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C. difficle spores in the environment of patients with C. difficile associated disease (CDAD) are difficult to eliminate. Bleach (5000 ppm) has been advocated as an effective disinfectant for the environmental surfaces of patients with CDAD. Few alternatives to bleach for non-outbreak conditions have been evaluated in controlled healthcare studies.
This study was a prospective clinical comparison during non-outbreak conditions of the efficacy of an accelerated hydrogen peroxide cleaner (0.5% AHP) to the currently used stabilized hydrogen peroxide cleaner (0.05% SHP at manufacturer recommended use-dilution) with respect to spore removal from toilets in a tertiary care facility. The toilets used by patients who had diarrhea with and without C. difficile associated disease (CDAD) were cultured for C. difficile and were monitored using an ultraviolet mark (UVM) to assess cleaning compliance on a daily basis 5 days per week. A total of 243 patients and 714 samples were analysed. The culture results were included in the analysis only if the UVM audit from the same day confirmed that the toilet had been cleaned.
Our data demonstrated that the efficacy of spore killing is formulation specific and cannot be generalized. The OxivirTB® AHP formulation resulted in statistically significantly (p = 0.0023) lower levels of toxigenic C. difficile spores in toilets of patients with CDAD compared to the SHP formulation that was routinely being used (28% vs 45% culture positive). The background level of toxigenic C. difficile spores was 10% in toilets of patients with diarrhea not due to CDAD. The UVM audit indicated that despite the enhanced twice-daily cleaning protocol for CDAD patients cleaning was not achieved on approximately 30 - 40% of the days tested.
Our data indicate that the AHP formulation evaluated that has some sporicidal activity was significantly better than the currently used SHP formulation. This AHP formulation provides a one-step process that significantly lowers the C. difficile spore level in toilets during non-outbreak conditions without the workplace safety concerns associated with 5000 ppm bleach.
Toxigenic Clostridium difficile causes a significant number of enteric infections world-wide [1-5]. In Manitoba, where C. difficile associated diarrhea (CDAD) is reportable, there were 985 cases of CDAD compared to 512 cases of all other enteric bacterial infections combined in 2007 . The incidence of CDAD ranges from 3.4 cases/1000 admissions up to 50 cases/1000 admissions [1,7]. The rates of CDAD per 100,000 population in the USA have almost doubled between 1996 and 2003 .
A major reservoir linked to nosocomial infections is thought to be the environment of healthcare facilities that are contaminated with the C. difficile spores shed by patients with CDAD [1,7,9,8,11]. The persistence of C. difficile spores has been well documented with toilets having the highest levels [1,9,12]. Reducing C. difficile spores from environmental sources is challenging as few surface disinfectant and/or cleaning agents have sporocidal activity in a short enough time-frame (e.g. 3 minutes) to be effective .
National guidelines in Canada do not recommend disinfectants for routine housekeeping  but many healthcare facilities use bleach at a 1:10 dilution (5,000 ppm) and increase cleaning from once to twice daily for patients with CDAD as per PIDAC[9,10,12,15]. Despite being widely accepted, neither Wilcox's original study  nor Eckstein's recent study  were able to demonstrate complete eradication of spores when 5,000 ppm bleach was used for cleaning/disinfecting toilet facilities of patients with CDAD. In most published studies, bleach at 5,000 ppm was combined with other heightened strategies such as improved housekeeping, enhanced compliance with infection control isolation precautions, and increased education . Although 5,000 ppm chlorine bleach is an effective sporicidal agent, there are significant workplace safety concerns related to using bleach and it requires a two step process (i.e. must be wiped off using water). There are no published studies that have audited cleaning compliance in conjunction with evaluating bleach alternatives (that have some sporicidal activity) that could be used for environmental cleaning of CDAD patient toilets during non-outbreak conditions.
The objective of this research was to determine if the presence of C. difficile spores in toilets of patients with CDAD could be reduced in non-outbreak conditions when a non-bleach based disinfecting agent that had some sporicidal activity was used for cleaning toilets. To ensure that the intervention was used the toilets were audited with UVM and only if the toilet had received cleaning was the culture date included in the overall analysis.
