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<strong>Antimicrobial</strong> <strong>resistance</strong><strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong>Annual report of the <strong>Europe</strong>an <strong>Antimicrobial</strong>Resistance Surveillance Network (EARS-Net)2011


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTThe <strong>Europe</strong>an Centre for Disease Prevention and Control (ECDC) wishesto thank all EARS-Net participat<strong>in</strong>g laboratories and hospitals <strong>in</strong> theMember States for provid<strong>in</strong>g data for this report.Furthermore, all EARS-Net participants and National EpidemiologicalContact Po<strong>in</strong>ts are acknowledged for facilitat<strong>in</strong>g data transferand provid<strong>in</strong>g valuable comments for this report. The ECDC’s staffmembers Silvia Sarbu and Dana Ursut, and WHONET representativeJohn Stell<strong>in</strong>g are acknowledged for data management and provid<strong>in</strong>gtechnical support to the participat<strong>in</strong>g countries.ECDC’s staff members Liselotte Diaz Högberg and Ole Heuer areacknowledged for the preparation of the report, and Christ<strong>in</strong>e Waltonat UK NEQAS is acknowledged for her contribution to Annex 1. Inaddition, the ECDC wishes to thank EARS-Net Coord<strong>in</strong>ation groupmembers Christian Giske, Hajo Grundmann, V<strong>in</strong>cent Jarlier, GunnarKahlmeter, Jolanta Miciuleviciene, Jos Monen, Gian Maria Rossol<strong>in</strong>i,Gunnar Skov Simonsen, Nienke van de Sande-Bru<strong>in</strong>sma and HelenaZemlickova for provid<strong>in</strong>g valuable comments and scientific advicedur<strong>in</strong>g the production of the report.Suggested citation for full report:<strong>Europe</strong>an Centre for Disease Prevention and Control. <strong>Antimicrobial</strong><strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011. Annual Report of the<strong>Europe</strong>an <strong>Antimicrobial</strong> Resistance Surveillance Network (EARS-Net).Stockholm: ECDC; 2012.Cover picture © istockphotoISSN 1831-9491ISBN 978-92-9193-398-3doi 10.2900/6551© <strong>Europe</strong>an Centre for Disease Prevention and Control, 2012.Reproduction is authorised, provided the source is acknowledged.ii


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011ContentsList of tables ................................................................................................................................................... ivList of figures ................................................................................................................................................. ivAbbreviations and acronyms ...................................................................................................................... viNational <strong>in</strong>stitutions/organisations participat<strong>in</strong>g <strong>in</strong> EARS-Net ........................................................ viiSummary ........................................................................................................................................................... 11 Introduction ................................................................................................................................................... 32 Data collection and analysis .................................................................................................................... 52.1 Data analysis ............................................................................................................................................... 62.2 Interpretation of the results .......................................................................................................................... 63 Demographic characteristics of cases of <strong>in</strong>vasive gram-negative <strong>in</strong>fections <strong>in</strong> <strong>Europe</strong>. . . . . . . . . . . 93.1. Introduction ................................................................................................................................................ 93.2. Material and methods .................................................................................................................................. 93.3 Results ....................................................................................................................................................... 103.4 Discussion .................................................................................................................................................. 114 <strong>Antimicrobial</strong> <strong>resistance</strong> <strong>in</strong> <strong>Europe</strong> ........................................................................................................ 134.1 Escherichia coli. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134.2 Klebsiella pneumoniae ................................................................................................................................ 234.3 Pseudomonas aerug<strong>in</strong>osa ........................................................................................................................... 344.4 Streptococcus pneumoniae ......................................................................................................................... 474.5 Staphylococcus aureus ................................................................................................................................. 554.6 Enterococci ................................................................................................................................................ 59References ...................................................................................................................................................... 69Annex 1 External quality assessment (EQA) exercise 2011 ................................................................ 69Annex 2 EARS-Net laboratory/hospital denom<strong>in</strong>ator data 2011 ........................................................ 75Country summary sheets ............................................................................................................................. 81iii


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SummaryThe results presented <strong>in</strong> this report are based on antimicrobial<strong>resistance</strong> data from <strong>in</strong>vasive isolates reportedto EARS-Net by 29 EU/EEA countries <strong>in</strong> 2012 (data referr<strong>in</strong>gto 2011), and on trend analyses of EARSS/EARS-Netdata reported by the participat<strong>in</strong>g countries dur<strong>in</strong>g theperiod 2008 to 2011.The results show a general <strong>Europe</strong>-wide <strong>in</strong>crease of antimicrobial<strong>resistance</strong> <strong>in</strong> the gram-negative pathogensunder <strong>surveillance</strong> (Escherichia coli, Klebsiella pneumoniaeand Pseudomonas aerug<strong>in</strong>osa), whereas theoccurrence of <strong>resistance</strong> <strong>in</strong> the gram-positive pathogens(Streptococcus pneumoniae, Staphylococcus aureus,Enterococcus faecium and Enterococcus faecalis) appearsto be stabilis<strong>in</strong>g or even decreas<strong>in</strong>g <strong>in</strong> some countries.For most pathogen–antimicrobial comb<strong>in</strong>ations, large<strong>in</strong>ter-country variations are evident.In 2011, the most alarm<strong>in</strong>g evidence of <strong>in</strong>creas<strong>in</strong>gantimicrobial <strong>resistance</strong> <strong>in</strong> <strong>Europe</strong> came from data oncomb<strong>in</strong>ed <strong>resistance</strong> (<strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides)<strong>in</strong> E. coli and <strong>in</strong> K. pneumoniae. For both of these pathogens,more than one third of the report<strong>in</strong>g countries hadsignificantly <strong>in</strong>creas<strong>in</strong>g trends of comb<strong>in</strong>ed <strong>resistance</strong>over the last four years.The high and <strong>in</strong>creas<strong>in</strong>g percentage of comb<strong>in</strong>ed <strong>resistance</strong>observed for K. pneumoniae means that for somepatients with life-threaten<strong>in</strong>g <strong>in</strong>fections, only a fewtherapeutic options rema<strong>in</strong> available, e.g. carbapenems.However s<strong>in</strong>ce 2010, carbapenem-<strong>resistance</strong> has<strong>in</strong>creased <strong>in</strong> a number of countries, further aggravat<strong>in</strong>gthe situation. For P. aerug<strong>in</strong>osa, comb<strong>in</strong>ed <strong>resistance</strong>is also common, with 15% of the isolates resistantto at least three of the antimicrobial classes under<strong>surveillance</strong>. The seem<strong>in</strong>gly unimpeded <strong>in</strong>crease ofantimicrobial <strong>resistance</strong> <strong>in</strong> the major gram-negativepathogens will unavoidably lead to loss of therapeutictreatment options.In parallel, other trends of antimicrobial <strong>resistance</strong>reported to EARS-Net <strong>in</strong>dicate that national effortson <strong>in</strong>fection control and conta<strong>in</strong>ment of <strong>resistance</strong> areeffective, as illustrated by the trends for meticill<strong>in</strong>resistantS. aureus (MRSA), antimicrobial-resistant S.pneumoniae and antimicrobial-resistant enterococci,for which the situation appears generally stable or evenimprov<strong>in</strong>g <strong>in</strong> some countries. For MRSA, these observationsare consistent with reports from the national<strong>surveillance</strong> programmes of some Member States andrecent scientific studies on the results of <strong>in</strong>fection controlefforts. Large <strong>in</strong>ter-country variations can be notedfor S. pneumoniae, but non-susceptibility to commonlyused antimicrobials has rema<strong>in</strong>ed relatively stable <strong>in</strong><strong>Europe</strong> dur<strong>in</strong>g recent years, and this observation wasconfirmed by the 2011 data.High-level am<strong>in</strong>oglycoside <strong>resistance</strong> <strong>in</strong> E. faecalisseems stable <strong>in</strong> <strong>Europe</strong> and several countries whichpreviously reported relatively high levels of <strong>resistance</strong>now have decreas<strong>in</strong>g trends. Likewise, the occurrenceof vancomyc<strong>in</strong>-<strong>resistance</strong> <strong>in</strong> E. faecium is stabilis<strong>in</strong>g ordecreas<strong>in</strong>g.For several antimicrobial–pathogen comb<strong>in</strong>ations, e.g.fluoroqu<strong>in</strong>olone-<strong>resistance</strong> <strong>in</strong> E. coli, K. pneumoniae, P.aerug<strong>in</strong>osa and for MRSA, a north-to-south gradient isevident <strong>in</strong> <strong>Europe</strong>. In general, lower <strong>resistance</strong> percentagesare reported <strong>in</strong> the north and higher percentages<strong>in</strong> the south of <strong>Europe</strong>. These geographical differencesmay reflect differences <strong>in</strong> <strong>in</strong>fection control practices andantimicrobial use <strong>in</strong> the report<strong>in</strong>g countries. Prudent useof antimicrobial agents and comprehensive <strong>in</strong>fectioncontrol measures should be cornerstones of effectiveprevention and control efforts aimed at reduc<strong>in</strong>g theselection and transmission of antimicrobial-resistantbacteria1


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT2


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011isolates of the same bacterial species from other sites,i.e. ur<strong>in</strong>ary tract <strong>in</strong>fections, pneumonia, wound <strong>in</strong>fections,etc.Case ascerta<strong>in</strong>ment of patients with bloodstream <strong>in</strong>fections(BSIs) is strongly l<strong>in</strong>ked to diagnostic habits andthe frequency with which blood cultures are taken.Therefore, variations <strong>in</strong> blood culture frequency (nondifferentialsampl<strong>in</strong>g) result <strong>in</strong> an <strong>in</strong>creas<strong>in</strong>g uncerta<strong>in</strong>tywhen compar<strong>in</strong>g <strong>resistance</strong> percentages between differenthospitals and countries. Extrapolations of EARS-Netdata as a measure of BSI <strong>in</strong>cidence could thereforeunderestimate the true value <strong>in</strong> countries with low bloodculture frequency.Differential sampl<strong>in</strong>g can occur if blood cultures are typicallyonly performed after empirical treatment showsno adequate therapeutic response. Predictably, thiswill lead to an overestimation of the percentage <strong>resistance</strong>by not <strong>in</strong>clud<strong>in</strong>g susceptible BSI isolates from thedenom<strong>in</strong>ator.For detailed <strong>in</strong>formation on national blood culture frequency,see Annex 2.Laboratory rout<strong>in</strong>es and capacityThe use of guidel<strong>in</strong>es for cl<strong>in</strong>ical breakpo<strong>in</strong>ts variesbetween countries <strong>in</strong> <strong>Europe</strong>, and <strong>in</strong> some <strong>in</strong>stanceseven between laboratories <strong>in</strong> the same country. As aresult the <strong>in</strong>terpretation of AST results may vary, atleast for <strong>resistance</strong> mechanisms produc<strong>in</strong>g MICs closeto the breakpo<strong>in</strong>ts. In addition, the use of microbiologicalbreakpo<strong>in</strong>ts may change over time, when breakpo<strong>in</strong>tprotocols are updated or changed. As data on quantitativemeasures (i.e. zone diameters <strong>in</strong> disk diffusiontests or MIC values) are not provided by all participat<strong>in</strong>glaboratories, only the reported S, I, and R results areconsidered for the analyses.The ability of the laboratory to identify the microorganismand its associated antimicrobial susceptibilitypattern may differ. All laboratories provid<strong>in</strong>g data forEARS-Net are offered participation <strong>in</strong> an annual ExternalQuality Assessment (EQA) exercise to assess the reliabilityof the laboratory test results.For more <strong>in</strong>formation on the EARS-Net EQA and laboratoryperformance, see Annex 1.7


