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A randomized controlled trial of chloroquine for the treatment of dengue in vietnamese adults

dc.contributor.authorVianney Tricouen_US
dc.contributor.authorNguyet Nguyen Minhen_US
dc.contributor.authorToi Pham vanen_US
dc.contributor.authorSue J. Leeen_US
dc.contributor.authorJeremy Farraren_US
dc.contributor.authorBridget Willsen_US
dc.contributor.authorHien Tinh Tranen_US
dc.contributor.authorCameron P. Simmonsen_US
dc.contributor.otherUCLen_US
dc.contributor.otherChurchill Hospitalen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T09:23:58Z
dc.date.available2018-09-24T09:23:58Z
dc.date.issued2010-08-01en_US
dc.description.abstractBackground:There is currently no licensed antiviral drug for treatment of dengue. Chloroquine (CQ) inhibits the replication of dengue virus (DENV) in vitro. Methods and Findings:A double-blind, randomized, placebo-controlled trial of CQ in 307 adults hospitalized for suspected DENV infection was conducted at the Hospital for Tropical Diseases (Ho Chi Minh City, Vietnam) between May 2007 and July 2008. Patients with illness histories of 72 hours or less were randomized to a 3-day course of CQ (n = 153) or placebo (n = 154). Laboratory-confirmation of DENV infection was made in 257 (84%) patients. The primary endpoints were time to resolution of DENV viraemia and time to resolution of DENV NS1 antigenaemia. In patients treated with CQ there was a trend toward a longer duration of DENV viraemia (hazard ratio (HR) = 0.80, 95% CI 0.62?1.05), but we did not find any difference for the time to resolution of NS1 antigenaemia (HR = 1.07, 95% CI 0.76?1.51). Interestingly, CQ was associated with a significant reduction in fever clearance time in the intention-to-treat population (HR = 1.37, 95% CI 1.08?1.74) but not in the per-protocol population. There was also a trend towards a lower incidence of dengue hemorrhagic fever (odds ratio = 0.60, PP 95% CI 0.34-1.04) in patients treated with CQ. Differences in levels of T cell activation or pro- or antiinflammatory plasma cytokine concentrations between CQ- and placebo-treated patients did not explain the trend towards less dengue hemorrhagic fever in the CQ arm. CQ was associated with significantly more adverse events, primarily vomiting. Conclusions:CQ does not reduce the durations of viraemia and NS1 antigenaemia in dengue patients. Further trials, with appropriate endpoints, would be required to determine if CQ treatment has any clinical benefit in dengue. © 2010 Tricou et al.en_US
dc.identifier.citationPLoS Neglected Tropical Diseases. Vol.4, No.8 (2010)en_US
dc.identifier.doi10.1371/journal.pntd.0000785en_US
dc.identifier.other2-s2.0-78149265507en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29581
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78149265507&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA randomized controlled trial of chloroquine for the treatment of dengue in vietnamese adultsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78149265507&origin=inwarden_US

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