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Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria

BACKGROUND: Malaria diagnosis using microscopy is currently the gold standard. However, malaria rapid diagnostic tests (mRDTs) were developed to simplify the diagnosis in regions without access to functional microscopy. AIM: The objective of this study was to compare the diagnostic accuracy of mRDT...

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Autores principales: Ogunfowokan, Oluwagbenga, Ogunfowokan, Bamidele A., Nwajei, Anthony I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380062/
https://www.ncbi.nlm.nih.gov/pubmed/32634015
http://dx.doi.org/10.4102/phcfm.v12i1.2212
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author Ogunfowokan, Oluwagbenga
Ogunfowokan, Bamidele A.
Nwajei, Anthony I.
author_facet Ogunfowokan, Oluwagbenga
Ogunfowokan, Bamidele A.
Nwajei, Anthony I.
author_sort Ogunfowokan, Oluwagbenga
collection PubMed
description BACKGROUND: Malaria diagnosis using microscopy is currently the gold standard. However, malaria rapid diagnostic tests (mRDTs) were developed to simplify the diagnosis in regions without access to functional microscopy. AIM: The objective of this study was to compare the diagnostic accuracy of mRDT CareStat(TM) with microscopy. SETTING: This study was conducted in the paediatric primary care clinic of the Federal Medical Centre, Asaba, Nigeria. METHODS: A cross-sectional study for diagnostic accuracy was conducted from May 2016 to October 2016. Ninety-eight participants were involved to obtain a precision of 5%, sensitivity of mRDT CareStat(TM) of 95% from published work and 95% level of confidence after adjusting for 20% non-response rate or missing data. Consecutive participants were tested using both microscopy and mRDT. The results were analysed using EPI Info Version 7. RESULTS: A total of 98 children aged 3–59 months were enrolled. Malaria prevalence was found to be 53% (95% confidence interval [CI] = 46% – 60%), whilst sensitivity and specificity were 29% (95% CI = 20% – 38%) and 89% (95% CI = 83% – 95%), respectively. The positive and negative predictive values were 75% (95% CI = 66.4% – 83.6%) and 53% (95% CI = 46% – 60%), respectively. CONCLUSION: Agreement between malaria parasitaemia using microscopy and mRDT positivity increased with increase in the parasite density. The mRDT might be negative when malaria parasite density using microscopy is low.
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spelling pubmed-73800622020-07-29 Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria Ogunfowokan, Oluwagbenga Ogunfowokan, Bamidele A. Nwajei, Anthony I. Afr J Prim Health Care Fam Med Original Research BACKGROUND: Malaria diagnosis using microscopy is currently the gold standard. However, malaria rapid diagnostic tests (mRDTs) were developed to simplify the diagnosis in regions without access to functional microscopy. AIM: The objective of this study was to compare the diagnostic accuracy of mRDT CareStat(TM) with microscopy. SETTING: This study was conducted in the paediatric primary care clinic of the Federal Medical Centre, Asaba, Nigeria. METHODS: A cross-sectional study for diagnostic accuracy was conducted from May 2016 to October 2016. Ninety-eight participants were involved to obtain a precision of 5%, sensitivity of mRDT CareStat(TM) of 95% from published work and 95% level of confidence after adjusting for 20% non-response rate or missing data. Consecutive participants were tested using both microscopy and mRDT. The results were analysed using EPI Info Version 7. RESULTS: A total of 98 children aged 3–59 months were enrolled. Malaria prevalence was found to be 53% (95% confidence interval [CI] = 46% – 60%), whilst sensitivity and specificity were 29% (95% CI = 20% – 38%) and 89% (95% CI = 83% – 95%), respectively. The positive and negative predictive values were 75% (95% CI = 66.4% – 83.6%) and 53% (95% CI = 46% – 60%), respectively. CONCLUSION: Agreement between malaria parasitaemia using microscopy and mRDT positivity increased with increase in the parasite density. The mRDT might be negative when malaria parasite density using microscopy is low. AOSIS 2020-06-17 /pmc/articles/PMC7380062/ /pubmed/32634015 http://dx.doi.org/10.4102/phcfm.v12i1.2212 Text en © 2020. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Ogunfowokan, Oluwagbenga
Ogunfowokan, Bamidele A.
Nwajei, Anthony I.
Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title_full Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title_fullStr Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title_full_unstemmed Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title_short Sensitivity and specificity of malaria rapid diagnostic test (mRDT CareStat(TM)) compared with microscopy amongst under five children attending a primary care clinic in southern Nigeria
title_sort sensitivity and specificity of malaria rapid diagnostic test (mrdt carestat(tm)) compared with microscopy amongst under five children attending a primary care clinic in southern nigeria
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380062/
https://www.ncbi.nlm.nih.gov/pubmed/32634015
http://dx.doi.org/10.4102/phcfm.v12i1.2212
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