Increasing prevalence of ertapenem-resistant, carbapenem-susceptible Enterobacteriaceae (ERE) in Singapore presents a major therapeutic problem. Our objective was to determine risk factors associated with the acquisition of ERE in hospitalized patients; to assess associated patient outcomes; and to describe the molecular characteristics of ERE.
A retrospective case-case-control study was conducted in 2009 at a tertiary care hospital. Hospitalized patients with ERE and those with ertapenem-sensitive Enterobacteriaceae (ESE) were compared with a common control group consisting of patients with no prior gram-negative infections. Risk factors analyzed included demographics; co-morbidities; instrumentation and antibiotic exposures. Two parallel multivariate logistic regression models were performed to identify independent variables associated with ERE and ESE acquisition respectively. Clinical outcomes were compared between ERE and ESE patients.
Twenty-nine ERE cases, 29 ESE cases and 87 controls were analyzed. Multivariate logistic regression showed that previous hospitalization (Odds ratio [OR], 10.40; 95% confidence interval [CI], 2.19–49.20) and duration of fluoroquinolones exposure (OR, 1.18 per day increase; 95% CI, 1.05–1.34) were unique independent predictors for acquiring ERE. Duration of 4th-generation cephalosporin exposure was found to predict for ESE acquisition (OR, 1.63 per day increase; 95% CI, 1.05–2.54). In-hospital mortality rates and clinical response rates were significantly different between ERE and ESE groups, however ERE infection was not a predictor of mortality. ERE isolates were clonally distinct. Ertapenem resistance was likely to be mediated by the presence of extended-spectrum β-lactamases or plasmid-borne AmpC in combination with impermeability due to porin loss and/or efflux pumps.
Citation: Teo J, Cai Y, Tang S, Lee W, Tan TY, Tan TT, et al. (2012) Risk Factors, Molecular Epidemiology and Outcomes of Ertapenem-Resistant, Carbapenem-Susceptible Enterobacteriaceae: A Case-Case-Control Study. PLoS ONE 7(3): e34254. https://doi.org/10.1371/journal.pone.0034254
Editor: Brad Spellberg, Los Angeles Biomedical Research Institute, United States of America
Received: September 15, 2011; Accepted: February 24, 2012; Published: March 26, 2012
Copyright: © 2012 Teo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported in part by research grants from the SingHealth Foundation (Singapore). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. No additional external funding received for this study.
Competing interests: The authors have declared that no competing interests exist.
Extended-spectrum β-lactamases (ESBL)-producing Enterobacteriaceae are major contributors to the mounting gram-negative resistance problem globally . Carbapenems are often the only remaining therapeutic options available for these serious ESBL-producing Enterobacteriaceae infections . Unfortunately, carbapenem resistance has also emerged as a result of selective pressure on Enterobacteriaceae . Whilst Singapore is not spared from this emergence, it is fortunate that overall rates of susceptibility to carbapenems remained fairly stable . However, since 2006, systemic surveillance of hospitals unexpectedly detected an increasing prevalence of Klebsiella pneumoniae and Escherichia coli clinical isolates that were resistant to ertapenem, but susceptible to group II carbapenems . This coincided with the increasing popularity of ertapenem as a treatment option for ESBL- and AmpC-producing Enterobacteriaceae infections, in spite of the lack of prospective comparative trials investigating its use in such infections.
Carbapnem resistance may be mediated by carbapenemases or metallo-β-lactamases ; or due to a combination of ESBL or AmpC β-lactamase production with impermeability caused by porin loss –. Enterobacteriaceae exhibiting low-level resistance to ertapenem, a Group I carbapenem, may still remain susceptible to Group II carbapenems such as imipenem and meropenem. The underlying resistance mechanisms in these unique ertapenem-resistant Enterobacteriaceae appear to differ from those isolates with universal resistance to all carbapenems – ertapenem permeability tends to be more affected by porin loss compared to other Group II carbapenems and ertapenem resistance is seldom carbapenemases-mediated , , .
