Original article

Risk factors for urinary tract infections due to ciprofloxacin-resistant Escherichia coli in a tertiary care urology department in Switzerland

J Nicoletti, S Kuster, T Sulser, B Ledergerber

DOI: https://doi.org/10.4414/smw.2010.13059
Publication Date: 15.07.2010
Swiss Med Wkly. 2010;140:w13059

Questions under study: Monitoring of antimicrobial resistance is a key component of antibiotic stewardship programs. In 2007, a significantly higher resistance rate of Escherichia coli to ciprofloxacin was found at the Department of Urology, University Hospital Zurich, Switzerland, when compared to other hospital units. Thus, we aimed to determine the risk factors for this increased fluoroquinolone resistance in outpatients and inpatients with urinary tract infection (UTI) or colonisation with E. coli.

We performed a cross sectional study including 275 patients of the Department
of Urology in whom E. coli was isolated
from urine or blood cultures between 01.01.2006 and 31.08.2007. Clinical
data were collected from patients’ records using a structured questionnaire.
Multivariable analysis was performed for the detection of risk factors.

Results: Ciprofloxacin-resistant E. coli was detected in 22% of patients. Risk factors for ciprofloxacin-resistant E. coli included prior use of fluoroquinolones (odds ratio [OR] (95% confidence intervals): 2.24 (1.08–4.62), p = 0.030), prior urinary tract catheterisation (OR: 2.41 (1.02–5.67), p = 0.044) and recurrent UTIs (OR: 2.26 (1.07–4.78), p = 0.032). 60.8% of all prescriptions in urinary tract infections were for fluoroquinolones, and this antibiotic class was the empiric antibiotic regimen of choice in 72.5% of all acute, uncomplicated, urinary tract infections.

Conclusions: The increasing prevalence of ciprofloxacin-resistant E. coli makes empiric therapy in UTIs with this agent questionable, especially in patients with one or several of the above mentioned risk factors. Due to the increasing resistance rate, continuous surveillance and susceptibility testing in individual patients, particularly with complicated UTIs, is indispensable for adequate therapy.

Key words: Escherichia coli; ciprofloxacin; fluoroquinolones; antibacterial drug resistance; urinary tract infections; urology


Urinary tract infections (UTIs) are common infections among inpatients and outpatients, ranking second only to respiratory infections, and thus, are a frequent cause for prescription of antibiotics [1]. Common pathogens causing uncomplicated UTIs are Escherichia coli (75–90% of UTIs) and Staphylococcus saprophyticus (5–15% of UTIs, particularly in younger women). Occasionally, Proteus mirabilis, Klebsiella spp. or enterococci are isolated from urine samples [2]. Fluoroquinolones are often prescribed empirically and as a first choice in patients with UTIs, achieving high concentrations in urine and showing a broad antibacterial spectrum. In 2000, fluoroquinolones were prescribed for treatment of acute, uncomplicated UTIs in Switzerland in 64% of cases [3]. Knowledge of the most frequent microorganisms and their susceptibility pattern are the basis for empirical antimicrobial therapy, especially in UTIs, as susceptibility testing is often not performed in the community setting. Unfortunately, this diagnostic and therapeutic approach is becoming more and more limited because of increasing resistance to commonly used antimicrobial drugs.

Across Europe, levels of antibiotic consumption show great variations [4], with the use of fluoroquinolones being highest in Portugal and Spain. As the emergence of resistance is associated with high antibiotic consumption [5, 6], it is not surprising that resistance to ciprofloxacin in E. coli shows great geographical variations, too, reaching high levels in southern Europe and low levels in northern European countries [6–8]. In addition to attentive monitoring of resistance patterns, the identification of risk factors for infections with resistant strains may contribute to improved empirical treatment. Factors associated with resistance to ciprofloxacin in E. coli reported in previous studies are urinary tract abnormalities, older age, previous antimicrobial therapy (especially quionolone therapy), urinary catheterisation, recurrent UTIs, male gender and presence of complicated UTI [9–13]. In our hospital, resistance rates of E. coli to ciprofloxacin in inpatients range from as low as 4.9% to as high as 35.5% across hospital units, and resistance rates at the Department of Urology have been shown to be significantly higher compared to other hospital units [14]. Resistance rates of in- and outpatients at our hospital ranged from 0 to 40% in 2008 [unpublished internal report].

