针对美国与 COVID-19 相关住院的初级系列和加强剂量疫苗有效性:基于阴性设计的实时研究。

Vaccine effectiveness of primary series and booster doses against covid-19 associated hospital admissions in the United States: living test negative design study.

机构信息

CDC COVID-19 Response Team, Atlanta, GA, USA.

Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

BMJ. 2022 Oct 11;379:e072065. doi: 10.1136/bmj-2022-072065.

Abstract

OBJECTIVE

To compare the effectiveness of a primary covid-19 vaccine series plus booster doses with a primary series alone for the prevention of hospital admission with omicron related covid-19 in the United States.

DESIGN

Multicenter observational case-control study with a test negative design.

SETTING

Hospitals in 18 US states.

PARTICIPANTS

4760 adults admitted to one of 21 hospitals with acute respiratory symptoms between 26 December 2021 and 30 June 2022, a period when the omicron variant was dominant. Participants included 2385 (50.1%) patients with laboratory confirmed covid-19 (cases) and 2375 (49.9%) patients who tested negative for SARS-CoV-2 (controls).

MAIN OUTCOME MEASURES

The main outcome was vaccine effectiveness against hospital admission with covid-19 for a primary series plus booster doses and a primary series alone by comparing the odds of being vaccinated with each of these regimens versus being unvaccinated among cases versus controls. Vaccine effectiveness analyses were stratified by immunosuppression status (immunocompetent, immunocompromised). The primary analysis evaluated all covid-19 vaccine types combined, and secondary analyses evaluated specific vaccine products.

RESULTS

Overall, median age of participants was 64 years (interquartile range 52-75 years), 994 (20.8%) were immunocompromised, 85 (1.8%) were vaccinated with a primary series plus two boosters, 1367 (28.7%) with a primary series plus one booster, and 1875 (39.3%) with a primary series alone, and 1433 (30.1%) were unvaccinated. Among immunocompetent participants, vaccine effectiveness for prevention of hospital admission with omicron related covid-19 for a primary series plus two boosters was 63% (95% confidence interval 37% to 78%), a primary series plus one booster was 65% (58% to 71%), and for a primary series alone was 37% (25% to 47%) (P<0.001 for the pooled boosted regimens compared with a primary series alone). Vaccine effectiveness was higher for a boosted regimen than for a primary series alone for both mRNA vaccines (BNT162b2 (Pfizer-BioNTech): 73% (44% to 87%) for primary series plus two boosters, 64% (55% to 72%) for primary series plus one booster, and 36% (21% to 48%) for primary series alone (P<0.001); mRNA-1273 (Moderna): 68% (17% to 88%) for primary series plus two boosters, 65% (55% to 73%) for primary series plus one booster, and 41% (25% to 54%) for primary series alone (P=0.001)). Among immunocompromised patients, vaccine effectiveness for a primary series plus one booster was 69% (31% to 86%) and for a primary series alone was 49% (30% to 63%) (P=0.04).

CONCLUSION

During the first six months of 2022 in the US, booster doses of a covid-19 vaccine provided additional benefit beyond a primary vaccine series alone for preventing hospital admissions with omicron related covid-19.

READERS' NOTE: This article is a living test negative design study that will be updated to reflect emerging evidence. Updates may occur for up to two years from the date of original publication.

摘要

目的

比较新冠病毒疫苗基础免疫系列加加强针与仅基础免疫系列对预防美国与奥密克戎相关的新冠病毒住院的效果。

设计

多中心观察性病例对照研究,采用阴性检测设计。

地点

美国 18 个州的医院。

参与者

2021 年 12 月 26 日至 2022 年 6 月 30 日期间因急性呼吸道症状入住 21 家医院的 4760 名成年人,期间奥密克戎变异株占主导地位。参与者包括 2385 名(50.1%)实验室确诊的新冠病毒(病例)和 2375 名(49.9%)新冠病毒检测阴性的患者(对照组)。

主要结果

主要结局是与仅基础免疫系列相比,基础免疫系列加加强针预防因新冠病毒住院的效果,比较病例与对照组中接种这些方案的疫苗接种者与未接种疫苗者的住院比值比。疫苗有效性分析按免疫抑制状态(免疫功能正常、免疫功能低下)分层。主要分析评估了所有新冠病毒疫苗类型的组合,次要分析评估了特定疫苗产品。

结果

总体而言,参与者的中位年龄为 64 岁(四分位距 52-75 岁),994 人(20.8%)免疫功能低下,85 人(1.8%)接种了一剂基础免疫系列加两剂加强针,1367 人(28.7%)接种了一剂基础免疫系列加一剂加强针,1875 人(39.3%)接种了一剂基础免疫系列,1433 人(30.1%)未接种疫苗。在免疫功能正常的参与者中,一剂基础免疫系列加两剂加强针预防奥密克戎相关新冠病毒住院的疫苗有效性为 63%(95%置信区间 37%至 78%),一剂基础免疫系列加一剂加强针为 65%(58%至 71%),一剂基础免疫系列为 37%(25%至 47%)(与仅基础免疫系列相比,所有加强针方案均有显著差异(P<0.001))。与仅基础免疫系列相比,加强针方案的疫苗有效性更高,包括两种 mRNA 疫苗(BNT162b2(辉瑞-生物科技):一剂基础免疫系列加两剂加强针为 73%(44%至 87%),一剂基础免疫系列加一剂加强针为 64%(55%至 72%),一剂基础免疫系列为 36%(21%至 48%)(P<0.001);mRNA-1273(Moderna):一剂基础免疫系列加两剂加强针为 68%(17%至 88%),一剂基础免疫系列加一剂加强针为 65%(55%至 73%),一剂基础免疫系列为 41%(25%至 54%)(P=0.001))。在免疫功能低下的患者中,一剂基础免疫系列加一剂加强针的疫苗有效性为 69%(31%至 86%),一剂基础免疫系列为 49%(30%至 63%)(P=0.04)。

结论

2022 年上半年,美国奥密克戎相关新冠病毒疫苗加强针在预防因新冠病毒住院方面比仅基础免疫系列更有优势。

读者注意事项

本文是一篇正在进行的阴性检测设计研究,将根据新出现的证据进行更新。原始发表日期起两年内可能会有更新。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f41/9551237/1aa15d1baade/adak072065.f1.jpg

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