期刊
INFECTION
卷 50, 期 2, 页码 531-536出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s15010-021-01712-8
关键词
COVID-19; Vaccine; Ad26; COV2; S; Vaccine-induced thrombotic thrombocytopenia; VITT; Thrombosis with thrombocytopenia syndrome; TTS; Cerebral venous sinus thrombosis; Thrombosis
This case report describes the first reported case of vaccine-induced immune thrombocytopenia (VITT) following Ad26.COV2.S vaccination outside the US. The importance of maintaining a high index of suspicion and early diagnosis and treatment in patients with symptoms compatible with VITT after receiving an adenovirus-vector-based SARS-CoV-2 vaccine is highlighted to improve prognosis and outcomes.
Purpose We reported the first described post Ad26.COV2.S (Janssen, Johnson & Johnson) vaccine-induced immune thrombocytopenia (VITT) case outside US. Case description CA young woman without any medical history presented association of deep vein thrombosis and thrombocytopenia at day 10 after vaccine injection. The patient was treated with low-molecular weight heparin at a first medical institution. Twelve days post Ad26.COV2.S vaccination, the patient was admitted at our hospital for neurological deterioration and right hemiplegia. Medical imaging using MRI showed thrombosis of the major anterior part of the sagittal superior sinus with bilateral intraparenchymal hemorrhagic complications. Screening tests for antibodies against platelet factor 4 (PF4)-heparin by rapid lateral flow immunoassay and chemiluminescence techniques were negative. Platelet activation test using heparin-induced multiple electrode aggregometry confirmed the initial clinical hypothesis. Despite immediate treatment with intravenous immunoglobulin, dexamethasone, danaparoid and attempted neurosurgery the patient evolved toward brain death. Conclusion Even though it is an extremely rare complication of vaccination physicians should maintain a high index of suspicion of VITT in patients who received an adenovirus-vector-based SARS-CoV-2 vaccine within the last 30 days with persistent complains compatible with VITT or thromboembolic event associated with thrombocytopenia. The diagnosis should not be excluded if the rapid anti-PF4 immunological nor chemiluminescence techniques yield negative results. An adapted functional assay should be performed to confirm the diagnosis. Early treatment with intravenous immunoglobulin and non-heparin anticoagulants is essential as delayed diagnosis and administration of appropriate treatment is associated with poor prognosis.
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