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT8


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20113 Demographic characteristics of cases of<strong>in</strong>vasive gram-negative <strong>in</strong>fections <strong>in</strong> <strong>Europe</strong>Experiences from EARSS/EARS-Net 2005–20113.1 IntroductionGram-negative bacteria (GNB) are a frequent cause ofserious <strong>in</strong>fections <strong>in</strong>clud<strong>in</strong>g bloodstream <strong>in</strong>fections(BSIs) 1 . <strong>Antimicrobial</strong>-resistant GNB have become animportant cl<strong>in</strong>ical and public health issue, hav<strong>in</strong>g asignificant impact on morbidity, mortality and healthrelatedcosts 2–6 . Trends reported from EARSS/EARS-Nethave shown a cont<strong>in</strong>uous <strong>in</strong>crease <strong>in</strong> the percentages ofantimicrobial-resistant GNB <strong>in</strong> many countries, <strong>in</strong>dicat<strong>in</strong>gthat the rise of resistant GNB <strong>in</strong> <strong>Europe</strong> is becom<strong>in</strong>ga serious public health problem that requires urgent andconcerted action. Antibiotic treatment options for multidrug-resistantGNB are often very limited and f<strong>in</strong>d<strong>in</strong>g anappropriate drug is an <strong>in</strong>creas<strong>in</strong>g challenge s<strong>in</strong>ce veryfew new antibiotics are expected to enter the market asthe older classes lose their efficacy 7 .An understand<strong>in</strong>g of the risk factors associated withantimicrobial-resistant GNB is essential to guide <strong>in</strong>terpretationof <strong>surveillance</strong> data and design effectivecontrol programmes, as antimicrobial-resistant GNB arereported to vary depend<strong>in</strong>g on geography, orig<strong>in</strong> of isolateand type of population under <strong>surveillance</strong> 8–12 . Datafrom EARSS/EARS-Net provide an important source of<strong>in</strong>formation on GNB <strong>in</strong> <strong>Europe</strong>, <strong>in</strong>clud<strong>in</strong>g <strong>in</strong>formationfrom over 471 000 GNB isolates from 29 EU/EEA countriescollected over seven years. Traditionally, data fromEARS-Net are presented by their temporal and spatialaspects and are not rout<strong>in</strong>ely analysed by the demographiccharacteristics of the cases. The exception isthe country summary sheets provided <strong>in</strong> the annualEARS-Net report present<strong>in</strong>g isolates by age group, genderand hospital department. However, annual nationaldata <strong>in</strong> most cases do not cover a sufficient number ofisolates to determ<strong>in</strong>e any significant differences <strong>in</strong> datastratified by major demographic characteristics.Here we used pooled EARSS/EARS-Net data from 2005to 2011 to describe general demographic characteristicsof GNB <strong>in</strong>fection cases reported to the network,and <strong>in</strong>vestigated demographic differences <strong>in</strong> <strong>resistance</strong>to major antimicrobial classes and for comb<strong>in</strong>ed <strong>resistance</strong>.This provides previously unpublished <strong>in</strong>formationon antimicrobial-resistant GNB epidemiology <strong>in</strong> <strong>Europe</strong>.3.2 Material and methodsData for the three GNB <strong>in</strong>cluded <strong>in</strong> EARS-Net (Klebsiellapneumoniae, Escherichia coli and Pseudomonas aerug<strong>in</strong>osa)reported from 2005 to 2011 were extractedfrom the EARS-Net (formerly EARSS) database at ECDC.Data were analysed by bacterial species and stratifiedaccord<strong>in</strong>g to patient’s age, gender, admission status andhospital department type. For age, data were grouped<strong>in</strong> four age strata: 0 to 4 years; 5 to 19 years; 20 to 64years and 65 years or older. Gender strata were femaleand male. Admission status was stratified accord<strong>in</strong>gto reported <strong>in</strong>patient and outpatient status at the timethe isolates were obta<strong>in</strong>ed. Hospital department typewas stratified as <strong>in</strong>tensive care units (ICUs) (for isolatesreported obta<strong>in</strong>ed from patients <strong>in</strong> adult or paediatricICUs) and other, non-ICU departments (<strong>in</strong>clud<strong>in</strong>gpatients from <strong>in</strong>ternal medic<strong>in</strong>e, paediatric, surgery,oncology, obstetrics/gynaecology, emergency, urology,<strong>in</strong>fectious disease and other departments).Report<strong>in</strong>g completeness differed for the variables. Age<strong>in</strong>formation was miss<strong>in</strong>g for 7% of all cases, with onecountry (Greece) provid<strong>in</strong>g age <strong>in</strong>formation for less thanhalf of the cases; gender <strong>in</strong>formation was miss<strong>in</strong>g for 7%of all cases with one country (Greece) provid<strong>in</strong>g gender<strong>in</strong>formation for less than half of their cases; admissionstatus was miss<strong>in</strong>g for 15% of all cases with threecountries (F<strong>in</strong>land, Iceland and Ireland) provid<strong>in</strong>g this<strong>in</strong>formation for less than half of their cases; and <strong>in</strong>formationon hospital department was miss<strong>in</strong>g for 26% ofthe cases with six countries (Belgium, F<strong>in</strong>land, Ireland,Luxembourg, Netherlands and United K<strong>in</strong>gdom) report<strong>in</strong>ghospital department for less than half of their cases.Significant differences <strong>in</strong> selected demographic characteristicsbetween two groups were determ<strong>in</strong>ed byChi 2 -test, and a p-value < 0.05 was considered statisticallysignificant.Mean percentages of AMR dur<strong>in</strong>g the study period<strong>in</strong>clud<strong>in</strong>g a 95% confidence <strong>in</strong>terval (CI) were calculatedper bacterial species for the total number of isolates,as well as for each demographic characteristic <strong>in</strong>cluded<strong>in</strong> the study. For E. coli and K. pneumoniae, <strong>resistance</strong>to third-generation cephalospor<strong>in</strong>s and comb<strong>in</strong>ed<strong>resistance</strong> (i.e. <strong>resistance</strong> to fluoroqu<strong>in</strong>olones, thirdgenerationcephalospor<strong>in</strong>s and am<strong>in</strong>oglycosides) were<strong>in</strong>cluded, and for P. aerug<strong>in</strong>osa <strong>resistance</strong> to carbapenemsand comb<strong>in</strong>ed <strong>resistance</strong> (i.e. <strong>resistance</strong> to threeor more of piperacill<strong>in</strong>±tazobactam, fluoroqu<strong>in</strong>olones,ceftazidime, am<strong>in</strong>oglycosides and carbapenems) were<strong>in</strong>cluded <strong>in</strong> the analysis.9


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT3.3 ResultsGeneral demographic characteristics ofreported isolatesA total of 471 596 <strong>in</strong>vasive isolates were <strong>in</strong>cluded <strong>in</strong> thestudy, of which E. coli were the majority, account<strong>in</strong>g for344 700 (73%) isolates, followed by K. pneumoniae at74 985 isolates (16%) and 51 911 (11%) P. aerug<strong>in</strong>osa isolates.The number of isolates for which <strong>in</strong>formation onage and gender was miss<strong>in</strong>g was higher for K. pneumoniaeand P. aerug<strong>in</strong>osa than E. coli.As shown <strong>in</strong> Table 3.1, the age distribution was skewedtowards the elderly population (aged 65 years or older)for all <strong>in</strong>cluded bacterial species. The highest percentageof isolates from the elderly was reported for E. coli(64%) and this was also the bacterium with the lowestpercentage of isolates from young children (0 to 4years). Escherichia coli were more frequent <strong>in</strong> femaleswhereas K. pneumoniae and P. aerug<strong>in</strong>osa were morefrequent <strong>in</strong> males.Inpatients represented the majority of cases for all bacteria,but the percentage was significantly lower for E.coli compared to the other two GNB (p


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Among <strong>in</strong>patients, isolates from ICU patients were significantlymore likely to be resistant to the studiedantimicrobial classes than isolates from other departments(non-ICU patients). The differences <strong>in</strong> <strong>resistance</strong>percentage between ICU and non-ICU patients were lessprom<strong>in</strong>ent for E. coli than K. pneumoniae and P. aerug<strong>in</strong>osa,but were significant for all three bacteria (Tables3.2, 3.3).3.4 DiscussionThis study is based on a unique dataset conta<strong>in</strong><strong>in</strong>g <strong>in</strong>formationfrom a large number of GNB isolates collectedfrom 29 <strong>Europe</strong>an countries over a seven-year period.For the first time, we present the demographic characteristicsof cases of <strong>in</strong>vasive GNB <strong>in</strong>fection as reportedto EARSS/EARS-Net, highlight<strong>in</strong>g differences <strong>in</strong> theepidemiological data l<strong>in</strong>ked to the isolates of E. coli, K.pneumoniae and P. aerug<strong>in</strong>osa <strong>in</strong> <strong>Europe</strong>.The rank order of the bacteria <strong>in</strong>cluded <strong>in</strong> this study wassimilar to that which has been reported elsewhere 4,13–15with the majority (70%) of the isolates be<strong>in</strong>g E. coli.There was a significant difference between the demographicprofile of cases with E. coli BSI and cases withBSI caused by K. pneumoniae or P. aerug<strong>in</strong>osa; a higherpercentage of isolates from the elderly, a majority offemale patients and a lower percentage of isolates from<strong>in</strong>patients and from ICU patients. Although data fromEARSS/EARS-Net do not provide sufficient <strong>in</strong>formationto determ<strong>in</strong>e the orig<strong>in</strong> of the <strong>in</strong>fection, these resultsmay partly be expla<strong>in</strong>ed by previously reported differences<strong>in</strong> the aetiology of <strong>in</strong>vasive E. coli <strong>in</strong>fections and ofK. pneumoniae and P. aerug<strong>in</strong>osa <strong>in</strong>fections. In severalstudies, E. coli has more frequently been associated withcommunity-acquired BSI than other GNB 16 and was moreoften associated with a ur<strong>in</strong>ary tract source 17 , especially<strong>in</strong> female patients 18 . This is <strong>in</strong> contrast to observationsfor <strong>in</strong>vasive isolates of K. pneumoniae and P. aerug<strong>in</strong>osaTable 3.2: Percentage (%) of isolates resistant to third-generation cephalospor<strong>in</strong>s (3GC R) and comb<strong>in</strong>ed <strong>resistance</strong>(comb<strong>in</strong>ed R) (<strong>resistance</strong> to fluoroqu<strong>in</strong>olones, third-generation cephalospor<strong>in</strong>s and am<strong>in</strong>oglycosides) for all cases andper demographic characteristic <strong>in</strong> <strong>in</strong>vasive isolates of E. coli and K. pneumoniae reported to EARSS/EARS-Net dur<strong>in</strong>gthe period 2005–2011 (95% CI given <strong>in</strong> parenthesis)E. coli K. pneumoniae3GC R Comb<strong>in</strong>ed R 3GC R Comb<strong>in</strong>ed RAll cases 6.7 (6.6-6.8) 2.9 (2.8-2.9) 35.3 (33.5-37.2) 17.5 (17.2-17.8)Age0 to 4 years 5.5 (5.0-6.1) 1.5 (1.2-1.8) 35.3 (33.5-37.2) 15.4 (14.0-16.8)5 to 19 years 5.7 (4.9-6.5) 2.1 (1.6-2.7) 24.5 (21.4-27.8) 13.6 (11.2-16.3)20 to 64 years 6.6 (6.4-6.7) 2.8 (2.7-2.9) 23.1 (22.5-23.6) 15.7 (15.2-16.2)65 years or older 6.5 (6.4-6.6) 2.7 (2.7-2.8) 17.0 (16.7-17.4) 11.0 (10.6-11.1)GenderMale 7.9 (7.7-8.0) 3.4 (3.3-3.5) 22.3 (21.9-22.7) 14.6 (14.2-15.0)Female 5.4 (5.3-5.5) 2.2 (2.1-2.2) 17.8 (17.3-18.3) 11.1 (10.7-11.5)Admission statusInpatient 7.1 (7.0-7.2) 3.0 (3.0-3.1) 29.0 (28.7-29.4) 20.0 (19.7-20.4)Outpatient 5.1 (4.9-5.3) 2.1 (2.0-2.3) 8.2 (7.5-9.0) 5.0 (4.4-5.6)Hospital departmentICU 9.8 (9.4-10.2) 3.9 (3.6-4.1) 51.7 (50.9-52.5) 37.1 (36.3-37.9)Other department 6.4 (6.4-6.5) 2.8 (2.7-2.9) 18.9 (18.6-19.2) 12.3 (12.0-12.6)Table 3.3: Percentage (%) <strong>resistance</strong> to carbapenems and comb<strong>in</strong>ed <strong>resistance</strong> (<strong>resistance</strong> to three or more antibioticclasses among piperacill<strong>in</strong>–tazobactam, ceftazidime, am<strong>in</strong>oglycosides and carbapenems) for all cases and perdemographic characteristic <strong>in</strong> <strong>in</strong>vasive isolates of P. aerug<strong>in</strong>osa reported to EARSS/EARS-Net dur<strong>in</strong>g the period2005–2011 (95% CI given <strong>in</strong> parenthesis)P. aerug<strong>in</strong>osaCarbapenem RComb<strong>in</strong>ed <strong>resistance</strong>All cases 18.8 (18.5-19.1) 15.6 (15.3-15.9)Age0 to 4 years 17.2 (15.3-19.3) 11.4 (9.7-13.0)5 to 19 years 17.1 (14.5-19.8) 11.1 (9.0-13.3)20 to 64 years 19.7 (19.1-20.4) 15.5 (15.0-16.0)65 years or older 11.5 (11.1-11.9) 9.5 (9.2-9.9)GenderMale 15.5 (15.1-15.9) 12.5 (12.1-12.9)Female 14.8 (14.3-15.4) 11.6 (11.1-12.1)Admission statusInpatient 20.8 (20.4-21.2) 17.5 (17.2-17.9)Outpatient 6.7 (5.8-7.7) 4.4 (3.7-5.1)Hospital departmentICU 32.5 (31.7-33.3) 27.9 (27.1-28.7)Other department 14.1 (13.7-14.5) 11.5 (11.2-11.8)11


