Title: EXTENDED SPECTRUM BETA-LACTAMASE (ESBL) RODUCING OLIFORMS Directorate: Infection Control Responsible for review: S Hoque, Consultant Microbiologist Infection Control Support Team Ratified by: Dr J Lowes, Medical Director Ms E Childs, Director of Nursing and Quality Paul Foster, Clinical Director of Pharmacy Ref: 0916 Version 2 Classification: Protocol Due for Review: 18/10/14 Document Control Applicability: All staff Torbay and Southern Devon Health and Care NHS Trust The Community Infection Control Team are available 09:00 – 17.00 Monday to Friday, excluding Bank Holidays. The Consultant Medical Microbiologist is available at all other times via Torbay Hospital switchboard or Derriford Hospital switchboard (Southams/Tavistock Community hospitals). South Devon Healthcare NHS Foundation Trust The Infection Control Team are available 08:30-17:00 Monday-Friday. Microbiologist is available at all other times via switchboard. The Consultant Medical CONTENTS 1 2 3 4 5 6 7 8 9 INTRODUCTION SPREAD PREVENTION AND CONTROL ISOLATION HAND HYGIENE AND ENVIROMENTAL MEASURES ESBL CARRIAGE/ SCREENING TREATMENT OF ESBL PRODUCING COLIFORM INFECTIONS DECOLONISATION OUTBREAKS REFERENCES AMENDMENTS Amendments: Proposals for amendment should be sent to Infection Control Appendix A – ESBL Patient information leaflet Appendix B – ESBL prescribing guidelines Collated by Clinical Effectiveness Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 1 of 11 1.0 INTRODUCTION Extended spectrum beta-lactamase producing coliforms are identified in the laboratory by their resistance to the beta-lactam antibiotic cefpodoxime. The gene for this resistance is carried on a plasmid which can be readily transmitted between similar strains. This resistance is partially inhibited by beta lactamase inhibitors (e.g. clavulinic acid), which distinguishes it from other mechanisms of resistance such as chromosomal (AmpC) resistance. Most ESBLs detected in the UK are of the CTX-M type and typically occur in Klebsiella pneumoniae and E.coli. The number of coliforms producing ESBLs is increasing at an alarming rate, particularly in South East England and the West Midlands. The clinical significance of these finding clinically is that ESBLs are resistant to penicillin’s and cefalosporins. In addition, they are frequently multiply resistant to other antibiotics such as trimethoprim, ciprofloxacin and even aminoglycosides. This situation is analogous to that of MRSA. ESBL producing coliforms are usually susceptible to Nitrofurantoin PO (suitable for uncomplicated UTI only), fosfomycin PO (available from pharmacy at SDHFT & Derriford) and carbapenems such as meropenem and ertapenem. There is a new type transferable antibiotic resistance in gram-negative organisms (including E.coli). NDM1(New Delhi Metallo-beta-lactamase 1) is named after the city that was visited by the patient in whom the first organism carrying this enzyme was isolated but this resistance has spread worldwide. NDM-1 is a new type of pasmid-mediated resistance that is active against all beta-lactamase, carbapenems and can also carry other resistance mechanisms and is readily transferable to other strains. Most ESBL & Metallo-beta-lactamase infections will be urinary tract or gut associated, although they may cause other infections e.g. Klebsiella pneumoniae can cause pneumonia. Infections with ESBLs are a concern for the following reasons: They are difficult to treat because they carry plasmids that confer resistance to many antibiotics. Patients may experience a delay in appropriate treatment because the microbe is resistant to first-line antibiotics. Patients may experience significantly longer hospital stays with increased costs. Patients with infections have an increased risk of death. The colonisation rate for K. pneumoniae is low in healthy individuals in the general population; however it is increased in hospitalised patients, especially during prolonged hospitalisation or antibiotic therapy. ESBLs are primarily identified in long-term care facilities and hospitals. The length of stay in an intensive care unit (with exposure to endemic strains) and health care manipulations, e.g. use of catheters, are associated with acquisition of ESBLs. The most successful pathogens causing healthcare-associated infections (HCAl) develop antibiotic resistance, have the ability to spread (transmissibility), and cause disease (virulence). HCAl caused by ESBLs are most often associated with intensive care units, oncology, burn and neonatal units, as well as receiving previous antibiotic therapy. Most colonised patients are asymptomatic and may be a source of transmission to others. 