Shelf life of sterilized packaged items stored in acute care hospital settings: factors for consideration

Prabha Lakhan BN, MN, PhD , Joan Faoagali MBChB, MPH, FRCPA , Rosemary Steinhardt BHSc, GradCertMngt, GradDipInfection Control , Dolly Olesen Grad Dip(Clinical Nursing Studies), MHSc(Infection Control)
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引用次数: 6

Abstract

Introduction

Reusable medical devices are sterilized and stored before their use in hospital settings. The length of time the sterilized item can be stored (shelf life) to maintain sterility has been discussed in the literature over the last four decades, with a shift to an event rather than time-related determination of shelf life. This paper reviews the evidence and provides a summary of some key issues for consideration when adopting event-related or time-based shelf life recommendations for packaged sterile items in Australian hospitals.

Discussion

Australian and international standards provide guidelines for procedures to be used for sterilization of reusable medical devices and storage conditions following sterilization. Reusable medical devices are sterilized by commercial manufacturers or sterilizing departments located in hospitals. Commercial manufacturers allocate expiry dates on sterilized items which should be respected, unless sterility is compromised by an event. The shelf life of items sterilized in hospital is debated, with growing support for event- rather than time-related sterility. Many factors determine whether event- or time-related shelf life should be followed. Well designed experimental studies into shelf life of sterilized items are lacking, with some small studies indicating that items can remain sterile for 12 to 24 months. Factors for consideration by hospitals are outlined and an algorithm to assist in implementation of event-related or time-based shelf life for reprocessed reusable medical devices is provided.

Conclusion

The method of determining shelf life in hospitals is dependent on adequacy of processes for sterilization, monitoring of sterility over time and storage conditions.

在急症护理医院储存的灭菌包装物品的保质期:需要考虑的因素
可重复使用的医疗器械在医院使用前要进行消毒和储存。在过去的四十年中,文献中讨论了灭菌物品可以储存的时间长度(保质期)以保持无菌,并转向事件而不是与时间相关的保质期决定。本文回顾了证据,并提供了一些关键问题的总结,当采用事件相关或基于时间的保质期建议包装无菌项目在澳大利亚医院考虑。讨论澳大利亚和国际标准为可重复使用医疗器械的灭菌程序和灭菌后的储存条件提供了指南。可重复使用的医疗器械由商业制造商或医院的消毒部门消毒。除非无菌性受到事件的影响,否则商业制造商应遵守灭菌物品的有效期。医院消毒物品的保质期一直备受争议,越来越多的人支持与事件有关而不是与时间有关的消毒。许多因素决定了是否应该遵循与事件或时间相关的保质期。设计良好的灭菌物品保质期实验研究缺乏,一些小型研究表明,物品可以保持无菌12至24个月。概述了医院应考虑的因素,并提供了一种算法,以协助实施与事件相关或基于时间的可重复使用医疗设备的保质期。结论确定医院药品货架期的方法取决于灭菌过程的充分性、无菌时间的监测和储存条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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