The goals of this study were (i) to determine resistance rates in outpatients and inpatients with UTIs, (ii) to assess prescribers’ choices for empirical antibiotic therapy, and (iii) to identify risk factors for infections due to ciprofloxacin-resistant E. coli in patients at the Department of Urology of the University Hospital Zurich, Switzerland.



The University Hospital in Zurich, Switzerland, is an 861 beds tertiary care teaching hospital. 36 beds are assigned to the Department of Urology. 1722 patients were admitted in 2006, accounting for 10412 bed-days (day of admission and day of discharge counted together as one bed-day) and a mean length of stay of 6.0 days. In the same year, 6514 patients were treated in the outpatient unit.


We performed a cross sectional study at the Department of Urology. All adult inpatients and outpatients were included in whom E. coli was isolated from clinical urinary samples or blood cultures (in case of clinical symptoms suggestive of urinary tract infection but negative urinary culture) in the study period from January 1, 2006 to August 31, 2007. Most of the in- and outpatients presenting with complicated urinary tract infections to the University Hospital Zurich are treated at the Department of Urology, except kidney transplant recipients. At our hospital, acute, uncomplicated urinary tract infections and women with acute, uncomplicated pyelonephritis are treated at the Department of Urology, the Department of Gynecology and Obstetrics, and at the Medical Emergency Department.

All specimens were tested in a central clinical microbiology laboratory (Institute of Medical Microbiology, University of Zurich). Bacteria were isolated from urine and blood cultures according to standard methods [15]. Antimicrobial susceptibility testing and screening for extended spectrum beta-lactamase (ESBL) was performed according to the Clinical and Laboratory Standards Institute (CLSI) [16]. Briefly, in the disk diffusion test, ciprofloxacin zone diameters of <15 mm and of >21 mm were considered resistant and susceptible, respectively; zones of 16–20 mm were considered as intermediately susceptible but were categorised as non-susceptible. Some strains were tested by a commercial microdilution test (Vitek2, BioMérieux, Marcy L’Étoile, France); minimal inhibitory concentrations (MIC) of ciprofloxacin of <1 mg/L and of >4 mg/L were considered susceptible and resistant, respectively; an MIC of 2 mg/L was intermediately susceptible but was categorised as non-susceptible. The screening test for ESBL was an inhibition zone of <22 mm against ceftazidime or of <27 mm against cefotaxime. Any synergy between amoxicillin/clavulanic acid and ceftazidime or cefepime (double disk method), or between piperacillin/tazobactam and cefotaxime in the disk diffusion test was also an indication for a confirmation test by Etest according to the prescription of the manufacturer (AB Biodisk, Solna, Sweden); a greater than twofold concentration decrease in an MIC for ceftazidime or cefepime, or for cefotaxime tested in combination with clavulanic acid versus its MIC when tested alone was confirmatory for ESBL. In accordance with the CLSI guidelines, all ESBL-producing E. coli strains were classified as resistant to all penicillins, cephalosporins and aztreonam regardless of the MICs determined for these drugs [16].

Demographic and clinical information of both in- and outpatients was collected from each patient by chart review using a structured questionnaire.


Bacterial counts with 104 colony forming units or more per millilitre of urine in asymptomatic patients were considered to represent asymptomatic bacteriuria. Acute, uncomplicated urinary tract infection was defined as symptomatic cystitis, characterised by frequency, dysuria, suprapubic pain and urgency in women with a normal urogenital tract. In men, symptomatic urinary tract infections were classified as complicated. Acute, uncomplicated pyelonephritis was defined as a parenchymatous infection of the kidney in women with normal urogenital tract who presented with flank pain and often fever. Complicated urinary tract infection was defined as symptomatic cystitis or pyelonephritis in men or women with functional or structural abnormalities of the urogenital tract. Any detection of E. coli in blood culture samples was considered significant bacteremia. Infections were considered nosocomial if the patient was hospitalised in an acute care centre for >48 hours prior to sample collection. One antibiotic course was defined as administration of at least one dose of any antibacterial agent. A time interval of >24 hours between the administration of two doses was defined to separate one course from another, unless certain conditions (e.g. renal insufficiency) justified a dose interval of >24 hours. The variable ‘recurrent UTIs’ was recorded according to the available information from patient history without definition of a threshold.

