Skip to main content

Catheter-associated bacterial flora in patients with benign prostatic hyperplasia: shift in antimicrobial susceptibility pattern



Men with urinary retention secondary to benign prostatic hyperplasia (BPH) are prone to genitourinary infections. Physicians should be aware of the current antimicrobial susceptibility pattern in this population if empirical treatment is needed. The goal of this study was to evaluate variations in prevalence, composition and antimicrobial susceptibility of bacterial flora in men with indwelling catheters subjected to surgery for BPH in chosen time periods since 1994. Necessary changes in empirical therapy were also assessed.


All patients with indwelling catheters admitted to a single urological center for BPH surgery in the years 1994–1996, 2004–2006, and 2011–2015 were considered. Catheterization times and results of urine cultures from samples collected at admission were evaluated. Susceptibility for selected antimicrobials was compared separately for Gram negative and Gram positive species. For each agent and for their combinations effectiveness of empirical therapy was calculated dividing the number of patients with bacteriuria susceptible to the agents by the total number of patients with bacteriuria.


Bacteriuria was present in 70% of 169, 72% of 132, and 69% of 156 men in the respective time periods. The incidence of Gram-positive strains increased from 10 to 37% (P < 0.001). Their susceptibility to amoxicillin/clavulanate was fluctuating (81, 61, 77%; P=NS). No vancomycin-resistant strain was present. Gram-negative flora composition was stable. Their susceptibility decreased to ciprofloxacin (70 to 53%; P = 0.01) and amoxicillin/clavulanate (56 to 37%; P < 0.01) while it increased to gentamycin (64 to 88%; P < 0.001) and co-trimoxazole (14 to 62%; P < 0.001); susceptibility to amikacin remained high (> 85%). Only two cases of resistance to carbapenems in 2004–2006 were found. In vitro effectiveness of amikacin + amoxicillin/clavulanate in empirical therapy was slowly decreasing (87 to 77%; P=NS). Imipenem was found the most effective single agent (90–95%) and its efficacy was even improved by adding vancomycin (97–98%).


Substantial rise in the incidence of Gram-positive species and fluctuations in antimicrobial susceptibility patterns were found. Empirical therapy of genitourinary infection in catheterized men with BPH should now involve antimicrobial agents effective both to Enterococci and Enterobacteriaceae. Periodic monitoring and publishing data on antimicrobial susceptibility for this population is necessary.

Peer Review reports


Catheter-associated urinary tract infection (CAUTI) is the most common of all healthcare-associated infections [1]. Despite best care and precautions, long-term catheterization is linked to an almost 100% risk of bacteriuria [2, 3], and up to 80% of catheter-associated strains are resistant to multiple drugs [4, 5]. Permanently or temporarily catheterized patients represent a significant proportion of urological ward patients, and knowledge about resistance patterns is crucial in emergencies when empirical treatment is started. Changes in CAUTI bacterial flora can also be used for monitoring drug resistance in the population because in this patient group, resistant pathogens accumulate as a result of biofilm formation, pressure from antibiotics used for prevention or treatment of CAUTI, and occasional contact with contaminated medical facilities.

Recent European Association of Urology guidelines state that empirical management of CAUTI should be carried out with broad-spectrum antibiotics based on local susceptibility patterns [6]. However, no reports are currently available on the susceptibility of catheterized patients according to the specific reason for catheterization.

Among patients treated at urological departments, the largest group consists of men with urinary retention caused by benign prostatic hyperplasia (BPH) who are admitted for surgical removal of obstruction. In this homogeneous group, we have monitored species composition and resistance patterns since 1994 and have already published on differences after one decade [7]. After another 10-year period, we decided to look again for new trends of resistance in this population. Thus, the primary goal of the current study was to examine the evolution of bacterial species distribution and antibiotic susceptibility patterns of strains isolated from urine of catheterized patients with BPH-related urine retention in a tertiary referral urology department in the last 20 years. The other equally important goal was to consider the necessary changes in the empirical therapy of genitourinary infections in this group of patients. 


Patients and data collection

This retrospective study was conducted at a single academic urological department according to the Declaration of Helsinki. All patients signed informed consent for using their results of routine tests carried out during hospitalization for research purposes. Microbiological data were analyzed for all patients with indwelling transurethral catheters scheduled for surgical treatment of BPH in three time periods: 1994–1996 (Period 1), 2004–2006 (Period 2), and 2011–2015 (Period 3). Patients with other types of obstruction or other methods of urine diversion were not analyzed. In addition, patients without reliable and up-to-date urine culture results were excluded. Data on the presence of bacteriuria, bacterial species, and their resistance to antibiotics as well as time of catheterization measured from installation until hospital admission were obtained from medical records.

