Publication:
Thiamin supplementation does not reduce the frequency of adverse events after anti-malarial therapy among patients with falciparum malaria in southern Laos

dc.contributor.authorMayfong Mayxayen_US
dc.contributor.authorManiphone Khanthavongen_US
dc.contributor.authorLorna Coxen_US
dc.contributor.authorOdai Sichanthongthipen_US
dc.contributor.authorMallika Imwongen_US
dc.contributor.authorTiengkham Pongvongsaen_US
dc.contributor.authorBouasy Hongvanthongen_US
dc.contributor.authorSamlane Phompidaen_US
dc.contributor.authorViengxay Vanisavethen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorPaul N. Newtonen_US
dc.contributor.otherMahosot Hospitalen_US
dc.contributor.otherUniversity of Health Sciencesen_US
dc.contributor.otherUniversity of Oxforden_US
dc.contributor.otherCentre of Malariologyen_US
dc.contributor.otherMRC Human Nutrition Researchen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSavannakhet Provincial Malaria Stationen_US
dc.date.accessioned2018-11-09T02:21:09Z
dc.date.available2018-11-09T02:21:09Z
dc.date.issued2014-07-15en_US
dc.description.abstractBackground: In a recent study one third of Lao patients presenting with uncomplicated Plasmodium falciparum malaria had biochemical evidence of thiamin deficiency, which was associated with a higher incidence of adverse events. Thiamin supplementation might, therefore, reduce adverse events in this population. Methods. An exploratory, double-blind, parallel group, placebo-controlled, superiority trial of thiamin supplementation in patients of all ages with uncomplicated and severe falciparum malaria was conducted in Xepon District, Savannakhet Province, southern Laos. Patients were randomly assigned to either oral thiamin 10 mg/day for 7 days immediately after standard anti-malarial treatment then 5 mg daily until day 42, or identical oral placebo. Results: After interim analyses when 630 patients (314 in thiamin and 316 in placebo groups) had been recruited, the trial was discontinued on the grounds of futility. On admission biochemical thiamin deficiency (alpha ≥ 25%) was present in 27% of patients and 9% had severe deficiency (alpha > 31%). After 42 days of treatment, the frequency of thiamin deficiency was lower in the thiamin (2%, 1% severe) compared to the placebo (11%, 3% severe) groups (p < 0.001 and p = 0.05), respectively. Except for diarrhoea, 7% in the placebo compared to 3% in the thiamin group (p = 0.04), and dizziness on day 1 (33% vs 25%, p = 0.045), all adverse events were not significantly different between the groups (p > 0.05). Clinical, haematological, and parasitological responses to treatment did not differ significantly between the two groups. Conclusion: Thiamin supplementation reduced biochemical thiamin deficiency among Lao malaria patients following anti-malarial drug treatment, but it did not reduce the frequency of adverse events after anti-malarial therapy or have any detected clinical or parasitological impact. Trial registration. ISRCTN 85411059. © 2014 Mayxay et al.; licensee BioMed Central Ltd.en_US
dc.identifier.citationMalaria Journal. Vol.13, No.1 (2014)en_US
dc.identifier.doi10.1186/1475-2875-13-275en_US
dc.identifier.issn14752875en_US
dc.identifier.other2-s2.0-84904077607en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/33959
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84904077607&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleThiamin supplementation does not reduce the frequency of adverse events after anti-malarial therapy among patients with falciparum malaria in southern Laosen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84904077607&origin=inwarden_US

Files

Collections