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In vivo susceptibility of Plasmodium falciparum to artesunate in Binh Phuoc Province, Vietnam.

机译:越南平富省恶性疟原虫对青蒿琥酯的体内敏感性。

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摘要

BACKGROUND: By 2009, there were worrying signs from western Cambodia that parasitological responses to artesunate-containing treatment regimens for uncomplicated Plasmodium falciparum malaria were slower than elsewhere which suggested the emergence of artemisinin resistance. Vietnam shares a long land border with Cambodia with a large number of migrants crossing it on a daily basis. Therefore, there is an urgent need to investigate whether there is any evidence of a change in the parasitological response to the artemisinin derivatives in Vietnam. METHODS: From August 2010 to May 2011, a randomized controlled clinical trial in uncomplicated falciparum malaria was conducted to compare two doses of artesunate (AS) (2mg/kg/day versus 4 mg/kg/day for three days) followed by dihydroartemisinin-piperaquine (DHA-PPQ) and a control arm of DHA-PPQ. The goal was characterization of the current efficacy of artesunate in southern Vietnam. The primary endpoint of this study was the parasite clearance half-life; secondary endpoints included the parasite reduction ratios at 24 and 48 hours and the parasite clearance time. RESULTS: 166 patients were recruited into the study. The median parasite clearance half-lives were 3.54 (AS 2mg/kg), 2.72 (AS 4mg/kg), and 2.98 hours (DHA-PPQ) (p=0.19). The median parasite-reduction ratio at 24 hours was 48 in the AS 2mg/kg group compared with 212 and 113 in the other two groups, respectively (p=0.02). The proportions of patients with a parasite clearance time of >72 hours for AS 2mg/kg, AS 4mg/kg and DHA-PPQ were 27%, 27%, and 22%, respectively. Early treatment failure occurred in two (4%) and late clinical failure occurred in one (2%) of the 55 patients in the AS 2mg/kg group, as compared with none in the other two study arms. The PCR-corrected adequate clinical and parasitological response (APCR) rates in the three groups were 94%, 100%, and 100% (p=0.04). CONCLUSIONS: This study demonstrated faster P. falciparum parasite clearance in southern Vietnam than in western Cambodia but slower clearance in comparison with historical data from Vietnam. Further studies to determine whether this represents the emergence of artemisinin resistance in this area are needed. Currently, the therapeutic response to DHA-PPQ remains satisfactory in southern Vietnam. TRIAL REGISTRATION: NTC01165372.
机译:背景:到2009年,柬埔寨西部地区出现令人担忧的迹象,表明对含青蒿琥酯的非复杂性恶性疟原虫疟疾治疗方案的寄生虫学反应要慢于其他地方,这表明青蒿素耐药性的出现。越南与柬埔寨有着漫长的陆地边界,每天都有大量移民越境。因此,迫切需要调查越南是否有任何证据表明对青蒿素衍生物的寄生虫学反应发生了变化。方法:从2010年8月至2011年5月,进行了一项无并发症恶性疟疾的随机对照临床试验,以比较两种剂量的青蒿琥酯(AS)(2mg / kg /天与4mg / kg /天,共三天),然后进行双氢青蒿素-哌喹(DHA-PPQ)和DHA-PPQ的控制臂。目标是表征越南南部青蒿琥酯目前的疗效。这项研究的主要终点是寄生虫清除半衰期。次要终点包括24小时和48小时的寄生虫减少率和寄生虫清除时间。结果:166名患者被纳入研究。中位寄生虫清除半衰期为3.54(AS 2mg / kg),2.72(AS 4mg / kg)和2.98小时(DHA-PPQ)(p = 0.19)。 AS 2mg / kg组在24小时时的中位数寄生虫减少率是48,而其他两组分别为212和113(p = 0.02)。 AS 2mg / kg,AS 4mg / kg和DHA-PPQ的寄生虫清除时间> 72小时的患者比例分别为27%,27%和22%。在AS 2mg / kg组的55名患者中,有2名(4%)发生了早期治疗失败,在2名(2%)中发生了晚期临床失败,而在其他两个研究组中则没有发生。经PCR校正的三组患者的临床和寄生虫学应答率(APCR)分别为94%,100%和100%(p = 0.04)。结论:本研究表明越南南部的恶性疟原虫寄生虫清除速度比柬埔寨西部快,但与越南的历史数据相比清除速度较慢。需要进一步研究以确定这是否代表该地区青蒿素耐药性的出现。目前,越南南部对DHA-PPQ的治疗反应仍然令人满意。试用注册:NTC01165372。

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