Urine culture collection and analysis

Urine samples for microbiological evaluation were collected during the first 12 h after admission, obtained from catheters during their replacement on ward. Bacterial strains and their resistance were evaluated if significant bacteriuria, defined as > 103 cfu/ml after 24-h incubation at 37 °C, was detected. Contamination was diagnosed when common nonpathogenic strains were grown or more than four strains were found. Bacteria were identified according to standard methods [8]. Isolates were speciated by routine procedures, which included colonial characteristics, Gram-staining, Vitek 2 or Vitek MS (bioMerieux, France) system assays. Susceptibility testing was performed with the disc diffusion method using Mueller Hinton II Agar (MHE, bioMerieux, France) or the VITEK 2 (bioMerieux, France) system. The choice of antimicrobial agents used in susceptibility testing depended on the species of bacteria and the year of examination. Interpretation of test results was based on the recommendations of the Clinical Laboratory Standards Institute to the 2012 and from 2012 to the present in accordance with European Committee on Antimicrobial Susceptibility Testing. Possible susceptibility test results were scored S (sensitive), I (intermediately sensitive), and R (resistant). In further analysis, strains were scored either as sensitive (S and I) or resistant (R).

As a result of differences in antibiotics included routinely in susceptibility testing between the periods of 2004–2006 and 2011–2015, comparative analysis of resistance was based only on drugs used in all analyzed periods and included in the case of Gram-negative bacteria: amoxicillin with clavulanic acid (amox/clav), cefuroxime, cefotaxime, ceftazidime, gentamicin, amikacin, imipenem, ciprofloxacin, cotrimoxazole, and nitrofurantoin. In the case of Gram-positive bacteria amox/clav, imipenem and vancomycin were analyzed. Additionally, for Enterococci, the most frequent among Gram-positive isolates, test for the resistance to the high levels of the aminoglycosides (HLAR) was performed using disc diffusion method with discs with gentamycin (120 micrograms) and streptomycin (300 micrograms). In the case of the representatives the Enterobacteriaceae family, test for the detection of the ESBL (Extended-Spectrum Beta-Lactamases) was performed, using discs diffusion method and discs with standard concentrations of aztreonam, ceftazidime, cefepime and amox/clav in the middle. The proportion of susceptible organisms was calculated by dividing the number of urinary isolates resistant to each antibiotic by the number of organisms tested against that antimicrobial agent.

Statistical analysis

Continuous variables are presented as medians accompanied by ranges or interquartile ranges. Differences among the periods (1994–1996, 2004–2006, and 2011–2015) were evaluated with the Mann–Whitney test for continuous variables and by the chi-square test for categorical variables (including strains and resistance patterns). Influence of catheterization time on bacteriuria occurrence and number of species isolated from a single urine sample was evaluated with Mann–Whitney and rho-Spearman tests, respectively. For all statistical analyses, a two-sided P value < 0.05 was considered statistically significant. Statistical analysis was performed using STATISTICA 12 (StatSoft, USA).


A total of 169, 132, and 156 patients hospitalized in 1994–1996 (Period 1), 2004–2006 (Period 2), and 2011–2015 (Period 3), respectively, met inclusion criteria. Bacteriuria was found in 119 (70%) individuals in Period 1, 95 (72%) in Period 2, and 107 (69%) in Period 3. Escherichia coli was the most prevalent uropathogen in all periods (22, 25, 27%), followed by Proteus mirabilis (14%) in the 90-ties, and Enterococcus faecalis in the Periods 2 (14%) and 3 (19%). All significant species are given in Table 1.

Table 1 Bacterial species isolated from urine of men with benign prostatic hyperplasia and indwelling catheters in given time periods

