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Increased resistance of gram-negative urinary pathogens after kidney transplantation

  • Johannes Korth1Email author,
  • Julia Kukalla1,
  • Peter-Michael Rath3,
  • Sebastian Dolff2,
  • Marco Krull4,
  • Hana Guberina2,
  • Anja Bienholz1,
  • Benjamin Wilde1,
  • Stefan Becker1,
  • Birgit Ross4,
  • Olympia Evdoxia Anastasiou5,
  • Andreas Kribben1 and
  • Oliver Witzke2
BMC NephrologyBMC series – open, inclusive and trusted201718:164

https://doi.org/10.1186/s12882-017-0580-z

Received: 9 November 2016

Accepted: 11 May 2017

Published: 19 May 2017

Abstract

Background

Urinary tract infection is the most common complication after kidney transplantation. It can cause severe sepsis and transplant loss. Emergence of drug resistance among gram-negative urinary pathogens is the current challenge for urinary tract infection treatment after kidney transplantation.

Methods

This study analyzes the antimicrobial susceptibility of gram-negative urinary pathogens after kidney transplantation from 2009 to 2012 at the Transplant Outpatient Clinic of the University Hospital Essen, Germany. Kidney transplant patients at the University Hospital Essen receive regular follow up examinations after transplantation. Midstream urines were examined for bacteriuria at each follow up visit.

Results

From 2009 to 2012 15.741 urine samples were obtained from 859 patients. In 2985 (19%) samples bacterial growth was detected. The most frequently detected gram-negative bacteria were E.coli 1109 (37%), Klebsiella spp. 242 (8%) and Pseudomonas aeruginosa 136 (4.5%). Klebsiella spp. showed a significant increase of resistance to trimethoprim-sulfamethoxazole by 19% (p = 0.02), ciprofloxacin by 15% (p = 0.01) and ceftazidime by 17% (p = 0.004). E.coli and P. aeruginosa isolates presented no significant differences of antimicrobial susceptibility to the analyzed antibiotics.

Conclusions

Antimicrobial resistance of Klebsiella spp. increased significant to trimethoprim-sulfamethoxazole, ciprofloxacin and ceftazidime from 2009 to 2012.

Keywords

Urinary tract infection Antimicrobial susceptibility Klebsiella spp. E.Coli, kidney transplantation Gram-negative urinary pathogens

Background

Urinary tract infection (UTI) is the most common infection after kidney transplantation [13]. It is also one of the most common causes for allograft failure, sepsis and mortality after transplantation. The risk for UTI after kidney transplantation is highest during the first year of transplantation with up to 60% [4]. Other risk factors are advanced age, female sex, diabetes mellitus and vesicoureteral reflux [5].

The incidence of drug resistant urinary pathogens seems to be increasing and has become a rising therapeutic challenge for clinicians. Drug resistant strains seem to have significant negative impact on the clinical course [69]. The rising incidence of resistant strains may be due to high antibiotic exposure. Antibiotic exposure could be identified as a risk factor for emerging resistance in gram-negative bacteria in other settings [10]. The antibiotic exposure after kidney transplantation is elevated due to treatment of asymptomatic bacteriuria (ASB) and pneumocystis pneumonia (PCP) prophylaxis.

The current treatment strategies of UTI after kidney transplantation are not defined or standardized. Most transplant center strategies include antibiotic treatment of ASB [11, 12]. The local UTI treatment strategy of the University Hospital Essen contains treatment of ASB as well [13].

This study investigates the prevalence of urinary pathogens and the resistance patterns in a cohort of kidney transplant patients during a period of 4 years (2009–2012) [1416].

Methods

Study population and design

The present study was conducted at the University Hospital Essen, Germany. It compares retrospectively the antimicrobial susceptibility of gram-negative uropathogens isolated from kidney transplant recipients older than 18 years from 2009 to 2012. Patients with at least one sample per year with antibiotic resistance were assigned to the antibiotic resistant group. Analysis focused on the most common gram-negative pathogens that cause UTI including E. coli, Klebsiella spp., and Pseudomonas aeruginosa [17]. The evaluated antibiotics were chosen based on the use in the local guidelines for treatment of UTI and pneumocystis prophylaxis. E. coli and Klebsiella spp. were analyzed for susceptibility to ceftazidime, piperacillin/tazobactam, ciprofloxacin and trimethoprim-sulfamethoxazole. P. aeruginosa was analyzed for susceptibility to ceftazidime, piperacillin and ciprofloxacin. To answer if a shift of complicated UTI after renal transplantation occurred during observation period, the cases of urosepsis due to gram negative pathogens were documented and correlated to the number of urine cultures with gram negative pathogens (E.coli, Klebsiella spp., P. aeruginosa). To determine recurrence of resistant urinary pathogens, the frequency of single and multiple detected E.coli and Klebsiella spp. isolates was recorded. The susceptibility to ceftazidime, piperacillin/tazobactam and ciprofloxacin was analyzed to evaluate if antimicrobial resistance was linked to recurrent pathogen detection. This study has been approved by ethics committee of the medical faculty of the University Duisburg-Essen (16–6952-BO).

