The Application of Digital PCR as a Reference Measurement Procedure to Support the Accuracy of Quality Assurance for Infectious Disease Molecular Diagnostic Testing

Nucleic acid amplification tests (NAATs) assist in the diagnosis of numerous infectious diseases. They are typically sensitive and specific and can be quickly developed and adapted. Far more challenging is the development of standards to ensure NAATs are performing within specification; reference ma...

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Veröffentlicht in:Clinical chemistry (Baltimore, Md.) Md.), 2024-12
Hauptverfasser: Falak, Samreen, O'Sullivan, Denise M, Cleveland, Megan H, Cowen, Simon, Busby, Eloise J, Devonshire, Alison S, Valiente, Esmeralda, Jones, Gerwyn M, Kammel, Martin, Milavec, Mojca, Vierbaum, Laura, Schellenberg, Ingo, Zeichhardt, Heinz, Kummrow, Andreas, Vallone, Peter M, Macdonald, Rainer, Huggett, Jim F
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Sprache:eng
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Zusammenfassung:Nucleic acid amplification tests (NAATs) assist in the diagnosis of numerous infectious diseases. They are typically sensitive and specific and can be quickly developed and adapted. Far more challenging is the development of standards to ensure NAATs are performing within specification; reference materials take time to develop and suitable reference measurement procedures (RMPs) have not been available. This study investigated digital PCR (dPCR) RMP delivery of traceability for NAAT external quality assessment (EQA). Three National Metrology Institutes (NMIs) applied reverse transcription (RT)-dPCR as a candidate RMP to estimate the RNA quantity in 32 independent severe acute respiratory syndrome coronavirus 2 materials. The results were combined to value assign the respective materials: 21 materials were used in 6 rounds of EQA over 17 months for 61 laboratories for COVID-19 testing results compared with reference values. The agreement between the 3 NMIs showed
ISSN:0009-9147
1530-8561
1530-8561
DOI:10.1093/clinchem/hvae187