2021
DOI: 10.1016/s0140-6736(21)00872-2
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Bilateral superior ophthalmic vein thrombosis, ischaemic stroke, and immune thrombocytopenia after ChAdOx1 nCoV-19 vaccination

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Cited by 117 publications
(130 citation statements)
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“…Finally, several international reports have been published highlighting the possibility of thrombohemorrhagic complications within the time interval of 5 to 16 days after the first dose of the adenoviral vector vaccine ChAdOx1-19 against COVID-19 [7][8][9]18]: these data confirmed that the analyzed cases may be definitively classified as AEFI caused by vaccination.…”
Section: Ihc Findings (Figure 3)mentioning
confidence: 52%
See 1 more Smart Citation
“…Finally, several international reports have been published highlighting the possibility of thrombohemorrhagic complications within the time interval of 5 to 16 days after the first dose of the adenoviral vector vaccine ChAdOx1-19 against COVID-19 [7][8][9]18]: these data confirmed that the analyzed cases may be definitively classified as AEFI caused by vaccination.…”
Section: Ihc Findings (Figure 3)mentioning
confidence: 52%
“…Moreover, in order to develop specific evidence-based items, an exhaustive review of the pertinent literature was performed. To date, several reports have been published reporting severe adverse effects (thrombosis and thrombocytopenia) after COVID-19 vaccination [7][8][9][16][17][18][19]. Each report was analyzed independently by each author of this article in order to identify specific items.…”
Section: Vaccine Characteristics and Exhaustive Review Of The Literaturementioning
confidence: 99%
“…Cases of thrombotic thrombocytopenia induced by coronavirus disease 2019 (COVID-19) vaccines have been reported recently [1][2][3]. Herein, we describe the first case of another critical disorder, hemophagocytic lymphohistiocytosis (HLH), in a healthy person after COVID-19 vaccination.…”
Section: To the Editormentioning
confidence: 94%
“…The presentation window after vaccination may span a broader time range that reported in the original case series, especially when underlying thrombotic events lead to milder, less acute clinical manifestations hence leading to delayed diagnosis. Furthermore, a non-specific, flu-like illness may precede or accompany the syndrome at the time of presentation [ 31 ]. A presumptive diagnosis of VITT is confirmed with the demonstration of circulating PF4/polyanion antibodies (usually with high optical density readings [ 1 , 2 ]) via enzyme-linked immunosorbent assay (ELISA), in the absence of prior heparin exposure.…”
Section: Diagnostic and Therapeutic Considerationsmentioning
confidence: 99%