4.6 Article

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

期刊

LIFE-BASEL
卷 12, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/life12020159

关键词

SARS-CoV-2; qPCR; lab automation; qc monitoring; high-throughput testing; data analysis

资金

  1. GSK
  2. Federal Government
  3. Deloitte Centre for Crisis Management
  4. CliniSys/MIPS Cyberlab & GLIMS development teams
  5. UgenTec development, support, data and customer success teams

向作者/读者索取更多资源

This article presents the rapid establishment of a standardized, multi-site, nation-wide COVID-19 screening program in Belgium and the implementation of a reliable, validated, high-volume workflow to overcome challenges caused by shortages of equipment and reagents.
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.

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