The clinical epidemiology of these ertapenem-resistant, Group II carbapenem-susceptible Enterobacteriaceae (ERE) is poorly understood. There have been several reports regarding the risk factors for acquisition of carbapenem-resistant Enterobacteriaceae –, but less so for ertapenem resistance in particular , . The intent of this study was to identify the risk factors associated with the acquisition of ERE among hospitalized patients, to compare the outcomes of patients with ERE with those with ertapenem-susceptible Enterobacteriaceae (ESE) infections, and to describe the molecular profile of ERE locally. Identification of factors contributing to the emergence of ERE among the hospitalized population is crucial in the design of effective strategies to prevent the development of such infections, as well as to avoid therapy failure by precluding empiric ertapenem use in this risk population.
Materials and Methods
The study was conducted at Singapore General Hospital, a 1,600-bedded acute tertiary care hospital between January 2009 to September 2009. The hospital is the largest of six public healthcare hospitals, and accounted for approximately 35% of recorded inpatient-days among them. Infection control policies remained unchanged during the study period. ERE prevalence remained stable and there was no indication of an outbreak during this period. Surveillance cultures to detect asymptomatic ERE colonization were not routinely performed in the institution. The study was reviewed and approved by the Singhealth institutional ethics review board. As this was a retrospective study, the need for an informed consent was waived by the ethics review board.
A retrospective parallel case-control study design was used to identify risk factors associated with the acquisition of ERE. The case-case-control design overcomes several limitations of the standard case-control design, particularly studies where patients infected with “susceptible phenotype” are elected as controls. In such case-control studies, effect measures of antibiotics active against the susceptible, but not the resistant phenotype, could be falsely inflated since the administration of these antibiotics close to the time of culture would have prevented the recovery of the susceptible phenotype, hence excluding these patients from the control group. The other advantages of the case-case-control methodology are described in detail elsewhere , .
The computerized records of the hospital's clinical microbiological laboratory were used to identify all clinical cultures positive for Enterobactaeriaceae. The first case group consisted of all adult inpatients (>18 years old) with microbiological cultures positive for ERE, regardless of whether the culture reflected a clinically-relevant infection or colonization. The second case group consisted of adult inpatients with microbiological cultures positive for ESE recorded within the same study period. In order to ensure that the two parallel case-control models were comparable, an equal number of (i) Enterobacteriaceae species type and (ii) specimen type were selected for each case group. Patients who had multiple cultures positive for Enterobacteriaceae were included only once and the “index” culture is the first Enterobacteriaceae specimen recorded during the stay that qualified each patient for inclusion into the two case groups.
Control group patients were adult inpatients admitted within the study period with no history of prior infection with Enterobacteriaceae or other gram-negative bacilli, but could have gram-positive infections. Three control patients were randomly identified and chosen from the hospital's computerized administrative source records for each ERE/ESE case patient.
An independent observer (a research assistant), blinded to the study's hypothesis/objectives, performed random selection of ESE case and control patients based solely on the respective inclusion and exclusion criteria provided to him. The first patient listed in the database who met the study criteria was selected and this process was continued until all ESE cases and controls patients were identified.
Data were sought from inpatient charts, electronic medical records, clinical microbiology laboratory computerized databases and collated in a structured data collection form by three trained reviewers. Variables analyzed as risk factors included: 1) demographics (age, gender); 2) presence of comorbid conditions and Charlson weighted co-morbidity index; 3) severity of illness as determined by APACHE II score; 4) hospitalization history such as previous hospital and nursing home stay, previous ICU stay, length of hospital stay prior to outcome of interest (defined as length of stay prior to Enterobacteriaceae isolation for case patients and total length of stay for controls); 5) exposure to invasive interventions (central lines, urinary catheters, drainage devices, invasive ventilation, dialysis, non-surgical invasive procedures such as endoscopic procedures, invasive surgery, dialysis); 6) receipt of immunosuppressive therapy (defined as receipt of >one dose of chemotherapy or immunosuppressants, or >14 days of corticosteroids at an equivalent daily dose of 20 mg prednisolone) and 7) antibiotics exposure (receipt of ≥one dose of various classes of antimicrobials). The number of invasive devices and cumulative duration of antibiotics were also tabulated. All variables were evaluated for an interval of 90 days prior to the occurrence of ERE/ESE for case patients or end of hospitalization for control patients.
