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dc.contributor.authorDavies, Simon J
dc.contributor.authorCaskey, Fergus J
dc.contributor.authorCoyle, David
dc.contributor.authorLindley, Elizabeth
dc.contributor.authorMacdonald, Jamie
dc.contributor.authorMitra, Sandip
dc.contributor.authorWilkie, Martin
dc.contributor.authorDavenport, Andrew
dc.contributor.authorFarrington, Ken
dc.contributor.authorDasgupta, Indranil
dc.contributor.authorOrmandy, Paula
dc.contributor.authorAndronis, Lazaros
dc.contributor.authorSolis-Trapala, Ivonne
dc.contributor.authorSim, Julius
dc.date.accessioned2018-10-23T01:40:29Z
dc.date.available2018-10-23T01:40:29Z
dc.date.issued2017-04-26
dc.identifier.citationDavies , S J , Caskey , F J , Coyle , D , Lindley , E , Macdonald , J , Mitra , S , Wilkie , M , Davenport , A , Farrington , K , Dasgupta , I , Ormandy , P , Andronis , L , Solis-Trapala , I & Sim , J 2017 , ' Rationale and design of BISTRO : a randomized controlled trial to determine whether bioimpedance spectroscopy-guided fluid management maintains residual kidney function in incident haemodialysis patients ' , BMC Nephrology , vol. 18 , no. 1 , pp. 138 . https://doi.org/10.1186/s12882-017-0554-1
dc.identifier.otherPURE: 13323704
dc.identifier.otherPURE UUID: d4631f10-e80a-4ff8-9f92-f6bc848dfb1e
dc.identifier.otherPubMed: 28441936
dc.identifier.otherPubMedCentral: PMC5405466
dc.identifier.otherScopus: 85018628624
dc.identifier.urihttp://hdl.handle.net/2299/20738
dc.description.abstractBACKGROUND: Preserved residual kidney function (RKF) and normal fluid status are associated with better patient outcomes in incident haemodialysis patients. The objective of this trial is to determine whether using bioimpedance technology in prescribing the optimal post-dialysis weight can reduce the rate of decline of RKF and potentially improve patient outcomes. METHODS/DESIGN: 516 pateints commencing haemodialysis, aged >18 with RKF of > 3 ml/min/1.73 m2 or a urine volume >500 ml per day or per the shorter inter-dialytic period will be consented and enrolled into a pragmatic, open-label, randomized controlled trial. The intervention is incorporation of bioimpedance spectroscopy (BI) determination of normally hydrated weight to set a post-dialysis target weight that limits volume depletion, compared to current standard practice. Clinicians and participants will be blinded to BI measures in the control group and a standardized record capturing management of fluid status will be used in all participants. Primary outcome is preservation of residual kidney function assessed as time to anuria (≤100 ml/day or ≤200 ml urine volume in the short inter-dialytic period). A sample size of 516 was based upon a cumulative incidence of 30% anuria in the control group and 20% in the treatment group and 11% competing risks (death, transplantation) over 10 months, with up to 2 years follow-up. Secondary outcomes include rate of decline in small solute clearance, significant adverse events, hospitalization, loss of vascular access, cardiovascular events and interventions, dialysis efficacy and safety, dialysis-related symptoms and quality of life. Economic evaluation will be carried out to determine the cost-effectiveness of the intervention. Analyses will be adjusted for patient characteristics and dialysis unit practice patterns relevant to fluid management. DISCUSSION: This trial will establish the added value of undertaking BI measures to support clinical management of fluid status and establish the relationship between fluid status and preservation of residual kidney function in incident haemodialysis patients. TRIAL REGISTRATION: ISCCTN Number: 11342007 , completed 26/04/2016; NIHR Portfolio number: CPMS31766; Sponsor: Keele University.en
dc.language.isoeng
dc.relation.ispartofBMC Nephrology
dc.subjectJournal Article
dc.titleRationale and design of BISTRO : a randomized controlled trial to determine whether bioimpedance spectroscopy-guided fluid management maintains residual kidney function in incident haemodialysis patientsen
dc.contributor.institutionBasic and Clinical Science Unit
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionDepartment of Pharmacy, Pharmacology and Postgraduate Medicine
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.1186/s12882-017-0554-1
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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