Median catheterization time was shortest in Period 1 (2 months), followed by Periods 2 and 3 (3 months). For patients with bacteriuria median catheterization time was longer than for those with negative urine cultures in Periods 1 (2 vs 1.75 months; P < 0.01) and 2 (3 vs 2 months; P < 0.05) but not in Period 3 (3 months in both). Frequently more than one species was isolated from urine of catheterized patients. Two or more species were present in 25 (21%), 37 (39%), and 35 (33%) patients of those with bacteriuria in consecutive Periods. In Periods 2 and 3, catheterization time was positively correlated with the number of isolated strains (rs = 0.3 P < 0.01 and rs = 0.25 P = 0.02 respectively), but no such correlation was found for Period 1 (rs = 0.18 P = 0.06). Gram-positive only bacteriuria was steadily growing. It was found in 10/119 (8%), 11/95 (11.6%), and in 18/107 (17%) patients of those with bacteriuria respectively. Mixed bacteriuria of Gram-negative and Gram-positive organisms was found in 2 (1.7%), 21 (22%) and 21 (19.6%) patients in the consecutive Periods. While all Gram-positive bacteria were susceptible to amox/clav and to imipenem in Period 1, in the following Periods resistant strains of Enterococcus faecium and Staphylococci were already reported, and susceptibility rate dropped by at least 20%. For Gram-negative species significant changes in both directions in susceptibility to various antimicrobial agents were noted. Detailed susceptibility patterns for Gram-negative and Gram-positive species for all Periods are presented in Table 2. The right choice of empirical therapy can be made with use of data presented in Table 3. It shows in vitro susceptibility patterns of whole bacterial flora identified in samples from individual patients to antibiotics and their combinations. Looking at data in this way amikacin was the most effective choice in Period 1 when susceptibility data for some antibiotics were not available for all patients. In the following Periods efficacy of amikacin alone dropped. In years 2004–06 and 2011–15 its combination with amox/clav was effective in around 80% of patients. At the same time imipenem was the most effective single agent (90–95%). Combination of imipenem with vancomycin increased susceptibility of the flora in specimen to maximum 98%.

Table 2 Susceptibility of Gram-negative and Gram-positive strains isolated from patients with indwelling catheters
Table 3 Susceptibility to selected antibiotics or their combinations of bacterial flora in patients with benign prostatic hyperplasia and indwelling catheters


This report is the first to specifically characterize bacteriuria in patients with urinary retention secondary to BPH. These patients require special attention of urologists because they are common in our departments, undergo transurethral procedures, that bear high risk of infectious complications and also they may be a source of contamination with multidrug resistance strains. Finally, during several weeks with a catheter, men are prone to infective complications, such as epididymitis, prostatitis, and symptomatic lower urinary tract infections (UTIs). As current urine culture is rarely available when complications arise, empirical therapy is usually implemented and knowledge of antimicrobial susceptibility pattern becomes crucial.

Our data show several characteristic trends in the composition and antimicrobial susceptibility of bacterial flora that occurred during the studied period. First, the percentage of Gram-positive bacteria increased significantly. Whereas in the 90’s it could be assumed that Gram-negative bacteria were responsible for vast majority of CAUTI (90% of patients had Gram-negative species only), later the percentage of patients contaminated with Gram-positive only or with mixed flora involving Gram-positive germs increased significantly. Gram-positive strains in Period 1 were few and all susceptible to amox/clav and imipenem. After ten years appearance of Enterococcus faecium and resistant Staphylococci caused that those agents had become less effective. At the same time susceptibility Gram-negative flora to fluoroquinolones decreased significantly while susceptibility to cotrimoxazole and gentamicin increased at the same time. The trend for fluoroquinolones has already been reported extensively and attributed to the enormous use of these antibiotics in medicine and in livestock breeding [9]. The improvement in the effectiveness of cotrimoxazole and gentamicin is probably related to lower popularity of both drugs but this issue was investigated to a lesser extent [10, 11]. Whether these trends are universal or not is hard to conclude as results reported by investigators vary.

Studies on antimicrobial resistance of bacteria causing catheter-associated infections are scarce, and none are focused on this specific group of patients. An analysis by Jiménez-Alcaide et al. included all patients with any type of urinary catheter or stent and symptomatic UTI hospitalized in 2012–2013 in a single urological ward [12]. About a quarter of their group consisted of patients with indwelling catheters on admission who might be considered similar to our patients. Another group analyzed samples of urine collected from unspecific catheterized patients in India with UTI symptoms [4]. Valuable data on CAUTI among patients in US acute care hospitals and inpatient rehabilitation facilities also come from reports from the US Centers for Disease Control and Prevention (CDC) National Healthcare Safety Network. A recent update covered the years 2011–2014 [1] and reported on over 138,000 CAUTI events. Data on bacteriuria in catheterized patients in nursing homes from a single Swedish county were presented in a cross-sectional study from 2011 [13], but in contrast to other studies, this group consisted mainly of asymptomatic women and men – only 7% used antibiotics when the sample was collected. However, age, sex, and time of catheterization (70% catheterized longer than 12 months) make this study significantly different from ours. Some CAUTI studies have focused on a specific bacteria species (e.g., Proteus spp. [14]) and others on specific resistance mechanisms (e.g., extended-spectrum beta-lactamase (ESBL) [15, 16]). In those reports, the groups also were not disease-specific, and time of catheterization was not reported.