A retrospective cohort study involving the same groups of ERE and ESE patients were conducted in order to evaluate the impact of ERE on clinical outcomes. All ERE and ESE patients who were considered having clinically relevant infections were included for outcome analyses. Infection was considered clinically relevant if Enterobacteriaceae were isolated from clinical specimens obtained from sterile sites (e.g. blood or pleural effusion); or if there was a presence of clinical symptoms or signs of infection consistent with the infecting Enterobacteriaceae; or antibiotic therapy was administered for the Enterobacteriaceae infection. Colonizers were excluded. For polymicrobial infections, patients were included only if the presence of ERE or ESE contributed to the decision for antibiotic treatment. Primary outcomes of interest were: (i) the final end-points of hospitalization i.e. discharge or mortality (in-hospital all-cause mortality), (ii) hospital length of stay after infection, (iii) 30-day readmission (defined as non-elective readmission within 30 days of discharge), and (iv) clinical response (defervescence, resolution of abnormalities of vital signs and infection markers, or resolution of symptoms specific to infection). Clinical improvement was presumed if patient was well enough to be discharged in patients where surrogate infection markers were not documented.
Carbapenem susceptibility was determined using disk diffusion and interpreted in accordance to the 2009 Clinical and Laboratory Standards Institute guidelines as per hospital's clinical microbiology laboratory protocol . Susceptibility testing for ertapenem and imipenem was part of laboratory's routine protocol, but not for meropenem. Enterobacteriaceae isolates with “intermediate” or “resistant” classification for ertapenem, but “susceptible” to class II carbapenems, were included in ERE case group. Fifteen clinical isolates were available for further molecular characterization. A conventional rep-polymerase chain reaction (PCR) method was used for clonal typing . PCR products were analyzed by chip-based microfluidic electrophoresis (Experion, Biorad, USA). Digitalized banding images were exported and cluster analysis was performed using Bionumerics 5.4 (AppliedMaths, Kortrijk, Belgium). The isolates were considered as indistinguishable (similarity of DNA fragment pattern >90%) or distinct (similarity of DNA fragment pattern <90%). Resistance gene analyses of ESBLs, plasmid-mediated AmpC genes, metallo-β-lactamases (MBLs) and Klebsiella pneumoniae carbapenemase (KPC) were performed using modified methods from previously published PCR protocols –.
Catergorical variables were presented as numbers and percentages, and were compared using the Χ2 or Fisher exact test, as appropriate. Continuous variables were presented as mean ± SD or median and range, and were compared using the Student's t test or the Mann-Whitney test, depending on the validity of the normality assumption.
In the risk factor analysis, multivariate logistic regression models were used to compare each case group to control group. Clinically plausible variables identified in the univariate analysis were included in a stepwise selection multivariate logistic regression model if P<0.1. The final model was chosen on basis of biologic plausibility. Odds ratios (OR) and 95% confidence intervals (CI) were calculated to evaluate the strength of any association. Results from the ERE-control model were compared with the ESE-control model to identify significant factors unique to each case group. In the outcomes analysis, ERE and ESE patients who died were compared with those who survived in order to determine risk factors predicting for in-hospital mortality via univariate and subsequently multivariate logistic regression analysis.
For all calculations, a 2-tailed P value of less than 0.05 was considered to reveal a statistical significant difference. Statistical analyses were performed using SPSS 17.0 (SPSS, Chicago, IL, USA).
