Santos Steven, Humbard Matthew, Lambrou Anastasia S, Lin Gary, Padilla Yamil, Chaitram Jasmine, Natrajan Muktha S, Kirking Hannah L, Courtney Sean, Del Guercio Kim, Roberts Seth, Gaspar Fraser, Iademarco Michael F, Hamel Joseph, Salerno Reynolds M
The Administration for Strategic Preparedness and Response, Washington, DC, USA.
The Administration for Strategic Preparedness and Response, Washington, DC, USA.
Lancet Public Health. 2025 Jan;10(1):e47-e57. doi: 10.1016/S2468-2667(24)00279-2.
Rapid, accessible, and accurate testing was paramount to an effective US COVID-19 response. Federal partners supported SARS-CoV-2 testing scale-up through an interagency-coordinated approach that focused on expanding supply chains, research and development, validation, and improving patient access. We aimed to provide an overview of the federal efforts to scale up the testing response and study the impact of scale-up.
In this descriptive analysis, we mapped federal partner activities and milestones using the US Government Testing and Diagnostics Working Group (TDWG) and participating agency and department data from Jan 1, 2020, to Dec 31, 2022. Tests produced (TDWG), reported test positivity (US Centers for Disease Control and Prevention [CDC]'s COVID-19 Electronic Laboratory Reporting system and the Federal Direct Report testing data), reported COVID-19 case counts (CDC), hospitalisations (Department of Health and Human Services Unified Hospital Data Surveillance System and the CDC's National Healthcare Safety Network), and deaths (CDC) were analysed over time. We then developed an agent-based model to evaluate the impact testing had on COVID-19 outcomes using different scenarios. The scenarios were (1) if efforts led to substantially fewer tests produced, (2) if scale-up was delayed, affecting test access, and (3) if efforts led to substantially more tests produced.
Approximately 6·7 billion SARS-CoV-2 tests, including over 1·5 billion laboratory-based, 1·9 billion point-of-care (POC), and 3·2 billion over-the-counter (OTC) tests, were produced, and approximately 2·7 billion tests were performed between Jan 1, 2020, and Dec 31, 2022. Testing capacity exhibited various expansion phases, with laboratory-based capacity growing from approximately 6 million tests per month in March, 2020 to approximately 34 million tests per month in July, 2020; POC increased to approximately 126 million tests per month by December, 2020, and OTC increased to approximately 986 million tests per month by February, 2022. Comparison between the baseline (actual) and delay-in-testing scenario suggests the increased testing capacity potentially saved upwards of 1·4 million lives and averted 7 million hospitalisations.
Our study suggests that early development, manufacturing, and distribution of tests had a great impact on reducing severe COVID-19 outcomes. These results highlight the importance of robust and rapid test development, production, and distribution when addressing future public health threats.
US Administration for Strategic Preparedness and Response and US Centers for Disease Control and Prevention.
快速、便捷且准确的检测对于美国有效应对新冠疫情至关重要。联邦合作伙伴通过跨部门协调的方法支持扩大新冠病毒检测规模,该方法聚焦于扩大供应链、研发、验证以及改善患者获取检测的途径。我们旨在概述联邦政府为扩大检测应对措施所做的努力,并研究扩大规模的影响。
在这项描述性分析中,我们利用美国政府检测与诊断工作组(TDWG)以及参与的机构和部门在2020年1月1日至2022年12月31日期间的数据,梳理联邦合作伙伴的活动和里程碑。分析了随时间推移的检测产出(TDWG)、报告的检测阳性率(美国疾病控制与预防中心[CDC]的新冠病毒电子实验室报告系统和联邦直接报告检测数据)、报告的新冠病例数(CDC)、住院人数(卫生与公众服务部统一医院数据监测系统和CDC的国家医疗安全网络)以及死亡人数(CDC)。然后,我们开发了一个基于主体的模型,以评估在不同情景下检测对新冠疫情结果的影响。这些情景包括:(1)如果努力导致检测产出大幅减少;(2)如果扩大规模延迟,影响检测获取;(3)如果努力导致检测产出大幅增加。
在2020年1月1日至2022年12月31日期间,共生产了约67亿次新冠病毒检测,包括超过15亿次基于实验室的检测、19亿次即时检测(POC)和32亿次非处方(OTC)检测,并且进行了约27亿次检测。检测能力呈现出不同的扩张阶段,基于实验室的能力从2020年3月的每月约600万次检测增长到2020年7月的每月约3400万次检测;即时检测到2020年12月增加到每月约1.26亿次检测,非处方检测到2022年2月增加到每月约9.86亿次检测。基线(实际)情景与检测延迟情景之间的比较表明,检测能力的提高可能挽救了超过140万人的生命,并避免了700万人住院。
我们的研究表明,检测的早期开发、生产和分发对减少新冠重症结果有很大影响。这些结果凸显了在应对未来公共卫生威胁时强大而快速的检测开发、生产和分发的重要性。
美国战略准备与应对管理局和美国疾病控制与预防中心。