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Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú

Plasmodium vivax is co-endemic with Plasmodium falciparum in Peru, and optimum management requires distinguishing these two species in the blood of patients. For the differential identification of P. vivax and other Plasmodium spp., the Loopamp(TM) Malaria Pan Detection Kit in combination with the L...

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Autores principales: Nolasco, Oscar, Infante, Beronica, Contreras-Mancilla, Juan, Incardona, Sandra, Ding, Xavier C., Gamboa, Dionicia, Torres, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Tropical Medicine and Hygiene 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543827/
https://www.ncbi.nlm.nih.gov/pubmed/32748776
http://dx.doi.org/10.4269/ajtmh.20-0212
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author Nolasco, Oscar
Infante, Beronica
Contreras-Mancilla, Juan
Incardona, Sandra
Ding, Xavier C.
Gamboa, Dionicia
Torres, Katherine
author_facet Nolasco, Oscar
Infante, Beronica
Contreras-Mancilla, Juan
Incardona, Sandra
Ding, Xavier C.
Gamboa, Dionicia
Torres, Katherine
author_sort Nolasco, Oscar
collection PubMed
description Plasmodium vivax is co-endemic with Plasmodium falciparum in Peru, and optimum management requires distinguishing these two species in the blood of patients. For the differential identification of P. vivax and other Plasmodium spp., the Loopamp(TM) Malaria Pan Detection Kit in combination with the Loopamp Malaria Pv Detection Kit (Eiken Chemical Co. Ltd., Tokyo, Japan) was used to evaluate 559 whole blood samples collected in 2017 from febrile patients with suspected malaria attending different health facilities in the Loreto region. The Loopamp Malaria Pan Detection Kit showed a sensitivity of 87.7% (95% CI: 83.5–91.9) and a specificity of 94.4% (95% CI: 91.9–96.9) and good agreement with PCR (Cohen’s kappa 0.8266, 95% CI: 0.7792–0.874). By comparison, the Loopamp Malaria Pv Detection Kit showed a similar sensitivity (84.4%, 95% CI: 79.0–89.7) and specificity (92.4%, 95% CI: 89.7–95.0) and substantial agreement with PCR (Cohen’s kappa: 0.7661, 95% CI: 0.7088–0.8234).
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spelling pubmed-75438272020-10-11 Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú Nolasco, Oscar Infante, Beronica Contreras-Mancilla, Juan Incardona, Sandra Ding, Xavier C. Gamboa, Dionicia Torres, Katherine Am J Trop Med Hyg Articles Plasmodium vivax is co-endemic with Plasmodium falciparum in Peru, and optimum management requires distinguishing these two species in the blood of patients. For the differential identification of P. vivax and other Plasmodium spp., the Loopamp(TM) Malaria Pan Detection Kit in combination with the Loopamp Malaria Pv Detection Kit (Eiken Chemical Co. Ltd., Tokyo, Japan) was used to evaluate 559 whole blood samples collected in 2017 from febrile patients with suspected malaria attending different health facilities in the Loreto region. The Loopamp Malaria Pan Detection Kit showed a sensitivity of 87.7% (95% CI: 83.5–91.9) and a specificity of 94.4% (95% CI: 91.9–96.9) and good agreement with PCR (Cohen’s kappa 0.8266, 95% CI: 0.7792–0.874). By comparison, the Loopamp Malaria Pv Detection Kit showed a similar sensitivity (84.4%, 95% CI: 79.0–89.7) and specificity (92.4%, 95% CI: 89.7–95.0) and substantial agreement with PCR (Cohen’s kappa: 0.7661, 95% CI: 0.7088–0.8234). The American Society of Tropical Medicine and Hygiene 2020-10 2020-08-03 /pmc/articles/PMC7543827/ /pubmed/32748776 http://dx.doi.org/10.4269/ajtmh.20-0212 Text en © The American Society of Tropical Medicine and Hygiene This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Articles
Nolasco, Oscar
Infante, Beronica
Contreras-Mancilla, Juan
Incardona, Sandra
Ding, Xavier C.
Gamboa, Dionicia
Torres, Katherine
Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title_full Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title_fullStr Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title_full_unstemmed Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title_short Diagnosis of Plasmodium vivax by Loop-Mediated Isothermal Amplification in Febrile Patient Samples from Loreto, Perú
title_sort diagnosis of plasmodium vivax by loop-mediated isothermal amplification in febrile patient samples from loreto, perú
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7543827/
https://www.ncbi.nlm.nih.gov/pubmed/32748776
http://dx.doi.org/10.4269/ajtmh.20-0212
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