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Endoscope-associated infections: A brief summary of the current state and views toward the future

机译:内窥镜相关感染:目前国家的简要摘要,对未来的观点

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World-wide reports of duodenoscope-associated outbreaks of multidrug resistant micro-organisms are an indication that transmission of infection via contaminated endoscopes occurs more frequently than previously thought. To reduce the incidence of endoscope contamination, open communication between manufacturers, institutions, and government agencies is urgently needed. Endoscope risk factor studies and thorough investigation of outbreaks by experts are instrumental in lowering and ultimately eliminating infections. These studies should yield improvements in endoscope design, endoscope reprocessing, as well as hospital surveillance and infection control measures. Current reprocessing methods have a very small margin of safety, allowing no room for error. Strictly following the manufacturer's instructions regarding reprocessing does not adequately guarantee complete removal of micro-organisms. New reprocessing measures to reduce contamination show promising results, but they are costly to implement and do not assure zero contamination risk. Redesign of endoscopes to facilitate better cleaning and ultimately sterilization instead of disinfection might provide a solution. Going forward, the focus should extend beyond the forceps elevator to include the entire instrument since every aspect of the duodenoscope can be contaminated by infectious organisms. Single-use duodeno-scopes would completely eliminate the risk of transmission of exogenous micro-organisms, but they not the Food and Drug Administration-approved, and are likely to be costly and of unproven efficacy. Indeed, balancing cost-effectiveness of any redesign or use of disposable endoscopes with the actual risk of transmitting exogenous micro-organisms will ultimately determine which solutions are adopted and utilized.
机译:世界范围内有关十二指肠镜相关耐多药微生物暴发的报告表明,通过受污染的内窥镜传播感染的频率比以前想象的要高。为了降低内窥镜污染的发生率,迫切需要制造商、机构和政府机构之间的公开沟通。内窥镜检查风险因素研究和专家对疫情的彻底调查有助于降低并最终消除感染。这些研究将改进内窥镜设计、内窥镜再处理以及医院监测和感染控制措施。目前的再处理方法安全性很低,不允许出现错误。严格遵守制造商关于再加工的说明并不能充分保证彻底去除微生物。减少污染的新的后处理措施显示出有希望的结果,但实施起来成本高昂,而且不能保证零污染风险。重新设计内窥镜,以便更好地清洁和最终灭菌,而不是消毒,这可能是一个解决方案。展望未来,重点应该超越镊子升降机,包括整个器械,因为十二指肠镜的每个方面都可能受到感染性有机体的污染。一次性使用十二指肠镜将完全消除外源性微生物传播的风险,但它们未经美国食品和药物管理局批准,且可能成本高昂且疗效未经证实。事实上,在一次性内窥镜的任何重新设计或使用的成本效益与传播外源性微生物的实际风险之间取得平衡,最终将决定采用和使用哪些解决方案。

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