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Ursodeoxycholic acid and artesunate in the treatment of severe falciparum malaria patients with jaundice

dc.contributor.authorSombat Treeprasertsuken_US
dc.contributor.authorUdomsak Silachamroonen_US
dc.contributor.authorSrivicha Krudsooden_US
dc.contributor.authorArun Huntrupen_US
dc.contributor.authorPlengsakoon Suwannakudten_US
dc.contributor.authorSuparp Vannaphanen_US
dc.contributor.authorPolrat Wilairatanaen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T09:36:14Z
dc.date.available2018-09-24T09:36:14Z
dc.date.issued2010-01-01en_US
dc.description.abstractBackground and Aims: Plasmodium falciparum (PF) infection can lead to severe complications. Ursodeoxycholic acid (UDCA) is increasingly used for the treatment of cholestatic liver diseases. The present study aims to determine the effects of combined UDCA and artesunate compared to placebo and artesunate on the improvement of liver tests in severe PF jaundiced patients. Methods: All severe PF jaundiced patients, aged ≥ 15 years and diagnosed as having severe malaria according to WHO 2000 criteria, were enrolled. Patients with evidence of biliary obstruction, other cholestatic liver diseases and those who were pregnant were excluded. Patients were randomized to receive either oral UDCA or placebo for 2 weeks in additional to artesunate. All patients were admitted for at least 14 days to monitor the result of the treatment. Results: Seventy-four severe PF malaria patients with jaundice were enrolled. Both groups had similar demographic and laboratory tests, with the exception being more males in the UDCA group than in the placebo group (P = 0.04). The median of percentage change of total bilirubin and aminotransferase levels at the end of weeks 1, 2, 3 and 4 showed no difference between the two groups. Only the median of percentage change of alkaline phosphatase at the end of week one compared with the baseline values showed less increment in the UDCA group than in the placebo group (P = 0.04). No serious adverse events were seen during the 4 weeks of follow up. Conclusions: In severe PF malaria patients with jaundice, combined therapy with UDCA and artesunate is safe, but does not significantly improve liver tests compared to placebo and artesunate. © 2010 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd.en_US
dc.identifier.citationJournal of Gastroenterology and Hepatology (Australia). Vol.25, No.2 (2010), 362-368en_US
dc.identifier.doi10.1111/j.1440-1746.2009.06007.xen_US
dc.identifier.issn14401746en_US
dc.identifier.issn08159319en_US
dc.identifier.other2-s2.0-76149085827en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29837
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=76149085827&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleUrsodeoxycholic acid and artesunate in the treatment of severe falciparum malaria patients with jaundiceen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=76149085827&origin=inwarden_US

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