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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/36072
Title: The challenges of introducing routine G6PD testing into radical cure: A workshop report
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
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
Keywords: Immunology and Microbiology;Medicine
Issue Date: 29-Sep-2015
Citation: Malaria Journal. Vol.14, No.1 (2015)
Abstract: © 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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942421382&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/36072
ISSN: 14752875
Appears in Collections:Scopus 2011-2015

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