Calculation of the Chronic Disease Score was performed according to McGregor et al. [17].

Statistical analysis

We used Stata (Version 10, StataCorp, College Station, Texas) for statistical analyses. Differences in group proportions were assessed by the Chi-square or Fisher’s exact test, and differences in medians were calculated with the Wilcoxon rank-sum test. Logistic regression analysis was performed to identify risk factors for acquisition of fluoroquinolone-resistant E. coli. In multivariable analysis, male gender and all variables revealing a p value <0.2 in univariable analysis were included. A p value <0.05 was considered statistically significant.

Ethics approval

The study was approved by the local ethics committee.


Patients and antibiotic prescriptions

275 patients were enrolled and a total of 345 urinary or blood culture samples were analysed. Patients’ characteristics, clinical presentation and microbiological findings are summarised in table 1. The median age (interquartile range (IQR)) of the 151 (55%) women and the 124 (45%) men was 56.8 (51.9–60.4) years. Of the population studied, 178 (65%) subjects were treated as outpatients and 97 (35%) as inpatients. The most common diagnosis was acute, uncomplicated UTI (80 (29%) patients), followed by complicated UTI (69 (25%) patients). Ciprofloxacin-resistant E. coli was isolated in 61 patients, representing 36% of all inpatients and 15% of outpatients.

174 out of 286 (60.8%) initial antibiotic prescriptions were for fluoroquinolones, 13% were for penicillins and 7% were for sulfamethoxazole-trimethoprim. Fluoroquinolones were the empiric antibiotic therapy of choice in 72.5% (58/80) of all acute, uncomplicated urinary tract infections, in 76.5% (13/17) of all episodes of acute, uncomplicated pyelonephritis and in 65.0% (52/80) of all complicated urinary tract infections. Penicillins accounted for 10.0%, 17.6% and 16.3%, respectively, and sulfamethoxazole-trimethoprim accounted for 12.5%, 5.9% and 8.8%, respectively.

Predictors of ciprofloxacin-resistant E. coli

The characteristics of patients with ciprofloxacin-resistant strains were compared with those of patients with a ciprofloxacin-susceptible strain (table 2). Significant predictors of ciprofloxacin-resistant E. coli in univariable analysis were inpatient status, recurrent UTIs, urolithiasis, foreign material (e.g. pigtail catheter) in the upper urinary tract, urinary catheter, prior use of fluoroquinolones, prior use of any antibiotics and prior treatment in the Department of Urology. To identify independent risk factors, a multivariable analysis was performed. Thereby, fluoroquinolone use in the preceding year (odds ratio [OR] (95% confidence intervals [CI]): 2.24 (1.08–4.62), p = 0.030), urinary tract catheterisation in the preceding year (OR: 2.41 (1.02–5.67), p = 0.044) and recurrent urinary tract infections (OR: 2.26 (1.07–4.78), p = 0.032) were found to be independently associated with infection or colonisation with a ciprofloxacin-resistant strain.

A further analysis of prior antibiotic use is depicted in table 3. Only one cycle of fluoroquinolone treatment in the preceding year significantly increased the odds of being infected or colonised with a ciprofloxacin-resistant E. coli strain (OR: 2.80 (1.51–5.22), p <0.001), whereas one cycle of any antibiotic in the prior 12 months did not (OR: 1.36 (0.73–2.53), p = 0.339). However, the odds were significantly increased when multiple antibiotic cycles were recorded (OR: 4.40 (2.36–8.20), p <0.001), regardless of the antibiotic class used.

Antibiotic susceptibility of E. coli resistant and susceptible to ciprofloxacin

The cumulative antibiograms of ciprofloxacin-resistant and ciprofloxacin-susceptible E. coli strains are shown in table 4. Of the 345 isolates, 94 (27%) were resistant to ciprofloxacin. Compared with susceptible strains, ciprofloxacin-resistant E. coli strains showed significantly increased resistance rates to all antimicrobials tested, except for piperacillin-tazobactam and carbapenems (meropenem and imipenem). Among ciprofloxacin-susceptible strains, resistance to ampicillin (28%), tetracycline (20%) and trimethoprim-sulfamethoxazole (16%) was most prevalent. Ciprofloxacin-resistant strains produced extended-spectrum beta-lactamases (ESBL) significantly more often than ciprofloxacin-susceptible strains (p <0.0001).

