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The effect of varying multidrug-resistence (MDR) definitions on rates of MDR gram-negative rods

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Abstract

Background

A multitude of definitions determining multidrug resistance (MDR) of Gram-negative organisms exist worldwide. The definitions differ depending on their purpose and on the issueing country or organization. The MDR definitions of the European Centre for Disease Prevention and Control (ECDC) were primarily chosen to harmonize epidemiological surveillance. The German Commission of Hospital Hygiene and Infection Prevention (KRINKO) issued a national guideline which is mainly used to guide infection prevention and control (IPC) measures. The Swiss University Hospital Zurich (UHZ) – in absentia of national guidelines – developed its own definition for IPC purposes. In this study we aimed to determine the effects of different definitions of multidrug-resistance on rates of Gram-negative multidrug-resistant organisms (GN-MDRO).

Methods

MDR definitions of the ECDC, the German KRINKO and the Swiss University Hospital Zurich were applied on a dataset comprising isolates of Escherichia coli, Klebsiella pneumoniae, Enterobacter sp., Pseudomonas aeruginosa, and Acinetobacter baumannii complex. Rates of GN-MDRO were compared and the percentage of patients with a GN-MDRO was calculated.

Results

In total 11′407 isolates from a 35 month period were included. For Enterobacterales and P. aeruginosa, highest MDR-rates resulted from applying the ‘ECDC-MDR’ definition. ‘ECDC-MDR’ rates were up to four times higher compared to ‘KRINKO-3/4MRGN’ rates, and up to six times higher compared to UHZ rates. Lowest rates were observed when applying the ‘KRINKO-4MRGN’ definitions. Comparing the ‘KRINKO-3/4MRGN’ with the UHZ definitions did not show uniform trends, but yielded higher rates for E. coli and lower rates for P. aeruginosa. On the patient level, the percentages of GN-MDRO carriers were 2.1, 5.5, 6.6, and 18.2% when applying the ‘KRINKO-4MRGN’, ‘UHZ-MDR’, ‘KRINKO-3/4MRGN’, and the ‘ECDC-MDR’ definition, respectively.

Conclusions

Different MDR-definitions lead to considerable variation in rates of GN-MDRO. Differences arise from the number of antibiotic categories required to be resistant, the categories and drugs considered relevant, and the antibiotic panel tested. MDR definitions should be chosen carefully depending on their purpose and local resistance rates, as definitions guiding isolation precautions have direct effects on costs and patient care.

Background

The number of gram-negative bacteria that are resistant to multiple antibiotics is on a constant rise and infections due to these resistant organisms pose an increasing threat to the achievements of modern medicine [1, 2]. Besides standard infection prevention precautions, most hospitals apply additional transmission-based precautions to reduce the spread of gram-negative multidrug-resistant organisms (GN-MDRO) from colonized or infected patients to others. Whether or not care for a patient with a GN-MDRO needs additional precautions deserves judgement about the organism’s clinical and epidemiological significance [3], as isolation precautions cause high direct and indirect costs, and were shown to negatively impact several dimensions of patient care [4, 5]. It is well known that the definitions of multidrug resistance (MDR) are neither harmonized between countries, nor between hospitals in the same country, nor do guidelines on infection prevention and control (IPC) standards for patients with GN-MDRO exist to date [6,7,8].

In Europe, a multitude of definitions for GN-MDRO with varying purposes do exist: The MDR definitions of the European Centre for Disease Prevention and Control (ECDC), published in 2011, were primarily chosen to harmonize epidemiological surveillance data across healthcare settings and countries [9]. The ECDC criteria define MDR as acquired non-susceptibility to at least one agent in three or more antimicrobial categories. Categories were constructed with the intent of placing antimicrobial agents into therapeutically relevant groups and each category is considered equally relevant.

