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Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination

BACKGROUND. The performance of Plasmodium falciparum–specific histidine-rich protein 2–based rapid diagnostic tests (RDTs) to evaluate suspected malaria in low-endemicity settings has not been well characterized. METHODS. Using dried blood spot samples from patients with suspected malaria at 37 heal...

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Autores principales: Ranadive, Nikhil, Kunene, Simon, Darteh, Sarah, Ntshalintshali, Nyasatu, Nhlabathi, Nomcebo, Dlamini, Nomcebo, Chitundu, Stanley, Saini, Manik, Murphy, Maxwell, Soble, Adam, Schwartz, Alanna, Greenhouse, Bryan, Hsiang, Michelle S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399938/
https://www.ncbi.nlm.nih.gov/pubmed/28369268
http://dx.doi.org/10.1093/cid/cix131
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author Ranadive, Nikhil
Kunene, Simon
Darteh, Sarah
Ntshalintshali, Nyasatu
Nhlabathi, Nomcebo
Dlamini, Nomcebo
Chitundu, Stanley
Saini, Manik
Murphy, Maxwell
Soble, Adam
Schwartz, Alanna
Greenhouse, Bryan
Hsiang, Michelle S.
author_facet Ranadive, Nikhil
Kunene, Simon
Darteh, Sarah
Ntshalintshali, Nyasatu
Nhlabathi, Nomcebo
Dlamini, Nomcebo
Chitundu, Stanley
Saini, Manik
Murphy, Maxwell
Soble, Adam
Schwartz, Alanna
Greenhouse, Bryan
Hsiang, Michelle S.
author_sort Ranadive, Nikhil
collection PubMed
description BACKGROUND. The performance of Plasmodium falciparum–specific histidine-rich protein 2–based rapid diagnostic tests (RDTs) to evaluate suspected malaria in low-endemicity settings has not been well characterized. METHODS. Using dried blood spot samples from patients with suspected malaria at 37 health facilities from 2012 to 2014 in the low-endemicity country of Swaziland, we investigated the diagnostic accuracy of histidine-rich protein 2–based RDTs using qualitative polymerase chain reaction (PCR) (nested PCR targeting the cytochrome b gene) and quantitative PCR as reference standards. To explore reasons for false-negative and/or false-positive results, we used pfhrp2/3-specific PCR and logistic regression analyses of potentially associated epidemiological factors. RESULTS. From 1353 patients, 93.0% of RDT-positive (n = 185) and 31.2% of RDT-negative samples (n = 340) were available and selected for testing. Compared with nested PCR, the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of RDTs were 51.7%, 94.1%, 67.3%, and 89.1%, respectively. After exclusion of samples with parasite densities <100/μL, which accounted for 75.7% of false-negative results and 33.3% of PCR-detectable infections, the sensitivity, specificity, PPV, and NPV were 78.8%, 93.7%, 62.3%, and 97.1%. Deletions of pfhrp2 were not detected. False-positivity was more likely during the second year and was not associated with demographics, recent malaria, health facility testing characteristics, or potential DNA degradation. CONCLUSIONS. In the low-transmission setting of Swaziland, we demonstrated low sensitivity of RDT for malaria diagnosis, owing to an unexpectedly high proportion of low-density infection among symptomatic subjects. The PPV was also low, requiring further investigation. A more accurate point-of-care diagnostic may be needed to support malaria elimination efforts.
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spelling pubmed-53999382017-04-28 Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination Ranadive, Nikhil Kunene, Simon Darteh, Sarah Ntshalintshali, Nyasatu Nhlabathi, Nomcebo Dlamini, Nomcebo Chitundu, Stanley Saini, Manik Murphy, Maxwell Soble, Adam Schwartz, Alanna Greenhouse, Bryan Hsiang, Michelle S. Clin Infect Dis Major Article BACKGROUND. The performance of Plasmodium falciparum–specific histidine-rich protein 2–based rapid diagnostic tests (RDTs) to evaluate suspected malaria in low-endemicity settings has not been well characterized. METHODS. Using dried blood spot samples from patients with suspected malaria at 37 health facilities from 2012 to 2014 in the low-endemicity country of Swaziland, we investigated the diagnostic accuracy of histidine-rich protein 2–based RDTs using qualitative polymerase chain reaction (PCR) (nested PCR targeting the cytochrome b gene) and quantitative PCR as reference standards. To explore reasons for false-negative and/or false-positive results, we used pfhrp2/3-specific PCR and logistic regression analyses of potentially associated epidemiological factors. RESULTS. From 1353 patients, 93.0% of RDT-positive (n = 185) and 31.2% of RDT-negative samples (n = 340) were available and selected for testing. Compared with nested PCR, the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of RDTs were 51.7%, 94.1%, 67.3%, and 89.1%, respectively. After exclusion of samples with parasite densities <100/μL, which accounted for 75.7% of false-negative results and 33.3% of PCR-detectable infections, the sensitivity, specificity, PPV, and NPV were 78.8%, 93.7%, 62.3%, and 97.1%. Deletions of pfhrp2 were not detected. False-positivity was more likely during the second year and was not associated with demographics, recent malaria, health facility testing characteristics, or potential DNA degradation. CONCLUSIONS. In the low-transmission setting of Swaziland, we demonstrated low sensitivity of RDT for malaria diagnosis, owing to an unexpectedly high proportion of low-density infection among symptomatic subjects. The PPV was also low, requiring further investigation. A more accurate point-of-care diagnostic may be needed to support malaria elimination efforts. Oxford University Press 2017-05-01 2017-03-27 /pmc/articles/PMC5399938/ /pubmed/28369268 http://dx.doi.org/10.1093/cid/cix131 Text en © The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Major Article
Ranadive, Nikhil
Kunene, Simon
Darteh, Sarah
Ntshalintshali, Nyasatu
Nhlabathi, Nomcebo
Dlamini, Nomcebo
Chitundu, Stanley
Saini, Manik
Murphy, Maxwell
Soble, Adam
Schwartz, Alanna
Greenhouse, Bryan
Hsiang, Michelle S.
Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title_full Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title_fullStr Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title_full_unstemmed Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title_short Limitations of Rapid Diagnostic Testing in Patients with Suspected Malaria: A Diagnostic Accuracy Evaluation from Swaziland, a Low-Endemicity Country Aiming for Malaria Elimination
title_sort limitations of rapid diagnostic testing in patients with suspected malaria: a diagnostic accuracy evaluation from swaziland, a low-endemicity country aiming for malaria elimination
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399938/
https://www.ncbi.nlm.nih.gov/pubmed/28369268
http://dx.doi.org/10.1093/cid/cix131
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