通过根本原因分析优化灭菌包装:纸塑袋密封缺陷的探讨。

Sixin Jiang, Liangying Yi, Yanhua Chen, Ruixue Hu
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引用次数: 0

摘要

背景纸塑灭菌袋在医疗保健中防止仪器污染是必不可少的。然而,这些袋的密封缺陷会危及患者的安全。为了解决这个问题,我们的研究使用了根本原因分析(RCA),旨在识别导致这些缺陷的因素,并提出实际的解决方案。通过这种方式,我们的目标是提高整个灭菌过程。材料与方法回顾性分析2020年7月至2021年6月(rca前,17563台)和2021年9月至2022年8月(rca后,18199台)在我院中央无菌供应科(CSSD)消毒并包装在纸塑袋中的35,762台器械。我们评估了RCA评分,包装人员对密封质量的看法,以及RCA实施前后的密封缺陷率。结果:密封缺陷的根本原因包括缺乏标准化的检验程序、包装台尺寸不合适、漏检、不正确的分配程序、人员培训不足以及储藏室和分配室之间的通窗采光不足。其中,缺乏标准化的检验程序,包装表尺寸小,漏检是统计上显著的危险因素(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimizing Sterilization Packaging through Root Cause Analysis: An Exploration into Sealing Defects of Paper-Plastic Pouches.

Optimizing Sterilization Packaging through Root Cause Analysis: An Exploration into Sealing Defects of Paper-Plastic Pouches.

Optimizing Sterilization Packaging through Root Cause Analysis: An Exploration into Sealing Defects of Paper-Plastic Pouches.

Optimizing Sterilization Packaging through Root Cause Analysis: An Exploration into Sealing Defects of Paper-Plastic Pouches.

BACKGROUND Paper-plastic sterilization pouches are essential in healthcare for preventing instrument contamination. However, sealing defects in these pouches can jeopardize patient safety. To address this issue, our study uses Root Cause Analysis (RCA), aiming to identify contributing factors to these defects and propose practical solutions. Through this, we aim to enhance the overall sterilization process. MATERIAL AND METHODS A retrospective analysis was conducted on 35,762 instruments sterilized and packaged in paper-plastic pouches at our hospital's Central Sterile Supply Department (CSSD) across two periods: July 2020 to June 2021 (pre-RCA, 17,563 instruments) and September 2021 to August 2022 (post-RCA, 18,199 instruments). We evaluated RCA scores, packaging personnel's perceptions of sealing quality, and sealing defect rates before and after RCA implementation. RESULTS Root causes for sealing defects included lack of a standardized inspection procedure, inadequately sized packing table, missed inspections, incorrect distribution procedures, inadequate staff training, and insufficient lighting through the pass-through window between storage and distribution rooms. Among these, lack of a standardized inspection procedure, small packing table size, and missed inspections were statistically significant risk factors (P<0.05). The sealing defect rate decreased from 0.15% pre-RCA implementation to 0.07% post-RCA implementation. CONCLUSIONS Implementing RCA has been shown to effectively enhance the CSSD staff's perception of sealing quality and significantly reduce the incidence of sealing defects in paper-plastic pouches. Thus, RCA serves as an invaluable tool for quality improvement in sterilization packaging processes.

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