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Microbiological surveillance post-reprocessing of flexible endoscopes used in digestive endoscopy: a national study.消化内镜检查中使用的软性内镜再处理后的微生物监测:一项全国性研究。
J Hosp Infect. 2023 Jan;131:139-147. doi: 10.1016/j.jhin.2022.09.024. Epub 2022 Oct 13.
2
Efficacy of a novel channel-cleaning ball brush for endoscope reprocessing: a randomized controlled trial.一种新型通道清洁球刷在内镜再处理中的效果:一项随机对照试验。
Clin Endosc. 2022 Sep;55(5):674-682. doi: 10.5946/ce.2021.210. Epub 2022 Aug 2.
3
Monitoring the Cleanliness of Reusable Surgical Instruments in Central Sterile Supply Department by Adenosine Triphosphate Method.采用三磷酸腺苷法监测中心供应室可重复使用手术器械的清洁度。
J AOAC Int. 2022 Apr 27;105(3):844-847. doi: 10.1093/jaoacint/qsab102.
4
Fungal biofilm architecture produces hypoxic microenvironments that drive antifungal resistance.真菌生物膜结构产生低氧微环境,从而导致抗真菌耐药性。
Proc Natl Acad Sci U S A. 2020 Sep 8;117(36):22473-22483. doi: 10.1073/pnas.2003700117. Epub 2020 Aug 26.
5
Work systems analysis of sterile processing: decontamination.无菌处理工作系统分析:消毒。
BMJ Qual Saf. 2020 Apr;29(4):320-328. doi: 10.1136/bmjqs-2019-009422. Epub 2019 Nov 13.
6
Challenges in achieving effective high-level disinfection in endoscope reprocessing.实现内镜再处理中有效高水平消毒的挑战。
Am J Infect Control. 2020 Mar;48(3):309-315. doi: 10.1016/j.ajic.2019.09.013. Epub 2019 Oct 31.
7
How clean is clean enough? An observational pilot study to assess central sterilization processing efficacy with adenosine triphosphate levels.清洁到何种程度才算足够清洁?一项使用三磷酸腺苷水平评估中心消毒处理效果的观察性试点研究。
Am J Infect Control. 2020 Apr;48(4):420-422. doi: 10.1016/j.ajic.2019.08.006. Epub 2019 Sep 11.
8
Complex design of surgical instruments as barrier for cleaning effectiveness, favouring biofilm formation.手术器械的复杂设计作为清洁效果的障碍,有利于生物膜的形成。
J Hosp Infect. 2019 Sep;103(1):e53-e60. doi: 10.1016/j.jhin.2018.11.001. Epub 2018 Nov 10.
9
An update on gastrointestinal endoscopy-associated infections and their contributing factors.胃肠内镜相关感染及其影响因素的最新研究进展。
Ann Clin Microbiol Antimicrob. 2018 Oct 10;17(1):36. doi: 10.1186/s12941-018-0289-2.
10
Reprocessing safety issues associated with complex-design orthopaedic loaned surgical instruments and implants.与复杂设计的骨科租借手术器械和植入物相关的再处理安全问题。
Injury. 2018 Nov;49(11):2005-2012. doi: 10.1016/j.injury.2018.09.006. Epub 2018 Sep 5.

吸引式金属管腔器械清洁质量的调查:一项横断面研究。

An investigation into cleaning quality of suction-type metal lumen instruments: a cross-sectional study.

作者信息

Wu Yuqi, Li Li

机构信息

First Hospital of China Medical University, Shenyang, China.

出版信息

Sci Rep. 2025 Jan 20;15(1):2492. doi: 10.1038/s41598-024-83215-8.

DOI:10.1038/s41598-024-83215-8
PMID:39833252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11746972/
Abstract

The highest unqualified cleaning rate of suction-type lumen instruments is a major challenge for a central sterile supply department (CSSD). However, A few comprehensive studies have analyzed the main factors affecting cleaning quality. In response, this study aimed to explore the current state and the factors affecting the cleaning quality of reused suction-type metal lumen instruments in CSSD. The results revealed that the qualified cleaning rates determined by the 5x magnifier visual inspection with light source method, OB reagent method, and ATP bioluminescence detection method were 94.2%, 72.6%, and 60.5%, respectively. The results also showed a significant difference between the three methods (X = 60.293, P < 0.001). Meanwhile, the binary logistic regression analysis revealed that the time interval between instrument recycling and cleaning, pollution level, pretreatment soaking time, cleaning technique, and the presence of visible bloodstains or dirt after pretreatment are independent risk factors that influence the cleaning quality of suction-type metal lumen instruments. Based on these results, the cleaning quality of suction-type metal lumen instruments needs further improvement.

摘要

吸引式腔镜器械的最高不合格清洗率是中央无菌供应室(CSSD)面临的一项重大挑战。然而,一些综合性研究分析了影响清洗质量的主要因素。对此,本研究旨在探讨CSSD中重复使用的吸引式金属腔镜器械的清洗质量现状及其影响因素。结果显示,采用带光源5倍放大镜目视检查法、OB试剂法和ATP生物发光检测法测定的合格清洗率分别为94.2%、72.6%和60.5%。结果还表明,这三种方法之间存在显著差异(X = 60.293,P < 0.001)。同时,二元逻辑回归分析显示,器械回收与清洗的时间间隔、污染程度、预处理浸泡时间、清洗技术以及预处理后可见血迹或污垢的存在是影响吸引式金属腔镜器械清洗质量的独立危险因素。基于这些结果,吸引式金属腔镜器械的清洗质量有待进一步提高。