C. difficile strain 726 was a clinical isolate that was used for spore preparation as described by Alfa et al . The spore preparation of ~106 spores/mL was stored in 45% alcohol and the same batch of spores was used for all testing.
The efficacy of various disinfectant solutions at killing spores of C. difficile was assessed using suspension and surface testing. The use of ATS (artificial test soil) as an organic challenge and the recovery of residual C. difficile spores from inoculated toilet seats by Rodac plates is described by Alfa et al . Five different chemical disinfectants were evaluated; PerDiem at 1:16 use-dilution (research based use-dilution that is not recommended by the manufacturer), OxivirTB® used directly (manufacturer's recommended use-dilution), Bleach at 500, 1000 and 5000 ppm. C. difficile spores (in ATS as an organic challenge) were used to inoculate the surface of a toilet seat (4 Log10 spores per site) and dried overnight. Each disinfectant was sprayed to completely wet the inoculated surface and allowed to remain in contact with the surface until completely dried (~10 minutes) with no surface wiping or allowed to remain in contact with the surface for 3 minutes followed by a manual wipe using sterile gauze that was pre-moistened with the same disinfectant. The level of residual viable spores was then assessed using the Rodac plate technique. Each experiment was performed in triplicate and each count was performed in triplicate. Results represent the mean ± standard deviation of all 9 counts. Toilet seats were inoculated with an organic challenge and spores as described in methods.
Each day the patient's toilet was assessed using Rodac plates containing CDMN agar (samples surface area of 25 cm2) for detection of the presence of C. difficile spores as described previously . The same Rodac plate was used to sequentially sample four areas of the toilet (underside of the toilet lid, toilet seat surface and underside, as well as the inside rim of the upper portion of the toilet bowl) for a total surface are of 100 cm2. The identification of isolates and the confirmation of toxin production was as previously described by Alfa et al .
OxivirTB® is an accelerated hydrogen peroxide (AHP) formulation that is marketed for use in healthcare, medical, industrial and institutional facilities. It has an M. tuberculosis label claim and is sold in a ready to use format that contains 0.5% AHP. The manufacturer recommended contact time is 1 minute. PerDiem is a stabilized hydrogen peroxide (SHP) that is used for routine housekeeping at 1:64 dilution (0.0469 final concentration of SHP at use-dilution of 1:64). There is no need for special PPE for either PerDiem or OxivirTB® at the use-dilutions and no wipe-off of residual disinfectant is needed. The manufacturer recommended contact time is 10 minutes for PerDiem. PerCept is a Hydrogen peroxide (HP) formulation that contains 7% HP that is to be diluted at 1:16, carries a broader spectrum of efficacy than PerDiem with a 5-minute contact time and is intended for disinfection of environmental surfaces and non-critical devices. In concentrate at 7%, this formulation has special PPE requirements; however, at the use dilution does not require special PPE. Bleach (5% household bleach containing 50,000 ppm chlorine) was also assessed at use-dilutions of 5,000 ppm, 1,000 ppm and 500 ppm (prepared fresh daily). Bleach does require special PPE at 5,000 ppm and also requires a wipe-off after appropriate contact time (no minimum manufacturer recommended contact time for household bleach).
Glitterbug lotion (Brevis Inc) was used as the UV-visible marker (UVM) on the undersides of the toilet seat as an audit to ensure housekeeping staff had cleaned the toilet. The value of UVM as an audit tool of cleaning compliance has been described by Alfa et al . If this marker was not removed it indicated that the toilet had not been cleaned as per the protocol therefore the culture results from the Rodac Plates taken on that day would not reflect the efficacy of the agent tested because it was not applied to the toilet. Only if the UVM was removed was the Rodac culture result included in the final data analysis.
