In the context of the SARS-CoV-2 pandemic, the laboratory based surveillance of COVID-19, together with the national hospital based surveillance [23] and mortality surveillance [21], was crucial to follow the evolution of the SARS-CoV-2 epidemic in Belgium. Monitoring the number of reported COVID-19 cases and performed tests in Belgium allowed to follow-up key indicators and trends, and allowed to provide this information to the different authorities for policy making.
The participation of CML’s in Belgium has been essential since the beginning of the epidemic. A rapid increasing number of CML’s throughout the country were able to perform COVID-19 diagnostic tests. As a result, the number of tests performed increased significantly from March to May 2020. Because the availability of large-scale testing is crucial for monitoring the progression of the epidemic, Belgium decided to also rely on a federal platform to increase testing capacities. This combined testing strategy is halfway between the German strategy relying on a clinical laboratory network and the centralized testing approach developed by the UK government [24, 25]. Thanks to both the increasing number of laboratories performing testing and the accompanied increasing laboratory test capacity, the testing strategy could be broadened at different stages during spring 2020. Overall, almost 10 million tests have been performed by the NRC, CML’s and federal platforms over 1 year (Belgium has 11.5 million inhabitants).
These efforts done by the laboratories to increase test capacity, as well as logistic improvements (with sampling facilities and between laboratories), also resulted in an improvement of the TAT between date of sampling and laboratory test result and the speed of reporting of these results to Sciensano to be used for surveillance and to initiate contact tracing. After the first wave, from the end of April to end of May 2020 there was an improvement of the TAT between sampling and result that was followed by an improvement of the speed of reporting to Sciensano in July-August 2020. As a result, from May to the end of August 2020 the TAT between sampling and reporting improved continuously to reach more than 75% of the test results that were reported at the latest the day after the day of sampling. The second wave, with a peak in October 2020, resulted in a high number of performed tests, impacting the sampling facilities and laboratories and resulting in an increase of the TAT between sampling and test result. In this context, it was decided to prioritize and temporary stop testing of asymptomatic high-risk contacts from week 44 to week 47. This resulted in a clear improvement again of the TAT. Following the control measures taken (most stringent measures on the 19th of October), the number of cases and the number of tests progressively declined starting from week 45 of 2020.
Since the end of November 2020, 90 to 95% of test results are reported at the latest the day after sampling. This high performance continued in January-February 2021 although there was an increase in the number of tests carried out, indicating the ability of the testing facilities and laboratories to quickly process and report a high number of tests.
Despite these achievements over the past year new challenges are arising for 2021. The data collection of laboratory test results has been modified in March 2021 to allow reporting of semi-quantitative interpretation of cycle threshold (Ct) values to gain knowledge on the dynamics of the epidemic [26]. Rapid diagnostic tools such as antigenic tests will be more broadly used for testing outside laboratories settings. It is essential that positive results of these tests are reported as systematically and as quickly as the laboratory reporting. These tests however also present limitations [27] and the involvement of the clinical laboratories will remain crucial for confirmation of test results and monitoring the laboratory test capacity and the positivity rate in 2021.
The real time integration of genomic data provided by CML’s and/or large sequencing platforms is another challenge that will be crucial to better track community spread and transmission chains. Genomic data will help to identify viral mutations, and combined with health data could inform about viral genome correlations with clinical outcomes [28]. Reporting of genomic data from testing facilities to Sciensano is possible since March 2021 to take up this challenge [29].
Finally, with the start of the vaccination campaign in Belgium in 2021, laboratories will be essential for the detection and monitoring of breakthrough cases post-vaccination. We can build on the experience and all the work done during the first year of the epidemic to meet these new challenges in 2021.