ABSTRACT ORIGINAL RESEARCH. Gunnar Kahlmeter. Jenny Åhman. Erika Matuschek

Similar documents
Defining Extended Spectrum b-lactamases: Implications of Minimum Inhibitory Concentration- Based Screening Versus Clavulanate Confirmation Testing

ABSTRACT INTRODUCTION

Lack of Change in Susceptibility of Pseudomonas aeruginosa in a Pediatric Hospital Despite Marked Changes in Antibiotic Utilization

EUCAST Subcommitee for Detection of Resistance Mechanisms (ESDReM)

A retrospective analysis of urine culture results issued by the microbiology department, Teaching Hospital, Karapitiya

THE SENSITIVITY OF PATHOGENS OF COMMUNITY-ACQUIRED URINARY TRACT INFECTIONS IN KARAGANDA Ye. A. Zakharova 1, Chesca Antonella 2, I. S.

Title: Antibacterial resistances in uncomplicated urinary tract infections in women: ECO * SENS II data from primary health care in Austria

Vaccine Evaluation Center, BC Children s Hospital Research Institute, 950 West 28 th Ave,

1. The preferred treatment option for an initial UTI episode in a 22-year-old female patient

Principles and Practice of Antimicrobial Susceptibility Testing. Microbiology Technical Workshop 25 th September 2013

Section of Infectious Diseases and Clinical Microbiology, Uppsala University, Uppsala, Sweden

Protocol for Surveillance of Antimicrobial Resistance in Urinary Isolates in Scotland

Suggestions for appropriate agents to include in routine antimicrobial susceptibility testing

a. 379 laboratories provided quantitative results, e.g (DD method) to 35.4% (MIC method) of all participants; see Table 2.

Mili Rani Saha and Sanya Tahmina Jhora. Department of Microbiology, Sir Salimullah Medical College, Mitford, Dhaka, Bangladesh

BSAC antimicrobial susceptibility

Crescent Journal of Medical and Biological Sciences Vol. 2, No. 2, Spring 2015, 48-52

European Committee on Antimicrobial Susceptibility Testing

ESBL Producers An Increasing Problem: An Overview Of An Underrated Threat

Antimicrobial Stewardship Strategy: Antibiograms

ESBL- and carbapenemase-producing microorganisms; state of the art. Laurent POIREL

Tandan, Meera; Duane, Sinead; Vellinga, Akke.


European Committee on Antimicrobial Susceptibility Testing

Summary of the latest data on antibiotic consumption in the European Union

Guidelines for Treatment of Urinary Tract Infections

January 2014 Vol. 34 No. 1

Prevalence of Extended Spectrum Beta- Lactamase Producers among Various Clinical Samples in a Tertiary Care Hospital: Kurnool District, India

PILOT STUDY OF THE ANTIMICROBIAL SUSCEPTIBILITY OF SHIGELLA IN NEW ZEALAND IN 1996

EUCAST recommended strains for internal quality control

Intrinsic, implied and default resistance

What s new in EUCAST methods?

EARS Net Report, Quarter

Sheffield User Group Day October Members of the BSAC Working party on Susceptibility Testing present:

ESBL Positive E. coli and K. pneumoneae are Emerging as Major Pathogens for Urinary Tract Infection

APPENDIX III - DOUBLE DISK TEST FOR ESBL

Prevalence of Extended-spectrum β-lactamase Producing Enterobacteriaceae Strains in Latvia

ESCMID Online Lecture Library. by author

Antimicrobial resistance (EARS-Net)

International Journal of Pharma and Bio Sciences ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF ESBL PRODUCING GRAM NEGATIVE BACILLI ABSTRACT

ORIGINAL ARTICLE. Focus Technologies, Inc., 1 Hilversum, The Netherlands, 2 Herndon, Virginia and 3 Franklin, Tennessee, USA

Original Article INTRODUCTION

Community-Acquired Urinary Tract Infection. (Etiology and Bacterial Susceptibility)

Routine internal quality control as recommended by EUCAST Version 3.1, valid from

