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The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa
The tiered laboratory framework for human immunodeficiency virus (HIV) viral load monitoring accommodates a range of HIV viral load testing platforms, with quality assessment critical to ensure quality patient testing. HIV plasma viral load testing is challenged by the instability of viral RNA. An a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911816/ https://www.ncbi.nlm.nih.gov/pubmed/33499162 http://dx.doi.org/10.3390/diagnostics11020160 |
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author | Noble, Lara Dominique Scott, Lesley Erica Bongwe, Asiashu Da Silva, Pedro Stevens, Wendy Susan |
author_facet | Noble, Lara Dominique Scott, Lesley Erica Bongwe, Asiashu Da Silva, Pedro Stevens, Wendy Susan |
author_sort | Noble, Lara Dominique |
collection | PubMed |
description | The tiered laboratory framework for human immunodeficiency virus (HIV) viral load monitoring accommodates a range of HIV viral load testing platforms, with quality assessment critical to ensure quality patient testing. HIV plasma viral load testing is challenged by the instability of viral RNA. An approach using an RNA stabilizing buffer is described for the Xpert(®) HIV-1 Viral Load (Cepheid) assay and was tested in remote laboratories in South Africa. Plasma panels with known HIV viral titres were prepared in PrimeStore molecular transport medium for per-module verification and per-instrument external quality assessment. The panels were transported at ambient temperatures to 13 testing laboratories during 2017 and 2018, tested according to standard procedures and uploaded to a web portal for analysis. A total of 275 quality assessment specimens (57 verification panels and two EQA cycles) were tested. All participating laboratories met study verification criteria (n = 171 specimens) with an overall concordance correlation coefficient (ρ(c)) of 0.997 (95% confidence interval (CI): 0.996 to 0.998) and a mean bias of −0.019 log copies per milliliter (cp/mL) (95% CI: −0.044 to 0.063). The overall EQA ρ(c) (n = 104 specimens) was 0.999 (95% CI: 0.998 to 0.999), with a mean bias of 0.03 log cp/mL (95% CI: 0.02 to 0.05). These panels are suitable for use in quality monitoring of Xpert(®) HIV-1 VL and are applicable to laboratories in remote settings. |
format | Online Article Text |
id | pubmed-7911816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79118162021-02-28 The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa Noble, Lara Dominique Scott, Lesley Erica Bongwe, Asiashu Da Silva, Pedro Stevens, Wendy Susan Diagnostics (Basel) Article The tiered laboratory framework for human immunodeficiency virus (HIV) viral load monitoring accommodates a range of HIV viral load testing platforms, with quality assessment critical to ensure quality patient testing. HIV plasma viral load testing is challenged by the instability of viral RNA. An approach using an RNA stabilizing buffer is described for the Xpert(®) HIV-1 Viral Load (Cepheid) assay and was tested in remote laboratories in South Africa. Plasma panels with known HIV viral titres were prepared in PrimeStore molecular transport medium for per-module verification and per-instrument external quality assessment. The panels were transported at ambient temperatures to 13 testing laboratories during 2017 and 2018, tested according to standard procedures and uploaded to a web portal for analysis. A total of 275 quality assessment specimens (57 verification panels and two EQA cycles) were tested. All participating laboratories met study verification criteria (n = 171 specimens) with an overall concordance correlation coefficient (ρ(c)) of 0.997 (95% confidence interval (CI): 0.996 to 0.998) and a mean bias of −0.019 log copies per milliliter (cp/mL) (95% CI: −0.044 to 0.063). The overall EQA ρ(c) (n = 104 specimens) was 0.999 (95% CI: 0.998 to 0.999), with a mean bias of 0.03 log cp/mL (95% CI: 0.02 to 0.05). These panels are suitable for use in quality monitoring of Xpert(®) HIV-1 VL and are applicable to laboratories in remote settings. MDPI 2021-01-22 /pmc/articles/PMC7911816/ /pubmed/33499162 http://dx.doi.org/10.3390/diagnostics11020160 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Noble, Lara Dominique Scott, Lesley Erica Bongwe, Asiashu Da Silva, Pedro Stevens, Wendy Susan The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title | The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title_full | The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title_fullStr | The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title_full_unstemmed | The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title_short | The Development of a Standardized Quality Assessment Material to Support Xpert(®) HIV-1 Viral Load Testing for ART Monitoring in South Africa |
title_sort | development of a standardized quality assessment material to support xpert(®) hiv-1 viral load testing for art monitoring in south africa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911816/ https://www.ncbi.nlm.nih.gov/pubmed/33499162 http://dx.doi.org/10.3390/diagnostics11020160 |
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