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Vaccine‐induced prothrombotic immune thrombocytopenia without thrombosis may not require immune modulatory therapy: A case report

BACKGROUND: Vaccine‐induced immune thrombotic thrombocytopenia (VITT) is a rare complication of the ChAdOx1 nCoV‐19 and Ad26.COV2.S COVID‐19 vaccines. It presents most commonly with severe thrombocytopenia and thrombotic complications with extremely high D‐dimer levels 5–30 days after vaccination. W...

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Detalles Bibliográficos
Autores principales: Lai, Chieh Min Benjamin, Lee, Agnes Y.Y., Parkin, Stephen B.I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115974/
https://www.ncbi.nlm.nih.gov/pubmed/35599706
http://dx.doi.org/10.1002/rth2.12716
Descripción
Sumario:BACKGROUND: Vaccine‐induced immune thrombotic thrombocytopenia (VITT) is a rare complication of the ChAdOx1 nCoV‐19 and Ad26.COV2.S COVID‐19 vaccines. It presents most commonly with severe thrombocytopenia and thrombotic complications with extremely high D‐dimer levels 5–30 days after vaccination. We report a patient who presented with mild thrombocytopenia and minimally elevated D‐dimer levels without thrombosis, but who tested positive for antiplatelet factor 4 (PF4) platelet‐activating antibodies on a PF4‐enhanced serotonin‐release assay. KEY CLINICAL QUESTION: Is immunomodulation necessary in patients who present without thrombosis? CLINICAL APPROACH AND CONCLUSIONS: Treatment with rivaroxaban alone was followed by platelet normalization despite persistence of anti‐PF4 antibodies. This case provides support that vaccination for COVID‐19 can induce a broad, heterogeneous prothrombotic disorder characterized by anti‐PF4 platelet‐activating antibodies that shares features with classical heparin‐induced thrombocytopenia (HIT) and autoimmune HIT syndromes and that immunomodulation may not be required in those without thrombosis.