Summary
Introduction.
Contamination of hospital surfaces plays an important role in the transmission of several healthcare-associated microorganisms, therefore methods for evaluating hospital surfaces' cleaning gain particular importance. Among these, there are visual inspection, quantitative microbiology, fluorescent markers and adenosine triphosphate (ATP) bioluminescence. The latter seems to provide interesting features, detecting the presence of ATP on surface (as Relative Light Units, RLU), a proxy of organic matter and microbial contamination. Several studies have investigated the effectiveness of this technology; with this research, we aim to summarize the most significant results.
Methods.
A systematic review was conducted. The keywords (namely, "ATP", "bioluminescence", "hospital" and "surfaces") were searched in PubMed/MEDLINE and Scopus databases, in order to find relevant data, from January 2000 to October 2014. After the selection, we globally considered 27 articles.
Results.
Most of the studies were conducted in United Kingdom and in USA. Different threshold RLU benchmark values were identified by analyzed studies. Fourteen of these researches compared the ATP bioluminescence with microbiological methods, 11 identified a significant correlation between the two methods, although poor or not complete for 5.
Discussion.
ATP bioluminescence is not a standardized methodology: each tool has different benchmark values, not always clearly defined. At the moment, we can say that the technique could be used to assess, in real time, hospital surfaces where cleanliness is required, but not sterility.
Key words: ATP Bioluminescence, Hospital Surfaces, Healthcare-Associated Infections
Introduction
Healthcare-associated infections (HAIs) represent an important and widespread cause of morbidity and mortality among patients. Over the past decades, various scientific evidences have accumulated, indicating that contamination of hospital surfaces plays an important role in the transmission and diffusion of several healthcareassociated microorganisms [1, 2]. In particular, the hospital environment contributes to the transmission of several nosocomial pathogens, such as Clostridium difficile, methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) [2, 3]. These bacteria could survive in this setting for a variable period, from hours to days and, in some cases, even months, and could contaminate the surfaces or the medical devices [4]. Consequently, pathogens could infect patients or contaminate the hands of healthcare staff and, then, patients [2].
Within this perspective, methods to assess hospital environments cleaning can be considered an integral part of infections prevention and control programs. Among these, the most known and used are: visual inspection, microbial methods, fluorescent markers and adenosine triphosphate (ATP) bioluminescence. The latter measures the presence of ATP on surfaces. The ATP bioluminescence consists in a swab, used to sample a standardized area, which, subsequently, is placed in a tool that uses the firefly enzyme "luciferase" to catalyze the conversion of ATP in Adenosine Monophosphate (AMP): this reaction results into an emission of light which is detected by the bioluminometer and quantified in Relative Light Unit (RLU). The presence of ATP on surface, obviously, is a proxy of organic matter and, consequently, of microbial contamination. This method has been used in food industries since over 30 years. Its use in the health care environment is growing, but it is still controversial, in that different tools consider different threshold values, and, therefore, this technique seems not to be standardized.
Several studies investigated the effectiveness and also evaluated the practical application of this technique in this setting. The aim of this study was to qualitatively synthesize and discuss the most significant results and implications of the applications of ATP bioluminescence in healthcare settings, reviewing the most recent scholarly literature.
Methods
We conducted a systematic review according to the "Preferred Reporting Items for Systematic Reviews and Meta-analyses" (PRISMA) guidelines [5]. The search strategy consisted in a string of keywords such as ATP, bioluminescence, bioluminometer, hospital, healthcare setting, surfaces, connected by proper Boolean operators. For this scope, the keywords were searched in PubMed/MEDLINE and Scopus databases, in order to find relevant data. Time filter was applied and only articles from January 2000 to October 2014 were considered. Only articles written in English or for which an English translated text was available were included. Using Scopus we searched the keywords, selecting the option "all fields", whilst for PubMed/MEDLINE medical subject headings (MeSH) terms were used. All the searches as well as the screening were made by two researches EC and GM independently. Any disagreement was discussed until consensus was reached.
We included all types of studies, except: i) not peerreviewed scholarly articles; ii) overview/review articles, which were excluded but scanned for including further potentially relevant studies, iii) articles not written in English language, iv) all laboratory studies, not conducted in health care settings, and v) articles lacking sufficient details or not pertinent with the aim of our review. Further, selected target journals were hand-searched for increasing the chance of getting relevant articles. For ensuring a high-quality of the included studies, we did not search in the grey literature.