Table 1Patient characteristics.
Total number of patients214 (100)61 (100) 
     Female121 (57)30 (50)0.312
     Male93 (43)31 (51)0.312
Age, median (95% CI)55.5 (49.2–58.1)63.8 (54.0–70.0)0.062
     Outpatients152 (71)26 (43)<0.001
     Inpatients62 (29)35 (57)<0.001
     Length of stay, days, median (95% CI)4 (4–6)7 (5–10)0.094
     Chronic Disease Score, median (95% CI)4.7 (3–5.5)3 (3–4)0.083
Clinical presentation   
     Asymptomatic bacteriuria41 (19)12 (20)1.000
     Asymptomatic bacteriuria with indwelling catheter18 (8)9 (15)0.148
     Acute, uncomplicated urinary tract infection74 (35)6 (10)<0.001
     Acute, uncomplicated pyelonephritis16 (7)1 (2)0.132
     Complicated urinary tract infection52 (24)28 (46)0.002
     Bacteremia0 (0)1 (2)0.222
     Other/unclear diagnosis13 (6)4 (7)1.000
Table 2Risk factors for urinary tract infections with ciprofloxacin-resistant E. coli.
Number of patients214 (100)61 (100)    
Male gender93 (43)31 (51)1.34 (0.76–2.38)0.3091.57 (0.77-3.17)0.212
Age >65 years78 (36)29 (48)1.58 (0.89–2.81)0.119 1.00 (0.50-2.01)0.995
In-hospital treatment62 (29)35 (57)3.30 (1.83–5.94)<0.0011.98 (0.95-4.12)0.069
Chronic Disease Score >3131 (50)16 (46)0.73 (0.32–1.70)0.470  
Diabetes mellitus15 (7)3 (5)0.69 (0.19–2.45)0.562  
Malignoma, non-urological4 (2)1 (2)0.88 (0.10–7.98)0.906  
Malignoma, urological18 (8) 10 (16)2.14 (0.93–4.91)0.074  
Nosocomial infection4 (2)1 (2)0.88 (0.10–7.98)0.906  
Recurrent urinary tract infection73 (34)33 (54)2.28 (1.28–4.05)0.0052.26 (1.07–4.78)0.032
Vesico-ureteral reflux1 (0)2 (3)7.22 (0.64–81.01)0.1093.77 (0.28–50.43)0.316
Benign prostatic hyperplasia225 (27)9 (29)1.30 (0.58–2.98)0.521  
Urolithiasis16 (7)10 (16) 2.43 (1.03–5.67) 0.0401.72 (0.61–4.85)0.303
Urologic surgery in last 12 months341 (19)27 (44)3.35 (1.82–6.16)<0.001  
Foreign material in upper urinary tract in last 12 months313 (6)12 (20)3.79 (1.63–8.81) 0.002  
Urinary catheter in last 12 months39 (18)33 (54)5.29 (2.87–9.75) <0.0012.41 (1.02–5.67)0.044
Fluoroquinoloneuse in last 12 months49 (23)36 (59)4.85 (2.66–8.85)<0.0012.24 (1.08–4.62)0.030
Use of other antibiotics in last 12 months56 (26)31 (51)2.92 (1.62–5.25)<0.0011.59 (0.79–3.20)0.195
Hospitalisation in Department of Urology in last 12 months22 (10)23 (38)5.28 (2.68–10.43)<0.0011.28 (0.50–3.26)0.607
Corticosteroids or other immunosuppressants in last 12 months9 (4)3 (5)1.18 (0.31–4.49) 0.810  
Renal insufficiency4 (2)3 (5)2.72 (0.59–12.48)0.1991.97 (0.32–12.06)0.464
Kidney transplant recipient1 (0)1 (2)3.55 (0.22–57.60)0.373   
HIV infection3 (1)1 (2)1.17(0.12–11.47)0.891  
1 inpatients, 2 in male patients, 3 these variables have been excluded in the multivariable analysis because of collinearity
Table 3Antibiotic treatment within the previous 365 days.
Total number of patients214 (100)61 (100)  
No prior treatment130 (61)14 (23)0.19 (0.10–0.37)<0.001
     1 cycle38 (18)23 (38)2.80 (1.51–5.22)0.001
     >1 cycle11 (5)13 (21) 5.00 (2.15–11.64)<0.001
All antibiotics    
     1 cycle51 (24) 19 (31)1.36 (0.73–2.53)0.339
     >1 cycle33 (15)28 (46) 4.40 (2.36–8.20)<0.001
Table 4Cumulative antibiograms of 345 E. coli isolates from 275 patients.
Ciprofloxacin251 (100)94 (100) 
Amoxicillin-clavulanate6 (2)17 (18)<0.001
Ampicillin71 (28)83 (90)<0.001
1st generation Cephalosporins9 (4)27 (29)<0.001
Gentamicin3 (1)39 (41)<0.001
Piperacillin-tazobactam5 (2)4 (4)0.262
Sulfamethoxazole and trimethoprim39 (16)57 (62)<0.001
Tetracycline50 (20)66 (72)<0.001
Tobramycin3 (1)18 (20)<0.001
Ceftazidime3 (1)12 (13)<0.001
Ceftriaxone1 (0)12 (13)<0.001
Meropenem5 (2)0 (0)0.329
Imipenem0 (0)0 (0)n.a.
Extended-Spectrum Beta-Lactamase producing strain 1 (0)10 (11)<0.001