2.0 SPREAD Selective antibiotic pressure leads to colonisation of patient’s bowel and skin with a risk of subsequent infection. Faecal colonisation may play a critical role in facilitating spread. Outbreaks associated with procedures, e.g., catheterisation, and contamination of medical devices has also been reported. Secondary spread in health care settings can readily occur through healthcare personnel hands. Endemic strains may persist in health care settings for years because of patient colonisation, environmental Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 2 of 11 Collated by Clinical Effectiveness contamination, and hand transmission. Infection prevention and control practices are essential to prevent spread and outbreaks of ESBL-producing coliforms. There are few expert recommendations to direct management of these microbes in healthcare settings and this policy will be re-evaluated on a regular basis to incorporate developing best practice. 3.0 PREVENTION AND CONTROL Health care workers (both hospital and community based) should be encouraged to promote practices known to reduce the spread of ESBLs. These fall into two broad groups, the first being good hand hygiene and cleanliness and the second being a restrictive approach to antibiotic prescribing, especially in the limitation of third generation cephalosporin use. These simple interventions can have a major influence on the impact of ESBLs in the health care setting. Appropriate use of antibiotics will greatly reduce the selection pressure for colonisation and infection with ESBLs. Those prescribing antibiotics in SDHFT should adhere to the Trust Antibiotic Guidelines (CG 0040 & CG1118). For those prescribing within the TSDHCT please adhere to your respective joint formulary: South Devon Joint Formulary – www.torbaycaretrust.nhs.uk/jointformulary or Plymouth Joint Formulary – http://plymouthformulary.nhs.uk/ . There should be a daily review of the need for continuation of antibiotics for all patients on antibiotics. In the situation where there is more than one case on a ward, the prescriber should consider avoiding cephalosporin use altogether in patients on the ward. In an outbreak situation, the Infection Control Support Team/Community Infection Control Team, Consultant Medical Microbiologist and/or Antimicrobial Pharmacist (Antimicrobial Pharmacist not available in TSDHCT) will suggest interim alternative antibiotic prescribing guidelines on a ward / unit. 4.0 ISOLATION 4.1 Use of Barrier Precautions Contact precautions in addition to other infection prevention measures, e.g., hand hygiene, environmental cleaning, and restriction of antibiotics, have been shown to be effective in preventing transmission in outbreak situations. Contact precautions are recommended for colonised/infected patients in facility-based health care settings. This includes the use of gloves and aprons/gowns. No additional precautions are required in outpatient or home care settings. Patients known to be colonised or infected with an ESBL producing coliforms must be managed in a single room. If this is not possible, then appropriate additional precautions will need to be discussed with the Infection Control Support Team/ Community Infection Control Team. 4.2 Type of isolation Single room, ideally with a hand wash basin and toilet. If a toilet is not available a commode must be used and be designated for the sole use of that patient. It must be thoroughly cleaned after each use. An isolation notice must be placed on the outer door of the single room. 4.3 Duration of isolation Isolation should be continued throughout the inpatient stay to reduce the risk of secondary spread. 4.4 Main infection source Faeces, urine, skin (moist sites). Collated by Clinical Effectiveness Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 3 of 11 4.5 Pathology specimens Normal procedures apply. Clinical details, recent and current antibiotic history must be written on the request form. 4.6 Protective clothing Always use plastic apron and gloves for direct patient contact or contact with the immediate environment and when handling body excretions/secretions. 4.7 Disposal of faeces/urine Use a side room toilet if possible, otherwise use a designated commode. 4.8 Disposal of clinical waste Yellow/Orange clinical waste bags 4.9 Cutlery/crockery Normal ward issue – machine dishwasher on ward or in central kitchen. 4.10 Medical equipment Patients must use designated equipment, which must be cleaned and disinfected on discharge. If unable to designate for the sole use of the patient, then equipment must be cleaned and disinfected prior to removal. Always ensure that the manufactures instructions are followed. 4.11 Linen Use a water-soluble red bag then put into the laundry’s red bag. 4.12 Room cleaning Rooms must be cleaned daily, paying special attention to dust-collecting areas and horizontal surfaces. 