Publication:
Comparison of artemether and chloroquine for severe malaria in Gambian children

dc.contributor.authorN. J. Whiteen_US
dc.contributor.authorF. Nostenen_US
dc.contributor.authorN. J. Whiteen_US
dc.contributor.authorD. Walleren_US
dc.contributor.authorN. J. Whiteen_US
dc.contributor.authorD. Walleren_US
dc.contributor.authorJ. Crawleyen_US
dc.contributor.authorD. Chapmanen_US
dc.contributor.authorD. Brewsteren_US
dc.contributor.authorB. M. Greenwooden_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCho Quan Hospitalen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherRoyal Victoria Teaching Hospital Gambiaen_US
dc.contributor.otherMedical Research Council Laboratories Gambiaen_US
dc.date.accessioned2018-08-10T08:47:37Z
dc.date.available2018-08-10T08:47:37Z
dc.date.issued1992-02-08en_US
dc.description.abstractArtemether is an oil-soluble methyl ether of artemesinin (qinghaosu). It has been studied extensively in China, where it has been shown to be rapidly effective in severe falciparum malaria. Nearly all the patients studied previously were adults. We have investigated the efficacy of artemether in children with moderate or severe falciparum malaria. In the preliminary study of moderately severe malaria, 30 Gambian children were randomised in pairs to receive either intramuscular artemether (4 mg/kg loading dose followed by 2 mg/kg daily) or intramuscular chloroquine ('Nivaquine') 3·5 mg base/kg every 6 h. Both drugs were well tolerated and rapidly effective. The times to parasite clearance were significantly shorter in the artemether recipients (mean 36·7 [SD 11·3] vs 48·4 [16·8] h, p<0·05). 43 children with severe malaria were then randomised to receive intramuscular treatment with the same regimens of artemether (n=21) or chloroquine (n=22) as used in the preliminary study. 8 children (19%) died. There were no significant differences between the two groups in the clinical, haematological, biochemical, or parasitological measures of therapeutic response in survivors and there was no evidence of local or systemic toxicity. Despite similar parasite counts on admission, clearance times overall were longer in severe malaria than in moderate malaria. Artemether is a well tolerated and rapidly effective parenteral treatment for severe malaria in children, and would be especially valuable in areas with chloroquine-resistant P falciparum. © 1992.en_US
dc.identifier.citationThe Lancet. Vol.339, No.8789 (1992), 317-321en_US
dc.identifier.doi10.1016/0140-6736(92)91644-Nen_US
dc.identifier.issn01406736en_US
dc.identifier.other2-s2.0-0026597469en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/22413
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026597469&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleComparison of artemether and chloroquine for severe malaria in Gambian childrenen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0026597469&origin=inwarden_US

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