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTwhich have been reported to orig<strong>in</strong>ate more frequentlyfrom healthcare-associated <strong>in</strong>fections and from patients<strong>in</strong> ICU 14 where BSIs with GNB often orig<strong>in</strong>ate from therespiratory or gastro<strong>in</strong>test<strong>in</strong>al tract 17–20 .For all GNB and all <strong>resistance</strong> types <strong>in</strong>cluded <strong>in</strong> thestudy, isolates from <strong>in</strong>patients had higher <strong>resistance</strong>levels than those from outpatients, and isolatesfrom ICU patients had significantly higher <strong>resistance</strong>percentages than isolates from patients from otherdepartments. These results are hardly surpris<strong>in</strong>g andsupport previous conclusions highlight<strong>in</strong>g risk factorsfor transmission of resistant bacteria <strong>in</strong> the hospitalenvironment. High antibiotic pressure, frequent use of<strong>in</strong>vasive devices and the challenge of ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g a highstandard of <strong>in</strong>fection control all contribute to <strong>in</strong>creasethe risk of patients acquir<strong>in</strong>g a healthcare-associated<strong>in</strong>fection with resistant bacteria 20 .Our results also revealed age- and gender-related differencesbetween <strong>resistance</strong> percentages. While thesedifferences were less prom<strong>in</strong>ent for E. coli than K. pneumoniaeand P. aerug<strong>in</strong>osa, they could be noted for allthree bacteria. Interest<strong>in</strong>gly, the age group where <strong>resistance</strong>percentages were the highest differed betweenbacteria. For K. pneumoniae and P. aerug<strong>in</strong>osa, <strong>resistance</strong>percentages were lower <strong>in</strong> isolates from the elderly(age ≥65 years) than <strong>in</strong> those from other age groups,whereas for E. coli <strong>resistance</strong> percentages were higheramong isolates from adults and the elderly than fromchildren. These differences are difficult to expla<strong>in</strong>, butmay be attributed to differences <strong>in</strong> the types of <strong>in</strong>fectioncaused by the bacteria as well as age-related differences<strong>in</strong> risk factors such as antimicrobial use and exposure tothe healthcare environment. A more <strong>in</strong>-depth analysis<strong>in</strong>clud<strong>in</strong>g additional cl<strong>in</strong>ical <strong>in</strong>formation is required <strong>in</strong>order to properly determ<strong>in</strong>e the role of the patient’s age<strong>in</strong> <strong>resistance</strong> percentages for the different bacteria.EARS-Net <strong>in</strong>clusion criteria address some of thepotential threats to data validity by only accept<strong>in</strong>g <strong>in</strong>formationfrom <strong>in</strong>vasive isolates and by exclud<strong>in</strong>g duplicatereports from the same patient and year. By pool<strong>in</strong>g <strong>in</strong>formationfrom a seven-year period, the large number ofobservations allowed for analysis of data by differentdemographic strata. However, pool<strong>in</strong>g national <strong>surveillance</strong>data to provide <strong>Europe</strong>an estimates will <strong>in</strong>creasethe risk of bias caused by <strong>in</strong>ter-country differences <strong>in</strong>population coverage, methods for data collection andspecimen process<strong>in</strong>g. As the population coverage for thecountries participat<strong>in</strong>g <strong>in</strong> EARS-Net varies considerably,<strong>in</strong>dividual countries will contribute differently to thecrude <strong>Europe</strong>an estimate. In addition, the percentageof miss<strong>in</strong>g <strong>in</strong>formation for the demographic variablesdiffered both between countries and between bacteria.The percentages of isolates miss<strong>in</strong>g <strong>in</strong>formation on ageand gender were considerably higher for K. pneumoniaeand P. aerug<strong>in</strong>osa than for E. coli. Although this maypartly <strong>in</strong>fluence the observed differences <strong>in</strong> age andgender distribution between the bacteria, it is unlikelythat it would fully expla<strong>in</strong> the observed demographicdifferences.In conclusion, document<strong>in</strong>g population-specific differences<strong>in</strong> <strong>resistance</strong> percentages and trends is importantto enable identification of high-risk groups and to formulatepolicies on screen<strong>in</strong>g, prevention and control ofAMR. Data from EARSS/EARS-Net <strong>in</strong>dicate that there aresignificant differences <strong>in</strong> the demographic profiles ofcases with <strong>in</strong>vasive GNB <strong>in</strong>fections <strong>in</strong> <strong>Europe</strong>, both forthe GNB <strong>in</strong>volved, and for the percentages of <strong>resistance</strong>to important antimicrobials <strong>in</strong>clud<strong>in</strong>g comb<strong>in</strong>ed <strong>resistance</strong>.However, due to the ecological nature of EARSS/EARS-Net data, our results should be <strong>in</strong>terpreted withcaution, and we encourage additional studies based ondata with more extensive cl<strong>in</strong>ical <strong>in</strong>formation to furtherexplore these differences.Provid<strong>in</strong>g representative population estimates is achallenge for any <strong>surveillance</strong> system 21,22 . The EARSS/12


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114 <strong>Antimicrobial</strong> <strong>resistance</strong> <strong>in</strong> <strong>Europe</strong>4.1 Escherichia coli4.1.1 Cl<strong>in</strong>ical and epidemiological importanceEscherichia coli is the gram-negative rod most frequentlyisolated from blood cultures. It is the mostfrequent cause of bacteraemia, community- and hospital-acquiredur<strong>in</strong>ary tract <strong>in</strong>fections, is associated withspontaneous and post-surgical peritonitis and with sk<strong>in</strong>and soft tissue <strong>in</strong>fections of polymicrobial aetiology,causes neonatal men<strong>in</strong>gitis and is one of the lead<strong>in</strong>gcausative agents <strong>in</strong> food-borne <strong>in</strong>fections worldwide.4.1.2 Resistance mechanismsIn E. coli, <strong>resistance</strong> to beta-lactams is mostly due toproduction of beta-lactamases, which hydrolyse thebeta-lactam r<strong>in</strong>g of beta-lactam antimicrobials, whichis crucial for <strong>in</strong>hibition of the penicill<strong>in</strong>-b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong>(PBP) targets. Resistance to broad-spectrum penicill<strong>in</strong>s,such as ampicill<strong>in</strong> or amoxicill<strong>in</strong>, is usually conferred byplasmid coded beta-lactamases ma<strong>in</strong>ly of the TEM typeand to a lesser extent of the SHV type, (whereby TEM-1accounts for up to 60% of am<strong>in</strong>openicill<strong>in</strong> <strong>resistance</strong>),while <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>sis mostly conferred by extended-spectrum beta-lactamases(ESBLs). The first ESBLs spread<strong>in</strong>g <strong>in</strong> E. coli werevariants of the TEM or SHV enzymes <strong>in</strong> which s<strong>in</strong>gle ormultiple am<strong>in</strong>oacid substitutions expand their hydrolys<strong>in</strong>gability to <strong>in</strong>clude third-generation cephalospor<strong>in</strong>s(<strong>in</strong> this report referr<strong>in</strong>g to cefotaxime, ceftriaxone andceftazidime), fourth-generation cephalospor<strong>in</strong>s andmonobactams. Dur<strong>in</strong>g the past decade, however, theseenzymes have largely been replaced by the CTX-M-typeESBLs, which are now the most common ESBLs <strong>in</strong> E. coli.Most ESBLs can be <strong>in</strong>hibited by beta-lactamase <strong>in</strong>hibitorssuch as clavulanic acid, sulbactam or tazobactam.More than 250 ESBL variants are known to date. Animportant factor <strong>in</strong> their global dom<strong>in</strong>ance is the widedissem<strong>in</strong>ation of particular plasmids or bacterial clonesproduc<strong>in</strong>g CTX-M-type ESBLs (e.g. CTX-M-15). Otherenzymes affect<strong>in</strong>g the susceptibility to third-generationcephalospor<strong>in</strong>s <strong>in</strong>clude plasmid-encoded variantsderived from some chromosomal AmpC-type beta-lactamases.CMY-2 is the most widespread enzyme belong<strong>in</strong>gto this group, which is still less common than ESBLs <strong>in</strong> E.coli <strong>in</strong> <strong>Europe</strong>, but frequently seen <strong>in</strong> the United States.An important threat that will require close <strong>surveillance</strong><strong>in</strong> the future is the emergence of carbapenem <strong>resistance</strong><strong>in</strong> E. coli, mediated by metallo-beta-lactamases (such asthe VIM or IMP enzymes, or the emerg<strong>in</strong>g NDM enzyme)or ser<strong>in</strong>e-carbapenemases (such as the KPC enzymes),provid<strong>in</strong>g <strong>resistance</strong> to most or all available beta-lactamFigure 4.1: Escherichia coli: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>s bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta13