Germany has a nationwide MDR definition, issued by the national German Commission of Hospital Hygiene and Infection Prevention (KRINKO) in 2012, which is primarily used to guide IPC measures [10]. The German KRINKO defines MDR according to resistance to commonly used agents to treat severe infections (i.e. antipseudomonal penicillins, extended spectrum cephalosporins, carbapenems and quinolones). It grades resistance by severity into multidrug resistance to three and four antibiotic categories. Isolation precautions are recommended for all patients with bacterial species resistant to four antibiotic categories. For patients with species resistant to three antibiotic categories, isolation precautions are warranted for patients on high-risk wards (e.g. hemato-oncology) with Escherichia coli, Klebsiella sp., Enterobacter sp., Pseudomonas aeruginosa, and Acinetobacter baumanii.

In Switzerland, no national consensus guidelines on MDR definitions exist to date. Therefore, the University Hospital Zurich (UHZ) developed its own definition in 2008. These definitions are based on clinical reasoning, local resistance rates, antibiotic use policies, and international expert proposals [11]. They are mainly used to guide IPC measures. The UHZ-guidelines define MDR as resistance to agents of three out of five antimicrobial categories including the aminoglycosides. Unlike the ECDC and KRINKO definitions, the UHZ also includes the ESBL-phenotype of Enterobacterales (except Escherichia coli) as MDR. E. coli ESBL is not considered a GN-MDRO following recommendations of the Swiss national center for infection control (Swissnoso) recommending standard precautions for this specific ESBL-producing species [12].

Differences in MDR definitions do have an impact on percentage of gram-negatives considered MDRO and, if used to guide IPC measures, on patients requiring isolation precautions. The primary aim of this study was to analyze the impact of the ECDC, KRINKO and UHZ definitions on the rate of GN-MDRO and the resulting number of patients characterized as GN-MDRO carriers. To describe the influence of the different MDR definition criteria, we applied the definition criteria of ECDC, KRINKO and UHZ on 11′407 isolates of five common gram-negative species isolated during a 35 month period in patients from the UHZ.

Methods

Setting

The University Hospital Zurich, Zurich, Switzerland, is an 950-bed tertiary-care teaching hospital covering all medical specialties except paediatrics and orthopaedics. All microbiologic samples are tested in the clinical microbiology laboratory of the Institute of Medical Microbiology, University of Zurich, Zurich, Switzerland. The Institute of Medical Microbiology collects all raw data of disk diffusion antimicrobial susceptibility testing (i.e. inhibition zone diameters) in a dedicated database (Sirweb, i2a, Montpellier, France), allowing re-analysis of the raw data.

Isolates and patients

Data from gram-negative rods isolated during a 35-month period from 1.1.2013 to 1.12.2015 were analysed. Species analysed comprised Escherichia coli, Klebsiella pneumoniae, Enterobacter sp., Pseudomonas aeruginosa, and Acinetobacter baumannii complex. In order to prevent the exclusion of potential MDR follow-up isolates which arise from selective pressure under therapy, we intentionally included all repeat isolates, neglecting guidelines for analysis and presentation of cumulative antibiograms advising inclusion of first isolates per patient only [13]. We only included isolates with a miminum of the following antibiotics tested (required for the ‘UHZ-2008’ definitions, see below): piperacillin/tazobactam, ceftriaxone (for Enterobacterales), ceftazidime, cefepime, ertapenem (for Enterobacterales), imipenem, meropenem, levofloxacin, ciprofloxacin, amikacin, tobramycin and gentamicin. In total, we included 11.407 isolates from 8.454 patients.

To assess the percentage of patients with colonisation or infection with a GN-MDRO, we divided the number of patients with at least one GN-MDRO by the total patient population included in the study.

