Enhanced monitoring of healthcare shower water in augmented and non-augmented care wards showing persistence of Pseudomonas aeruginosa despite remediation work.

IF 2.4 4区 医学 Q3 MICROBIOLOGY
Özge Yetiş, Shanom Ali, Kush Karia, Paul Bassett, Peter Wilson
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引用次数: 0

Abstract

Introduction. Pseudomonas aeruginosa in healthcare shower waters presents a high risk of infection to immune-suppressed patients; identifying the colonization-status of water outlets is essential in preventing acquisition.Hypothesis/Gap Statement. Testing frequencies may be insufficient to capture presence/absence of contamination in healthcare waters between sampling and remediation activities. Standardization of outlets may facilitate the management and control of P. aeruginosa.Aim. This study aims to monitor shower waters and drains for P. aeruginosa in augmented and non-augmented healthcare settings every 2 weeks for a period of 7 months during remedial actions.Methodology. All shower facilities were standardized to include antimicrobial silver-impregnated showerhead/hose units, hose-length fixed to 0.8 m and replaced every 3 months. Standard hospital manual decontamination/disinfection occurred daily. Thermostatic-mixer-valves (TMVs) were replaced and disinfected if standard remediation unsuccessful.Results. Of 560 shower and drain samples collected over 14 time-points covering 7 months, P. aeruginosa colonized 40 %(4/10; non-augmented) and 80 %(8/10; augmented-care) showers in the first week. For each week elapsed, new outlets became contaminated with P. aeruginosa by 18-19 % (P<0.001) in shower waters (OR=1.19; CI=1.09-1.31) and drains (OR=1.18; CI=1.09-1.30). P. aeruginosa occurrence in shower water was associated with subsequent colonization of the corresponding drain and vice versa (chi-square; P<0.001) with simultaneous contamination present in 31 %(87/280) of areas. TMV replacement was ineffective in eradicating colonisation in ~83 % of a subset (6/20; three per ward) of contaminated showers.Conclusions. We demonstrate the difficulties in eradicating P. aeruginosa from hospital plumbing, particularly when contamination is no longer sporadic. Non-augmented care settings are reservoirs of P. aeruginosa and should not be overlooked in outbreak investigations. Antimicrobial-impregnated materials may be ineffective once colonization with P. aeruginosa is established beyond the hose and head. Reducing hose-length insufficient to prevent cross-contamination from shower drains. P. aeruginosa colonization can be transient in both drain and shower hose/head. Frequent microbiological monitoring suggests testing frequencies following HTM04-01 guidelines are insufficient to capture the colonization-status of healthcare waters between samples. Disinfection/decontamination is recommended to minimize bioburden and the effect of remediation should be verified with microbiological monitoring. Where standard remediation did not remove P. aeruginosa contamination, intensive monitoring supported justifying replacement of showers and contiguous plumbing.

加强监测保健淋浴水在扩大和非扩大护理病房显示铜绿假单胞菌的持久性,尽管补救工作。
介绍。保健淋浴水中的铜绿假单胞菌对免疫抑制的患者有很高的感染风险;确定出水口的定植状态对于预防感染至关重要。假设/差距语句。在取样和补救活动之间,检测频率可能不足以捕捉保健用水中是否存在污染。标准化的网点可方便铜绿假单胞菌的管理和控制。本研究旨在监测增建和非增建医疗机构淋浴水和排水管中铜绿假单胞菌的感染情况,每两周监测一次,为期7个月。所有淋浴设施都标准化了,包括浸银抗菌淋浴喷头/软管单元,软管长度固定为0.8米,每3个月更换一次。每天进行标准的医院人工去污/消毒。如果标准修复不成功,则更换恒温混合器阀(tmv)并进行消毒。在7个月的14个时间点收集的560份淋浴室和排水管样本中,铜绿假单胞菌定植率为40% (4/10;非增广)和80% (8/10;增强护理)第一周的淋浴。每过一周,新的出口被铜绿假单胞菌污染的比例为18- 19% (pp)。淋浴水中铜绿假单胞菌的出现与随后相应排水管的定植有关,反之亦然(卡方;PConclusions。我们证明了从医院管道根除铜绿假单胞菌的困难,特别是当污染不再是零星的。非强化护理机构是铜绿假单胞菌的宿主,在疫情调查中不应忽视。一旦铜绿假单胞菌在软管和头部外定植,抗菌浸渍材料可能无效。缩短软管长度,不足以防止淋浴排水管的交叉污染。铜绿假单胞菌在排水管和淋浴软管/喷头中的定植可能是短暂的。频繁的微生物监测表明,遵循HTM04-01指南的检测频率不足以捕获样本之间医疗用水的定植状态。建议进行消毒/去污以尽量减少生物负担,并应通过微生物监测验证修复效果。在标准补救措施不能消除铜绿假单胞菌污染的地方,强化监测支持更换淋浴和连续管道的合理性。
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来源期刊
Journal of medical microbiology
Journal of medical microbiology 医学-微生物学
CiteScore
5.50
自引率
3.30%
发文量
143
审稿时长
4.5 months
期刊介绍: Journal of Medical Microbiology provides comprehensive coverage of medical, dental and veterinary microbiology, and infectious diseases. We welcome everything from laboratory research to clinical trials, including bacteriology, virology, mycology and parasitology. We publish articles under the following subject categories: Antimicrobial resistance; Clinical microbiology; Disease, diagnosis and diagnostics; Medical mycology; Molecular and microbial epidemiology; Microbiome and microbial ecology in health; One Health; Pathogenesis, virulence and host response; Prevention, therapy and therapeutics
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