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治疗维持性血液透析患者导管相关血流感染的干预措施。

Interventions for treating catheter-related bloodstream infections in people receiving maintenance haemodialysis.

机构信息

Department of Vascular and Endovascular Surgery, Federal University of Sao Paulo, Sao Paulo, Brazil.

出版信息

Cochrane Database Syst Rev. 2022 Apr 1;4(4):CD013554. doi: 10.1002/14651858.CD013554.pub2.

Abstract

BACKGROUND

Patients with kidney failure require vascular access to receive maintenance haemodialysis (HD), which can be achieved by an arteriovenous fistula or a central venous catheter (CVC). CVC use is related to frequent complications such as venous stenosis and infection. Venous stenosis occurs mainly due to trauma caused by the entrance of the catheter into the venous lumen and repeated contact with the vein wall.  A biofilm, a colony of irreversible adherent and self-sufficient micro-organisms embedded in a self-produced matrix of exopolysaccharides, is associated with the development of infections in patients with indwelling catheters. Despite its clinical relevance, the treatment of catheter-related bloodstream infections (CRBSIs) in patients receiving maintenance HD remains controversial, especially regarding catheter management. Antibiotic lock solutions may sterilise the catheter, treat the infection and prevent unnecessary catheter procedures. However, such treatment may also lead to antibiotic resistance or even clinical worsening in certain more virulent pathogens. Catheter removal and delayed replacement may remove the source of infection, improving infectious outcomes, but this approach may also increase vascular access stenosis, thrombosis or both, or even central vein access failure. Catheter guidewire exchange attempts to remove the source of infection while maintaining access to the same vein and, therefore, may improve clinical outcomes and preserve central veins for future access.

OBJECTIVES

To assess the benefits and harms of different interventions for CRBSI treatment in patients receiving maintenance HD through a permanent CVC, such as systemic antibiotics alone or systemic antibiotics combined with either lock solutions or catheter guidewire exchange or catheter replacement.

SEARCH METHODS

We searched the Cochrane Kidney and Transplant Register of Studies up to 21 December 2021 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register were identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Register (ICTRP) Search Portal, and ClinicalTrials.gov.

SELECTION CRITERIA

We included all randomised controlled trials (RCTs) and quasi-RCTs evaluating the management of CRBSI in permanent CVCs in people receiving maintenance HD.

DATA COLLECTION AND ANALYSIS

Two authors independently selected studies for inclusion, assessed their risk of bias, and performed data extraction. Results were expressed as risk ratios (RR) or hazard ratios (HR) for dichotomous outcomes and mean difference (MD) for continuous outcomes, with their 95% confidence intervals (CI). The certainty of the evidence was assessed using GRADE.

MAIN RESULTS

We identified two RCTs and one quasi-RCT that enrolled 760 participants addressing the treatment of CRBSIs in people (children and adults) receiving maintenance HD through CVC. No two studies compared the same interventions. The quasi-RCT compared two different lock solutions (tissue plasminogen activator (TPA) and heparin) with concurrent systemic antibiotics. One RCT compared systemic antibiotics alone and in association with an ethanol lock solution, and the other compared systemic antibiotics with different catheter management strategies (guidewire exchange versus removal and replacement). The overall certainty of the evidence was downgraded due to the small number of participants, high risk of bias in many domains, especially randomisation, allocation, and other sources of bias, and missing outcome data. It is uncertain whether an ethanol lock solution used with concurrent systemic antibiotics improved CRBSI eradication compared to systemic antibiotics alone (RR 1.61, 95% CI 1.16 to 2.23) because the certainty of this evidence is very low. There were no reported differences between the effects of TPA and heparin lock solutions on cure rates (RR 0.92, 95% CI 0.74 to 1.15) or between catheter guidewire exchange versus catheter removal with delayed replacement, expressed as catheter infection-free survival (HR 0.88, 95% CI 0.43 to 1.79). To date, no results are available comparing other interventions. Outcomes such as venous stenosis and/or thrombosis, antibiotic resistance, death, and adverse events were not reported.

AUTHORS' CONCLUSIONS: Currently, there is no available high certainty evidence to support one treatment over another for CRBSIs. The benefit of using ethanol lock treatment in combination with systemic antibiotics compared to systemic antibiotics alone for CRBSIs in patients receiving maintenance HD remains uncertain due to the very low certainty of the evidence. Hence, further RCTs to identify the benefits and harms of CRBSI treatment options are needed. Future studies should unify CRBSI and cure definitions and improve methodological design.

