Abstract

Rapid and accurate laboratory diagnosis of SARS-CoV-2 infection is crucial for the management of COVID-19 patients and control of the spread of the virus. At the start of the COVID-19 pandemic, Bangladesh had only one government molecular laboratory where real-time RT-PCR would be performed to diagnose SARS-CoV-2 infection. With the increasing number of suspected cases requiring confirmation diagnostic testing, there is a requirement to expand capacity for large-scale testing quickly. The government of Bangladesh established over 100 molecular laboratories within one year to test COVID-19. To expand the testing capacity, the government was compelled to recruit laboratory staff with limited experience and technical expertise, especially in molecular assays, to process specimens, interpret results, troubleshoot. As a result, the risk of diagnostic errors, such as cross-contamination, increased, potentially undermining the efficacy of public health policies, public health response, surveillance programs, and restrictive measures aimed toward containing the outbreak. In this piece, we discuss the different sources of cross-contamination in the COVID-19 RT-PCR laboratories and proffer practical preventive measures to avoid them.

Highlights

  • The coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 has triggered a global public health emergency

  • Rapid and accurate laboratory diagnosis of SARS-CoV-2 infection is crucial for the management of COVID-19 patients and control of the spread of the virus

  • We discuss the different sources of crosscontamination in the COVID-19 Reverse transcriptase-polymerase chain reaction (RT-PCR) laboratories and proffer practical

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Summary

Introduction

The coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 has triggered a global public health emergency. This included the set-up of the necessary instruments and test kits and personnel recruitment. This article will focus on the risk of cross-contamination in the testing laboratories in Bangladesh, a country like other low-income countries, which had to quickly ramp up capacity with limited resources [4]. With these notes from the field, we discuss the various sources of contamination in COVID-19 RT-PCR laboratories and provide efficient, effective, and feasible solutions to address these issues

Methodology
Preanalytical Considerations
Analytical Concerns
Post Analytical Considerations
Conclusion

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