| Literature DB >> 18567436 |
Noppadon Tangpukdee1, Srivicha Krudsood, Vipa Thanachartwet, Chaweewan Pengruksa, Nanthaporn Phophak, Shigeyuki Kano, Guoqiao Li, Gary M Brittenham, Sornchai Looareesuwan, Polrat Wilairatana.
Abstract
To determine the efficacy, safety and tolerability of an alternative short-course, artemisinin-based combination therapy for acute uncomplicated Plasmodium falciparum malaria, we compared Artequick--a fixed-dosed combination of artemisinin (80 mg), piperaquine (400 mg), and primaquine (4 mg), per tablet--with a standard regimen of artesunate-mefloquine. A total of 130 patients were randomly assigned to treatment with an orally administered, once-daily, 3-day regimen of either Artequick (Group A: 3.2 mg/Kg/day of artemisinin, 16 mg/Kg/day of piperaquine, and 0.16 mg/Kg/day of primaquine) or artesunate-mefloquine (Group B: artesunate, 4 mg/Kg/day, with mefloquine, 8 mg/Kg/day). Patients receiving each regimen had a rapid clinical and parasitological response. All treatments were well tolerated, and no serious adverse effects occurred. No significant differences were found in fever- and parasite-clearance times between the two study groups. The 28-day cure rates were similarly high, at 98.5% and 100%, in groups A and B, respectively. We conclude that Artequick was as effective and well tolerated as artesunate-mefloquine and could be used as an alternative treatment for multidrug-resistant Plasmodium falciparum malaria in Southeast Asia.Entities:
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Year: 2008 PMID: 18567436 PMCID: PMC3129605
Source DB: PubMed Journal: Southeast Asian J Trop Med Public Health ISSN: 0125-1562 Impact factor: 0.267