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根据基于年龄的剂量方案,给患有 的儿童服用磷酸萘酚喹的剂量。

Doses of primaquine administered to children with according to an age-based dose regimen.

机构信息

Pharmacy Faculty, Para Federal University , Belem, Brazil.

Global Health Division, Menzies School of Health Research and Charles Darwin University , Darwin, Australia.

出版信息

Pathog Glob Health. 2020 Oct;114(7):388-392. doi: 10.1080/20477724.2020.1799166. Epub 2020 Jul 24.

DOI:10.1080/20477724.2020.1799166
PMID:32705964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7580727/
Abstract

Primaquine is still the first-line drug to eliminate hypnozoites of . The therapeutic efficacy is related to the total dose administered. In several endemic areas, the drug is administered for children in an age-based regimen, which can lead to inadequate exposure, increasing the rates of recurrence of the infection. The present study aims to describe the mg/kg total dose of primaquine administered to children for treatment for vivax malaria when an age-based regimen is used and to measure the plasma concentrations of primaquine and carboxyprimaquine. A total of 85 children were included in the study. The total dose of primaquine administered based on mg/kg had a median value of 3.22 mg/kg. The percentage of patients with a total dose below the required dose of 3.5 mg/kg was 55.75%. The median primaquine maximum concentration was 94 ng/ml. For carboxy-primaquine, the median maximum concentration was 375 ng/ml. The results suggest that age-based dosing regimens likely lead to substantial under-dosing of primaquine, which is evident in the youngest children and is reflected in decreased levels of primaquine and carboxy-primaquine in plasma samples 13.

摘要

伯氨喹仍然是消除间日疟休眠子的一线药物。疗效与给予的总剂量有关。在几个流行地区,儿童按年龄组给药,这可能导致剂量不足,增加感染复发率。本研究旨在描述在使用年龄组方案治疗间日疟时,儿童接受的伯氨喹毫克/公斤总剂量,并测量伯氨喹和羧基伯氨喹的血浆浓度。共有 85 名儿童纳入研究。基于 mg/kg 的伯氨喹总剂量中位数为 3.22 mg/kg。总剂量低于 3.5 mg/kg 所需剂量的患者百分比为 55.75%。伯氨喹最大浓度中位数为 94ng/ml。对于羧基伯氨喹,最大浓度中位数为 375ng/ml。结果表明,基于年龄的剂量方案可能导致伯氨喹的大量剂量不足,这在最小的儿童中尤为明显,反映在血浆样本中伯氨喹和羧基伯氨喹的水平降低。

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Malar J. 2019 Jan 22;18(1):18. doi: 10.1186/s12936-019-2644-y.
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Primaquine ineligibility in anti-relapse therapy of Plasmodium vivax malaria: the problem of G6PD deficiency and cytochrome P-450 2D6 polymorphisms.在间日疟原虫抗复发治疗中禁用伯氨喹:G6PD 缺乏症和细胞色素 P-450 2D6 多态性的问题。
Malar J. 2018 Jan 22;17(1):42. doi: 10.1186/s12936-018-2190-z.
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Age, Weight, and Genotype Are Major Determinants of Primaquine Pharmacokinetics in African Children.年龄、体重和基因型是非洲儿童中伯氨喹药代动力学的主要决定因素。
Antimicrob Agents Chemother. 2017 Apr 24;61(5). doi: 10.1128/AAC.02590-16. Print 2017 May.
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BMC Med. 2016 Oct 27;14(1):171. doi: 10.1186/s12916-016-0701-8.
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