Susceptibility testing, detection of resistance mechanisms and species identification

Only data collected during routine diagnostic testing was included in this study. For susceptibility testing, the disc diffusion method according to Kirby-Bauer was used. Antibiotic discs were obtained from i2a (Montpellier, France). Susceptibility testing was done on Mueller-Hinton agar (Becton-Dickinson, Franklin Lakes, NJ, USA) using MacFarland 0.5 from overnight cultures followed by incubation at 35 °C for 16-18 h. Inhibition zone diameters were determined and recorded in the automated Sirweb/Sirscan system (i2a) and interpreted according to EUCAST 2015 guidelines [14]. When EUCAST provided no interpretation guidelines for the tested antibiotics, CLSI 2015 guidelines were applied [15]: ceftriaxone, cefepime, ceftazidime and piperacillin/tazobactam for A. baumannii complex, fosfomycin for the Enterobacterales, minocycline and tetracycline for Enterobacterales and A. baumannii complex. Since July 2015 susceptibility to ciprofloxacin and levofloxacin of Enterobacterales was inferred from the susceptibility from norfloxacin. Intermediate susceptibility is interpreted as resistant.

ESBL production was phenotypically detected by using screening cut-off values for cephalosporines, followed by phenotypic confirmation with combination-disk and double-disk synergy tests and, in non-distinctive cases, molecular detection of ESBL genes [16, 17]. Carbapenemase production was phenotypically detected by using screening cut-off values for meropenem, followed by phenotypic confirmation with combination disk tests and molecular detection of carbepenemase genes [16, 18, 19].

Species identification was performed by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) by the direct transfer-formic acid method using Bruker Biotyper MALDI-TOF MS System (Bruker corporation) [20].

MDR-definitions of ECDC, KRINKO and UHZ

The three different MDR definitions per bacterial species are depicted in Tables 1, 2 and 3.

Table 1 Definition criteria and antibiotic panel for Enterobacterales (Escherichia coli, Klebsiella pneumoniae and Enterobacter sp.)
Table 2 Definition criteria and antibiotic panel for Pseudomonas aeruginosa
Table 3 Definition criteria and antibiotic panel for Acinetobacter baumannii complex

ECDC definitions, published by Magiorakos et al. in 2011 [9]: The ECDC definitions define multidrug-resistance, ‘ECDC-MDR’, by non-susceptibility to at least one agent in three or more of 17 antimicrobial categories for Enterobacterales, of eight categories for P. aeruginosa, and of nine categories for A. baumanii.

German KRINKO definitions, published in 2012 [10]: The definition includes two MDR categories, ‘KRINKO-3MRGN’ and ‘KRINKO-4MRGN’ (MRGN = “Multiresistente gramnegative Stäbchen”, English: “multiresistant gram-negative rods”). Antibiotics and/or drug categories that are considered relevant for the MDR-definition are i) piperacillin, ii) cephalosporins (cefotaxime (or cefepime for P.aeruginosa), ceftazidime) iii) ciprofloxacin, and iv) carbapenems (meropenem and imipenem). ‘KRINKO-3MRGN’ and ‘KRINKO-4MRGN’ is defined by resistance to three and four categories, respectively. Carbapenemase production automatically defines ‘KRINKO-4MRGN’. Other genotypic or phenotypic test results are not considered relevant. As bacteria of both MDR categories trigger isolation precautions, we created the category KRINKO-3/4MRGN comprising species of KRINKO-3MRGN and KRINKO-4MRGN.

UHZ-definitions, developed in 2008: The UHZ-definitions classify bacteria to ‘UHZ-MDR’ by nonsusceptibility to one or several agents of at least three out of five drug categories. In addition, ESBL producing bacteria (except E. coli) and carbapenamase producing bacteria are always classified as ‘UHZ-MDR’, irrespective of the reported susceptibilities.

Adaptions due to local antibiotic panel

As the Institute of Medical Microbiology of the University of Zurich tested piperacillin/tazobactam but not piperacillin alone (which is required in the KRINKO definitions), piperacillin resistance of Enterobacterales and A. baumanii complex was inferred from resistance to cefotaxime or ceftazidime as it is advised from the German KRINKO [21]. For the same reason, cefotaxime was replaced by ceftriaxone for the KRINKO definitions.

