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平衡试验(balANZ 试验)的原理和设计:一项比较低 GDP、中性 pH 值与标准腹膜透析液对残余肾功能保护作用的随机对照试验。

Rationale and design of the balANZ trial: a randomised controlled trial of low GDP, neutral pH versus standard peritoneal dialysis solution for the preservation of residual renal function.

机构信息

Department of Renal Medicine, Princess Alexandra Hospital, Brisbane, Australia.

出版信息

BMC Nephrol. 2010 Sep 16;11:25. doi: 10.1186/1471-2369-11-25.

Abstract

BACKGROUND

The main hypothesis of this study is that neutral pH, low glucose degradation product (GDP) peritoneal dialysis (PD) fluid better preserves residual renal function in PD patients over time compared with conventional dialysate.

METHODS/DESIGN: Inclusion criteria are adult PD patients (CAPD or APD) aged 18-81 years whose first dialysis was within 90 days prior to or following enrolment and who have a residual GFR ≥ 5 ml/min/1.73 m2, a urine output ≥ 400 ml/day and an ability to understand the nature and requirements of this trial. Pregnant or lactating patients or individuals with an active infection at the time of enrolment, a contra-indication to PD or participation in any other clinical trial where an intervention is designed to moderate rate of change of residual renal function are excluded. Patients will be randomized 1:1 to receive either neutral pH, low GDP dialysis solution (Balance) or conventional dialysis solution (Stay.safe) for a period of 2 years. During this 2 year study period, urinary urea and clearance measurements will be performed at 0, 3, 6, 9, 12, 18 and 24 months. The primary outcome measure will be the slope of residual renal function decline, adjusted for centre and presence of diabetic nephropathy. Secondary outcome measures will include time from initiation of peritoneal dialysis to anuria, peritoneal small solute clearance, peritoneal transport status, peritoneal ultrafiltration, technique survival, patient survival, peritonitis rates and adverse events. A total of 185 patients has been recruited into the trial.

DISCUSSION

This investigator-initiated study has been designed to provide evidence to help nephrologists determine the optimal dialysis solution for preserving residual renal function in PD patients.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry Number: ACTRN12606000044527.

摘要

背景

本研究的主要假设是,与传统透析液相比,中性 pH 值、低葡萄糖降解产物 (GDP) 的腹膜透析 (PD) 液在较长时间内可更好地保留 PD 患者的残余肾功能。

方法/设计:纳入标准为年龄在 18-81 岁之间的成年 PD 患者(CAPD 或 APD),其首次透析在入组前或入组后 90 天内进行,且残余肾小球滤过率 (GFR)≥5ml/min/1.73m2,尿量≥400ml/天,且能理解本试验的性质和要求。排除妊娠或哺乳期患者、入组时存在活动性感染、有 PD 禁忌证或参加任何旨在调节残余肾功能变化率的干预临床试验的个体。患者将以 1:1 的比例随机接受中性 pH 值、低 GDP 透析液(Balance)或传统透析液(Stay.safe)治疗,为期 2 年。在这 2 年的研究期间,将在 0、3、6、9、12、18 和 24 个月时进行尿尿素和清除率测量。主要结局指标将是残余肾功能下降的斜率,调整中心和糖尿病肾病的存在。次要结局指标包括从开始腹膜透析到无尿、腹膜小分子清除率、腹膜转运状态、腹膜超滤、技术生存率、患者生存率、腹膜炎发生率和不良事件的时间。该试验共招募了 185 名患者。

讨论

这项由研究者发起的研究旨在提供证据,帮助肾病学家确定保留 PD 患者残余肾功能的最佳透析液。

试验注册

澳大利亚新西兰临床试验注册中心编号:ACTRN12606000044527。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7024/2954914/4d72fdd84acf/1471-2369-11-25-1.jpg

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