Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT) by A Third Dose of Chadox1 Ncov-19 (Astrazeneca) After BNT162b2 (Pfizer–BioNTech)

Costa Rc
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引用次数: 1

Abstract

An atypical case of VITT was described resulting from a vaccination schedule where the third booster with ChAdOx1 nCoV-19 (AstraZeneca) was administered. The patient received a complete vaccination schedule with two doses of Pfizer–BioNTech (BNT162b2) without any complications before the third dose. However, the patient has developed an infrequent yet extreme prothrombotic; hypercoagulable state caused by platelet-activating anti-platelet factor 4 (PF4) antibodies. This phenomenon is typically triggered by the proximate administration of an adenoviral vector vaccine against COVID-19. The patient’s symptoms began ten days after taking the third dose of the ChAdOx1 nCoV-19 vaccine (AstraZeneca). His main complaints when hospitalized were severe headaches and right abdominal pain. The blood tests and MRI scan imaging findings were very characteristic of VITT, and a rare cerebral venous sinus thrombosis was found. Also, a markedly elevated D-dimer and strong positive PF4-dependent enzyme- immunoassay test results were documented. Due to discerning clinical suspicion, this patient was rapidly treated with immunoglobulin infusion for two days and oral steroids for three days. Subsequently, he was anticoagulated with the new oral anticoagulant edoxaban after platelet numbers recovery. In a few days, platelets normalized, and D-dimer levels decreased, while anti- PF4-dependent enzyme-immunoassay test results showed a slow decline. He was discharged taking oral edoxaban without any squeal.
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第三剂Chadox1 Ncov-19(阿斯利康)继BNT162b2(辉瑞- biontech)后疫苗诱导的免疫性血小板减少症(VITT)
报告了一例非典型VITT病例,这是由于接种了含有ChAdOx1 nCoV-19(阿斯利康)的第三种增强剂的疫苗接种计划造成的。患者在第三剂前接受了两剂辉瑞- biontech (BNT162b2)的完整疫苗接种计划,无任何并发症。然而,患者发生了罕见但极端的血栓前病变;血小板活化抗血小板因子4 (PF4)抗体引起的高凝状态。这种现象通常是由就近接种针对COVID-19的腺病毒载体疫苗引发的。患者在服用第三剂ChAdOx1 nCoV-19疫苗(阿斯利康)10天后开始出现症状。他住院时的主诉是严重头痛和右腹痛。血液检查和MRI扫描成像结果非常具有VITT的特征,并发现罕见的脑静脉窦血栓形成。此外,d -二聚体明显升高,pf4依赖性酶免疫测定结果呈强阳性。由于临床怀疑,该患者迅速接受免疫球蛋白输注2天,口服类固醇3天治疗。随后,在血小板计数恢复后,使用新的口服抗凝剂依多沙班进行抗凝治疗。几天后,血小板恢复正常,d -二聚体水平下降,而抗pf4依赖性酶免疫测定结果显示缓慢下降。他口服依多沙班出院,没有任何尖叫声。
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