Infection control in the post-antibiotic era
Stephanie J. DancerDepartment of Microbiology, Hairmyres Hospital, East Kilbride, Lanarkshire G75 8RG, UK. Email: stephanie.dancer@lanarkshire.scot.nhs.uk
Healthcare Infection 18(2) 51-60 https://doi.org/10.1071/HI12042
Submitted: 27 September 2012 Accepted: 8 January 2013 Published: 10 April 2013
Journal Compilation © Australian Infection Control Association 2013
Abstract
There are enormous challenges facing infection control in the 21st century. Countries across the world are confronted by ageing populations, restricted healthcare resources, demands for modern medicine and increasing antimicrobial resistance. Problem pathogens in the community are set to invade hospitals, and those created in hospitals are seeding into the community. Continued consumption of antimicrobial agents is generating and consolidating resistance to nearly all classes of drugs. New resistance mechanisms arising in one locality rapidly spread across the ‘global village’ courtesy of migration, conflict and international travel. We are facing unprecedented threats to the management of infection both in healthcare and communities across the world. This review summarises the current challenges for infection control and proposes a range of solutions encompassing novel strategies and technologies aimed at protecting us against untreatable infection.
Additional keywords: antimicrobial stewardship, decontamination, healthcare-associated infection, hospital hygiene, infection control.
Implications
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This opinion piece summarises current challenges for the prevention and control of infection.
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It proposes a range of novel strategies and technologies aimed at protecting us against untreatable infection.
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We need to prepare for a world without antibiotics.
Introduction
Infection control faces radical challenges at the beginning of the third millennium.1 Infection remains the second most common cause of death worldwide, with healthcare-associated infection (HAI) affecting at least 1 in 10 patients admitted into hospital. Advanced healthcare increases the risk of infection – with invasive technologies and immunosuppression – while fuelling high patient expectations of modern medicine.2 Most countries are experiencing ageing populations, along with continued restrictions on healthcare resources.3 Healthcare tourism, along with migrant workers, refugees, business and holiday travellers illustrate the ease by which pathogens traverse the aptly named ‘global village’.4
These socioeconomic, medical and population issues have coincided with the present backdrop of steadily-increasing antimicrobial resistance.3,5,6 Some pathogens are termed multi-drug resistant (MDR), with a few treatment choices; others, with one major drug class available, are classified ‘extreme-resistant’ (XDR); and finally, there are organisms termed ‘pan-resistant (PDR), because there are no remaining agents with which to treat patients.7
Additional organisms attract attention by virtue of pathogenic determinants and/or superlative transmission ability. These include Clostridium difficile and a wide range of viruses.3,8 Resistance issues have already been heralded with C. difficile (low-level resistance to metronidazole) and some influenza strains appear to be developing resistance to oseltamivir.9,10 As for norovirus, new genotypes regularly appear, causing a wave of outbreaks across a region, which then spread elsewhere.11 Such genomic plasticity illustrates a persistent threat, because it means that viruses could mutate into a strain impossible to contain, particularly if combined with exceptional virulence.12 Indeed, all microbial categories have this capacity for mutation.
Despite current concern over resistance, antimicrobial development and immunotherapy appear to have frozen.13,14 There are economic reasons for this, since short-term anti-infectives do not generate much profit, but it is possible that there are only a finite number of microbial targets accessible for antimicrobial exploration.15 It is also the case that regulatory bodies are not necessarily helping smooth the tortuous pathway from drug discovery to licensing.16
With diminishing options for treating infection, control of transmissible pathogens has ignited international interest.17 Multiple organisations have begun to formulate policies, but these efforts are challenged on every level by national, political, criminal and economic restraints.5,17–19 Without international recognition and collaboration, successful interventions in one part of the world will ultimately be compromised by control deficits in another. This article highlights current problems with microbial pathogens and offers a range of strategies for the future delivery of infection control. A return to the pre-antibiotic era, when normal healthy people died from infection, is not inevitable, even if a 21st century solution for treating infection takes its time to emerge.
Current problems with control methods
Healthcare
Solutions for controlling healthcare-associated infection are not all possible, practical, affordable, acceptable or even evidence-based.20 The usual response is to implement a ‘bundle’ of infection-control strategies, and hope that the overall effect will have the desired result.20–22 Exactly what effect each individual strategy has against a particular pathogen is usually unknown because we lack this level of evidence. Post-outbreak analysis often only provides a cause-and-effect relationship rather than data supporting single interventions. Thus, designing infection-control studies is fraught with confounders as well as being subject to ethical constraints.23
Formulating guidelines and policies on infection control has never been so popular but stating what we should do, and doing what is stated, can be a world apart on a busy ward.24,25 When clinical staff are overstretched, time for patient care is compromised, and integral to this is infection control.26,27 Good practice is reliant on personal choices. The ‘zero tolerance’ policy aimed at healthcare workers and their hand hygiene practices has not necessarily resulted in 100% compliance and there are compelling reasons for its failure.28,29 In addition, the success of antimicrobial stewardship programs depends on support by committed prescribers.30
Outside of outbreak situations, routine infection control remains low priority, since it is impossible to cost something that may not happen.31,32 By its very nature, infection prevention conflicts with the priorities of managers, keen to lower the overheads of their organisations.33,34 Running a hospital at 100% bed occupancy, for example, or underestimating staffing levels, is an invitation for pathogens to spread.33,35 Infection-control practitioners must engage with management and convince them of the importance of early implementation of control activities.36 It is unacceptable that avoidable fatalities have to occur before anyone takes any notice of hygiene deficits. Ultimately, the responsibility of determining the quality of healthcare rests with governing bodies at national level.37
Whilst many hospitals have set up epidemiology and surveillance programs to aid infection control, the components of these may lack definition, which means that surveillance data cannot be compared between countries, or even between regions.3 Similar problems exist at molecular level, where strain types may be disputed by international agencies and impede global attempts at monitoring spread.38
Community
Poor infection control encourages and concentrates pathogen reservoirs in hospitals, which eventually permits spillage into the community. Since the street between the hospital and the community runs both ways, patients colonised or infected with hospital organisms then return them back to hospital.2,39,40 Carriers contaminate the healthcare environment, which serves as a reservoir for others.41 In contrast, pathogens originating in the community are capable of spreading through hospitals following introduction by both staff and patients.42 Resistant coliforms can be acquired through different community reservoirs and carried long-term in the gut, particularly amongst the elderly.40,43 Older patients do not retain immunological defences capable of eradicating these microbes, which results in an accumulation of pathogens among people who frequently, and ultimately, require healthcare.
Patients not only desire the best and most modern of treatments, they also expect a ‘pill for every ill’, which makes it difficult to withhold antimicrobial drugs for the worried well. Time constraints in community clinics do not permit the explanation, reassurance and education required for non-infected patients, especially parents who want something for a sick child.44 Indeed, rigid stewardship in the community occasionally compromises the management of a patient who really does need timely antimicrobial therapy.45 This is compounded by poor access to diagnostic microbiology laboratories, which forces clinicians to prescribe broad-spectrum therapy and ultimately encourages antimicrobial resistance.46
There seems to be a current trend for waging war on the germs.47,48 Germs are a ‘buzzword’ for a danger that people wish to eliminate from their surroundings.47 This has resulted in a flourishing market of antibacterial products for use in the community.49,50 Antibacterial products were developed to prevent transmission of pathogens among patients, particularly in hospitals, but they are now being added to products used in healthy households, even though additional health benefits have not been demonstrated.51 Some antibacterial agents promote resistance and cross-resistance antibiotics.52,53 We should remember that ‘nature abhors a vacuum and will fill it up if she can’; this means that using microbiocidal products might remove susceptible microbes, but the space created could attract a new population of something worse.46,48 We cannot rid ourselves of bacteria.