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011agents. Another grow<strong>in</strong>g family of ESBLs comprises theOXA-type enzymes that confer <strong>resistance</strong> to ampicill<strong>in</strong>and cefalot<strong>in</strong> and are characterised by their high hydrolyticactivity aga<strong>in</strong>st oxacill<strong>in</strong> and cloxacill<strong>in</strong> and the factthat they are poorly <strong>in</strong>hibited by clavulanic acid. Thisfamily also <strong>in</strong>cludes some enzymes with carbapenemaseactivity (e.g. OXA-48), which have recently emerged <strong>in</strong>E. coli and other enterobacteriaceae and confer reducedsusceptibility to carbapenems and <strong>resistance</strong> to penicill<strong>in</strong>s,but not to the expanded-spectrum cephalospor<strong>in</strong>s.Increas<strong>in</strong>gly common is also the f<strong>in</strong>d<strong>in</strong>g of E. coli stra<strong>in</strong>swhich produce multiple beta-lactamases.Fluoroqu<strong>in</strong>olones <strong>in</strong>teract with DNA gyrase andtopoisomerase IV, which are enzymes that regulateconformational changes <strong>in</strong> the bacterial chromosomedur<strong>in</strong>g replication and transcription. This <strong>in</strong>teractionleads to the irreversible <strong>in</strong>hibition of the enzyme activityfollowed by DNA fragmentation and eventually to celldeath. Resistance to fluoroqu<strong>in</strong>olones arises throughstepwise mutations <strong>in</strong> the cod<strong>in</strong>g regions of the gyrasesubunits (gyrA and gyrB) and DNA topoisomerase IV(parC). Accumulation of mutations <strong>in</strong> several of thesegenes <strong>in</strong>creases the MIC <strong>in</strong> a stepwise manner. Low-level<strong>resistance</strong> to fluoroqu<strong>in</strong>olones may also arise throughchanges <strong>in</strong> outer membrane por<strong>in</strong>s or from upregulationof efflux pumps, result<strong>in</strong>g <strong>in</strong> lower outer membranepermeability and higher efflux, respectively. In recentyears, several plasmid-mediated qu<strong>in</strong>olone <strong>resistance</strong>mechanisms have also been identified, <strong>in</strong>clud<strong>in</strong>g theQnr prote<strong>in</strong>s, which protect DNA topoisomerases fromqu<strong>in</strong>olone b<strong>in</strong>d<strong>in</strong>g, the AAC(6’)-Ib-cr enzyme, which<strong>in</strong>activates some fluoroqu<strong>in</strong>olones by acetylation, andthe QepA efflux pump, which effluxes hydrophilic qu<strong>in</strong>olones.These mechanisms are a concern becausethis type of <strong>resistance</strong> is transferable and because oftheir frequent association with CTX-M and CMY-typeenzymes <strong>in</strong>activat<strong>in</strong>g third-generation cephalospor<strong>in</strong>s.Additionally they are believed to <strong>in</strong>crease the risk ofchromosomal mutations.Am<strong>in</strong>oglycosides block prote<strong>in</strong> synthesis by b<strong>in</strong>d<strong>in</strong>gto the ribosomes, which are <strong>in</strong>volved <strong>in</strong> the translationof RNA <strong>in</strong>to prote<strong>in</strong>s, and are also able to damagethe outer membrane of gram-negative rods. Resistanceto am<strong>in</strong>oglycosides can be due to targeted modification(methylation) of the large ribosomal subunit,which excludes am<strong>in</strong>oglycoside molecules, or byam<strong>in</strong>oglycoside-modify<strong>in</strong>g enzymes that acetylate,adenylate or phosphorylate their target molecules andthereby neutralise the biological effect of am<strong>in</strong>oglycosides.Of particular concern is ArmA 16S that conferspan-<strong>resistance</strong> to am<strong>in</strong>oglycosides, and is frequentlyaccompany<strong>in</strong>g carbapenemases.4.1.3 ResultsAm<strong>in</strong>openicill<strong>in</strong>s• For 2011, 28 countries reported 57 920 isolates,of which 32 110 (55.4%) were resistant toTable 4.1: Escherichia coli: number and percentage of <strong>in</strong>vasive isolates resistant to am<strong>in</strong>openicill<strong>in</strong>s, third-generationcephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides and comb<strong>in</strong>ed <strong>resistance</strong>*, <strong>in</strong>clud<strong>in</strong>g 95% confidence <strong>in</strong>tervals(95% CI), by country, EU/EEA countries, 2011CountryAm<strong>in</strong>openicill<strong>in</strong>s Third-gen. cephalospor<strong>in</strong>s Fluoroqu<strong>in</strong>olones Am<strong>in</strong>oglycosides Comb<strong>in</strong>ed <strong>resistance</strong>N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI)Austria 3 148 50.3 (49-52) 3 160 9.1 (8-10) 3 162 22.3 (21-24) 3 144 7.4 (7-8) 3 121 2.6 (2-3)Belgium 3 507 58.7 (57-60) 3 985 6.0 (5-7) 3 549 21.5 (20-23) 3 831 9.3 (8-10) 3 331 1.4 (1-2)Bulgaria 152 60.5 (52-68) 179 22.9 (17-30) 179 30.2 (24-37) 179 17.3 (12-24) 179 10.1 (6-15)Cyprus 134 77.6 (70-84) 138 36.2 (28-45) 137 47.4 (39-56) 138 23.9 (17-32) 137 18.2 (12-26)Czech Republic 2 683 60.7 (59-63) 2 684 11.4 (10-13) 2 682 23.5 (22-25) 2 674 8.8 (8-10) 2 667 3.7 (3-4)Denmark 3 638 47.9 (46-50) 2 532 8.5 (7-10) 3 583 14.1 (13-15) 3 638 6.4 (6-7) 2 529 3.0 (2-4)Estonia 0 . 90 12.2 (6-21) 312 9.9 (7-14) 314 4.8 (3-8) 89 1.1 (0-6)F<strong>in</strong>land 1 826 36.3 (34-39) 2 419 5.1 (4-6) 2 420 10.8 (10-12) 2 420 5.3 (4-6) 2 419 2.7 (2-3)France 8 784 55.1 (54-56) 8 479 8.2 (8-9) 8 694 17.9 (17-19) 8 742 7.9 (7-8) 8 428 2.6 (2-3)Germany 3 638 52.3 (51-54) 3 642 8.0 (7-9) 3 636 23.7 (22-25) 3 645 7.6 (7-9) 3 631 3.6 (3-4)Greece 1 297 54.5 (52-57) 1 435 14.9 (13-17) 1 433 26.6 (24-29) 1 434 16.8 (15-19) 1 431 10.8 (9-13)Hungary 991 64.7 (62-68) 1 224 15.1 (13-17) 1 213 31.2 (29-34) 1 226 14.8 (13-17) 1 209 8.3 (7-10)Iceland 129 48.1 (39-57) 130 6.2 (3-12) 121 14.0 (8-22) 129 6.2 (3-12) 120 0.8 (0-5)Ireland 2 118 69.5 (68-72) 2 166 9.0 (8-10) 2 153 22.9 (21-25) 2 158 10.2 (9-12) 2 148 3.6 (3-4)Italy 1 530 67.1 (65-69) 1 870 19.8 (18-22) 1 899 40.5 (38-43) 1 985 18.3 (17-20) 1 745 10.3 (9-12)Latvia 130 54.6 (46-63) 132 15.9 (10-23) 131 16.8 (11-24) 132 11.4 (7-18) 131 9.2 (5-15)Lithuania 383 47.8 (43-53) 385 7.0 (5-10) 381 12.9 (10-17) 382 9.7 (7-13) 378 2.4 (1-4)Luxembourg 353 52.1 (47-57) 353 8.2 (6-12) 353 24.1 (20-29) 354 8.2 (6-12) 353 2.8 (1-5)Malta 219 53.0 (46-60) 219 12.8 (9-18) 219 32.0 (26-39) 219 15.5 (11-21) 219 9.6 (6-14)Netherlands 4 425 48.5 (47-50) 4 408 5.7 (5-6) 4 427 14.3 (13-15) 4 431 7.8 (7-9) 4 400 2.2 (2-3)Norway 2 617 39.1 (37-41) 2 523 3.6 (3-4) 2 505 9.0 (8-10) 2 470 4.1 (3-5) 2 259 1.2 (1-2)Poland 934 62.0 (59-65) 938 11.7 (10-14) 1 141 27.3 (25-30) 1 171 8.4 (7-10) 902 4.0 (3-5)Portugal 1 963 56.5 (54-59) 1 901 11.3 (10-13) 1 917 27.2 (25-29) 1 962 16.1 (14-18) 1 891 7.5 (6-9)Romania 22 68.2 (45-86) 91 22.0 (14-32) 46 30.4 (18-46) 46 19.6 (9-34) 46 10.9 (4-24)Slovakia 608 68.6 (65-72) 738 31.0 (28-35) 737 41.9 (38-46) 738 17.9 (15-21) 737 12.9 (11-16)Slovenia 1 002 53.9 (51-57) 1 002 8.8 (7-11) 1 002 20.7 (18-23) 1 002 9.8 (8-12) 1 002 4.1 (3-6)Spa<strong>in</strong> 5 592 65.6 (64-67) 5 600 12.0 (11-13) 5 597 34.5 (33-36) 5 603 14.8 (14-16) 5 594 4.9 (4-6)Sweden 1 023 34.8 (32-38) 3 939 3.0 (3-4) 3 295 7.9 (7-9) 3 203 3.7 (3-4) 2 844 1.0 (1-1)United K<strong>in</strong>gdom 5 074 62.8 (61-64) 5 182 9.6 (9-10) 5 564 17.5 (17-19) 5 661 8.2 (7-9) 5 005 3.6 (3-4)* Comb<strong>in</strong>ed <strong>resistance</strong> def<strong>in</strong>ed as be<strong>in</strong>g resistant to third-generation cephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides.15


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTTable 4.2: Escherichia coli: number of <strong>in</strong>vasive isolatesresistant to third-generation cephalospor<strong>in</strong>s (3GCREC)and percentage of extended spectrum beta-lactamase(ESBL)-positive among these isolates, as ascerta<strong>in</strong>edby the participat<strong>in</strong>g laboratories, EU/EEA countries,2011CountryNumber oflaboratoriesNumber of3GCREC%ESBLAustria 27 237 91.1Bulgaria 12 30 93.3Czech Republic 42 305 89.5Denmark 3 45 71.1Estonia 5 11 100France 16 99 83.8Germany 12 190 92.1Hungary 9 44 100Ireland 26 189 82Latvia 5 21 90.5Lithuania 8 27 100Luxembourg 5 29 96.6Poland 33 98 85.7Portugal 14 159 97.5Slovakia 7 154 83.1Slovenia 9 88 94.3Spa<strong>in</strong> 26 381 88.5Only data from laboratories consistently report<strong>in</strong>g the ESBL test results for allisolates identified as resistant to third-generation cephalospor<strong>in</strong>s and fromcountries with at least 10 of such isolates were selected for the analysis.am<strong>in</strong>openicill<strong>in</strong>s. The number of isolates with relevantAST <strong>in</strong>formation reported per country ranged from 22to 8 784 (Table 4.1).• The percentages of resistant isolates <strong>in</strong> the report<strong>in</strong>gcountries ranged from 34.8% (Sweden) to 77.6%(Cyprus). Seven countries reported 25-50%, while therema<strong>in</strong><strong>in</strong>g 21 countries reported resistant percentagesabove 50% (Table 4.1).• Trends for the period 2008–2011 were calculatedfor 27 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trendswere observed for eight countries (Belgium, Cyprus,Denmark, Greece, Hungary, Italy, Spa<strong>in</strong> and Sweden).For Belgium, Italy and Sweden the trends were not significantwhen consider<strong>in</strong>g only data from laboratoriesreport<strong>in</strong>g consistently for all four years (Figure 4.4).• Significantly decreas<strong>in</strong>g trends were observed for twocountries (Germany and Lithuania); however, thesetrends were not significant when consider<strong>in</strong>g onlylaboratories report<strong>in</strong>g consistently for all four years(Figure 4.4).Third-generation cephalospor<strong>in</strong>s• For 2011, 29 countries reported 61 544 isolates, ofwhich 5 619 (9.1%) were resistant to third-generationcephalospor<strong>in</strong>s. The number of isolates with relevantAST <strong>in</strong>formation reported per country ranged from 90to 8 479 (Table 4.1).• The percentages of resistant isolates <strong>in</strong> the report<strong>in</strong>gcountries ranged from 3.0% (Sweden) to 36.2%(Cyprus). Two countries reported <strong>resistance</strong> percentagesbelow 5%, 13 countries reported 5-10%,12 countries reported 10-25%, and two countriesreported above 25% (Table 4.1 and Figure 4.5).• Trends for the period 2008–2011 were calculatedfor 28 countries. Significant <strong>in</strong>creas<strong>in</strong>g trends wereobserved <strong>in</strong> 18 of 28 countries. For three countries(Italy, the Netherlands, and Poland), the trends didnot rema<strong>in</strong> significant when consider<strong>in</strong>g only datafrom laboratories report<strong>in</strong>g consistently for all fouryears (Figure 4.5).• None of the 28 report<strong>in</strong>g countries had decreas<strong>in</strong>gtrends of <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>sover the last four years (Figure 4.5).Extended-spectrum beta-lactamase (ESBL)• Among E. coli isolates resistant to third-generationcephalospor<strong>in</strong>s, a large percentage was ascerta<strong>in</strong>edas ESBL-positive by the participat<strong>in</strong>g laboratories<strong>in</strong> 2011. Fourteen of 17 countries reported between85% and 100% ESBL-positive isolates among isolatesresistant to third-generation cephalospor<strong>in</strong>s (Table4.2).Fluoroqu<strong>in</strong>olones• For 2011, 29 countries reported 62 488 isolates ofwhich 13 075 (20.9%) were resistant to fluoroqu<strong>in</strong>olones.The number of isolates with relevant AST<strong>in</strong>formation reported by the countries ranged from 46to 8 694 (Table 4.1).• The percentages of resistant isolates <strong>in</strong> the report<strong>in</strong>gcountries ranged from 7.9% (Sweden) to 47.4%(Cyprus). Three countries reported <strong>resistance</strong> percentagesbelow 10%, 15 countries reported 10-25% and 11countries reported above 25% (Table 4.1 and Figure4.2)• Trends for the period 2008–2011 were calculated for28 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for 11 countries. For Italy and Poland, thesetrends were not significant when consider<strong>in</strong>g onlydata from laboratories report<strong>in</strong>g consistently dur<strong>in</strong>gall four years (Figure 4.6).• Significantly decreas<strong>in</strong>g trends were observed forthe Czech Republic and Sweden; however, the trendsfor these two countries were not significant whenconsider<strong>in</strong>g only data from laboratories report<strong>in</strong>g consistentlyfor all four years (Figure 4.6).Am<strong>in</strong>oglycosides• For 2011, 29 countries reported 63 031 isolates ofwhich 5 867 (9.3%) were resistant to am<strong>in</strong>oglycosides.The number of isolates with relevant AST <strong>in</strong>formationreported by the countries ranged from 46 to 8 742(Table 4.1).• The percentages of resistant isolates <strong>in</strong> the report<strong>in</strong>gcountries ranged from 3.7% (Sweden) to 23.9%(Cyprus). Three countries reported <strong>resistance</strong> percentagesbelow 5%, 14 countries reported 5-10%, 12countries reported above 10% (Table 4.1 and Figure4.3).• Trends for the period 2008–2011 were calculated for28 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends were16