In contrast, our study reports on a very well-defined group of men with one urological condition, catheterized for a period of several weeks to months. It also offers a 20-year perspective on changes in microbial composition and antimicrobial resistance in a single center, which is unique among papers on CAUTI. Due to the lack of more similar studies, it was decided to compare our results with the aforementioned analyses. A high rate of Gram-positive bacteria in catheter-associated flora was confirmed in some of the mentioned studies (16% [1], 21% [8], 31% [12]) but not all (2% [4]), which may reflect geographical variability. Gram-positive bacteria reported in our series are highly susceptible to amox/clav. However, in the male genitourinary tract, this antibiotic, as well as ampicillin, is not always effective because of low penetration to prostatic tissue [17, 18]. Instead high penetrability has been confirmed for carbapenems and vancomycin [19, 20]. Moreover, E. faecalis resistance to amox/clav was already reported to be as high as 20% [12]. With an increasing number of vancomycin-resistant enterococci (VRE) - colonized patients in our department (data on file) and reported by other groups (8% [1]), we predict that BPH patients with catheters colonized by these germs will soon appear.

The choice of antibiotic for treatment of Gram-negative species is a much more difficult task. Rising resistance to fluoroquinolones means that this group, which penetrates very well to prostatic tissue, should not be used any more for empirical treatment of complicated UTIs. A significant decrease in resistance to cotrimoxazole still does not mean that this drug can replace fluoroquinolones. Among agents available in oral formulations, none can be used without urine culture. Despite methodological differences, a high resistance to fluoroquinolones and cotrimoxazole is convincingly confirmed by other studies (17% [13], 33% [1], 50% [12]). The ESBL prevalence of 20% in our group presents the same level as US and Spanish hospitalized patients with CAUTI [1, 12] and among European participants in the SMART study [21]. Toner et al. found that an indwelling catheter almost doubles the risk for ESBL-producing strains in urine [22]. Susceptibility to amikacin among Gram-negative species is still high, but significant prevalence of Enterococci makes this drug poor choice if used alone. Carbapenems is the last resort, however, as in the case of VRE, we can predict growth in the number of carbapenemase-producing strains in the near future. At the Spanish urological department, resistance against amikacin was less frequent than against carbapenems (3% vs 10% for E. coli) [12]. The US CDC has reported similar numbers [1]. An older global study on nosocomial UTI showed highest susceptibility to imipenem [23]. A low prevalence of two species, Acinetobacter baumanii and Klebsiella pneumoniae, which are the most common producers of carbapenemase, may explain the difference between our results and those in other reports cited here. Apart from geographical variations, exposure to hospital strains also may be a reason. Although our patients visited only outpatient clinics before they entered the ward for surgery, patients from other studies usually were recruited among already hospitalized populations, some of them after urological procedures. In Swedish nursing homes, carbapenemase-bearing strains were also not reported [13]. Considering antimicrobial resistance, our results can be placed between those obtained from hospitalized patients [1, 12] and patients in Swedish decentralized geriatric care facilities where strict adherence to the Swedish Strategic Programme against Antibiotic Resistance recommendations is a rule.

There are some limitations of this study. The main one is the fact that the data come from a single center. Differences in species composition and susceptibility between different continents, countries and centers result from local patterns of antibiotics use, hygienic conditions, migration, or the time of the average catheterization time. Similar analyses should be performed locally in other centers and promotion of this issue was one of our additional goal. Another weakness is the heterogeneous composition of antibiograms. Therefore, only a few antibiotics were repeatedly evaluated in the three Periods studied. Also, we did not have the original minimum inhibitory concentration data and the standard of susceptibility is different prior to and after 2010.

Although our findings do not refer strictly to the situation in other countries and other clinical conditions, we think that taking into account the trends identified in other studies, the significance of these results remains broadly relevant.