Study procedures

After transplantation all patients receive regular follow up examinations at the Transplant Outpatient Clinic of the University Hospital Essen. Midstream urines were obtained for urine culture at each follow up visit. Samples were transported to the Institute of Medical Microbiology within 4 h for analysis. Samples were cultured using standard media with semi quantification. Cultured bacteria were identified (MALDI-TOF) and susceptibility testing was performed using the VITEK system. Patients suffering UTI or ASB got empirical treatment according to the local UTI treatment strategy. All patients were treated with low-dose trimethoprim-sulfamethoxazole for pneumocystis (PCP) prophylaxis for at least 6 month after transplantation. To confirm the adherence to local guidelines the defined daily dose (ddd) from 2010 to 2012 of trimethoprim-sulfamethoxazole, ciprofloxacin, cefuroxime and amoxicillin/clavulanate was documented. For 2012 the ddd of nitrofurantoin was recorded as well. Data for nitrofurantoin from 2009 to 2011 are not available.

Local UTI treatment strategy

Enterococcus spp. is frequently detected during the first 12 weeks after kidney transplantation [18]. Therefore empirical UTI treatment differs based on the time of occurrence after transplantation. Patients suffering from UTI symptoms during the first 2 months after transplantation received oral ciprofloxacin for 7 days. After the third month of transplantation, therapy was initiated with oral cefuroxime for 7 days. The antibiotic treatment was adjusted to the microbiological findings. Patients with urosepsis were initially treated with piperacillin/tazobactam and therapy was then adjusted according to the microbiological findings. The local guideline includes treatment of ASB according to results of the urinary culture test results [13].

Definitions

Asymptomatic bacteriuria (ASB) was defined as pathogen detection >100.000 CFU/ml with presence of leukocytes (>100/μl) in urine in patients without UTI symptoms [13]. The diagnosis of UTI required the presence of symptoms like dysuria and pollakisuria combined with leucocyturia and/or positive nitrite test.

Statistical analysis

The statistical analysis was performed with Graph Pad Prism V6.0. Chi-square test and fisher exact test were used between groups comparison.

Results

From 2009 to 2012 a large number of 15.741 urine samples were obtained from 859 patients (324 (38%) male, 535 (62%) female). The average age of the patients was 54 years. Bacterial growth was detected in 2985 of 15.741 (19%) samples. In 2009 911/3931 (23%), in 2010 667/4310 (16%), in 2011 652/3566 (18%), and in 2012 755/3934 (19%) were tested positive.

Species distribution of gram-negative uropathogens

The most frequently detected gram-negative bacteria were E.coli 1109/2985 (37%; 2009: n = 240; 2010 n = 300; 2011 n = 255; 2012 n = 314), Klebsiella spp. 242/2985 (8%; 2009: n = 68; 2010 n = 54; 2011 n = 42; 2012 n = 78) and P. aeruginosa 136/2985 (4.5%; 2009: n = 33; 2010 n = 32; 2011 n = 34; 2012 n = 37). No significant difference in the prevalence of the analyzed pathogens was detected (Table 1).
Table 1

Isolated gram negative urinary pathogens in kidney transplant patients from 2009 to 2012

Gram negative urinary pathogens in kidney transplant patients 2009–2012

 

E. coli

Enterobacter cloacae

Citrobacter spp.

Klebsiella spp.

Morganella spp.

