The challenges of introducing routine G6PD testing into radical cure: A workshop report

© 2015 Ley et al. The only currently available drug that effectively removes malaria hypnozoites from the human host is primaquine. The use of 8-aminoquinolines is hampered by haemolytic side effects in glucose-6-phosphate dehydrogenase (G6PD) deficient individuals. Recently a number of qualitative...

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Main Authors: Benedikt Ley, Nick Luter, Fe Esperanza Espino, Angela Devine, Michael Kalnoky, Yoel Lubell, Kamala Thriemer, J. Kevin Baird, Eugenie Poirot, Nolwenn Conan, Chong Chee Kheong, Lek Dysoley, Wasif Ali Khan, April G. Dion-Berboso, Germana Bancone, Jimee Hwang, Ritu Kumar, Ric N. Price, Lorenz Von Seidlein, Gonzalo J. Domingo
Other Authors: Menzies School of Health Research
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/36072
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spelling th-mahidol.360722018-11-23T17:35:24Z The challenges of introducing routine G6PD testing into radical cure: A workshop report Benedikt Ley Nick Luter Fe Esperanza Espino Angela Devine Michael Kalnoky Yoel Lubell Kamala Thriemer J. Kevin Baird Eugenie Poirot Nolwenn Conan Chong Chee Kheong Lek Dysoley Wasif Ali Khan April G. Dion-Berboso Germana Bancone Jimee Hwang Ritu Kumar Ric N. Price Lorenz Von Seidlein Gonzalo J. Domingo Menzies School of Health Research PATH Seattle Research Institute of Tropical Medicine Mahidol University Eijkman-Oxford Clinical Research Unit Nuffield Department of Clinical Medicine University of California, San Francisco Malaria Consortium Kementerian Kesihatan Malaysia National Center for Parasitology, Entomology and Malaria Control National Institute of Public Health International Centre for Diarrhoeal Disease Research Bangladesh University of the Philippines Manila Shoklo Malaria Research Unit Centers for Disease Control and Prevention Immunology and Microbiology Medicine © 2015 Ley et al. The only currently available drug that effectively removes malaria hypnozoites from the human host is primaquine. The use of 8-aminoquinolines is hampered by haemolytic side effects in glucose-6-phosphate dehydrogenase (G6PD) deficient individuals. Recently a number of qualitative and a quantitative rapid diagnostic test (RDT) format have been developed that provide an alternative to the current standard G6PD activity assays. The WHO has recently recommended routine testing of G6PD status prior to primaquine radical cure whenever possible. A workshop was held in the Philippines in early 2015 to discuss key challenges and knowledge gaps that hinder the introduction of routine G6PD testing. Two point-of-care (PoC) test formats for the measurement of G6PD activity are currently available: qualitative tests comparable to malaria RDT as well as biosensors that provide a quantitative reading. Qualitative G6PD PoC tests provide a binomial test result, are easy to use and some products are comparable in price to the widely used fluorescent spot test. Qualitative test results can accurately classify hemizygous males, heterozygous females, but may misclassify females with intermediate G6PD activity. Biosensors provide a more complex quantitative readout and are better suited to identify heterozygous females. While associated with higher costs per sample tested biosensors have the potential for broader use in other scenarios where knowledge of G6PD activity is relevant as well. The introduction of routine G6PD testing is associated with additional costs on top of routine treatment that will vary by setting and will need to be assessed prior to test introduction. Reliable G6PD PoC tests have the potential to play an essential role in future malaria elimination programmes, however require an improved understanding on how to best integrate routine G6PD testing into different health settings. 2018-11-23T10:15:34Z 2018-11-23T10:15:34Z 2015-09-29 Article Malaria Journal. Vol.14, No.1 (2015) 10.1186/s12936-015-0896-8 14752875 2-s2.0-84942421382 https://repository.li.mahidol.ac.th/handle/123456789/36072 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942421382&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Benedikt Ley
Nick Luter
Fe Esperanza Espino
Angela Devine
Michael Kalnoky
Yoel Lubell
Kamala Thriemer
J. Kevin Baird
Eugenie Poirot
Nolwenn Conan
Chong Chee Kheong
Lek Dysoley
Wasif Ali Khan
April G. Dion-Berboso
Germana Bancone
Jimee Hwang
Ritu Kumar
Ric N. Price
Lorenz Von Seidlein
Gonzalo J. Domingo
The challenges of introducing routine G6PD testing into radical cure: A workshop report
description © 2015 Ley et al. The only currently available drug that effectively removes malaria hypnozoites from the human host is primaquine. The use of 8-aminoquinolines is hampered by haemolytic side effects in glucose-6-phosphate dehydrogenase (G6PD) deficient individuals. Recently a number of qualitative and a quantitative rapid diagnostic test (RDT) format have been developed that provide an alternative to the current standard G6PD activity assays. The WHO has recently recommended routine testing of G6PD status prior to primaquine radical cure whenever possible. A workshop was held in the Philippines in early 2015 to discuss key challenges and knowledge gaps that hinder the introduction of routine G6PD testing. Two point-of-care (PoC) test formats for the measurement of G6PD activity are currently available: qualitative tests comparable to malaria RDT as well as biosensors that provide a quantitative reading. Qualitative G6PD PoC tests provide a binomial test result, are easy to use and some products are comparable in price to the widely used fluorescent spot test. Qualitative test results can accurately classify hemizygous males, heterozygous females, but may misclassify females with intermediate G6PD activity. Biosensors provide a more complex quantitative readout and are better suited to identify heterozygous females. While associated with higher costs per sample tested biosensors have the potential for broader use in other scenarios where knowledge of G6PD activity is relevant as well. The introduction of routine G6PD testing is associated with additional costs on top of routine treatment that will vary by setting and will need to be assessed prior to test introduction. Reliable G6PD PoC tests have the potential to play an essential role in future malaria elimination programmes, however require an improved understanding on how to best integrate routine G6PD testing into different health settings.
author2 Menzies School of Health Research
author_facet Menzies School of Health Research
Benedikt Ley
Nick Luter
Fe Esperanza Espino
Angela Devine
Michael Kalnoky
Yoel Lubell
Kamala Thriemer
J. Kevin Baird
Eugenie Poirot
Nolwenn Conan
Chong Chee Kheong
Lek Dysoley
Wasif Ali Khan
April G. Dion-Berboso
Germana Bancone
Jimee Hwang
Ritu Kumar
Ric N. Price
Lorenz Von Seidlein
Gonzalo J. Domingo
format Article
author Benedikt Ley
Nick Luter
Fe Esperanza Espino
Angela Devine
Michael Kalnoky
Yoel Lubell
Kamala Thriemer
J. Kevin Baird
Eugenie Poirot
Nolwenn Conan
Chong Chee Kheong
Lek Dysoley
Wasif Ali Khan
April G. Dion-Berboso
Germana Bancone
Jimee Hwang
Ritu Kumar
Ric N. Price
Lorenz Von Seidlein
Gonzalo J. Domingo
author_sort Benedikt Ley
title The challenges of introducing routine G6PD testing into radical cure: A workshop report
title_short The challenges of introducing routine G6PD testing into radical cure: A workshop report
title_full The challenges of introducing routine G6PD testing into radical cure: A workshop report
title_fullStr The challenges of introducing routine G6PD testing into radical cure: A workshop report
title_full_unstemmed The challenges of introducing routine G6PD testing into radical cure: A workshop report
title_sort challenges of introducing routine g6pd testing into radical cure: a workshop report
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/36072
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