Study of drug resistance pattern of principal ESBL producing urinary isolates in an urban hospital setting in Eastern India

Clinical and Economic Impact of Urinary Tract Infections Caused by Escherichia coli Resistant Isolates

Should we test Clostridium difficile for antimicrobial resistance? by author

National Surveillance of Antimicrobial Resistance

Risk factors for extended-spectrum b-lactamase positivity in uropathogenic Escherichia coli isolated from community-acquired urinary tract infections

Campylobacter infections in EU/EEA and related AMR

Summary of the latest data on antibiotic resistance in the European Union

Background and Plan of Analysis

Quelle politique antibiotique pour l Europe? Dominique L. Monnet

Safe Patient Care Keeping our Residents Safe Use Standard Precautions for ALL Residents at ALL times

THE NAC CHALLENGE PANEL OF ISOLATES FOR VERIFICATION OF ANTIBIOTIC SUSCEPTIBILITY TESTING METHODS

Summary of the latest data on antibiotic consumption in the European Union

Florida Health Care Association District 2 January 13, 2015 A.C. Burke, MA, CIC

Compliance of manufacturers of AST materials and devices with EUCAST guidelines

PROTOCOL for serotyping and antimicrobial susceptibility testing of Salmonella test strains

Marc Decramer 3. Respiratory Division, University Hospitals Leuven, Leuven, Belgium

Infections - Oral Treatment Options?

Compliance of manufacturers of AST materials and devices with EUCAST guidelines

Streptococcus pneumoniae. Oxacillin 1 µg as screen for beta-lactam resistance

CLSI vs. EUCAST. What is EUCAST? Structure of EUCAST CLSI. Where they fit? SASCM WORKSHOP 5/24/2014

Antimicrobial susceptibility of Salmonella, 2016

Comparative Assessment of b-lactamases Produced by Multidrug Resistant Bacteria

Antibiotic Updates: Part II

Antimicrobial resistance of Escherichia coli urinary isolates in the Veterans Affairs Healthcare. System

Antimicrobial Susceptibility Profile of E. coli Isolates Causing Urosepsis: Single Centre Experience

جداول میکروارگانیسم های بیماریزای اولویت دار و آنتی بیوتیک های تعیین شده برای آزمایش تعیین حساسیت ضد میکروبی در برنامه مهار مقاومت میکروبی

Michael Hombach*, Guido V. Bloemberg and Erik C. Böttger

Helen Heffernan and Rosemary Woodhouse Antibiotic Reference Laboratory

Cephalosporins, Quinolones and Co-amoxiclav Prescribing Audit

JMSCR Vol 05 Issue 07 Page July 2017

Antimicrobial practice. Laboratory antibiotic susceptibility reporting and antibiotic prescribing in general practice

How is Ireland performing on antibiotic prescribing?

Understanding the Hospital Antibiogram

ESCMID Online Lecture Library. by author

by author ESCMID Online Lecture Library EUCAST The European Committee on Antimicrobial Susceptibility Testing September 2010

2015 Antimicrobial Susceptibility Report

Original Article. Suthan Srisangkaew, M.D. Malai Vorachit, D.Sc.

INCIDENCE OF BACTERIAL COLONISATION IN HOSPITALISED PATIENTS WITH DRUG-RESISTANT TUBERCULOSIS

Help with moving disc diffusion methods from BSAC to EUCAST. Media BSAC EUCAST

What is the problem? Latest data on antibiotic resistance

Antibiotic Reference Laboratory, Institute of Environmental Science and Research Limited (ESR); August 2017

Cipro for klebsiella uti

Antibiotic Susceptibility of Common Bacterial Pathogens in Canine Urinary Tract Infections

IMPORTANCE OF GLOBAL HARMONIZATION OF ANTIMICROBIAL SUSCEPTIBILITY TESTING IN CANADA FOR DEFINING ANTIMICROBIAL RESISTANCE

Please distribute a copy of this information to each provider in your organization.