During the study period, 29 patients with ERE, 29 patients with ESE and 87 controls were identified. Of the ERE species included in the study, Klebsiella spp. (16/29, 55.2%) was most commonly identified, while Escherichia coli (5/29, 17.2%) and Enterobacter spp. (8/29, 27.6%) accounted for the remaining ERE species. Urine (12/29, 41.4%) was the most common site which ERE were isolated from, followed by blood (6/29, 20.7%), abdominal tissues/fluids (6/29, 20.7%), respiratory secretions (3/29, 10.3%) and skin and soft tissue wounds (2/29, 6.9%) (Table 1). Of the 29 ERE isolates, 20 (69.0%) were resistant to ertapenem and 9 (31.0%) were intermediate. These ERE isolates exhibited multi-drug resistance – 100% was resistant to ceftriaxone and amoxicillin-clavulanate; 97% to piperacillin-tazobactam; 79% to ciprofloxacin; and 76% to cefepime. However, ERE remained relatively susceptible to amikacin (3% resistant) and gentamicin (41% resistant).
The demographic characteristics and co-morbidities of the case and control patients are shown in Table 2. Overall, ERE and ESE case patients were fairly similar in baseline characteristics to the control group respectively. However, ERE patients were more likely to have cardiovascular and hepatic diseases, while ESE patients were older, more likely to have hepatic and renal diseases and had a higher Charlson co-morbidity index, when compared to the control group.
Comparing ERE cases to controls, ERE patients were significantly more likely to have been previously exposed to the hospital environment and various instrumentation or interventions, and had longer hospital stays prior outcome of interest (Table 3). Likewise ESE patients had longer hospital stays prior outcome of interest when compared to controls. However, unlike ERE cases, only exposure to central lines and urinary catheters were significantly different between the ESE and control groups.
More than 70% of patients in each group received some form of antibiotic in the 90 days prior to the outcome of interest (Table 4). ERE patients received significantly longer durations of all classes of antibiotics investigated, with the exception of penicillin, when compared to controls. In contrast, there were no significant differences in antibiotic exposures between ESE patients and controls, with the exception of the receipt of 4th-generation cephalosporins.
Risk factor analysis
The results for the multivariate analyses of the ERE-control and ESE-control models are presented in Table 5. When the two models were contrasted, previous hospital stay and longer exposures of fluoroquinolone use were unique significant predictors of ERE acquisition, while duration of exposure to 4th-generation cephalosporins was the only unique significant predictor of ESE acquisition.
Twenty-six patients with ERE and 27 patients with ESE were considered to have clinically-relevant Enterobacteriaceae infections and were receiving antibiotic therapy for these infections. In-hospital mortality was significantly higher in the ERE group (P = 0.04) (Table 6). ERE patients also had a poorer clinical response rate (P = 0.04).
Table 7 showed the results of univariate analysis for risk factors associated with in-hospital mortality among the ERE and ESE-infected patients. In-hospital mortality was associated with malignancy, high APACHE II score, isolation of Enterobacteriaceae in blood and ERE infection. However, none of these variables remained significant when introduced into the multivariate model.
Fifteen isolates (15/29, 51.7%) were available for further molecular work-up, which included nine K. pneumoniae, four E. cloacae, one E. aerogenes and one E.coli (Table 1). Clonality testing of K. pneumoniae and E. cloacae isolates showed clonally-distinct populations respectively. Ertapenem resistance was not mediated by carbapenemases or MBLs in all three species. Overall, 80% (12/15) of tested isolates had beta-lactamases (TEM-1, SHV-1, SHV-11, SHV-12, SHV-50, CTX-M-1) or AmpC genes of the DHA-type alone or in combinations.
Infection with carbapenem-resistant Enterobacteriaceae (CRE) is emerging as an important challenge in health-care settings . While there are a number of studies relating to CRE in general, information pertaining to ERE is scarcer. Our study evaluated the potential risk factors and outcomes for the acquisition of ERE in hospitalized patients. We found that previous hospital stay and increased durations of prior fluoroquinolone therapy appeared to be associated with ERE acquisition. In addition, higher mortality rates and poorer clinical response rates were observed in ERE-infected patients.
