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辉瑞-生物科技和莫德纳 COVID-19 疫苗在医护人员中的疫苗有效性的临时估计 - 2021 年 1 月至 3 月,美国 33 个地点。

Interim Estimates of Vaccine Effectiveness of Pfizer-BioNTech and Moderna COVID-19 Vaccines Among Health Care Personnel - 33 U.S. Sites, January-March 2021.

出版信息

MMWR Morb Mortal Wkly Rep. 2021 May 21;70(20):753-758. doi: 10.15585/mmwr.mm7020e2.

DOI:10.15585/mmwr.mm7020e2
PMID:34014909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8136422/
Abstract

Throughout the COVID-19 pandemic, health care personnel (HCP) have been at high risk for exposure to SARS-CoV-2, the virus that causes COVID-19, through patient interactions and community exposure (1). The Advisory Committee on Immunization Practices recommended prioritization of HCP for COVID-19 vaccination to maintain provision of critical services and reduce spread of infection in health care settings (2). Early distribution of two mRNA COVID-19 vaccines (Pfizer-BioNTech and Moderna) to HCP allowed assessment of the effectiveness of these vaccines in a real-world setting. A test-negative case-control study is underway to evaluate mRNA COVID-19 vaccine effectiveness (VE) against symptomatic illness among HCP at 33 U.S. sites across 25 U.S. states. Interim analyses indicated that the VE of a single dose (measured 14 days after the first dose through 6 days after the second dose) was 82% (95% confidence interval [CI] = 74%-87%), adjusted for age, race/ethnicity, and underlying medical conditions. The adjusted VE of 2 doses (measured ≥7 days after the second dose) was 94% (95% CI = 87%-97%). VE of partial (1-dose) and complete (2-dose) vaccination in this population is comparable to that reported from clinical trials and recent observational studies, supporting the effectiveness of mRNA COVID-19 vaccines against symptomatic disease in adults, with strong 2-dose protection.

摘要

在整个 COVID-19 大流行期间,医护人员(HCP)因与患者接触和社区暴露(1)而面临感染 SARS-CoV-2(导致 COVID-19 的病毒)的高风险。免疫实践咨询委员会建议将医护人员列为 COVID-19 疫苗接种的优先人群,以维持关键服务的提供,并减少医疗机构内感染的传播(2)。两种 mRNA COVID-19 疫苗(辉瑞-BioNTech 和 Moderna)早期分发给医护人员,使我们能够在真实环境中评估这些疫苗的有效性。正在进行一项病例对照研究,以评估 33 个美国站点的 25 个美国州的医护人员中 mRNA COVID-19 疫苗对有症状疾病的有效性(VE)。中期分析表明,一剂(首剂后 14 天至第二剂后 6 天测量)的 VE 为 82%(95%置信区间[CI] = 74%-87%),经年龄、种族/族裔和潜在医疗条件调整。两剂的调整 VE 为 94%(95% CI = 87%-97%)(第二剂后≥7 天测量)。在该人群中,部分(一剂)和完全(两剂)疫苗接种的 VE 与临床试验和最近的观察性研究报告的结果相似,支持 mRNA COVID-19 疫苗对成年人有症状疾病的有效性,具有强大的两剂保护作用。

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