PerDiem at a 1:64 use-dilution was used for routine cleaning of patient toilets. The toilet cleaning instructions required that all surfaces (including the underside of the toilet lid and seat) be sprayed to entirely wet the toilet surfaces. The solution was to be in contact with the toilet surface while the housekeeper finished cleaning the other areas of the bathroom (observational studies indicated that this required from 3 - 5 minutes). The toilet was then to be wiped using a cloth wetted with the same use-dilution PerDiem solution. The toilet was cleaned last and the cleaning cloth was not to be used for any other cleaning - it was sent for laundering. The toilet was to be cleaned once per day. The enhanced housekeeping protocol (twice daily cleaning) used by this hospital was for toilets of patients who were on isolation precautions due to CDAD. PerDiem at the standard 1:64 use-dilution was used for the enhanced protocol. The cloths used for all cleaning were cotton material of varying thickness made from old bedsheets.
Patients with diarrhoea were enrolled in 3 Arms as shown in Figure Figure1.1. No samples were taken from the patients and only the patient's toilet was evaluated. The Research and Ethics committee approved that informed consent of patients who used the toilet evaluated was not needed. The hospital site where this study was undertaken was a 450 bed acute care facility. All housekeeping staff were informed that a study was being done that included a UVM audit, however, they were not notified which wards or patient rooms would be assessed. It was made clear to the housekeepers that no punitive action would result from the audits performed during this study. The healthcare facility had dedicated housekeepers for each ward. Staff were instructed and signs were placed in the toilets clearly indicating that the bottles of cleaner were not be removed or changed and that only these specific bottles were to be used for the cleaning. Each day the research staff checked the rooms to ensure the proper agent was being used. The diagnostic test results for all stool samples submitted to the diagnostic lab for C. difficile toxin testing were reviewed on a daily basis and the toilet of each patient enrolled was prospectively evaluated for 5 days of sampling unless patient died or was discharged before the five samples were collected.
Data was entered into an excel spreadsheet and some statistical analysis determined using GraphPad Instat Program.
The objective was to select a cleaning agent that had microbial killing ability that did not require an additional rinse step after application and had some C. difficile sporicidal activity within a short period of time. The selected formulation would then be used for a prospective clinical study. Preliminary in vitro testing (Figure (Figure2)2) of various disinfectant formulations using simulated-use suspension testing in the absence of an organic challenge indicated that the OxivirTB® formulation provided a 2-3 Log10 kill of C. difficile spores after only 1 minute exposure. The suspension killing for OxivirTB® was not as efficient as that achieved for bleach 5000 ppm but was equivalent to bleach 1000 ppm after 1 min. The other HP formulations tested did not have efficient spore killing ability within 1 - 5 mins. Further testing of the efficacy of C. difficile spore killing on surfaces in the presence of an organic challenge were also preformed (Figure (Figure3).3). If a spray and wipe cleaning process was used 5000 ppm bleach was the most effective, whereas if no wiping was performed then OxivirTB® and 5000 ppm bleach were not statistically different in their spore killing ability. Since the objective was to identify an alternative to 5000 ppm bleach, the OxivirTB® formulation was selected for the intervention study as it had rapid (but not complete) sporicidal activity yet does not require special PPE and does not need the additional step of being wiped off with water (i.e. is a one step process).
The efficiency of detection of C. difficile spores on surfaces by Rodac plates containing CDMN agar was assessed using a known concentration of spores inoculated and dried onto plastic, tin-foil and toilet seat surfaces (Table (Table11).
The ward intervention study (Figure (Figure1)1) was undertaken between December 2005 and July 2007. Patients in Arms 1, and 2 were prospectively followed while on isolation precautions for at least 1 week post diagnosis of CDAD unless discharged earlier or taken off of isolation precautions. Patients in Arm 3 (not on isolation) were prospectively followed for at least 1 week unless discharged earlier. Although patients who are treated for CDAD are known to shed spores for prolonged periods, the expectation was that the time of highest likelihood of having C. difficile spores shed into the toilet was during the first week post-diagnosis.