Cipro for gram positive cocci in urine

Quality assurance of antimicrobial susceptibility testing

Best Practice Guidelines for Treatment of Uncomplicated UTIs in Women While Decreasing Risk of Antibiotic Resistance

EXTENDED-SPECTRUM BETA-LACTAMASE (ESBL) TESTING

What is new in 2011: Methods and breakpoints in relation to subcommittees and expert groups. by author. Gunnar Kahlmeter, Derek Brown

Surveillance for Antimicrobial Resistance and Preparation of an Enhanced Antibiogram at the Local Level. janet hindler

CONTAGIOUS COMMENTS Department of Epidemiology

Why fosfomycin trometamol as first line therapy for uncomplicated UTI?

An Approach to Appropriate Antibiotic Prescribing in Outpatient and LTC Settings?

Initiatives taken to reduce antimicrobial resistance in DK and in the EU in the health care sector

Fluoroquinolone Resistance Among Gram-Negative Urinary Tract Pathogens: Global Smart Program Results,

Transcription:

Infect Dis Ther (2015) 4:417 423 DOI 10.1007/s40121-015-0095-5 ORIGINAL RESEARCH Antimicrobial Resistance of Escherichia coli Causing Uncomplicated Urinary Tract Infections: A European Update for 2014 and Comparison with 2000 and 2008 Gunnar Kahlmeter. Jenny Åhman. Erika Matuschek To view enhanced content go to www.infectiousdiseases-open.com Received: September 2, 2015 / Published online: October 27, 2015 The Author(s) 2015. This article is published with open access at Springerlink.com ABSTRACT Introduction: The objective of this study was to provide an update on the resistance of Escherichia coli in women with acute uncomplicated urinary tract infections (UTIs) in France, Germany, Spain, Sweden, and the United Kingdom (UK) to mecillinam [amdinocillin (United States Adopted Name)], amoxicillin clavulanic acid, cefadroxil, nitrofurantoin, ciprofloxacin, and trimethoprim, and to compare the results with resistance in the ECO.SENS I and II surveys in 2000 and 2008, respectively. Methods: The susceptibility of E. coli in France (166 isolates), Germany (133 isolates), Spain (169 isolates), Sweden (137 isolates), and the UK (124 isolates) was determined by disc diffusion according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) Electronic supplementary material The online version of this article (doi:10.1007/s40121-015-0095-5) contains supplementary material, which is available to authorized users. G. Kahlmeter (&) J. Åhman E. Matuschek Department of Clinical Microbiology, Central Hospital, Växjö, Sweden e-mail: gunnar.kahlmeter@kronoberg.se breakpoints and methodology. Resistance rates were compared using Fisher s exact test, 2-tailed, with P\ 0.05 indicating statistical significance. Results: Since 2000, there has been a significant increase in resistance to cefadroxil in Germany (1% to 12%) and Spain (3% to 8%), to ciprofloxacin in Germany (2% to 21%), Spain (15% to 31%), Sweden (0% to 7%), and the UK (1% to 15%), to trimethoprim in Germany (23% to 37%), Spain (25% to 37%), Sweden (9% to 17%), and the UK (13% to 46%), to mecillinam in Spain (1% to 6.5%), and to nitrofurantoin in the UK (0% to 6%); there was also a significant decrease in resistance to nitrofurantoin in Spain (4% to 0%). Since 2008, there has been a significant increase in resistance to ciprofloxacin in Sweden (3% to 15%) and the UK (1% to 15%), and to trimethoprim (13% to 46%) and nitrofurantoin (0% to 6%) in the UK. Conclusion: E. coli isolates from women with acute uncomplicated UTIs have increasing antimicrobial resistance, particularly to ciprofloxacin and trimethoprim. However, resistance to mecillinam and nitrofurantoin mostly remains low. Funding: LEO Pharma.