Between 1994 and 2015 substantial rise in the incidence of Gram-positive species in catheter-associated bacterial flora was discovered. This fact, together with fluctuations in antimicrobial susceptibility patterns, make necessary a switch in empirical therapy of CAUTI from Gram-negative targeted agents to therapy effective also to Gram-positive species [24].The choice of drugs in the empirical treatment of genitourinary infection in a male with a catheter was and still is limited to amikacin or carbapenems for Enterobacteriaceae and amox/clav, carbapenems or vancomycin for Enterococci. The final choice depends on the localization and severity of infection as well as renal function. Monitoring of catheter-associated bacteria resistance patterns reflects trends in the outpatient population, and these surveillance efforts should be continued independent from monitoring hospital-acquired infections.



Benign prostatic hyperplasia


Catheter-associated urinary tract infection


US Centers for Disease Control and Prevention


Extended-Spectrum Beta-Lactamases


Resistance to the high levels of the aminoglycosides


Urinary tract infection


Vancomycin-Resistant Enterococci


  1. 1.

    Weiner LM, Webb AK, Limbago B, et al. Antimicrobial-resistant pathogens associated with healthcare-associated infections: summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2011-2014. Infect Control Hosp Epidemiol. 2016;37:1288–301.

    Article  Google Scholar 

  2. 2.

    Warren JW. Catheter-associated urinary tract infections. Int J Antimicrob Agents. 2001;17:299–303.

    CAS  Article  Google Scholar 

  3. 3.

    Wilde MH. Urinary tract infection in people with long-term urinary catheters. J Wound Ostomy Cont Nurs Off Publ Wound Ostomy Cont Nurses Soc. 2003;30:314–23.

    Google Scholar 

  4. 4.

    Subramanian P, Shanmugam N, Sivaraman U, Kumar S, Selvaraj S. Antiobiotic resistance pattern of biofilm-forming uropathogens isolated from catheterised patients in Pondicherry. India Australas Med J. 2012;5:344–8.

    Article  Google Scholar 

  5. 5.

    Bi X-C, Zhang B, Ye Y-K, et al. Pathogen incidence and antibiotic resistance patterns of catheter-associated urinary tract infection in children. J Chemother Florence Italy. 2009;21:661–5.

    Article  Google Scholar 

  6. 6.

    Grabe M, Bartoletti R, Bjerklund-Johansen T.E., et al. Guidelines on urological infections. European Association of Urology, Arnhem (2015).

  7. 7.

    Zapała Ł, Dybowski B, Bres-Niewada E, Sonczyk A, Adamska A, Borkowski A. Bacterial flora of lower urinary tract in men with indwelling catheters in years 1994-1996 and 2004-2006. Urologia Polska. 2008;61:240–5.

    Google Scholar 

  8. 8.

    Balows A. Manual of clinical microbiology: Elsevier; 2000.

  9. 9.

    Dalhoff A. Resistance surveillance studies: a multifaceted problem—the fluoroquinolone example. Infection. 2012;40(3):239–62.

    CAS  Article  Google Scholar 

  10. 10.

    Batra P, Deo V, Mathur P, Gupta AK. Cotrimoxazole, a wonder drug in the era of multiresistance: case report and review of literature. J Lab Physicians. 2017;9(3):210–3.

    CAS  Article  Google Scholar 

  11. 11.

    Park JJ, Seo YB, Lee J. Antimicrobial susceptibilities of Enterobacteriaceae in community-acquired urinary tract infections during a 5-year period: a single hospital study in Korea. Infection & Chemotherapy. 2017;49(3):184–93.

    Article  Google Scholar 

  12. 12.

    Jiménez-Alcaide E, Medina-Polo J, García-González L, et al. Healthcare-associated urinary tract infections in patients with a urinary catheter: risk factors, microbiological characteristics and patterns of antibiotic resistance. Arch Esp Urol. 2015;68:541–50.

    PubMed  Google Scholar 

  13. 13.

    Jonsson K, Claesson BEB, Hedelin H. Urine cultures from indwelling bladder catheters in nursing home patients: a point prevalence study in a Swedish county. Scand J Urol Nephrol. 2011;45:265–9.

    Article  Google Scholar 

  14. 14.

    Moryl M, Torzewska A, Jałmuzna P, Rózalski A. Analysis of Proteus mirabilis distribution in multi-species biofilms on urinary catheters and determination of bacteria resistance to antimicrobial agents. Pol J Microbiol. 2013;62:377–84.

    PubMed  Google Scholar 

  15. 15.

    Spadafino JT, Cohen B, Liu J, Larson E. Temporal trends and risk factors for extended-spectrum beta-lactamase-producing Escherichia coli in adults with catheter-associated urinary tract infections. Antimicrob Resist Infect Control. 2014;3:39.

