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用于腹膜透析的生物相容性透析液。

Biocompatible dialysis fluids for peritoneal dialysis.

作者信息

Htay Htay, Johnson David W, Wiggins Kathryn J, Badve Sunil V, Craig Jonathan C, Strippoli Giovanni Fm, Cho Yeoungjee

机构信息

Department of Renal Medicine, Singapore General Hospital, 20 College Street, Singapore, Singapore, 169856.

出版信息

Cochrane Database Syst Rev. 2018 Oct 26;10(10):CD007554. doi: 10.1002/14651858.CD007554.pub3.

Abstract

BACKGROUND

Biocompatible peritoneal dialysis (PD) solutions, including neutral pH, low glucose degradation product (GDP) solutions and icodextrin, have previously been shown to favourably influence some patient-level outcomes, albeit based on generally sub-optimal quality studies. Several additional randomised controlled trials (RCT) evaluating biocompatible solutions in PD patients have been published recently. This is an update of a review first published in 2014.

OBJECTIVES

This review aimed to look at the benefits and harms of biocompatible PD solutions in comparison to standard PD solutions in patients receiving PD.

SEARCH METHODS

The Cochrane Kidney and Transplant Specialised Register was searched up to 12 February 2018 through contact with the Information Specialist using search terms relevant to this review. Studies in the Specialised Register are identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Register Search Portal and ClinicalTrials.gov.

SELECTION CRITERIA

All RCTs and quasi-RCTs in adults and children comparing the effects of biocompatible PD solutions (neutral pH, lactate-buffered, low GDP; neutral pH, bicarbonate(± lactate)-buffered, low GDP; glucose polymer (icodextrin)) in PD were included. Studies of amino acid-based solutions were excluded.

DATA COLLECTION AND ANALYSIS

Two authors extracted data on study quality and outcomes. Summary effect estimates were obtained using a random-effects model, and results were expressed as risk ratios and 95% confidence intervals (CI) for categorical variables, and mean differences (MD) or standardised mean differences (SMD) and 95% CI for continuous variables.

MAIN RESULTS

This review update included 42 eligible studies (3262 participants), including six new studies (543 participants). Overall, 29 studies (1971 participants) compared neutral pH, low GDP PD solution with conventional PD solution, and 13 studies (1291 participants) compared icodextrin with conventional PD solution. Risk of bias was assessed as high for sequence generation in three studies, allocation concealment in three studies, attrition bias in 21 studies, and selective outcome reporting bias in 16 studies.Neutral pH, low GDP versus conventional glucose PD solutionUse of neutral pH, low GDP PD solutions improved residual renal function (RRF) preservation (15 studies, 835 participants: SMD 0.19, 95% CI 0.05 to 0.33; high certainty evidence). This approximated to a mean difference in glomerular filtration rate of 0.54 mL/min/1.73 m (95% CI 0.14 to 0.93). Better preservation of RRF was evident at all follow-up durations with progressively greater preservation observed with increasing follow up duration. Neutral pH, low GDP PD solution use also improved residual urine volume preservation (11 studies, 791 participants: MD 114.37 mL/day, 95% CI 47.09 to 181.65; high certainty evidence). In low certainty evidence, neutral pH, low GDP solutions may make little or no difference to 4-hour peritoneal ultrafiltration (9 studies, 414 participants: SMD -0.42, 95% CI -0.74 to -0.10) which approximated to a mean difference in peritoneal ultrafiltration of 69.72 mL (16.60 to 122.00 mL) lower, and may increase dialysate:plasma creatinine ratio (10 studies, 746 participants: MD 0.01, 95% CI 0.00 to 0.03), technique failure or death compared with conventional PD solutions. It is uncertain whether neutral pH, low GDP PD solution use led to any differences in peritonitis occurrence, hospitalisation, adverse events (6 studies, 519 participants) or inflow pain (1 study, 58 participants: RR 0.51, 95% CI 0.24 to 1.08).Glucose polymer (icodextrin) versus conventional glucose PD solutionIn moderate certainty evidence, icodextrin probably reduced episodes of uncontrolled fluid overload (2 studies, 100 participants: RR 0.30, 95% CI 0.15 to 0.59) and augmented peritoneal ultrafiltration (4 studies, 102 participants: MD 448.54 mL/d, 95% CI 289.28 to 607.80) without compromising RRF (4 studies, 114 participants: SMD 0.12, 95% CI -0.26 to 0.49; low certainty evidence) which approximated to a mean creatinine clearance of 0.30 mL/min/1.73m higher (0.65 lower to 1.23 higher) or urine output (3 studies, 69 participants: MD -88.88 mL/d, 95% CI -356.88 to 179.12; low certainty evidence). It is uncertain whether icodextrin use led to any differences in adverse events (5 studies, 816 participants) technique failure or death.

