 18 months [80,81]
Recurrence Higher propensity for re-developing anti-PF4/heparin antibodies upon intra-operative heparin re-exposure. However, redevelopment of HIT is rare [74,76,77] A subset of patients shows persistent thrombocytopenia and platelet-activating antibodies, with some cases of recurrent thrombosis and thrombocytopenia [80,82]
Recommended treatment Non-heparin anticoagulant [42] IVIG [17]