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Table 4.3: Escherichia coli: overall <strong>resistance</strong> and <strong>resistance</strong> comb<strong>in</strong>ations among <strong>in</strong>vasive isolates tested aga<strong>in</strong>stam<strong>in</strong>openicill<strong>in</strong>s, fluoroqu<strong>in</strong>olones, third-generation cephalospor<strong>in</strong>s and am<strong>in</strong>oglycosides (n=54 338), EU/EEAcountries, 2011Resistance pattern Number of isolates % of totalFully susceptible 22 586 41.6S<strong>in</strong>gle <strong>resistance</strong> (to <strong>in</strong>dicated drug classes)Total (all s<strong>in</strong>gle <strong>resistance</strong>) 19 293 35.5Am<strong>in</strong>openicill<strong>in</strong>s 17 954 33Fluoroqu<strong>in</strong>olones 1 236 2.3Am<strong>in</strong>oglycosides 103 0.2Resistance to two classes of antimicrobial drugsTotal (all two classes comb<strong>in</strong>ations) 6 457 11.9Am<strong>in</strong>openicill<strong>in</strong>s + fluoroqu<strong>in</strong>olones 4 610 8.5Am<strong>in</strong>openicill<strong>in</strong>s + third-generation cephalospor<strong>in</strong>s 964 1.8Am<strong>in</strong>openicill<strong>in</strong>s + am<strong>in</strong>oglycosides 797 1.5Fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 86 0.2Resistance to three classes of antimicrobial drugsTotal (all three classes comb<strong>in</strong>ations) 3 864 7.1Am<strong>in</strong>openicill<strong>in</strong>s + fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 1 867 3.4Am<strong>in</strong>openicill<strong>in</strong>s + third-generation cephalospor<strong>in</strong>s + fluoroqu<strong>in</strong>olones 1 796 3.3Am<strong>in</strong>openicill<strong>in</strong>s + third-generation cephalospor<strong>in</strong>s + am<strong>in</strong>oglycosides 201 0.4Resistance to four classes of antimicrobial drugsAm<strong>in</strong>openicill<strong>in</strong>s + third-generation cephalospor<strong>in</strong>s + fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 2 138 3.9Only data from isolates tested aga<strong>in</strong>st all four antimicrobial classes were <strong>in</strong>cluded <strong>in</strong> the analysis.observed for 11 countries. For Belgium, Hungary, Italyand Portugal the trends did rema<strong>in</strong> significant whenconsider<strong>in</strong>g only data from laboratories consistentlyreport<strong>in</strong>g for all four years (Figure 4.7).• A significantly decreas<strong>in</strong>g trend of am<strong>in</strong>oglycoside<strong>resistance</strong> was observed only for one country(Bulgaria) (Figure 4.7).Carbapenems• For 2011, 28 countries reported 59 326 isolates, ofwhich 25 (0.04%) were resistant to carbapenems.The number of isolates with relevant AST <strong>in</strong>formationreported by the countries ranged from 1 to 8 503.Eleven countries reported one or more resistantisolate(s) <strong>in</strong> 2011. The majority of the resistant isolates(10 isolates; 40%) were reported by Greece.Comb<strong>in</strong>ed <strong>resistance</strong>• For 2011, 29 countries reported 58 945 E. coli isolatestested for <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>s,fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides. Thenumber of isolates with relevant AST <strong>in</strong>formationreported by the countries ranged from 46 to 8 428(Table 4.1).• The percentage of isolates with comb<strong>in</strong>ed <strong>resistance</strong>to third-generation cephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olonesand am<strong>in</strong>oglycosides) reported by the countriesranged from 0.8% (Iceland) to 18.2% (Cyprus). Onecountry reported a <strong>resistance</strong> percentage below 1%,18 countries reported 1–5%, four countries reported5–10%, and six countries reported above 10% (Table4.1 and Figure 4.8).• Trends for the period 2008–2011 were calculated for28 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for 13 countries. For Belgium, Italy, theNetherlands and Poland, the trends did not rema<strong>in</strong> significantwhen consider<strong>in</strong>g only data from laboratoriesreport<strong>in</strong>g consistently for all four years (Figure 4.8).• Significantly decreas<strong>in</strong>g trends were observed forBulgaria and Malta. For Bulgaria, the trend did notrema<strong>in</strong> significant when consider<strong>in</strong>g only data fromlaboratories report<strong>in</strong>g consistently for all four years.• More detailed <strong>in</strong>formation on the most frequent <strong>resistance</strong>phenotypes <strong>in</strong> E. coli is presented <strong>in</strong> Table 4.3.4.1.4 Discussion and conclusions<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>in</strong> E. coli requires close attentionas the percentages of isolates resistant to commonlyused antimicrobials cont<strong>in</strong>ue to <strong>in</strong>crease throughout<strong>Europe</strong>. Especially worrisome is the <strong>in</strong>crease of <strong>resistance</strong>to third-generation cephalospor<strong>in</strong>s and comb<strong>in</strong>ed<strong>resistance</strong> to at least three antimicrobial classes, forwhich many countries reported significantly <strong>in</strong>creas<strong>in</strong>gtrends dur<strong>in</strong>g the period 2008–2011.Although EARS-Net data on ESBL production rema<strong>in</strong><strong>in</strong>complete, a large percentage of third-generationcephalospor<strong>in</strong>-resistant E. coli was reported as ESBLpositive.Presence of ESBL production and comb<strong>in</strong>ed<strong>resistance</strong> is a serious public health concern s<strong>in</strong>ce itseverely limits the number of treatment alternatives forpatients with life-threaten<strong>in</strong>g <strong>in</strong>fections. In addition,<strong>in</strong>creas<strong>in</strong>g comb<strong>in</strong>ed <strong>resistance</strong> and spread of ESBLmay lead to <strong>in</strong>creased use of carbapenems, favour<strong>in</strong>gthe further dissem<strong>in</strong>ation of carbapenemase-produc<strong>in</strong>gEnterobacteriaceae (CPE).Prudent antimicrobial use and comprehensive <strong>in</strong>fectioncontrol measures should be the cornerstones of<strong>in</strong>terventions aim<strong>in</strong>g to prevent selection and transmissionof resistant bacteria, <strong>in</strong>clud<strong>in</strong>g E. coli. A recent riskassessment on the spread of CPE published by ECDC<strong>in</strong> 2011 emphasises that the use of standard precautions,especially adherence to hand hygiene policies,is fundamental to prevent transmission of any multidrug-resistantorganisms, not only CPE, <strong>in</strong> healthcaresett<strong>in</strong>gs 23 .17


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.5: Escherichia coli: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>s, by country,EU/EEA countries, 2008–2011SENO (>)FI (>)NL (>*)2008200920102011BEIS (>)LTDE (>)FR (>)LUDK (>)SI (>)IE (>)Country codeAT (>)UK (>)PTCZPL (>*)ES (>)EE (>)MTEL (>)HU (>)LVIT (>*)ROBGCY (>)0 5 10 15 20 25 30 35 40% third-generation cephalospor<strong>in</strong> <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Slovakia) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends,respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.19


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.6: Escherichia coli: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to fluoroqu<strong>in</strong>olones, by country, EU/EEAcountries, 2008–2011SE ()2008200920102011LTIS (>)DK (>)NLLVUKFR (>)SI (>)BE (>)Country codeATIECZ ()PTPL (>*)BGROHU (>)MTES (>)IT (>*)CY0 10 20 30 40 50% fluoroqu<strong>in</strong>olone <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Slovakia) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends,respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.20


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.7: Escherichia coli: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to am<strong>in</strong>oglycosides, by country, EU/EEAcountries, 2008–2011SE (>)NOEEFI (>)2008200920102011ISDK (>)ATDENL (>)FR (>)UKLUPLCountry codeCZBE (>*)LTSIIELVHU (>*)ES (>)MTPT (>*)ELBG (*)ROCY (>)0 5 10 15 20 25 30 35% am<strong>in</strong>oglycoside <strong>resistance</strong>Countries not report<strong>in</strong>g data (Slovakia) for all four years were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends,respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.21


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.8: Escherichia coli: trends of <strong>in</strong>vasive isolates with comb<strong>in</strong>ed <strong>resistance</strong> (resistant to fluoroqu<strong>in</strong>olones, thirdgenerationcephalospor<strong>in</strong>s and am<strong>in</strong>oglycosides), by country, EU/EEA countries, 2008–2011ISSEEENO2008200920102011BE (>*)NL (>*)LTATFR (>)FI (>)LUDK (>)DECountry codeUKIE (>)CZPL (>*)SI (>)ES (>)PTHU (>)LVMT ()ROCY (>)0 5 10 15 20% comb<strong>in</strong>ed <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Slovakia) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends,respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.22


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114.2 Klebsiella pneumoniae4.2.1 Cl<strong>in</strong>ical and epidemiological importanceBacteria of the genus Klebsiella are frequent colonisersof the gastro<strong>in</strong>test<strong>in</strong>al tract <strong>in</strong> humans, but may also befound on sk<strong>in</strong>, <strong>in</strong> the oropharynx and upper airways <strong>in</strong>hospitalised <strong>in</strong>dividuals. Klebsiella pneumoniae is associatedwith opportunistic <strong>in</strong>fections <strong>in</strong> <strong>in</strong>dividuals withimpaired immune systems, such as diabetic, alcoholicand hospitalised patients with <strong>in</strong>dwell<strong>in</strong>g devices. Themost common sites of <strong>in</strong>fection are the ur<strong>in</strong>ary tractand the respiratory tract. Organisms such as K. pneumoniaecan spread rapidly, from the gastro<strong>in</strong>test<strong>in</strong>altract of patients and via the hands of hospital personnelto colonise other patients, lead<strong>in</strong>g to nosocomialoutbreaks. Klebsiella pneumoniae is the second mostfrequent cause of gram-negative bloodstream <strong>in</strong>fectionsafter Escherichia coli. The mortality rates of pneumoniacaused by K. pneumoniae can be high even when appropriateantimicrobial treatment is given. However, thisalso depends on the severity of the underly<strong>in</strong>g condition.4.2.2 Resistance mechanismsSimilar to E. coli, K. pneumoniae can be resistant to multipleantimicrobials, and <strong>resistance</strong> traits are frequentlyacquired through plasmids. However, <strong>in</strong> contrast to E.coli, K. pneumoniae has a chromosomally encoded SHVbeta-lactamase and is thus <strong>in</strong>tr<strong>in</strong>sically resistant to am<strong>in</strong>openicill<strong>in</strong>s.Moreover, this organism readily acquiresplasmid-mediated <strong>resistance</strong> determ<strong>in</strong>ants. Many novelESBL variants were <strong>in</strong>itially identified <strong>in</strong> K. pneumoniaeand were only subsequently found <strong>in</strong> E. coli. S<strong>in</strong>ce the<strong>resistance</strong> mechanisms do not differ significantly fromthose described for E. coli, readers should refer to the E.coli section (4.1, above) for further details. Carbapenemshave been widely used <strong>in</strong> many countries due to the<strong>in</strong>creas<strong>in</strong>g rate of ESBL-produc<strong>in</strong>g Enterobacteriaceaewith a consequent impact on the emergence of<strong>resistance</strong> to these antimicrobials, especially <strong>in</strong> K. pneumoniae.KPC carbapenemase-produc<strong>in</strong>g clones of K.pneumoniae have been observed <strong>in</strong> the United States,Greece, Italy and Israel, and similar stra<strong>in</strong>s are nowspread<strong>in</strong>g <strong>in</strong> several <strong>Europe</strong>an countries while plasmidsencod<strong>in</strong>g the VIM metallo-carbapenemase are frequent<strong>in</strong> K. pneumoniae <strong>in</strong> Greece. A new type of plasmidic carbapenemase,the New Delhi metallo-beta-lactamase 1(NDM-1), has been observed <strong>in</strong> patients return<strong>in</strong>g fromthe Indian subcont<strong>in</strong>ent. The bla OXA-48 gene codes for anoxacill<strong>in</strong>ase (OXA-48) that causes <strong>resistance</strong> to penicill<strong>in</strong>and reduces susceptibility to carbapenems, but not toexpanded-spectrum cephalospor<strong>in</strong>s. The level of <strong>resistance</strong>is often low and such stra<strong>in</strong>s are thus frequentlymissed <strong>in</strong> laboratories us<strong>in</strong>g automated AST systems. Acomb<strong>in</strong>ation of OXA-48-like enzymes with ESBLs suchas CTX-M15 can occur <strong>in</strong> Klebsiella spp. and can result<strong>in</strong> a highly drug-resistant phenotype. S<strong>in</strong>gle clones withsuch comb<strong>in</strong>ations have caused hospital outbreaks <strong>in</strong>several <strong>Europe</strong>an countries.Figure 4.9: Klebsiella pneumoniae: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s, by country, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta23


