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Initiating renal replacement therapy through incremental haemodialysis: Protocol for a randomized multicentre clinical trial

机译:通过增量血液透析激​​发肾置换疗法:随机化多期临床试验的议定书

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BACKGROUND:Thrice-weekly haemodialysis is the usual dose when starting renal replacement therapy; however, this schedule is no longer appropriate since it does not consider residual renal function. Several reports have suggested the potential benefit of beginning haemodialysis less frequently and incrementally increasing the dose as the residual renal function decreases. However, all the data published so far are from observational studies. Thus, this clinical trial avoids any potential selection bias and will assess the possible benefits that have been observed in observational studies.METHODS/DESIGN:This report describes the study protocol of a randomized prospective multi-centre open-label clinical trial to evaluate whether starting renal replacement therapy with twice-weekly haemodialysis sessions preserves residual renal function better than the standard thrice-weekly regimen. We also explore other clinical parameters, such as concentrations of uremic toxins, dialysis doses, control of anaemia, removal of medium-weight uremic toxins, nutritional status, quality of life, hospital admissions and mortality. Only incident haemodialysis patients who can maintain a urea clearance rate KrU ≥ 2.5?mL/min/1.73?msup2/sup are eligible. Patient recruitment began on 1 January 2017 and will last for 2 years or until the required sample size has been recruited to ensure the established statistical power has been reached. The minimum follow-up period will be 1 year. Anuric patients with acute renal failure and patients who return to haemodialysis after a kidney transplant failure are excluded. It has been calculated that 44 patients should be recruited into each group to achieve a power of 80% in a two-sided comparison of means with a usual significance level of 0.05. A time-to-event analysis will estimate the probability of kidney function survival in both groups using the Kaplan-Meier method. Survival curves will be compared with log-rank tests. This survival analysis will be complemented with a proportional hazard model to estimate the hazard ratio of kidney function survival adjusted for any confounding factors. Analyses will be carried out in accordance with the intention-to-treat principle.DISCUSSION:The incremental initiation of dialysis may preserve residual renal function better than the conventional treatment, with similar or higher survival rates, as reported by observational studies. To our knowledge, this is the first clinical trial to evaluate whether initiating renal replacement therapy with twice-weekly haemodialysis sessions preserves residual renal function better than beginning with the standard thrice-weekly regimen.TRIAL REGISTRATION:ClinicalTrials.gov, NCT03302546. Registered on 5 October 2017.
机译:背景:三次每周血液透析是在开始肾替代疗法时通常的剂量;但是,本时间表不再适当,因为它不考虑残余肾功能。几份报告表明,在剩余肾功能下降时,开始血液透析的潜在益处较少,增加剂量。但是,到目前为止发布的所有数据都来自观察性研究。因此,该临床试验避免了任何潜在的选择偏差,并将评估在观察性研究中观察到的可能益处。方法/设计:本报告描述了随机预期多中心开放标签临床试验的研究方案,以评估是否启动肾置换疗法两次两次血液透析疗程,比标准的三次每周方案更好地保持残留的肾功能。我们还探讨了其他临床参数,如尿毒毒素浓度,透析剂量,贫血控制,去除中等重量尿毒症毒素,营养状况,生活质量,医院入学和死亡。只有入射的血液透析患者可以维持尿素清除率KRU≥2.5?ml / min / 1.73?m 2 符合条件。患者招聘始于2017年1月1日,并将持续2年或招募所需的样品规模以确保已达成既定的统计权。最低后续期间将是1年。患有急性肾功能衰竭的抗病患者和患有肾移植失败后恢复血液透析的患者。已经计算出44名患者应招募到每组的每组患者,以达到常见意义水平为0.05的双面比较的80%的力量。使用Kaplan-Meier方法估算两组肾功能存活的概率分析。将曲线与日志秩检验进行比较。这种存活分析将与比例危害模型补充,以估计对任何混淆因素调整的肾功能存活的危害比。分析将按照意图对待原则进行.Discssion:透析的增量启动可能比常规治疗更好地保持残留的肾功能,并且通过观察研究报告的存在类似或更高的存活率。据我们所知,这是第一项评估发起肾脏替代治疗的临床试验两次血液透析会话是否比以标准的三周期的开始更好地保留残留的肾功能.TRIAL注册:ClinicalTrials.gov,NCT03302546。 2017年10月5日注册。

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