Proteus mirabilis

Serratia marescens

Pseudomonas aeroginosa

Stenotrophomonas maltophilia

n = 544

2009

n/y

300

18

21

68

28

65

7

33

4

%/y

55,1%

3,3%

3,9%

12,5%

5,1%

11,9%

1,3%

6,1%

0,7%

n = 444

2010

n/y

240

17

23

54

20

51

5

32

2

%/y

54,1%

3,8%

5,2%

12,2%

4,5%

11,5%

1,1%

7,2%

0,5%

n = 424

2011

n/y

255

19

19

42

13

35

5

34

2

%/y

60,1%

4,5%

4,5%

9,9%

3,1%

8,3%

1,2%

8,0%

0,5%

n = 538

2012

n/y

314

25

15

78

15

49

2

37

3

%/y

58,4%

4,6%

2,8%

14,5%

2,8%

9,1%

0,4%

6,9%

0,6%

Increase/decrease

ns

ns

ns

ns

ns

ns

ns

ns

ns

ns not significant, n/y number of detected pathogens per year, %/y prevalence

Defined daily doses (ddd) of antibiotics prescribed in 2010 and 2012

In total 7091 defined daily doses (ddd) of antibiotics were prescribed in 2010 and 7259 ddd were prescribed in 2012. The most frequently prescribed antibiotics were trimethoprim-sulfamethoxazole (2010 ddd: 3933, 55%; 2012 ddd: 3180, 44%), ciprofloxacin (2010 ddd: 857, 12%; 2012 ddd: 794, 11%) and cefuroxime (2010 ddd: 1347, 19%; 2012 ddd: 916, 13%). In 2012, nitrofurantoin was one of the most prescribed antibiotics with 13% (ddd: 924). Amoxicillin/clavulanate (2010 ddd: 81, 1%; 2012 ddd: 258, 4%) were prescribed less in both years. The remaining prescriptions (13 and 16%) of ddd in 2010 and 2012 were antibiotics without primary indication for UTI treatment. Overall, the total amount of prescribed antibiotics in 2010 was not different compared to the antibiotics prescribed in 2012. Trimethoprim-sulfamethoxazole and cefuroxim were less frequently prescribed in 2012 (−11 and −6%) as compared to 2010. The prescription of ciprofloxacin was not different between the years 2010 and 2012 (−1%). Amoxicillin/clavulanate prescriptions increased slightly fromm 2010 to 2012 with +3%. The amount of nitrofurantoin ddd in 2012 cannot be compared because data was not available in 2010.

Antimicrobial susceptibility of Klebsiella spp., E.coli and Pseudomonas aeruginosa

Klebsiella spp. presented a significant increase of resistance to trimethoprim-sulfamethoxazole (p = 0.02; 2009 32%, 2010 33%, 2011 41%, 2012 51%), ciprofloxacin (p = 0.01; 2009 6%, 2010 15%, 2011 14%, 2012 21%) and ceftazidime (p = 0.004; 2009 6%, 2010 9%, 2011 14%, 2012 23%). The antimicrobial susceptibility to piperacillin/tazobactam was not significantly different (p = 0.50; 2009 16%, 2010 23%, 2011 20%, 2012 21%) (Fig. 1).
Fig. 1

Displays the prevalence of urinary Klebsiella spp. and E.coli antibiotic resistance in kidney transplant recipients from 2009 to 2012. Klebsiella spp. resistance to ceftazidime, ciprofloxacin and trimethoprim-sulfamethoxazole increased significantly. The increase in resistance to piperacillin/tazobactam was not significant. E.coli isolates showed no significant increase or decrease in antibiotic resistance

The E.coli isolates presented no significant difference of antimicrobial susceptibility to trimethoprim-sulfamethoxazole (p = 0.22; 2009 55%, 2010 56%, 2011 62%, 2012 60%), ciprofloxacin (p = 0.98; 2009 34%, 2010 36%, 2011 33%, 2012 34%), ceftazidime (p = 0.48; 2009 13%, 2010, 18%, 2011 18%, 2012 14%) and piperacillin/tazobactam (p = 0.11; 2009 16%, 2010 23%, 2011 20%, 2012 21%) (Fig. 1).

P. aeruginosa isolates presented no significant difference of antimicrobial susceptibility to ciprofloxacin (p = 0.40; 2009 30%, 2010 19%, 2011 24%, 2012 22%), ceftazidime (p = 0.62; between 3 and 5%) and piperacillin (p = 0.90; between 6 and 5%) (Fig. 2).
Fig. 2

Displays the prevalence of urinary Pseudomonas aeruginosa antibiotic resistance in kidney transplant recipients from 2009 to 2012. No shift in resistance to piperacillin, ceftazidime and ciprofloxacin was observed

ESBL phenotypes

In 2009 44/3931 (1%) ESBL phenotypes were isolated. In 2012, the isolates with an ESBL phenotype remained stable with 48/3934 (1%). The number of ESBL producing Klebsiella spp. isolates and chinolone resistance increased significantly between 2009 and 2012 (p = 0.009; 2009 1/44 (2%), 2010 3/46 (7%), 2011 5/41 (12%), 2012 11/48 (11%) (Fig. 3). No significant difference was observed in ESBL producing E.coli with chinolone resistance (2009 36/44 (82%), 2010 35/46 (76%), 2011 32/41 (78%), 2012 35/48 (73%)). Between 2009 and 2012, only a single case with ESBL producing P. aeruginosa showing chinolone and carbapenem resistance was detected in our cohort of kidney transplant patients.
Fig. 3

