首页> 外文OA文献 >Efficacy of chloroquine, chloroquine plus sulphadoxine-pyrimethamine, and amodiaquine for treatment of vivax malaria in Bangka island, Indonesia: a randomized trial
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Efficacy of chloroquine, chloroquine plus sulphadoxine-pyrimethamine, and amodiaquine for treatment of vivax malaria in Bangka island, Indonesia: a randomized trial

机译:氯喹,氯喹加硫代胺 - 吡米甲胺和氨基胺治疗曼卡岛,印度尼西亚的疟疾治疗疗效:随机试验

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摘要

Plasmodium vivax malaria resistant to chloroquine is alarming in Indonesia and has been also reported in other countries. An alternative drug is needed. The study was a prospective evaluation and a comparative study of the therapeutic efficacy of chloroquine 25 mg base/kg bw for 3 days (CQ3, n=75), CQ3 plus sulfadoxine-pyrimethamine based on pyrimethamine dosage of 1.25 mg/kg bw single dose (SP1) [CQ3+SP1, n=84] and amodiaquine 25 mg base/kg bw for 3 days (AQ3, n=83) in symptomatic vivax malaria patients in children and adults. The new version of 2001 WHO test system was used in this study. PCR for genotyping was also done to validate and confirm the treatment outcomes. The therapeutic efficacy of CQ3, CQ3+SP1 and AQ3 on day 14 were very high (94.4%, 97.4% and 98.8%), and dropped on day 28 (81.7%, 87.2% and 96.2% by evaluable analysis; 78.9%. 82.0% and 92.5% after confirmation with PCR; and 74.7%, 78.0% and 90.2% by intention to treat analysis). Most of the ACPR cases (>96%) showed hematological recovery. Gametocyte carriages were documented on day 7 (2.9%, 1.3% and 1.2%), day 14 (4.3%, 1.3% and 1.2%) and day 28 (6.6%, 4.2% and none) in CQ3, CQ3+SP1 and AQ3 groups. Of these 3 regimens, AQ3 showed a better therapeutic efficacy than CQ3 and combined CQ3+SP1 by day 28. Introducing primaquine at the beginning of treatment day or giving a radical treatment in vivax malaria may improve the cure rate. (Med J Indones 2008; 17: 96-106)Keywords: P.vivax, chloroquine, sulfadoxine-pyrimethamine,amodiaquine, artesunate
机译:间日疟对氯喹耐药印尼是惊人的,并已在其他国家也报告。需要一种替代药物。该研究是一项前瞻性的评估和氯喹25mg的碱/ kg体重的3天的治疗功效的比较研究(CQ3,N = 75),CQ3加磺胺多辛 - 乙胺嘧啶基于1.25 mg / kg体重的单剂量的乙胺嘧啶剂量(SP1)[CQ3 + SP1中,n = 84]和阿莫地25毫克碱/ kg体重用于对症间日疟患者在儿童和成人3天(AQ3中,n = 83)。 2001年,世界卫生组织测试系统的新版本在本研究中使用。 PCR基因分型也做了验证和确认的治疗结果。 CQ3的治疗功效,CQ3 + SP1和AQ3第14天非常高(94.4%,97.4%和98.8%),并滴在被评估的分析28天(81.7%,87.2%和96.2%; 78.9%82.0 %,并用PCR确认后为92.5%;和74.7%,78.0%和意向治疗分析90.2%)。大多数的ACPR例(> 96%)显示出造血功能恢复。配子体支架被记录在CQ3,CQ3 + SP1和AQ37天(2.9%,1.3%和1.2%),14天(4.3%,1.3%和1.2%)和第28天(6.6%,4.2%和无)组。这些3个方案的,AQ3表现出更好的治疗效果比CQ3和组合CQ3 + SP1由第28天,在治疗一天的开始引入伯氨喹或给予在间日疟自由基处理可以提高治愈率。 (医学杂志Indones 2008; 17:96-106)关键词:间日疟原虫,氯喹,磺胺多辛 - 乙胺嘧啶,阿莫地喹,青蒿琥酯

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