    Article  Google Scholar 

  16. 16.

    Bonkat G, Müller G, Braissant O, et al. Increasing prevalence of ciprofloxacin resistance in extended-spectrum-β-lactamase-producing Escherichia coli urinary isolates. World J Urol. 2013;31:1427–32.

    CAS  Article  Google Scholar 

  17. 17.

    Klotz T, Braun M, Bin Saleh A, Orlovski M, Engelmann U. Penetration of a single infusion of ampicillin and sulbactam into prostatic tissue during transurethral prostatectomy. Int Urol Nephrol. 1999;31:203–9.

    CAS  Article  Google Scholar 

  18. 18.

    Madden T, Doble A, Aliyu SH, Neal DE. Infective complications after transrectal ultrasound-guided prostate biopsy following a new protocol for antibiotic prophylaxis aimed at reducing hospital-acquired infections. BJU Int. 2011;108(10):1597–602.

    CAS  Article  Google Scholar 

  19. 19.

    Wang H, Chen Z, Zhu Y, Wang T, Wu X. Penetrability and therapeutic effect of vancomycin to the prostates of rats with bacterial prostatitis (BP) or BPH-BP. Zhonghua Nan Ke Xue Natl J Androl. 2006;12:490–5.

    CAS  Google Scholar 

  20. 20.

    Charalabopoulos K, Karachalios G, Baltogiannis D, Charalabopoulos A, Giannakopoulos X, Sofikitis N. Penetration of antimicrobial agents into the prostate. Chemotherapy. 2003;49(6):269–79.

    CAS  Article  Google Scholar 

  21. 21.

    Morrissey I, Hackel M, Badal R, Bouchillon S, Hawser S, Biedenbach D. A review of ten years of the study for monitoring antimicrobial resistance trends (SMART) from 2002 to 2011. Pharm Basel Switz. 2013;6:1335–46.

    Google Scholar 

  22. 22.

    Toner L, Papa N, Aliyu SH, Dev H, Lawrentschuk N, Al-Hayek S. Extended-spectrum beta-lactamase-producing Enterobacteriaceae in hospital urinary tract infections: incidence and antibiotic susceptibility profile over 9 years. World J Urol. 2016;34:1031–7.

    CAS  Article  Google Scholar 

  23. 23.

    Tandogdu Z, Cek M, Wagenlehner F, et al. Resistance patterns of nosocomial urinary tract infections in urology departments: 8-year results of the global prevalence of infections in urology study. World J Urol. 2014;32:791–801.

    CAS  PubMed  Google Scholar 

  24. 24.

    Wagenlehner FM, Cek M, Naber KG, Kiyota H, Bjerklund-Johansen TE. Epidemiology, treatment and prevention of healthcare-associated urinary tract infections. World J Urol. 2012;30:59–67.

    CAS  Article  Google Scholar 

Download references


Not applicable.


No funding was obtained for this study.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

Author information




All authors listed on the manuscript have contributed significantly to the study. Each author made substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data; has been involved in drafting the manuscript or revising it critically for important intellectual content; has given final approval of the version to be published. Each author have participated sufficiently in the work to take public responsibility for appropriate portions of the content and agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. BD - conception and design, acquisition of data, analysis and interpretation of data; PZ - conception and design, acquisition of data, analysis and interpretation of data; EBN - conception and design acquisition of data, analysis and interpretation of data; ŁZ - conception and design acquisition of data, analysis and interpretation of data; NMZ - acquisition of data, analysis and interpretation of data; SP - acquisition of data, analysis and interpretation of data; GM – analysis and interpretation of data; supervision; PR - analysis and interpretation of data; superivison. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Piotr Zapała.

Ethics declarations

Competing interest

The authors declare that they have no competing interests.

Ethics approval and consent to participate

This is a retrospective study. For this type of study formal consent is not required based on policy of Ethical Committee by Medical University of Warsaw. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

All patients signed informed consent for using their results of routine tests carried out during hospitalization for research purposes.

Consent for publication

Not applicable.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted 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. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Dybowski, B.A., Zapała, P., Bres-Niewada, E. et al. Catheter-associated bacterial flora in patients with benign prostatic hyperplasia: shift in antimicrobial susceptibility pattern. BMC Infect Dis 18, 590 (2018).

Download citation


  • Antimicrobial Susceptibility Patterns
  • Benign Prostatic Hyperplasia (BPH)
  • Catheterization Time
  • Genitourinary Infections
  • Effective Single Agent