To ensure the cleaning agents (both AHP and SHP) were applied to the toilets, a UV visible marker (UVM) was used on the underside of the toilet seat following the protocol of Alfa et al . Our data (Figure (Figure4)4) showed 30 to 41% of the toilets had a UVM score of 3 indicating the marker was not removed, therefore, not cleaned according to the housekeeping protocol. The overall average UVM scores were 1.48, 1.40, 1.48 and 1.63 for Arms 1, 2, and 3 respectively (not significantly different by ANOVA, p = 0.4253). To ensure reliable conclusions, the data on C. difficile culture results was stratified based on UVM audits. Figure Figure55 summarizes the data for C. difficile detection in Arms 1, 2, and 3 for samples collected from toilets where the UVM confirmed there had been some level of cleaning (i.e. UVM <3) versus when the UVM was 3 (no cleaning). Arm 1 (intervention agent) had significantly lower spore levels compared to Arm 2 (currently used protocol).
Our study is the first to incorporate UVM as an audit to confirm that cleaning of the toilet was done during the assessment of an alternative cleaning formulation. Our data indicated that the compliance with the housekeeping cleaning policy (i.e. UVM score <3) was about 60% which is consistent with what has been previously reported in regular as well as ICU rooms [19-21]. Despite the policy requiring cleaning of toilets twice per day for patients with CDAD, this was not being achieved 40% of the time. Recently a number of published reports [18,22-24] have indicated that the currently accepted benchmark of "visibly clean" is an inadequate audit approach in healthcare facilities. Alternative audit tools suggested include ATP bioluminescence and culture [22,23] with cleaning considered inadequate at ATP levels ≥ 500 RLU/cm2 or when culture showed >1 cfu/cm2 of C. difficile. Although using ATP based audit tools [22-24], or culture may provide a more direct measure of the residual bioburden, the UVM method provides an inexpensive and easy method for sites to accurately audit cleaning compliance (i.e. physical wiping of the surface) and this assessment is critical when comparing a possible alternative disinfecting/cleaning agent to a current agent.
Although Rodac plates containing CDMN provide excellent recovery of C. difficile spores from toilet surfaces (86%), it should be noted that C. difficile spores in a patient-used toilet will not be evenly distributed and our Rodac sampling method (sampled 100 cm2) represented only about 10% of the total toilet surface area that could be contaminated. Dispite this caveat the Rodac sampling method provides a good indication of the level of spore contamination as it samples the sites most likely to be contaminated after patient-use or after the contents of a bedpan are disposed of in the toilet.
The daily monitoring of C. difficile spores in the patient toilet using Rodac plates provided direct assessment of the impact of the cleaning agent on spore removal/killing. Physical cleaning is not sufficient alone to eliminate spores and use of a disinfectant may be needed to provide an efficient means of reducing the level of environmental spores. Although chlorine releasing agents are optimal for spore killing even 5,000 ppm bleach has been reported as not totally effective [1,7,9,23]. The previous published clinical studies did not have audits to ensure cleaning compliance, as such the suboptimal results obtained using 5,000 ppm bleach (up to ~20% still having C. difficile) may be due to lack of housekeeping compliance. However,  Eckstein reported that even when research staff performed the cleaning that 5000 ppm bleach was not totally effective at eradicating C. difficile spores from patient toilets (10% still having C. difficile). Our data indicated that although bleach at 500 to 5,000 ppm was effective at killing C. difficile spores in suspension in 5 minutes, it was not as effective when surface testing in the presence of an organic challenge was used. Perez et al  have shown that 5,000 ppm bleach needs 5 - 8 mins to provide a 6 Log10 reduction in C. difficile spores. OxivirTB® was as effective as 5000 ppm bleach when tested on surfaces with an organic challenge without physical wiping (neither was completely effective without wiping). Perez et al's  data also support the value of AHP for C. difficile spore killing. However, the formulation they tested is designed for medical device reprocessing and therefore requires special PPE as well as a second wipe with water to remove the AHP residuals. Neither the AHP formulation (OxivirTB) or the SHP formulation (PerDiem) used for the current study require special PPE or a second wipe to remove residuals. There have been published reports that the use of AHP disinfecting cleaners have been associated with outbreak control and reduced rates of CDAD .
