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IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients.

dc.contributor.authorDeira, Javier
dc.contributor.authorSuárez, Miguel A
dc.contributor.authorLópez, Francisca
dc.contributor.authorGarcía-Cabrera, Emilio
dc.contributor.authorGascón, Antonio
dc.contributor.authorTorregrosa, Eduardo
dc.contributor.authorGarcía, Giannina E
dc.contributor.authorHuertas, Jorge
dc.contributor.authorde la Flor, Jose C
dc.contributor.authorPuello, Suleya
dc.contributor.authorGómez-Raja, Jonathan
dc.contributor.authorGrande, Jesús
dc.contributor.authorLerma, José L
dc.contributor.authorCorradino, Carlos
dc.contributor.authorMusso, Carlos
dc.contributor.authorRamos, Manuel
dc.contributor.authorMartín, Jesús
dc.contributor.authorBasile, Carlo
dc.contributor.authorCasino, Francesco G
dc.date.accessioned2023-01-25T10:27:48Z
dc.date.available2023-01-25T10:27:48Z
dc.date.issued2019-01-09
dc.description.abstractMost people who make the transition to renal replacement therapy (RRT) are treated with a fixed dose thrice-weekly hemodialysis réegimen, without considering their residual kidney function (RKF). Recent papers inform us that incremental hemodialysis is associated with preservation of RKF, whenever compared with conventional hemodialysis. The objective of the present controlled randomized trial (RCT) is to determine if start HD with one sessions per week (1-Wk/HD), it is associated with better patient survival and other safety parameters. IHDIP is a multicenter RCT experimental open trial. It is randomized in a 1:1 ratio and controlled through usual clinical practice, with a low intervention level and non-commercial. It includes 152 incident patients older than 18 years, with a RRF of ≥4 ml/min/1.73 m2, measured by renal clearance of urea (KrU). The intervention group includes 76 patients who will start with incremental HD (1-Wk/HD). The control group includes 76 patients who will start with thrice-weekly hemodialysis régimen. The primary outcome is assessing the survival rate, while the secondary outcomes are the morbidity rate, the clinical parameters, the quality of life and the efficiency. This study will enable to know the number of sessions a patient should receive when starting HD, depending on his RRF. The potentially important clinical and financial implications of incremental hemodialysis warrant this RCT. U.S. National Institutes of Health, ClinicalTrials.gov . Number: NCT03239808 , completed 13/04/2017. Foundation for Training and Research of Health Professionals of Extremadura.
dc.identifier.doi10.1186/s12882-018-1189-6
dc.identifier.essn1471-2369
dc.identifier.pmcPMC6325813
dc.identifier.pmid30626347
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325813/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1186/s12882-018-1189-6
dc.identifier.urihttp://hdl.handle.net/10668/13401
dc.issue.number1
dc.journal.titleBMC nephrology
dc.journal.titleabbreviationBMC Nephrol
dc.language.isoen
dc.organizationÁrea de Gestión Sanitaria de Jerez, Costa Noroeste y Sierra de Cádiz
dc.organizationHospital Costa del Sol
dc.organizationAGS - Jerez, Costa Noroeste y Sierra de Cáidz
dc.page.number8
dc.pubmedtypeClinical Trial Protocol
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectIncremental haemodialysis progressive hemodialysis
dc.subjectOnce-weekly haemodialysis
dc.subjectRandomized clinical trial
dc.subjectTwice-weekly haemodialysis
dc.subject.meshCreatinine
dc.subject.meshHumans
dc.subject.meshKidney
dc.subject.meshMulticenter Studies as Topic
dc.subject.meshOutcome Assessment, Health Care
dc.subject.meshProspective Studies
dc.subject.meshRandomized Controlled Trials as Topic
dc.subject.meshRenal Dialysis
dc.subject.meshUrea
dc.titleIHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number20
dspace.entity.typePublication

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