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紧急启动腹膜透析与常规启动腹膜透析治疗慢性肾脏病患者的比较。

Urgent-start peritoneal dialysis versus conventional-start peritoneal dialysis for people with chronic kidney disease.

机构信息

Department of Renal Medicine, Singapore General Hospital, Singapore, Singapore.

Department of Nephrology, Princess Alexandra Hospital, Woolloongabba, Australia.

出版信息

Cochrane Database Syst Rev. 2020 Dec 15;12(12):CD012913. doi: 10.1002/14651858.CD012913.pub2.

Abstract

BACKGROUND

Urgent-start peritoneal dialysis (PD), defined as initiation of PD within two weeks of catheter insertion, has been emerging as an alternative mode of dialysis initiation for patients with chronic kidney disease (CKD) requiring urgent dialysis without established permanent dialysis access. Recently, several small studies have reported comparable patient outcomes between urgent-start and conventional-start PD.

OBJECTIVES

To examine the benefits and harms of urgent-start PD compared with conventional-start PD in adults and children with CKD requiring long-term kidney replacement therapy.

SEARCH METHODS

We searched the Cochrane Kidney and Transplant Register of Studies up to 25 May 2020 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register are identified through searches of CENTRAL, MEDLINE, EMBASE, conference proceedings, the International Clinical Trials Register (ICTRP) Search Portal, and ClinicalTrials.gov. For non-randomised controlled trials, MEDLINE (OVID) (1946 to 27 June 2019), EMBASE (OVID) (1980 to 27 June 2019), Clinical Trials Register (ICTRP) Search Portal and ClinicalTrials.gov (up to 27 June 2019) were searched.

SELECTION CRITERIA

All randomised controlled trials (RCTs) and non-RCTs comparing the outcomes of urgent-start PD (within 2 weeks of catheter insertion) and conventional-start PD ( ≥ 2 weeks of catheter insertion) treatment in children and adults CKD patients requiring long-term dialysis were included. Studies without a control group were excluded.

DATA COLLECTION AND ANALYSIS

Data were extracted and quality of studies were examined by two independent authors. The authors contacted investigators for additional information. Summary estimates of effect were examined using random-effects model and results were presented as risk ratios (RR) with 95% confidence intervals (CI) as appropriate for the data. The certainty of evidence for individual outcome was assessed using the GRADE approach.

MAIN RESULTS

A total of 16 studies (2953 participants) were included in this review, which included one multicentre RCT (122 participants) and 15 non-RCTs (2831 participants): 13 cohort studies (2671 participants) and 2 case-control studies (160 participants). The review included unadjusted data for analyses due to paucity of studies reporting adjusted data. In low certainty evidence, urgent-start PD may increase dialysate leak (1 RCT, 122 participants: RR 3.90, 95% CI 1.56 to 9.78) compared with conventional-start PD which translated into an absolute number of 210 more leaks per 1000 (95% CI 40 to 635). In very low certainty evidence, it is uncertain whether urgent-start PD increases catheter blockage (4 cohort studies, 1214 participants: RR 1.33, 95% CI 0.40 to 4.43; 2 case-control studies, 160 participants: RR 1.89, 95% CI 0.58 to 6.13), catheter malposition (6 cohort studies, 1353 participants: RR 1.63, 95% CI 0.80 to 3.32; 1 case-control study, 104 participants: RR 3.00, 95% CI 0.64 to 13.96), and PD dialysate flow problems (3 cohort studies, 937 participants: RR 1.44, 95% CI 0.34 to 6.14) compared to conventional-start PD. In very low certainty evidence, it is uncertain whether urgent-start PD increases exit-site infection (2 cohort studies, 337 participants: RR 1.43, 95% CI 0.24 to 8.61; 1 case-control study, 104 participants RR 1.20, 95% CI 0.41 to 3.50), exit-site bleeding (1 RCT, 122 participants: RR 0.70, 95% CI 0.03 to 16.81; 1 cohort study, 27 participants: RR 1.58, 95% CI 0.07 to 35.32), peritonitis (7 cohort studies, 1497 participants: RR 1.00, 95% CI 0.68 to 1.46; 2 case-control studies, participants: RR 1.09, 95% CI 0.12 to 9.51), catheter readjustment (2 cohort studies, 739 participants: RR 1.27, 95% CI 0.40 to 4.02), or reduces technique survival (1 RCT, 122 participants: RR 1.09, 95% CI 1.00 to 1.20; 8 cohort studies, 1668 participants: RR 0.90, 95% CI 0.76 to 1.07; 2 case-control studies, 160 participants: RR 0.92, 95% CI 0.79 to 1.06). In very low certainty evidence, it is uncertain whether urgent-start PD compared with conventional-start PD increased death (any cause) (1 RCT, 122 participants: RR 1.49, 95% CI 0.87 to 2.53; 7 cohort studies, 1509 participants: RR 1.89, 95% CI 1.07 to 3.3; 1 case-control study, 104 participants: RR 0.90, 95% CI 0.27 to 3.02; very low certainty evidence). None of the included studies reported on tunnel tract infection.