4.13 Visitors Visitors with only social contact need not wear protective clothing but should wash their hands on leaving the room. Alcohol based hand rubs are also effective against ESBL producing coliforms. 5.0 HAND HYGIENE AND ENVIRONMENTAL MEASURES 5.1 Patient to patient transfer of microorganisms via the hands of healthcare workers is thought to be the main mode of transmission for ESBLs, although some ESBL outbreaks have been attributed to contaminated medical devices (e.g. ultrasound gel). Hand hygiene is a simple and effective infection prevention and control intervention. Hand washing with soap and water is effective; however alcohol hand rubs are a quick and accessible alternative when hands are not visibly soiled and are very effective at killing ESBLs when used correctly. Improving hand hygiene compliance will significantly reduce the risk of healthcare associated infection. 5.2 Commodes, toilets, wheelchairs, floors, sinks, linen and medical devices may all become contaminated. ESBL producing coliforms survive best in moist environments. Following discharge or transfer, thorough terminal cleaning of furniture and the room is required. The curtains must also be changed. 6.0 ESBL CARRIAGE/ SCREENING Patients with known ESBL carriage should have their records flagged consistent with established policies. This will include an alert on the inside cover of their notes as well as on the IHCS screen. As with other alert organisms/conditions, this needs to be routinely checked for all inpatient admissions or outpatient assessments/procedures. Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 4 of 11 Collated by Clinical Effectiveness Upon readmission consider screening for ESBL. Sites most often sampled for carriage are those where coliforms are typically found - perianal/rectal and urine. Patients with persistent carriage (e.g. 3 consecutive positive samples taken at least a week apart and the continuation of ESBL-associated risk factors) do not require continued screening during an admission. Precautionary measures are required and should be maintained. It is reasonable to re-screen during the admission if there are changes in ESBL-associated risk factors. Re-screening should be determined on an individual patient basis. Factors to consider include: continuing use of antibiotics predicted invasive interventions proposed removal of precautions On patient transfer, the receiving healthcare facility should be informed about a patient’s ESBL carriage as with any antimicrobial-resistant microorganism. Screening of health care workers is not recommended. The only exception would be if there is epidemiological evidence of transmission from a suspected common source, where screening of personnel may be warranted as part of the investigation. This would only be undertaken following consultation between the Infection Control Support Team/Community Infection Control Team, Occupational Health and the Clinical Director/ Matron covering the area concerned. 7.0 TREATMENT OF ESBL PRODUCING COLIFORM INFECTIONS Medical staff should review the requirement for antibiotic(s). Inappropriate use of antibiotics may encourage colonisation and secondary infection. Asymptomatic patients do not require treatment nor those with resolving and very mild symptoms. If treatment is required, please discuss treatment with a Consultant Microbiologist or Antimicrobial Pharmacist ( not in the Community). Treatment guidelines are currently being produced but any serious infection that may be due to ESBLs should include antibiotics to which the organism is known to be susceptible. Most ESBLs are susceptible to meropenem IV. 8.0 OUTBREAKS If there is an outbreak (two or more acquired cases), patient screening will be used for control purposes. Identified cases should be placed in single rooms and full contact precautions followed (see section 3). Patients in close proximity to colonised/infected patients should be screened for asymptomatic carriage. Continue to screen exposed patients weekly until the outbreak ends (e.g. 2-4 weeks with no further cases or colonisations). The Devon Health Protection Unit will be notified should such a course of action be taken. Outbreaks of infection caused by ESBL producing coliforms will be reported as serious untoward incidents associated with infection. Collated by Clinical Effectiveness Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 5 of 11 Appendix A Patient Information about ESBLs What are ESBLs? This stands for Extended Spectrum Beta-Lactamases - which is a name used for a group of bacteria1 that are resistant to many commonly used antibiotics. These bacteria are usually found in the bowel, where they live quite happily without causing any problem. They are no more likely to cause infection than other bacteria found within everyone’s bowel. However, occasionally they end up in a place where they