Nasopharyngeal temperature probes: is South Africa’s current decontamination process adequate?

R. Davids, C. Cilliers
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引用次数: 0

Abstract

Background: The standard practice in many institutions incorporates nasopharyngeal probes for temperature monitoring in patients undergoing general anaesthesia. Current disinfection guidelines for these devices are not clear and they are poorly adhered to. In South Africa, these temperature probes are reused and subjected to unstandardized decontamination processes. This study sought to investigate nasopharyngeal temperature probes as possible source for cross-contamination, and assess the efficacy of current disinfection practices for these probes. Methodology: This was an analytical double-blind randomized study of 4 different disinfection protocols for 48 nasopharyngeal temperature probes. The probes were randomized to disinfection protocols that included water wash, dry wipe, hibitane® and cidex® wash. After decontamination by the respective protocol, the probes were aseptically placed in nutrient broths, manually agitated and removed, and the broths were then inoculated onto blood agar plates. After 48 hours of aerobic culture incubation at 37oC, plates were examined for growth and bacteria identified using automated bioMérieux Vitek-2 microbial identification system. Chi square and logistic regression analyses were used to assess bacterial contamination rates of the disinfected probes, in order to infer the efficacy of the decontamination processes. Results: Of the 48 nasopharyngeal temperature probes disinfected by the different protocols, 22 (45.8%) had bacterial contamination, with frequency of isolation for coagulase negative staphylococci (44%), Bacillus cereus (20%), Staphylococcus aureus (10%), Enterobacter cloaca (7%), Pseudomonas aeruginosa (4%), Pseudomonas fluorescens (3%), Acinetobacter baumannii (3%), amongst other bacterial species. Dry wipe, and water and soap methods, had statistically significant higher contamination rates of 83.3% and 66.7% than hibitane® and cidex®, with 25.0% and 8.3% respectively (X2=17.69, p<0.0001). The odds of contamination when water-wipe was used as a cleaning method was 6 times (OR=6.000; 95% CI=1.018-35.374, p=0.048) that of hibitane® method while the odds for dry-wipe was 15 times (OR=15.000, 95% CI=2.024-111.174, p=0.008). No statistically significant difference was observed in the contamination rates between cidex® and hibitane® disinfection methods(OR=0.273, 95% CI=0.024-3.093, p=0.294). Conclusion: These data shows that nasopharyngeal temperature probes are possible source of cross-contamination and pathogen transmission due to inadequacy of the decontamination processes for these temperature probes.
鼻咽温度探头:南非目前的去污过程是否足够?
背景:许多机构的标准做法包括在接受全身麻醉的患者中使用鼻咽探头进行体温监测。目前这些设备的消毒指南不明确,而且没有得到很好的遵守。在南非,这些温度探头被重复使用,并受到非标准化的净化过程。本研究旨在调查鼻咽温度探头作为交叉污染的可能来源,并评估当前对这些探头的消毒措施的有效性。方法:这是一项分析性双盲随机研究,对48个鼻咽温度探头进行4种不同的消毒方案。将探针随机分配到水清洗、干擦、hibitane®和cidex®清洗的消毒方案中。通过相应的方案去污后,将探针无菌放置在营养肉汤中,手动搅拌并取出,然后将肉汤接种到血琼脂板上。37℃好氧培养48小时后,检测培养皿的生长情况,并使用自动biom rieux Vitek-2微生物鉴定系统鉴定细菌。使用卡方和逻辑回归分析评估消毒探针的细菌污染率,以推断消毒过程的有效性。结果:48个经不同方案消毒的鼻咽温度探头中,有22个(45.8%)存在细菌污染,检出凝固酶阴性葡萄球菌(44%)、蜡样芽孢杆菌(20%)、金黄色葡萄球菌(10%)、阴沟肠杆菌(7%)、铜绿假单胞菌(4%)、荧光假单胞菌(3%)、鲍曼不动杆菌(3%)等细菌。干擦法和水皂法的污染率分别为83.3%和66.7%,高于hibitane®和cidex®的25.0%和8.3% (X2=17.69, p<0.0001)。当使用水擦拭作为清洁方法时,污染的几率是6倍(OR=6.000;95% CI=1.018 ~ 35.374, p=0.048),而干擦法的比值为15倍(OR=15.000, 95% CI=2.024 ~ 111.174, p=0.008)。cidex®和hibitane®消毒方法的污染率差异无统计学意义(OR=0.273, 95% CI=0.024-3.093, p=0.294)。结论:这些数据表明,由于鼻咽温度探头净化过程不完善,可能是交叉污染和病原体传播的来源。
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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