Curtain twitchers should beware

curtains

A study published in ICHE by a team from the University of Iowa evaluated the effectiveness of antimicrobial impregnated hospital curtains. The powerful double-blinded RCT study design of 15 standard curtains and 15 curtains impregnated with a metal-alloy based ‘complex element compound (CEC)’ meant there was no doubt that the differences between the two study arms were due to the curtains. The antimicrobial CEC curtains took longer to become contaminated (14 vs. 2 days) but were not significantly less contaminated in the later culture results.

The authors conclude that the ‘Use of privacy curtains with antimicrobial properties could increase the time between washings and may potentially play a role in decreasing pathogen transmission.’

The list of pathogens cultured from the curtains during the study is compelling: MRSA, VRE, Acinetobacter species, methicillin-susceptible S.aureus, E. coli, Pseudomonas species, Klebsiella species, vancomycin-susceptible enterococci, Enterobacter species, Leclercia adecarboxylata, Pantoea agglomerans, Stenotrophomonas maltophilia, Proteus mirabilis, Serratia plymuthica, Sphingomonas paucimobilis, and Citrobacter freundii. These findings highlight the importance of curtains as a potential reservoir for pathogen transmission.

In terms of study limitations, there were some structural differences between the curtains (woven vs. knitted) that could have contributed to the difference between the groups. Also, it would have been useful to know more about the exact chemical composition of the complex element compound (CEC) used. Finally, the authors did not assess contamination with C. difficile spores and effectiveness of the chemical compound used against spores seems unlikely.

I wonder how often privacy curtains are changed on average? As with any other antimicrobial intervention, the product is only as good as the practice. This study provides some useful data on a novel product that could help to reduce the overall burden of microbial contamination in healthcare facilities and, in doing so, contribute to increased patient safety.

Article citation: Schweizer M, Graham M, Ohl M et al. Novel hospital curtains with antimicrobial properties: a randomized, controlled trial. Infect Control Hosp Epidemiol 2012; 33: 1081-5.

Why boys and girls should keep the toilet seat down

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A charming study evaluated the risk of aerosolisation of Clostridium difficle spores through toilet flushing and the potential for resulting environmental contamination. Sure enough, using a faecal suspension to simulate diarrhea caused by C. difficile, investigators found that air and surfaces surrounding the toilet were contaminated with C. difficile spores when the toilet was flushed with the lid up. So, the advice is to close the lid when you flush the toilet to avoid aersolisation spread of gastrointestinal pathogens. One added complication though: many hospital toilets do not have lids, so the authors concluded by discouraging the use of lidless toilets.

Article citation: Best EL, Sandoe JA, Wilcox MH. Potential for aerosolization of Clostridium difficile after flushing toilets: the role of toilet lids in reducing environmental contamination risk. J Hosp Infect 2012; 80: 1-5.

Hydrogen peroxide vapour vs. aerosol

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There has been an awful lot of discussion out in the field about various hydrogen peroxide systems used for “no-touch” automated room disinfection. Comparison of different systems through assessment of individual studies is tricky because different methods are used to assess the effectiveness of the products. Thus, the only way to get an accurate comparison of different technologies is through head-to-head comparisons.

A recently published study compared a hydrogen peroixde vapour (HPV) system (Bioquell) with an aerosolised hydrogen peroxide (aHP) system (ASP Glosair). The independent study was performed by researchers at St. Georges’ Hospital Testing was performed in a 50m3 room with a 13m3 anteroom, representing a single occupancy room with bathroom. For both systems it was found that rooms must be sealed to prevent leakage and room re-entry must be led by a hand held sensor to ensure safety. HPV generally achieved a 6-log reduction of spore BIs and in-house prepared test discs inoculated with MRSA, Clostridium difficile and Acineotbacter baumannii, whereas aHP generally achieved a 4-log reduction or less. The aHP system had reduced efficacy against the catalase-positive A. baumannii with a <2-log reductions in the majority of room locations. HPV was able to penetrate soiling more effectively than aHP and uneven distribution of the active agent within the enclosure was evident for aHP but not for HPV.

It is difficult to produce a laboratory challenge that is truly representative of field conditions, but the authors did a thorough job and used several different ways to measure the efficacy of the products, concluding that ‘the HPV system was safer to operate, slightly faster and achieved a greater level of biological inactivation than the aHP system.’

Article citation: Fu TY, Gent P, Kumar V. Efficacy, efficiency and safety aspects of hydrogen peroixde vapour and aerosolized hydrogen peroixde room disinfection systems. J Hosp Infect 2012; 80: 199-205.

Do biofilms on dry hospital surfaces change how we think about hospital disinfection?

An important paper published in the Journal of Hospital Infection has identified biofilms on dry hospital surfaces. Biofilms are known to be important in several areas of medicine including indwelling medical devices and endoscope tubing, usually associated with surface-water interfaces. However, it was unclear whether biofilms formed on dry hospital surfaces. The study by Vickery et al. ‘destructively sampled’ several hospital surfaces after cleaning and disinfection using bleach (i.e. cut the materials out of the hospital environment and took them to the lab for analysis). Scanning electron microscopy was used to examine the surfaces for biofilms, which were identified on 5/6 surfaces: a curtain, a blind cord, a plastic door, a wash basin and a reagent bucket. Furthermore, MRSA was identified in the biofilm on three of the surfaces.

biofilm

Could it be that we have missed or underestimated the importance of biofilms on dry hospital surfaces? Biofilms could explain why vegetative bacteria can survive on dry hospital surfaces for so long, be part of the reason why they are so difficult to remove or inactivate using disinfectants (bacteria in biofilms can be 1000x more difficult to kill than corresponding planktonic bacteria) and explain to some degree the difficulty in recovering environmental pathogens by surface sampling.

Biofilms are clearly not the only reason for failures in hospital disinfection given the difficulty in achieving adequate distribution and contact time using manual methods, but these findings may have implications for infection control practices within hospitals and on the choice of the appropriate disinfectants used to decontaminate surfaces.

Article citation: Vickery K, Deva A, Jacombs A, Allan J, Valente P, Gosbell IB. Presence of biofilm containing viable multiresistant organisms despite terminal cleaning on clinical surfaces in an intensive care unit. J Hosp Infect 2012; 80: 52-55.

Image courtesy of the Lewis Lab at Northeastern University. Image created by Anthony D’Onofrio, William H. Fowle, Eric J. Stewart and Kim Lewis