Statistical analyses

Differences in group proportions were assessed using Fisher’s exact test. We used Stata (Version 15.1, StataCorp, College Station, Texas) for statistical analyses. In order to address incidental findings associated with multiple testing, only P-values <.001 were considered statistically significant.

Results

We included 4′300 isolates of E. coli, 1′161 isolates of K. pneumoniae, 610 isolates of Enterobacter sp., 5′158 isolates of P. aeruginosa and 178 isolates of A. baumannii complex into the analysis. Susceptibility rates for all relevant antibiotics are shown in Additional file 1: Figure S1.

Isolates classified as GN-MDRO

The percentages of isolates per species fulfilling the different MDR definitions are shown in Fig. 1a-e. E.coli, K. pneumonia, Enterobacter sp. and P.aeruginosa had highest rates of multidrug resistance when analysed according to the ‘ECDC-MDR’ definitions and lowest rates when applying the ‘KRINKO-4MRGN’ definitions. Interestingly, the ‘KRINKO-3/4MRGN’ definitions did not result in uniformly lower or higher MDR rates as compared to UHZ-definitions. Among Enterobacterales the ‘KRINKO-3/4MRGN’ definitions caused higher rates in MDR E. coli, whereas in K. pneumonia and Enterobacter sp. rates were comparable. By contrast, the ‘KRINKO-3/4MRGN’ lead to a lower percentage of MDR P. aeruginosa. In A. baumanii complex all four definitions lead to comparable MDR rates. P-values of all comparisons are shown in the Additional file 2: Table S1.

Fig. 1
figure1

Percentages of isolates and patients fulfilling the respective GN-MDRO criteria. Light grey bars are the percentage of isolates classified as GN-MDRO according to the respective definition criteria. Grey bars are the percentage of patients who ever had an isolate fulfilling the respective definition criteria. The definition criteria are shown in Tables 1, 2 and 3. ECDC-MDR, multidrug resistance according to the European Centre for Disease Prevention and Control; GN-MDRO, Gram-negative multirdrug resistant organisms; KRINKO-3/4MRGN, multidrug resistance defined as resistance to three or four antibiotic categories according to the German Commission of Hospital Hygiene and Infection Prevention; KRINKO-4MRGN, multidrug resistance defined as resistance to four antibiotic categories according to the German Commission of Hospital Hygiene and Infection Prevention; UHZ-MDR, multidrug resistance according to University Hospital Zurich guidelines

Patients with a GN-MDRO

The percentage of patients colonised or infected with any GN-MDRO is depicted in Fig. 1f. The percentage is highest with 18.2% (95% confidence interval (CI), 17.4–19.0%) when applying the ‘ECDC-MDR’ definition and lowest with 2.1% (95% CI, 1.8–2.4%) when applying the ‘KRINKO-4MRGN’ definition. From the definitions used to guide IPC measures, the ‘KRINKO-3/4MRGN’ definition lead to highest percentages.

Discussion

This study demonstrated major differences in rates of GN-MDRO when applying the four definitions of the ECDC, the German KRINKO and the Swiss UHZ. Highest rates of 32–46% for Enterobacterales, P. aeruginosa and A. baumannii were found when applying the ‘ECDC-MDR’ definitions, which were primarily chosen to harmonize epidemiological surveillance data and are defined by acquired resistance to at least one antibiotic of any three drug categories. Lowest rates were induced by applying the ‘KRINKO-4MRGN’ definition - definitions requiring resistance in all four relevant drug categories. On the patient level, the ‘ECDC-MDR’ definitions lead to around thrice as many patients with GN-MDRO compared to the ‘UHZ-MDR’ and the ‘KRINKO-3/4MRGN’ criteria, and around nine times as many patients compared to the ‘KRINKO-4MRGN’ criteria.