Whilst affluent countries exercise their choice of disinfectant, there are places in the world which lack even basic sanitation and clean water. This compromises hygiene, facilitates infection and furthers the spread of resistant pathogens.54,55 Underfunded or inaccessible healthcare also encourages the creation of resistant organisms, such as tuberculosis, with transmission facilitated by social and housing deficits, HIV and war zones.56 Benefits accrued from antimicrobial restrictions and infection-control policies will be eroded by practices elsewhere in the world. Without international understanding and cooperation, national strategies are compromised when people purchase antimicrobial agents over-the-counter from local pharmacists or from internet sources.57–59 There exists a ‘black market’ for ‘antimicrobial’ medicines, for anyone keen enough to pay. The sudden emergence or recognition of a novel ‘superbug’ reignites irrational behaviour, reminiscent of long-gone quackery.60
Veterinary and agricultural contributions
The consequences of antimicrobial exposure outside hospitals do not originate solely from human consumption because industry, agriculture and the veterinary profession also use antibiotics in various ways.46 Resistant organisms are shed in excreta without antimicrobial pressures.61 Faeces entering, or bypassing, sewage systems can disperse organisms throughout the wider environment and sewage acts as a suitable vehicle for the transmission of resistance genes.55,62 Antibiotics given to animals contribute towards emergence of resistant bacteria in people, some of which may cause disease.63–65 The ST398 strain of methicillin-resistant Staphylococcus aureus (MRSA) that causes skin infections and sepsis in farm workers has evolved its resistance profile within a farm animal reservoir.65
Other resistant organisms originating in livestock enter the food chain and can be shown on foodstuffs at point of sale.43 A Dutch study demonstrates the spread of antibiotic-resistant E. coli from animals to people, firstly farmers and ultimately meat consumers.66 Similar findings have been reported from the UK.67 The US Food and Drug Administration recently announced new restrictions on using preventive antibiotics in livestock, but the rules cover a subset of drugs constituting just 0.2 per cent of antibiotics used on farms.68 As a result they are not expected to have much effect.69
Veterinary contribution does not rest solely on antimicrobial consumption or pathogen reservoirs, but with infection control practices as well.70 Hygiene measures are required to limit the transmission of resistant organisms between animals, just as they are for humans.71–73 Since some infection control practices in human healthcare remain controversial, similar evidence-based activities to limit spread among animals will take time to become established.
Short-term control policies
There are practices that could be implemented or improved in the short-term, in order to minimise transmission of resistant organisms. These strategies are already employed to a greater or lesser extent within healthcare systems throughout the world. They include cleaning, screening, hand hygiene, barrier and contact precautions, antimicrobial stewardship, surveillance, laboratory access, education, monitoring and feedback, research, managerial engagement, national policy making, and international collaboration.74 If these activities are already in place, what more could we do to deter antimicrobial resistance and transmissible infection?
Hygiene
Given that impeding transmission reduces the risk of infection, hygiene is key, with emphasis on prevention, rather than control.48 Failed or faltering hand hygiene campaigns can be re-ignited with repeated educational and advertising campaigns, supported by personal electronic reminders.75 The hospital environment can receive the attention it has needed for years, with targeted and revised cleaning strategies for general surfaces and clinical equipment.76,77 We should initiate scientific monitoring of surface-level cleanliness in hospitals, with application of infection risk-based standards similar to that in the food industry.78–80 Cleaning in healthcare will thus achieve a status never witnessed before, with a tiered professional structure based on certified courses for janitorial staff. These could include practical and accredited qualifications aimed at decontamination of clinical equipment and other surfaces currently cleaned by nurses.81 Sufficient cleaning hours, determined by staff and patient consortia, can be implemented throughout the healthcare system despite current lack of evidence.78
All hospitals should increase the proportion of single en-suite rooms, with isolation units for pan-resistant pathogens and novel ventilation methods, such as air ionisers and high-intensity UV light.82,83 There could be greater use of silver and similar non-antibiotic coatings for clinical equipment and devices.84 ‘Natural’ products such as hydrogen peroxide, ozone, steam and electrolysed water can be integrated into cleaning and decontamination strategies, despite concern over the efficacy of some.78,85,86 Healthcare facilities could also make good use of natural (cross) ventilation and the germicidal properties of sunlight, since earlier work on these appears to have been forgotten.87,88 Use of antiseptics or disinfectants shown to encourage cross-resistance with antibiotics should be discouraged in healthcare facilities.51–53
To assist the campaign for cleaner hospitals, there are antimicrobial surfaces and easy-clean furniture, but despite future promise, traditional cleaning methods should not be relaxed even if the whole hospital is coated with bioactive veneer.78,89,90 No one single process will remove all relevant microbial soil from the hospital. Coating constituents can wear off, degrade, or simply fail due to accumulation of organic soil. There might be health and safety issues, including toxic effects on the environment. Futuristic surfaces might seem appropriate for a 21st century hospital, but they could proffer false assurance if not properly tested over time. All require a comprehensive assessment in association with patient outcome before widespread adoption for healthcare.78
Antimicrobial stewardship
Antimicrobial stewardship requires further restrictions, with electronic monitoring, mixed prescribing and diagnostic frameworks aimed at reducing anti-infective use in hospital and community.91 It takes courage to say ‘no’ to a request for antimicrobials, but if a patient is systemically well, the benefits of treatment for the individual should be weighed against safeguarding treatment options for future patients.92,93 Antibiotic prophylaxis should be regarded as a privilege. Prescribing penalties for clinicians, along with financial incentives, would focus management on reducing antimicrobial consumption.93,94 Other initiatives are mandatory antimicrobial restrictions and testing in veterinary practices and agriculture, including imported livestock and foods, implemented and monitored on a global basis. Food producers should not use growth-promoting antimicrobial agents. There is no strong evidence of actual economic benefit and the potential for harm from antimicrobial resistance is high.95,96 International understanding, cooperation and support will be required to terminate over-the-counter drugs, electronic purchase and exchange of surveillance and research data.2,18
Laboratories, surveillance and screening
Good access to routine diagnostic laboratories requires continued support, with rapid diagnostic molecular methods introduced into routine practice.97 Electronic transmission of data will deliver results to clinicians for immediate appropriate management.98 For countries lacking accessible laboratories, the resources required should become a national priority, with additional support from charitable healthcare organisations. One affluent country could ‘adopt’ another of similar population and help construct an infection-control framework including laboratories, computer technology and data capture.
International agencies should agree on standardised definitions for surveillance in order to compare and contrast resistance rates all over the world.3,7,99 Screening may be expensive, and vulnerable to definition, but you cannot control what you do not know about. There has been much debate over MRSA screening. Perhaps it is time to introduce routine screening for other resistant microbes, with programs reflecting local hotspots or burgeoning risk depending on geography, institution and speciality.100
Education
Implementation of these strategies requires robust educational grounding for healthcare workers and the general public. Public health personnel could initiate and supervise structured delivery of mandatory hygiene education for school children and students, with courses made available for mothers, teachers, food handlers, farmers and people who work with animals, beauticians, sports coaches, supermarket and food shop staff, amongst others.101 Infection-control education can be strengthened within student curricula, and introduced for healthcare-staffing groups who have not previously been included. Advertising campaigns using national and local media would support this, extolling the benefits from restricting antimicrobial agents and keeping hands and surfaces clean, although no government will be able to challenge domestic squalor of necessity, design or choice.16,102
Research
Relevant research initiatives need higher status, with better-quality original studies, surveillance, epidemiological investigation, drug discovery and trials, industry and business partnerships, and international cooperation.1,2,17,18,23 Current emphasis on cancer and heart disease has meant that hygiene projects have not, so far, received the priority they deserve. Escalating drug-resistant infection should encourage work on phage-based therapies,103,104 antimicrobial peptides,105–107 bacterial interference,108 probiotics, toll-like receptor and quorum sensing blockers,109 nanoparticles,110 bacterial reversal agents,111,112 novel vaccines and immunotherapy,113,114 maggots,115 tea tree oil,116 and potential antimicrobial constituents in herbs, spices and foodstuffs, amongst other innovations.117 Almost certainly, scientists will return to the soil-searching of old in pursuit of new antimicrobial agents.118
Managerial and political engagement
Managerial responsibilities regarding infection control should continue to be formalised with professional networking to ignite and maintain political interest.36 Healthcare data on quality, outcome and mortality from regional managers delivered on a regular and timely basis should be accessible to the public, and serve to focus the political agenda. Once MRSA became an electoral issue in the UK, screening, surveillance and mandatory reporting helped prioritise its control with nationwide benefit.119 National leaders should identify an independent forum for long-term policy planning, including support for assisting research innovation into practice.36 International collaboration already exists but needs encouragement, commitment and support from institutional heads and politicians.
Infection control in the future
The initiatives described make the most of what is already known. Should these be insufficient, then we require additional interventions to aid control. Some of the following suggestions may seem incredible now, but not for a world without antibiotics. Most are unsupported by scientific evidence.
Healthcare
Perhaps the most contentious proposal is the premise that all prescribers should have a supplementary antimicrobial-prescribing licence. Challenging doctors’ and veterinarians’ right to prescribe will not be popular. It is likely that electronic prescribing with in-built antimicrobial alerts will be introduced, with formal regulation and monitoring. If antibiotics become obsolete, it is hoped that there would be other types of anti-infective drugs forthcoming.107,110 We can be confident that human initiative will prevail.120 Use of new agents should be severely restricted and monitored if resistance is biologically possible.