Only two case-control studies investigating ERE have been published. Risk factors implicated in these studies included: ICU stay, exposure to invasive medical devices, and antibiotic exposure, specifically cephalosporin and carbapenem use , . Our study, on the other hand, identified previous hospital stay as a significant independent predictor of ERE acquisition. This is not surprising as this factor has been widely acknowledged to be associated with the acquisition of several different types of antibiotic-resistant organisms such as multi-drug resistant Acinetobacter baumanni, and Pseudomonas aeruginosa , . Previously hospitalized patients will have a higher likelihood of exposure to nosocomial organisms through horizontal transmission among patients. Furthermore, previous hospital stay could be a surrogate marker of prior antibiotic exposure.
Long durations of fluoroquinolone exposure were also associated with the acquisition of ERE in our study. This association offers biologic plausibility. Ertapenem resistance is commonly mediated by the production of AmpC/ESBL enzymes coupled with a deficiency in expression of the outer membrane proteins (OMPs) –. In our study, 80% of available isolates tested identified ESBL/AmpC as the prevalent mechanisms. There is a possibility that fluoroquinolone use has resulted in a selective pressure for these ESBL-producing Enterobacteriaceae in our institution. In this population of ESBL-producing Enterobacteriaceae, there could be an ertapenem-resistant subpopulation with deficiency in porin expression. This phenomenon has been demonstrated by Leavitt et al., where 1–2% of ESBL-producing Klebsiella pneumonia in the study was found to be lacking in OMPK36 . Further constant and cumulative antibiotic exposures, including ertapenem and the other carbapenems use, then exert a selective pressure for these ESBL-producing Enterobacteriaceae associated with porin loss, or facilitate the activation of mechanisms leading to porin loss, resulting in the predomination of ertapenem-resistant phenotypes.
Our study did highlight some key differences when compared to the other ERE and CRE risk factor studies whereby poor functional status; ICU stay; presence of biliary drains and invasive ventilation; prior beta-lactams, anti-pseudomonal penicillins and carbapenem exposure were identified as predictors –. These discrepancies in findings were not unexpected since the profiles of study organisms were largely different - some studies included both colonized patients and those with clinically-relevant infections; and sites and species of infecting organisms also varied. The resulting epidemiological characteristics and resistance mechanisms of study organisms were hence diverse. For instance, isolates from Israel had a mix of KPC- and ESBL-producers with porin loss , ; carbapenem-resistant strains from Greece were likely to be MBL-producers ; US isolates consisted of KPC-producers –; while our local isolates were predominantly ESBL-producers, likely with porin loss. This diversity in carbapenem resistance mechanisms may be associated with distinct clinical risk factors, in particular prior antibiotic exposure, explaining the differences between the studies.
Not surprisingly, we showed that there is a significant difference in in-hospital mortality and clinical response between the ERE and ESE group. However, ERE infection was not found to be a significant predictor of in-hospital mortality in the multivariate analysis, probably due to the confounding effect of severity of illness. A more extensive study with a larger sample size would have to be undertaken to better characterize the clinical outcomes.
Our study presented with several limitations. First, this is a retrospective study with a small sample size – only 29 cases in each case group were collected, limiting the power of the study. However, almost all adult hospitalized patients with an ERE during the study period were included. Molecular characterization of ERE was further limited to only 15 available isolates, hence results may not have been representative of the true distribution of resistance mechanisms locally. In addition, controls were not screened for Enterobacteriaceae by active surveillance, some patients with unrecognized Enterobacteriaceae colonization may be misclassified as non-infected control patients. Our study also did not seek to distinguish between colonization and infection with and ERE isolate, which could present very different epidemiological and clinical characteristics, and hence different risk factors.
