Ali S, Muzslay M, Bruce M, Jeanes A, Moore G, Wilson A P R
Clinical Microbiology and Virology, University College London Hospitals NHS Foundation Trust, London, UK.
Clinical Microbiology and Virology, University College London Hospitals NHS Foundation Trust, London, UK.
J Hosp Infect. 2016 May;93(1):70-7. doi: 10.1016/j.jhin.2016.01.016. Epub 2016 Feb 9.
Hydrogen peroxide vapour (HPV) disinfection systems are being used to reduce patients' exposure to hospital pathogens in the environment. HPV whole-room aerial disinfection systems may vary in terms of operating concentration and mode of delivery.
To assess the efficacy of two HPV systems (HPS1 and HPS2) for whole-room aerial disinfection of single isolation rooms (SIRs).
Ten SIRs were selected for manual terminal disinfection after patient discharge. Test coupons seeded with biological indicator (BI) organisms [∼10(6) colony-forming units (cfu) of meticillin-resistant Staphylococcus aureus (MRSA) or Klebsiella pneumoniae, or ∼10(5)cfu Clostridium difficile 027 spores] prepared in a soil challenge were placed at five locations per room. For each cycle, 22 high-frequency-touch surfaces in SIRs were sampled with contact plates (∼25cm(2)) before and after HPV decontamination, and BIs were assayed for the persistence of pathogens.
Approximately 95% of 214 sites were contaminated with bacteria after manual terminal disinfection, with high numbers present on the SIR floor (238.0-352.5cfu), bed control panel (24.0-33.5cfu), and nurse call button (21.5-7.0cfu). Enhanced disinfection using HPV reduced surface contamination to low levels: HPS1 [0.25cfu, interquartile range (IQR) 0-1.13] and HPS2 (0.5cfu, IQR 0-2.0). Both systems demonstrated similar turnaround times (∼2-2.5h), and no differences were observed in the efficacy of the two systems against BIs (C. difficile ∼5.1log10 reduction; MRSA/K. pneumoniae ∼6.3log10 reduction). Despite different operating concentrations of hydrogen peroxide, MRSA persisted on 27% of coupons after HPV decontamination.
Enhanced disinfection with HPV reduces surface contamination left by manual terminal cleaning, minimizing the risks of cross-contamination. The starting concentration and mode of delivery of hydrogen peroxide may not improve the efficacy of decontamination in practice, and therefore the choice of HPV system may be based upon other considerations such as cost, convenience and logistics.
过氧化氢蒸汽(HPV)消毒系统正用于减少患者在医院环境中接触病原体。HPV全室空气消毒系统在操作浓度和输送方式方面可能存在差异。
评估两种HPV系统(HPS1和HPS2)对单人隔离病房(SIR)进行全室空气消毒的效果。
选择10间SIR在患者出院后进行人工终末消毒。将接种了生物指示剂(BI)微生物[耐甲氧西林金黄色葡萄球菌(MRSA)或肺炎克雷伯菌约10(6)菌落形成单位(cfu),或艰难梭菌027孢子约10(5)cfu]的测试 coupons 置于土壤挑战中制备,每个房间放置在五个位置。对于每个周期,在HPV去污前后,用接触板(约25cm(2))对SIR中的22个高频接触表面进行采样,并检测BIs中病原体的持久性。
人工终末消毒后,214个位点中约95%被细菌污染,SIR地板(238.0 - 352.5cfu)、病床控制面板(24.0 - 33.5cfu)和护士呼叫按钮(21.5 - 7.0cfu)上细菌数量较多。使用HPV进行强化消毒可将表面污染降低到低水平:HPS1[0.25cfu,四分位间距(IQR)0 - 1.13]和HPS2(0.5cfu, IQR 0 - 2.0)。两种系统的周转时间相似(约2 - 2.5小时),两种系统对BIs的消毒效果未观察到差异(艰难梭菌约减少5.1log10;MRSA/肺炎克雷伯菌约减少6.3log10)。尽管过氧化氢的操作浓度不同,但HPV去污后MRSA仍在27%的coupons上存活。
用HPV进行强化消毒可减少人工终末清洁后留下的表面污染,将交叉污染风险降至最低。过氧化氢的起始浓度和输送方式在实际中可能不会提高去污效果,因此HPV系统的选择可基于其他考虑因素,如成本、便利性和物流。