首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Patients' adherence and clinical effectiveness of a 14-day course of primaquine when given with a 3-day chloroquine in patients with Plasmodium vivax at the Thai-Myanmar border
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Patients' adherence and clinical effectiveness of a 14-day course of primaquine when given with a 3-day chloroquine in patients with Plasmodium vivax at the Thai-Myanmar border

机译:在泰国-缅甸边境的间日疟原虫患者中,给予3天的氯喹联合14天疗程的伯氨喹的患者依从性和临床有效性

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摘要

Primaquine is the only antimalarial drug available for eradicating the hypnozoite stage of Plasmodium vivax to prevent the disease from recurring. However, one limitation of its clinical use is the long treatment course of 14 days, which may result in poor patients' adherence and low treatment efficacy. The aim of the current study was to assess patients' adherence and the clinical effectiveness of the unsupervised standard 14-day primaquine regimen (daily dose of 15 mg base/kg body weight daily for 14 days) when given together with 3-day chloroquine (25 mg base/kg body weight over 3 days). The study was conducted in 85 patients with P. vivax malaria in a malaria endemic area along the Thai Myanmar border. Patients' adherence to primaquine therapy was assessed based on primaquine concentrations in finger-prick dried blood spot (DBS) samples alongside patients' self-reporting on drug administration and pill counting methods. Results suggest high rate of patients' adherence to this 14-day primaquine regimen (95-98% based on primaquine concentrations in DBS on days 3, 7, and 14 of treatment, and 100% based on patients' self-reporting and pill counting methods. Clinical effectiveness was 100% during the 42-day follow-up. (C) 2015 Elsevier B.V. All rights reserved.
机译:primaquine是唯一可用于消除间日疟原虫次生子期以预防疾病复发的抗疟药。但是,其临床使用的局限性是治疗期长达14天,这可能导致患者依从性差和治疗效果差。本研究的目的是评估与3天氯喹(3,4-二甲基环己基环戊烯醚)联合使用的无监督标准14天伯氨喹方案(每日剂量15 mg碱/ kg体重,每天14天)的患者依从性和临床有效性。 25毫克/千克体重,持续3天)。该研究在泰国缅甸边境沿线的疟疾流行地区对85名间日疟原虫进行了研究。根据手指刺干血斑(DBS)样品中的伯氨喹浓度以及患者对药物管理和药丸计数方法的自我报告,评估患者对伯氨喹治疗的依从性。结果表明,患者对这种为期14天的伯氨喹方案的依从性较高(95%至98%基于治疗3、7和14天时DBS中伯氨喹的浓度,而100%基于患者的自我报告和药丸计数方法:在42天的随访中,临床有效性为100%(C)2015 Elsevier BV保留所有权利。

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