Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries
<p>Primaquine is the only available antimalarial drug which kills dormant liver stages of Plasmodium vivax and Plasmodium ovale malarias and therefore prevents their relapse (“radical cure”). It is also the only generally available antimalarial which rapidly sterilises mature P. falciparum gam...
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| Format: | Journal article |
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Public Library of Science
2018
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| _version_ | 1797079880804859904 |
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| author | Recht, J Ashley, E White, N |
| author_facet | Recht, J Ashley, E White, N |
| author_sort | Recht, J |
| collection | OXFORD |
| description | <p>Primaquine is the only available antimalarial drug which kills dormant liver stages of Plasmodium vivax and Plasmodium ovale malarias and therefore prevents their relapse (“radical cure”). It is also the only generally available antimalarial which rapidly sterilises mature P. falciparum gametocytes. Radical cure requires extended courses of primaquine (usually 14 days; total dose 3.5-7mg/kg) whereas transmissibility reduction in falciparum malaria requires a single dose (formerly 0.75mg/kg, now a single low dose (SLD) of 0.25mg/kg is recommended). The main adverse effect of primaquine is dose-dependent haemolysis in glucose-6-phosphate dehydrogenase (G6PD) deficiency, the most common human enzymopathy. X-linked mutations conferring varying degrees of G6PD deficiency are prevalent throughout malaria endemic regions. Phenotypic screening tests usually detect <30% of normal G6PD activity identifying nearly all male hemizygotes and female homozygotes, and some heterozygotes. Unfortunately G6PD screening is usually unavailable at point of care and as a consequence radical cure is greatly underused. As both haemolytic risk (determined by the prevalence and severity of G6PD deficiency polymorphisms) and relapse rates vary there has been considerable uncertainty in both policies and practices related to G6PD testing and use of primaquine for radical cure.</p><p> Review of available information on the prevalence and severity of G6PD variants together with countries’ policies for the use of primaquine and G6PD testing confirms a wide range of practices. There remains lack of consensus on the requirement for G6PD testing before prescribing primaquine radical cure regimens. Despite substantially lower haemolytic risks, implementation of SLD primaquine as a P. falciparum gametocytocide also varies. In Africa, a few countries have recently adopted SLD primaquine, yet many with areas of low seasonal transmission do not use primaquine as an antimalarial at all. Most countries which recommended the higher 0.75mg/kg single primaquine dose for falciparum malaria (e.g. most countries in the Americas) have not changed their recommendation. Some vivax malaria endemic countries where G6PD testing is generally unavailable have adopted the once weekly radical cure regimen (0.75mg/kg/week for 8 weeks) known to be safer in less severe G6PD deficiency variants. There is substantial room for improvement in radical cure policies and practices. </p> |
| first_indexed | 2024-03-07T00:52:10Z |
| format | Journal article |
| id | oxford-uuid:86c31701-22e3-441f-bc84-6b84f85ac143 |
| institution | University of Oxford |
| last_indexed | 2024-03-07T00:52:10Z |
| publishDate | 2018 |
| publisher | Public Library of Science |
| record_format | dspace |
| spelling | oxford-uuid:86c31701-22e3-441f-bc84-6b84f85ac1432022-03-26T22:06:13ZUse of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countriesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:86c31701-22e3-441f-bc84-6b84f85ac143Symplectic Elements at OxfordPublic Library of Science2018Recht, JAshley, EWhite, N<p>Primaquine is the only available antimalarial drug which kills dormant liver stages of Plasmodium vivax and Plasmodium ovale malarias and therefore prevents their relapse (“radical cure”). It is also the only generally available antimalarial which rapidly sterilises mature P. falciparum gametocytes. Radical cure requires extended courses of primaquine (usually 14 days; total dose 3.5-7mg/kg) whereas transmissibility reduction in falciparum malaria requires a single dose (formerly 0.75mg/kg, now a single low dose (SLD) of 0.25mg/kg is recommended). The main adverse effect of primaquine is dose-dependent haemolysis in glucose-6-phosphate dehydrogenase (G6PD) deficiency, the most common human enzymopathy. X-linked mutations conferring varying degrees of G6PD deficiency are prevalent throughout malaria endemic regions. Phenotypic screening tests usually detect <30% of normal G6PD activity identifying nearly all male hemizygotes and female homozygotes, and some heterozygotes. Unfortunately G6PD screening is usually unavailable at point of care and as a consequence radical cure is greatly underused. As both haemolytic risk (determined by the prevalence and severity of G6PD deficiency polymorphisms) and relapse rates vary there has been considerable uncertainty in both policies and practices related to G6PD testing and use of primaquine for radical cure.</p><p> Review of available information on the prevalence and severity of G6PD variants together with countries’ policies for the use of primaquine and G6PD testing confirms a wide range of practices. There remains lack of consensus on the requirement for G6PD testing before prescribing primaquine radical cure regimens. Despite substantially lower haemolytic risks, implementation of SLD primaquine as a P. falciparum gametocytocide also varies. In Africa, a few countries have recently adopted SLD primaquine, yet many with areas of low seasonal transmission do not use primaquine as an antimalarial at all. Most countries which recommended the higher 0.75mg/kg single primaquine dose for falciparum malaria (e.g. most countries in the Americas) have not changed their recommendation. Some vivax malaria endemic countries where G6PD testing is generally unavailable have adopted the once weekly radical cure regimen (0.75mg/kg/week for 8 weeks) known to be safer in less severe G6PD deficiency variants. There is substantial room for improvement in radical cure policies and practices. </p> |
| spellingShingle | Recht, J Ashley, E White, N Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title | Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title_full | Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title_fullStr | Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title_full_unstemmed | Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title_short | Use of primaquine and glucose-6-phosphate dehydrogenase deficiency testing: divergent policies and practices in malaria endemic countries |
| title_sort | use of primaquine and glucose 6 phosphate dehydrogenase deficiency testing divergent policies and practices in malaria endemic countries |
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