Exploration of in vivo efficacy of artemether-lumefantrine against uncomplicated Plasmodium falciparum malaria in under fives in Tabora region, Tanzania

• Published in: Malaria journal Vol. 12; no. 1; p. 60
• Main Authors: Joseph, Deokary, Kabanywanyi, Abdunoor M, Hulser, Ruth, Premji, Zulfiqarali, Minzi, Omary Ms, Mugittu, Kefas
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 11-02-2013; BioMed Central
• Subjects: Antimalarials - pharmacokinetics; Antimalarials - therapeutic use; Artemisinins - pharmacokinetics; Artemisinins - therapeutic use; Child, Preschool; Chromatography, High Pressure Liquid; Colleges & universities; Drug Combinations; Drug therapy; Drug therapy, Combination; Ethanolamines - pharmacokinetics; Ethanolamines - therapeutic use; Female; Fluorenes - pharmacokinetics; Fluorenes - therapeutic use; Health aspects; Health facilities; High performance liquid chromatography; Humans; Infant; Malaria; Malaria, Falciparum - drug therapy; Male; Plasma - chemistry; Plasmodium falciparum; Tanzania; Treatment Outcome; Tanzania
• ISSN: 1475-2875; 1475-2875
• DOI: 10.1186/1475-2875-12-60

Tanzania adopted artemether-lumefantrine (AL) as first-line drug for uncomplicated malaria in 2006. Recently, there was an anecdotal report on high malaria recurrence rate following AL treatment in in the (urban and peri-urban), western part of Tanzania. The current report is an exploratory study to carefully and systematically assess AL efficacy in the area.
Between June and August 2011, a total of 1,126 patients were screened for malaria, 33 had malaria, of which 20 patients met inclusion criteria and were enrolled and treated with standard dose of AL as recommended in the WHO protocol. Treated patients were followed up for 28 days to assess treatment responses. Before treatment (Day 0) and post-treatment (Day 7) plasma lumefantrine levels were determined to assess prior AL use and ascertain parasites exposure to adequate plasma leveles of lumefantrine, respectively.
The cure rate was 100%. All Day 0 plasma lumefantrine were below HPLC detectable level. The median Day 7 lumefantrine concentration was 404, (range, 189-894 ng/ml). Six out of 20 patients (30%) were gametocytaemic and all cleared gametocytes by Day 14. One patient showed an increase in gametocytes from four on Day 0 to 68, per 500 WBC on Day 2.
Artemether lumefantrine is highly efficacious against uncomplicated Plasmodium falciparum malaria. The elevation of gametocytaemia despite AL treatment needs to be evaluated in a larger study.