Publication:
Comparative clinical trial of artesunate suppositories and oral artesunate in combination with mefloquine in the treatment of children with acute falciparum malaria

dc.contributor.authorA. Sabchareonen_US
dc.contributor.authorP. Attanathen_US
dc.contributor.authorP. Chanthavanichen_US
dc.contributor.authorP. Phanuaksooken_US
dc.contributor.authorV. Prarinyanupharben_US
dc.contributor.authorY. Poonpanichen_US
dc.contributor.authorD. Mookmaneeen_US
dc.contributor.authorP. Teja-Isavadharmen_US
dc.contributor.authorD. G. Heppneren_US
dc.contributor.authorT. G. Breweren_US
dc.contributor.authorT. Chongsuphajaisiddhien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThong Pha Phum Hospitalen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherU. States Army Med. Res. Inst. I.en_US
dc.date.accessioned2018-07-04T08:08:26Z
dc.date.available2018-07-04T08:08:26Z
dc.date.issued1998-01-01en_US
dc.description.abstractA randomized pilot study to compare the safety and efficacy of artesunate suppositories (15 mg/kg/day for three days) versus oral artesunate (6 mg/kg/day for three days), both in combination with mefloquine (25 mg/kg), was conducted in 52 Thai children with uncomplicated multidrug-resistant falciparum malaria. Forty-five patients (87%) had a full 28-day follow-up in the hospital to assess efficacy and exclude reinfection. Mean [range] times to fever clearance of the two groups were similar (42 hr [15-104] versus 42 hr [6-119]). Artesunate suppositories resulted in significantly longer times to achieve 50% and 90% reductions of the initial parasite counts (17 and 26 hr versus 9 and 15 hr; P < 0.05 and P < 0.001). Time [range] to parasite clearance was longer in the artesunate suppositories group (42 hr [14-93] versus 35 hr [16-69]), but the difference was not significant. The cure rates by days 28 were not significantly different, 92% for artesunate suppository- treated patients and 100% for oral artesunate-treated patients. Both drug regimens are safe and effective. Further studies are needed to characterize the pharmacokinetic properties and the optimum regimen of artesunate suppositories for the treatment of severe malaria.en_US
dc.identifier.citationAmerican Journal of Tropical Medicine and Hygiene. Vol.58, No.1 (1998), 11-16en_US
dc.identifier.doi10.4269/ajtmh.1998.58.11en_US
dc.identifier.issn00029637en_US
dc.identifier.other2-s2.0-0031917554en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/18415
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031917554&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleComparative clinical trial of artesunate suppositories and oral artesunate in combination with mefloquine in the treatment of children with acute falciparum malariaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0031917554&origin=inwarden_US

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