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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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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