Department of Medical Research (Lower Myanmar), Yangon, The Republic of the Union of Myanmar.
PLoS One. 2013;8(3):e57689. doi: 10.1371/journal.pone.0057689. Epub 2013 Mar 8.
Plasmodium falciparum resistance to artemisinins, the first line treatment for malaria worldwide, has been reported in western Cambodia. Resistance is characterized by significantly delayed clearance of parasites following artemisinin treatment. Artemisinin resistance has not previously been reported in Myanmar, which has the highest falciparum malaria burden among Southeast Asian countries.
A non-randomized, single-arm, open-label clinical trial of artesunate monotherapy (4 mg/kg daily for seven days) was conducted in adults with acute blood-smear positive P. falciparum malaria in Kawthaung, southern Myanmar. Parasite density was measured every 12 hours until two consecutive negative smears were obtained. Participants were followed weekly at the study clinic for three additional weeks. Co-primary endpoints included parasite clearance time (the time required for complete clearance of initial parasitemia), parasite clearance half-life (the time required for parasitemia to decrease by 50% based on the linear portion of the parasite clearance slope), and detectable parasitemia 72 hours after commencement of artesunate treatment. Drug pharmacokinetics were measured to rule out delayed clearance due to suboptimal drug levels.
The median (range) parasite clearance half-life and time were 4.8 (2.1-9.7) and 60 (24-96) hours, respectively. The frequency distributions of parasite clearance half-life and time were bimodal, with very slow parasite clearance characteristic of the slowest-clearing Cambodian parasites (half-life longer than 6.2 hours) in approximately 1/3 of infections. Fourteen of 52 participants (26.9%) had a measurable parasitemia 72 hours after initiating artesunate treatment. Parasite clearance was not associated with drug pharmacokinetics.
A subset of P. falciparum infections in southern Myanmar displayed markedly delayed clearance following artemisinin treatment, suggesting either emergence of artemisinin resistance in southern Myanmar or spread to this location from its site of origin in western Cambodia. Resistance containment efforts are underway in Myanmar.
Australian New Zealand Clinical Trials Registry ACTRN12610000896077.
恶性疟原虫对青蒿素类药物的耐药性已在柬埔寨西部报道,青蒿素类药物是全球治疗疟疾的一线药物。耐药性的特征是在青蒿素类药物治疗后寄生虫清除明显延迟。此前,在东南亚国家中疟疾负担最高的缅甸尚未报告青蒿素耐药性。
在缅甸南部的高当,进行了一项非随机、单臂、开放性临床试验,评估青蒿琥酯单药治疗(每天 4 毫克/千克,共 7 天)对急性血涂片阳性恶性疟原虫感染的成年人的疗效。每 12 小时测量一次寄生虫密度,直到连续两次涂片阴性。参与者在研究诊所每周随访 3 周。主要终点包括寄生虫清除时间(初始寄生虫血症完全清除所需的时间)、寄生虫清除半衰期(根据寄生虫清除斜率的线性部分,寄生虫血症减少 50%所需的时间)和青蒿琥酯治疗开始后 72 小时可检测到寄生虫血症。测量药物药代动力学以排除因药物水平不理想导致的清除延迟。
中位数(范围)寄生虫清除半衰期和时间分别为 4.8(2.1-9.7)和 60(24-96)小时。寄生虫清除半衰期和时间的分布呈双峰型,约 1/3 的感染中存在非常缓慢的寄生虫清除,这是柬埔寨最慢清除寄生虫的特征(半衰期长于 6.2 小时)。在 52 名参与者中,有 14 名(26.9%)在开始青蒿琥酯治疗后 72 小时可检测到寄生虫血症。寄生虫清除与药物药代动力学无关。
在缅甸南部,部分恶性疟原虫感染在青蒿素类药物治疗后清除明显延迟,这表明青蒿素耐药性在缅甸南部出现,或者从柬埔寨西部的起源地传播到该地区。缅甸正在进行耐药性控制措施。
澳大利亚和新西兰临床试验注册中心 ACTRN12610000896077。