Cleveland Clinic Akron General, Department of Emergency Medicine, Akron, OH, USA; Northeast Ohio Medical University, Rootstown, OH, USA.
Cleveland Clinic Akron General, Department of Emergency Medicine, Akron, OH, USA; Northeast Ohio Medical University, Rootstown, OH, USA.
Am J Emerg Med. 2021 Nov;49:441.e3-441.e4. doi: 10.1016/j.ajem.2021.05.001. Epub 2021 May 4.
The U.S. Food and Drug Administration (FDA) recently issued an Emergency Use Authorization (EUA) for two highly effective Sars-CoV-2 (COVID-19) vaccines from Pfizer-BioNTech and Moderna. More recently, EUA was granted for the Johnson and Johnson COVID-19 vaccine which uses traditional virus-based technology. In this vaccine, researchers added the gene for the coronavirus spike protein to modified Adenovirus 26 and named it Ad26.COV2-S. Nearly 7 million doses of the Ad26.COV2-S have been administered as of mid-April 2021. Recently the Federal Drug Administration and Center for Disease Control and Prevention reviewed data involving six reported cases in the United States of cerebral venous sinus thrombosis in combination with thrombocytopenia in people who received the vaccination. All cases were in women between 18 and 48, with symptoms developing six to 13 days after vaccination. A recent study in the United Kingdom reported similar events in 23 patients age 21 to 77, 61% of which were female, with cases of presumed vaccine induced thrombosis and thrombocytopenia occurring six to 24 days after vaccination. We report a 62-year-old female who presented to the emergency department (ED) with acute onset of altered mental status. She had received the Ad26.COV2-S vaccine 37 days prior to ED presentation. She developed thrombotic thrombocytopenic purpura (TTP) and no other cause was found. To our knowledge this is the first case in the United States of thrombotic thrombocytopenic purpura after receiving the Ad26.COV2-S COVID-19 vaccine.
美国食品和药物管理局(FDA)最近发布了辉瑞-生物技术公司和 Moderna 两种高度有效的 SARS-CoV-2(COVID-19)疫苗的紧急使用授权(EUA)。最近,强生 COVID-19 疫苗也获得了 EUA,该疫苗采用传统的基于病毒的技术。在这种疫苗中,研究人员将冠状病毒刺突蛋白的基因添加到改良的腺病毒 26 中,并将其命名为 Ad26.COV2-S。截至 2021 年 4 月中旬,已经接种了近 700 万剂 Ad26.COV2-S。最近,美国食品和药物管理局和疾病控制与预防中心审查了涉及在美国接种疫苗的 6 例报告病例的脑静脉窦血栓形成合并血小板减少的数据。所有病例均发生在 18 至 48 岁的女性中,症状在接种疫苗后 6 至 13 天出现。最近在英国的一项研究报告了 23 例年龄在 21 至 77 岁的患者出现类似事件,其中 61%为女性,接种疫苗后 6 至 24 天发生疑似疫苗诱导的血栓形成和血小板减少。我们报告了一例 62 岁女性,她因精神状态突然改变而到急诊科就诊。她在急诊科就诊前 37 天接种了 Ad26.COV2-S 疫苗。她发生了血栓性血小板减少性紫癜(TTP),没有发现其他原因。据我们所知,这是首例在美国接种 Ad26.COV2-S COVID-19 疫苗后发生血栓性血小板减少性紫癜的病例。