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT4.2.3 ResultsThird-generation cephalospor<strong>in</strong>s• For 2011, 29 countries reported 15 052 K. pneumoniaeisolates of which 4 538 (30.1%) were resistant to thirdgenerationcephalospor<strong>in</strong>s. The number of isolateswith relevant AST <strong>in</strong>formation reported by the countriesranged from 25 to 1 665.• The percentages of isolates reported as resistantranged from 2.3% (Sweden) to 81.0% (Bulgaria). Threecountries reported <strong>resistance</strong> percentages below 5%,four countries reported 5–10%, six countries reported10–25%, 10 countries reported 25–50%, and six countriesreported above 50% (Figure 4.9, Table 4.4).• Trends for the period 2008–2011 were calculated for25 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for 10 countries. For Italy, the trend did notrema<strong>in</strong> significant when consider<strong>in</strong>g only data fromlaboratories report<strong>in</strong>g consistently for all four years(Figure 4.14).• None of the report<strong>in</strong>g countries had significantlydecreas<strong>in</strong>g trends of <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s (Figure 4.14).Extended-spectrum beta-lactamase (ESBL)• N<strong>in</strong>eteen countries were <strong>in</strong>cluded <strong>in</strong> the calculationof ESBL percentages for K. pneumoniae. Datawere only <strong>in</strong>cluded from laboratories report<strong>in</strong>g ESBLtest results for all isolates identified as resistant tothird-generation cephalospor<strong>in</strong>s, and only from countrieswith at least 10 of such isolates.• The percentage of K. pneumoniae isolates found tobe resistant to third-generation cephalospor<strong>in</strong>s andascerta<strong>in</strong>ed by the participat<strong>in</strong>g laboratories as ESBLproducers, ranged from 65.2% to 100%. The percentagesof isolates ascerta<strong>in</strong>ed as ESBL producers werereported by 19 countries (Table 4.5).Fluoroqu<strong>in</strong>olones• For 2011, 29 countries reported 15 329 isolates, ofwhich 4 668 (30.5%) were resistant to fluoroqu<strong>in</strong>olones.The number of isolates with relevant AST<strong>in</strong>formation reported per country ranged from 10 to1 683 (Table 4.4).• The percentage of isolates found to be resistantranged from 1.9% (Sweden) to 72.2% (Greece). Fivecountries reported <strong>resistance</strong> percentages below 5%,two countries reported 5-10, seven countries reported10–25%, eight countries reported 25–50%, and sevencountries reported above 50% (Figure 4.10, Table 4.4).• Trends for the period 2008–2011 were calculated for25 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for 10 countries. For Luxembourg, the trendwas not significant when consider<strong>in</strong>g only data fromlaboratories report<strong>in</strong>g consistently for all four years(Figure 4.15).Figure 4.10: Klebsiella pneumoniae: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to fluoroqu<strong>in</strong>olones, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta24


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011• Significantly decreas<strong>in</strong>g trends were observed for twocountries (Denmark and Sweden) (Figure 4.15).Am<strong>in</strong>oglycosides• For 2011, 29 countries reported 15 367 isolates, ofwhich 4 020 (26.2%) were resistant to am<strong>in</strong>oglycosides.The number of isolates with relevant AST<strong>in</strong>formation reported per country ranged from 10 to1 688.• The percentages of resistant isolates reported bythe countries ranged from zero (Iceland) to 71.7%(Bulgaria). Five countries reported resistant percentagesbelow 5%, seven countries reported 5–10%, fourcountries reported 10–25%, eight countries reported25–50%, and five countries reported above 50%(Figure 4.11, Table 4.4).• Trends for the period 2008–2011 were calculated for25 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for six countries (Greece, Hungary, Italy,France, Malta and Portugal). For Italy, the trend wasnot significant when consider<strong>in</strong>g only data fromlaboratories report<strong>in</strong>g consistently for all four years(Figure 4.16).• None of the report<strong>in</strong>g countries had significantlydecreas<strong>in</strong>g trends of am<strong>in</strong>oglycoside <strong>resistance</strong>.Carbapenems• For 2011, 28 countries reported 14 594 isolates, ofwhich 1 323 (9.1%) were resistant to carbapenems.The number of isolates with relevant AST <strong>in</strong>formationreported by the countries ranged from 10 to 1 640.Fifteen countries reported one or more resistantisolate(s) <strong>in</strong> 2011. The majority of the resistant isolates(1 115 isolates; 84.3%) were reported by Greece,followed by Italy (164 isolates; 26.7%) and Cyprus (13isolates; 15.7%).• The percentage of isolates resistant to carbapenemsreported by the countries ranged from zero (13countries) to 68.2% (Greece). Twenty-three countriesreported <strong>resistance</strong> percentages below 1%, two countriesreported 1–5%, one country reported 10–25%,and two countries reported above 25% (Figure 4.12and Table 4.4).• Trends for the period 2008–2011 were calculated for22 countries (Figure 4.17). Significantly <strong>in</strong>creas<strong>in</strong>gtrends were observed for three countries (Greece,Hungary and Italy).• Significantly decreas<strong>in</strong>g trends were only observed forNorway. This trend was not significant when <strong>in</strong>clud<strong>in</strong>gonly data from laboratories report<strong>in</strong>g consistentlythroughout the period.Figure 4.11: Klebsiella pneumoniae: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to am<strong>in</strong>oglycosides, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta25


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTComb<strong>in</strong>ed <strong>resistance</strong>• For 2011, 29 countries reported 14 532 isolates testedfor susceptibility to third-generation cephalospor<strong>in</strong>s,fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides. The numberof isolates with relevant AST <strong>in</strong>formation reported percountry ranged from 10 to 1 647.• The percentages of isolates with comb<strong>in</strong>ed <strong>resistance</strong>to third-generation cephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olonesand am<strong>in</strong>oglycosides reported by the countriesranged from zero (Iceland) to 64.1% (Greece). Threecountries reported <strong>resistance</strong> percentages below 1%,eight countries reported 1–5%, two countries reported5–10%, four countries reported 10–25%, ten countriesreported 25–50%, and two countries reported above50% (Figure 4.13, Table 4.4).• Trends for the period 2008–2011 were calculatedfor 25 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends ofcomb<strong>in</strong>ed <strong>resistance</strong> were observed for 10 countries(Figure 4.18).• A significantly decreas<strong>in</strong>g trend was only observedfor the United K<strong>in</strong>gdom. This trend was not significantwhen consider<strong>in</strong>g only data from laboratories report<strong>in</strong>gconsistently for all four years (Figure 4.18).• More detailed <strong>in</strong>formation on the most frequent <strong>resistance</strong>phenotypes <strong>in</strong> K. pneumoniae is presented <strong>in</strong>Table 4.6.4.2.4 Discussion and conclusion<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>in</strong> K. pneumoniae is a publichealth concern of <strong>in</strong>creas<strong>in</strong>g importance <strong>in</strong> <strong>Europe</strong>.Resistance to third-generation cephalospor<strong>in</strong>s <strong>in</strong>creasedsignificantly <strong>in</strong> several countries dur<strong>in</strong>g the period2008–2011. Comb<strong>in</strong>ed <strong>resistance</strong> is common and<strong>in</strong>creas<strong>in</strong>g <strong>in</strong> several <strong>Europe</strong>an countries, with 22.3% ofthe isolates <strong>in</strong> 2011 resistant to at least three antimicrobialclasses.Similar to reports for E. coli, ESBL production among K.pneumoniae with <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>swas very common. Besides the beta-lactams,ESBL producers are also commonly resistant to otherantimicrobial classes, complicat<strong>in</strong>g the treatment ofserious <strong>in</strong>fections caused by these bacteria.Further dim<strong>in</strong>ish<strong>in</strong>g the available options for antimicrobialtreatment is the <strong>in</strong>creas<strong>in</strong>g percentage ofcarbapenem-resistant K. pneumoniae <strong>in</strong> some <strong>Europe</strong>ancountries. This situation is of particular concern as thecarbapenems are among the few effective antimicrobialsavailable for the treatment of <strong>in</strong>fections caused bymultidrug-resistant K. pneumoniae.Although <strong>in</strong>formation on carbapenemase production isvery limited <strong>in</strong> EARS-Net, data from scientific publicationsand enhanced <strong>surveillance</strong> established by someTable 4.4: Klebsiella pneumoniae: number and percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides, carbapenems and comb<strong>in</strong>ed <strong>resistance</strong>*, <strong>in</strong>clud<strong>in</strong>g 95%confidence <strong>in</strong>tervals (95%CI), by country, EU/EEA countries, 2011CountryThird-gen. cephalospor<strong>in</strong>s Fluoroqu<strong>in</strong>olones Am<strong>in</strong>oglycosides Carbapenems Comb<strong>in</strong>ed <strong>resistance</strong>N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI)Austria 795 13.3 (11-16) 797 16.6 (14-19) 790 7.2 (6-9) 610 0.2 (0-1) 785 4.1 (3-6)Belgium 668 13.6 (11-16) 663 14.9 (12-18) 608 8.1 (6-11) 646 0.3 (0-1) 587 4.9 (3-7)Bulgaria 121 81.0 (73-88) 121 51.2 (42-60) 120 71.7 (63-80) 116 0.0 (0-3) 120 45.8 (37-55)Cyprus 83 41.0 (30-52) 83 36.1 (26-47) 83 27.7 (18-39) 83 15.7 (9-25) 83 25.3 (16-36)Czech Republic 1 287 48.3 (45-51) 1 287 52.8 (50-56) 1 283 44.7 (42-48) 1 193 0.1 (0-0) 1 283 36.0 (33-39)Denmark 637 11.1 (9-14) 888 11.6 (10-14) 908 5.8 (4-8) 589 0.0 (0-1) 633 4.9 (3-7)Estonia 43 39.5 (25-56) 91 22.0 (14-32) 90 12.2 (6-21) 73 0.0 (0-5) 42 19.0 (9-34)F<strong>in</strong>land 319 3.4 (2-6) 319 3.8 (2-6) 319 1.9 (1-4) 318 0.0 (0-1) 319 1.9 (1-4)France 1 654 25.3 (23-28) 1 683 28.0 (26-30) 1 688 23.6 (22-26) 1 640 0.0 (0-0) 1 647 19.5 (18-21)Germany 519 12.5 (10-16) 519 14.1 (11-17) 518 8.9 (7-12) 512 0.0 (0-1) 518 6.9 (5-9)Greece 1 665 75.8 (74-78) 1 635 72.2 (70-74) 1 649 69.0 (67-71) 1 636 68.2 (66-70) 1 630 64.1 (62-66)Hungary 431 53.1 (48-58) 420 51.0 (46-56) 430 53.0 (48-58) 413 1.9 (1-4) 417 46.0 (41-51)Iceland 26 7.7 (1-25) 24 4.2 (0-21) 26 0.0 (0-13) 0 . 24 0.0 (0-14)Ireland 304 7.6 (5-11) 303 8.9 (6-13) 304 7.6 (5-11) 302 0.3 (0-2) 303 3.3 (2-6)Italy 627 45.9 (42-50) 597 45.7 (42-50) 661 34.6 (31-38) 615 26.7 (23-30) 566 32.9 (29-37)Latvia 65 38.5 (27-51) 63 38.1 (26-51) 65 33.8 (23-47) 65 0.0 (0-6) 63 33.3 (22-46)Lithuania 137 60.6 (52-69) 137 54.7 (46-63) 137 55.5 (47-64) 19 0.0 (0-18) 137 43.1 (35-52)Luxembourg 48 35.4 (22-51) 48 33.3 (20-48) 48 29.2 (17-44) 48 0.0 (0-7) 48 27.1 (15-42)Malta 52 13.5 (4-24) 52 13.5 (6-26) 52 9.6 (3-21) 52 3.8 (0-13) 52 3.8 (0-13)Netherlands 720 8.1 (6-10) 728 7.3 (6-9) 729 8.1 (6-10) 722 0.3 (0-1) 720 4.3 (3-6)Norway 421 2.9 (1-5) 427 3.5 (2-6) 426 2.8 (1-5) 443 0.0 (0-1) 374 0.8 (0-2)Poland 278 59.7 (54-66) 369 57.7 (53-63) 383 47.5 (42-53) 376 0.5 (0-2) 259 37.1 (31-43)Portugal 616 35.4 (32-39) 617 36.3 (33-40) 619 31.5 (28-35) 580 0.3 (0-1) 614 20.8 (18-24)Romania 25 44.0 (24-65) 10 30.0 (7-65) 10 50.0 (19-81) 10 0.0 (0-31) 10 30.0 (7-65)Slovakia 463 68.0 (64-72) 462 70.6 (66-75) 463 66.1 (62-70) 432 0.7 (0-2) 462 62.1 (58-67)Slovenia 232 30.2 (24-37) 232 35.3 (29-42) 232 22.0 (17-28) 232 0.0 (0-2) 232 19.8 (15-26)Spa<strong>in</strong> 1 145 13.4 (11-15) 1 145 17.0 (15-19) 1 145 10.5 (9-12) 1 144 0.3 (0-1) 1 145 8.3 (7-10)Sweden 736 2.3 (1-4) 624 1.9 (1-3) 602 1.7 (1-3) 900 0.0 (0-0) 545 0.7 (0-2)United K<strong>in</strong>gdom 935 5.3 (4-7) 985 4.6 (3-6) 979 4.3 (3-6) 825 0.4 (0-1) 914 2.1 (1-3)* Comb<strong>in</strong>ed <strong>resistance</strong> def<strong>in</strong>ed as be<strong>in</strong>g resistant to third-generation cephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olone and am<strong>in</strong>oglycosides.26