MDR definitions differ between agencies, countries, and even between hospitals in a particular country [7]. A survey among members of the SHEA Research network in 2012/2013 showed that among 66 hospitals, there were 22 different MDR definitions for Enterobacterales [7]. The survey also revealed that the most commonly selected definition of MDR for Enterobacterales, A. baumannii complex and P. aeruginosa was resistance to three or more classes of antimicrobials. A literature review in 2006 showed that various definitions are used for the terms MDR A. baumannii complex and P. aeruginosa [22]. MacKinnon et al. evaluated the effects of applying three MDR classification metrics on E. coli isolates from chicken abattoir surveillance samples and showed that rates were highest when the isolates were non-susceptible to ≥3 antibiotic drugs (53.3%), followed by non-susceptible to ≥3 antibiotic categories (i.e. the ‘ECDC-MDR’ definition, 49.4%), and ≥ 3 antibiotic classes (38.5%) [23].

All definitions evaluated in the current study – irrespective if used for surveillance reasons or to guide IPC-precautions - use a ‘category approach’. As expected, the more categories are required to be resistant, the less isolates are considered GN-MDRO. This explains the lowest rates by applying the ‘KRINKO-4MRGN’ definition defined by resistance to all four tested categories. Regarding definition criteria requiring resistance to three drug categories (‘ECDC-MDR’, ‘KRINKO-3/4MRGN’, UHZ-definitions), differences arise from the number of categories taken into consideration, and the number of drugs in the respective drug category required to be resistant. As expected, the ‘ECDC-MDR’ definitions – with highest number of relevant drug categories (i.e. up to 17 categories compared to four or five in Enterobacterales) and lowest number of antibiotics required to be resistant per drug category (i.e. one antibiotic compared to up to three) - lead to considerably higher rates of GN-MDRO than the other two definition criteria. The difference between UHZ-MDR and KRINKO-3/4MRGN E. coli (7.8% vs. 11.3%) may be driven by E.coli ESBL producing species that fulfill the ‘KRINKO-3/4MRGN’ definition, but do not meet the UHZ-MDR definitions: Although the UHZ criteria generally consider ESBL-producing strains - detected phenotypically or genotypically - as GN-MDRO, regardless of whether the strains fulfill the ‘UHZ-MDR’ criteria otherwise, the E. coli ESBL isolated are treated as an exception. E.coli are not per se considered UHZ-MDR because E.coli has a demonstrated lower transmission potential than other Enterobacterales, and hence bear a lesser potential for outbreaks [24, 25]. In comparison, e.g. K. pneumoniae shows a clear trend to spread clonally within healthcare institutions, and K. pneumoniae ESBL are considered UZH-MDR irrespective ot other drug resistances being presented or not [26].

When applying the three definition criteria used to guide IPC measures (both KRINKO and the UHZ definition) on the patient level, only 2% of patients are colonized or infected with bacteria fulfilling the ‘KRINKO-4MRGN’ definitions. The UHZ-definition and the ‘KRINKO-3/4MRGN’ definition lead to 5.6 and 6.6% of patients with an GN-MDRO, respectively. The difference between the UHZ-definitions and the ‘KRINKO-3/4MRGN’ definition is driven by the difference in MDR E. coli, the only species in which UHZ-definitions showed lower results than KRINKO-3/4MRGN. This relative difference of 16% between UHZ- and ‘KRINKO-3/4MRGN’ definitions still is considerable when taking into account that most hospitals would assign patients with GN-MDRO to a single room and ask for resource intensive isolation precautions. A study by Tran et al. showed that patients isolated for methicillin resistant Staphylococcus aureus in comparison to non-isolated patients had longer lengths of hospital stay, stayed in hospital longer than expected, and had higher costs [5]. Direct costs of isolation precautions in a Swiss hospital were calculated to sum up to 158 $ per day [4].

