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递增式血液透析启动肾脏替代治疗的随机多中心临床试验方案

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

机构信息

Servicio de Nefrología, Hospital Universitario Ramón y Cajal, IRYCIS, Madrid, Spain.

Departamento de Medicina, Universidad de Alcala, Alcalá de Henares, Madrid, Spain.

出版信息

Trials. 2020 Feb 19;21(1):206. doi: 10.1186/s13063-020-4058-0.

Abstract

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 m 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.

摘要

背景

开始肾脏替代治疗时,每周三次的血液透析是常用剂量;然而,由于这种方案没有考虑到残余肾功能,因此已不再适用。有几项报告表明,随着残余肾功能的下降,减少血液透析频率并逐渐增加剂量可能具有潜在的益处。然而,迄今为止所有发表的数据均来自观察性研究。因此,本临床试验避免了任何潜在的选择偏倚,并将评估观察性研究中观察到的可能益处。

方法/设计:本报告描述了一项随机前瞻性多中心开放标签临床试验的研究方案,以评估每周两次血液透析治疗开始肾脏替代治疗是否比标准每周三次方案更能保留残余肾功能。我们还探讨了其他临床参数,如尿毒症毒素浓度、透析剂量、贫血控制、中分子量尿毒症毒素清除、营养状况、生活质量、住院和死亡率。只有能够维持尿素清除率 KrU≥2.5ml/min/1.73m 的新发生血液透析患者有资格入组。患者招募于 2017 年 1 月 1 日开始,持续 2 年或直至招募到所需的样本量以确保达到既定的统计效力。最低随访期为 1 年。急性肾衰竭无尿患者和肾移植失败后重新开始血液透析的患者除外。根据双侧均值比较的常用意义水平 0.05 和 80%的效力计算,每组应招募 44 例患者。采用 Kaplan-Meier 方法估计两组的肾功能生存率。生存曲线将通过对数秩检验进行比较。该生存分析将通过比例风险模型进行补充,以根据任何混杂因素调整肾功能生存的风险比。分析将根据意向治疗原则进行。

讨论

正如观察性研究报告的那样,与传统治疗相比,递增性开始透析可能会更好地保留残余肾功能,且生存率相似或更高。据我们所知,这是首个评估每周两次血液透析开始肾脏替代治疗是否比标准每周三次方案更能保留残余肾功能的临床试验。

试验注册

ClinicalTrials.gov,NCT03302546。于 2017 年 10 月 5 日注册。

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