Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia

Abstract Background The sensitivity of rapid diagnostic tests (RDTs) for malaria is inadequate for detecting low-density, often asymptomatic infections, such as those that can occur when screening pregnant women for malaria. The performance of the Alere™ Ultra-sensitive Malaria Ag Plasmodium falcipa...

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Main Authors: Vera T. Unwin, Rukhsana Ahmed, Rintis Noviyanti, Agatha M. Puspitasari, Retno A. S. Utami, Leily Trianty, Theda Lukito, Din Syafruddin, Jeanne R. Poespoprodjo, Maria A. Santana-Morales, Feiko O. Ter Kuile, Emily R. Adams
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Malaria Journal
Subjects:
Online Access:https://doi.org/10.1186/s12936-020-3110-6
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spelling doaj-c7e681ab7d3846c0b5cfcc79054455b02021-01-17T12:55:49ZengBMCMalaria Journal1475-28752020-01-011911810.1186/s12936-020-3110-6Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in IndonesiaVera T. Unwin0Rukhsana Ahmed1Rintis Noviyanti2Agatha M. Puspitasari3Retno A. S. Utami4Leily Trianty5Theda Lukito6Din Syafruddin7Jeanne R. Poespoprodjo8Maria A. Santana-Morales9Feiko O. Ter Kuile10Emily R. Adams11Department of Tropical Disease Biology and Department of Clinical Sciences, Liverpool School of Tropical MedicineDepartment of Tropical Disease Biology and Department of Clinical Sciences, Liverpool School of Tropical MedicineMalaria Pathogenesis Laboratory, Eijkman Institute of Molecular BiologyMalaria Pathogenesis Laboratory, Eijkman Institute of Molecular BiologyMalaria Pathogenesis Laboratory, Eijkman Institute of Molecular BiologyMalaria Pathogenesis Laboratory, Eijkman Institute of Molecular BiologyClinesiaMalaria Pathogenesis Laboratory, Eijkman Institute of Molecular BiologyMimika District Health Authority, District Government BuildingUniversity Institute of Tropical Diseases and Public Health of the Canary Islands, University of la LagunaDepartment of Tropical Disease Biology and Department of Clinical Sciences, Liverpool School of Tropical MedicineDepartment of Tropical Disease Biology and Department of Clinical Sciences, Liverpool School of Tropical MedicineAbstract Background The sensitivity of rapid diagnostic tests (RDTs) for malaria is inadequate for detecting low-density, often asymptomatic infections, such as those that can occur when screening pregnant women for malaria. The performance of the Alere™ Ultra-sensitive Malaria Ag Plasmodium falciparum RDT (uRDT) was assessed retrospectively in pregnant women in Indonesia. Methods The diagnostic performance of the uRDT and the CareStart™ Malaria HRP2/pLDH VOM (Plasmodium vivax, Plasmodium ovale and Plasmodium malariae) Combo RDT (csRDT) were assessed using 270 stored red blood cell pellets and plasma samples from asymptomatic pregnant women. These included 112 P. falciparum negative and 158 P. falciparum positive samples detected by a composite test (qPCR, LAMP, nPCR) as reference standard. Diagnostic indicators: sensitivity, specificity, negative predictive value (NPV), positive predictive value (PPV), diagnostic odds ratio (DOR) and the level of agreement (kappa) were calculated for comparison. Results Compared with the reference test, the uRDT had a sensitivity of 19.6% (95% CI 13.9–26.8) and specificity of 98.2% (93.1–99.7%). The csRDT was 22.8% (16.7–30.3) sensitive and 95.5% (89.4–98.3) specific for P. falciparum infections. Performance of the uRDT was non-significantly different to the csRDT (p = 0.169). RDT outcome was stratified by qPCR cycling threshold (Ct), and performance of the RDTs was found to be comparable across parasite loads. Conclusion The uRDT performed similarly to the currently used csRDTs in detecting P. falciparum infections in asymptomatic pregnant women. In these settings, molecular diagnostics are currently the most sensitive for malaria.https://doi.org/10.1186/s12936-020-3110-6MalariaDiagnosticsPregnancyRapid diagnostic testDiagnostic performanceMolecular techniques
collection DOAJ
language English
format Article
sources DOAJ
author Vera T. Unwin
Rukhsana Ahmed
Rintis Noviyanti
Agatha M. Puspitasari
Retno A. S. Utami
Leily Trianty
Theda Lukito
Din Syafruddin
Jeanne R. Poespoprodjo
Maria A. Santana-Morales
Feiko O. Ter Kuile
Emily R. Adams
spellingShingle Vera T. Unwin
Rukhsana Ahmed
Rintis Noviyanti
Agatha M. Puspitasari
Retno A. S. Utami
Leily Trianty
Theda Lukito
Din Syafruddin
Jeanne R. Poespoprodjo
Maria A. Santana-Morales
Feiko O. Ter Kuile
Emily R. Adams
Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
Malaria Journal
Malaria
Diagnostics
Pregnancy
Rapid diagnostic test
Diagnostic performance
Molecular techniques
author_facet Vera T. Unwin
Rukhsana Ahmed
Rintis Noviyanti
Agatha M. Puspitasari
Retno A. S. Utami
Leily Trianty
Theda Lukito
Din Syafruddin
Jeanne R. Poespoprodjo
Maria A. Santana-Morales
Feiko O. Ter Kuile
Emily R. Adams
author_sort Vera T. Unwin
title Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
title_short Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
title_full Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
title_fullStr Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
title_full_unstemmed Use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in Indonesia
title_sort use of a highly-sensitive rapid diagnostic test to screen for malaria in pregnancy in indonesia
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2020-01-01
description Abstract Background The sensitivity of rapid diagnostic tests (RDTs) for malaria is inadequate for detecting low-density, often asymptomatic infections, such as those that can occur when screening pregnant women for malaria. The performance of the Alere™ Ultra-sensitive Malaria Ag Plasmodium falciparum RDT (uRDT) was assessed retrospectively in pregnant women in Indonesia. Methods The diagnostic performance of the uRDT and the CareStart™ Malaria HRP2/pLDH VOM (Plasmodium vivax, Plasmodium ovale and Plasmodium malariae) Combo RDT (csRDT) were assessed using 270 stored red blood cell pellets and plasma samples from asymptomatic pregnant women. These included 112 P. falciparum negative and 158 P. falciparum positive samples detected by a composite test (qPCR, LAMP, nPCR) as reference standard. Diagnostic indicators: sensitivity, specificity, negative predictive value (NPV), positive predictive value (PPV), diagnostic odds ratio (DOR) and the level of agreement (kappa) were calculated for comparison. Results Compared with the reference test, the uRDT had a sensitivity of 19.6% (95% CI 13.9–26.8) and specificity of 98.2% (93.1–99.7%). The csRDT was 22.8% (16.7–30.3) sensitive and 95.5% (89.4–98.3) specific for P. falciparum infections. Performance of the uRDT was non-significantly different to the csRDT (p = 0.169). RDT outcome was stratified by qPCR cycling threshold (Ct), and performance of the RDTs was found to be comparable across parasite loads. Conclusion The uRDT performed similarly to the currently used csRDTs in detecting P. falciparum infections in asymptomatic pregnant women. In these settings, molecular diagnostics are currently the most sensitive for malaria.
topic Malaria
Diagnostics
Pregnancy
Rapid diagnostic test
Diagnostic performance
Molecular techniques
url https://doi.org/10.1186/s12936-020-3110-6
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