In hospitals, futuristic strategies might include robot healthcare delivery; or user-friendly ‘space’ suits to shield staff managing infected patients. Staff and patients would be further protected by compulsory shower and changing facilities when traversing different hospital wards or units (as occurs in food factories). Could staff be irradiated with a microbiocidal light source, if safe for human health? Even ordinary sunlight has untapped capacity for decontamination.88 There is no doubt that hand hygiene compliance will become a major issue – if it isn’t already – with mandatory monitoring and video surveillance in clinical areas.75,121 It is hoped that disciplinary issues on hygiene misdemeanours do not escalate into witch hunts, encouraged by ensuing panic over untreatable infection.
Given the potential for airborne transmission, novel ventilation systems will be needed to deliver frequent air-changes based on clinical risk. Accurate airflow visualisation techniques are essential to understand how aerosolised or airborne infection may be dispersed and, equally importantly, how it may be prevented.122 Less well-resourced healthcare facilities will contemplate outdoor wards and clinics, as regularly practiced before the discovery of antibiotics.87 There could be 24 h specialist infection-control cleaning teams, using steam, UV light and hydrogen peroxide when necessary, supplementing high frequency manual cleaning with or without bio-coated surfaces.78,89
Hospitals would benefit from multiple isolation ‘bubble’ room design, with antechamber, separate ventilation, plumbing and waste disposal systems, and strip-panel delivery of germicidal light in these rooms and other patient areas.83 In the diagnostic laboratory, tests could be devolved to critical areas within the hospital, such as polymerase chain reaction microarrays and other rapid molecular techniques for routine use in emergency departments.123 These might render the benefits from electronic transfer of clinical data obsolete, but not necessarily quicker diagnosis of infected wounds using electronic ‘nose’ or glowing wound technology.124
Natural resources can and should be used to run our hospitals, with minimal adverse effects on the environment. Microbiocidal properties of sunlight, air and water can be exploited and delivered where possible. If homes and healthcare continue to rely upon disinfectants, nature’s ‘balloon’ expands to fill the vacuum. There is no guarantee that the microbes which proliferate will always be controlled by disinfectants, nor, indeed, by current antimicrobial agents.48,125
Community
In the community, national and private laboratory resources will prioritise infection research, investigating bioengineering, pathogen transmission, disinfectant testing, antimicrobial surfaces, coatings, cements & textiles, and cleaning equipment & methods. No doubt business and industry will create marketable items for ‘eliminating’ infection risk in peoples’ homes and elsewhere.47 Supermarkets will make use of UVC-based decontamination of consumables and bio-coated wrappers for both raw and processed food. Environmental health teams will use species-specific pathogen adenosine triphosphate (ATP)-detecting kits for food-producing premises, cafes and restaurants. Community health centres will create their own infection-control strategies, with specialist nurses responsible for managing patients in a variety of community healthcare settings.126 A framework of guidelines, policies and procedures for outbreak detection, contact tracing and intervention will be overseen by public health teams, supported by diagnostic laboratories and local clinical staff.127
Mobile decontamination and cleaning firms will provide hygiene services for the community, with automatic drive-in washer-disinfectors for public transport and ambulances. Local community initiatives will provide hygiene and health evening classes, with find-and-treat vans roaming the streets for patients with MDR tuberculosis and other infections.128 Whole families can be quarantined at home, if one or more members are sick, with computer technology aiding education and job commitments. Public health legislation will support incarceration of people with untreatable transmissible infection, similar to the situation with syphilis a century ago.56 Travellers might have to undergo quarantine conditions, depending on origin and destination, or perhaps people might choose simply to stay at home. The prospect of untreatable malaria would quickly remove the gloss from an exotic holiday.
Veterinary and agricultural interventions will be monitored with systematic surveillance programs shared across the world, with regular updates and international reporting.129,130 Perhaps a long time coming, but nonetheless welcome, would be a global strategy to provide clean water for everyone. The obvious addition to this would be a complete ban on routine and emergency sewage discharge into free-flowing water courses or the sea, with appropriate sewage management for all countries.54
Conclusion
Darwinian evolution will compromise all our antimicrobial policies over time. Microbes readily exchange survival mechanisms between themselves, as well as from environmental sources.131 The latter will always be capable of producing a resistance mechanism against any biological agent introduced into clinical practice.46,132 Once selected, the capability for resistance persists long-term whether or not the original stimulus continues.133 Resistant organisms so generated then spread throughout the world in a chosen niche accelerated by 21st century trends, travel and technology. This is well illustrated by the recent appearance of New Delhi metallo-β-lactamase enterobacteria (NDM-1), complete with encoded carbapenemase. The emergence of this gene is a catastrophe, because it edges bacteria to the brink of being completely untreatable. Since the gene resides in organisms that colonise people without necessarily causing symptoms, NDM-1 has been a hidden assault, crossing borders and entering hospitals without being detected.4,134
The real challenge for infection control over the next few years will be raising its profile to those not actively involved in healthcare. Engaging policy makers and budget holders at all levels will require repeated debate, since investment in infection control will hardly be a priority in the current economic climate. Action depends upon altruistic individuals with vision, who can influence political drive, governmental mandate and international collaboration. People will die from untreatable infection before the resources are found to control activities and research.
There is still time to prepare for a world without antibiotics. The need to revisit hygiene values of the past will not set pulses racing in an age of microchips and space travel.135,136 We have a duty to reverse complacency over infection prevention and control in the 21st century.
Conflict of interests
The author has received past funding for hospital cleaning studies, and non-recurring lectureship fees and conference support from Pfizer, Novartis and Janssen-Cilag.
Funding
No funding was received towards the writing of this article.
Acknowledgement
The author wishes to acknowledge infection control staff at the Royal Hobart hospital, for advice regarding the specialist cleaning initiative.
References
[1] Macías AE, Ponce-de-Leon S. Infection control: old problems and new challenges. Arch Med Res 2005; 36 637–45.| Infection control: old problems and new challenges.Crossref | GoogleScholarGoogle Scholar | 16216645PubMed |
[2] Gastmeier P. Healthcare-associated versus community-acquired infections: a new challenge for science and society. Int J Med Microbiol 2010; 300 342–5.
| Healthcare-associated versus community-acquired infections: a new challenge for science and society.Crossref | GoogleScholarGoogle Scholar | 20452277PubMed |
[3] Sydnor ER, Perl TM. Hospital epidemiology and infection control in acute-care settings. Clin Microbiol Rev 2011; 24 141–73.
| Hospital epidemiology and infection control in acute-care settings.Crossref | GoogleScholarGoogle Scholar | 21233510PubMed |
[4] Wilson ME, Chen LH. NDM-1 and the role of travel in its dissemination. Curr Infect Dis Rep 2012; 14 213–26.
| NDM-1 and the role of travel in its dissemination.Crossref | GoogleScholarGoogle Scholar | 22419230PubMed |
[5] Carlet J, Collignon P, Goldmann D, Goossens H, Gyssens IC, Harbarth S, et al Society’s failure to protect a precious resource: antibiotics. Lancet 2011; 378 369–71.
| Society’s failure to protect a precious resource: antibiotics.Crossref | GoogleScholarGoogle Scholar | 21477855PubMed |
[6] Chan M. Antimicrobial resistance: no action today means no cure tomorrow. Geneva, Switzerland: World Health Organization; 2011. Available from: http://www.who.int/dg/speeches/2011/WHD_20110407/en/index.html [verified 22 March 2013].
