| 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 |