Displays the prevalence of urinary Klebsiella spp. and E.coli ESBL isolates in kidney transplant recipients from 2009 to 2012. The prevalence of Klebsiella ESBL isolates with chinolone resistance increased significantly. The prevalence of E.coli ESBL isolates remained constant

Urosepsis after renal transplantation

In 51 renal transplant patients, urosepsis due to gram-negative pathogens (E.coli, Klebsiella spp., P. aeruginosa) was diagnosed from 2009 to 2012. The number of cases with urosepsis normalized to the number of urinary cultures with gram-negative pathogens did not change between 2009 and 2012 (2009 2%; 2010 4%; 2011 4%, 2012 4%). In 36 out of 51 (70%) cases with urosepsis E.coli was detected, in 10/51 (20%) cases Klebsiella spp. was detected and in 5/51 (10%) cases P. aeruginosa was detected. The percentage of cases with E.coli detected in urosepsis showed an increase from 2009 to 2010 from 60 to 92%, and decreased to 2012 with 56%. Over the same time period, the percentage of patients with urosepsis and Klebsiella spp. increased from 10 to 38% (given as percentage of all cases with gram negative urosepsis in the respective year). In contrast, P. aeruginosa isolates in urosepsis cases decreased from 2009 with 30% to 2012 with 6%.

Recurrent pathogen detection and antimicrobial susceptibility

E.coli was detected in 1109 urinary cultures during observation time from 2009 to 2012. In 654 cases, cultures were only once positive whereas 455 (41%) cultures were repeatedly positive in more than one urinary culture per year. Antimicrobial resistance to ceftazidime was detected in 45 (7%) of single positive cultures vs. 139 (31%) in multiple positive cultures. Antimicrobial resistance to ciprofloxacin was detected in 133 (21%) of all single positive cultures vs. 248 (54%) in multiple positive cultures. In addition, resistance to piperacillin/tazobactam was detected in 53 (8%) of all single positive cultures vs. 167 (36%) in multiple positive cultures. Klebsiella spp. were detected in 242 urinary cultures during observation time from 2009 to 2012. One hundred sixty-two (67%) were once positive and 80 (33%) were positive in multiple urinary cultures per year. Antimicrobial resistance to ceftazidime was detected in 9 (6%) of single positive cultures vs. 24 (30%) in multiple positive cultures. Antimicrobial resistance to ciprofloxacin was detected in 9 (6%) of single positive cultures vs. 25 (30%) in multiple positive cultures. Moreover, resistance to piperacillin/tazobactam was detected in 23 (13%) of single positive cultures vs. 25 (39%) in multiple positive cultures.

Discussion

In the present study, we found that the species-specific prevalence of urinary tract infections remained stable between 2009 and 2012 in our cohort of renal transplant patients. Interestingly, the resistance pattern of E.coli and P. aeruginosa did not significantly shift over time. In contrast, the prevalence of ESBL producing and chinolone-resistant Klebsiella spp. increased steadily between 2009 and 2012.

In the literature E.coli is the most detected gram negative pathogen causing UTI with up to 38% [19, 20]. This can be confirmed with our present data. In addition no difference of the species distribution was detected from 2009 to 2012. The most frequent prescription of trimethoprim-sulfamethoxazole, ciprofloxacin and cefuroxime reflects the adherence to local guidelines for i. Pneumocystis pneumonia prophylaxis and ii. UTI. The lesser prescription of trimethoprim-sulfamethoxazole in 2012 compared to 2010 (−11%) is based on its primary use for Pneumocystis pneumonia prophylaxis in our center. It reflects the deceasing number of renal transplantations in Germany from 2010 to 2012 with −12,8% [21]. The high rate of nitrofurantoin ddd in 2012 shows the influence of clinical (practice) guidelines for uncomplicated UTI published in 2011 by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases which recommends nitrofurantoin for uncomplicated UTI [22]. Furthermore nitrofurantoin may represent the use for ESBL-producing E. coli, as it shows to be an efficacious agent for UTI caused by ESBL-producing E. coli [23].

Resistance of gram-negative strains increased during the last decades. Pathogens with distinct resistance against multiple groups of antibiotics are associated with increased mortality, longer hospital stays, and higher hospital costs [24, 25]. In our cohort, the prevalence of multi-resistant Klebsiella spp. increased steadily whereas E.coli as well as P. aeruginosa showed no significant change in resistance pattern. The increase of multi-resistant Klebsiella spp. isolates did not seem to have an impact on the number of urosepsis cases per year in our cohort, although the amount of Klebsiella spp. isolated in urosepsis cases increased steadily. Interestingly, increasing resistance of gram negative isolates has been observed in other cohorts, too [6, 16, 2628]. In general, previous antibiotic exposure and increased broad-spectrum antibiotic consumption could be identified as risk factors for increasing resistance. After solid organ transplantation (SOT) additional risk factors are delayed graft function, diabetes mellitus and relapsing UTI [26, 29, 30]. Therefore we hypothesize that rising antimicrobial resistance of gram negative pathogens could be influenced by the present UTI treatment strategy.

