Jacobson Barry Frank, Schapkaitz Elise, Takalani Azwi, Rowji Pradeep Frank, Louw Vernon, Opie Jessica, Bekker Linda Gail, Garrett Nigel, Goga Ameena, Reddy Tarylee, Zuma Nonhlanhla Yende, Sanne Ian, Seocharan Ishen, Peter Jonny, Robinson Michelle, Collie Shirley, Khan Amber, Takuva Simbarashe, Gray Glenda
Molecular Medicine and Haematology, University of the Witwatersrand Johannesburg Faculty of Health Sciences, Johannesburg, South Africa.
Hutchinson Centre Research Institute of South Africa (HCRISA), Chris Hani Baragwanath Hospital, Johannesburg, South Africa.
BMJ Med. 2023 Mar 23;2(1):e000302. doi: 10.1136/bmjmed-2022-000302. eCollection 2023.
To assess the rates of vascular thrombotic adverse events in the first 35 days after one dose of the Ad26.COV2.S vaccine (Janssen/Johnson & Johnson) in healthcare workers in South Africa and to compare these rates with those observed in the general population.
Open label, single arm, phase 3B study.
Sisonke study, South Africa, 17 February to 15 June 2021.
The Sisonke cohort of 477 234 healthcare workers, aged ≥18 years, who received one dose of the Ad26.COV2.S vaccine.
Observed rates of venous arterial thromboembolism and vaccine induced immune thrombocytopenia and thrombosis in individuals who were vaccinated, compared with expected rates, based on age and sex specific background rates from the Clinical Practice Research Datalink GOLD database (database of longitudinal routinely collected electronic health records from UK primary care practices using Vision general practice patient management software).
Most of the study participants were women (74.9%) and median age was 42 years (interquartile range 33-51). Twenty nine (30.6 per 100 000 person years, 95% confidence interval 20.5 to 44.0) vascular thrombotic events occurred at a median of 14 days (7-29) after vaccination. Of these 29 participants, 93.1% were women, median age 46 (37-55) years, and 51.7% had comorbidities. The observed to expected ratios for cerebral venous sinus thrombosis with thrombocytopenia and pulmonary embolism with thrombocytopenia were 10.6 (95% confidence interval 0.3 to 58.8) and 1.2 (0.1 to 6.5), respectively. Because of the small number of adverse events and wide confidence intervals, no conclusions were drawn between these estimates and the expected incidence rates in the population.
Vaccine induced immune thrombocytopenia and thrombosis after one dose of the Ad26.COV2.S vaccine was found in only a few patients in this South African population of healthcare workers. These findings are reassuring if considered in terms of the beneficial effects of vaccination against covid-19 disease. These data support the continued use of this vaccine, but surveillance is recommended to identify other incidences of venous and arterial thromboembolism and to improve confidence in the data estimates.
ClinicalTrials.gov NCT04838795.
评估南非医护人员接种一剂Ad26.COV2.S疫苗(杨森/强生公司)后35天内血管血栓形成不良事件的发生率,并将这些发生率与普通人群中观察到的发生率进行比较。
开放标签、单臂、3B期研究。
2021年2月17日至6月15日在南非进行的Sisonke研究。
Sisonke队列中的477234名年龄≥18岁的医护人员,他们接种了一剂Ad26.COV2.S疫苗。
根据临床实践研究数据链GOLD数据库(使用Vision全科患者管理软件从英国初级医疗实践中纵向常规收集的电子健康记录数据库)中按年龄和性别划分的背景发生率,比较接种疫苗个体中静脉动脉血栓栓塞、疫苗诱导的免疫性血小板减少症和血栓形成的观察发生率与预期发生率。
大多数研究参与者为女性(74.9%),中位年龄为42岁(四分位间距33 - 51岁)。接种疫苗后中位14天(7 - 29天)发生了29例(每10万人年30.6例,95%置信区间20.5至44.0)血管血栓形成事件。在这29名参与者中,93.1%为女性,中位年龄46岁(37 - 55岁),51.7%患有合并症。伴有血小板减少症的脑静脉窦血栓形成和伴有血小板减少症的肺栓塞的观察与预期比率分别为10.6(95%置信区间0.3至58.8)和1.2(0.1至6.5)。由于不良事件数量较少且置信区间较宽,这些估计值与人群中预期发病率之间未得出结论。
在南非这群医护人员中,仅少数患者出现了接种一剂Ad26.COV2.S疫苗后疫苗诱导的免疫性血小板减少症和血栓形成。如果从接种疫苗预防新冠疾病的有益效果方面考虑,这些发现令人安心。这些数据支持继续使用该疫苗,但建议进行监测以识别静脉和动脉血栓栓塞的其他发生率,并提高对数据估计的可信度。
ClinicalTrials.gov NCT04838795