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首页> 外文期刊>Journal of Tropical Pediatrics >Therapeutic efficacy and effect on gametocyte carriage of an artemisinin and a non-based combination treatment in childrenn with uncomplicated P. falciparum malaria, living in an area with high-level chloroquine resistance
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Therapeutic efficacy and effect on gametocyte carriage of an artemisinin and a non-based combination treatment in childrenn with uncomplicated P. falciparum malaria, living in an area with high-level chloroquine resistance

机译:生活在高氯喹耐药地区的单纯性恶性疟原虫疟疾儿童的青蒿素和非基础联合治疗对青蒿素的治疗功效和影响

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Combination therapy with artemesinin or non-artemesinin-based antimalarials (ACTs or NACTs) are known to retard the development and progression of drug resistance in Plasmodium falciparum (P. falciparum). The optimal antimalarial combinations in Africa are yet unknown. We evaluate the therapeutic efficacy and effects on gametocyte carriage of Artemether–Lumefantrine (AL) and Amodiaquine–Sulfalene/Pyrimethamine (ASP) in children with P. falciparum malaria in an endemic area. One-hundred and thirty-nine children aged ≤10 years with uncomplicated P. falciparum malaria were enrolled. The primary end points were adequate clinical and parasitological response (ACPR), late parasitological failure(LPF), late clinical failure (LCF) and early treatment failure (ETF). Polymerase chain reaction (PCR)-corrected cure rates on days 14–42 and gametocyte carriage rates were determined. Fever clearance time was significantly shorter (P = 0.009) with ASP, but parasite clearance time was similar with both regimens. Day 28 cure rates were 91.4 and 89.9% (PCR-corrected) for AL and ASP respectively. Both regimens were well tolerated. Overall, gametocyte carriage before and following treatment were similar. Both combinations were found effective and comparable for treatment of acute, uncomplicated, P. falciparum malaria.
机译:已知与青蒿素或非青蒿素类抗疟药(ACT或NACT)联合使用可延缓恶性疟原虫(恶性疟原虫)耐药性的发展和进程。非洲的最佳抗疟疾组合尚不清楚。我们评估了流行区恶性疟原虫患儿的蒿甲醚-卢美他汀(AL)和阿莫地喹-亚砜/乙胺(ASP)对配子体运输的治疗效果和效果。入选了139例年龄≤10岁的未患恶性疟原虫疟疾的儿童。主要终点是充分的临床和寄生虫学响应(ACPR),晚期寄生虫学衰竭(LPF),晚期临床失败(LCF)和早期治疗失败(ETF)。确定了聚合酶链反应(PCR)在14-42天时的治愈率和配子细胞的转运率。 ASP的发烧清除时间明显缩短(P = 0.009),但两种方案的寄生虫清除时间均相似。第28天的AL和ASP治愈率分别为91.4%和89.9%(经PCR校正)。两种方案均耐受良好。总体而言,治疗前后的配子细胞转运相似。发现这两种组合物对于治疗急性,简单的恶性疟原虫疟疾均有效且具有可比性。

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    《Journal of Tropical Pediatrics》 |2010年第6期|p.398-406|共9页
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