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The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings
Measurement of HIV-1 viral load (VL) is essential for monitoring antiretroviral treatment (ART) efficacy. The preferred specimen type for VL is plasma, but in remote settings where collection and preservation of plasma many not be possible, dried blood spots (DBS) are often used instead. A new speci...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10306227/ https://www.ncbi.nlm.nih.gov/pubmed/37379313 http://dx.doi.org/10.1371/journal.pgph.0002099 |
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author | Kiyaga, Charles Makoha, Caroline Nkugwa, Ivan Okiira, Christopher Okwir, Richard Gebreab, Sirak Zenebe Suarez, Patricia Rodriguez-Ventosa LaBrot, Benjamin Durán, Ana Carrasco |
author_facet | Kiyaga, Charles Makoha, Caroline Nkugwa, Ivan Okiira, Christopher Okwir, Richard Gebreab, Sirak Zenebe Suarez, Patricia Rodriguez-Ventosa LaBrot, Benjamin Durán, Ana Carrasco |
author_sort | Kiyaga, Charles |
collection | PubMed |
description | Measurement of HIV-1 viral load (VL) is essential for monitoring antiretroviral treatment (ART) efficacy. The preferred specimen type for VL is plasma, but in remote settings where collection and preservation of plasma many not be possible, dried blood spots (DBS) are often used instead. A new specimen collection matrix, the cobas plasma separation card (PSC, Roche Diagnostics Solutions), enables specimen preparation from a finger prick or venous blood, using a multi-layer absorption and filtration design that results in a specimen similar to dried plasma. We sought to confirm the correlation between VL results obtained using PSC prepared from venous blood to those from plasma or DBS, as well as PSC prepared with capillary blood from a finger prick. PSC, DBS and plasma were prepared with blood from HIV-1 infected persons attending a primary care clinic in Kampala, Uganda. VL in PSC and plasma was measured using cobas HIV-1 (Roche Diagnostics), while VL in DBS was measured with RealTime HIV-1 (Abbott Diagnostics). The correlation between VL from plasma and PSC made from capillary or venous blood was high (regression coefficient of determination r(2) between 0.87 and 0.91), and there was good agreement based on mean bias (-0.14 to 0.24 log(10) copies/mL) and classification of VL above or below 1000 copies/mL (91.4% agreement). In contrast, VL from DBS was lower than plasma or PSC (mean bias 0.51 to 0.63 log(10) copies/mL) and not as well correlated (r(2) 0.78 to 0.81, 75.1–80.5% agreement). These results confirm the utility of PSC as an alternative specimen type for HIV-1 viral load measurement in areas where preparation and optimal storage or shipment of plasma is an obstacle to provision of treatment and care of HIV-1 infected people. |
format | Online Article Text |
id | pubmed-10306227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103062272023-06-29 The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings Kiyaga, Charles Makoha, Caroline Nkugwa, Ivan Okiira, Christopher Okwir, Richard Gebreab, Sirak Zenebe Suarez, Patricia Rodriguez-Ventosa LaBrot, Benjamin Durán, Ana Carrasco PLOS Glob Public Health Research Article Measurement of HIV-1 viral load (VL) is essential for monitoring antiretroviral treatment (ART) efficacy. The preferred specimen type for VL is plasma, but in remote settings where collection and preservation of plasma many not be possible, dried blood spots (DBS) are often used instead. A new specimen collection matrix, the cobas plasma separation card (PSC, Roche Diagnostics Solutions), enables specimen preparation from a finger prick or venous blood, using a multi-layer absorption and filtration design that results in a specimen similar to dried plasma. We sought to confirm the correlation between VL results obtained using PSC prepared from venous blood to those from plasma or DBS, as well as PSC prepared with capillary blood from a finger prick. PSC, DBS and plasma were prepared with blood from HIV-1 infected persons attending a primary care clinic in Kampala, Uganda. VL in PSC and plasma was measured using cobas HIV-1 (Roche Diagnostics), while VL in DBS was measured with RealTime HIV-1 (Abbott Diagnostics). The correlation between VL from plasma and PSC made from capillary or venous blood was high (regression coefficient of determination r(2) between 0.87 and 0.91), and there was good agreement based on mean bias (-0.14 to 0.24 log(10) copies/mL) and classification of VL above or below 1000 copies/mL (91.4% agreement). In contrast, VL from DBS was lower than plasma or PSC (mean bias 0.51 to 0.63 log(10) copies/mL) and not as well correlated (r(2) 0.78 to 0.81, 75.1–80.5% agreement). These results confirm the utility of PSC as an alternative specimen type for HIV-1 viral load measurement in areas where preparation and optimal storage or shipment of plasma is an obstacle to provision of treatment and care of HIV-1 infected people. Public Library of Science 2023-06-28 /pmc/articles/PMC10306227/ /pubmed/37379313 http://dx.doi.org/10.1371/journal.pgph.0002099 Text en © 2023 Kiyaga et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kiyaga, Charles Makoha, Caroline Nkugwa, Ivan Okiira, Christopher Okwir, Richard Gebreab, Sirak Zenebe Suarez, Patricia Rodriguez-Ventosa LaBrot, Benjamin Durán, Ana Carrasco The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title | The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title_full | The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title_fullStr | The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title_full_unstemmed | The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title_short | The plasma separation card as a novel solution for enhancing central laboratory capability for HIV-1 viral load monitoring in limited-access settings |
title_sort | plasma separation card as a novel solution for enhancing central laboratory capability for hiv-1 viral load monitoring in limited-access settings |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10306227/ https://www.ncbi.nlm.nih.gov/pubmed/37379313 http://dx.doi.org/10.1371/journal.pgph.0002099 |
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