418 Infect Dis Ther (2015) 4:417 423 Keywords: Amoxicillin clavulanic acid; Antimicrobial resistance; Susceptibility; Cefadroxil; Ciprofloxacin; Escherichia coli; Mecillinam; Nitrofurantoin; Trimethoprim; Urinary isolates; Urinary tract infections INTRODUCTION Antimicrobial resistance (AMR) in clinically important pathogens, such as Escherichia coli, is of continuing concern [1]. Changes in resistance levels are best monitored by prospective, multi-national, surveillance programs, employing standardized procedures to collect the isolates and determine their antimicrobial susceptibility [2]. The ECO.SENS (The pan-european Escherichia coli sensitivity survey) project was the first such study to investigate the antimicrobial susceptibility of E. coli in acute uncomplicated urinary tract infections (UTIs) in women. It was first conducted between 1999 and 2000, involving 1417 isolates from 4734 women in 17 countries [3], and again in 2008 involving 903 isolates from 1697 women in 5 countries [4]. We report here an update on the antimicrobial susceptibility of isolates of similar origin from five countries which participated in either both or one of the previous surveys representing areas of Europe with varying AMR problems. METHODS The selection of patients and procedures involved has been reported previously and are summarized only briefly here [3, 4]. Methodological differences if any are described. The study involved isolates of E. coli from non-hospitalized females aged 18 years and over, with symptoms of acute uncomplicated lower UTI, which included any or all of the following: frequency, dysuria, urgency, and suprapubic pain. In France (14 centers), Spain (3 centers), Sweden (1 center), and the United Kingdom (UK; 2 centers), all isolates were from patients in primary healthcare. In Germany (four centers), isolates were from women attending hospital clinics and the laboratory had difficulties guaranteeing the community origin of the isolates. Isolates were sent to the Department of Clinical Microbiology at the Central Hospital, Växjö, Sweden. Their antimicrobial susceptibility to mecillinam [amdinocillin (United States Adopted Name)], amoxicillin clavulanic acid, cefadroxil (as a screen for cephalosporin resistance, particularly ESBL production), nitrofurantoin, ciprofloxacin, and trimethoprim was determined by disc diffusion using the European Committee on Antimicrobial Susceptibility Testing (EUCAST) methodology and breakpoints [5, 6]. Isolates resistant to the first-generation cephalosporin, cefadroxil, were investigated for production of extended-spectrum beta-lactamase (ESBL) by double disc synergy testing using cefotaxime with and without clavulanic acid and ceftazidime with and without clavulanic acid. Resistance rates were compared to those obtained in 2000, for all countries and to those obtained in 2008 for Sweden and the UK for all antimicrobials with the exception of amoxicillin clavulanic acid. The methodology for determining susceptibility to amoxicillin clavulanic acid in the current study was different from that used in the previous studies [7]. Statistical comparison was by Fisher s exact test, 2-tailed, with P\0.05 indicating statistical significance. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation at the