shouldn’t be and then it does cause an infection, for example, a urinary tract infection. This can still be treated with antibiotics, but it does mean a different choice of antibiotics from the ones that would normally be used. How are ESBLs spread? It isn’t quite clear why ESBLs are suddenly starting to become a problem now and where most people get them from. The most important route is likely to be through poor hand hygiene, but poorly maintained or cleaned clinical and living areas may be significant in some cases. People with urinary catheters and those who are taking antibiotics are more likely to pick them up. How are they treated? If you have ESBLs in your bowel, you are likely to carry them for a long time and there is no ‘treatment’ for this. You will only be treated if you are showing signs of infection, for example, a high temperature with burning pain when passing urine. If antibiotic tablets / syrups can be used, this would obviously be the first choice. However, antibiotics in tablet or syrup form will not work against all ESBLs and it may then require treatment with injectable antibiotics even if you are not seriously ill. If this is the case, we would hope that a nurse could come out from the hospital and give you the antibiotic once a day in your own home. Are ESBLs a big problem? In South Devon we Screen patients regularly for these bacteria Take steps to ensure patient get the right antibiotics wherever they are Make sure all local doctors know about ESBLs We do all this because we know there have been problems elsewhere in Britain when this has not been done. Some of the correct antibiotics are very expensive and this is also an issue for the NHS. What if I do have to come into hospital? You will be nursed in a side room to reduce the risk of environmental contamination and so reduce the risk of spreading it to others. Please remind staff as soon as you come into hospital that you have had an ESBL in the past. 1 The most common bacteria in this group are species of Klebsiella or Escherichia coli (E. coli) – although the strains involved are quite different from the E. coli O157 found in food poisoning. Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 6 of 11 Collated by Clinical Effectiveness Will my hospital treatment be affected? No. You will be allowed to attend other departments for investigations as normal. You will have any operation or procedure that you need, as normal. The only difference is that, if you do get an infection whilst you are in hospital, the doctors are likely to choose a different antibiotic to treat you. How can I prevent the spread of ESBL? Good hand hygiene, especially after using the toilet and when looking after people with urinary catheters. Maintaining a clean home. Taking antibiotics only when they are really necessary. Should I change my lifestyle? No. You should live your life as normal. With good basic hygiene, as described above, you should put absolutely no restrictions on your family or social life, secure in the knowledge that you are not placing your friends or family at risk. There is no need to avoid young children, or sick or elderly relatives and friends. And remember, you are no more likely to get an infection than anyone else - but if you do get an infection, remind the doctor that you have had ESBLs before so that they can choose the right antibiotic for you. These bacteria have been around for years, the only difference is that they have learnt to stand up for themselves against some antibiotics! If you require further advice after reading this leaflet, please contact; In hospital: Lynn Kelly Infection Control Nurse Torbay Hospital 01803 655757 In the community: Consultants in Communicable Disease Control (01803) 861849 Community Infection Control Team: (01803) 210547/210548 References: International Infection Control Council – Best Infection Control Practices for Patients with Extended Spectrum BetaLactamase Enterobacteriacae – C Friedman, S Callery, A Jeanes, P Piaskowski, L Scott (representing the International Infection Control Council) and members of the Best Practices Expert Panel and Reviewer It is very hard to find good information about ESBLs on the internet, but here are two places to start; http://www.phls.co.uk/infections/topics_az/esbl/q_and_a.htm http://www.cbc.ca/news/background/hospital-infections/esbl_bacteria.html ESBLs/Infection Control/SDHC/06.06 Collated by Clinical Effectiveness Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 7 of 11 Appendix B A guide to the management of ESBLs Dr Tony Maggs V1.0 Jan 2006 What are ESBLs? ESBL stands for “Extended Spectrum Beta-Lactamase producer”, and the bacteria included in this category are usually coliform bacteria. For a long time now, many coliforms have been resistant to antibiotics such as amoxicillin