[7] Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect 2012; 18 268–81.
| Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance.Crossref | GoogleScholarGoogle Scholar | 21793988PubMed |
[8] Clements AC, Magalhães RJ, Tatem AJ, Paterson DL, Riley TV. Clostridium difficile PCR ribotype 027: assessing the risks of further worldwide spread. Lancet Infect Dis 2010; 10 395–404.
| Clostridium difficile PCR ribotype 027: assessing the risks of further worldwide spread.Crossref | GoogleScholarGoogle Scholar | 20510280PubMed |
[9] Baines SD, O’Connor R, Freeman J, Fawley WN, Harmanus C, Mastrantonio P, et al Emergence of reduced susceptibility to metronidazole in Clostridium difficile. J Antimicrob Chemother 2008; 62 1046–52.
| Emergence of reduced susceptibility to metronidazole in Clostridium difficile.Crossref | GoogleScholarGoogle Scholar | 18693234PubMed |
[10] Wang B, Taylor J, Ratnamohan M, McPhie K, Kesson A, Dixit R, et al Frequency of oseltamivir resistance in Sydney, during the Newcastle outbreak of community transmitted oseltamivir-resistant influenza A (H1N1)pdm09 virus, Australia, June to August 2011. Euro Surveill 2012; 17 20 210
[11] Marshall JA, Bruggink LD. The dynamics of norovirus outbreak epidemics: recent insights. Int J Environ Res Public Health 2011; 8 1141–9.
| The dynamics of norovirus outbreak epidemics: recent insights.Crossref | GoogleScholarGoogle Scholar | 21695033PubMed |
[12] Osterholm MT. Preparing for the next pandemic. N Engl J Med 2005; 352 1839–42.
| Preparing for the next pandemic.Crossref | GoogleScholarGoogle Scholar | 15872196PubMed |
[13] Freire-Moran L, Aronsson B, Manz C, Gyssens IC, So AD, Monnet DL, et al ECDC-EMA Working Group Critical shortage of new antibiotics in development against multidrug-resistant bacteria-Time to react is now. Drug Resist Updat 2011; 14 118–24.
| Critical shortage of new antibiotics in development against multidrug-resistant bacteria-Time to react is now.Crossref | GoogleScholarGoogle Scholar | 21435939PubMed |
[14] Theuretzbacher U. Accelerating resistance, inadequate antibacterial drug pipelines and international responses. Int J Antimicrob Agents 2012; 39 295–9.
| Accelerating resistance, inadequate antibacterial drug pipelines and international responses.Crossref | GoogleScholarGoogle Scholar | 22341298PubMed |
[15] Cormican M, Vellinga A. Existing classes of antibiotics are probably the best we will ever have. BMJ 2012; 344 e3369
| Existing classes of antibiotics are probably the best we will ever have.Crossref | GoogleScholarGoogle Scholar | 22589509PubMed |
[16] Appelbaum PC. 2012 and beyond: potential for the start of a second pre-antibiotic era? J Antimicrob Chemother 2012; 67 2062–8.
| 2012 and beyond: potential for the start of a second pre-antibiotic era?Crossref | GoogleScholarGoogle Scholar | 22687888PubMed |
[17] Carlet JM, Jarlier V, Harbarth S, Voss A, Goossens H, Pittet D, et al Ready for a world without antibiotics? The Pensieres antibiotic resistance call to action. Antimicrob Resist Infect Control 2012; 1 11
| Ready for a world without antibiotics? The Pensieres antibiotic resistance call to action.Crossref | GoogleScholarGoogle Scholar |
[18] Dettenkofer M, Ammon A, Astagneau P, Dancer SJ, Gastmeier P, Harbarth S, et al Infection control - a European research perspective for the next decade. Report from a symposium held in Freiburg, Germany. J Hosp Infect 2011; 77 7–10.
| Infection control - a European research perspective for the next decade. Report from a symposium held in Freiburg, Germany.Crossref | GoogleScholarGoogle Scholar | 21145620PubMed |
[19] Delepierre A, Gayot A, Carpentier A. Update on counterfeit antibiotics worldwide; Public health risks. Med Mal Infect 2012; 42 247–55.
| 22621827PubMed |
[20] Marwick C, Davey P. Care bundles: the holy grail of infectious risk management in hospital? Curr Opin Infect Dis 2009; 22 364–9.
| Care bundles: the holy grail of infectious risk management in hospital?Crossref | GoogleScholarGoogle Scholar | 19506477PubMed |
[21] Bull A, Wilson J, Worth LJ, Stuart RL, Gillespie E, Waxman B, et al A bundle of care to reduce colorectal surgical infections: an Australian experience. J Hosp Infect 2011; 78 297–301.
| A bundle of care to reduce colorectal surgical infections: an Australian experience.Crossref | GoogleScholarGoogle Scholar | 21664720PubMed |
[22] Anthony T, Murray BW, Sum-Ping JT, Lenkovsky F, Vornik VD, Parker BJ, et al Evaluating an evidence-based bundle for preventing surgical site infection: a randomized trial. Arch Surg 2011; 146 263–9.
| Evaluating an evidence-based bundle for preventing surgical site infection: a randomized trial.Crossref | GoogleScholarGoogle Scholar | 21079110PubMed |
[23] Stone SP, Cooper BS, Kibbler CC, Cookson BD, Roberts JA, Medley GF, et al The ORION statement: guidelines for transparent reporting of outbreak reports and intervention studies of nosocomial infection. J Antimicrob Chemother 2007; 59 833–40.
| The ORION statement: guidelines for transparent reporting of outbreak reports and intervention studies of nosocomial infection.Crossref | GoogleScholarGoogle Scholar | 17387116PubMed |
[24] Gould D, Chamberlain A. The use of a ward-based educational teaching package to enhance nurses’ compliance with infection control procedures. J Clin Nurs 1997; 6 55–67.
| The use of a ward-based educational teaching package to enhance nurses’ compliance with infection control procedures.Crossref | GoogleScholarGoogle Scholar | 9052110PubMed |
[25] Cocanour CS, Peninger M, Domonoske BD, Li T, Wright B, Valdivia A, et al Decreasing ventilator-associated pneumonia in a trauma ICU. J Trauma 2006; 61 122–30.
| Decreasing ventilator-associated pneumonia in a trauma ICU.Crossref | GoogleScholarGoogle Scholar | 16832259PubMed |
[26] Cimiotti JP, Aiken LH, Sloane DM, Wu ES. Nurse staffing, burnout, and healthcare-associated infection. Am J Infect Control 2012; 40 486–90.
| Nurse staffing, burnout, and healthcare-associated infection.Crossref | GoogleScholarGoogle Scholar | 22854376PubMed |
[27] Dancer SJ. Infection control from the other side: a patient’s perspective. J Hosp Infect 2012; 80 189–91.
| Infection control from the other side: a patient’s perspective.Crossref | GoogleScholarGoogle Scholar | 22226910PubMed |
[28] Beggs CB, Noakes CJ, Shepherd SJ, Kerr KG, Sleigh PA, Banfield K. The influence of nurse cohorting on hand hygiene effectiveness. Am J Infect Control 2006; 34 621–6.
| The influence of nurse cohorting on hand hygiene effectiveness.Crossref | GoogleScholarGoogle Scholar | 17161736PubMed |
[29] Smith SJ, Young V, Robertson C, Dancer SJ. Cross-transmission audit of environmental surfaces, clinical equipment and patient: who touches what? J Hosp Infect 2012; 80 206–11.
| Cross-transmission audit of environmental surfaces, clinical equipment and patient: who touches what?Crossref | GoogleScholarGoogle Scholar | 22297169PubMed |
[30] Owens RC, Shorr AF, Deschambeault AL. Antimicrobial stewardship: shepherding precious resources. Am J Health Syst Pharm 2009; 66 S15–22.
| Antimicrobial stewardship: shepherding precious resources.Crossref | GoogleScholarGoogle Scholar | 19502223PubMed |
[31] Rampling A, Wiseman S, Davis L, Hyett AP, Walbridge AN, Payne GC, et al Evidence that hospital hygiene is important in the control of methicillin-resistant Staphylococcus aureus. J Hosp Infect 2001; 49 109–16.
| Evidence that hospital hygiene is important in the control of methicillin-resistant Staphylococcus aureus.Crossref | GoogleScholarGoogle Scholar | 11567555PubMed |
[32] Mehtar S. How to cost and fund an infection control programme. J Hosp Infect 1993; 25 57–69.
| How to cost and fund an infection control programme.Crossref | GoogleScholarGoogle Scholar | 7901275PubMed |
[33] Clements A, Halton K, Graves N, Pettitt A, Morton A, Looke D, et al Overcrowding and understaffing in modern health-care systems: key determinants in meticillin-resistant Staphylococcus aureus transmission. Lancet Infect Dis 2008; 8 427–34.
| Overcrowding and understaffing in modern health-care systems: key determinants in meticillin-resistant Staphylococcus aureus transmission.Crossref | GoogleScholarGoogle Scholar | 18582835PubMed |
[34] Lim S, Closson T, Howard G, Gardam M. Collateral damage: the unforeseen effects of emergency outbreak policies. Lancet Infect Dis 2004; 4 697–703.
| Collateral damage: the unforeseen effects of emergency outbreak policies.Crossref | GoogleScholarGoogle Scholar | 15522682PubMed |
[35] Kaier K, Mutters NT, Frank U. Bed occupancy rates and hospital-acquired infections-should beds be kept empty? Clin Microbiol Infect 2012; 18 941–5.
