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介入技术感染控制实践评估:安全注射实践和使用单剂量药物小瓶的最佳证据综合。

Assessment of infection control practices for interventional techniques: a best evidence synthesis of safe injection practices and use of single-dose medication vials.

机构信息

Pain Management Center of Paducah, Paducah, KY, and University of Louisville, Louisville, KY, USA.

出版信息

Pain Physician. 2012 Sep-Oct;15(5):E573-614.

PMID:22996856
Abstract

BACKGROUND

It is universally accepted that transmission of bloodborne pathogens during health care procedures continues to occur because of the use of unsafe and improper injection, infusion, and medication administration practices by health care professionals in various clinical settings. This resulted in development of multiple guidelines based on case reports; however, these case reports are confounded by multiple factors without causal relationship to a single factor. Even then, single-dose vials used for multiple patients have been singled out and became the focus of infection control policies resulting in inordinate expenses for practices without improving patient safety. The cost of implementation of single dose vial policy in interventional pain management for drugs alone may cost $750 million, whereas with single use radional gloves may exceed $1 billion per year.

STUDY DESIGN

Best evidence synthesis.

OBJECTIVE

To critically appraise and synthesize the literature on infection control practices for interventional techniques, including safe injection and medication vial utilization.

METHODS

The available literature on infection control practices was reviewed. Due to the nature of the studies involved, with the majority being case reports, and a few prospective evaluations, quality assessment and clinical relevance criteria were not applied. Data sources included relevant literature identified through searches of PubMed and EMBASE from 1966 through June 2012, literature from the Centers for Disease Control and Prevention (CDC), the U.S. Food and Drug Administration (FDA), and manual searches of the bibliographies of known primary and review articles.

OUTCOME MEASURES

The primary outcome measure was correlating infection to a breach of standards in infection control practices. The secondary objective was to assess the contribution of single-dose vials independently for infection.

RESULTS

A total of 60 reports met inclusion criteria, with 16 reports related to pain management and other procedures, of which 9 reports were attributed to issues related to interventional techniques. Based on an estimated 37 infections occurring during 200 million interventional techniques from 1997 through 2011, the rate of infection is speculated to be one infection for every 5 million interventional pain management procedures. However, if 10 times more infections are estimated, the infection rate appears to be one infection for every 500,000 interventional pain management procedures. The evidence is good for infection related to a breach of infection control practices. There is good evidence that contamination of multi-dose or single-dose vials can contribute to infection. There was poor evidence that the use of single-dose vials on multiple patients with appropriate infection control practices cause infection in interventional pain management.

LIMITATIONS

The limitations of this comprehensive best evidence synthesis include the paucity of literature and dependence of governmental agencies on their literature without applying Institute of Medicine (IOM) criteria for guideline synthesis.

CONCLUSION

There is good evidence that any breach of sterile practice may result in serious and life threatening infections. There is poor evidence for single-dose vials as a sole factor causing infections when used in multiple patients in interventional pain management settings.

摘要

背景

众所周知,由于医护人员在各种临床环境中使用不安全和不当的注射、输液和药物管理操作,在医疗过程中继续发生血源性病原体的传播。这导致了基于病例报告的多项指南的制定;然而,这些病例报告受到多种因素的影响,这些因素之间没有因果关系。即便如此,单次剂量小瓶已被单独挑出,并成为感染控制政策的焦点,这导致了实践费用的不合理增加,而患者的安全性却没有提高。仅在介入性疼痛管理中实施单次剂量小瓶政策的成本可能就高达 7.5 亿美元,而使用一次性放射性手套每年可能超过 10 亿美元。

研究设计

最佳证据综合。

目的

批判性评估和综合介入技术感染控制实践的文献,包括安全注射和药物小瓶的使用。

方法

对感染控制实践的相关文献进行了回顾。由于所涉及的研究大多是病例报告,只有少数是前瞻性评估,因此没有应用质量评估和临床相关性标准。资料来源包括通过搜索 PubMed 和 EMBASE 从 1966 年到 2012 年 6 月期间确定的相关文献,疾病控制和预防中心(CDC)、美国食品和药物管理局(FDA)的文献以及已知原始和综述文章的参考文献的手工搜索。

主要结果测量

主要结果测量是将感染与感染控制实践标准的违反相关联。次要目标是评估单剂量小瓶对感染的独立贡献。

结果

共有 60 份报告符合纳入标准,其中 16 份报告与疼痛管理和其他程序有关,其中 9 份报告与介入技术有关的问题有关。根据 1997 年至 2011 年期间估计的 2 亿次介入技术中发生的 37 次感染,感染率推测为每 500 万次介入性疼痛管理程序发生一次感染。然而,如果估计感染增加 10 倍,感染率似乎为每 50 万次介入性疼痛管理程序发生一次感染。证据表明感染与违反感染控制实践有关。有充分的证据表明多剂量或单剂量小瓶的污染会导致感染。有证据表明,在介入性疼痛管理中,在适当的感染控制措施下,将单剂量小瓶用于多名患者不会导致感染。

局限性

本综合最佳证据综合的局限性包括文献匮乏以及政府机构依赖其文献,而没有应用医学研究所(IOM)的指南综合标准。

结论

任何违反无菌操作的行为都可能导致严重的、危及生命的感染。在介入性疼痛管理中,当将单次剂量小瓶用于多名患者时,证据不足表明单次剂量小瓶是导致感染的唯一因素。

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