IF 4.5 3区 医学 Q2 IMMUNOLOGY
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引用次数: 0

摘要

重要性在目前奥米克龙流行和加强免疫的时代,评估全人群接种 COVID-19 疫苗的风险效益比仍然具有现实意义。对接种/感染后的死亡风险和心血管事件的评估通常是在较温和的奥米克龙出现和加强型疫苗推出之前进行的。方法:2022 年 1 月 6 日至 12 月 31 日(奥米克龙传播为主)对年龄≥18 岁的新加坡成年人进行的回顾性队列研究。使用经人口统计学/并发症调整的 Cox 回归模型来估算接种/感染 SARS-CoV-2 后 0-180 天与接种后 180 天的全因死亡和心血管事件风险。接种疫苗后的风险期按之前 180 天内是否感染 SARS-CoV-2 进一步分层;同样,感染后的风险期按感染前 180 天内是否接种疫苗进一步分层。记录了 23,028 例死亡和 54,017 例心脏事件。接种疫苗后,所有年龄层的全因死亡率/心血管事件风险都没有升高。相反,与接种疫苗后 180 天的个人时间相比,老年人(≥60 岁)在感染后 180 天内的全因死亡率仍然较高。对于 180 天前接种疫苗的老年人,疫苗突破性 SARS-CoV-2 感染的死亡风险仅在感染后 60 天内升高,超过 60 天后则不再升高。所有年龄段的人群在感染任何 SARS-CoV-2 后 1-2 个月内发生心血管事件的风险都有所升高,感染后 180 天的老年人发生心血管事件的风险更高(调整后危险比,aHR = 1.18,95 %CI = 1.04-1.34)。结论在 Omicron 时代,接种任何剂量的 mRNA 疫苗后 180 天内,未观察到全因死亡率或心血管事件风险增加;接种疫苗降低了老年人急性期后的心血管风险。在 Omicron 期间,接种疫苗的风险效益比仍为正值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of death and cardiovascular events following COVID-19 vaccination or positive SARS-CoV-2 test amongst adult Singaporeans during omicron transmission

Importance

Assessing population-wide risk-benefit ratio of COVID-19 vaccination remains relevant in the current era of Omicron endemicity and boosting. Assessments of mortality risk and cardiovascular events post-vaccination/infection were generally made prior to emergence of milder Omicron and booster rollout.

Methods

Retrospective cohort study from 6th January to 31st December 2022 (Omicron-predominant transmission), amongst adult Singaporeans aged ≥18 years. Cox regression models adjusted for demographics/comorbidities were used to estimate risk of all-cause mortality and cardiovascular events 0–180 days post-mRNA vaccination/SARS-CoV-2 infection, compared to >180 days post-mRNA vaccination. Risk periods post-vaccination were further stratified by presence/absence of SARS-CoV-2 infection in the preceding 180 days; similarly, risk periods post-infection were further stratified by vaccination in the 180 days preceding infection.

Results

3,137,210 adults participated, with 2,047,008 vaccine doses administered (99 % being booster doses) and 1,189,846 infections. 23,028 deaths and 54,017 cardiac events were recorded. No elevated risk of all-cause mortality/cardiovascular events was observed across all age strata post-vaccination. Conversely, all-cause mortality post-infection remained elevated up to >180 days in older adults (≥60 years), compared to person-time > 180 days post-vaccination. For vaccine-breakthrough SARS-CoV-2 infection in older adults vaccinated <180 days prior, risk of mortality was only elevated up to 60 days post-infection, but not beyond. Elevated risk of cardiovascular events 1–2 months after any SARS-CoV-2 infection was observed across all age strata, with elevated risk observed in older adults >180 days post-infection (adjusted-hazards-ratio, aHR = 1.18, 95 %CI = 1.04–1.34). Preceding vaccination within 180 days prior to infection attenuated this risk, with no significantly elevated post-acute risk of cardiovascular events (>180 days: aHR = 1.10, 95 %CI = 0.95–1.07).

Conclusion

No increased risk of all-cause mortality or cardiovascular events was observed up to 180 days after any mRNA vaccination dose in the Omicron era; vaccination attenuated post-acute cardiovascular risk in older adults. The risk-benefit ratio of vaccination remained positive during Omicron.

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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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