Table I reports our search strategy.
Tab. I.
strategy item | Details |
---|---|
Keywords | Adenosine triphosphate, ATP, bioluminescence, bioluminometer, surfaces, hospital |
Databases | PubMed/MEDLINE, Scopus |
Inclusion criteria | Studies investigating the applications and effectiveness of ATP bioluminescence Studies conducted in healthcare settings |
Exclusion criteria | Studies not carried out in healthcare settings Studies lacking sufficient details Studies not pertinent with the aim of this review Study design: overview/review articles |
Time filter | January 2000-October 2014 |
Language filter | Only articles written in English |
Target journals | American Journal of Infection Control; British Journal of Infection Control; Healthcare Infection; Infection control and hospital epidemiology: the official journal of the Society of Hospital Epidemiologists of America; International journal of hygiene and environmental health; Journal of Infection Control; Journal of Occupational and Environmental Hygiene |
Tab. II.
Author/year | Country | Setting | Sample | RLU benchmark | Correlation RLU/CFU | Brand bioluminometer |
---|---|---|---|---|---|---|
Ali et al., 2012 [6] | UK | Hospital | 60 samples pre and 60 post cleaning | 250 | Not investigated | Not reported |
Amin et al., 2014 [16] | U.S. | Clinic ophtalmology ward | 396 samples pre and 396 post cleaning | 250 | Not investigated | 3M Clean-Trace ATP System |
Amodio et al., 2013 [25] | Italy | Teaching hospital | 193 surfaces postcleaning | 100 | Poor (R2=0.29) | Luminocontrol II (PBI internarnational, Milano) |
Andersen et al., 2008 [29] | Norway | Teaching hospital | 96 samples pre and 96 post cleaning | 100, 500 | Not investigated | ATP Biotrace Clean-Trace system; Hygiena System |
Anderson et al., 2011 [7] | UK | Hospital surgical ward | 44 samples post-cleaning | 100 | Not investigated | SystemSure Plus system (Hygiena Int. Ltd) |
Aycicek et al., 2015 [26] | Turkey | Hospital kitchen | 280 from 14 surfaces | Not reported | Significant (κ = 0.249) | Pd-10 kikkoman Co, Japan |
Boyce et al., 2009 [17] | U.S. | Teaching hospital | 510 samples pre and 503 post cleaning | 250 | From poor to moderate (r from 0.356 to 0.649) | 3M Clean-Trace ATP System |
Boyce et al., 2011 [18] | U.S. | Teaching hospital | 500 samples pre and 500 post cleaning | 250 | Not significant | 3M Clean-Trace ATP System |
Branch-Elliman et al., 2014 [19] | U.S. | Hospital | 820 samples post clearing | 300 | Not investigated | 3M Clean-Trace NG Luminometer |
Cooper et al., 2007 [8] | UK | 4 hospital | 552 samples pre and 547 post cleaning | 500 | Significant | Biotrace Cleantrace system |
Ferreira et al., 2011 [31] | Brazil | Hospital | 100 samples post clearing | 500 | Not significant | 3M Clean-Trace ATP System |
Gillespie et al., 2012 [30] | Australia | Hospital | 50 samples pre and 50 post cleaning | Not reported | Not investigated | Not reported |
Gold et al., 2013 [20] | U.S. | Intensive Care Unit (ICU) | Postcleaning. Number of surfaces not specified | 45 | Not investigated | Ruholf ATO Complete contamination Monitoring System |
Gordon et al., 2014[3] | Canada | Teaching hospital | 15 HTOs in 36 patients rooms (first day) and in 37 patients room (second day) | 1000 | Not investigated | Not reported |
Griffith et al., 2008 [9] | UK | Hospital | 31 sites postcleaning | 500 | Not reported | Biotrace Clean-Trace system |
Havill et al., 2011 [21] | U.S. | Teaching hospital | 300 samples from 101 rolling blood pressure unit | 250 | Not investigated | 3M Clean-Trace ATP System |
Lewis et al., 2008 [10] | UK | Teaching hospital | 180 samples post cleaning | 250 | Significant | Biotrace International, Ltd, Brigend, UK |
Luick et al., 2013 [22] | U.S. | Teaching hospital | 250 surfaces pre and post cleaning | Not reported | Not significant | Accupoint HC (Neogen) |
Malik et al., 2003 [11] | UK | 4 hospitals | non specified the samples number. Sampling done postcleaning | 500 | Significant | Biotrace Cleantrace system |
Mulvey et al., 2011 [13] | UK | Teaching hospital | 90 samples pre and post cleaning | 250 | Significant | Hygiena system |
Moore et al., 2010 [12] | UK | Teaching hospital | 90 samples pre and 90 post cleaning | 250, 500 | Not investigated | 3M Clean-Trace Clinical Hygiene Monitoring System |