Infect Dis Ther (2015) 4:417 423 419 respective institutions and with the Helsinki Declaration of 1964, as revised in 2013. No patient identifiers other than sex and age were recorded and, as such, informed consent was not required for inclusion in this study. RESULTS Percentage susceptibilities to the agents tested are shown in Table 1. When compared to the results from 2000, there were instances where resistance had increased significantly in 2014, as follows: Germany showed a significant increase in resistance to cefadroxil (1.4% to 12.0%; P\0.001), ciprofloxacin (2.2% to 20.2%; P\0.0001), and trimethoprim (22.5% to 36.8%; P\0.05); Spain showed a significant increase in resistance to mecillinam (1.0% to 6.5%; P\0.01), cefadroxil (3.1% to 8.3%; P\0.05), ciprofloxacin (14.7% to 30.8%; P\0.001), and trimethoprim (25.1% to 37.3%; P\0.05); Sweden showed a significant increase in resistance to ciprofloxacin (0% to 7.3%; P\0.001) and trimethoprim (8.8% to 16.9%; P\0.05); and the UK showed a significant increase in resistance to ciprofloxacin (0.6% to 15.3%; P\0.0001), trimethoprim (13.3% to 46.0%; P\0.0001), and nitrofurantoin (0% to 5.6%; P\0.01). Spain also showed a significant decrease in resistance to nitrofurantoin (4.2% to 0%; P\0.01). Resistance in 2014 was significantly greater than that recorded in 2008 in the UK with a significant increase in resistance to ciprofloxacin (0.5% to 15.3%; P\ 0.0001), nitrofurantoin (0% to 5.6%; P\0.01), and trimethoprim (14.9% to 46.0%; P\0.0001). Overall there were 35 (4.8%) isolates positive for ESBL production. The incidence in each country was 2.4% in France, 10.5% in Germany, 4.7% in Spain, 2.9% in Sweden, and 4.0% in the UK. DISCUSSION E. coli from women with acute uncomplicated UTIs in 2014 showed high levels of resistance to ciprofloxacin, trimethoprim, and amoxicillin clavulanic acid. Significantly greater resistance when compared to similar isolates from both 2000 and 2008 was noted for ciprofloxacin and trimethoprim. The current study is particularly important in that it enables trends in resistance to be compared over a 15-year period, as opposed to the usual surveys which take only a snapshot at a specific time. When compared to 2000, ciprofloxacin and trimethoprim resistance had increased in Germany, Spain, Sweden, and the UK. Resistance had similarly increased to ciprofloxacin and trimethoprim in the UK since 2008. There were only minor differences in methodology between the first two surveys and that reported here. The surveys in 2000 and 2008 involved many centers in each country [3, 4]. In contrast, the latest study was truly multi-center only in France, whereas samples from the other countries came from up to four centers. No upper age limit was imposed on patients in the current study, whereas an upper age limit of 65 years was specified previously. Despite these differences, the three surveys had very important similarities. All involved women with acute uncomplicated UTIs. Urine samples in all three surveys were obtained from women in primary healthcare, with the exception of Germany in the current study, where most of the isolates were from women attending

420 Infect Dis Ther (2015) 4:417 423 Table 1 Percentage susceptibility of Escherichia coli isolated from women with acute uncomplicated urinary tract infection in 2000, 2008, and 2014 Country Year No. of isolates Mecillinam Amoxicillin clavulanic acid Cefadroxil Nitrofurantoin Ciprofloxacin Trimethoprim France 2014 166 97.0 94.0 97.0 100 95.2 82.5 2000 199 98.5 NA a 99.0 99.0 98 84.4 Germany 2014 133 97.0 91.7 88.0 97.7 79.7 b 63.2 2000 138 97.8 NA a 98.6 99.3 97.8 77.5 Spain 2014 169 93.5 79.9 91.7 100 69.2 62.7 2000 191 99.0 NA a 96.9 95.8 85.3 74.9 Sweden 2014 137 98.5 94.3 97.1 98.5 92.7 b 83.1 b 2008 203 99.5 NA a 98.5 100 97.5 83.7 2000 193 98.4 NA a 94.8 100 100 91.2 United Kingdom 2014 124 95.2 86.3 95.2 94.4 84.7 54.0 2008 201 99.0 NA a 98.5 100 99.5 85.1 2000 180 98.3 NA a 98.3 100 99.4 86.7 a b See text for why data for amoxicillin clavulanic acid are not applicable (NA) Additional 1% intermediate susceptibility