In contrast to other reports, the shift of resistance pattern was limited to Klebsiella spp. in our cohort; the resistance pattern of other gram-negative pathogens remained unchanged over time. The reason why increased antibiotic resistance was limited to Klebsiella spp. isolates in our cohort remains unknown.

In our cohort, recurrent pathogen detection was linked to a higher rate of antimicrobial resistant E.coli and Klebsiella spp. detection. Recurrent detection of resistant pathogens may be due to insufficient first-line treatment, since quinolones and cephalosporins are included in the local UTI treatment guideline. Further more in literature MDR pathogens are frequent in kidney recipients with recurrent UTI [19]. This could be another explanation for the association of resistant pathogen detection in multiple urinary cultures, because renal transplant patients with recurrent or persistent UTI receive intensive follow up monitoring including repeated urinary cultures.

To challenge pathogen resistance, the reduction of antibiotic exposure is currently under discussion. The impact of the rational use of antibiotics on antimicrobial susceptibility remains controversial. A swedish study could not show an influence of rational antibiotic use on penicillin-resistant Streptococcus pneumoniae, although reduction of antibiotic use could be observed [31]. One prospective study of kidney transplant recipients with ASB showed no greater incidence of multi-drug resistant pathogens in patients receiving treatment for ASB compared to patients remaining untreated [32]. However, this study was limited to 115 patients and a follow up of 24 months.

Though, the majority of studies showed that resistance can be reduced by introducing antimicrobial stewardship programs [33, 34]. The stewardship programs recommend the use of the antibiotics with the narrowest spectrum possible. In addition limitation of the therapy duration is recommended.

However, in patients after SOT, reduction of antibiotic exposure is challenging. Trimethoprim-sulfamethoxazole prophylaxis is used for Pneumocystis pneumonia prophylaxis. The prophylaxis is crucial for survival after SOT [35]. Therefore it cannot be suspended, although it is associated with increased amoxicillin and trimethoprim-sulfamethoxazole resistance in gram-negative bacteria [36]. Even in our study, resistance of Klebsiella spp. isolates to trimethoprim-sulfamethoxazole increased significantly.

There are additional strategies to reduce antibiotic exposure and to strengthen rational antibiotic treatment. The differentiation between UTI and ASB should be implemented in future strategies. UTI after renal transplantation has a great impact on the transplant outcome. Gołębiewska et al. evaluated the influence of UTIs on renal graft function in a cohort of 209 adult renal transplant recipients. They observed 322 UTI episodes in 111 patients, including asymptomatic bacteriuria, lower and upper UTIs and urosepsis. Graft function was significantly worse in patients suffering from UTI [37]. Furthermore Pelle et al. investigated in a cohort of 177 renal transplant recipients that patients with upper UTIs (acute pyelonephritis) exhibited a decrease in creatinine clearance compared to patients with uncomplicated UTI 1 year after transplantation, which was still persistent 4 years after transplantation [18]. In addition Dharnidharka et al. investigated that the risk for graft loss after early UTI was elevated in a cohort of under aged renal transplant patients [38]. Therefore treatment for UTI is warrantable. In the context of “choosing wisely”, the antibiotic treatment of ASB is controversial [39]. A Cochrane Renal Group’s Specialized Register analysis could not find a clinical benefit of ASB treatment [40]. Even in the cohort of kidney transplant patients, treatment strategies for ASB are currently changing. However, untreated ASB within the first 3 months of transplantation has been identified as an independent risk factor for acute cellular rejection. [41]. In contrast ASB is not associated with short-term graft function impairment [42]. Therefore, treatment should be considered early after transplantation but maybe obsolete at a later time point [43]. Alternatively, patients with ASB could be monitored. Treatment should be initiated in case of decreasing kidney function or UTI symptoms [41]. This strategy may prevent unnecessary antibiotic exposure.

Conclusions

This study found a concerning increase of antimicrobial resistance to commonly used antibiotic agents among gram-negative uropathogens isolated from kidney transplant recipients during an observation period of 4 years (2009–2012). Antimicrobial resistance of Klebsiella spp. to trimethoprim-sulfamethoxazole, ciprofloxacin and ceftazidime increased significantly from 2009 to 2012. Local treatment strategies of urinary tract infections and PCP prophylaxis may have influenced increased antimicrobial resistance.