because they posess a ß-lactamase enzyme which breaks down the antibiotic and renders it useless. However, ESBLs have a new form of this ß-lactamase enzyme which now allows them to destroy a much greater range of ß-lactam antibiotics, including most cephalosporins and penicillins. In addition, and not directly related to their ß-lactamase enzyme, these tend to be more antibiotic resistant strains generally and they are often resistant to other non-ß-lactam antibiotics as well, such as ciprofloxacin and gentamicin. Does it matter clinically? These bacteria are probably no more likely to cause infections than any other coliform, but when infections do occur they can be more difficult to treat with antibiotics. As coliforms cause over 90% of community acquired urinary tract infections, not surprisingly ESBLs are seen most commonly in this area and they raise the prospect of a simple urinary tract infection which can only be treated by intravenous antibiotics. How big a problem is it? ESBLs can be identified in the laboratory. In 2012 about 4% of coliforms causing UTIs have been ESBLs. However, as UTIs are so common, this represents a significant number of infections. Who is at risk of ESBL infection? The risk factors for urinary tract infection with ESBLs are the same as for UTIs generally. As with other antibiotic-resistant organisms, those who receive antibiotics frequently are most likely to acquire ESBLs, although we are seeing small numbers of ESBL infections in younger patients without a history of repeated or recent antibiotic usage. There does not seem to be any association with previous hospital stays, but patients in nursing homes are over-represented in the figures. How should the infection control issues be addressed? The infection control precautions are broadly similar to those used for MRSA, with a particular emphasis on hand cleansing before and after clinical contact, but with no restrictions in terms of social contact. Given their importance in UTI, scrupulous attention should be paid to urinary catheter care including the use of a new pair of gloves for each patient for catheter bag emptying or other manipulation, and hand cleansing following the removal of all gloves. Any patient with an ESBL UTI is likely to have the organism within their gut but, unlike MRSA, there is no decolonisation programme; therefore good infection control practices are important all the time and not just when someone is known to have a current ESBLrelated infection. Patients who have had an ESBL infection will have their notes marked / a PAS computer flag set to help future empirical antibiotic choice / nursing. Within hospitals, it would be sensible to place known ESBL patients in side-rooms; within nursing homes, it would be best not to allow known colonised or infected clients to share rooms with catheterised clients who have not had problems with ESBLs. As ever, all antibiotics should carry a health warning and they should only be used where the benefits outweigh the risks. Treatment of ESBL infections The great majority of infections are simple urinary tract infections in patients being managed in the community. If the symptoms are not severe, repeat the urine sample; a significant number of these infections may clear spontaneously without the need for any antibiotics. If the bacteriuria is persistent with relatively mild but significant symptoms, if the organism is sensitive to it, then use nitrofurantoin (50 mg qds O: enteric coated formulations are preferable to avoid GI disturbance) or fosfomycin PO (available from SDHFT and Derriford pharmacies). In moderate / severe infection AND if a patient is <65 years of age, use ciprofloxacin (500 md bd O) if the organism is sensitive to ciprofloxacin. Ertapenem (1g od IV) can be used and administered by the MAT team (SDHFT) or other hospital services (TSDHCT) if ciprofloxacin-resistant (or if .65 years or a history of C.difficile) but ertapenem sensitive. Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 8 of 11 Collated by Clinical Effectiveness In the community, for patients who have previously had ESBL problems themselves or are from a nursing home where a number of residents have had such problems, empirical choice of antibiotics for a new UTI should be as above, and there should be lower threshold for sending urine samples to the lab. If you refer a patient to hospital from a nursing home where you know there have been a number of ESBL problems, please mention this on your referral letter. In hospitals, for patients who have previously had ESBL problems themselves or are from a nursing home where a number of residents have had such problems, if there are severe symptoms consistent with a Gram negative infection meropenem (1g tds IV) should be part of their empirical therapy. Please discuss