Infect Dis Ther (2015) 4:417 423 421 hospital clinics. Antimicrobial susceptibility was performed at the same laboratory for all three studies. Susceptibility in the current study was determined using EUCAST breakpoints and standardized methodology [5, 6]. The methodology used in the current study was different to that used previously, as it used a different medium and inoculum as specified by EUCAST. However, the zone diameter breakpoints were the same for all antimicrobials with the exception of amoxicillin clavulanic acid [5 7]. The most recent guidelines for amoxicillin clavulanic acid use a fixed concentration of clavulanic acid and apply specifically to urinary isolates [5, 6]. The new susceptibility breakpoint for isolates from UTIs is defined as an amoxicillin minimum inhibitory concentration of B32 mg/l. Due to these differences in methodology it is impossible and inappropriate to compare the resistance rates for this antimicrobial between on one hand 2014 and on the other 2000 and 2008. However, it is acceptable to compare the results from the three surveys for all other antimicrobials. Statistical comparison is also acceptable, although for the reasons discussed above, one should not place too much emphasis upon the degrees of statistical significance found. Our results and the trends observed are comparable to those observed elsewhere over a similar timescale. In France, resistance to amoxicillin clavulanic acid [8] and trimethoprim sulfamethoxazole [8, 9] has been highlighted, and there are similar reports from Germany [10, 11], along with resistance to cephalosporins [10]. Resistance to quinolones and trimethoprim sulfamethoxazole in Spain is well documented [12, 13]. Although antimicrobial susceptibility in E. coli isolates in Sweden is generally high, trimethoprim resistance levels have been a cause for concern [14]. Similarly, the high level of trimethoprim resistance in the UK is well documented [15]. The Antimicrobial Resistance Epidemiological Survey on Cystitis (ARESC) study in Europe and Brazil, which involved similar patients to those in our study, noted that susceptibility to E. coli of over 90% was found for mecillinam, nitrofurantoin, and fosfomycin only [16]. Although fosfomycin was not tested in our latest study, consistent and high susceptibility of E. coli in all countries was similarly noted for mecillinam and nitrofurantoin. Interestingly, investigation of 34 isolates of E. coli resistant to either mecillinam or nitrofurantoin from the first ECO.SENS study in 2000 indicated the low probability of future clonal spread of resistance to these agents [17]. Our update has confirmed no major increase in mecillinam or nitrofurantoin resistance has taken place in the last 15 years. ESBL production was recorded in 35 (4.8%) isolates. This is greater than that recorded previously in the 2008 ECO.SENS study (1.2% of isolates), suggesting that the frequency of ESBL-producing E. coli in the community is increasing. The incidence was less than 5% in all countries except Germany, where it was 10.5%, where isolates were from women attending hospital clinics. The continuing and increasing resistance to ciprofloxacin and trimethoprim is disturbing and impacts on the choice of therapy for women with acute uncomplicated UTIs, particularly in domiciliary practice, where treatment is usually empirical. Antimicrobial susceptibility surveys such as the ECO.SENS and ARESC are essential and provide the most appropriate information on which to base such treatment. Our data, and that of others, indicate that mecillinam, nitrofurantoin, and

422 Infect Dis Ther (2015) 4:417 423 fosfomycin are suitable options for empirical therapy of women with acute uncomplicated UTI. These are old agents with indications limited to lower uncomplicated UTIs. Interest in the redevelopment of these old agents has awakened with the galloping resistance to other agents and with the lack of new agents [18]. CONCLUSIONS E. coli isolates from women with acute uncomplicated UTIs showed a significant increase in AMR since 2000 to ciprofloxacin and trimethoprim (Germany, Spain, Sweden, and the UK). Susceptibility to mecillinam and nitrofurantoin remains high. The ECO.SENS and ARESC studies indicate that suitable agents for empirical treatment of acute cystitis include mecillinam, nitrofurantoin, and fosfomycin. ACKNOWLEDGMENTS The article processing charges for this study were funded by Leo Pharma, Denmark. Colleagues Jordi Vila, Rafael Canton and Luis Martinez-Martinez (Spain), Sören Gatermann (Germany), Karen Bowker and Mandy Wootton (UK), and Vincent Jarlier (France) are thanked for organizing the collection of isolates in the respective countries. This material was presented in part at the 25th European Congress of Clinical Microbiology and Infectious Disease, Copenhagen, Denmark, April 25 28, 2015. The assistance of Paul Menday in the statistical analysis and preparation of this manuscript is acknowledged. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval for the version to be published. Disclosures. Gunnar Kahlmeter, Jenny Åhman, and Erika Matuschek declare that they have no conflict of interest. Compliance with ethics guidelines. All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation at the respective institutions and with the Helsinki Declaration of 1964, as revised in 2013. No patient identifiers other than sex and age were recorded and, as such, informed consent was not required for inclusion in this study. Open Access. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/ by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. REFERENCES 1. Allocati N, Masulli M, Alexeyev MF, Di Ilio C. Escherichia coli in Europe: an overview. Int J Environ Res Public Health. 2013;10:6235 54. 2. The Microbial Threat. Copenhagen: Invitational EU Conference, Denmark, September 1998 (Workshops 7 8 September). 3. Kahlmeter G. An international survey of the antimicrobial susceptibility of pathogens from acute uncomplicated urinary tract infections: the ECO.SENS project. J Antimicrob Chemother. 2003;51:69 76. 4. Kahlmeter G, Poulsen HO. Antimicrobial susceptibility of Escherichia coli from