| Bed occupancy rates and hospital-acquired infections-should beds be kept empty?Crossref | GoogleScholarGoogle Scholar | 22757765PubMed |
[36] National Institute for Health & Clinical Excellence (NICE). Prevention and control of healthcare-associated infections: quality improvement guide. London: NICE; 2011. Available from: http://publications.nice.org.uk/prevention-and-control-of-healthcare-associated-infections-ph36 [verified 22 March 2013]
[37] Borg MA. Could the incidence of healthcare infections in Europe simply be a reflection of overall quality standards? J Hosp Infect 2012; 82 141–2.
| Could the incidence of healthcare infections in Europe simply be a reflection of overall quality standards?Crossref | GoogleScholarGoogle Scholar | 22999640PubMed |
[38] Larsen MV, Cosentino S, Rasmussen S, Friis C, Hasman H, Marvig RL, et al Multilocus sequence typing of total-genome-sequenced bacteria. J Clin Microbiol 2012; 50 1355–61.
| Multilocus sequence typing of total-genome-sequenced bacteria.Crossref | GoogleScholarGoogle Scholar | 22238442PubMed |
[39] Burke L, Humphreys H, Fitzgerald-Hughes D. The revolving door between hospital and community: extended-spectrum beta-lactamase-producing Escherichia coli in Dublin. J Hosp Infect 2012; 81 192–8.
| The revolving door between hospital and community: extended-spectrum beta-lactamase-producing Escherichia coli in Dublin.Crossref | GoogleScholarGoogle Scholar | 22658893PubMed |
[40] Denkinger CM, Grant AD, Denkinger M, Gautam S, D’Agata EMC. Increased multidrug resistance among the elderly on admission to the hospital-a 12 year surveillance study. Arch Gerontol Geriatr 2013; 56 227–30.
| Increased multidrug resistance among the elderly on admission to the hospital-a 12 year surveillance study.Crossref | GoogleScholarGoogle Scholar | 22682422PubMed |
[41] Touati A, Zenati K, Brasme L, Benallaoua S, de Champs C. Extended-spectrum beta-lactamase characterisation and heavy metal resistance of Enterobacteriaceae strains isolated from hospital environmental surfaces. J Hosp Infect 2010; 75 78–9.
| Extended-spectrum beta-lactamase characterisation and heavy metal resistance of Enterobacteriaceae strains isolated from hospital environmental surfaces.Crossref | GoogleScholarGoogle Scholar | 20227789PubMed |
[42] Skov R, Christiansen K, Dancer SJ, Daum RS, Dryden M, Huang YC, et al Update on the prevention and control of community-acquired meticillin-resistant Staphylococcus aureus (CA-MRSA). Int J Antimicrob Agents 2012; 39 193–200.
| Update on the prevention and control of community-acquired meticillin-resistant Staphylococcus aureus (CA-MRSA).Crossref | GoogleScholarGoogle Scholar | 22226649PubMed |
[43] van den Bogaard AE, Stobberingh EE. Epidemiology of resistance to antibiotics; links between animals and humans. Int J Antimicrob Agents 2000; 14 327–35.
| Epidemiology of resistance to antibiotics; links between animals and humans.Crossref | GoogleScholarGoogle Scholar | 10794955PubMed |
[44] Verheij TJ. The antibiotic revolution should be more focused. Br J Gen Pract 2009; 59 716–7.
| The antibiotic revolution should be more focused.Crossref | GoogleScholarGoogle Scholar | 19843417PubMed |
[45] Kieran I, Lyttle M, Leroi M. Successful antibiotic stewardship: are we a victim of our own success? ANZ J Surg 2011; 81 488–9.
| Successful antibiotic stewardship: are we a victim of our own success?Crossref | GoogleScholarGoogle Scholar | 22295363PubMed |
[46] Dancer SJ. How antibiotics can make us sick. Review of the lesser-known adverse effects of antibiotic chemotherapy. Lancet Infect Dis 2004; 4 611–9.
| How antibiotics can make us sick. Review of the lesser-known adverse effects of antibiotic chemotherapy.Crossref | GoogleScholarGoogle Scholar | 15451489PubMed |
[47] Levy SB. Antibacterial household products: cause for concern. Emerg Infect Dis 2001; 7 512–5.
| Antibacterial household products: cause for concern.Crossref | GoogleScholarGoogle Scholar | 11485643PubMed |
[48] Sattar SA. Reducing the health impact of infectious agents: the significance of preventive strategies. GMS Krankenhhyg Interdiszip 2007; 2 Doc06
| 20200667PubMed |
[49] D’Arcy N. Antimicrobials in plastics: a global review. Plast Addit Compd 2001; 3 12–5.
| Antimicrobials in plastics: a global review.Crossref | GoogleScholarGoogle Scholar |
[50] Braid JJ, Wale MCJ. The antibacterial activity of triclosan-impregnated storage boxes against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Bacillus cereus and Shewanella putrefaciens in conditions simulating domestic use. J Antimicrob Chemother 2002; 49 87–94.
| The antibacterial activity of triclosan-impregnated storage boxes against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Bacillus cereus and Shewanella putrefaciens in conditions simulating domestic use.Crossref | GoogleScholarGoogle Scholar | 11751771PubMed |
[51] Aiello AE, Larson EL, Levy SB. Consumer antibacterial soaps: effective or just risky? Clin Infect Dis 2007; 45 S137–47.
| Consumer antibacterial soaps: effective or just risky?Crossref | GoogleScholarGoogle Scholar | 17683018PubMed |
[52] Akimitsu N, Hamamoto H, Inoue R, Shoji M, Akamine A, Takemori K, et al Increase in resistance of methicillin-resistant Staphylococcus aureus to beta-lactams caused by mutations conferring resistance to benzalkonium chloride, a disinfectant widely used in hospitals. Antimicrob Agents Chemother 1999; 43 3042–3.
| 10651623PubMed |
[53] Naparstek L, Carmeli Y, Chmelnitsky I, Banin E, Navon-Venezia S. Reduced susceptibility to chlorhexidine among extremely-drug-resistant strains of Klebsiella pneumoniae. J Hosp Infect 2012; 81 15–9.
| Reduced susceptibility to chlorhexidine among extremely-drug-resistant strains of Klebsiella pneumoniae.Crossref | GoogleScholarGoogle Scholar | 22463977PubMed |
[54] Curtis V, Schmidt W, Luby S, Florez R, Touré O, Biran A. Hygiene: new hopes, new horizons. Lancet Infect Dis 2011; 11 312–21.
| Hygiene: new hopes, new horizons.Crossref | GoogleScholarGoogle Scholar | 21453872PubMed |
[55] Silva J, Castillo G, Callejas L, Lopez H, Olmos J. Frequency of transferable multiple antibiotic resistance among coliform bacteria isolated from a treated sewage effluent in Antofagasta, Chile. Electron J Biotechnol 2006; 9 534–40.
| Frequency of transferable multiple antibiotic resistance among coliform bacteria isolated from a treated sewage effluent in Antofagasta, Chile.Crossref | GoogleScholarGoogle Scholar |
[56] Gandhi NR, Nunn P, Dheda K, Schaaf HS, Zignol M, van Soolingen D, et al Multidrug-resistant and extensively drug-resistant tuberculosis: a threat to global control of tuberculosis. Lancet 2010; 375 1830–43.
| Multidrug-resistant and extensively drug-resistant tuberculosis: a threat to global control of tuberculosis.Crossref | GoogleScholarGoogle Scholar | 20488523PubMed |
[57] Kobaidze K, Salakaia A, Blumberg HM. Over the counter availability of antituberculosis drugs in Tbilisi, Georgia in the setting of a high prevalence of MDR-TB. Interdiscip Perspect Infect Dis 2009; 2009 513 609
| Over the counter availability of antituberculosis drugs in Tbilisi, Georgia in the setting of a high prevalence of MDR-TB.Crossref | GoogleScholarGoogle Scholar |
[58] Khan AU, Nordmann P. Spread of carbapenemase NDM-1 producers: the situation in India and what may be proposed. Scand J Infect Dis 2012; 44 531–5.
| Spread of carbapenemase NDM-1 producers: the situation in India and what may be proposed.Crossref | GoogleScholarGoogle Scholar | 22497308PubMed |
[59] Zarb P, Goossens H. Human use of antimicrobial agents. Rev Sci Tech 2012; 31 121–33.
| 22849272PubMed |
[60] Young JH. The Toadstool Millionaires: A Social History of Patent Medicines in America before Federal Regulation. Princeton, NJ: Princeton University Press; 1961.