As with many antimicrobial resistance epidemiological studies, selection bias and confounding are issues of concern. The use of controls without prior gram-negative bacillary infection, and with possible gram-positive infection only, may have introduced a selection bias towards potentially healthier controls. Furthermore, there is a concern that use of such a control group may not represent the true source population for the cases, and will not allow the differentiation between ERE-specific risk factors and risk factors relating to gram-negative bacilli infections in general. Missing information on antibiotic treatments and instrumentation at private healthcare providers prior admission, and the lack of electronic randomization procedures could have also contributed to selection bias. Finally, case and control patients were not matched due to difficulties in obtaining matched controls for two different case groups. This led to differences in certain variables such as length of stay prior to outcome of interest, severity of illness and age between the groups, all of which could potentially confound the interpretation of results. The differences in the median lengths of stay prior to outcome of interest between the ERE group and the two other groups, is a possible study limitation. However, it is also debatable, as a significantly longer hospitalization may be needed to acquire ERE. Future studies should be designed to control for these differences in length of stay.
In conclusion, we found that ERE infection was associated with previous hospital stay and increased duration of prior fluoroquinolone therapy, notwithstanding the above limitations. Patients with ERE infection experienced higher in-hospital mortality rates and poorer clinical response. ERE represent a major clinical and infection control challenge. Evidently, more active interventions and research in this area is required to curb the problem. In particular, the introduction of preventive measures such as antimicrobial stewardship to help reduce unnecessary fluoroquinolones use may help to attenuate the risk of ERE infections. Nosocomial transmission is a critical factor in the context of carbapenem-resistant Enterobacteriaceae, and risk of horizontal transmission during hospitalization can be alleviated by active surveillance, good infection control practices such as hand hygiene and cohorting measures. Further investigations on mechanisms of resistance and clonal spread, as well as a more detailed analysis of clinical outcomes are warranted for a better understanding of the current problem.
The authors thank Dr Sarah Staedke for her valuable suggestions and critique of this research work and Ms Nur Syahidah Bte Amran for her technical assistance in the molecular epidemiologic investigations. These data were presented in part at the 51st Interscience Conference on Antimicrobial Agents and Chemotherapy, Boston, USA, 2010.
Conceived and designed the experiments: JT ALK WL. Performed the experiments: JT YYC SST. Analyzed the data: JT ALK. Contributed reagents/materials/analysis tools: TTT TYT. Wrote the paper: JT ALK.
- 1. Winokur PL, Canton R, Casellas JM, Legakis N (2001) Variations in the prevalence of strains expressing an extended-spectrum beta-lactamase phenotype and characterization of isolates from Europe, the Americas, and the Western Pacific region. Clin Infect Dis 2001 32(Suppl 2): S94–103.
- 2. Endimiani A, Luzzaro F, Perilli M, Lombardi G, Colì A, et al. (2004) Bacteremia due to Klebsiella pneumoniae isolates producing the TEM-52 extended-spectrum beta-lactamase: treatment outcome of patients receiving imipenem or ciprofloxacin. Clin Infect Dis 38: 243–51.
- 3. Mackenzie FM, Forbes KJ, Dorai-John T, Amyes SG, Gould IM (1997) Emergence of a carbapenem-resistant Klebsiella pneumoniae. Lancet 350(9080): 783.
- 4. Tan TY, Hsu LY, Koh TH, Ng LS, Tee NW, et al. (2008) Antibiotic resistance in gram-negative bacilli: a Singapore perspective. Ann Acad Med Singapore 37(10): 819–25.
- 5. Hsu LY, Tan TY, Tam VH, Kwa A, Fisher DA, et al. (2010) Surveillance and correlation of antibiotic prescription and resistance of Gram-negative bacteria in Singaporean hospitals. Antimicrob Agents Chemother 54(3): 1173–8.
- 6. Walsh TR (2010) Emerging carbapenemases: a global perspective. Int J Antimicrob Agents 36(S3): 8–14.
- 7. Doumith M, Ellington MJ, Livermore DM, Woodford N (2009) Molecular mechanisms disrupting porin expression in ertapenem-resistant Klebsiella and Enterobacter spp. clinical isolates from the UK. J Antimicrob Chemother 63: 659–667.
