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首页> 外文期刊>The Internet Journal of Infectious Diseases >Efficacy of Arthemether – Lumenfantrine against Uncomplicated Plasmodium falciparum Malaria in Infants and Children in Uyo, Nigeria
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Efficacy of Arthemether – Lumenfantrine against Uncomplicated Plasmodium falciparum Malaria in Infants and Children in Uyo, Nigeria

机译:蒿甲醚的功效– Lumefantrine对尼日利亚乌约的婴幼儿单纯性恶性疟原虫疟疾的预防作用

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Coartem is recently approved artemisinin- based tablet that provides effective antimalarial treatment for children in many sub-saharan countries. This study evaluates the efficacy of this drug in 120 children weighing 5-25kg with uncomplicated falciparum malaria in Uyo. Six doses of coartem were given over 3 days with follow up at 7, 14 and 28 days. Treatment rapidly cleared parasitaemia and fever. The overall 28-day cure was 80.1%. Cure rate at 7 and 14 days exceeded 90%. No severe adverse side-effects, clinical failures or parasitological failures were observed among these patient. Coartem therefore appear efficacious for the treatment of uncomplicated malaria in Nigeria. Introduction Malaria is one of the most serious diseases in the tropics claiming millions of lives yearly. Malaria in Africa mainly due to a blood parasite, Plasmodium falciparum. Children under the age of five years and pregnant women are the most afflicted with this debilitating disease. The problem of malaria is compounded by the declining sensitivity of P. falciparum to the array of available antimalarial drugs1. Resistance to antimalarial is responsible for an increase in morbidity and mortality in many sub-saharan countries2. In Nigeria malaria is identified as the most prevalent type of infective and parasitic disease3. Estimates show that this parasitic disease accounts for no less than 300,000 deaths from more than 20 million clinical attacks while 10-20% of hospital admissions are due to malaria. The problem of malaria in Nigeria is complicated by the emergence of drug resistant malaria parasites. As a response to increasing levels of resistance to antimalarials drug, World Health Organisation recommends that all countries experiencing resistance to conventional monotherapies such as chloroquine, amodiaquine or sulfadoxine – Pyrimethamine (SP) should use combination therapies preferably those containing artemisnin derivatives (ACTs – artemisinin based combination therapies) for falciparum malaria4.Artemether – Lumefantrine also known under the brand name coartemR is a new artemisinin – containing fixed combination antimalarial treatment that has proved to be well tolerated and highly effective against Plamodium falciparum 5. The goal of chemotherapy in malaria is often to effect a clinical cure or parasitological clearance or to limit the development of drug resistance6. Accurate and effective surveillance systems for monitoring antimalarial drug efficacy have been recognized as an essential basis for decisions on the use of drug. The main purpose of this study was to ascertain the therapeutic efficacy of coartem in the treatment of uncomplicated P. falciparum malaria in Uyo, South Eastern Nigeria. The data obtained from this study would provide useful information for future management of uncomplicated falciparum malaria in Nigeria. Material And Methods Study SiteThe study was carried out between July and December, 2007 in Uyo, Southern Nigeria. Uyo is located on latitude 5003' North and longitude 7057' East. It is the capital city of Akwa Ibom State Nigeria. Akwa Ibom State is located within the lowland coastal plain region of Nigeria between latitude 4032' and 5053' North and longitude 7025' and 8025' East. The state lies on the Eastern Niger Delta and shares the hot humid tropical climate of the region marked by two distinct seasons – dry (November to March) and wet (April to October) seasons. As in the entire country malaria is endemic and the transmission is intense (stable) and peaks during the rainy season. PatientsThis study followed the World Health Organisation7 recommendation, for the in-vivo investigations of antimalarial drug efficacy, in terms of treatment, follow up and data analysis. The study was conducted in children with fever weighing 5-25kg, who were attending Nedeke Paediatrics Specialist Hospital, Uyo, using the WHO 28 day in-vivo protocol, patients, were enrolled in the study, if they satisfied the following inclusion crite
机译:复方蒿甲醚是最近批准的基于青蒿素的片剂,可为许多撒哈拉以南国家的儿童提供有效的抗疟疾治疗。这项研究评估了该药物对Uyo地区120例体重5-25kg并发单纯性恶性疟疾的儿童的疗效。在3天内给予六剂复方蒿甲醚,并在7、14和28天进行随访。治疗迅速清除了寄生虫血症和发烧。 28天总治愈率为80.1%。 7天和14天的治愈率超过90%。这些患者中未观察到严重的不良副作用,临床失败或寄生虫学失败。因此,复方蒿甲醚似乎对治疗尼日利亚的单纯性疟疾有效。简介疟疾是热带地区最严重的疾病之一,每年夺去数百万人的生命。非洲的疟疾主要归因于血液寄生虫恶性疟原虫。五岁以下的儿童和孕妇最容易患上这种令人衰弱的疾病。恶性疟原虫对现有抗疟药的敏感性下降,加剧了疟疾问题。在许多撒哈拉以南国家,对疟疾的耐药性导致发病率和死亡率增加2。在尼日利亚,疟疾被确定为最流行的传染病和寄生虫病3。估计显示,这种寄生虫病导致超过2000万例临床发作的死亡人数不少于300,000,而住院的10-20%是由于疟疾。尼日利亚的疟疾问题由于耐药疟疾寄生虫的出现而变得复杂。为了应对日益增加的抗疟药耐药性,世界卫生组织建议所有对常规单一疗法(例如氯喹,氨二喹或磺胺多辛-乙胺嘧啶)产生抗药性的国家都应使用组合疗法,最好使用那些含有青蒿素衍生物(ACTs-青蒿素的药物)蒿甲醚– Lumefantrine,也以商品名coartemR着名,是一种新的青蒿素–包含固定的联合抗疟疾治疗,已被证明对恶性疟原虫5具有很好的耐受性和高度有效。疟疾化疗的目标通常是进行临床治愈或寄生虫清除或限制耐药性的发展6。公认的用于监测抗疟药功效的准确有效的监测系统是决定药物使用的必要基础。这项研究的主要目的是确定复方蒿甲醚在尼日利亚东南部乌约的单纯性恶性疟原虫疟疾的治疗中的疗效。从这项研究中获得的数据将为将来在尼日利亚控制简单的恶性疟疾提供有用的信息。材料和方法研究地点该研究于2007年7月至12月在尼日利亚南部的乌约进行。乌约位于北纬5003',东经7057'。它是阿克瓦伊博姆州尼日利亚的首都。阿夸伊博姆州位于尼日利亚低地沿海平原地区,北纬4032'和5053',东经7025'和8025'。该州位于尼日尔东部三角洲,并享有该地区炎热潮湿的热带气候,其特征在于两个明显的季节-干燥(11月至3月)和潮湿(4月至10月)季节。与整个国家一样,疟疾是地方病,传播很强烈(稳定),在雨季达到高峰。患者本研究遵循了世界卫生组织的建议7,用于就治疗,随访和数据分析方面进行抗疟药功效的体内研究。这项研究是根据WHO 28天的体内实验方案,对正在乌尤内德克儿科专科医院就诊的5-25kg的发烧儿童进行的,如果他们满足以下纳入标准,则将其纳入研究范围

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