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Randomised controlled trial to determine the efficacy and safety of prescribed water intake to prevent kidney failure due to autosomal dominant polycystic kidney disease (PREVENT-ADPKD)

dc.contributor.authorWong, Annette T. Y.
dc.contributor.authorMannix, Carly
dc.contributor.authorGrantham, Jared J.
dc.contributor.authorAllman-Farinelli, Margaret
dc.contributor.authorBadve, Sunil V.
dc.contributor.authorBoudville, Neil
dc.contributor.authorByth, Karen
dc.contributor.authorChan, Jessie
dc.contributor.authorCoulshed, Susan
dc.contributor.authorEdwards, Marie E.
dc.contributor.authorJiang, Simon
dc.date.accessioned2019-04-28T23:45:57Z
dc.date.available2019-04-28T23:45:57Z
dc.date.issued2018
dc.date.updated2019-03-12T07:34:48Z
dc.description.abstractIntroduction: Maintaining fluid intake sufficient to reduce arginine vasopressin (AVP) secretion has been hypothesised to slow kidney cyst growth in autosomal dominant polycystic kidney disease (ADPKD). However, evidence to support this as a clinical practice recommendation is of poor quality. The aim of the present study is to determine the long-term efficacy and safety of prescribed water intake to prevent the progression of height-adjusted total kidney volume (ht-TKV) in patients with chronic kidney disease (stages 1–3) due to ADPKD. Methods and analysis: A multicentre, prospective, parallel-group, open-label, randomised controlled trial will be conducted. Patients with ADPKD (n=180; age ≤65 years, estimated glomerular filtration rate (eGFR) ≥30 mL/min/1.73 m2) will be randomised (1:1) to either the control (standard treatment+usual fluid intake) or intervention (standard treatment+prescribed fluid intake) group. Participants in the intervention arm will be prescribed an individualised daily fluid intake to reduce urine osmolality to ≤270 mOsmol/kg, and supported with structured clinic and telephonic dietetic review, self-monitoring of urine-specific gravity, short message service text reminders and internet-based tools. All participants will have 6-monthly follow-up visits, and ht-TKV will be measured by MRI at 0, 18 and 36 months. The primary end point is the annual rate of change in ht-TKV as determined by serial renal MRI in control vs intervention groups, from baseline to 3 years. The secondary end points are differences between the two groups in systemic AVP activity, renal disease (eGFR, blood pressure, renal pain), patient adherence, acceptability and safety. Ethics and dissemination: The trial was approved by the Human Research Ethics Committee, Western Sydney Local Health District. The results will inform clinicians, patients and policy-makers regarding the long-term safety, efficacy and feasibility of prescribed fluid intake as an approach to reduce kidney cyst growth in patients with ADPKD.en_AU
dc.description.sponsorshipThe development and commencement of the trial was funded by University of Sydney Bridging Grants (2014, 2016), Westmead Medical Research Foundation, the Western Sydney Local Health District and an investigator-initiated research grant from Danone Nutricia Research (France).en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn2044-6055en_AU
dc.identifier.urihttp://hdl.handle.net/1885/160671
dc.language.isoen_AUen_AU
dc.provenanceThis is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/ licenses/by/4.0/en_AU
dc.publisherBMJ Publishing Groupen_AU
dc.rights© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018en_AU
dc.sourceBMJ Openen_AU
dc.titleRandomised controlled trial to determine the efficacy and safety of prescribed water intake to prevent kidney failure due to autosomal dominant polycystic kidney disease (PREVENT-ADPKD)en_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue1en_AU
local.contributor.affiliationWong, Annette T Y, University of Sydneyen_AU
local.contributor.affiliationMannix, Carly, University of Sydneyen_AU
local.contributor.affiliationGrantham, Jared J, Kansas University Medical Centeren_AU
local.contributor.affiliationAllman-Farinelli, Margaret, University of Sydneyen_AU
local.contributor.affiliationBadve, Sunil V, St George Hospitalen_AU
local.contributor.affiliationBoudville, Neil, University of Western Australiaen_AU
local.contributor.affiliationByth, Karen, Westmead Hospitalen_AU
local.contributor.affiliationChan, Jessie, McCloud Consulting Groupen_AU
local.contributor.affiliationCoulshed, Susan, North Shore Nephrologyen_AU
local.contributor.affiliationEdwards, Marie E, Mayo Clinicen_AU
local.contributor.affiliationJiang, Simon, College of Health and Medicine, ANUen_AU
local.contributor.authoruidJiang, Simon, u3365929en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor110312 - Nephrology and Urologyen_AU
local.identifier.absseo920119 - Urogenital System and Disordersen_AU
local.identifier.ariespublicationu4485658xPUB2457en_AU
local.identifier.citationvolume8en_AU
local.identifier.doi10.1136/bmjopen-2017-018794en_AU
local.identifier.scopusID2-s2.0-85045311682
local.identifier.thomsonID000431743500128
local.publisher.urlhttps://authors.bmj.com/open-access/en_AU
local.type.statusPublished Versionen_AU

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