Infect Dis Ther (2015) 4:417 423 423 community-acquired urinary tract infections in Europe: the ECO.SENS study revisited. Int J Antimicrob Agents. 2012;39:45 51. 5. The European Committee on Antimicrobial Susceptibility Testing. EUCAST Disk Diffusion Test Manual. v 4.0; 2014. http://www.eucast.org. 6. The European Committee on Antimicrobial Susceptibility Testing. Breakpoint tables for interpretation of MICs and zone diameters. Version 4.0; 2014. http://www.eucast.org. 7. The Swedish Reference Group for Antibiotics (SRGA) and its subcommittee on antibiotics (SRGA-M). http://www.srga.org. 8. Lobet B, Valot A, Cattoir V, et al. Comparison of antimicrobial susceptibility of 1217 Escherichia coli isolates from women with hospital and community acquired urinary tract infections (Article in French). Presse Med. 2008;37:46 50. 9. Neuzillet V, Naber KG, Schito G, et al. French results of the ARESC study: clinical aspects and epidemiology of antimicrobial resistance in female patients with cystitis. Implications for therapy. Med Mal Infect. 2012;42:66 75. 10. Kresken M, Pfeifer Y, Hafner D, et al. Occurrence of multidrug resistance to oral antibiotics among Escherichia coli urine isolates from outpatient departments in Germany: extended-spectrum beta-lactamases and the role of fosfomycin. Int J Antimicrob Agents. 2014;44:295 300. 11. Schmiemann G, Gagyor I, Hummers-Pradier E, et al. Resistance profiles of urinary tract pathogens in general practice an observational study. BMC Urol. 2012;21 33. 12. Garcia Garcia ML, Munoz Bellido JL, Garcia Rodriguez JA, et al. In vitro susceptibility of community-acquired urinary tract pathogens to commonly used antimicrobial agents in Spain: a comparative multicenter study (2002 2004). J Chemother. 2007;19:263 70. 13. Gobernado M, Valdes L, Alos JI, et al. Antimicrobial susceptibility of clinical Escherichia coli isolates from uncomplicated cystitis in women over a 1-year period in Spain. Rev Esp Quimoter. 2007;20:68 76. 14. Lindback H, Lindback J, Sylvan S, Melhus A. Low frequency of antibiotic resistance among urine isolates of Escherichia coli in the community, despite a major hospital outbreak with Klebsiella pneumoniae producing CTS-M-15 in Uppsala County. Scand J Infect Dis. 2010;42:243 8. 15. Bean DC, Krahe D, Wareham DW. Antimicrobial resistance in community and nosocomial Escherichia coli urinary tract isolates, London 2005 2006. Ann Clin Microbiol Antimicrob. 2008;7:13. 16. Schito GC, Naber KG, Botto H, et al. The ARESC study: an international survey on the antimicrobial resistance of pathogens involved in uncomplicated urinary tract infections. Int J Antimicrob Agents. 2009;34:407 13. 17. Poulsen HO, Johansson A, Granholm S, Kahlmeter G, Sundqvist M. High genetic diversity of nitrofurantoin or mecillinam resistant Escherichia coli indicates low propensity for clonal spread. J Antimicrob Chemother. 2013;68:1974 7. 18. Theuretzbacher U, Van Bambeke F, Canton R, et al. Reviving old antibiotics. J Antimicrob Chemother. 2015;70(8):2177 81.