首页> 外文OA文献 >An open, randomized comparison of artesunate plus mefloquine vs. dihydroartemisinin-piperaquine for the treatment of uncomplicated Plasmodium falciparum malaria in the Lao People's Democratic Republic (Laos).
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An open, randomized comparison of artesunate plus mefloquine vs. dihydroartemisinin-piperaquine for the treatment of uncomplicated Plasmodium falciparum malaria in the Lao People's Democratic Republic (Laos).

机译:青蒿琥酯加甲氟喹与二氢青蒿素-哌喹用于治疗老挝人民民主共和国(老挝)单纯性恶性疟原虫的开放式,随机对照。

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摘要

OBJECTIVE: To determine the efficacy and safety of oral dihydroartemisinin-piperaquine (DP, Artekin) in the treatment of uncomplicated Plasmodium falciparum malaria in southern Laos. METHODS: An open, randomized clinical trial of oral artesunate-mefloquine (AM) vs. DP in 220 patients with acute uncomplicated falciparum malaria in Savannakhet Province, Laos. RESULTS: The 42-day cure rates (95% CI), as determined by survival analysis and adjusted for reinfection, were excellent and similar for the two groups [99 (94-100)% and 100 (100-100)% for AM and DP, respectively]. The median (range) fever and parasite clearance times for the AM and DP groups were also similar [20 (4-63) h and 2 (1-4) days vs. 20 (7-57) and 2 (1-4) days, logrank P = 0.4 and 0.17, respectively]. There were more patients with at least one potential side effect following treatment in the AM group when compared with the DP group [64/110 (58%) vs. 48/110 (44%), respectively, P = 0.031]. CONCLUSION: Dihydroartemisinin-piperaquine did not have superior efficacy to AM for the treatment of uncomplicated falciparum malaria in Laos but was associated with fewer adverse effects.
机译:目的:确定口服二氢青蒿素-哌喹(DP,Artekin)治疗老挝南部单纯性恶性疟原虫的疗效和安全性。方法:在老挝沙湾拿吉省进行的220例急性单纯性恶性疟疾患者中,口服青蒿琥酯-甲氟喹(AM)与DP的开放性随机临床试验。结果:通过生存分析确定并经重新感染调整的42天治愈率(95%CI)对于两组而言是极好且相似的[AM分别为99(94-100)%和100(100-100)%和DP分别]。 AM和DP组的中值(范围)发烧和寄生虫清除时间也相似[20(4-63)h和2(1-4)天,而20(7-57)和2(1-4)天天,logrank P分别为0.4和0.17]。与DP组相比,AM组中治疗后至少有一种潜在副作用的患者更多[分别为64/110(58%)和48/110(44%),P = 0.031]。结论:双氢青蒿素-哌喹对老挝单纯性恶性疟疾的治疗效果不及AM,但不良反应较少。

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