The aim of this study was to identify risk factors for colonisation or infection with ciprofloxacin-resistant E. coli in patients treated at the Department of Urology of the University Hospital Zurich. Our analysis demonstrated that 22% of the population under study was infected or colonised with ciprofloxacin-resistant E. coli. Recurrent urinary tract infections, urinary catheterisation within the last 12 months and use of fluoroquinolones in the last 12 months turned out to be independently associated with ciprofloxacin-resistant strains. Those resistant strains were often also resistant to other antibiotics, mostly against ampicillin (90%) and tetracyclin (72%). Fluoroquinolones turned out to be the most frequently prescribed antibiotics for treatment of acute uncomplicated UTI, acute uncomplicated pyelonephritis and complicated UTI.

Our study documents risk factors for UTIs caused by ciprofloxacin-resistant E. coli in patients at a tertiary care urology centre. The population studied is exceptional in respect to the high prevalence of diseases that facilitate urinary tract infections, for example urinary tract obstructions, or foreign material in the upper and lower urinary tract. The study has several limitations. Internal validity may be reduced, as measurement bias might have been introduced by collecting demographic and medical information by chart review. Charts of outpatients are usually not as detailed as those of inpatients, probably accounting for systematic deviations in the availability of information. Recall bias might have been introduced as patients with underlying urinary tract disorders might more appropriately report their antibiotic treatment history. In outpatients, antibiotic therapy for UTI is usually started empirically and cultures are only performed if the patient fails to respond to treatment, has recurrent episodes of UTI or has complicated UTI [18, 19]. Thus, data on resistance rates based on laboratory surveillance may overestimate the true levels of antibiotic resistance in the community, accounting for selection bias. However, since most urinary samples obtained at the Department of Urology are sent for bacterial culture, the 22% resistance rate of E. coli to ciprofloxacin is likely to be a realistic number for the population under study. Generalisation of these results may be restricted as these data were collected in a single hospital department in one geographic area during an 18 months period. The odds ratios may be different in other settings, even within Switzerland.

Risk factors for ciprofloxacin-resistant E. coli in UTIs have been presented by other authors [9–13]. The results of our study are in agreement with risk factors previously reported, with prior exposure to fluoroquinolones being the most commonly described factor to increase risk. Whereas other authors tried to find an association with the presence of a urinary catheter at the time of detection of the ciprofloxacin-resistant strain [11, 12], we included prior urinary tract catheterisation within one year as a possible risk factor. However, multivariable analysis did not reveal prior urinary tract catheterisation as an independent risk factor. In contrast, Arslan et al. found an association between ciprofloxacin resistance and complicated UTIs, including those patients with urinary catheters in situ [10]. Others have been able to show a correlation between age (50 years and 65 years or older, respectively) and fluoroquinolone resistance [9–11], whereas we could not. Differences between studies may have arisen due to different settings, different populations under study, and, to some extent, disregard of collinearity and cocausality in multivariable analyses.

