Wellcome Trust-Mahosot Hospital-Oxford University Tropical Medicine Research Collaboration, Mahosot Hospital, Vientiane, Lao PDR.
Malar J. 2012 Jun 8;11:184. doi: 10.1186/1475-2875-11-184.
The Lao Government changed the national policy for uncomplicated Plasmodium falciparum malaria from chloroquine to artemether-lumefantrine (AL) in 2005. Since then, no information on AL efficacy has been reported. With evidence of resistance to artemisinin derivatives in adjacent Cambodia, there has been a concern as to AL efficacy. Monitoring of AL efficacy would help the Lao Government to make decisions on appropriate malaria treatment.
The efficacy of a three-day, twice daily oral artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in Xepon District, Savannakhet Province, southern Laos was studied over 42 days follow-up. This was part of a trial of thiamin supplementation in falciparum malaria.
Of 630 patients with P. falciparum enrolled in the trial of thiamin treatment, 549 (87%, 357 children ≤15 years and 192 adults) were included in this study. The per protocol 42-day cure rates were 97% (524/541) [96% (337/352) for children and 99% (187/189) for adults, p = 0.042]. By conventional intention-to-treat analysis, the 42-day cure rates adjusted for re-infection, were 97% (532/549) [96% (342/357) in children and 99% (190/192) in adults, p = 0.042]. The proportion of patients who remained parasitaemic at day 1 after treatment was significantly higher in children [33% (116/356)] compared to adults [15% (28/192)] (p < 0.001) and only one adult patient had detectable parasitaemia on day 2. There were no serious adverse events. Potential side effects after treatment were reported more commonly in adults (32%) compared to children (15%) (p < 0.001). Patients with recrudescent infections were significantly younger, had longer mean time to fever clearance, and had longer median time to parasite clearance compared to those who were cured.
The current nationally-recommended anti-malarial treatment (artemether-lumefantrine) remains highly efficacious for the treatment of uncomplicated falciparum malaria five years after introduction in Laos. Regular monitoring is required in case artemisinin-resistant P. falciparum parasites should appear.
ISRCTN85411059.
2005 年,老挝政府将复杂型恶性疟的国家治疗方案从氯喹改为青蒿琥酯-甲氟喹(AL)。此后,一直没有关于 AL 疗效的信息报告。鉴于毗邻的柬埔寨出现了对青蒿素衍生物的耐药性,人们开始担心 AL 的疗效。监测 AL 的疗效将有助于老挝政府就适当的疟疾治疗做出决策。
在老挝南部色贡省 Xepon 区进行了为期 42 天的随访,评估了三天两次口服青蒿琥酯-甲氟喹治疗无并发症恶性疟的疗效。这是一项关于补充硫胺素治疗恶性疟的试验的一部分。
在参加硫胺素治疗试验的 630 名感染恶性疟的患者中,有 549 名(87%,357 名≤15 岁的儿童和 192 名成人)被纳入本研究。基于方案的 42 天治愈率为 97%(524/541)[96%(337/352)为儿童,99%(187/189)为成人,p=0.042]。通过常规意向治疗分析,调整再感染后,42 天的治愈率为 97%(532/549)[96%(342/357)为儿童,99%(190/192)为成人,p=0.042]。治疗后第 1 天仍有寄生虫血症的患者比例,儿童(33%,116/356)明显高于成人(15%,28/192)(p<0.001),且仅 1 名成年患者在第 2 天出现可检测到的寄生虫血症。无严重不良事件发生。治疗后成人(32%)比儿童(15%)更常报告潜在的副作用(p<0.001)。复发性感染患者的年龄明显更小,退热时间的平均时间更长,寄生虫清除时间的中位数也更长。
在老挝引入五年后,目前国家推荐的抗疟治疗药物(青蒿琥酯-甲氟喹)对治疗无并发症恶性疟仍然非常有效。应定期监测,以防出现对青蒿素的恶性疟寄生虫耐药。
ISRCTN85411059。