- 8. Jacoby GA, Mills DM, Chow N (2004) Role of beta-lactamases and porins in resistance to ertapenem and other beta-lactams in Klebsiella pneumoniae. Antimicrob Agents Chemother 48(8): 3203–6.
- 9. Szabó D, Silveira F, Hujer AM, Bonomo RA, Hujer KM, et al. (2006) Outer membrane protein changes and efflux pump expression together may confer resistance to ertapenem in Enterobacter cloacae. Antimicrob Agents Chemother 50(8): 2833–5.
- 10. Leavitt A, Chmelnitsky I, Colodner R, Ofek I, Carmeli Y, et al. (2009) Ertapenem resistance among extended-spectrum-β-lactamase-producing Klebsiella isolates. J Clin Microbiol 47(4): 969–74.
- 11. Wu JJ, Wang LR, Liu YF, Chen HM, Yan JJ (2011) Prevalence and characteristics of ertapenem-resistant Klebsiella pneumoniae isolates in a Taiwanese university hospital. Microb Drug Resist 17(2): 259–66.
- 12. García-Fernández A, Miriagou V, Papagiannitsis CC, Giordano A, Venditti M, et al. (2010) An ertapenem-resistant ESBL-producing Klebsiella pneumoniae clone carries a novel OmpK36 porin variant. Antimicrob Agents Chemother 54: 4178–4184.
- 13. Falagas ME, Rafailidis PI, Kofteridis D, Virtzili S, Chelvatzoglou FC, et al. (2007) Risk factors of carbapenem-resistant Klebsiella pneumoniae infections: a matched case control study. J Antimicrob Chemother 60(5): 1124–30.
- 14. Schwaber MJ, Klarfeld-Lidji S, Navon-Venezia S, Schwartz D, Leavitt A, et al. (2008) Predictors of carbapenem-resistant Klebsiella pneumoniae acquisition among hospitalized adults and effect of acquisition on mortality. Antimicrob Agents Chemother 52(3): 1028–1033.
- 15. Jeon MH, Choi SH, Kwak YG, Chung JW, Lee SO, et al. (2008) Risk factors for the acquisition of carbapenem-resistant Escherichia coli among hospitalized patients. Diagn Microbiol Infect Dis 62(4): 402–6.
- 16. Hussein K, Sprecher H, Mashiach T, Oren I, Kassis I, et al. (2009) Carbapenem resistance among Klebsiella pneumoniae isolates: risk factors, molecular characteristics, and susceptibility patterns. Infect Control Hosp Epidemiol 30(7): 666–71.
- 17. Mouloudi E, Protonotariou E, Zagorianou A, Iosifidis E, Karapanagiotou A, et al. (2010) Bloodstream infections caused by metallo-β-lactamase/Klebsiella pneumoniae carbapenemase-producing K. pneumoniae among intensive care unit patients in Greece: risk factors for infection and impact of type of resistance on outcomes. Infect Control Hosp Epidemiol 31(12): 1250–6.
- 18. Patel , Harrington S, Dihmess A, Woo B, Masoud R, et al. (2011) Clinical epidemiology of carbapenem-intermediate or -resistant Enterobacteriaceae. J Antimicrob Chemother 66(7): 1600–8.
- 19. Kritsotakis EI, Tsioutis C, Roumbelaki M, Christidou A, Gikas A (2011) Antibiotic use and the risk of carbapenem-resistant extended-spectrum-β-lactamase-producing Klebsiella pneumoniae infection in hospitalized patients: results of a double case-control study. J Antimicrob Chemother 66(6): 1383–91.
- 20. Hyle EP, Ferraro MJ, Silver M, Lee H, Hooper DC (2010) Ertapenem-resistant Enterobacteriaceae: risk factors for acquisition and outcomes. Infect Control Hosp Epidemiol 31(12): 1242–9.
- 21. Orsi GB, García-Fernández A, Giordano A, Venditti C, Bencardino A, et al. (2011) Risk factors and clinical significance of ertapenem-resistant Klebsiella pneumoniae in hospitalised patients. J Hosp Infect 78(1): 54–8.
