Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
ICES, Toronto, Ontario, Canada.
Clin Infect Dis. 2023 Feb 18;76(4):640-648. doi: 10.1093/cid/ciac634.
A major goal of coronavirus disease 2019 (COVID-19) vaccination is to prevent severe outcomes (hospitalizations and deaths). We estimated the effectiveness of messenger RNA (mRNA) and ChAdOx1 COVID-19 vaccines against severe outcomes in 4 Canadian provinces between December 2020 and September 2021.
We conducted this multiprovincial, retrospective, test-negative study among community-dwelling adults aged ≥18 years in Ontario, Quebec, British Columbia, and Manitoba using linked provincial databases and a common study protocol. Multivariable logistic regression was used to estimate province-specific vaccine effectiveness against COVID-19 hospitalization and/or death. Estimates were pooled using random-effects models.
We included 2 508 296 tested participants, with 31 776 COVID-19 hospitalizations and 5842 deaths. Vaccine effectiveness was 83% after a first dose and 98% after a second dose against both hospitalization and death (separately). Against severe outcomes, effectiveness was 87% (95% confidence interval [CI], 71%-94%) ≥84 days after a first dose of mRNA vaccine, increasing to 98% (95% CI, 96%-99%) ≥112 days after a second dose. Vaccine effectiveness against severe outcomes for ChAdOx1 was 88% (95% CI, 75%-94%) ≥56 days after a first dose, increasing to 97% (95% CI, 91%-99%) ≥56 days after a second dose. Lower 1-dose effectiveness was observed for adults aged ≥80 years and those with comorbidities, but effectiveness became comparable after a second dose. Two doses of vaccines provided very high protection for both homologous and heterologous schedules and against Alpha, Gamma, and Delta variants.
Two doses of mRNA or ChAdOx1 vaccine provide excellent protection against severe outcomes.
2019 年冠状病毒病(COVID-19)疫苗接种的主要目标是预防严重后果(住院和死亡)。我们估计了信使 RNA(mRNA)和 ChAdOx1 COVID-19 疫苗在 2020 年 12 月至 2021 年 9 月期间在加拿大 4 个省预防严重后果的有效性。
我们通过省级数据库的链接和共同的研究方案,在安大略省、魁北克省、不列颠哥伦比亚省和马尼托巴省进行了这项多省、回顾性、测试阴性研究,研究对象为年龄≥18 岁的社区居民。我们使用多变量逻辑回归来估计各省 COVID-19 住院和/或死亡的疫苗效力。使用随机效应模型对估计值进行汇总。
我们纳入了 2508296 名接受检测的参与者,其中 31776 例 COVID-19 住院,5842 例死亡。第一剂后,针对住院和死亡(分别),疫苗效力为 83%,第二剂后为 98%。针对严重后果,mRNA 疫苗第一剂后≥84 天的效力为 87%(95%置信区间 [CI],71%-94%),第二剂后≥112 天的效力为 98%(95% CI,96%-99%)。ChAdOx1 针对严重后果的疫苗效力在第一剂后≥56 天为 88%(95% CI,75%-94%),第二剂后≥56 天为 97%(95% CI,91%-99%)。≥80 岁的成年人和有合并症的成年人的一剂疫苗有效性较低,但第二剂后效果相当。两剂疫苗对同源和异源接种方案以及 Alpha、Gamma 和 Delta 变异株均提供了极高的保护。
两剂 mRNA 或 ChAdOx1 疫苗对严重后果提供了极好的保护。