首页> 外文OA文献 >CV8, a new combination of dihydroartemisinin, piperaquine, trimethoprim and primaquine, compared with atovaquone-proguanil against falciparum malaria in Vietnam
【2h】

CV8, a new combination of dihydroartemisinin, piperaquine, trimethoprim and primaquine, compared with atovaquone-proguanil against falciparum malaria in Vietnam

机译:CV8,一种双氢青蒿素,哌喹,甲氧苄啶和伯氨喹的新组合,与阿托伐醌-鸟嘌呤相比,在越南对抗恶性疟疾

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

OBJECTIVES To study a new combination, based on dihydroartemisinin and piperaquine (CV8) and atovaquone/proguanil (Malarone) for treatment of uncomplicated falciparum malaria in Vietnam. METHODS Vietnamese adults with falciparum malaria were allocated randomly to treatment with dihydroartemisinin/piperaquine/trimethoprim/primaquine 256/2560/720/40 mg (CV8, n = 84) or Malarone 3000/1200 mg (n = 81), both over 3 days. Patients were followed-up for 28 days. RESULTS All patients recovered rapidly. The mean (95% CI) parasite elimination half-life of CV8 was 6.8 h (6.2-7.4) and of Malarone 6.5 h (6.1-6.9) (P = 0.4). Complete parasite clearance time was 35 (31-39) and 34 h (31-38) (P = 0.9). The 28-day cure rate was 94% and 95%, respectively (odds ratio 0.84, 95% CI 0.18-3.81). No significant side-effects were found. CONCLUSION CV8 and Malarone are effective combinations against multi-drug resistant falciparum malaria. CV8 has the advantage of a low price
机译:目的研究一种基于双氢青蒿素和哌喹(CV8)和阿托伐醌/丙胍(马拉隆)的新组合,用于治疗越南的单纯性恶性疟疾。方法越南成年人恶性疟原虫被随机分配接受双氢青蒿素/哌喹/甲氧苄氨苄/伯氨喹256/2560/720/40 mg(CV8,n = 84)或Malarone 3000/1200 mg(n = 81)的治疗,均为三天。对患者进行了28天的随访。结果所有患者均迅速康复。 CV8的平均(95%CI)寄生虫消除半衰期为6.8 h(6.2-7.4),而Malarone为6.5 h(6.1-6.9)(P = 0.4)。完全的寄生虫清除时间为35(31-39)和34 h(31-38)(P = 0.9)。 28天治愈率分别为94%和95%(几率0.84、95%CI 0.18-3.81)。没有发现明显的副作用。结论CV8和Malarone是对抗多重耐药性恶性疟疾的有效组合。 CV8具有价格低廉的优势

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号