EPI-PHARE Scientific Interest Group in Epidemiology of Health Products (French National Agency for the Safety of Medicines and Health Products - ANSM, French National Health Insurance - CNAM), Saint-Denis, France, and Faculté de Pharmacie, Université Paris-Saclay, Châtenay-Malabry, France (J.B.).
EPI-PHARE Scientific Interest Group in Epidemiology of Health Products (French National Agency for the Safety of Medicines and Health Products - ANSM, French National Health Insurance - CNAM), Saint-Denis, France (M.J.J., M.B., B.B., J.D., S.L.V., A.W., R.D.).
Ann Intern Med. 2022 Sep;175(9):1250-1257. doi: 10.7326/M22-0988. Epub 2022 Aug 23.
The BNT162b2 (Pfizer-BioNTech) vaccine has been shown to be safe with regard to risk for severe cardiovascular events (such as myocardial infarction [MI], pulmonary embolism [PE], and stroke) in persons aged 75 years or older. Less is known about the safety of other COVID-19 vaccines or outcomes in younger populations.
To assess short-term risk for severe cardiovascular events (excluding myocarditis and pericarditis) after COVID-19 vaccination in France's 46.5 million adults younger than 75 years.
Self-controlled case series method adapted to event-dependent exposure and high event-related mortality.
France, 27 December 2020 to 20 July 2021.
All adults younger than 75 years hospitalized for PE, acute MI, hemorrhagic stroke, or ischemic stroke ( = 73 325 total events).
Linkage between the French National Health Data System and COVID-19 vaccine databases enabled identification of hospitalizations for cardiovascular events (MI, PE, or stroke) and receipt of a first or second dose of the Pfizer-BioNTech, mRNA-1273 (Moderna), Ad26.COV2.S (Janssen), or ChAdOx1 nCoV-19 (Oxford-AstraZeneca) vaccine. The relative incidence (RI) of each cardiovascular event was estimated in the 3 weeks after vaccination compared with other periods, with adjustment for temporality (7-day periods).
No association was found between the Pfizer-BioNTech or Moderna vaccine and severe cardiovascular events. The first dose of the Oxford-AstraZeneca vaccine was associated with acute MI and PE in the second week after vaccination (RI, 1.29 [95% CI, 1.11 to 1.51] and 1.41 [CI, 1.13 to 1.75], respectively). An association with MI in the second week after a single dose of the Janssen vaccine could not be ruled out (RI, 1.75 [CI, 1.16 to 2.62]).
It was not possible to ascertain the relative timing of injection and cardiovascular events on the day of vaccination. Outpatient deaths related to cardiovascular events were not included.
In persons aged 18 to 74 years, adenoviral-based vaccines may be associated with increased incidence of MI and PE. No association between mRNA-based vaccines and the cardiovascular events studied was observed.
None.
已有研究表明,BNT162b2(辉瑞-生物科技)疫苗在 75 岁及以上人群中接种后,严重心血管事件(如心肌梗死[MI]、肺栓塞[PE]和中风)的风险较低。然而,对于其他 COVID-19 疫苗或较年轻人群中的结局的安全性知之甚少。
评估法国 4650 万 75 岁以下成年人接种 COVID-19 疫苗后短期内发生严重心血管事件(不包括心肌炎和心包炎)的风险。
适应于事件相关暴露和高事件相关死亡率的自我对照病例系列方法。
法国,2020 年 12 月 27 日至 2021 年 7 月 20 日。
所有因 PE、急性 MI、出血性中风或缺血性中风而住院的年龄小于 75 岁的成年人(共 73325 例总事件)。
法国国家卫生数据系统与 COVID-19 疫苗数据库的链接可识别心血管事件(MI、PE 或中风)的住院情况和第一剂或第二剂辉瑞-生物科技、mRNA-1273(Moderna)、Ad26.COV2.S(Janssen)或 ChAdOx1 nCoV-19(牛津-阿斯利康)疫苗的接种情况。与其他时期相比,在接种后 3 周内,通过调整时间性(7 天周期),估计每种心血管事件的相对发病率(RI)。
辉瑞-生物科技或 Moderna 疫苗与严重心血管事件之间未发现关联。牛津-阿斯利康疫苗的第一剂与接种后第 2 周的急性 MI 和 PE 相关(RI,分别为 1.29 [95%CI,1.11 至 1.51] 和 1.41 [CI,1.13 至 1.75])。单剂量 Janssen 疫苗接种后第 2 周 MI 的关联不能排除(RI,1.75 [CI,1.16 至 2.62])。
无法确定疫苗接种当天注射和心血管事件的相对时间。未纳入与心血管事件相关的门诊死亡。
在 18 至 74 岁人群中,腺病毒疫苗可能与 MI 和 PE 发生率增加有关。未观察到 mRNA 疫苗与研究中的心血管事件之间存在关联。
无。