Sherlock et al., 2009 [14] | UK | Two hospital wards | 120 sample pre and 120 post cleaning | 500 | Not investigated | 3M International Ltd, Brigend, UK |
Smith et al., 2013 [23] | U.S. | Hospital | 10 samples in 10 rooms pre and post-cleaning | 250 | Significant only precleaning | 3M Clean-Trace ATP System |
Smith et al., 2013 [24] | U.S. | Hospital | 18 samples pre-cleaning in 10 rooms | 250 | Significant | 3M Clean-Trace ATP System |
Watanabe et al., 2014 [27] | Japan | Three hospital of different sizes | 752 samples post cleaning | 127 | Poor (r = 0.287) | 3M Clean-Trace ATP System |
Willis et al., 2007 [15] | UK | Hospital | 108 samples post cleaning | 100(surfaces), 300 (floor) | Poor (r = 0.15) | Hygiena system |
Zambrano et al., 2014 [28] | Chile | Teaching hospital | 198 samples pre and post cleaning | Not reported | Not investigated | Lightning MVPTM (Arquimed) |
From each included study, we collected information about: i) the surname of the first author of the article and the year of publication; ii) the country where the research was carried out, iii) the setting in which the investigation was performed; iv) the samples used in the investigation; v) the RLU benchmark value discerning between clean and dirty surfaces (when investigated and reported), vi) the type of bioluminometers used, and vii) whether an eventual correlation between bioluminescence and microbiological methods existed (in terms of correlation coefficients, such as Pearson's coefficient, Spearman's rank coefficient, concordance κ coefficient or R2). The effect size of the correlation coefficient, when reported, was interpreted using the following rule of thumb: very high positive (or negative) if ranging from 0.90 to 1.00 (or ranging from -0.90 to -1.00): high positive (or negative) if ranging from 0.70 to 0.90 (or ranging from -0.70 to -0.90), moderate positive (or negative) if ranging from 0.50 to 0.70 (or ranging from -0.50 to -0.70), low/poor positive (or negative) if ranging from 0.30 to 0.50 (or ranging from -0.30 to -0.50), and little/no correlation if ranging from 0.00 to 0.30 (or ranging from 0.00 to -0.30). In the case the exact correlation coefficient was not indicated, we reported whether the correlation was statistically significant or not, on the basis of the p-value. Data extraction was carried out by two reviewers independently. In case of discrepancy, any disagreement was solved by discussion until consensus was reached or a third reviewer was involved.
Results
Using PubMed/MEDLINE we found 19 studies, 4 of which were judged not relevant for our investigation and one was a review, examining 12 papers, already found by our research. The final number of studies considered using PubMed/MEDLINE was 14. Therefore, in Scopus we found 315 papers, and only 27 were useful for the review. As such, the final number of studied included in the review was 27 (Fig. 1).
Concerning the data extracted, all studies were conducted in health care settings. Most of them were carried out in United Kingdom (UK) (10/27) [6- 15]; 9 of them were performed in USA [16-24], 1 in Italy [25], Turkey [26], Japan [27], Chile [28], Canada [3], Norway [29], Australia [30] and Brazil [31]. Eleven researches monitored the surfaces after cleaning [3, 7, 9-11, 15, 19, 20, 25, 27, 31], one before [23], 13 both pre and post cleaning [6, 8, 12-14, 16-18, 22, 24, 28- 30] and in the remaining two studies this information was not reported [21, 26]. Twenty-three studies (85.2%) identified a RLU benchmark value, discerning between clean and dirty surfaces. This value corresponded to 250 for 10 studies [6, 10, 12, 13, 16-18 21, 23, 24], to 500 for 7 researches [8, 9, 11, 12, 14, 29, 31], to 100 for 4 studies [7, 15, 25, 29], to 300 for 2 studies [15, 19]; 127 [27], 1000 [3] and to 45 [20] for one study, respectively. Moore et al. [12] identified two threshold values: 250 and 500 RLU. Andersen et al. [29] used two different tools and, so, considered two different values: 500 RLU for ATP Biotrace Cleantrace system and 100 for Hygiena System. Another paper considered as cutoff 100 RLU for several patient rooms surfaces and 300 RLU for floors [15]. Details about RLU threshold values for each type of bioluminometers are shown in Figure 2. Figure 3 shows the benchmark values according to geographical provenance of studies.
