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Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya

BACKGROUND: In Kenya, access to early infant diagnosis and viral load monitoring services for HIV patients on ART is significantly hampered by sample transportation challenges and long turnaround times. Near patient care testing technologies have the potential to obviate such constraints. The Cephei...

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Autores principales: Bwana, Priska, Ageng’o, Joshua, Mwau, Matilu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430374/
https://www.ncbi.nlm.nih.gov/pubmed/30901343
http://dx.doi.org/10.1371/journal.pone.0213865
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author Bwana, Priska
Ageng’o, Joshua
Mwau, Matilu
author_facet Bwana, Priska
Ageng’o, Joshua
Mwau, Matilu
author_sort Bwana, Priska
collection PubMed
description BACKGROUND: In Kenya, access to early infant diagnosis and viral load monitoring services for HIV patients on ART is significantly hampered by sample transportation challenges and long turnaround times. Near patient care testing technologies have the potential to obviate such constraints. The Cepheid GeneXpert was launched in 2010 as a TB assay and in 2014 as a potential point of care HIV viral load assay. Whereas it is widely is used for TB in Kenya, its utility for HIV testing has not been evaluated. OBJECTIVE: To investigate the performance and usability characteristics of the GeneXpert HIV-1 qualitative and quantitative assay. METHODS: This was a cross sectional study among 911 HIV Exposed infants and 310 HIV positive adults. Existing machines used for routine TB diagnosis were used in this study. The diagnostic accuracy of the qualitative assay was assessed using Roche CAP/CTM while the quantitative assay was assessed using with Abbott m2000 as the reference assays respectively. Statistical analysis was done using Stata/MP Version 14 for Mac. Concordance values and misclassification were calculated at the clinical cutoff of 1000 cp/ml. RESULTS: The sensitivity, specificity and accuracy of the GeneXpert HIV-1 qualitative assay were 99.23% (95% CI 97.24–99.90%), 98.91% (95% CI 97.76–99.55%) and 99.00% respectively. For the quantitative assay, they were 92.50% (95% CI 79.61–98.43%), 100.00% and 97.00% respectively. All 30 (100%) users reported that the GeneXpert machine was easy to use, workflow was simple and TB diagnosis was not negatively affected. In our hands, the median turn-around time for an individual qualitative and quantitative test was 90 minutes. A total of 58 (4.34%) errors and 28 (2.10%) invalid outcomes were experienced; 44 (3.29%) tests did not run to completion due to power outages. CONCLUSION: GeneXpert HIV-1 qualitative and quantitative assay is an accurate test for the diagnosis of HIV in infants and for viral load monitoring. At the point of care, the GeneXpert machine’s simple work flow, ease of use and short test turnaround time present the potential to improve access to HIV testing and viral load monitoring. To integrate HIV diagnosis into the existing GeneXpert platforms for TB Diagnosis, there is need to scale up the infrastructure and to change the way work is done.
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spelling pubmed-64303742019-04-02 Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya Bwana, Priska Ageng’o, Joshua Mwau, Matilu PLoS One Research Article BACKGROUND: In Kenya, access to early infant diagnosis and viral load monitoring services for HIV patients on ART is significantly hampered by sample transportation challenges and long turnaround times. Near patient care testing technologies have the potential to obviate such constraints. The Cepheid GeneXpert was launched in 2010 as a TB assay and in 2014 as a potential point of care HIV viral load assay. Whereas it is widely is used for TB in Kenya, its utility for HIV testing has not been evaluated. OBJECTIVE: To investigate the performance and usability characteristics of the GeneXpert HIV-1 qualitative and quantitative assay. METHODS: This was a cross sectional study among 911 HIV Exposed infants and 310 HIV positive adults. Existing machines used for routine TB diagnosis were used in this study. The diagnostic accuracy of the qualitative assay was assessed using Roche CAP/CTM while the quantitative assay was assessed using with Abbott m2000 as the reference assays respectively. Statistical analysis was done using Stata/MP Version 14 for Mac. Concordance values and misclassification were calculated at the clinical cutoff of 1000 cp/ml. RESULTS: The sensitivity, specificity and accuracy of the GeneXpert HIV-1 qualitative assay were 99.23% (95% CI 97.24–99.90%), 98.91% (95% CI 97.76–99.55%) and 99.00% respectively. For the quantitative assay, they were 92.50% (95% CI 79.61–98.43%), 100.00% and 97.00% respectively. All 30 (100%) users reported that the GeneXpert machine was easy to use, workflow was simple and TB diagnosis was not negatively affected. In our hands, the median turn-around time for an individual qualitative and quantitative test was 90 minutes. A total of 58 (4.34%) errors and 28 (2.10%) invalid outcomes were experienced; 44 (3.29%) tests did not run to completion due to power outages. CONCLUSION: GeneXpert HIV-1 qualitative and quantitative assay is an accurate test for the diagnosis of HIV in infants and for viral load monitoring. At the point of care, the GeneXpert machine’s simple work flow, ease of use and short test turnaround time present the potential to improve access to HIV testing and viral load monitoring. To integrate HIV diagnosis into the existing GeneXpert platforms for TB Diagnosis, there is need to scale up the infrastructure and to change the way work is done. Public Library of Science 2019-03-22 /pmc/articles/PMC6430374/ /pubmed/30901343 http://dx.doi.org/10.1371/journal.pone.0213865 Text en © 2019 Bwana et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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
Bwana, Priska
Ageng’o, Joshua
Mwau, Matilu
Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title_full Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title_fullStr Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title_full_unstemmed Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title_short Performance and usability of Cepheid GeneXpert HIV-1 qualitative and quantitative assay in Kenya
title_sort performance and usability of cepheid genexpert hiv-1 qualitative and quantitative assay in kenya
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430374/
https://www.ncbi.nlm.nih.gov/pubmed/30901343
http://dx.doi.org/10.1371/journal.pone.0213865
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