...
首页> 外文期刊>Malaria Journal >Monitoring Plasmodium vivax chloroquine sensitivity along China-Myanmar border of Yunnan Province, China during 2008–2013
【24h】

Monitoring Plasmodium vivax chloroquine sensitivity along China-Myanmar border of Yunnan Province, China during 2008–2013

机译:2008-2013年间中国云南省中缅边境间日疟原虫氯喹敏感性监测

获取原文

摘要

Background Plasmodium vivax is the most widespread of the malaria parasites infecting human hosts. In malaria-eliminating settings, both imported and local malaria predominantly occurs in border areas, and most of them are P. vivax. Chloroquine (CQ) is the first-line drug for P. vivax treatment in China. To understand CQ sensitivity in P. vivax, in vivo monitoring of CQ resistance was conducted along the China-Myanmar border from 2008 to 2013. Methods Eligible patients with mono-infections of P. vivax were recruited to this study after obtaining full informed consent. CQ tablets for different categories of kg body weight ranges were given once a day for three days. Patients were followed up for 28 days. PCR was conducted to distinguish between re-infection and recrudescence, to confirm the Plasmodium species. The data were entered and analysed by the Kaplan-Meier method. Treatment outcome and sensitivity were classified according to the WHO recommended standards. Results 603 patients were completed valid follow-up. The fever clearance time and asexual parasite clearance times were, respectively, 22.2?±?10.2 and 38.1?±?12.6 hours. 594 (98.5%) patients were adequate clinical and parasitological response (ACPR), and nine (1.5%) patients, who were late clinical failure (LCF) or resistant response level I (RI), were imported from the neighbouring districts of Myanmar. Conclusion In terms of efficacy, CQ is still effective for vivax malaria treatment. Plasmodium vivax CQ sensitivity had not significantly changed along the China-Myanmar border of Yunnan Province, China.
机译:背景间日疟原虫是感染人类宿主的最广泛的疟原虫。在消除疟疾的地区,进口和局部疟疾都主要发生在边境地区,其中大多数是间日疟原虫。氯喹(CQ)是中国间日疟原虫治疗的一线药物。为了了解间日疟原虫的CQ敏感性,于2008年至2013年在中缅边境进行了对CQ耐药性的体内监测。方法在获得完全知情同意后,将符合条件的间日疟原虫单一感染患者纳入本研究。每天一次,每千克体重范围使用一次CQ片剂,持续三天。对患者进行了28天的随访。进行PCR以区分再感染和再发,以确认疟原虫种类。输入数据并通过Kaplan-Meier方法进行分析。治疗结果和敏感性根据WHO推荐标准进行分类。结果603例患者均完成了有效的随访。发烧清除时间和无性寄生虫清除时间分别为22.2±±10.2小时和38.1±±12.6小时。 594(98.5%)例患者具有足够的临床和寄生虫学反应(ACPR),并且有9例(1.5%)患者为晚期临床衰竭(LCF)或I级抗药性(RI),来自缅甸附近地区。结论就疗效而言,CQ仍可有效治疗间日疟。在中国云南省的中缅边境,间日疟原虫的CQ敏感性没有显着变化。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

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