Our study has limitations. First, it was conducted in a low prevalence country for GN-MDRO and our results might not be similarly applicable to higher prevalence regions. Second, the antibiotic panel tested has a critical influence on resistance rates, especially for the ‘ECDC-MDR” definition. Broadly speaking, the higher the number of antibiotics on the panel the higher the probability that an isolate is considered ‘ECDC-MDR’. The ECDC emphazises the necessity of testing an adequate number of antimicrobial agents in order to effectively apply the ECDC-definitions, but even in a high-income country like Switzerland, the antibiotic panel tested for Enterobacterales is smaller than the proposed ECDC panel. This is due to financial restrictions that force clinical laboratories to work at least cost-neutral. Also, manufacturers of microdilution assays often preset the antibiotic panel tested. These facts extrinsicaly cause differences in ‘ECDC-MDR’ rates and preclude comparisons between hospitals with different antibiotic panel. Still, as we were unable to identify other studies trying to answer this research question, our study provides unique data demonstrating the difference of GN-MDRO rates after applying diverse resistance definitions to a “real-world” clinical database with a “real-world” antibiotic panel.

Conclusion

By demonstrating that rates of gram-negatives classified as MDRO differ considerably depending on the applied MDR-criteria, we consider choosing definition criteria carefully depending on their purpose to be of high importance. For determining definitions directing isolation precautions, local resistance rates and epidemiological priorities as well as available resources should be taken into consideration. The additional effort and costs of isolation precautions should be in due proportion to the expected benefit. GN-MDRO abundantly present in the population likely do not require isolation precautions. MDR definitions should be consistent, clearly communicated, and reviewed regularly. More studies applying the different definitions on datasets from high prevalence regions or testing the effects of other definitions would provide useful information to further get insight in the landscape of GN-MDRO worldwide. Additionally, the effect of EUCASTs new definitions of susceptibility testing categories would be interesting to evaluate [27].

Availability of data and materials

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

Abbreviations

ECDC-MDR:

Multidrug resistance according to ECDC definitions

MDR:

Multidrug resistance

ECDC:

European Centre for Disease Prevention and Control

GN-MDRO:

Gram-negative multidrug-resistant organisms

IPC:

Infection prevention and control

KRINKO:

German Commission of Hospital Hygiene and Infection Prevention (German: Kommission für Krankenhaushygiene und Infektionsprävention)

KRINKO-3/4MRGN:

Multidrug resistance to three or four drug categories according to KRINKO definitions

KRINKO-3MRGN:

Multidrug resistance to three drug categories according to KRINKO definitions

KRINKO-4MRGN:

Multidrug resistance to four drug categories according to KRINKO definitions

MDR:

Multidrug resistance

UHZ:

University Hospital Zurich

UHZ-MDR:

Multidrug resistance according to the University Hospital Zurich guidelines

References

  1. 1.

    Glasner C, Albiger B, Buist G, Tambic Andrasevic A, Canton R, Carmeli Y, et al. Carbapenemase-producing Enterobacteriaceae in Europe: a survey among national experts from 39 countries, February 2013. Euro Surveill. 2013;18(28):20525.

  2. 2.

    Antimicrobial resistance surveillance in Europa. ECDC-Homepage: http://ecdc.europa.eu/en/publications/Publications/antimicrobial-resistance-europe-2014.pdf, last Accessed January 2019.

  3. 3.

    2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings. CDC. http://www.cdc.gov/hicpac/pdf/isolation/Isolation2007.pdf, last Accessed Jan 2019.

  4. 4.

    Roth JA, Hornung-Winter C, Radicke I, Hug BL, Biedert M, Abshagen C, et al. Direct costs of a contact isolation day: a prospective cost analysis at a Swiss University hospital. Infect Control Hosp Epidemiol. 2018;39(1):101–3.

  5. 5.