摘要

背景

肾衰竭患者需要血管通路来接受维持性血液透析(HD),这可以通过动静脉瘘或中央静脉导管(CVC)来实现。CVC 的使用与静脉狭窄和感染等频繁并发症有关。静脉狭窄主要是由于导管进入静脉腔和反复接触静脉壁而引起的创伤。生物膜是一种不可逆转的附着和自给自足的微生物群落,嵌入在由细胞外多糖组成的自产生基质中,与留置导管患者感染的发展有关。尽管具有临床相关性,但维持性血液透析患者的导管相关血流感染(CRBSI)的治疗仍存在争议,尤其是关于导管管理。抗生素锁定溶液可以对导管进行消毒,治疗感染并防止不必要的导管程序。然而,这种治疗方法也可能导致抗生素耐药性,甚至在某些更具毒力的病原体中导致临床恶化。导管拔除和延迟更换可能会去除感染源,改善感染结局,但这种方法也可能增加血管通路狭窄、血栓形成或两者兼而有之,甚至导致中央静脉通路失败。导管导丝交换试图在保留相同静脉通路的同时去除感染源,因此可能会改善临床结局并为未来的通路保留中央静脉。

目的

通过永久性 CVC 评估治疗维持性 HD 患者 CRBSI 的不同干预措施的益处和危害,例如单独使用全身抗生素或全身抗生素联合使用锁定溶液或导管导丝交换或导管更换。

搜索方法

我们通过与信息专家联系,使用与本综述相关的搜索词,在 Cochrane 肾脏和移植登记处的研究中搜索至 2021 年 12 月 21 日。通过搜索 CENTRAL、MEDLINE 和 EMBASE、会议记录、国际临床试验注册平台(ICTRP)搜索门户和 ClinicalTrials.gov 来确定登记处的研究。

选择标准

我们纳入了所有随机对照试验(RCT)和准随机对照试验,评估了永久性 CVC 中 CRBSI 的管理在接受维持性 HD 的人群中的应用。

数据收集和分析

两名作者独立选择纳入的研究,评估其偏倚风险,并进行数据提取。结果表示为二分类结局的风险比(RR)或风险比(HR),连续结局的均数差(MD),及其 95%置信区间(CI)。使用 GRADE 评估证据的确定性。

主要结果

我们确定了两项 RCT 和一项准 RCT,共纳入 760 名参与者,旨在治疗通过 CVC 接受维持性 HD 的人群(儿童和成人)的 CRBSI。没有两项研究比较相同的干预措施。准 RCT 比较了两种不同的锁定溶液(组织纤溶酶原激活剂(TPA)和肝素)与同时使用全身抗生素。一项 RCT 比较了单独使用全身抗生素与使用乙醇锁定溶液联合使用,另一项 RCT 比较了全身抗生素与不同的导管管理策略(导丝交换与拔除和更换)。由于参与者数量少、许多领域(特别是随机化、分配和其他来源的偏倚以及缺失结局数据)的偏倚风险高,以及结局数据缺失,因此证据的总体确定性被降级。不确定乙醇锁定溶液与全身抗生素联合使用是否比单独使用全身抗生素更能提高 CRBSI 根除率(RR 1.61,95%CI 1.16 至 2.23),因为该证据的确定性非常低。TPA 和肝素锁定溶液对治愈率的影响(RR 0.92,95%CI 0.74 至 1.15)或导管导丝交换与延迟更换相比导管感染无生存(HR 0.88,95%CI 0.43 至 1.79)之间没有差异。迄今为止,尚无比较其他干预措施的结果。静脉狭窄和/或血栓形成、抗生素耐药性、死亡和不良事件等结局未报告。

作者结论

目前,没有高质量证据支持一种治疗方法优于另一种治疗方法,用于治疗接受维持性 HD 的患者的 CRBSI。由于证据的确定性非常低,因此,使用乙醇锁定治疗与全身抗生素联合治疗与单独使用全身抗生素相比,在治疗接受维持性 HD 的患者的 CRBSI 方面的益处仍然不确定。因此,需要进一步的 RCT 来确定 CRBSI 治疗选择的益处和危害。未来的研究应统一 CRBSI 和治愈的定义,并改进方法设计。

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