Evidence mapPaperPMID 18545693Full record

ArticlePloS one2008

Safety profile of L-arginine infusion in moderately severe falciparum malaria.

Tsin W Yeo, Daniel A Lampah, Retno Gitawati, Emiliana Tjitra, Enny Kenangalem, Donald L Granger, J Brice Weinberg, Bert K Lopansri, Ric N Price, David S Celermajer and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00147368 (Pharmacokinetic-Pharmacodynamic Study of Adjunctive Arginine in Falciparum Malaria), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00147368 phase1 / phase2completednot on this map

Pharmacokinetic-Pharmacodynamic Study of Adjunctive Arginine in Falciparum Malaria

TypeinterventionalSponsorMenzies School of Health ResearchRan2005 to 2007Enrolled50ConditionsMalaria, FalciparumArmsintravenous (IV) arginine
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 31 citations in OpenAlex.

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  15. An Introduction to Pharmacotherapy for Inborn Errors of Metabolism.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 5 countries.

Tsin W YeoInternational Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Daniel A Lampah
Retno Gitawati
Emiliana Tjitra
Enny Kenangalem
Donald L Granger
J Brice Weinberg
Bert K Lopansri
Ric N Price
David S Celermajer
Stephen B Duffull
Nicholas M Anstey
Ministry of Health · IDMenzies School of Health Research · AUUniversity of Utah · USDuke Medical Center · USRoyal Darwin Hospital · AURoyal Prince Alfred Hospital · AUUniversity of Otago · NZ

Funding

Wellcome TrustWellcome Trust ICRG GR071614MA
6 · The paper itself

Abstract

backgroundL-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

findingsIn 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 12 g 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 registrationClinicalTrials.gov NCT00147368.

Indexed as

AdultArginineBlood GlucoseBlood PressureDose-Response Relationship, DrugElectrolytesHumansHydrogen-Ion ConcentrationInfusions, IntravenousMalaria, FalciparumArginineBlood GlucoseElectrolytes

Identifiers

PMID18545693
PMCPMC2405947
OpenAlexW1983318517

What Socratic holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.