Falade C O, Dada-Adegbola H O, Ogunkunle O O, Oguike M C, Nash O, Ademowo O G
Department of Pharmacology, Therapeutics, University of Ibadan, Ibadan, Nigeria.
Med Princ Pract. 2014;23(3):204-11. doi: 10.1159/000360578. Epub 2014 Apr 8.
To evaluate the comparative efficacy and safety of artemether-lumefantrine (AL), artesunate-amodiaquine (ASAQ) and artesunate-amodiaquine-chlorpheniramine (AQC) for the treatment of acute uncomplicated malaria among Southwest Nigerian children.
One hundred and sixty children aged 6 months to 14 years with acute uncomplicated malaria were randomized to AL (n = 53), ASAQ (n = 53), or AQC (n = 54). Enrollees were seen daily on days 0-3 and then on days 7, 14, 21, 28 and 42 for clinical and parasitological evaluations. Paired samples of genomic DNA at enrolment and at the time of recurrent parasitaemia were genotyped using nested PCR to distinguish between reinfection and recrudescence. Detailed haematological and biochemical evaluations were carried out in a subset of enrollees on days 0, 7 and 28 as part of a safety evaluation.
Of the 160 children, 144 (90%) completed the study. The mean fever clearance times and parasite clearance times for AL, ASAQ and AQC were comparable (p = 0.94 and p = 0.122, respectively). On day 14, the adequate clinical and parasitological response (ACPR) for AL and AQC was 100% and for ASAQ it was 90% (p = 0.39). The PCR-uncorrected results on days 28 and 42 and the ACPR-corrected results on day 42 were similar for all drugs (p = 0.62 and p = 0.56, respectively). AQC resulted in the best parasite clearance and haematological recovery on day 2 (p = 0.022 and p = 0.018, respectively). Biochemical parameters were not adversely affected by the three artemisinin-based combination therapies (ACTs) and these were well tolerated.
The three ACTs were efficacious and safe, but AQC resulted in a better haematological recovery on day 2 and higher cure rates throughout the study period.
评估蒿甲醚-本芴醇(AL)、青蒿琥酯-阿莫地喹(ASAQ)和青蒿琥酯-阿莫地喹-氯苯那敏(AQC)治疗尼日利亚西南部儿童急性非复杂性疟疾的相对疗效和安全性。
160名年龄在6个月至14岁的急性非复杂性疟疾儿童被随机分为AL组(n = 53)、ASAQ组(n = 53)或AQC组(n = 54)。在第0至3天每天对入组者进行观察,然后在第7、14、21、28和42天进行临床和寄生虫学评估。使用巢式PCR对入组时和复发性寄生虫血症时的配对基因组DNA样本进行基因分型,以区分再感染和复发。作为安全性评估的一部分,在第0、7和28天对一部分入组者进行了详细的血液学和生化评估。
在这160名儿童中,144名(90%)完成了研究。AL、ASAQ和AQC的平均退热时间和寄生虫清除时间相当(分别为p = 0.94和p = 0.122)。在第14天,AL和AQC的充分临床和寄生虫学反应(ACPR)为100%,ASAQ为90%(p = 0.39)。所有药物在第28天和第42天的PCR未校正结果以及第42天的ACPR校正结果相似(分别为p = 0.62和p = 0.56)。AQC在第2天导致最佳寄生虫清除和血液学恢复(分别为p = 0.022和p = 0.018)。三种基于青蒿素的联合疗法(ACTs)对生化参数没有不利影响,且耐受性良好。
三种ACTs有效且安全,但AQC在第2天导致更好的血液学恢复,并且在整个研究期间治愈率更高。