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首页> 外文期刊>Malaria Journal >Therapeutic efficacy of artemether-lumefantrine on treatment of uncomplicated Plasmodium falciparum mono-infection in an area of high malaria transmission in Zambia
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Therapeutic efficacy of artemether-lumefantrine on treatment of uncomplicated Plasmodium falciparum mono-infection in an area of high malaria transmission in Zambia

机译:蒿甲醚-氟美汀治疗赞比亚疟疾高发地区单纯性恶性疟原虫单株感染的治疗效果

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Background Anti-malarial drug resistance continues to be a leading threat to ongoing malaria control efforts and calls for continued monitoring of the efficacy of these drugs in order to inform national anti-malarial drug policy decision-making. This study assessed the therapeutic efficacy and safety of artemether-lumefantrine (AL)(Coartem?) for the treatment of uncomplicated Plasmodium falciparum malaria in two sentinel high malaria transmission districts in the Eastern Province of Zambia in persons aged six months and above, excluding women aged 12 to 18 years. Methods This was an observational cohort of 176 symptomatic patients diagnosed with uncomplicated Plasmodium falciparum mono-infection. A World Health Organization (WHO)-standardized 28-day assessment protocol was used to assess clinical and parasitological responses to directly observed AL treatment of uncomplicated malaria. DNA polymerase chain reaction (PCR) analysis for molecular markers of AL resistance was conducted on positive blood samples and differentiated recrudescence from re-infections of the malaria parasites. Results All patients (CI 97.6-100) had adequate clinical and parasitological responses to treatment with AL. At the time of enrolment, mean slide positivity among study participants was 71.8% and 55.2% in Katete and Chipata, respectively. From a mean parasite density of 55,087, 98% of the study participants presented with zero parasitaemia by day 3 of the study. Fever clearance occurred within 24 hours of treatment with AL. However mean parasite density declines were most dramatic in participants in the older age. No adverse reactions to AL treatment were observed during the study. Conclusion AL remains a safe and efficacious drug for the treatment of uncomplicated Plasmodium falciparum malaria in Zambia, endemic for malaria, with some provinces experiencing high transmission intensity. However, the delayed parasite clearance in younger patients calls for further sentinel and periodical monitoring of AL efficacy in different areas of the country.
机译:背景技术抗疟药耐药性仍然是对正在进行的疟疾控制工作的主要威胁,并呼吁继续监测这些药物的功效,以便为国家抗疟药政策决策提供依据。本研究评估了赞比亚东部省两个前哨高疟疾传播区中六个月及以上年龄的人群(女性除外)使用蒿甲醚-荧光粉(AL)(Coartem?)治疗单纯性恶性疟原虫疟疾的疗效和安全性。年龄12至18岁。方法这是对176例经诊断为单纯性恶性疟原虫单一感染的有症状患者的观察性队列。使用世界卫生组织(WHO)标准化的28天评估协议,评估对直接观察到的AL对复杂性疟疾治疗的临床和寄生虫学反应。在阳性血液样本上进行了AL抵抗分子标记的DNA聚合酶链反应(PCR)分析,并从疟原虫的再次感染中区分了复发。结果所有患者(CI 97.6-100)对AL治疗均具有足够的临床和寄生虫学反应。入学时,研究参与者的平均滑坡阳性率在凯特和奇帕塔分别为71.8%和55.2%。在平均寄生虫密度为55,087的情况下,到研究的第3天,有98%的研究参与者呈现出零寄生虫血症。在AL治疗后24小时内发烧。但是,平均寄生虫密度下降在老年参与者中最为明显。在研究过程中未观察到对AL治疗的不良反应。结论AL仍然是一种安全有效的药物,可用于治疗疟疾流行的赞比亚单纯性恶性疟原虫疟疾,有些省的传播强度很高。但是,年轻患者中寄生虫清除的延迟要求在该国不同地区进一步定期和定期监测AL的疗效。

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