During the study period, local guidelines of the University Hospital Zurich recommended a three day course of norfloxacin or trimethoprim/sulfamethazol for the treatment of acute, uncomplicated UTI in young women, and a 5 day course in men. Ciprofloxacin was only recommended as a first-line agent in the treatment of uncomplicated acute pyelonephritis. The results of our study show that those recommendations were not followed properly, as ciprofloxacin turned out to be the most frequently prescribed antibiotic for treatment of acute, uncomplicated UTIs. The fact that ciprofloxacin is often given inappropriately is alarming. However, as there is no evidence that norfloxacin has a lower capacity than ciprofloxacin to select for fluoroquinolone resistant strains, it cannot be assumed that following the institutional guidelines would have resulted in a lower prevalence of fluoroquinolone resistant strains of E. coli. Naber et al. demonstrated that most participants (microbiologists, infectious disease clinicians and clinicians with an interest in the management of UTIs) underestimated fluoroquinolone use in the management of acute, uncomplicated lower UTI and that they considered the high level of usage to be inappropriate from a societal perspective (risk of increased resistance) [3]. This suggests that part of decreasing the usage of fluoroquinolones is to inform clinicians about their high prescription rate as they tend to underestimate their use and are sometimes not aware of the high selection pressure. In the study by Van Hees et al. about strategies to optimise the use of ciprofloxacin, it could be shown that the numbers of inappropriate prescriptions can be reduced and the quality of prescriptions improved by educational interventions [20]. Similar investigations by Feucht et al. demonstrated that education of physicians resulted in an increase in appropriate empiric antibiotic use, a decrease in duration of inappropriate use, and a decrease in duplicate gram-negative coverage [21].

Across Europe, fluoroquinolone resistance rates show large differences, being generally high in southern Europe and low in northern European countries [6, 7]. These geographical variations are also seen in antibiotic consumption [4, 6, 22], which is being recognised as the main cause of emerging resistance [11, 23, 24]. Those international differences may be explained by different antimicrobial guidelines as well as cultural, demographic and socioeconomic factors, for instance, over-the-counter sales or physicians’ and patients’ attitudes to antibiotics. In 2002, Switzerland was the country with the lowest antibiotic consumption in the community in Europe. However, fluoroquinolones accounted for a share of 20.1% thereof, which is a much higher proportion compared to an average of 7.3% in the other European countries [25]. Although antibiotic consumption in our country is still considered to be low, continuous monitoring of resistance development is essential to adapt guidelines for empirical antimicrobial therapy. In 2008, according to the SEARCH database (Sentinel Surveillance of Antibiotic Resistance in Switzerland), the rate of non-susceptible E. coli to older fluoroquinolones in urogenital infections of inpatients and outpatients aged ≥15 years reached 17.2% and 17.1%, respectively [26].

To halt the process of resistance development, susceptibility testing to first-generation fluoroquinolones (e.g. nalidixic acid) may be considered, as they indicate single mutation in the gyrA-gene whereof at least two are needed to provide relevant resistance to later generation fluoroquinolones [27–29]. It has previously been suggested that selection pressure could be reduced by refraining from fluorquinolone use when resistance to nalidixic acid is detected in order to decelerate the accumulation of single mutations [11, 27, 29]. Nonetheless, resistance of E. coli is not only selected by the use of fluoroquinolones, but also by the use of unrelated antimicrobial classes including ampicillin, amoxicillin, trimethoprim or sulfamethoxazole alone, and trimethoprim-sulfamethoxazole [7]. Therefore, to decrease selection pressure to those ‘classic’ antibiotics, more frequent use of other antibiotics, for example nitrofurantion and fosfomycin, may be considered. In complicated UTIs, microbiological testing is essential to ensure adequate therapy because of high resistance rates.

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Joëlle Nicolettia*,
Stefan P. Kustera*, Tullio Sulserb,
Reinhard Zbindenc, Christian Ruefa,
Bruno Ledergerbera, Rainer Webera

a Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland
b Department of Urology, University Hospital Zurich, Zurich, Switzerland
c Institute of Medical Microbiology, University of Zurich, Zurich, Switzerland

* Contributed equally.

The authors declare no financial or commercial conflict of interest.

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Prof. Dr. med. Rainer Weber

Division of Infectious Diseases and Hospital Epidemiology University Hospital Zurich

University of Zurich

Raemistrasse 100

CH-8091 Zurich


E-Mail: rainer.weber@usz.ch