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高样本通量下可靠且可扩展的新冠病毒定量聚合酶链反应检测:比利时倡议的经验教训

Reliable and Scalable SARS-CoV-2 qPCR Testing at a High Sample Throughput: Lessons Learned from the Belgian Initiative.

作者信息

Van Vooren Steven, Grayson James, Van Ranst Marc, Dequeker Elisabeth, Laenen Lies, Janssen Reile, Gillet Laurent, Bureau Fabrice, Coppieters Wouter, Devos Nathalie, Hengchen Benjamin, Wattiau Pierre, Méhauden Sibylle, Verlinden Yvan, Van Baelen Kurt, Pattery Theresa, Valentin Jean-Pierre, Janssen Kris, Geraerts Martine, Smeraglia John, Hellemans Jan, Wytynck Pieter, Mestdagh Pieter, Besbrugge Nienke, Höfer René, Nollet Friedel, Vandesompele Jo, De Smet Pieter, Lebon John, Vandewynckele Emmanuel, Verstrepen Steven, Uten Wouter, Capron Arnaud, Malonne Hugues, Poels Jeroen, André Emmanuel

机构信息

UgenTec, Inc., Cambridge, MA 02138, USA.

Department of Microbiology, Immunology and Transplantation, KU Leuven, B-3000 Leuven, Belgium.

出版信息

Life (Basel). 2022 Jan 21;12(2):159. doi: 10.3390/life12020159.

Abstract

We present our approach to rapidly establishing a standardized, multi-site, nation-wide COVID-19 screening program in Belgium. Under auspices of a federal government Task Force responsible for upscaling the country's testing capacity, we were able to set up a national testing initiative with readily available resources, putting in place a robust, validated, high-throughput, and decentralized qPCR molecular testing platform with embedded proficiency testing. We demonstrate how during an acute scarcity of equipment, kits, reagents, personnel, protective equipment, and sterile plastic supplies, we introduced an approach to rapidly build a reliable, validated, high-volume, high-confidence workflow based on heterogeneous instrumentation and diverse assays, assay components, and protocols. The workflow was set up with continuous quality control monitoring, tied together through a clinical-grade information management platform for automated data analysis, real-time result reporting across different participating sites, qc monitoring, and making result data available to the requesting physician and the patient. In this overview, we address challenges in optimizing high-throughput cross-laboratory workflows with minimal manual intervention through software, instrument and assay validation and standardization, and a process for harmonized result reporting and nation-level infection statistics monitoring across the disparate testing methodologies and workflows, necessitated by a rapid scale-up as a response to the pandemic.

摘要

我们介绍了在比利时迅速建立标准化、多地点、全国性新冠病毒筛查计划的方法。在负责扩大该国检测能力的联邦政府特别工作组的支持下,我们利用现有资源启动了一项全国检测计划,建立了一个强大、经过验证、高通量且分散的定量聚合酶链反应(qPCR)分子检测平台,并嵌入了能力验证测试。我们展示了在设备、试剂盒、试剂、人员、防护设备和无菌塑料用品严重短缺的情况下,我们如何引入一种方法,基于异构仪器以及多样的检测方法、检测组件和方案,迅速构建一个可靠、经过验证、高容量、高可信度的工作流程。该工作流程通过持续的质量控制监测来设置,并通过一个临床级信息管理平台整合在一起,用于自动化数据分析、跨不同参与地点的实时结果报告、质量控制监测,以及将结果数据提供给申请医生和患者。在本概述中,我们阐述了在应对疫情迅速扩大规模所必需的情况下,通过软件、仪器和检测验证及标准化,以及统一结果报告和国家层面感染统计监测流程,以最少人工干预优化高通量跨实验室工作流程所面临的挑战,这些工作流程涉及不同的检测方法和工作流程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/703a/8879918/8d313641b3e3/life-12-00159-g001.jpg

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