Endoscope channel drying, storage, and conditions after reprocessing: How safe are they in clinical practice?

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Abstract

Introduction and aims

Adequate drying and proper storage of flexible endoscopes are essential for maintaining quality in their reprocessing. The aim of the present study was to evaluate the drying stages, storage, and channel conditions of endoscopes through borescope inspection.

Material and methods

The personnel responsible for endoscope reprocessing were interviewed. Storage conditions at 10 endoscopy facilities were inspected and an internal examination of the channels and ports of the stored equipment was carried out, utilizing a borescope. A total of 74 stored endoscope channels were evaluated.

Results

Only 10% of the facilities inspected utilized transport cases for storage and only 10% had rooms exclusively used for storage. Sixty percent of the facilities did not perform any shelf-life control. All the channels evaluated were scratched and fluids were present on 69% of them.

Conclusions

Endoscope reprocessing can be improved through the implementation of drying and storage control and validation tools, as well as the use of borescopes and periodic clinical audits.

内窥镜通道的干燥、储存和再处理后的条件:它们在临床实践中的安全性如何?
导言和目的柔性内窥镜的充分干燥和适当储存对保持其再处理质量至关重要。本研究旨在通过内窥镜检查评估内窥镜的干燥阶段、储存和通道条件。对 10 家内窥镜检查机构的储存条件进行了检查,并使用内窥镜对储存设备的通道和端口进行了内部检查。结果只有 10%的受检机构使用运输箱进行存储,只有 10%的机构有专门用于存储的房间。60%的机构没有进行任何保质期控制。结论通过实施干燥和储存控制及验证工具,以及使用内窥镜和定期临床审核,可以改进内窥镜的再处理。
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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