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Validation of Dried Tube Sample Format Quality Controls for the Monitoring of Viral Load and Blood Screening Assays.
Dimech, Wayne; Vincini, Giuseppe; Davies, Kylie; Karakaltsas, Marina; van Cauwalaert, Natasha Dubois; Guichet, Emilande; Koppelman, Marco; Cabuang, Liza.
Afiliación
  • Dimech W; National Serology Reference Laboratory, 4(th)Floor Healy Building, 41 Victoria Parade, FITZROY 3065, Victoria, Australia. Electronic address: wayne@nrlquality.org.au.
  • Vincini G; National Serology Reference Laboratory, 4(th)Floor Healy Building, 41 Victoria Parade, FITZROY 3065, Victoria, Australia.
  • Davies K; National Serology Reference Laboratory, 4(th)Floor Healy Building, 41 Victoria Parade, FITZROY 3065, Victoria, Australia.
  • Karakaltsas M; National Serology Reference Laboratory, 4(th)Floor Healy Building, 41 Victoria Parade, FITZROY 3065, Victoria, Australia.
  • van Cauwalaert ND; Solthis, 14-34 Avenue Jean-Jaurès, 75019, Paris, France.
  • Guichet E; Solthis, 14-34 Avenue Jean-Jaurès, 75019, Paris, France.
  • Koppelman M; Sanquin, Plesmanlaan 125, 1066 CX, Amsterdam, Netherlands.
  • Cabuang L; National Serology Reference Laboratory, 4(th)Floor Healy Building, 41 Victoria Parade, FITZROY 3065, Victoria, Australia.
J Virol Methods ; 285: 113957, 2020 11.
Article en En | MEDLINE | ID: mdl-32805272
HIV viral load (VL) and donor screening assays experience variation and require quaity assurance (QA). NRL sought to confirm a dried tube sample format (HIVDTS) sample type for use in quality control (QC) programs for HIV molecular testing. 50 µL of HIV supernatant at 1 × 105 copies per millilitre (copies/mL)) was dried for 48 hours at room temperature. Post-production and shipped integrity studies were undertaken. Dried HIVDTS was reconstituted in PBS buffer and tested in HIV VL (six participants) or blood screening assays (four participants). Results were entered into NRL's QC monitoring software (EDCNet™) for analysis. The mean of 224 VL results when HIVDTS QCs were tested in Biocentric HIV GENERIC Charge Virale assay was 4.54 log10 copies/mL, with the percentage coefficient of variation (CV%) ranging from 1.75 to 13.20%. The mean Ct value for HIVDTS QCs tested on Roche Cobas MPX assay results was 28.71 (range 28.33 to 29.14), with CV% ranging from 1.56 to 3.98%. The study confirms HIVDTS QCs can effectively monitor the performance of HIV molecular testing and offers a cheaper alternative to commercial QC samples that require cold-chain shipping on dry ice and UN3373 conditions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Control de Calidad / Infecciones por VIH / VIH-1 / Carga Viral / Pruebas con Sangre Seca Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: J Virol Methods Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Control de Calidad / Infecciones por VIH / VIH-1 / Carga Viral / Pruebas con Sangre Seca Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: J Virol Methods Año: 2020 Tipo del documento: Article