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Safety Profile of L-Arginine Infusion in Moderately Severe Falciparum Malaria

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dc.contributor.author Weinberg, J Brice en_US
dc.date.accessioned 2011-06-21T17:31:24Z
dc.date.available 2011-06-21T17:31:24Z
dc.date.issued 2008 en_US
dc.identifier.citation Yeo,Tsin W.;Lampah,Daniel A.;Gitawati,Retno;Tjitra,Emiliana;Kenangalem,Enny;Granger,Donald L.;Weinberg,J. Brice;Lopansri,Bert K.;Price,Ric N.;Celermajer,David S.;Duffull,Stephen B.;Anstey,Nicholas M.. 2008. Safety Profile of L-Arginine Infusion in Moderately Severe Falciparum Malaria. Plos One 3(6): e2347-e2347. en_US
dc.identifier.issn 1932-6203 en_US
dc.identifier.uri http://hdl.handle.net/10161/4494
dc.description.abstract Background: L-arginine infusion improves endothelial function in malaria but its safety profile has not been described in detail. We assessed clinical symptoms, hemodynamic status and biochemical parameters before and after a single L-arginine infusion in adults with moderately severe malaria. Methodology and Findings: In an ascending dose study, adjunctive intravenous L-arginine hydrochloride was infused over 30 minutes in doses of 3 g, 6 g and 12 g to three separate groups of 10 adults hospitalized with moderately severe Plasmodium falciparum malaria in addition to standard quinine therapy. Symptoms, vital signs and selected biochemical measurements were assessed before, during, and for 24 hours after infusion. No new or worsening symptoms developed apart from mild discomfort at the intravenous cannula site in two patients. There was a dose-response relationship between increasing mg/kg dose and the maximum decrease in systolic (rho = 0.463; Spearman's, p = 0.02) and diastolic blood pressure (r = 0.42; Pearson's, p = 0.02), and with the maximum increment in blood potassium (r = 0.70, p < 0.001) and maximum decrement in bicarbonate concentrations (r = 0.53, p = 0.003) and pH (r = 0.48, p = 0.007). At the highest dose (12 g), changes in blood pressure and electrolytes were not clinically significant, with a mean maximum decrease in mean arterial blood pressure of 6 mmHg (range: 0-11; p < 0.001), mean maximal increase in potassium of 0.5 mmol/L (range 0.2-0.7 mmol/L; p, 0.001), and mean maximal decrease in bicarbonate of 3 mEq/L (range 1-7; p < 0.01) without a significant change in pH. There was no significant dose-response relationship with blood phosphate, lactate, anion gap and glucose concentrations. All patients had an uncomplicated clinical recovery. Conclusions/Significance: Infusion of up to 12g of intravenous L-arginine hydrochloride over 30 minutes is well tolerated in adults with moderately severe malaria, with no clinically important changes in hemodynamic or biochemical status. Trials of adjunctive L-arginine can be extended to phase 2 studies in severe malaria. Trial Registration: ClinicalTrials.gov NCT00147368 en_US
dc.language.iso en_US en_US
dc.publisher PUBLIC LIBRARY SCIENCE en_US
dc.relation.isversionof doi:10.1371/journal.pone.0002347 en_US
dc.subject biology en_US
dc.subject multidisciplinary sciences en_US
dc.title Safety Profile of L-Arginine Infusion in Moderately Severe Falciparum Malaria en_US
dc.title.alternative en_US
dc.description.version Version of Record en_US
duke.date.pubdate 2008-6-11 en_US
duke.description.endpage e2347 en_US
duke.description.issue 6 en_US
duke.description.startpage e2347 en_US
duke.description.volume 3 en_US
dc.relation.journal Plos One en_US

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