[61] Calva JJ, Sifuentes-Osornio J, Ceron C. Antimicrobial resistance in fecal flora: longitudinal community based surveillance of children from urban Mexico. Antimicrob Agents Chemother 1996; 40 1699–702.
| 8807065PubMed |
[62] French GL, Ling J, Chow KL, Mark KK. Occurrence of multiple antibiotic resistance and R-plasmids in gram-negative bacteria isolated from faecally contaminated fresh-water streams in Hong Kong. Epidemiol Infect 1987; 98 285–99.
| Occurrence of multiple antibiotic resistance and R-plasmids in gram-negative bacteria isolated from faecally contaminated fresh-water streams in Hong Kong.Crossref | GoogleScholarGoogle Scholar | 3595747PubMed |
[63] Smith DL, Harris AD, Johnson JA. Animal antibiotic use has an early but important impact on the emergence of antibiotic resistance in human commensal bacteria. Proc Natl Acad Sci USA 2002; 99 6434–9.
| Animal antibiotic use has an early but important impact on the emergence of antibiotic resistance in human commensal bacteria.Crossref | GoogleScholarGoogle Scholar | 11972035PubMed |
[64] Levy SB, Fitzgerald GB, Macone AB. Changes in intestinal flora of farm personnel after introduction of a tetracycline-supplemented feed on a farm. N Engl J Med 1976; 295 583–8.
| Changes in intestinal flora of farm personnel after introduction of a tetracycline-supplemented feed on a farm.Crossref | GoogleScholarGoogle Scholar | 950974PubMed |
[65] Price LB, Stegger M, Hasman H, Aziz M, Larsen J, Andersen PS, et al Staphylococcus aureus CC398: host adaptation and emergence of methicillin resistance in livestock. MBiol 2012; 3 e00 305–11.
[66] van den Bogaard AE, London N, Driessen C, Stobberingh EE. Antibiotic resistance of faecal Escherichia coli in poultry, poultry farmers and poultry slaughterers. J Antimicrob Chemother 2001; 47 763–71.
| Antibiotic resistance of faecal Escherichia coli in poultry, poultry farmers and poultry slaughterers.Crossref | GoogleScholarGoogle Scholar | 11389108PubMed |
[67] Warren RE, Ensor VM, O’Neill P, Butler V, Taylor J, Nye K, et al Imported chicken meat as a potential source of quinolone-resistant Escherichia coli producing extended-spectrum beta-lactamases in the UK. J Antimicrob Chemother 2008; 61 504–8.
| Imported chicken meat as a potential source of quinolone-resistant Escherichia coli producing extended-spectrum beta-lactamases in the UK.Crossref | GoogleScholarGoogle Scholar | 18222958PubMed |
[68] FDA. Guidance for industry: The judicious use of medically important antimicrobial drugs in food-producing animals. Rockville, MD: Food and Drug Administration; 2012. Available from: http://www.fda.gov/downloads/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/UCM216936.pdf [verified 22 March 2013]
[69] Marshall M. Farmyard antibiotics linked to superbugs. New Scientist 2012; 2853: 22 February.
[70] Bergström K, Nyman G, Widgren S, Johnston C, Grönlund-Andersson U, Ransjö U. Infection prevention and control interventions in the first outbreak of methicillin-resistant Staphylococcus aureus infections in an equine hospital in Sweden. Acta Vet Scand 2012; 54 14
| Infection prevention and control interventions in the first outbreak of methicillin-resistant Staphylococcus aureus infections in an equine hospital in Sweden.Crossref | GoogleScholarGoogle Scholar | 22401493PubMed |
[71] Sieber S, Gerber V, Jandova V, Rossano A, Evison JM, Perreten V. Evolution of multidrug-resistant Staphylococcus aureus infections in horses and colonized personnel in an equine clinic between 2005 and 2010. Microb Drug Resist 2011; 17 471–8.
| Evolution of multidrug-resistant Staphylococcus aureus infections in horses and colonized personnel in an equine clinic between 2005 and 2010.Crossref | GoogleScholarGoogle Scholar | 21875361PubMed |
[72] Catry B, Van Duijkeren E, Pomba MC, Greko C, Moreno MA, Pyörälä S, et al Scientific Advisory Group on Antimicrobials (SAGAM) Reflection paper on MRSA in food-producing and companion animals: epidemiology and control options for human and animal health. Epidemiol Infect 2010; 138 626–44.
| Reflection paper on MRSA in food-producing and companion animals: epidemiology and control options for human and animal health.Crossref | GoogleScholarGoogle Scholar | 20141646PubMed |
[73] Wegener HC. Danish initiatives to improve the safety of meat products. Meat Sci 2010; 84 276–83.
| Danish initiatives to improve the safety of meat products.Crossref | GoogleScholarGoogle Scholar | 20374786PubMed |
[74] Damani N. Manual of Infection Prevention and Control. 3rd edn. Oxford, UK: Oxford University Press; 2012.
[75] Cheng VC, Tai JW, Ho SK, Chan JF, Hung KN, Ho PL, et al Introduction of an electronic monitoring system for monitoring compliance with Moments 1 and 4 of the WHO “My 5 Moments for Hand Hygiene” methodology. BMC Infect Dis 2011; 11 151
| Introduction of an electronic monitoring system for monitoring compliance with Moments 1 and 4 of the WHO “My 5 Moments for Hand Hygiene” methodology.Crossref | GoogleScholarGoogle Scholar | 21612666PubMed |
[76] Dancer SJ. Mopping up hospital infection. J Hosp Infect 1999; 43 85–100.
| Mopping up hospital infection.Crossref | GoogleScholarGoogle Scholar | 10549308PubMed |
[77] 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 52–5.
| Presence of biofilm containing viable multiresistant organisms despite terminal cleaning on clinical surfaces in an intensive care unit.Crossref | GoogleScholarGoogle Scholar | 21899921PubMed |
[78] Dancer SJ. Hospital cleaning in the 21st Century. Eur J Clin Microbiol Infect Dis 2011; 30 1473–81.
| Hospital cleaning in the 21st Century.Crossref | GoogleScholarGoogle Scholar | 21499954PubMed |
[79] Dancer SJ. How do we assess hospital cleaning? A proposal for microbiological standards for surface hygiene in hospitals. J Hosp Infect 2004; 56 10–5.
| How do we assess hospital cleaning? A proposal for microbiological standards for surface hygiene in hospitals.Crossref | GoogleScholarGoogle Scholar | 14706265PubMed |
[80] Griffith C. HACCP and the management of healthcare associated infections: are there lessons to be learnt from other industries? Int J Health Care Qual Assur Inc Leadersh Health Serv 2006; 19 351–67.
| HACCP and the management of healthcare associated infections: are there lessons to be learnt from other industries?Crossref | GoogleScholarGoogle Scholar | 16961100PubMed |
[81] Anderson RE, Young V, Stewart M, Robertson C, Dancer SJ. Cleanliness audit of clinical surfaces and equipment: Who cleans what? J Hosp Infect 2011; 78 178–81.
| Cleanliness audit of clinical surfaces and equipment: Who cleans what?Crossref | GoogleScholarGoogle Scholar | 21497943PubMed |
[82] Moore G, Ali S, FitzGerald G, Muzslay M, Atkinson S, Smith S, et al SmartIdeas Research Student Group, Wilson AP. Ward assessment of SmartIdeas project: bringing source isolation to the patient. J Hosp Infect 2010; 76 103–7.
| SmartIdeas Research Student Group, Wilson AP. Ward assessment of SmartIdeas project: bringing source isolation to the patient.Crossref | GoogleScholarGoogle Scholar | 20561713PubMed |
[83] Maclean M, MacGregor SJ, Anderson JG, Woolsey GA, Coia JE, Hamilton K, et al Environmental decontamination of a hospital isolation room using high-intensity narrow-spectrum light. J Hosp Infect 2010; 76 247–51.
| Environmental decontamination of a hospital isolation room using high-intensity narrow-spectrum light.Crossref | GoogleScholarGoogle Scholar | 20864210PubMed |
[84] Saint S, Elmore JG, Sullivan SD, Emerson SS, Koepsell TD. The efficacy of silver alloy-coated urinary catheters in preventing urinary tract infection: a meta-analysis. Am J Med 1998; 105 236–41.
| The efficacy of silver alloy-coated urinary catheters in preventing urinary tract infection: a meta-analysis.Crossref | GoogleScholarGoogle Scholar | 9753027PubMed |
[85] Falagas ME, Thomaidis PC, Kotsantis IK, Sgouros K, Samonis G, Karageorgopoulos DE. Airborne hydrogen peroxide for disinfection of the hospital environment and infection control: a systematic review. J Hosp Infect 2011; 78 171–7.
