Publication:
Artemisinin: Large community studies

dc.contributor.authorFranÇis Nostenen_US
dc.contributor.otherShoklo Malaria Research Uniten_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-02-27T04:26:44Z
dc.date.available2018-02-27T04:26:44Z
dc.date.issued1994-01-01en_US
dc.description.abstractProspective randomized trials with oral artemisinin derivatives have been conducted in over 1000 patients to determine the optimum treatment of multi-drug resistant falciparum malaria on the Thai-Burmese border. These drugs have proved valuable in 3 settings, (i) Primary treatment of uncomplicated malaria in combination with mefloquine, when they accelerate the rate of recovery, eliminate the risk of dangerous early failures, and if given for 3 d or more improve overall cure rates; (ii) treatment of recrudescent infections, which otherwise have a high failure rate; and (iii)oral treatment of patients with high parasitaemias (≥4%) but no clinical evidence of severity (a group who would usually receive parenteral quinine). The parenteral formulation of artemether is absorbed if given rectally, and this may offer a practical alternative method of treating severe malaria in rural areas. © 1994 Oxford University Press.en_US
dc.identifier.citationTransactions of the Royal Society of Tropical Medicine and Hygiene. Vol.88, (1994), 45-46en_US
dc.identifier.doi10.1016/0035-9203(94)90472-3en_US
dc.identifier.issn18783503en_US
dc.identifier.issn00359203en_US
dc.identifier.other2-s2.0-0028277862en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/9590
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028277862&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleArtemisinin: Large community studiesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0028277862&origin=inwarden_US

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