Evidence map›Paper›PMID 31805104›Full record

Trial reportPloS one2019

Citric-acid dialysate improves the calcification propensity of hemodialysis patients: A multicenter prospective randomized cross-over trial.

Karlien J Ter Meulen, Marijke J E Dekker, Andreas Pasch, Natascha J H Broers, Frank M van der Sande, Jeroen B van der Net, Constantijn J A M Konings, Isabelle M Gsponer, Matthias D N Bachtler, Adelheid Gauly and 2 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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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 3 institutions in 2 countries.

Karlien J Ter MeulenDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.ORCID 0000-0001-7035-6326
Marijke J E DekkerDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Andreas PaschCalciscon AG, Nidau, Switzerland.
Natascha J H BroersDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Frank M van der SandeDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Jeroen B van der NetDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Constantijn J A M KoningsDepartment of Internal Medicine, Division of Nephrology, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.
Isabelle M GsponerCalciscon AG, Nidau, Switzerland.
Matthias D N BachtlerCalciscon AG, Nidau, Switzerland.
Adelheid GaulyFresenius Medical Care, Bad Homburg, Germany.
Bernard CanaudFresenius Medical Care, Bad Homburg, Germany.
Jeroen P KoomanDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Maastricht University · NLRadboud University Nijmegen · NLFresenius Medical Care (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe concentration of dialysate calcium (dCa) has been suggested to affect vascular calcification, but evidence is scarce. Calcification propensity reflects the intrinsic capacity of serum to prevent calcium and phosphate to precipitate. The use of citric-acid dialysate may have a beneficial effect on the calcification propensity due to the chelating effect on calcium and magnesium. The aim of this study was to compare the intradialytic and short-term effects of haemodialysis with either standard acetic-acid dialysate with dCa1.50 (A1.5) or dCa1.25 (A1.25), as well as citric-acid dialysate with dCa1.50 (C1.5) in bicarbonate dialysis on the calcification propensity of serum.

methodsChronic stable hemodialysis patients were included. This multicenter randomized cross-over study consisted out of a baseline week (A1.5), followed by the randomized sequence of A1.25 or C1.5 for one week after which the alternate treatment was provided after a washout week with A1.5. Calcification propensity of serum was assessed by time-resolved nephelometry where the T50 reflects the transition time between formation of primary and secondary calciprotein particles.

resultsEighteen patients (median age 70 years) completed the study. Intradialytic change in T50 was increased with C1.5 (121 [90-152]min) compared to A1.25 (83 [43-108]min, p<0.001) and A1.5 (66 [18-102]min, p<0.001). During the treatment week, predialysis T50 increased significantly from the first to the third session with C1.5 (271 [234-291] to 280 [262-339]min, p = 0.002) and with A1.25 (274 [213-308] to 307 [256-337]min, p<0.001), but not with A1.5 (284 [235-346] to 300 [247-335]min, p = 0.33).

conclusionCalcification propensity, as measured by the change in T50, improved significantly during treatment in C1.5 compared to A1.25 and A1.5. Long-term studies are needed to investigate the effects of different dialysate compositions concentrations on vascular calcification and bone mineral disorders.

Indexed as

AgedCalciumCitric AcidFemaleHemodynamicsHumansMaleProspective StudiesRenal DialysisTime FactorsVascular CalcificationCalciumCitric Acid

Identifiers

PMID31805104
PMCPMC6894765
OpenAlexW2993953294

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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 OpenQuestion graph.