| Airborne hydrogen peroxide for disinfection of the hospital environment and infection control: a systematic review.Crossref | GoogleScholarGoogle Scholar | 21392848PubMed |
[86] Meakin NS, Bowman C, Lewis M, Dancer SJ. Cleaning efficacy between in-use disinfectant and electrolysed water in an English residential care home. J Hosp Infect 2012; 80 122–7.
| Cleaning efficacy between in-use disinfectant and electrolysed water in an English residential care home.Crossref | GoogleScholarGoogle Scholar | 22196853PubMed |
[87] Escombe AR, Oeser CC, Gilman RH, Navincopa M, Ticona E, Pan W, et al Natural ventilation for the prevention of airborne contagion. PLoS Med 2007; 4 e68
| Natural ventilation for the prevention of airborne contagion.Crossref | GoogleScholarGoogle Scholar | 17326709PubMed |
[88] Hobday RA. Sunlight therapy and solar architecture. Med Hist 1997; 41 455–72.
| Sunlight therapy and solar architecture.Crossref | GoogleScholarGoogle Scholar | 9536618PubMed |
[89] Page K, Wilson M, Parkin IP. Antimicrobial surfaces and their potential in reducing the role of the inanimate environment in the incidence of hospital-acquired infections. J Mater Chem 2009; 19 3819–31.
| Antimicrobial surfaces and their potential in reducing the role of the inanimate environment in the incidence of hospital-acquired infections.Crossref | GoogleScholarGoogle Scholar |
[90] Kent J. Using design to reduce cross infection. Nurs Times 2009; 105 37
| 19835200PubMed |
[91] Doron S, Davidson LE. Antimicrobial stewardship. Mayo Clin Proc 2011; 86 1113–23.
| Antimicrobial stewardship.Crossref | GoogleScholarGoogle Scholar | 22033257PubMed |
[92] Price DJ, Sleigh JD. Control of infection due to Klebsiella aerogenes in a neurosurgical unit by withdrawal of all antibiotics. Lancet 1970; 296 1213–5.
| Control of infection due to Klebsiella aerogenes in a neurosurgical unit by withdrawal of all antibiotics.Crossref | GoogleScholarGoogle Scholar |
[93] Garau J.. Impact of antibiotic restrictions: the ethical perspective. Clin Microbiol Infect 2006; 12 16–24.
| 16827821PubMed |
[94] Eggleston K, Zhang R, Zeckhauser RJ. The global challenge of antimicrobial resistance: insights from economic analysis. Int J Environ Res Public Health 2010; 7 3141–9.
| The global challenge of antimicrobial resistance: insights from economic analysis.Crossref | GoogleScholarGoogle Scholar | 20948953PubMed |
[95] Collignon P, Wegener HC, Braam P, Butler CD. The routine use of antibiotics to promote animal growth does little to benefit protein undernutrition in the developing world. Clin Infect Dis 2005; 41 1007–13.
| The routine use of antibiotics to promote animal growth does little to benefit protein undernutrition in the developing world.Crossref | GoogleScholarGoogle Scholar | 16142667PubMed |
[96] Collignon P, Powers JH, Chiller TM, Aidara-Kane A, Aarestrup FM. World Health Organization ranking of antimicrobials according to their importance in human medicine: a critical step for developing risk management strategies for the use of antimicrobials in food production animals. Clin Infect Dis 2009; 49 132–41.
| World Health Organization ranking of antimicrobials according to their importance in human medicine: a critical step for developing risk management strategies for the use of antimicrobials in food production animals.Crossref | GoogleScholarGoogle Scholar | 19489713PubMed |
[97] Leggieri N, Rida A, François P, Schrenzel J. Molecular diagnosis of bloodstream infections: planning to (physically) reach the bedside. Curr Opin Infect Dis 2010; 23 311–9.
| 20592531PubMed |
[98] Kusano N. Hospital infection control in the 21st century–importance of network for hospital infection control and role of clinical laboratory. Rinsho Byori 2001; 49 801–3.
| 11573290PubMed |
[99] Paterson DL, Doi Y. A step closer to extreme drug resistance (XDR) in gram-negative bacilli. Clin Infect Dis 2007; 45 1179–81.
| A step closer to extreme drug resistance (XDR) in gram-negative bacilli.Crossref | GoogleScholarGoogle Scholar | 17918079PubMed |
[100] Grundmann H, Klugman KP, Walsh T, Ramon-Pardo P, Sigauque B, Khan W, et al A framework for global surveillance of antibiotic resistance. Drug Resist Updat 2011; 14 79–87.
| A framework for global surveillance of antibiotic resistance.Crossref | GoogleScholarGoogle Scholar | 21482177PubMed |
[101] McNulty CA, Cookson BD, Lewis MA. Education of healthcare professionals and the public. J Antimicrob Chemother 2012; 67 i11–8.
| Education of healthcare professionals and the public.Crossref | GoogleScholarGoogle Scholar | 22855873PubMed |
[102] Bloomfield SF. Gastrointestinal disease in the domestic setting: What are the Issues? J Infect 2001; 43 23–9.
[103] Parracho HM, Burrowes BH, Enright MC, McConville ML, Harper DR. The role of regulated clinical trials in the development of bacteriophage therapeutics. J Mol Genet Med 2012; 6 279–86.
| 22872803PubMed |
[104] Abedon ST, Kuhl SJ, Blasdel BG, Kutter EM. Phage treatment of human infections. Bacteriophage 2011; 1 66–85.
| Phage treatment of human infections.Crossref | GoogleScholarGoogle Scholar | 22334863PubMed |
[105] Zhang L, Parente J, Harris SM, Woods DE, Hancock RE, Falla TJ. Antimicrobial peptide therapeutics for cystic fibrosis. Antimicrob Agents Chemother 2005; 49 2921–7.
| Antimicrobial peptide therapeutics for cystic fibrosis.Crossref | GoogleScholarGoogle Scholar | 15980369PubMed |
[106] Masuda Y, Zendo T, Sonomoto K. New type non-lantibiotic bacteriocins: circular and leaderless bacteriocins. Benef Microbes 2012; 3 3–12.
| New type non-lantibiotic bacteriocins: circular and leaderless bacteriocins.Crossref | GoogleScholarGoogle Scholar | 22348904PubMed |
[107] Aoki W, Kuroda K, Ueda M. Next generation of antimicrobial peptides as molecular targeted medicines. J Biosci Bioeng 2012; 114 365–70.
| Next generation of antimicrobial peptides as molecular targeted medicines.Crossref | GoogleScholarGoogle Scholar | 22658802PubMed |
[108] Bibel DJ, Aly R, Bayles C, Strauss WG, Shinefield HR, Maibach HI. Competitive adherence as a mechanism of bacterial interference. Can J Microbiol 1983; 29 700–3.
| Competitive adherence as a mechanism of bacterial interference.Crossref | GoogleScholarGoogle Scholar | 6411317PubMed |
[109] van Delden C, Köhler T, Brunner-Ferber F, François B, Carlet J, Pechère JC. Azithromycin to prevent Pseudomonas aeruginosa ventilator-associated pneumonia by inhibition of quorum sensing: a randomized controlled trial. Intensive Care Med 2012; 38 1118–25.
| Azithromycin to prevent Pseudomonas aeruginosa ventilator-associated pneumonia by inhibition of quorum sensing: a randomized controlled trial.Crossref | GoogleScholarGoogle Scholar | 22527075PubMed |
[110] Guzman M, Dille J, Godet S. Synthesis and antibacterial activity of silver nanoparticles against gram-positive and gram-negative bacteria. Nanomedicine 2012; 8 37–45.
| Synthesis and antibacterial activity of silver nanoparticles against gram-positive and gram-negative bacteria.Crossref | GoogleScholarGoogle Scholar | 21703988PubMed |
[111] Carey BE, Dancer SJ. Reversing methicillin resistance in MRSA using a bacterial transforming agent. J Antimicrob Chemother 2006; 58 455–7.
| Reversing methicillin resistance in MRSA using a bacterial transforming agent.Crossref | GoogleScholarGoogle Scholar | 16787954PubMed |
[112] Hiramatsu K, Igarashi M, Morimoto Y, Baba T, Umekita M, Akamatsu Y. Curing bacteria of antibiotic resistance: reverse antibiotics, a novel class of antibiotics in nature. Int J Antimicrob Agents 2012; 39 478–85.
