首页> 外文期刊>BMC Nephrology >Rationale and design of the Sodium Lowering In Dialysate (SoLID) trial: a randomised controlled trial of low versus standard dialysate sodium concentration during hemodialysis for regression of left ventricular mass
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Rationale and design of the Sodium Lowering In Dialysate (SoLID) trial: a randomised controlled trial of low versus standard dialysate sodium concentration during hemodialysis for regression of left ventricular mass

机译:透析液(固体)试验中降低钠的基本原理和设计:血液透析期间血液透析中低与标准透析钠浓度的随机对照试验,左心室肿块回归

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Background The current literature recognises that left ventricular hypertrophy makes a key contribution to the high rate of premature cardiovascular mortality in dialysis patients. Determining how we might intervene to ameliorate left ventricular hypertrophy in dialysis populations has become a research priority. Reducing sodium exposure through lower dialysate sodium may be a promising intervention in this regard. However there is clinical equipoise around this intervention because the benefit has not yet been demonstrated in a robust prospective clinical trial, and several observational studies have suggested sodium lowering interventions may be deleterious in some dialysis patients. Methods/design The Sodium Lowering in Dialysate (SoLID) study is funded by the Health Research Council of New Zealand. It is a multi-centre, prospective, randomised, single-blind (outcomes assessor), controlled parallel assignment 3-year clinical trial. The SoLID study is designed to study what impact low dialysate sodium has upon cardiovascular risk in dialysis patients. The study intends to enrol 118 home hemodialysis patients from 6 sites in New Zealand over 24 months and follow up each participant over 12 months. Key exclusion criteria are: patients who dialyse more frequently than 3.5 times per week, pre-dialysis serum sodium of Discussion The SoLID study is designed to clarify the effect of low dialysate sodium upon the cardiovascular outcomes of dialysis patients. The study results will provide much needed information about the efficacy of a cost effective, economically sustainable solution to a condition which is curtailing the lives of so many dialysis patients. Trial registration Australian and New Zealand Clinical Trials Registry number: ACTRN12611000975998
机译:背景技术目前的文献认识到左心室肥大对透析患者的高早期心血管死亡率进行了关键贡献。确定如何在透析人群中介入改善左心室肥厚已成为一个研究优先事项。通过低透析液钠降低钠暴露可能是这方面的有希望的干预。然而,围绕这种干预有临床设备,因为在强大的前瞻性临床试验中尚未证明益处,并且在一些透析患者中​​,几项观察性研究表明降低干预措施可能是有害的。方法/设计透析液(固体)研究中降低的钠由新西兰卫生研究委员会资助。它是一个多中心,前瞻性,随机单盲(结果评估员),受控并行分配3年临床试验。实验研究旨在研究透析患者心血管风险对低透析液的影响。该研究计划在新西兰的6个地点注入118名家庭血液透析患者超过24个月,并在12个月内跟进每个参与者。关键排除标准是:透析比每周3.5倍透析的患者,透析血清讨论钠固体研究旨在阐明低透析液钠对透析患者心血管结果的影响。研究结果将提供有关成本效益,经济可持续的解决方案对削减如此多的透析患者的生命的情况的效果的效果。审判登记澳大利亚和新西兰临床试验登记号:ACTRN12611000975998

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