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011EU Member States <strong>in</strong>dicate an <strong>in</strong>crease <strong>in</strong> the spreadof carbapenemase-produc<strong>in</strong>g Enterobacteriaceae (CPE)<strong>in</strong> <strong>Europe</strong> <strong>in</strong> recent years, with reports of travel-relatedcases, autochthonous cases and outbreaks. ECDC issuedtwo risk assessments target<strong>in</strong>g CPE dur<strong>in</strong>g 2011 23,24 ,emphasis<strong>in</strong>g the need for implementation of <strong>in</strong>fectioncontrol measures such as active patient screen<strong>in</strong>g andadditional hygiene precautions for the care of CPEpositivepatients. In addition, countries are encouragedto develop national guidance on how to stop the spreadof CPE with<strong>in</strong> their country, and to actively report casesof CPE by mak<strong>in</strong>g confirmed cases notifiable to nationalpublic health authorities. These <strong>in</strong>terventions wouldnot only target CPE but also affect the general spreadof AMR.Table 4.5: Klebsiella pneumoniae: number of <strong>in</strong>vasiveisolates resistant to third-generation cephalospor<strong>in</strong>s(3GCRKP) and percentage (%) extended-spectrum betalactamase(ESBL)-positive among these isolates, asascerta<strong>in</strong>ed by participat<strong>in</strong>g laboratories, by country,EU/EEA countries, 2011CountryNumber oflaboratoriesNumber of3GCRKP%ESBLAustria 24 57 75.4Bulgaria 11 53 96.2Czech Republic 44 621 87.3Denmark 3 10 80Estonia 4 17 100France 24 114 98.2Germany 10 40 97.5Hungary 9 91 100Ireland 13 23 65.2Italy 7 40 100Latvia 5 22 90.9Lithuania 9 83 100Luxembourg 4 17 82.4Netherlands 9 26 92.3Poland 32 151 96Portugal 14 135 93.3Slovakia 4 176 90.3Slovenia 8 70 98.6Spa<strong>in</strong> 24 89 86.5Only data from laboratories consistently report<strong>in</strong>g ESBL test results for allisolates identified as resistant to third-generation cephalospor<strong>in</strong>s and fromcountries with at least 10 of such isolates were selected for the analysis.Table 4.6: Klebsiella pneumoniae: overall <strong>resistance</strong> and <strong>resistance</strong> comb<strong>in</strong>ations among <strong>in</strong>vasive isolates testedaga<strong>in</strong>st fluoroqu<strong>in</strong>olones, third-generation cephalospor<strong>in</strong>s and am<strong>in</strong>oglycosides (n=14 532), by country, EU/EEAcountries, 2011Resistance pattern Number of isolates % of totalFully susceptible 9 239 63.6S<strong>in</strong>gle <strong>resistance</strong> (to <strong>in</strong>dicated drug classes)Total (all s<strong>in</strong>gle <strong>resistance</strong>) 987 6.8Fluoroqu<strong>in</strong>olones 517 3.6Third-generation cephalospor<strong>in</strong>s 338 2.3Am<strong>in</strong>oglycosides 132 0.9Resistance to two classes of antimicrobial drugsTotal (all two classes comb<strong>in</strong>ations) 1 065 7.3Third-generation cephalospor<strong>in</strong>s + fluoroqu<strong>in</strong>olones 567 3.9Third-generation cephalospor<strong>in</strong>s + am<strong>in</strong>oglycosides 299 2.1Fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 199 1.4Resistance to three classes of antimicrobial drugsThird-generation cephalospor<strong>in</strong>s + fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 3 241 22.3Only data from isolates tested aga<strong>in</strong>st all three antimicrobial classes were <strong>in</strong>cluded <strong>in</strong> the analysis.27


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.14: Klebsiella pneumoniae: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to third-generation cephalospor<strong>in</strong>s, bycountry, EU/EEA countries, 2008–2011SENOFI (>)UK2008200920102011IEISNLDKMT (>)DEAT (>)ESCountry codeFR (>)SIPT (>)LULVEE (>)CYIT (>*)CZHU (>)LT (>)EL (>)BG0 20 40 60 80 100% third-generation cephalospor<strong>in</strong> <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Poland and Romania)were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong>the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.29


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.15: Klebsiella pneumoniae: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to fluoroqu<strong>in</strong>olones, by country, EU/EEA countries, 2008–2011SE ()FR (>)LU (>*)SI (>)CYPT (>)LVIT (>)HU (>)BGCZLT (>)EL (>)0 10 20 30 40 50 60 70 80% fluoroqu<strong>in</strong>olone <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Poland and Romania)were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong>the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.30


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.16: Klebsiella pneumoniae: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to am<strong>in</strong>oglycosides, by country, EU/EEAcountries, 2008–2011ISSEFINO2008200920102011UKDKATIENLDEMT (>)ESCountry codeEESIFR (>)CYLUPT (>)LVIT (>*)CZHU (>)LTEL (>)BG0 10 20 30 40 50 60 70 80% am<strong>in</strong>oglycoside <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Poland and Romania)were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong>the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.31


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.17: Klebsiella pneumoniae: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to carbapenems, by country, EU/EEAcountries, 2008–2011LVEEBG2008200920102011SIFRSEDKFINO ()MTCYIT (>)EL (>)0 10 20 30 40 50 60 70 80% carbapenem <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium, Iceland and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Lithuania,Luxembourg, Poland and Romania) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trend, respectively. Theasterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.32


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.18: Klebsiella pneumoniae: trends of <strong>in</strong>vasive isolates with comb<strong>in</strong>ed <strong>resistance</strong> (third-generationcephalospor<strong>in</strong>s, fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides), by country, EU/EEA countries, 2008–2011ISSENOFI2008200920102011UK ()Country codeEE (>)FR (>)SIPT (>)CYLU (>)IT (>)LVCZ (>)LT (>)BGHU (>)EL (>)0 10 20 30 40 50 60 70 80% comb<strong>in</strong>ed <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Poland and Romania)were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trend, respectively. The asterisks <strong>in</strong>dicate significant trends <strong>in</strong>the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.33