| Curing bacteria of antibiotic resistance: reverse antibiotics, a novel class of antibiotics in nature.Crossref | GoogleScholarGoogle Scholar | 22534508PubMed |
[113] Christaki E, Opal SM, Keith JC, Kessimian N, Palardy JE, Parejo NA, et al A monoclonal antibody against RAGE alters gene expression and is protective in experimental models of sepsis and pneumococcal pneumonia. Shock 2011; 35 492–8.
| A monoclonal antibody against RAGE alters gene expression and is protective in experimental models of sepsis and pneumococcal pneumonia.Crossref | GoogleScholarGoogle Scholar | 21263385PubMed |
[114] Roux D, Pier GB, Skurnik D. Magic bullets for the 21st century: the reemergence of immunotherapy for multi- and pan-resistant microbes. J Antimicrob Chemother 2012; 67 2785–7.
| Magic bullets for the 21st century: the reemergence of immunotherapy for multi- and pan-resistant microbes.Crossref | GoogleScholarGoogle Scholar | 22899807PubMed |
[115] Jaklic D, Lapanje A, Zupancic K, Smrke D, Gunde-Cimerman N. Selective antimicrobial activity of maggots against pathogenic bacteria. J Med Microbiol 2008; 57 617–25.
| Selective antimicrobial activity of maggots against pathogenic bacteria.Crossref | GoogleScholarGoogle Scholar | 18436596PubMed |
[116] Carson CF, Hammer KA, Riley TV. Melaleuca alternifolia (Tea Tree) oil: a review of antimicrobial and other medicinal properties. Clin Microbiol Rev 2006; 19 50–62.
| Melaleuca alternifolia (Tea Tree) oil: a review of antimicrobial and other medicinal properties.Crossref | GoogleScholarGoogle Scholar | 16418522PubMed |
[117] Wachtel-Galor S, Benzie IFF. Chapter 1. Herbal medicine: an introduction to its history, usage, regulation, current trends, and research needs. In: Benzie IFF, Wachtel-Galor S, eds. Herbal Medicine: Biomolecular and Clinical Aspects. 2nd edn. Boca Raton, FL: CRC Press; 2011.
[118] Bhullar K, Waglechner N, Pawlowski A, Koteva K, Banks ED, Johnston MD, et al Antibiotic resistance is prevalent in an isolated cave microbiome. PLoS ONE 2012; 7 e34 953
| Antibiotic resistance is prevalent in an isolated cave microbiome.Crossref | GoogleScholarGoogle Scholar |
[119] Haustein T, Gastmeier P, Holmes A, Lucet JC, Shannon RP, Pittet D, et al Use of benchmarking and public reporting for infection control in four high-income countries. Lancet Infect Dis 2011; 11 471–81.
| Use of benchmarking and public reporting for infection control in four high-income countries.Crossref | GoogleScholarGoogle Scholar | 21616457PubMed |
[120] Behnken S, Hertweck C. Anaerobic bacteria as producers of antibiotics. Appl Microbiol Biotechnol 2012; 96 61–7.
| Anaerobic bacteria as producers of antibiotics.Crossref | GoogleScholarGoogle Scholar | 22854892PubMed |
[121] Armellino D, Hussain E, Schilling ME, Senicola W, Eichorn A, Dlugacz Y, et al Using high-technology to enforce low-technology safety measures: the use of third-party remote video auditing and real-time feedback in healthcare. Clin Infect Dis 2012; 54 1–7.
| Using high-technology to enforce low-technology safety measures: the use of third-party remote video auditing and real-time feedback in healthcare.Crossref | GoogleScholarGoogle Scholar | 22109950PubMed |
[122] Tang JW, Noakes CJ, Nielsen PV, Eames I, Nicolle A, Li Y, et al Observing and quantifying airflows in the infection control of aerosol- and airborne-transmitted diseases: an overview of approaches. J Hosp Infect 2011; 77 213–22.
| Observing and quantifying airflows in the infection control of aerosol- and airborne-transmitted diseases: an overview of approaches.Crossref | GoogleScholarGoogle Scholar | 21194796PubMed |
[123] Sibley CD, Peirano G, Church DL. Molecular methods for pathogen and microbial community detection and characterization: current and potential application in diagnostic microbiology. Infect Genet Evol 2012; 12 505–21.
| Molecular methods for pathogen and microbial community detection and characterization: current and potential application in diagnostic microbiology.Crossref | GoogleScholarGoogle Scholar | 22342514PubMed |
[124] Gibson TD, Hulbert JN, Prosser OC, Pavlou AK. Not to be sniffed at. Microbiol Today 2000; 27 14–7.
[125] Hegstad K, Langsrud S, Lunestad BT, Scheie AA, Sunde M, Yazdankhah SP. Does the wide use of quaternary ammonium compounds enhance the selection and spread of antimicrobial resistance and thus threaten our health? Microb Drug Resist 2010; 16 91–104.
| Does the wide use of quaternary ammonium compounds enhance the selection and spread of antimicrobial resistance and thus threaten our health?Crossref | GoogleScholarGoogle Scholar | 20370507PubMed |
[126] Flanagan E, Chopra T, Mody L. Infection prevention in alternative health care settings. Infect Dis Clin North Am 2011; 25 271–83.
| Infection prevention in alternative health care settings.Crossref | GoogleScholarGoogle Scholar | 21316005PubMed |
[127] Wiese-Posselt M, Heuck D, Draeger A, Mielke M, Witte W, Ammon A, et al Successful termination of a furunculosis outbreak due to lukS-lukF-positive, methicillin-susceptible Staphylococcus aureus in a German village by stringent decolonization, 2002–2005. Clin Infect Dis 2007; 44 e88–95.
| Successful termination of a furunculosis outbreak due to lukS-lukF-positive, methicillin-susceptible Staphylococcus aureus in a German village by stringent decolonization, 2002–2005.Crossref | GoogleScholarGoogle Scholar | 17479931PubMed |
[128] Jit M, Stagg HR, Aldridge RW, White PJ, Abubakar I, Find and Treat Evaluation Team Dedicated outreach service for hard to reach patients with tuberculosis in London: observational study and economic evaluation. BMJ 2011; 343 d5376
| Dedicated outreach service for hard to reach patients with tuberculosis in London: observational study and economic evaluation.Crossref | GoogleScholarGoogle Scholar | 22067473PubMed |
[129] Orand JP. Antimicrobial resistance and the standards of the World Organisation for Animal Health. Rev Sci Tech 2012; 31: 335–42, 325–34.
[130] Collignon P. The importance of a One Health Approach to preventing the development and spread of antibiotic resistance. Curr Top Microbiol Immunol 2012; In press
| The importance of a One Health Approach to preventing the development and spread of antibiotic resistance.Crossref | GoogleScholarGoogle Scholar | 22692831PubMed |
[131] Domingues S, Harms K, Fricke WF, Johnsen PJ, da Silva GJ, Nielsen KM. Natural transformation facilitates transfer of transposons, integrons and gene cassettes between bacterial species. PLoS Pathog 2012; 8 e1002 837
| Natural transformation facilitates transfer of transposons, integrons and gene cassettes between bacterial species.Crossref | GoogleScholarGoogle Scholar |
[132] Wright GD. Antibiotic resistance in the environment: a link to the clinic? Curr Opin Microbiol 2010; 13 589–94.
| Antibiotic resistance in the environment: a link to the clinic?Crossref | GoogleScholarGoogle Scholar | 20850375PubMed |
[133] Salyers AA, Amábile-Cuevas CF. Why are antibiotic resistance genes so resistant to elimination? Antimicrob Agents Chemother 1997; 41 2321–5.
| 9371327PubMed |
[134] Williamson DA, Sidjabat HE, Freeman JT, Roberts SA, Silvey A, Woodhouse R, et al Identification and molecular characterisation of New Delhi metallo-β-lactamase-1 (NDM-1) and NDM-6-producing Enterobacteriaceae from New Zealand hospitals. Int J Antimicrob Agents 2012; 39 529–33.
| Identification and molecular characterisation of New Delhi metallo-β-lactamase-1 (NDM-1) and NDM-6-producing Enterobacteriaceae from New Zealand hospitals.Crossref | GoogleScholarGoogle Scholar | 22526013PubMed |
[135] Wellcome Collection. Dirt: The filthy reality of everyday life. London, UK: Wellcome Collection; 2011. Available from: http://www.wellcomecollection.org/whats-on/exhibitions/dirt.aspx [verified 22 March 2013]
[136] Dancer SJ. Back to cleanliness [rapid response to: F. Godlee, Next to cleanliness]. BMJ 2008; 336: 0.1. Available from: http://www.bmj.com/rapid-response/2011/11/01/back-cleanliness [verified 22 March 2013]