Abbreviations

ASB: 

asymptomatic bacteriuria

CFU: 

colony forming units

ddd: 

defined daily dose

ESBL: 

Extended Spectrum β Lactamase

PCP: 

Pneumocystis pneumonia

SOT: 

solid organ transplantation

spp.: 

species

UTI: 

Urinary tract infection

Declarations

Acknowledgments

The authors would like to thank Alexandra Dragaqina and Anne Kamp for help with data collection and professional technical assistance.

Funding

Not applicable.

Availability of data and materials

The datasets analyzed during the current study is available from the corresponding author on reasonable request.

Authors’ contributions

JOK, JUK, PMR, OW and BW participated in the performance of the research, in research design, interpretation of data and in the writing of the paper. OA and AK provided analytic tools, participated in the analysis, interpretation of data and participated in the writing of the paper. SD, MK, HG, AB, SB and BR participated in the performance of research, interpretation of data and in the writing of the paper. All authors read and approved the final manuscript.

Competing interests

Johannes Korth has received sponsorship to attend international conferences from Roche, Astellas and Novartis. Benjamin Wilde has received advisory board honoraria from TEVA and Cytosorbents; he has also received travel funding from Alexion Pharma, Astellas, Chiesi, Novartis, Pfizer, Roche, Sanofi, TEVA und Wyeth. Oliver Witzke has received research funds and/or honoraria from Alexion, Astellas, Bristol-Myers Squibb, Chiesi, Janssen-Cilag, MSD, Novartis, Pfizer, Roche and Shire.

Consent for publication

Not applicable.

Ethics approval and consent to participate

This study has been approved by ethics committee of the medical faculty of the University Duisburg-Essen (16–6952-BO).

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Authors’ Affiliations

(1)
Department of Nephrology, University Hospital Essen, University Duisburg-Essen
(2)
Department of Infectious Diseases, University Hospital Essen, University Duisburg-Essen
(3)
Institute for Medical Microbiology, University Hospital Essen, University Duisburg-Essen
(4)
Institute of Hygiene, University Hospital Essen, University Duisburg-Essen
(5)
Department of Gastroenterology, University Hospital Essen, University Duisburg-Essen

