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Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis

INTRODUCTION: Early infant diagnosis (EID) and prompt linkage to care are critical to minimise the high morbidity and mortality associated with infant HIV infection. Attrition in the “EID cascade” is common; however, point-of-care (POC) EID assays with same-day result could facilitate prompt linkage...

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Autores principales: Hsiao, Nei-yuan, Dunning, Lorna, Kroon, Max, Myer, Landon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816318/
https://www.ncbi.nlm.nih.gov/pubmed/27032094
http://dx.doi.org/10.1371/journal.pone.0152672
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author Hsiao, Nei-yuan
Dunning, Lorna
Kroon, Max
Myer, Landon
author_facet Hsiao, Nei-yuan
Dunning, Lorna
Kroon, Max
Myer, Landon
author_sort Hsiao, Nei-yuan
collection PubMed
description INTRODUCTION: Early infant diagnosis (EID) and prompt linkage to care are critical to minimise the high morbidity and mortality associated with infant HIV infection. Attrition in the “EID cascade” is common; however, point-of-care (POC) EID assays with same-day result could facilitate prompt linkage of HIV-infected infant to treatment. Despite a number of POC EID assays in development, few have been independently evaluated and data on new technologies are urgently needed to inform policy. METHODS: We compared Alere q 1/2 Detect POC system laboratory test characteristics with the local standard of care (SOC), Roche CAP/CTM HIV-1 qualitative PCR in an independent laboratory-based evaluation in Cape Town, South Africa. Routinely EID samples collected between November 2013 and September 2014 were each tested by both SOC and POC systems. Repeat testing was done to troubleshoot any discrepancy between POC and SOC results. RESULTS: Overall, 1098 children with a median age of 47 days (IQR, 42–117) were included. Birth PCR (age <7 days) comprised of 8% (n = 92) tests while 56% (n = 620) of children tested as part of routine EID (ages 6–14 weeks). In the overall direct comparison, Alere q Detect achieved sensitivity of 95.5% (95% CI, 91.7–97.9%) and a specificity of 99.8% (95% CI, 99.1–100%). Following repeat testing of discordant samples and exclusion of any inconclusive results, the POC assay sensitivity and specificity were 96.9% (95% CI 93.4–98.9%) and 100% (lower 95% CI 98%) respectively. Among birth PCR tests the POC assay had slightly lower sensitivity (93.3% vs 96.5% in routine EID) and higher assay error rate (10% vs 5% in samples of older children, p = 0.04). CONCLUSION: Our results indicate this POC assay performs well for EID in the laboratory. The high specificity and thus high positive predictive value would suggest a positive POC result may be adequate for immediate infant ART initiation. While POC testing for EID may have particular utility for birth testing at delivery facilities, the lower sensitivity and error rate requires further attention, as does field implementation of POC EID technologies in other clinical care settings.
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spelling pubmed-48163182016-04-14 Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis Hsiao, Nei-yuan Dunning, Lorna Kroon, Max Myer, Landon PLoS One Research Article INTRODUCTION: Early infant diagnosis (EID) and prompt linkage to care are critical to minimise the high morbidity and mortality associated with infant HIV infection. Attrition in the “EID cascade” is common; however, point-of-care (POC) EID assays with same-day result could facilitate prompt linkage of HIV-infected infant to treatment. Despite a number of POC EID assays in development, few have been independently evaluated and data on new technologies are urgently needed to inform policy. METHODS: We compared Alere q 1/2 Detect POC system laboratory test characteristics with the local standard of care (SOC), Roche CAP/CTM HIV-1 qualitative PCR in an independent laboratory-based evaluation in Cape Town, South Africa. Routinely EID samples collected between November 2013 and September 2014 were each tested by both SOC and POC systems. Repeat testing was done to troubleshoot any discrepancy between POC and SOC results. RESULTS: Overall, 1098 children with a median age of 47 days (IQR, 42–117) were included. Birth PCR (age <7 days) comprised of 8% (n = 92) tests while 56% (n = 620) of children tested as part of routine EID (ages 6–14 weeks). In the overall direct comparison, Alere q Detect achieved sensitivity of 95.5% (95% CI, 91.7–97.9%) and a specificity of 99.8% (95% CI, 99.1–100%). Following repeat testing of discordant samples and exclusion of any inconclusive results, the POC assay sensitivity and specificity were 96.9% (95% CI 93.4–98.9%) and 100% (lower 95% CI 98%) respectively. Among birth PCR tests the POC assay had slightly lower sensitivity (93.3% vs 96.5% in routine EID) and higher assay error rate (10% vs 5% in samples of older children, p = 0.04). CONCLUSION: Our results indicate this POC assay performs well for EID in the laboratory. The high specificity and thus high positive predictive value would suggest a positive POC result may be adequate for immediate infant ART initiation. While POC testing for EID may have particular utility for birth testing at delivery facilities, the lower sensitivity and error rate requires further attention, as does field implementation of POC EID technologies in other clinical care settings. Public Library of Science 2016-03-31 /pmc/articles/PMC4816318/ /pubmed/27032094 http://dx.doi.org/10.1371/journal.pone.0152672 Text en © 2016 Hsiao 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
Hsiao, Nei-yuan
Dunning, Lorna
Kroon, Max
Myer, Landon
Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title_full Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title_fullStr Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title_full_unstemmed Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title_short Laboratory Evaluation of the Alere q Point-of-Care System for Early Infant HIV Diagnosis
title_sort laboratory evaluation of the alere q point-of-care system for early infant hiv diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816318/
https://www.ncbi.nlm.nih.gov/pubmed/27032094
http://dx.doi.org/10.1371/journal.pone.0152672
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