...
首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Icodextrin Versus Glucose Solutions for the Once-Daily Long Dwell in Peritoneal Dialysis: An Enriched Systematic Review and Meta-analysis of Randomized Controlled Trials
【24h】

Icodextrin Versus Glucose Solutions for the Once-Daily Long Dwell in Peritoneal Dialysis: An Enriched Systematic Review and Meta-analysis of Randomized Controlled Trials

机译:Icodextrin 与葡萄糖溶液对腹膜透析中每日一次的长期停留:随机对照试验的丰富系统评价和荟萃分析

获取原文
获取原文并翻译 | 示例

摘要

Rationale Objective: The efficacy and safety of icodextrin versus glucose-only peritoneal dialysis (PD) regimens is unclear. The aim of this study was to compare once-daily long-dwell icodextrin versus glucose among patients with kidney failure undergoing PD. Study Design: Systematic review of randomized controlled trials (RCTs), enriched with unpublished data from investigator-initiated and industry-sponsored studies. Setting Study Populations: Individuals with kidney failure receiving regular PD treatment enrolled in clinical trials of dialysate composition. Selection Criteria for Studies: Medline, Embase, CENTRAL, Ichushi Web, 10 Chinese databases, clinical trials registries, conference proceedings, and citation lists from inception to November 2018. Further data were obtained from principal investigators and industry clinical study reports. Data Extraction: 2 independent reviewers selected studies and extracted data using a prespecified extraction instrument. Analytic Approach: Qualitative synthesis of demographics, measurement scales, and outcomes. Quantitative synthesis with Mantel-Haenszel risk ratios (RRs), Peto odds ratios (ORs), or (standardized) mean differences (MDs). Risk of bias of included studies at the outcome level was assessed using the Cochrane risk-of-bias tool for RCTs. Results: 19 RCTs that enrolled 1,693 participants were meta-analyzed. Ultrafiltration was improved with icodextrin (medium-term MD, 208.92 95 CI, 99.69-318.14 mL/24 h; high certainty of evidence), reflected also by fewer episodes of fluid overload (RR, 0.43 95 CI, 0.24-0.78; high certainty). Icodextrin-containing PD probably decreased mortality risk compared to glucose-only PD (Peto OR, 0.49 95 CI, 0.24-1.00; moderate certainty). Despite evidence of lower peritoneal glucose absorption with icodextrin-containing PD (medium-term MD, -40.84 95 CI, -48.09 to -33.59 g/long dwell; high certainty), this did not directly translate to changes in fasting plasma glucose (-0.50 95 CI, -1.19 to 0.18 mmol/L; low certainty) and hemoglobin A(1c) levels (-0.14 95 CI, -0.34 to 0.05; high certainty). Safety outcomes and residual kidney function were similar in both groups; health-related quality-of-life and pain scores were inconclusive. Limitations: Trial quality was variable. The followup period was heterogeneous, with a paucity of assessments over the long term. Mortality results are based on just 32 events and were not corroborated using time-to-event analysis of individual patient data. Conclusions: Icodextrin for once-daily long-dwell PD has clinical benefit for some patients, including those not meeting ultrafiltration targets and at risk for fluid overload. Future research into patient-centered outcomes and cost-effectiveness associated with icodextrin is needed.
机译:基本原理和目标:icodextrin与仅葡萄糖腹膜透析(PD)方案的疗效和安全性尚不清楚。本研究的目的是比较接受 PD 的肾衰竭患者中每日一次的长停留伊考特糊精与葡萄糖。 研究设计:随机对照试验 (RCT) 的系统评价,丰富了来自研究者发起和行业赞助研究的未发表数据。环境和研究人群:接受常规PD治疗的肾衰竭患者参加了透析液成分的临床试验。研究纳入标准:Medline、Embase、CENTRAL、Ichushi Web、10个中文数据库、临床试验注册库、会议论文集、2018年11月引文列表。从主要研究人员和行业临床研究报告中获得了进一步的数据。资料提取:2名独立评价员选择研究并使用预先指定的提取工具提取资料。分析方法:人口统计学、测量量表和结果的定性综合。使用 Mantel-Haenszel 风险比 (RR)、Peto 比值比 (OR) 或(标准化)平均差 (MD) 进行定量综合。使用Cochrane随机对照试验偏倚风险工具评估纳入研究在结局水平上的偏倚风险。 结果:对19项RCTs进行了meta分析,共纳入了1,693名受试者。icodextrin(中期MD,208.92 [95% CI,99.69-318。14] 毫升/24 小时;证据质量高),也反映在液体超负荷的发生次数较少(RR,0.43 [95% CI,0.24-0.78];高质量证据)。与仅含葡萄糖的PD相比,含Icodextrin的PD可能降低了死亡风险(Peto OR,0.49 [95% CI,0.24-1.00];中等质量证据)。尽管有证据表明含艾考特霉素的PD腹膜葡萄糖吸收较低(中期MD,-40.84 [95% CI,-48.09至-33.59] g/长期停留;高质量证据),但这并不能直接转化为空腹血糖(-0.50 [95% CI,-1.19至0.18] mmol/L;低质量证据)和血红蛋白A(1c)水平(-0.14% [95% CI,-0.34%至0.05%];高质量证据)的变化。两组的安全性结局和残余肾功能相似;与健康相关的生活质量和疼痛评分尚无定论。局限性:试验质量参差不齐。随访期是异质的,缺乏长期评估。死亡率结果仅基于 32 个事件,并且未使用个体患者数据的事件发生时间分析进行证实。结论:Icodextrin 治疗每日一次长期停留 PD 对一些患者具有临床益处,包括未达到超滤目标且有液体超负荷风险的患者。未来需要研究以患者为中心的结果和与 icodextrin 相关的成本效益。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号