    Tran K, Bell C, Stall N, Tomlinson G, McGeer A, Morris A, et al. The effect of hospital isolation precautions on patient outcomes and cost of care: a multi-site, retrospective, propensity score-matched cohort study. J Gen Intern Med. 2017;32(3):262–8.

  6. 6.

    Muller J, Voss A, Kock R, Sinha B, Rossen JW, Kaase M, et al. Cross-border comparison of the Dutch and German guidelines on multidrug-resistant gram-negative microorganisms. Antimicrob Resist Infect Control. 2015;4:7.

  7. 7.

    Drees M, Pineles L, Harris AD, Morgan DJ. Variation in definitions and isolation procedures for multidrug-resistant gram-negative bacteria: a survey of the Society for Healthcare Epidemiology of America research network. Infect Control Hosp Epidemiol. 2014;35(4):362–6.

  8. 8.

    Gysin DV, Cookson B, Saenz H, Dettenkofer M, Widmer AF. Infections ESGfN. Variability in contact precautions to control the nosocomial spread of multi-drug resistant organisms in the endemic setting: a multinational cross-sectional survey. Antimicrob Resist Infect Control. 2018;7:81.

  9. 9.

    Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268–81.

  10. 10.

    Hygienemassnahmen bei Infektionen oder Besiedlung mit multiresistenten gramnegativen Stäbchen; Empfehlungen der Kommission für Kranknehaushygiene und Infektionsprävention (KRINKO) beim Robert Koch Institut (RKI); https://www.rki.de/DE/Content/Infekt/Krankenhaushygiene/Kommission/Downloads/Gramneg_Erreger.pdf?__blob=publicationFile; last Accessed Jan 2019.

  11. 11.

    Kuster SP, Ruef C, Zbinden R, Gottschalk J, Ledergerber B, Neuber L, et al. Stratification of cumulative antibiograms in hospitals for hospital unit, specimen type, isolate sequence and duration of hospital stay. J Antimicrob Chemother. 2008;62(6):1451–61.

  12. 12.

    Swissnoso; “Enterobacteriaceae mit Breitspektrum Beta-Laktamasen (ESBL) im Spital: Neue Empfehlungen Swissnoso 2014”, https://www.swissnoso.ch/fileadmin/swissnoso/Dokumente/6_Publikationen/Bulletin_Artikel_D/v18_2_2014-03_Swissnoso_Bulletin_de.pdf, last Accessed Sept 2019.

  13. 13.

    Hindler JF, Stelling J. Analysis and presentation of cumulative antibiograms: a new consensus guideline from the clinical and laboratory standards institute. Clin Infect Dis. 2007;44(6):867–73.

  14. 14.

    European committee on Antimicrobial Susceptibility testing. Breakpoint tables for interpretation of MICs and zone diameters. Version 5.0. http://www.eucast.org/fileadmin/src/media/PDFs/EUCAST_files/Breakpoint_tables/v_5.0_Breakpoint_Table_01.pdf; last Accessed Jan 2019.

  15. 15.

    Performance standards for antimicrobial susceptibility testing: twenty-fifth informational supplement, Sample. CLSI, January 2015. http://www.medsci.cn/webeditor/uploadfile/201505/20150518150013313.pdf, last Accessed Jan 2019.

  16. 16.

    European committee on antimicriobial susceptibility testing (EUCAST): EUCAST guidelines for detection of resistance mechanisms and specific resistances of clinical and/or epidemiological importance , Version 1.0.; http://www.eucast.org/resistance_mechanisms/; last Accessed Sept 2019.

  17. 17.

    Bloemberg GV, Polsfuss S, Meyer V, Bottger EC, Hombach M. Evaluation of the AID ESBL line probe assay for rapid detection of extended-spectrum beta-lactamase (ESBL) and KPC carbapenemase genes in Enterobacteriaceae. J Antimicrob Chemother. 2014;69(1):85–90.

  18. 18.