Fourteen papers (51.8%) [8, 10, 11, 13, 15, 17, 18, 22-27, 31] compared the effectiveness of ATP bioluminescence to assess hospital surfaces' cleaning with microbiological methods; in particular, these studies evaluated the correlation between RLU and Aerobic Colony Counts (ACC). Three of these studies have shown no correlation between the two compared methodologies [18, 22 31], whilst the remaining 11 have highlighted a correlation [8, 10, 11, 13, 15, 17, 23-27], although it is poor/ moderate according to 4 studies [15, 17, 25, 27] and one found only a pre-cleaning correlation [24].
Discussion
Contamination of hospital surfaces plays an important role in the transmission of several healthcare-associated microorganisms. In this perspective, methods for evaluating hospital surfaces' cleaning gain importance. Each of these methods show advantages and disadvantages, and directives indicating the most appropriate method to use in different health care settings do not exist. The ATP bioluminescence seems to provide interesting perspectives, detecting the presence of ATP on surfaces (as Relative Light Units, RLU), a proxy of organic matter and microbial contamination. The present review showed the ATP bioluminescence is not a standardized method for assessing cleanliness; each tool had different benchmark values, ranging from 45 RLU to 1000 RLU. The most used values were 250 and 500 RLU. It is also interesting to note that for the same brand of bioluminometer different threshold values were considered.
The country where the studies were conducted may have influenced the choice of the RLU cutoff values, for example in the U.S. the most often used value corresponded to 500 RLU. The tool used in most studies was 3M Clean-Trace ATP System, following by Hygiena system and Biotrace Cleantrace System.
These differences among the benchmark values make difficult the comparisons between measurements carried out with different tools [15].
A large majority of studies was conducted in UK and in USA, probably because in these Countries there is a growing interest about environmental hospital hygiene and methods to assess it. Furthermore, it should be noted that among 14 studies investigating the correlation between ATP bioluminescence and microbiological methods, 11 have found a significant correlation, although poor, or partial, for 5 papers. ATP bioluminescence would not seem to be a methodology very accurate in detecting bacteria. In addition, it provides a quantification of all organic material, including bacteria, but it also identifies others organic matters such as urine, milk and blood, which is a limiting aspect of the methods and is rather difficult to overcome [10].
Another limitation of this technique could be the residues of detergent or disinfectants on the surfaces [32], which may require rinsing of these surfaces before the use [33].
Despite of these considerations, some advantages of this technique can be listed, such as the possibility to provide real-time results (within 20 seconds of sampling), its simplicity of use (which makes possible the adoption of the method not only by trained healthcare staff), and the quantitative results. The latter allows comparisons between pre- and post-cleaning or between different surfaces.
Our study has a number of shortcoming that should be properly recognized. Despite the broad and systematic search, the main limitations of this study could be found in the selection of papers written only in English language and, therefore, in the possibility of having missed some relevant papers, which, considering the novelty of the technique, could be found, instead, in the "grey literature". On the other hand, it should be expected that the quality of the latter papers would be inferior to those present in the scholarly peer-reviewed indexed literature. Concerning the main implications of the current study, we can conclude that the use of this technique could produce better results after a proper validation/standardization. To achieve this aim a multi-phase approach should be followed: i) to clarify the methods of sanitizing or disinfecting performed on each surfaces before the controls made with the bioluminometer; ii) to select the most appropriate surfaces where the analysis have to be conducted (for example "high risk objects" such as toilet seats, basins, door handles); iii) to choose the bioluminometer among the different brands available; iv) to calibrate the instruments studying the correlation between CFU and RLU, identifying the best threshold value (higher sensitivity and specificity) [33] which discriminates between clean and dirt surfaces.
Conclusions
In conclusion, the ATP bioluminescence could be considered a practical, useful method to assess hospital hygiene, performing better than visual inspection (namely, Bacharach scale, bassoumeter, and glossmeter), if properly adopted, also being aware of its possible limits.
ACKNOWLEDGMENTS
The authors thank Dr Nicola Bragazzi for his helpful suggestions.
The authors declare that there is no conflict of interest regarding the publication of this paper.
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