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一项关于急性护理儿科患者中心静脉导管及导管部位有效管理的系统评价。

A systematic review for effective management of central venous catheters and catheter sites in acute care paediatric patients.

作者信息

Lee Olive Kin Eng, Johnston Linda

机构信息

Intensive Care Unit, The Royal Children's Hospital, The University of Melbourne, School of Nursing, Parkville, Victoria, Australia 3051.

出版信息

Worldviews Evid Based Nurs. 2005;2(1):4-13; discussion 14-5. doi: 10.1111/j.1524-475X.2005.04085.x.

DOI:10.1111/j.1524-475X.2005.04085.x
PMID:17040550
Abstract

BACKGROUND

Central venous catheters (CVCs) have provided many benefits in modern-day medical practice; however, they also put patients at risk of catheter-related complications. Numerous studies have been carried out in relation to the management of central venous catheters with conflicting results. While there were several systematic reviews of central venous catheter-related issues, it is clear that there was no systematic review of CVC-related studies specific to the paediatric population in the acute care setting.

OBJECTIVE

To present the best available evidence for effective management of central venous catheters and catheter sites in the prevention and/or reduction of catheter-related complications in hospitalised paediatric patients.

METHODS

A systematic review was undertaken according to the approach of the Centre for Reviews and Dissemination (CRD; http://www.york.ac.uk/inst/crd).

DATA SOURCE

Literature was identified by electronic searching of Cochrane Library, MEDLINE, CINAHL, HealthSTAR, and CancerLit; checking references of all review articles; hand searching of key relevant journals and conference proceedings; and contact with expert informants, medical suppliers, and pharmaceutical companies.

INCLUSION/EXCLUSION CRITERIA: The review included randomised and non-randomised controlled trials conducted with hospitalised paediatric patients. Studies that included mixed adult and paediatric populations and mixed hospitalised and home care settings were excluded.

DATA EXTRACTION

Two independent reviewers extracted data onto a standard data extraction form, with differences resolved by discussion.

QUALITY ASSESSMENT

The quality assessment of retrieved studies included: study design, the degree to which systematic bias was avoided or minimised, the degree to which the assessment was "blind," the degree to which follow up was completed.

DATA SYNTHESIS

Quantitative pooling of studies was not feasible due to the diversity of interventions and outcome measures between similar studies. A narrative account of the study characteristics and results was therefore undertaken.

RESULTS

Thirty-eight randomised and quasi-randomised controlled trials were retrieved for critical appraisal. Of these, 32 were excluded from the review because the studies did not meet the inclusion criteria and some lacked reporting of appropriate data. Six studies met the criteria with interventions such as antibiotic flushes, antiseptic skin preparations, and dressing materials.

CONCLUSION

Quality of reporting was generally lacking. Statistical pooling of results was not possible due to diversity in the reporting of outcomes. There was no evidence to make recommendations on the degree of barrier precautions and the type of aseptic technique to be used at the time of catheter insertion in the paediatric population to prevent catheter-related infection. There was insufficient evidence to support the routine use of an antibiotic flushing solution. There was a lack of randomised controlled trial (RCT) evidence on the benefit of heparin flushes, the use of in-line filters, the frequency of fluid administration set changes, or the type of dressing to use and the frequency of dressing changes. There was some evidence to suggest that chlorhexidine lotion is superior to povidone iodine as a cutaneous antiseptic at the catheter insertion site. However, no recommendation can be made for the use of chlorhexidine in neonates less than 2 weeks old or in premature infants. This systematic review concluded that there is an urgent need for well-designed randomised controlled trials with sufficient power to determine the effectiveness of various interventions in relation to management of CVCs.

摘要

背景

中心静脉导管(CVC)在现代医学实践中带来了诸多益处;然而,它们也使患者面临与导管相关并发症的风险。关于中心静脉导管的管理已开展了大量研究,但结果相互矛盾。虽然已有几项关于中心静脉导管相关问题的系统评价,但显然尚无针对急性护理环境中儿科患者的CVC相关研究的系统评价。

目的

提供最佳现有证据,以有效管理中心静脉导管及导管部位,预防和/或减少住院儿科患者的导管相关并发症。

方法

根据评价与传播中心(CRD;http://www.york.ac.uk/inst/crd)的方法进行系统评价。

数据来源

通过电子检索Cochrane图书馆、MEDLINE、CINAHL、HealthSTAR和CancerLit来识别文献;检查所有综述文章的参考文献;手工检索关键相关期刊和会议论文集;并与专家信息提供者、医疗供应商和制药公司联系。

纳入/排除标准:该评价纳入了针对住院儿科患者进行的随机和非随机对照试验。排除了包含成人和儿科混合人群以及住院和家庭护理混合环境的研究。

数据提取

两名独立评价者将数据提取到标准数据提取表上,通过讨论解决分歧。

质量评估

对检索到的研究的质量评估包括:研究设计、避免或最小化系统偏差的程度、评估“盲法”的程度、随访完成的程度。

数据综合

由于相似研究之间干预措施和结局指标的多样性,对研究进行定量汇总不可行。因此,对研究特征和结果进行了叙述性描述。

结果

检索到38项随机和半随机对照试验进行批判性评价。其中,32项被排除在评价之外,因为这些研究不符合纳入标准,且一些研究缺乏适当数据的报告。六项研究符合标准,其干预措施包括抗生素封管、皮肤消毒制剂和敷料材料。

结论

报告质量普遍欠佳。由于结局报告的多样性,无法对结果进行统计汇总。没有证据就儿科患者在导管插入时预防导管相关感染所需的屏障预防措施程度和无菌技术类型提出建议。没有足够的证据支持常规使用抗生素封管溶液。缺乏关于肝素封管、使用在线过滤器、更换输液装置的频率、使用的敷料类型和更换敷料的频率的益处的随机对照试验(RCT)证据。有一些证据表明,在导管插入部位,洗必泰洗剂作为皮肤消毒剂优于聚维酮碘。然而,对于小于2周龄新生儿或早产儿使用洗必泰,无法提出建议。该系统评价得出结论认为,迫切需要设计良好、有足够效力的随机对照试验,以确定各种干预措施对CVC管理的有效性。

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