Carr Peter J, Higgins Niall S, Cooke Marie L, Mihala Gabor, Rickard Claire M
Emergency Medicine, School of Medicine, The University of Western Australia, 2nd Floor, R Block, QE11 Medical Centre, Nedlands, Australia, 6009.
Cochrane Database Syst Rev. 2018 Mar 20;3(3):CD011429. doi: 10.1002/14651858.CD011429.pub2.
Most people admitted to hospitals worldwide require a vascular access device (VAD). Hundreds of millions of VADs are inserted annually in the USA with reports of over a billion peripheral intravenous catheters used annually worldwide. Numerous reports suggest that a team approach for the assessment, insertion, and maintenance of VADs improves clinical outcomes, the patient experience, and healthcare processes.
To compare the use of the vascular access specialist team (VAST) for VAD insertion and care to a generalist model approach for hospital or community participants requiring a VAD in terms of insertion success, device failure, and cost-effectiveness.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 1); Ovid MEDLINE (1950 to 7 February 2018); Ovid Embase (1980 to 7 February 2018); EBSCO CINAHL (1982 to 7 February 2018); Web of Science Conference Proceedings Citation Index - Science and Social Science and Humanities (1990 to 7 February 2018); and Google Scholar. We searched the following trial registries: Australian and New Zealand Clinical Trials Register (www.anzctr.org.au); ClinicalTrials.gov (www.clinicaltrials.gov); Current Controlled Trials (www.controlled-trials.com/mrct); HKU Clinical Trials Registry (www.hkclinicaltrials.com); Clinical Trials Registry - India (ctri.nic.in/Clinicaltrials/login.php); UK Clinical Trials Gateway (www.controlled-trials.com/ukctr/); and the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP) (www.who.int/trialsearch). We searched all databases on 7 February 2018.
We planned to include randomized controlled trials (RCTs) that evaluated the effectiveness of VAST or specialist inserters for their impact on clinical outcomes.
We used standard methodological procedures recommended by Cochrane and used Covidence software to assist with file management.
We retrieved 2398 citations: 30 studies were eligible for further examination of their full text, and we found one registered clinical trial in progress. No studies could be included in the analysis or review. We assigned one study as awaiting classification, as it has not been accepted for publication.
AUTHORS' CONCLUSIONS: This systematic review failed to locate relevant published RCTs to support or refute the assertion that vascular access specialist teams are superior to the generalist model. A vascular access specialist team has advanced knowledge with regard to insertion techniques, clinical care, and management of vascular access devices, whereas a generalist model comprises nurses, doctors, or other designated healthcare professionals in the healthcare facility who may have less advanced insertion techniques and who care for vascular access devices amongst other competing clinical tasks. However, this conclusion may change once the one study awaiting classification and one ongoing study are published. There is a need for good-quality RCTs to evaluate the efficacy of a vascular access specialist team approach for vascular access device insertion and care for the prevention of failure.
全球大多数住院患者都需要血管通路装置(VAD)。在美国,每年有数亿个VAD被插入,据报道全球每年使用超过10亿个外周静脉导管。大量报告表明,采用团队方式进行VAD的评估、插入和维护可改善临床结局、患者体验及医疗流程。
比较血管通路专科团队(VAST)进行VAD插入和护理与通科模式方法(针对医院或社区中需要VAD的参与者)在插入成功率、装置故障及成本效益方面的差异。
我们检索了Cochrane对照试验中心注册库(CENTRAL;2018年第1期);Ovid MEDLINE(1950年至2018年2月7日);Ovid Embase(1980年至2018年2月7日);EBSCO CINAHL(1982年至2018年2月7日);Web of Science会议论文引文索引 - 科学与社会科学及人文科学(1990年至2018年2月7日);以及谷歌学术。我们检索了以下试验注册库:澳大利亚和新西兰临床试验注册库(www.anzctr.org.au);ClinicalTrials.gov(www.clinicaltrials.gov);当前对照试验(www.controlled-trials.com/mrct);香港大学临床试验注册库(www.hkclinicaltrials.com);印度临床试验注册库(ctri.nic.in/Clinicaltrials/login.php);英国临床试验网关(www.controlled-trials.com/ukctr/);以及世界卫生组织国际临床试验注册平台(WHO ICTRP)(www.who.int/trialsearch)。我们于2018年2月7日检索了所有数据库。
我们计划纳入评估VAST或专科插入人员对临床结局影响的有效性的随机对照试验(RCT)。
我们采用Cochrane推荐的标准方法程序,并使用Covidence软件辅助文件管理。
我们检索到2398条引文:30项研究符合进一步全文审查的条件,我们发现有一项注册临床试验正在进行中。没有研究可纳入分析或综述。我们将一项研究列为待分类,因为它尚未被接受发表。
本系统评价未能找到相关的已发表RCT来支持或反驳血管通路专科团队优于通科模式这一论断。血管通路专科团队在插入技术、临床护理及血管通路装置管理方面拥有先进知识,而通科模式由医疗机构中的护士、医生或其他指定的医疗专业人员组成,他们可能插入技术不够先进,且在处理其他竞争临床任务的同时还要护理血管通路装置。然而,一旦这项待分类研究和一项正在进行的研究发表,这一结论可能会改变。需要高质量的RCT来评估血管通路专科团队方法在血管通路装置插入和护理以预防失败方面的疗效。