References

  1. Adamska Z, Karczewski M, Cichańska L, Więckowska B, Małkiewicz T, Mahadea D, et al. Bacterial infections in renal transplant recipients. Transplant Proc. 2015;47:1808–12.View ArticlePubMedGoogle Scholar
  2. Lyerová L, Viklický O, Nemcová D, Teplan V. The incidence of infectious diseases after renal transplantation: a single-centre experience. Int J Antimicrob Agents. 2008;31(Suppl 1):S58–62.View ArticlePubMedGoogle Scholar
  3. Witzke O, Schmidt C, Kohnle M, Lütkes P, Philipp T, Heemann U. Impact of febrile infections on the long-term function of kidney allografts. J Urol. 2001;166:2048–52.View ArticlePubMedGoogle Scholar
  4. Veroux M, Giuffrida G, Corona D, Gagliano M, Scriffignano V, Vizcarra D, et al. Infective complications in renal allograft recipients: epidemiology and outcome. Transplant Proc. 2008;40:1873–6.Google Scholar
  5. Chuang P, Parikh CR, Langone A. Urinary tract infections after renal transplantation: a retrospective review at two US transplant centers. Clin Transpl. 2005;19:230–5.View ArticleGoogle Scholar
  6. Bodro M, Sabé N, Tubau F, Lladó L, Baliellas C, Roca J, et al. Risk factors and outcomes of bacteremia caused by drug-resistant ESKAPE pathogens in solid-organ transplant recipients. Transplantation. 2013;96:843–9.View ArticlePubMedGoogle Scholar
  7. Kuo H-T, Ye X, Sampaio MS, Reddy P, Bunnapradist S. Cytomegalovirus serostatus pairing and deceased donor kidney transplant outcomes in adult recipients with antiviral prophylaxis. Transplantation. 2010;90:1091–8.View ArticlePubMedGoogle Scholar
  8. Bergamasco MD, Barroso Barbosa M, de Oliveira GD, Cipullo R, Moreira JCM, Baia C, et al. Infection with Klebsiella Pneumoniae carbapenemase (KPC)-producing K. Pneumoniae in solid organ transplantation. Transpl Infect Dis. 2012;14:198–205.View ArticlePubMedGoogle Scholar
  9. de Gouvêa EF, Martins IS, Halpern M, Ferreira ALP, Basto ST, Gonçalves RT, et al. The influence of carbapenem resistance on mortality in solid organ transplant recipients with Acinetobacter Baumannii infection. BMC Infect Dis. 2012;12:351.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Hu Y, Ping Y, Li L, Xu H, Yan X, Dai H. A retrospective study of risk factors for carbapenem-resistant Klebsiella Pneumoniae acquisition among ICU patients. J Infect Dev Ctries. 2016;10:208–13.View ArticlePubMedGoogle Scholar
  11. Gołębiewska JE, Dębska-Ślizień A, Rutkowski B. Treated asymptomatic bacteriuria during first year after renal transplantation. Transpl Infect Dis. 2014;16:605–15.View ArticlePubMedGoogle Scholar
  12. Pilmis B, Scemla A, Join-Lambert O, Mamzer M-F, Lortholary O, Legendre C, et al. ESBL-producing enterobacteriaceae-related urinary tract infections in kidney transplant recipients: incidence and risk factors for recurrence. Infect Dis (London, England). 2015;47:714–8.Google Scholar
  13. Becker S, Witzke O, Rübben H, Kribben A. Harnwegsinfektionen nach Nierentransplantation. Urologe. 2011;50:53–6.View ArticlePubMedGoogle Scholar
  14. Senger SS, Arslan H, Azap OK, Timurkaynak F, Cağir U, Haberal M. Urinary tract infections in renal transplant recipients. Transplant Proc. 2007;39:1016–7.View ArticlePubMedGoogle Scholar
  15. Valera B, Gentil MA, Cabello V, Fijo J, Cordero E, Cisneros JM. Epidemiology of urinary infections in renal transplant recipients. Transplant Proc. 2006;38:2414–5.View ArticlePubMedGoogle Scholar
  16. Origüen J, Fernández-Ruiz M, López-Medrano F, Ruiz-Merlo T, González E, Morales JM, et al. Progressive increase of resistance in Enterobacteriaceae urinary isolates from kidney transplant recipients over the past decade: narrowing of the therapeutic options. Transpl Infect Dis. 2016;18:575–84.View ArticlePubMedGoogle Scholar
  17. Parasuraman R, Julian K. Urinary tract infections in solid organ transplantation. Am J Transplant. 2013;13(Suppl 4):327–36.View ArticlePubMedGoogle Scholar
  18. Pellé G, Vimont S, Levy PP, Hertig A, Ouali N, Chassin C, et al. Acute pyelonephritis represents a risk factor impairing long-term kidney graft function. Am J Transplant. 2007;7:899–907.View ArticlePubMedGoogle Scholar
  19. Bodro M, Sanclemente G, Lipperheide I, Allali M, Marco F, Bosch J, et al. Impact of antibiotic resistance on the development of recurrent and relapsing symptomatic urinary tract infection in kidney recipients. Am J Transplant. 2015;15:1021–7.View ArticlePubMedGoogle Scholar
  20. Rossignol L, Vaux S, Maugat S, Blake A, Barlier R, Heym B, et al. Incidence of urinary tract infections and antibiotic resistance in the outpatient setting: a cross-sectional study. Infection (Springer Berlin Heidelberg). 2017;45:33–40.Google Scholar
  21. DEUTSCHE STIFTUNG ORGANTRANSPLANTATION. Organ donation and transplantation in Germany 2012. :https://www.dso.de/.Google Scholar
  22. Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG, et al. International clinical practice guidelines for the treatment of acute uncomplicated cystitis and Pyelonephritis in women: a 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. Clin Infect Dis (Oxford University Press). 2011;52:e103–20.View ArticleGoogle Scholar