Our study is the first to provide data that a one stage cleaning process using an AHP (0.5%) formulation can significantly reduce the load of C. difficile spores in the toilets of patients with CDAD during non-outbreak conditions. Our study demonstrated that the AHP intervention resulted in toilet spore levels (27.8%) nearly equivalent to those found when Eckstein et al  used 5,000 ppm bleach (~20%). It is critical that for "intervention studies" that cleaning compliance is audited. If the toilet has not been cleaned, results should not be included in the analysis of the intervention as the conclusions may be misleading.
Panessa  et al have reported that despite not being metabolically active, spores do attach to surfaces especially when sporulation is initiated. This ability of spores to attach combined with lack of cleaning compliance by housekeeping staff may be the basis for accumulation of spores and high positivity rates in toilets and high-touch areas of the rooms of patients with CDAD [1,7,9,11,26]. Despite a housekeeping policy requiring enhanced frequency of cleaning (twice per day) for CDAD patient isolation rooms, C. difficile spores were still detected in approximately 50% of toilets. Although this may be partly due to the housekeeping protocol not stipulating 10 minutes contact time with the use-dilution of PerDiem (as per manufacturer's contact time recommendations) it is unlikely that re-wetting the surface to provide 10 minutes contact time would have improved elimination of C. difficile spores as our preliminary testing showed that this formulation had essentially no ability to kill C. difficile spores even after 20 minutes exposure in suspension testing. The lack of ability of PerDiem (routinely used throughout the hospital) to eliminate spores may also explain why the background level of C. difficile is 10% even in rooms of patients without CDAD. Alternatively, this may be the lowest environmental level of C. difficile spores that can be achieved in healthcare facilities as our background level of 10% was similar to the residual level of spores when research staff did toilet cleaning in patient rooms using 5,000 ppm bleach . The efficacy of any cleaning/disinfecting agent tested is dependent on physical action. We recommend that healthcare facilities need to ensure that adequate time is allowed for cleaning of patient rooms and that adequate audits are used to ensure compliance with the cleaning protocol.
In conclusion, our data demonstrated that the use of an agent with some sporicidal activity for cleaning resulted in significantly reduced C. difficle spore levels in toilets of patients with CDAD during non-outbreak conditions. Infection transmission within healthcare will remain problematic if the role of housekeeping remains undervalued and if they are not provided with adequate audit tools such as UVM to ensure sustained cleaning compliance.
The ECR and all funds for this study were provided by Advanced Sterilization Products, a Division of Ethicon, a Johnson and Johnson company. MJA has undertaken contract research projects (unrelated to the current publication) for a variety of companies including; 3 M, bioMerieux, Olympus, Case Medical, Intelligent Hospital Systems, Johnson & Johnson, Novaflux, STERIS and Virox. No monies from the current or past research contracts have gone to MJA, they were administered through the St. Boniface Research Centre and were used for research related expenses only. MJA has been a sponsored conference speaker for numerous conferences and she has acted as a paid consultant for preparation of a one time literature review for STERIS in 2003 and for providing a one time educational microbiology workshop for 3 M staff in 2006.
The other authors have not acted as consultants and have no financial or other link with any company.
MA conceived the protocol and was involved in data analysis and had a primary role in manuscript writing. EL & GH were involved in data analysis and manuscript writing. AW, CD & PD were involved in ward sampling, data analysis and manuscript proofing. All authors have read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
Funds for this study were provided by Manitoba Medical Services Foundation as well as an unrestricted research grant from Virox Technologies Inc. and JohnsonDiversey Inc. All AHP used for this study was provided by Virox Inc. The support and help of Nila MacFarlane, Diane Robson, Leslie Klass and Janice Kennedy of the Infection Control Department is acknowledged. The expertise and technical support for culture of the environmental samples by the Clinical Microbiology laboratory staff at the St. Boniface General Hospital is acknowledged. The support and advice provided by Michelle MacRae, Louise Beulow-Smith and the housekeeping staff at St. Boniface General Hospital is acknowledged. The statistical advice from Dr. Doug Staley (biostatistician, Univerisity of Manitoba) is acknowledged.