- 22. Kaye KS, Harris AD, Samore M, Carmeli Y (2005) The case-case-control study design: addressing the limitations of risk factor studies for antimicrobial resistance. Infect Control Hosp Epidemiol 26(4): 346–51.
- 23. Harris AD, Karchmer TB, Carmeli Y, Samore MH (2001) Methodological principles of case-control studies that analyze risk factors for antibiotic resistance: a systematic review. Clin Infect Dis 32: 1055–1061.
- 24. Clinical and Laboratory Standards Institute (CLSI) (2009) Performance standards for antimicrobial susceptibility testing – 19th informational supplement. Wayne, PA: CLSI; CLSI document M100–S19.
- 25. Dombek PE, Johnson LK, Zimmerley ST, Sadowsky MJ (2000) Use of repetitive DNA sequences and the PCR to differentiate Escherichia coli isolates from human and animal sources. Appl Environ Microbiol 66(6): 2572–7.
- 26. Monstein HJ, Ostholm-Balkhed A, Nilsson MV, Nilsson M, Dornbusch K, et al. (2007) Multiplex PCR amplification assay for the detection of blaSHV, blaTEM and blaCTX-M genes in Enterobacteriaceae. APMIS 115(12): 1400–8.
- 27. Hindiyeh M, Smollen G, Grossman Z, Ram D, Davidson Y, et al. (2008) Rapid detection of blaKPC carbapenemase genes by real-time PCR. J Clin Microbiol 2008;46(9): 2879–83.
- 28. Ellington MJ, Kistler J, Livermore DM, Woodford N (2007) Multiplex PCR for rapid detection of genes encoding acquired metallo-β-lactamases. J Antimicrob Chemother 59(2): 321–2.
- 29. Woodford N, Fagan EJ, Ellington MJ (2006) Multiplex PCR for rapid detection of genes encoding CTX-M extended-spectrum β-lactamases. J Antimicrob Chemother 57: 154–5.
- 30. Perez-Perez FJ, Hanson ND (2002) Detection of plasmid-mediated AmpC β-lactamase genes in clinical isolates by using multiplex PCR. J Clin Microbiol 40: 2153–62.
- 31. Schwaber MJ, Carmeli Y (2008) Carbapenem-resistant Enterobacteriaceae: a potential threat. JAMA 300: 2911–3.
- 32. Eagye KJ, Kuti JL, Nicolau DP (2009) Risk factors and outcomes associated with isolation of meropenem high-level-resistant Pseudomonas aeruginosa. Infect Control Hosp Epidemiol 30(8): 746–52.
- 33. Baran G, Erbay A, Bodur H, Ongürü P, Akinci E, et al. (2008) Risk factors for nosocomial imipenem-resistant Acinetobacter baumannii infections. Int J Infect Dis 12(1): 16–21.
- 34. Ikonomidis A, Tokatlidou D, Kristo I, Sofianou D, Tsakris A, et al. (2005) Outbreaks in distinct regions due to a single Klebsiella pneumoniae clone carrying a bla VIM-1 metallo β-lactamase gene. J Clin Microbiol 43(10): 5344–7.
- 35. Bradford PA, Bratu S, Urban C, Visalli M, Mariano N, et al. (2004) Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 β-lactamases in New York City. Clin Infect Dis 39: 55–60.
- 36. Bratu S, Landman D, Haag R, Recco R, Eramo A, et al. (2005) Rapid spread of carbapenem-resistant Klebsiella pneumoniae in New York City: a new threat to our antibiotic armamentarium. Arch Intern Med 165: 1430–1435.
- 37. Woodford N, Tierno PM Jr, Young K, Tysall L, Palepou MF, et al. (2004) Outbreak of Klebsiella pneumoniae producing a new carbapenem-hydrolyzing class A β-lactamase, KPC-3, in a New York Medical Center. Antimicrob Agents Chemother 48(12): 4793–9.