AUTHORS' CONCLUSIONS: In patients with CKD who require dialysis urgently without ready-to-use dialysis access in place, urgent-start PD may increase the risk of dialysate leak and has uncertain effects on catheter blockage, malposition or readjustment, PD dialysate flow problems, infectious complications, exit-site bleeding, technique survival, and patient survival compared with conventional-start PD.

摘要

背景

紧急启动腹膜透析(PD)定义为在导管插入后两周内开始 PD,它已成为一种替代模式,适用于需要紧急透析但尚未建立永久性透析通路的慢性肾脏病(CKD)患者。最近,几项小型研究报告了紧急启动 PD 和常规启动 PD 之间可比的患者结局。

目的

在需要长期肾脏替代治疗的成人和儿童 CKD 患者中,比较紧急启动 PD 与常规启动 PD 的益处和危害。

检索方法

我们通过与信息专家联系,使用与本综述相关的检索词,检索了截至 2020 年 5 月 25 日的 Cochrane 肾脏病和移植登记册中的研究。登记册中的研究通过对 CENTRAL、MEDLINE、EMBASE、会议论文集、国际临床试验注册中心(ICTRP)搜索门户和 ClinicalTrials.gov 的搜索确定。对于非随机对照试验,检索了 MEDLINE(OVID)(1946 年至 2019 年 6 月 27 日)、EMBASE(OVID)(1980 年至 2019 年 6 月 27 日)、临床试验登记册(ICTRP)搜索门户和 ClinicalTrials.gov(截至 2019 年 6 月 27 日)。

选择标准

所有比较紧急启动 PD(导管插入后 2 周内)和常规启动 PD(导管插入后 ≥ 2 周)治疗需要长期透析的儿童和成人 CKD 患者结局的随机对照试验(RCT)和非随机对照试验均纳入研究。没有对照组的研究被排除在外。

数据收集和分析

两名独立作者提取数据并检查研究质量。作者联系研究人员以获取更多信息。使用随机效应模型评估汇总估计效应,并以适当的风险比(RR)和 95%置信区间(CI)呈现结果。使用 GRADE 方法评估个别结局证据的确定性。

主要结果

本综述共纳入 16 项研究(2953 名参与者),包括一项多中心 RCT(122 名参与者)和 15 项非 RCT(2831 名参与者):13 项队列研究(2671 名参与者)和 2 项病例对照研究(160 名参与者)。由于缺乏报告调整数据的研究,本综述纳入了未经调整的数据进行分析。在低确定性证据中,与常规启动 PD 相比,紧急启动 PD 可能会增加透析液渗漏(1 项 RCT,122 名参与者:RR 3.90,95%CI 1.56 至 9.78),这意味着每 1000 人中有 210 人以上会发生更多的渗漏(95%CI 40 至 635)。在极低确定性证据中,目前尚不确定紧急启动 PD 是否会增加导管阻塞(4 项队列研究,1214 名参与者:RR 1.33,95%CI 0.40 至 4.43;2 项病例对照研究,160 名参与者:RR 1.89,95%CI 0.58 至 6.13)、导管位置不当(6 项队列研究,1353 名参与者:RR 1.63,95%CI 0.80 至 3.32;1 项病例对照研究,104 名参与者:RR 3.00,95%CI 0.64 至 13.96)和 PD 透析液流动问题(3 项队列研究,937 名参与者:RR 1.44,95%CI 0.34 至 6.14)与常规启动 PD 相比。在极低确定性证据中,目前尚不确定紧急启动 PD 是否会增加出口部位感染(2 项队列研究,337 名参与者:RR 1.43,95%CI 0.24 至 8.61;1 项病例对照研究,104 名参与者:RR 1.20,95%CI 0.41 至 3.50)、出口部位出血(1 项 RCT,122 名参与者:RR 0.70,95%CI 0.03 至 16.81;1 项队列研究,27 名参与者:RR 1.58,95%CI 0.07 至 35.32)、腹膜炎(7 项队列研究,1497 名参与者:RR 1.00,95%CI 0.68 至 1.46;2 项病例对照研究,参与者:RR 1.09,95%CI 0.12 至 9.51)、导管调整(2 项队列研究,739 名参与者:RR 1.27,95%CI 0.40 至 4.02)或降低技术生存率(1 项 RCT,122 名参与者:RR 1.09,95%CI 1.00 至 1.20;8 项队列研究,1668 名参与者:RR 0.90,95%CI 0.76 至 1.07;2 项病例对照研究,160 名参与者:RR 0.92,95%CI 0.79 至 1.06)。在极低确定性证据中,目前尚不确定紧急启动 PD 是否会增加任何原因导致的死亡(1 项 RCT,122 名参与者:RR 1.49,95%CI 0.87 至 2.53;7 项队列研究,1509 名参与者:RR 1.89,95%CI 1.07 至 3.3;1 项病例对照研究,104 名参与者:RR 0.90,95%CI 0.27 至 3.02;极低确定性证据)。纳入的研究均未报告隧道感染。

作者结论

在需要紧急透析且尚未建立可用透析通路的 CKD 患者中,与常规启动 PD 相比,紧急启动 PD 可能会增加透析液渗漏的风险,且对导管阻塞、位置不当或调整、PD 透析液流动问题、感染性并发症、出口部位出血、技术生存率和患者生存率的影响不确定。

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