with consultant microbiologist if you are considering ertapenem or meropenem treatment in patients with previous penicillin hypersensitivity / renal failure. For patients with known previous ESBL problems, if you would normally give antibiotic prophylaxis for a given procedure using a drug such as co-amoxiclav or cefuroxime, a single dose of gentamicin or imipenem should be used in its place. Contact consultant microbiologist for further discussion. Ertapenem and the MAT team If needed, the MAT team is available to give ertapenem intravenously in the community to patients whose symptoms are not sufficiently severe to warrant hospital admission. Patients should be asked about penicillinhypersensitivity and severe renal dysfunction noted, and so their suitability for ertapenem treatment before referral. The drug will then be prescribed at South Devon Healthcare Trust, and the treatment given and monitored by the MAT team, before handing care back to the relevant general practitioner. The MAT team can be reached on (01803) 655776 or via long distance pager (07699 664766). For the areas not covered by the MAT team this service would need to be arranged with the prescriber and the appropriate Community Hospital team. Who to contact for further advice? For advice about treatment; Dr Paul Turner / Dr Tony Maggs Dr S Hoque Consultant Microbiologists Torbay Hospital (01803) 654990 Dr James Greig Consultant Microbiologist Derriford Hospital Plymouth 0845 1558155 Dr Peter Jenks Consultant Microbiologist Derriford Hospital Plymouth 0845 1558155 Collated by Clinical Effectiveness For Acute advice on infection control issues; Lynn Kelly Infection Control Nurse Torbay Hospital, (01803) 655757 Surgery, nursing and patients’ homes: Local Consultants in Communicable Disease Control (CCDC) (01803) 861849 For Community infection control advice contact: Community Infection Control Team: Bay House Nicholson Road Torquay (01803 210547/210548) Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 9 of 11 Protocols & Guidelines – Document Control This is a controlled document. It should not be altered in any way without the express permission of the author or their representative. On receipt of a new version, please destroy all previous versions. Ref: 0916 Title: Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Date of Issue: Version: 18 October 2012 Next Review Date: 16 September 2014 1 Dr S Hoque, Consultant Microbiologist Infection Control Support Team Infection Control Protocol All staff The guidance contained in this document is intended to be inclusive for all patients within the clinical group specified, regardless of age, disability, gender, gender identity, sexual orientation, race and ethnicity & religion or belief. Yes Author: Index: Classification: Applicability: Equality Impact: Evidence based: International Infection Control Council Best Infection Control Practices for Patients with Extended Spectrum Beta Lactamase Enterobacteriacae. Available via http://www.chica.org References: D M Livermore, N Woodford. Guidance to diagnostic laboratories: Laboratory Detection and Reporting of Bacteria with Extended-spectrum R-lactamases. Health Protection Agency, London, 2004. Available via http://www.hpa.org.uk Investigations into multi-drug resistant ESBL producing Escherichia coli strains causing infections in England. Available via http://www.hpa.org.uk Produced following audit: Audited: Approval Route: No No See ratification Date Approved: 11October 2012 Ms E Childs, Director of Nursing & Quality Approved By: Dr S Smith, Medical Director Paul Foster, Clinical Director of Pharmacy Links or overlaps with other policies: 0040 –Adult Emperical Antimicrobial Guidelines: 1118 Paediatric Empirical Antimicrobial Guidelines All SDHCF Trust strategies, policies and procedure documents. RATIFICATION: Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 10 of 11 Collated by Clinical Effectiveness PUBLICATION HISTORY: Issue 1 Date 29 June 2006 Status New 1 16 October 2008 Date Change 1 25 September 2009 1 16 September 2010 Document Info Added Date Change 18 October 2012 Revised 22 January 2013 TSDHCT Community Aspects Included. 2 2 Collated by Clinical Effectiveness Authorised Paul Turner, Consultant Microbiologist Ms E Childs, Director of Nursing & Quality Dr S Smith, Medical Director Medicines Governance Group Paul Turner, Consultant Microbiologist Infection Control Support Team Ms E Childs, Director of Nursing and Quality, Dr S Smith, Medical Director, Medicines Governance Group Dr J Lowes, Medical Director MS E Childs, Director of Nursing & Governance Paul Foster, Clinical Director of Pharmacy Anne Harding Community Infection Control Nurse. Extended Spectrum Beta-Lactamase (ESBL) Producing Coliforms Page 11 of 11
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