Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/39454
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dc.contributor.authorPolkinghorne K.R.en
dc.contributor.authorToussaint N.D.en
dc.contributor.authorBlair S.en
dc.contributor.authorLau K.K.en
dc.contributor.authorKerr P.en
dc.contributor.authorMorgan J.G.en
dc.contributor.authorStrauss B.J.en
dc.contributor.authorLian M.en
dc.contributor.authorMasterson R.en
dc.date.accessioned2021-05-14T13:27:54Zen
dc.date.available2021-05-14T13:27:54Zen
dc.date.copyright2017en
dc.date.created20170222en
dc.date.issued2017-02-22en
dc.identifier.citationHemodialysis International. 21 (1) (pp 19-28), 2017. Date of Publication: 01 Jan 2017.en
dc.identifier.issn1492-7535en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/39454en
dc.description.abstractIntroduction: Higher calcium dialysate is recommended for quotidian nocturnal hemodialysis (NHD) (>=6 nights/week) to maintain bone health. It is unclear what the optimal calcium dialysate concentration should be for alternate night NHD. We aimed to determine the effect of low calcium (LC) versus high calcium (HC) dialysate on cardiovascular and bone parameters in this population. Method(s): A randomized controlled trial where participants were randomized to LC (1.3 mmol/L, n = 24) or HC dialysate (1.6 or 1.75 mmol/L, n = 26). Primary outcome was change in mineral metabolism markers. Secondary outcomes included change in vascular calcification (VC) scores [CT abdominal aorta (AA) and superficial femoral arteries (SFA)), pulse wave velocity (PWV), bone mineral density (BMD) and left ventricular mass index (LVMI) over 12 months. Finding(s): In the LC group, pre-dialysis ionised calcium decreased -0.12 mmol/L (-0.18-0.06, P = 0.0001) and PTH increased 16 pmol/L (3.5-28.5, p = 0.01) from baseline to 12 months with no significant change in the HC group. In both groups, there was no progression of VC in AA or SFA and no change in PWV, LVMI or BMD. At 12 months, calcimimetics were prescribed in a higher percentage in the LC vs. HC groups (45.5% vs. 10.5%) with a lower proportion of the HC group being prescribed calcitriol (31.5% vs. 72%). Discussion(s): Although dialysate calcium prescription influenced biochemical parameters it was not associated with difference in progression of VC between HC and LC groups. An important finding was the potential impact of alternate night NHD in attenuating progression of VC and inducing stabilisation of LVMI and PWV.Copyright © 2016 International Society for Hemodialysisen
dc.languageEnglishen
dc.languageenen
dc.publisherBlackwell Publishing Inc. (E-mail: subscrip@blackwellpub.com)en
dc.relation.ispartofHemodialysis Internationalen
dc.titleLow versus high dialysate calcium concentration in alternate night nocturnal hemodialysis: A randomized controlled trial.en
dc.typeArticleen
dc.identifier.affiliationNephrologyen
dc.identifier.affiliationRadiologyen
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/hdi.12452en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid27364375 [http://www.ncbi.nlm.nih.gov/pubmed/?term=27364375]en
dc.identifier.source613084562en
dc.identifier.institution(Masterson, Lian, Toussaint) Department of Nephrology, The Royal Melbourne Hospital, Parkville, VIC, Australia (Masterson, Toussaint) Department of Medicine, University of Melbourne, Parkville, VIC, Australia (Blair, Polkinghorne, Kerr) Department of Nephrology, Monash Medical Centre, Clayton, VIC, Australia (Polkinghorne, Strauss, Kerr) Department of Medicine, Monash University, Clayton, VIC, Australia (Lau) Department of Radiology, Monash Medical Centre, Clayton, VIC, Australia (Morgan) Department of Cardiology, The Royal Melbourne Hospital, Parkville, VIC, Australiaen
dc.description.addressR. Masterson, Department of Nephrology, The Royal Melbourne Hospital, Parkville, VIC, Australia. E-mail: Rosemary.Masterson@mh.org.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2017 Elsevier B.V., All rights reserved.en
dc.subect.keywordsbone mineral metabolism dialysate calcium concentration nocturnal hemodialysis vascular calcificationen
dc.identifier.authoremailMasterson R.; Rosemary.Masterson@mh.org.auen
dc.identifier.affiliationext(Masterson, Lian, Toussaint) Department of Nephrology, The Royal Melbourne Hospital, Parkville, VIC, Australia-
dc.identifier.affiliationext(Masterson, Toussaint) Department of Medicine, University of Melbourne, Parkville, VIC, Australia-
dc.identifier.affiliationext(Polkinghorne, Strauss, Kerr) Department of Medicine, Monash University, Clayton, VIC, Australia-
dc.identifier.affiliationext(Morgan) Department of Cardiology, The Royal Melbourne Hospital, Parkville, VIC, Australia-
dc.identifier.affiliationmh(Blair, Polkinghorne, Kerr) Department of Nephrology, Monash Medical Centre, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Lau) Department of Radiology, Monash Medical Centre, Clayton, VIC, Australia-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptNephrology-
crisitem.author.deptNephrology-
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