Primaquine for Plasmodium vivax malaria treatment - Authors' reply.
Primaquine for Plasmodium vivax malaria treatment - Authors' reply.
复制标题
伯氨喹用于治疗间日疟原虫疟疾 - 作者的回复。
DOI:
10.1016/s0140-6736(20)30217-8
复制
发表时间:
2020
期刊:
影响因子:
--
通讯作者:
Price RN
中科院分区:
文献类型:
--
作者:
Price RN
We agree with Harin Karunajeewa and Robert James that radical cure of Plasmodium vivax malaria needs to be deployed more widely. The question is, how do we achieve this? Shortening the treatment course and thereby improving adherence is an important step in the right direction. 1 Primaquine regimens are usually extended over 14 days to reduce the daily dose and thereby improve tolerability and safety. The main adverse event risk is haemolysis in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. The primary reason why the prolonged regimen is still recommended is the lack of G6PD testing in vivax-endemic countries. 2 Novel point-of-care G6PD tests herald a new era, in which the use of different dosing regimens can be explored. 3, 4 We also agree that the adverse effects of 8-aminoquinolines should not be trivialised, but equally they should not be exaggerated. The adverse events following the 7 day primaquine regimen in the IMPROV study5 give rise to caution; however, we believe that they can be mitigated by pointof-care screening for G6PD deficiency, administering primaquine with food to reduce abdominal pain, and promoting awareness and understanding of the haemolytic risk so that patients