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维持性血液透析患者使用含葡萄糖与不含葡萄糖透析液的比较:一项多中心随机对照研究——GLUMO研究的研究方案

Glucose-containing vs. glucose-free dialysate for patients with maintenance hemodialysis: Study protocol for a multicenter randomized controlled study-GLUMO study.

作者信息

Zhou Zhifeng, Xu Qing, He Xin, Ou Santao, Zhang Ling

机构信息

Department of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, Chengdu, China.

Department of Nephrology, Chengdu Kangfu Kidney Disease Hospital, Chengdu, China.

出版信息

PLoS One. 2025 Aug 11;20(8):e0330155. doi: 10.1371/journal.pone.0330155. eCollection 2025.

Abstract

PURPOSE

To mitigate the risk of infection and disordered blood lipid metabolism, glucose-free dialysate is widely utilized in China and European countries. While glucose-free dialysis does not necessarily lead to hypoglycemia, several other metabolic adjustments must occur to maintain normal blood glucose levels. Additionally, glucose-free dialysis may also increase the loss of amino acids and the susceptibility to hypotension and cardiovascular events. Incorporating an appropriate amount of glucose into the dialysate can help to offset the insufficient blood glucose during hemodialysis (HD), potentially reducing the incidence of hypoglycemia. Currently, the efficacy and safety of glucose-containing dialysate during HD remain contentious, and this study will be conducted to evaluate the efficacy and safety of 5.5 mmol/L glucose-containing dialysate for maintenance HD patients.

STUDY DESIGN AND METHODS

A multicenter, prospective, open-label, parallel-group, randomized controlled trial (RCT) will be conducted at more than 30 dialysis centers in China. Approximately 600 participants undergoing maintenance HD will be enrolled. Eligible patients will be randomly assigned to two groups, receiving either glucose-containing dialysate or glucose-free dialysate for HD at a 1:1 ratio, determined by a central computer-generated randomized sequence. The primary outcome is the incidence of the major cardiovascular and cerebrovascular adverse events (MACCE). Secondary outcomes are all-cause mortality, incidence of intradialytic hypotension (IDH), incidence of hypoglycemia, blood pressure and blood glucose variability, dysfunction of vascular access, cardiac function and fatigue level. Outcome assessors and data analysts will be blinded. All data will be analyzed using either intention-to-treat or per-protocol analysis methods.

DISCUSSION

The results of this study will provide evidence on the efficacy and safety of 5.5 mmol/L glucose-containing dialysate for maintenance HD patients, and will provide valuable insights for future dialysate selection and the enhancement of dialysis treatment prescriptions.

TRIAL REGISTRATION NUMBER

ChiCTR2400083153.

摘要

目的

为降低感染风险和血脂代谢紊乱风险,无糖透析液在中国和欧洲国家被广泛使用。虽然无糖透析不一定会导致低血糖,但必须进行其他一些代谢调整以维持正常血糖水平。此外,无糖透析还可能增加氨基酸流失以及低血压和心血管事件的易感性。在透析液中加入适量葡萄糖有助于弥补血液透析(HD)期间血糖不足,可能降低低血糖的发生率。目前,含葡萄糖透析液在血液透析期间的疗效和安全性仍存在争议,本研究将评估5.5 mmol/L含葡萄糖透析液用于维持性血液透析患者的疗效和安全性。

研究设计和方法

将在中国30多个透析中心进行一项多中心、前瞻性、开放标签、平行组、随机对照试验(RCT)。将招募约600名接受维持性血液透析的参与者。符合条件的患者将被随机分为两组,以1:1的比例接受含葡萄糖透析液或无糖透析液进行血液透析,由中央计算机生成的随机序列确定。主要结局是主要心血管和脑血管不良事件(MACCE)的发生率。次要结局包括全因死亡率、透析中低血压(IDH)发生率、低血糖发生率、血压和血糖变异性、血管通路功能障碍、心脏功能和疲劳程度。结局评估者和数据分析者将设盲。所有数据将使用意向性分析或符合方案分析方法进行分析。

讨论

本研究结果将为5.5 mmol/L含葡萄糖透析液用于维持性血液透析患者的疗效和安全性提供证据,并将为未来透析液的选择和透析治疗处方的改进提供有价值的见解。

试验注册号

ChiCTR2400083153。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87ac/12338788/d4e5e1dd80b4/pone.0330155.g001.jpg

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