AUTHORS' CONCLUSIONS: This updated review strengthens evidence that neutral pH, low GDP PD solution improves RRF and urine volume preservation with high certainty. These effects may be related to increased peritoneal solute transport and reduced peritoneal ultrafiltration, although the evidence for these outcomes is of low certainty due to significant heterogeneity and suboptimal methodological quality. Icodextrin prescription increased peritoneal ultrafiltration and mitigated uncontrolled fluid overload with moderate certainty. The effects of either neutral pH, low GDP solution or icodextrin on peritonitis, technique survival and patient survival remain uncertain and require further high quality, adequately powered RCTs.

摘要

背景

生物相容性腹膜透析(PD)液,包括中性pH值、低葡萄糖降解产物(GDP)的溶液和艾考糊精,此前已被证明对一些患者层面的结局有有利影响,尽管基于的研究质量普遍欠佳。最近又发表了几项评估PD患者使用生物相容性溶液的随机对照试验(RCT)。这是2014年首次发表的一篇综述的更新版。

目的

本综述旨在探讨与标准PD液相比,生物相容性PD液在接受PD治疗的患者中的益处和危害。

检索方法

通过与信息专家联系,使用与本综述相关的检索词,检索截至2018年2月12日的Cochrane肾脏和移植专业注册库。专业注册库中的研究通过检索CENTRAL、MEDLINE和EMBASE、会议论文集、国际临床试验注册搜索门户和ClinicalTrials.gov来识别。

入选标准

纳入所有比较生物相容性PD液(中性pH值、乳酸缓冲、低GDP;中性pH值、碳酸氢盐(±乳酸)缓冲、低GDP;葡萄糖聚合物(艾考糊精))在PD中作用的成人和儿童RCT及半RCT。排除基于氨基酸溶液的研究。

数据收集与分析

两位作者提取了关于研究质量和结局的数据。使用随机效应模型获得汇总效应估计值,结果以分类变量的风险比和95%置信区间(CI)表示,连续变量以均值差(MD)或标准化均值差(SMD)及95%CI表示。

主要结果

本综述更新纳入了42项合格研究(3262名参与者),包括6项新研究(543名参与者)。总体而言,29项研究(1971名参与者)比较了中性pH值、低GDP的PD液与传统PD液,13项研究(1291名参与者)比较了艾考糊精与传统PD液。在三项研究中序列生成的偏倚风险被评估为高,三项研究中分配隐藏的偏倚风险为高,21项研究中有失访偏倚,16项研究中有选择性结局报告偏倚。

中性pH值、低GDP与传统葡萄糖PD液

使用中性pH值、低GDP的PD液可改善残余肾功能(RRF)的保留(15项研究,835名参与者:SMD 0.19,95%CI为0.05至0.33;高确定性证据)。这相当于肾小球滤过率的平均差异为0.54 mL/min/1.73m²(95%CI为0.14至0.93)。在所有随访期间,RRF的保留情况均较好,且随着随访时间的延长,保留情况逐渐改善。使用中性pH值、低GDP的PD液还可改善残余尿量的保留(11项研究,791名参与者:MD为114.37 mL/天,95%CI为47.09至181.65;高确定性证据)。在低确定性证据中,中性pH值、低GDP的溶液对4小时腹膜超滤可能几乎没有影响(9项研究,414名参与者:SMD -0.42,95%CI为-0.74至-0.10),这相当于腹膜超滤的平均差异低69.72 mL(16.60至122.00 mL),与传统PD液相比,可能会增加透析液:血浆肌酐比值(10项研究,746名参与者:MD 0.01,95%CI为0.00至0.03)、技术失败或死亡。尚不确定使用中性pH值、低GDP的PD液是否会导致腹膜炎发生率、住院率、不良事件(6项研究,519名参与者)或流入痛(1项研究,58名参与者:RR 0.51,95%CI为0.24至1.08)有任何差异。

葡萄糖聚合物(艾考糊精)与传统葡萄糖PD液

在中等确定性证据中,艾考糊精可能减少了液体超负荷失控的发作次数(2项研究,100名参与者:RR 0.30,95%CI为0.15至0.59),并增加了腹膜超滤(4项研究,102名参与者:MD为448.54 mL/天,95%CI为289.28至607.80),且不影响RRF(4项研究,114名参与者:SMD 0.12,95%CI为-0.26至0.49;低确定性证据),这相当于肌酐清除率平均高0.30 mL/min/1.73m²(低0.65至高1.23)或尿量(3项研究,69名参与者:MD -88.88 mL/天,95%CI为-356.88至179.12;低确定性证据)。尚不确定使用艾考糊精是否会导致不良事件(5项研究,816名参与者)、技术失败或死亡有任何差异。

作者结论

本更新综述强化了证据,即中性pH值、低GDP的PD液能高度确定地改善RRF和尿量保留。这些作用可能与腹膜溶质转运增加和腹膜超滤减少有关,尽管由于显著的异质性和欠佳的方法学质量,这些结局的证据确定性较低。艾考糊精处方能中等确定地增加腹膜超滤并减轻液体超负荷失控。中性pH值、低GDP溶液或艾考糊精对腹膜炎、技术存活和患者存活的影响仍不确定,需要进一步高质量、有足够样本量的RCT。

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