    Maurer FP, Castelberg C, Quiblier C, Bloemberg GV, Hombach M. Evaluation of carbapenemase screening and confirmation tests with Enterobacteriaceae and development of a practical diagnostic algorithm. J Clin Microbiol. 2015;53(1):95–104.

  19. 19.

    Bloemberg GV, Braun-Kiewnick A, Tedrup J, Meijerink C, Durer E, Ritter C, et al. Evaluation of the AID carbapenemase line probe assay for rapid detection and identification of carbapenemase genes in gram-negative bacilli. J Antimicrob Chemother. 2017;72(7):1948–54.

  20. 20.

    Schulthess B, Brodner K, Bloemberg GV, Zbinden R, Bottger EC, Hombach M. Identification of gram-positive cocci by use of matrix-assisted laser desorption ionization-time of flight mass spectrometry: comparison of different preparation methods and implementation of a practical algorithm for routine diagnostics. J Clin Microbiol. 2013;51(6):1834–40.

  21. 21.

    Antworten auf häufig gestellte Fragen im Zusammenhang mit der Klassifikation von 3MRGN und 4MRGN durch mikrobiologische Laboratorien. http://memiserf.medmikro.ruhr-uni-bochum.de/nrz/FAQ_zu_MRGN-Klassifikation_20130123.pdf.

  22. 22.

    Falagas ME, Koletsi PK, Bliziotis IA. The diversity of definitions of multidrug-resistant (MDR) and pandrug-resistant (PDR) Acinetobacter baumannii and Pseudomonas aeruginosa. J Med Microbiol. 2006;55(Pt 12):1619–29.

  23. 23.

    MacKinnon MC, Pearl DL, Carson CA, Parmley EJ, McEwen SA. Comparison of annual and regional variation in multidrug resistance using various classification metrics for generic Escherichia coli isolated from chicken abattoir surveillance samples in Canada. Prev Vet Med. 2018;154:9–17.

  24. 24.

    Freeman JT, Nimmo J, Gregory E, Tiong A, De Almeida M, McAuliffe GN, et al. Predictors of hospital surface contamination with extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae: patient and organism factors. Antimicrob Resist Infect Control. 2014;3(1):5.

  25. 25.

    Hilty M, Betsch BY, Bogli-Stuber K, Heiniger N, Stadler M, Kuffer M, et al. Transmission dynamics of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the tertiary care hospital and the household setting. Clin Infect Dis. 2012;55(7):967–75.

  26. 26.

    Harris AD, Perencevich EN, Johnson JK, Paterson DL, Morris JG, Strauss SM, et al. Patient-to-patient transmission is important in extended-spectrum beta-lactamase-producing Klebsiella pneumoniae acquisition. Clin Infect Dis. 2007;45(10):1347–50.

  27. 27.

    European committee on antimicriobial susceptibility testing (EUCAST): New definitions of S, I and R. http://www.eucast.org/newsiandr/, last Accessed Feb 2019.

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Acknowledgements

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Funding

AW is supported by the academic career program “Filling the gap” of the Medical Faculty of the University of Zurich.

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AW and MH designed the study. AW and MH acquired the data, and AW and SPK performed the statistical analysis. AW, MH, SPK, MM, and RZ analyzed and interpreted the data. AW drafted the manuscript, and MH, SPK, MM, and RZ provided critical review of the manuscript for important intellectual content. All authors agree with the content and conclusions of this manuscript. All authors read and approved the final manuscript

Correspondence to Aline Wolfensberger.

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Wolfensberger, A., Kuster, S.P., Marchesi, M. et al. The effect of varying multidrug-resistence (MDR) definitions on rates of MDR gram-negative rods. Antimicrob Resist Infect Control 8, 193 (2019) doi:10.1186/s13756-019-0614-3

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Keywords

  • MDRO
  • gram-negatives
  • Multidrug-resistance
  • ECDC
  • KRINKO