Suppr超能文献

加拿大安大略省 BNT162b2 和 mRNA-1273 新冠病毒疫苗对有症状的 SARS-CoV-2 感染和严重新冠病毒感染结局的有效性:阴性检测设计研究。

Effectiveness of BNT162b2 and mRNA-1273 covid-19 vaccines against symptomatic SARS-CoV-2 infection and severe covid-19 outcomes in Ontario, Canada: test negative design study.

机构信息

ICES, Toronto, ON, Canada.

Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.

出版信息

BMJ. 2021 Aug 20;374:n1943. doi: 10.1136/bmj.n1943.

Abstract

OBJECTIVE

To estimate the effectiveness of mRNA covid-19 vaccines against symptomatic infection and severe outcomes (hospital admission or death).

DESIGN

Test negative design study.

SETTING

Ontario, Canada between 14 December 2020 and 19 April 2021.

PARTICIPANTS

324 033 community dwelling people aged ≥16 years who had symptoms of covid-19 and were tested for SARS-CoV-2.

INTERVENTIONS

BNT162b2 (Pfizer-BioNTech) or mRNA-1273 (Moderna) vaccine.

MAIN OUTCOME MEASURES

Laboratory confirmed SARS-CoV-2 by reverse transcription polymerase chain reaction (RT-PCR) and hospital admissions and deaths associated with SARS-CoV-2 infection. Multivariable logistic regression was adjusted for personal and clinical characteristics associated with SARS-CoV-2 and vaccine receipt to estimate vaccine effectiveness against symptomatic infection and severe outcomes.

RESULTS

Of 324 033 people with symptoms, 53 270 (16.4%) were positive for SARS-CoV-2 and 21 272 (6.6%) received at least one dose of vaccine. Among participants who tested positive, 2479 (4.7%) were admitted to hospital or died. Vaccine effectiveness against symptomatic infection observed ≥14 days after one dose was 60% (95% confidence interval 57% to 64%), increasing from 48% (41% to 54%) at 14-20 days after one dose to 71% (63% to 78%) at 35-41 days. Vaccine effectiveness observed ≥7 days after two doses was 91% (89% to 93%). Vaccine effectiveness against hospital admission or death observed ≥14 days after one dose was 70% (60% to 77%), increasing from 62% (44% to 75%) at 14-20 days to 91% (73% to 97%) at ≥35 days, whereas vaccine effectiveness observed ≥7 days after two doses was 98% (88% to 100%). For adults aged ≥70 years, vaccine effectiveness estimates were observed to be lower for intervals shortly after one dose but were comparable to those for younger people for all intervals after 28 days. After two doses, high vaccine effectiveness was observed against variants with the E484K mutation.

CONCLUSIONS

Two doses of mRNA covid-19 vaccines were observed to be highly effective against symptomatic infection and severe outcomes. Vaccine effectiveness of one dose was observed to be lower, particularly for older adults shortly after the first dose.

摘要

目的

评估 mRNA 新冠疫苗对有症状感染和严重结局(住院或死亡)的有效性。

设计

阴性测试设计研究。

地点

加拿大安大略省,2020 年 12 月 14 日至 2021 年 4 月 19 日。

参与者

324033 名居住在社区、年龄≥16 岁的有新冠症状且接受过 SARS-CoV-2 检测的人群。

干预措施

BNT162b2(辉瑞-生物科技)或 mRNA-1273(莫德纳)疫苗。

主要观察指标

通过逆转录聚合酶链反应(RT-PCR)检测到实验室确诊的 SARS-CoV-2 以及与 SARS-CoV-2 感染相关的住院和死亡。多变量逻辑回归调整了与 SARS-CoV-2 和疫苗接种相关的个人和临床特征,以估计疫苗对有症状感染和严重结局的有效性。

结果

在 324033 名有症状的人群中,53270 人(16.4%)SARS-CoV-2 检测呈阳性,21272 人(6.6%)至少接种了一剂疫苗。在检测呈阳性的参与者中,2479 人(4.7%)住院或死亡。一剂疫苗接种后≥14 天的疫苗有效性为 60%(95%置信区间 57%至 64%),从一剂后 14-20 天的 48%(41%至 54%)增加到 35-41 天的 71%(63%至 78%)。两剂疫苗接种后≥7 天的疫苗有效性为 91%(89%至 93%)。一剂疫苗接种后≥14 天的疫苗对住院或死亡的有效性为 70%(60%至 77%),从一剂后 14-20 天的 62%(44%至 75%)增加到≥35 天的 91%(73%至 97%),而两剂疫苗接种后≥7 天的疫苗有效性为 98%(88%至 100%)。对于≥70 岁的成年人,一剂疫苗接种后短期观察到的疫苗有效性估计值较低,但在 28 天后所有间隔时间内,与年轻人的疫苗有效性相当。两剂疫苗接种后,对 E484K 突变的变异体观察到高疫苗有效性。

结论

两剂 mRNA 新冠疫苗对有症状感染和严重结局非常有效。一剂疫苗的有效性较低,尤其是在老年人第一剂疫苗接种后不久。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19dd/8377789/42441652703e/chuh066601.f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验