  23. 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(7):1031–7.Google Scholar
  24. Slama TG. Gram-negative antibiotic resistance: there is a price to pay. Crit Care. 2008;12(Suppl 4):S4.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Filius PMG, Gyssens IC, Kershof IM, Roovers PJE, Ott A, Vulto AG, et al. Colonization and resistance dynamics of gram-negative bacteria in patients during and after hospitalization. Antimicrob Agents Chemother. 2005;49:2879–86.View ArticlePubMedPubMed CentralGoogle Scholar
  26. Tsai M-H, Chu S-M, Hsu J-F, Lien R, Huang H-R, Chiang M-C, et al. Risk factors and outcomes for multidrug-resistant gram-negative bacteremia in the NICU. Pediatrics. 2014;133:e322–9.View ArticlePubMedGoogle Scholar
  27. Sanchez GV, Master RN, Karlowsky JA, Bordon JM. In vitro antimicrobial resistance of urinary Escherichia Coli isolates among U.S. outpatients from 2000 to 2010. Antimicrob Agents Chemother. 2012;56:2181–3.View ArticlePubMedPubMed CentralGoogle Scholar
  28. Yang Y-S, Ku C-H, Lin J-C, Shang S-T, Chiu C-H, Yeh K-M, et al. Impact of extended-spectrum β-lactamase-producing Escherichia Coli and Klebsiella Pneumoniae on the outcome of community-onset bacteremic urinary tract infections. J Microbiol Immunol Infect. 2010;43:194–9.View ArticlePubMedGoogle Scholar
  29. Espinar MJ, Miranda IM, Costa-De-Oliveira S, Rocha R, Rodrigues AG, Pina-Vaz C. Urinary tract infections in kidney transplant patients due to Escherichia Coli and Klebsiella Pneumoniae-producing extended-spectrum β-lactamases: risk factors and molecular epidemiology. PLoS One. 2015;10:1–11.View ArticleGoogle Scholar
  30. Kahlmeter G. Prevalence and antimicrobial susceptibility of pathogens in uncomplicated cystitis in Europe. The ECO.SENS study. Int J Antimicrob Agents. 2003;22(Suppl 2):49–52.View ArticlePubMedGoogle Scholar
  31. Mölstad S, Erntell M, Hanberger H, Melander E, Norman C, Skoog G, et al. Sustained reduction of antibiotic use and low bacterial resistance: 10-year follow-up of the Swedish Strama programme. Lancet Infect Dis. 2008;8:125–32.View ArticlePubMedGoogle Scholar
  32. Origüen J, López-Medrano F, Fernández-Ruiz M, Polanco N, Gutiérrez E, González E, et al. Should asymptomatic bacteriuria be systematically treated in kidney transplant recipients? Results from a randomized controlled trial. Am J Transplant. 2016;16:2943.View ArticlePubMedGoogle Scholar
  33. Lee C-R, Cho IH, Jeong BC, Lee SH. Strategies to minimize antibiotic resistance. Int J Environ Res Public Health. 2013;10:4274–305.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Dagan R, Barkai G, Givon-Lavi N, Sharf AZ, Vardy D, Cohen T, et al. Seasonality of antibiotic-resistant streptococcus pneumoniae that causes acute otitis media: a clue for an antibiotic-restriction policy? J Infect Dis. 2008;197:1094–102.View ArticlePubMedPubMed CentralGoogle Scholar
  35. Iriart X, Challan Belval T, Fillaux J, Esposito L, Lavergne R-A, Cardeau-Desangles I, et al. Risk factors of Pneumocystis pneumonia in solid organ recipients in the era of the common use of posttransplantation prophylaxis. Am J Transplant. 2015;15:190–9.View ArticlePubMedGoogle Scholar
  36. Singh R, Bemelman FJ, Hodiamont CJ, Idu MM, Ten Berge IJM, Geerlings SE. The impact of trimethoprim-sulfamethoxazole as Pneumocystis jiroveci pneumonia prophylaxis on the occurrence of asymptomatic bacteriuria and urinary tract infections among renal allograft recipients: a retrospective before-after study. BMC Infect Dis (BioMed Central Ltd). 2016;16:90.View ArticleGoogle Scholar
  37. Gołębiewska JE, Dębska-Ślizień A, Rutkowski B. Urinary tract infections during the first year after renal transplantation: one center’s experience and a review of the literature. Clin Transpl. 2014;28:1263–70.View ArticleGoogle Scholar
  38. Dharnidharka VR, Agodoa LY, Abbott KC. Effects of urinary tract infection on outcomes after renal transplantation in children. Clin J Am Soc Nephrol (American Society of Nephrology). 2006;2:100–6.View ArticleGoogle Scholar
  39. Fätkenheuer G, Jung N. Treatment of asymptomatic Bacteriuria. Clin Infect Dis. 2016;62:1190.View ArticlePubMedGoogle Scholar
  40. Zalmanovici Trestioreanu A, Lador A, Sauerbrun-Cutler M-T, Leibovici L. Antibiotics for asymptomatic bacteriuria. Cochrane Database Syst Rev. 2015;4:CD009534.PubMedGoogle Scholar
  41. Singh R, Geerlings SE, Bemelman FJ. Asymptomatic bacteriuria and urinary tract infections among renal allograft recipients. Curr Opin Infect Dis. 2015;28:112–6.View ArticlePubMedGoogle Scholar
  42. Bodro M, Sanclemente G, Lipperheide I, Allali M, Marco F, Bosch J, et al. Impact of urinary tract infections on short-term kidney graft outcome. Clin Microbiol Infect. 2015;21:1104.e1–8.View ArticleGoogle Scholar
  43. Lee JR, Bang H, Dadhania D, Hartono C, Aull MJ, Satlin M, et al. Independent risk factors for urinary tract infection and for subsequent bacteremia or acute cellular rejection: a single-center report of 1166 kidney allograft recipients. Transplantation. 2013;96:732–8.View ArticlePubMedGoogle Scholar

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