Dr. Brill und Partner GmbH Institut für Hygiene und Mikrobiologie, Hamburg, Germany.
Dr. Brill und Partner GmbH Institut für Hygiene und Mikrobiologie, Hamburg, Germany.
J Hosp Infect. 2023 Nov;141:17-24. doi: 10.1016/j.jhin.2023.08.006. Epub 2023 Aug 19.
In the clinical setting, surface disinfection is an important measure to reduce the risk of cross transmission of micro-organisms and the risk of nosocomial infections. Standardized methods can be used to evaluate disinfection procedures, as well as the effectiveness of the active ingredients used for disinfection. However, despite standardization, the results of such methodologies are still determined by several factors, and incorrect results may lead to invalid assumptions about the effectiveness of a disinfectant, posing significant health risks for patients and health personnel.
The objective of this study was to evaluate several determinants for the recovery of Pseudomonas aeruginosa and other test organisms to establish their influence on the results of standardized disinfection methodologies, and to find Gram-negative strains that can be used as suitable replacements for P. aeruginosa.
The effects of inoculum application method, drying time, temperature and carrier material on the survival and recovery of the test organisms were evaluated using Student's t-test, one-way analysis of variance and Tukey's multiple comparison test.
Temperature, drying time, application method and carrier material were found to affect the recovery of P. aeruginosa cells significantly, and therefore influence the outcome of the methodologies used. This study also showed thatP. aeruginosa could be replaced with the Gram-negative species Acinetobacter baumannii, a test organism used in many standardized methodologies, which responds better under the same circumstances and has a behaviour similar to that of P. aeruginosa in disinfectant efficacy tests.
在临床环境中,表面消毒是降低微生物交叉传播风险和医院感染风险的重要措施。可以使用标准化方法来评估消毒程序以及用于消毒的有效成分的有效性。然而,尽管已经标准化,但这些方法的结果仍然受到几个因素的影响,不正确的结果可能导致对消毒剂有效性的无效假设,从而对患者和医务人员的健康构成重大风险。
本研究的目的是评估几种因素对铜绿假单胞菌和其他测试菌回收的影响,以确定它们对标准化消毒方法结果的影响,并找到可作为铜绿假单胞菌合适替代品的革兰氏阴性菌株。
使用学生 t 检验、单因素方差分析和 Tukey 多重比较检验评估接种物应用方法、干燥时间、温度和载体材料对测试菌存活和回收的影响。
发现温度、干燥时间、应用方法和载体材料显著影响铜绿假单胞菌细胞的回收,从而影响所用方法的结果。本研究还表明,革兰氏阴性菌鲍曼不动杆菌可以替代许多标准化方法中使用的测试菌铜绿假单胞菌,在相同情况下,该菌的反应更好,并且在消毒剂功效测试中的行为与铜绿假单胞菌相似。