Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, United States.
Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States.
Vaccine. 2024 Mar 7;42(7):1731-1737. doi: 10.1016/j.vaccine.2024.02.032. Epub 2024 Feb 22.
Although previous studies found no-increased mortality risk after COVID-19 vaccination, residual confounding bias might have impacted the findings. Using a modified self-controlled case series (SCCS) design, we assessed the risk of non-COVID-19 mortality, all-cause mortality, and four cardiac-related death outcomes after primary series COVID-19 vaccination.
We analyzed all deaths between December 14, 2020, and August 11, 2021, among individuals from eight Vaccine Safety Datalink sites. Demographic characteristics of deaths in recipients of COVID-19 vaccines and unvaccinated individuals were reported. We conducted SCCS analyses by vaccine type and death outcomes and reported relative incidences (RI). The observation period for death spanned from the dates of emergency use authorization to the end of the study period (August 11, 2021) without censoring the observation period upon death. We pre-specified a primary risk interval of 28-day and a secondary risk interval of 14-day after each vaccination dose. Adjusting for seasonality in mortality analyses is crucial because death rates vary over time. Deaths among unvaccinated individuals were included in SCCS analyses to account for seasonality by incorporating calendar month in the models.
For Pfizer-BioNTech (BNT162b2), RIs of non-COVID-19 mortality, all-cause mortality, and four cardiac-related death outcomes were below 1 and 95 % confidence intervals (CIs) excluded 1 across both doses and both risk intervals. For Moderna (mRNA-1273), RI point estimates of all outcomes were below 1, although the 95 % CIs of two RI estimates included 1: cardiac-related (RI = 0.78, 95 % CI, 0.58-1.04) and non-COVID-19 cardiac-related mortality (RI = 0.80, 95 % CI, 0.60-1.08) 14 days after the second dose in individuals without pre-existing cancer and heart disease. For Janssen (Ad26.COV2.S), RIs of four cardiac-related death outcomes ranged from 0.94 to 0.98 for the 14-day risk interval, and 0.68 to 0.72 for the 28-day risk interval and 95 % CIs included 1.
Using a modified SCCS design and adjusting for temporal trends, no-increased risk was found for non-COVID-19 mortality, all-cause mortality, and four cardiac-related death outcomes among recipients of the three COVID-19 vaccines used in the US.
尽管先前的研究并未发现 COVID-19 疫苗接种后死亡率风险增加,但残余混杂偏倚可能影响了研究结果。本研究采用改良的自我对照病例系列(SCCS)设计,评估了 COVID-19 疫苗初级系列接种后非 COVID-19 死亡率、全因死亡率和四项与心脏相关的死亡结局的风险。
我们分析了 2020 年 12 月 14 日至 2021 年 8 月 11 日期间来自 8 个疫苗安全数据链接站点的所有死亡病例。报告 COVID-19 疫苗接种者和未接种者死亡病例的人口统计学特征。我们按疫苗类型和死亡结局进行 SCCS 分析,并报告相对发病率(RI)。死亡的观察期从紧急使用授权日期开始至研究结束(2021 年 8 月 11 日),在死亡后不截断观察期。我们预先指定了初级风险间隔期为接种后 28 天,次级风险间隔期为 14 天。由于死亡率随时间而变化,因此在死亡率分析中调整季节性至关重要。将未接种者的死亡纳入 SCCS 分析中,通过在模型中纳入日历月来考虑季节性。
对于辉瑞-生物科技(BNT162b2),两种剂量和两种风险间隔期内,非 COVID-19 死亡率、全因死亡率和四项与心脏相关的死亡结局的 RI 均低于 1,95%置信区间(CI)排除了 1。对于 Moderna(mRNA-1273),所有结局的 RI 点估计值均低于 1,尽管两个 RI 估计值的 95%CI 包括 1:心脏相关(RI=0.78,95%CI,0.58-1.04)和非 COVID-19 心脏相关死亡率(RI=0.80,95%CI,0.60-1.08)在无既往癌症和心脏病的个体中,第二次接种后 14 天。对于杨森(Ad26.COV2.S),四项与心脏相关的死亡结局的 14 天风险间隔期的 RI 范围为 0.94 至 0.98,28 天风险间隔期的 RI 范围为 0.68 至 0.72,95%CI 包含 1。
本研究采用改良的 SCCS 设计,并调整了时间趋势,结果显示,在美国使用的三种 COVID-19 疫苗接种者中,未发现非 COVID-19 死亡率、全因死亡率和四项与心脏相关的死亡结局风险增加。