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Operational feasibility of appropriate radical cure of Plasmodium vivax with tafenoquine or primaquine after semi-quantitative G6PD testing in Ethiopia: a mixed methods study

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dc.contributor.author Ethiopian Food and Drug Authority
dc.date.accessioned 2026-02-24T07:25:52Z
dc.date.available 2026-02-24T07:25:52Z
dc.date.issued Feb 2024
dc.identifier.uri http://repository.iphce.org/xmlui/handle/123456789/5330
dc.description.abstract Primaquine (PQ) and tafenoquine (TQ) can be used for the radical cure (RC) of P. vivax malaria. PQ requires a 14-day dose, compared to a single-day dose for TQ, which is likely to improve patient adherence to the treatment. However, a significant safety concern with both TQ and PQ is the high risk of acute hemolytic anemia (AHA) in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency. WHO recommends that “the G6PD status of patients should be used to guide administration of PQ & TQ for preventing relapse. The aim of the study is to investigate whether it is operationally feasible to provide appropriate radical cure (RC) treatment after semi-quantitative G6PD testing to P. vivax patients who are eligible for RC based on the national treatment guidelines en_US
dc.language.iso en_US en_US
dc.subject Malaria en_US
dc.title Operational feasibility of appropriate radical cure of Plasmodium vivax with tafenoquine or primaquine after semi-quantitative G6PD testing in Ethiopia: a mixed methods study en_US
dc.type Report en_US


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