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Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community
BACKGROUND: The Democratic Republic of the Congo (DRC) is one of the five countries carrying half of global malaria burden with children 0–5 years old being most at risk. Rapid diagnostic tests (RDTs) are currently routinely used for the detection of Plasmodium infection in health centres and may be...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248466/ https://www.ncbi.nlm.nih.gov/pubmed/25108305 http://dx.doi.org/10.1186/1475-2875-13-308 |
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author | Ilombe, Gillon Maketa, Vivi Mavoko, Hypolite Muhindo da Luz, Raquel Inocêncio Lutumba, Pascal Van geertruyden, Jean-Pierre |
author_facet | Ilombe, Gillon Maketa, Vivi Mavoko, Hypolite Muhindo da Luz, Raquel Inocêncio Lutumba, Pascal Van geertruyden, Jean-Pierre |
author_sort | Ilombe, Gillon |
collection | PubMed |
description | BACKGROUND: The Democratic Republic of the Congo (DRC) is one of the five countries carrying half of global malaria burden with children 0–5 years old being most at risk. Rapid diagnostic tests (RDTs) are currently routinely used for the detection of Plasmodium infection in health centres and may be a useful tool for population-based survey. METHODS: This study assessed, in a stable transmission zone of Kinshasa, whether a HRP2-based RDT matches the selection criteria of the National Malaria Control Programme (NMCP), DRC and assessed the most relevant fever threshold in this context. RESULTS: RDTs and microscopy were concordant in 84.3% and 83.4% children in the health centre and at the community level, respectively. The sensitivity was high (>95%), but the specificity was too low and lower in the community (66.9%; 95%CI: 58.5-75.2) compared to the HC (79.4%; 95%CI: 75.7-83.2). The estimated parasitic threshold of 5,414 parasites/μl was with a sensitivity of 63.3% and a specificity of 71.8% not very discriminative, and thus not a threshold. CONCLUSION: HRP-based RDT gives a satisfactory proxy to estimate and monitor malaria endemicity, but the low specificity, far below the selection criteria of the NMCP, DRC is problematic for use in a clinical setting. |
format | Online Article Text |
id | pubmed-4248466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42484662014-12-02 Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community Ilombe, Gillon Maketa, Vivi Mavoko, Hypolite Muhindo da Luz, Raquel Inocêncio Lutumba, Pascal Van geertruyden, Jean-Pierre Malar J Research BACKGROUND: The Democratic Republic of the Congo (DRC) is one of the five countries carrying half of global malaria burden with children 0–5 years old being most at risk. Rapid diagnostic tests (RDTs) are currently routinely used for the detection of Plasmodium infection in health centres and may be a useful tool for population-based survey. METHODS: This study assessed, in a stable transmission zone of Kinshasa, whether a HRP2-based RDT matches the selection criteria of the National Malaria Control Programme (NMCP), DRC and assessed the most relevant fever threshold in this context. RESULTS: RDTs and microscopy were concordant in 84.3% and 83.4% children in the health centre and at the community level, respectively. The sensitivity was high (>95%), but the specificity was too low and lower in the community (66.9%; 95%CI: 58.5-75.2) compared to the HC (79.4%; 95%CI: 75.7-83.2). The estimated parasitic threshold of 5,414 parasites/μl was with a sensitivity of 63.3% and a specificity of 71.8% not very discriminative, and thus not a threshold. CONCLUSION: HRP-based RDT gives a satisfactory proxy to estimate and monitor malaria endemicity, but the low specificity, far below the selection criteria of the NMCP, DRC is problematic for use in a clinical setting. BioMed Central 2014-08-09 /pmc/articles/PMC4248466/ /pubmed/25108305 http://dx.doi.org/10.1186/1475-2875-13-308 Text en © Ilombe et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ilombe, Gillon Maketa, Vivi Mavoko, Hypolite Muhindo da Luz, Raquel Inocêncio Lutumba, Pascal Van geertruyden, Jean-Pierre Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title | Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title_full | Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title_fullStr | Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title_full_unstemmed | Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title_short | Performance of HRP2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
title_sort | performance of hrp2-based rapid test in children attending the health centre compared to asymptomatic children in the community |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248466/ https://www.ncbi.nlm.nih.gov/pubmed/25108305 http://dx.doi.org/10.1186/1475-2875-13-308 |
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