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT4.3 Pseudomonas aerug<strong>in</strong>osa4.3.1 Cl<strong>in</strong>ical and epidemiological importancePseudomonas aerug<strong>in</strong>osa is a non-ferment<strong>in</strong>g gramnegativebacterium that is ubiquitous <strong>in</strong> aquaticenvironments <strong>in</strong> nature. It is an opportunistic pathogenfor plants, animals and humans, and is a major anddreaded cause of <strong>in</strong>fection <strong>in</strong> hospitalised patients withlocalised or systemic impairment of immune defences,be<strong>in</strong>g a common cause of hospital-acquired pneumonia(<strong>in</strong>clud<strong>in</strong>g ventilator-associated pneumonia), bloodstreamand ur<strong>in</strong>ary tract <strong>in</strong>fections. Because of itsubiquity, its enormous versatility and <strong>in</strong>tr<strong>in</strong>sic toleranceto many detergents, dis<strong>in</strong>fectants and antimicrobialcompounds, it is difficult to control P. aerug<strong>in</strong>osa <strong>in</strong>hospitals and <strong>in</strong>stitutional environments. Moreover, P.aerug<strong>in</strong>osa is a frequent cause of sk<strong>in</strong> <strong>in</strong>fections suchas folliculitis and otitis externa among recreational andcompetitive swimmers. In patients with cystic fibrosis, P.aerug<strong>in</strong>osa causes severe bacterial complication lead<strong>in</strong>gto chronic colonisation and <strong>in</strong>termittent exacerbation ofthe condition with, for example, bronchiolitis and acuterespiratory distress syndrome. F<strong>in</strong>ally, P. aerug<strong>in</strong>osa iscommonly found <strong>in</strong> burn units, and <strong>in</strong> these locations itis almost impossible to eradicate colonis<strong>in</strong>g stra<strong>in</strong>s withclassic <strong>in</strong>fection control procedures.4.3.2 Resistance mechanismPseudomonas aerug<strong>in</strong>osa is <strong>in</strong>tr<strong>in</strong>sically resistant tothe majority of antimicrobial agents due to its selectiveability to exclude various molecules from penetrat<strong>in</strong>g itsouter membrane. The antimicrobial classes that rema<strong>in</strong>active <strong>in</strong>clude some fluoroqu<strong>in</strong>olones (e.g. ciprofloxac<strong>in</strong>and levofloxac<strong>in</strong>), am<strong>in</strong>oglycosides (e.g. gentamic<strong>in</strong>,tobramyc<strong>in</strong> and amikac<strong>in</strong>), some beta-lactams (piperacill<strong>in</strong>–tazobactam,ceftazidime, cefepime, imipenem,doripenem and meropenem) and colist<strong>in</strong>. Resistance ofP. aerug<strong>in</strong>osa to these agents can be acquired throughone or more of several mechanisms:• mutational modification of antimicrobial targets suchas topoisomerases or ribosomal prote<strong>in</strong>s, whichconfer <strong>resistance</strong> to fluoroqu<strong>in</strong>olones and am<strong>in</strong>oglycosides,respectively;• mutational derepression of the chromosomallycoded AmpC beta-lactamase, that can confer <strong>resistance</strong>to penicill<strong>in</strong>s and cephalospor<strong>in</strong>s active aga<strong>in</strong>stPseudomonas spp., and which is not <strong>in</strong>hibited bytazobactam;• mutational loss of outer membrane prote<strong>in</strong>s prevent<strong>in</strong>gthe uptake of antimicrobial agents such ascarbapenems;Table 4.7: Pseudomonas aerug<strong>in</strong>osa: number and percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> topiperacill<strong>in</strong>(±tazobactam), ceftazidime fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides, carbapenems and comb<strong>in</strong>ed <strong>resistance</strong>*,<strong>in</strong>clud<strong>in</strong>g 95% confidence <strong>in</strong>tervals, by country, EU/EEA countries, 2011Piperacill<strong>in</strong>±CountrytazobactamCeftazidime Fluoroqu<strong>in</strong>olones Am<strong>in</strong>oglycosides CarbapenemsComb<strong>in</strong>ed<strong>resistance</strong>*N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI) N %R (95%CI)Austria 528 13.6 (11-17) 498 10.6 (8-14) 511 18.6 (15-22) 535 13.3 (11-16) 538 13.6 (11-17) 537 10.6 (8-14)Belgium 376 15.4 (12-19) 417 8.9 (6-12) 397 21.2 (17-26) 332 14.2 (11-18) 459 10.7 (8-14) 417 11.0 (8-14)Bulgaria 43 23.3 (12-39) 39 30.8 (17-48) 47 29.8 (17-45) 48 33.3 (20-48) 48 29.2 (17-44) 48 25.0 (14-40)Cyprus 51 19.6 (10-33) 51 23.5 (13-37) 51 13.7 (6-26) 51 15.7 (7-29) 51 43.1 (29-58) 51 19.6 (10-33)Czech Republic 448 22.1 (18-26) 448 20.3 (17-24) 448 33.9 (30-39) 448 24.1 (20-28) 448 13.2 (10-17) 448 21.2 (18-25)Denmark 405 5.4 (3-8) 402 5.2 (3-8) 403 6.9 (5-10) 404 2.2 (1-4) 403 5.5 (3-8) 404 3.2 (2-5)Estonia 3 0.0 (0-71) 4 0.0 (0-60) 16 6.3 (0-30) 14 0.0 (0-23) 12 8.3 (0-38) 12 0.0 (0-26)F<strong>in</strong>land 164 14.0 (9-20) 168 8.3 (5-14) 185 14.6 (10-21) 221 3.6 (2-7) 221 10.4 (7-15) 185 5.9 (3-10)France 1 572 22.5 (20-25) 1 466 16.0 (14-18) 1 554 27.0 (25-29) 1 598 21.0 (19-23) 1 622 20.0 (18-22) 1 621 18.9 (17-21)Germany 386 14.8 (11-19) 386 9.1 (6-12) 385 18.2 (14-22) 386 11.7 (9-15) 386 9.8 (7-13) 387 7.2 (5-10)Greece 923 31.1 (28-34) 930 37.4 (34-41) 933 38.8 (36-42) 935 37.8 (35-41) 900 54.0 (51-57) 935 38.4 (35-42)Hungary 599 10.7 (8-13) 604 11.9 (9-15) 599 20.4 (17-24) 605 17.9 (15-21) 604 21.2 (18-25) 604 12.3 (10-15)Iceland 17 5.9 (0-29) 17 5.9 (0-29) 16 6.3 (0-30) 17 0.0 (0-20) 17 5.9 (0-29) 17 5.9 (0-29)Ireland 172 2.9 (1-7) 181 4.4 (2-9) 179 6.1 (3-11) 181 3.9 (2-8) 180 6.1 (3-11) 181 3.3 (1-7)Italy 233 21.9 (17-28) 303 16.2 (12-21) 318 26.1 (21-31) 279 20.4 (16-26) 316 20.6 (16-25) 313 17.3 (13-22)Latvia 11 9.1 (0-41) 11 9.1 (0-41) 12 25.0 (5-57) 12 25.0 (5-57) 12 8.3 (0-38) 12 8.3 (0-38)Lithuania 30 13.3 (4-31) 29 20.7 (8-40) 30 16.7 (6-35) 30 13.3 (4-31) 30 20.0 (8-39) 30 10.0 (2-27)Luxembourg 32 15.6 (5-33) 32 9.4 (2-25) 32 18.8 (7-36) 32 15.6 (5-33) 32 15.6 (5-33) 32 15.6 (5-33)Malta 42 23.8 (11-38) 42 11.9 (4-26) 42 19.0 (9-35) 42 33.3 (18-48) 42 23.8 (11-38) 42 23.5 (11-38)Netherlands 391 6.4 (4-9) 434 4.6 (3-7) 434 7.1 (5-10) 434 4.6 (3-7) 431 3.5 (2-6) 434 3.0 (2-5)Norway 142 4.9 (2-10) 146 3.4 (1-8) 147 5.4 (2-10) 147 0.0 (0-2) 148 4.1 (2-9) 148 1.4 (0-5)Poland 191 31.4 (25-39) 142 23.2 (17-31) 194 30.4 (24-37) 191 33.5 (27-41) 184 24.5 (18-31) 194 25.8 (20-33)Portugal 522 19.0 (16-23) 526 15.2 (12-19) 516 25.6 (22-30) 526 15.2 (12-19) 505 19.8 (16-24) 525 16.2 (13-20)Romania 6 66.7 (22-96) 8 62.5 (24-91) 8 75.0 (35-97) 9 66.7 (30-93) 9 66.7 (30-93) 9 66.7 (30-93)Slovakia 264 41.3 (35-47) 248 25.0 (20-31) 264 58.7 (53-65) 264 50.8 (45-57) 249 30.5 (25-37) 265 39.6 (34-46)Slovenia 118 12.7 (7-20) 118 7.6 (4-14) 118 9.3 (5-16) 118 7.6 (4-14) 118 23.7 (16-32) 118 10.2 (5-17)Spa<strong>in</strong> 833 6.4 (5-8) 836 8.9 (7-11) 838 24.2 (21-27) 839 18.7 (16-22) 839 16.3 (14-19) 839 12.6 (10-15)Sweden 289 4.2 (2-7) 378 5.3 (3-8) 344 5.8 (4-9) 234 0.9 (0-3) 390 7.7 (5-11) 379 1.8 (1-4)United K<strong>in</strong>gdom 557 4.3 (3-6) 578 4.8 (3-7) 585 6.2 (4-8) 590 3.4 (2-5) 540 5.6 (4-8) 587 2.6 (1-4)* Comb<strong>in</strong>ed <strong>resistance</strong> def<strong>in</strong>ed as be<strong>in</strong>g resistant to three or more antibiotic classes among piperacill<strong>in</strong>±tazobactam, ceftazidime, fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosidesand carbapenems.34


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011• mutational upregulation of efflux systems, that canconfer <strong>resistance</strong> to beta-lactams, fluoroqu<strong>in</strong>olonesand am<strong>in</strong>oglycosides; and• acquisition of plasmid-mediated <strong>resistance</strong> genescod<strong>in</strong>g for various beta-lactamases and am<strong>in</strong>oglycoside-modify<strong>in</strong>genzymes that can confer <strong>resistance</strong>to various beta-lactams <strong>in</strong>clud<strong>in</strong>g carbapenems (e.g.metallo-beta-lactamases) and am<strong>in</strong>oglycosides, orcod<strong>in</strong>g for rRNA ribosomal methylases that can conferhigh-level <strong>resistance</strong> to all am<strong>in</strong>oglycosides.4.3.3 ResultsPiperacill<strong>in</strong> (± tazobactam)• For 2011, 29 countries reported 9 348 isolates, ofwhich 1 538 (16.5%) were resistant to piperacill<strong>in</strong>(±tazobactam). The number of isolates with relevantAST <strong>in</strong>formation reported per country ranged from 3 to1 572. Two countries (Estonia and Romania) reportedfewer than 10 isolates and are thus not shown <strong>in</strong>Figure 4.19.• The percentages of resistant isolates reported bythe countries ranged from zero (Estonia) to 66.7%(Romania). Five countries reported <strong>resistance</strong> percentageslower than 5%, five countries reported 5–10%, 15countries reported 10–25%, three countries reported25–50%, and one country reported above 50% (Figure4.19 and Table 4.7).• Trends for the period 2008–2011 were calculated for23 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for six countries (Austria, Denmark, F<strong>in</strong>land,France, Sweden and United K<strong>in</strong>gdom). For F<strong>in</strong>land, thetrend was not significant when consider<strong>in</strong>g only datafrom laboratories report<strong>in</strong>g consistently throughoutthe period (Figure 4.25).• Significantly decreas<strong>in</strong>g trends were observed forthree countries (Bulgaria, Hungary and Malta). ForBulgaria and Hungary, the trends were not significantwhen consider<strong>in</strong>g only data from laboratories report<strong>in</strong>gconsistently throughout the period (Figure 4.25).Ceftazidime• For 2011, 29 countries reported 9 442 isolates, ofwhich 1 338 (14.2%) were resistant to ceftazidime.The number of isolates with relevant AST <strong>in</strong>formationreported per country ranged from 4 to 1 466. Twocountries (Estonia and Romania) reported fewer than10 isolates and are thus not <strong>in</strong>cluded <strong>in</strong> Figure 4.20.• The percentages of resistant isolates reported bythe countries ranged from zero (Estonia) to 62.5%(Romania). Five countries reported <strong>resistance</strong> percentageslower than 5%, 10 countries reported 5–10%, 10countries reported 10–25%, three countries reported25–50%, and one country reported above 50% (Figure4.20, Table 4.7).Figure 4.19: Pseudomonas aerug<strong>in</strong>osa: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to piperacill<strong>in</strong>±tazobactam,by country, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta35


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT• Trends for the period 2008–2011 were calculated for23 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for Austria and France (Figure 4.26).• Significantly decreas<strong>in</strong>g trends were observed for theCzech Republic and Malta (Figure 4.26).Fluoroqu<strong>in</strong>olones• For 2011, 29 countries reported 9 606 isolates, ofwhich 2 159 (22.5%) were resistant to fluoroqu<strong>in</strong>olones.The number of isolates with relevant AST<strong>in</strong>formation reported per country ranged from 8 to1 554. One country (Romania) reported fewer than 10isolates and is thus not <strong>in</strong>cluded <strong>in</strong> Figure 4.21.• The percentages of resistant isolates reported bythe countries ranged from 5.4% (Norway) to 75.0%(Romania). N<strong>in</strong>e countries reported <strong>resistance</strong> percentagesof 5–10%, 10 countries reported 10–25%,eight countries reported 25–50%, and two countriesreported above 50% (Figure 4.21, Table 4.7).• Trends for the period 2008–2011 were calculated for21 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for three countries (Austria, Denmark andFrance). For France, the trend was not significant when<strong>in</strong>clud<strong>in</strong>g only data from laboratories report<strong>in</strong>g consistentlyfor all four years (Figure 4.27).• Significantly decreas<strong>in</strong>g trends were observed forseven countries (Czech Republic, Cyprus, Greece,Hungary, Ireland, Italy and Slovenia). For Hungary andItaly, the trends were not significant when consider<strong>in</strong>gonly data from laboratories report<strong>in</strong>g consistently forall four years (Figure 4.27).Am<strong>in</strong>oglycosides• For 2011, 29 countries reported 9 522 isolates, ofwhich 1 690 (17.7%) were resistant to am<strong>in</strong>oglycosides.The number of isolates with relevant AST <strong>in</strong>formationreported per country ranged from 9 to 1 598. Onecountry (Romania) reported fewer than 10 isolates andis thus not <strong>in</strong>cluded <strong>in</strong> Figure 4.22).• The percentage of resistant isolates reported by thecountries ranged from zero (Estonia, Iceland andNorway) to 66.7% (Romania). Four countries reported<strong>resistance</strong> percentages lower than 1%, five countriesreported 1–5%, one country reported 5–10%, 12countries reported 10–25%, five countries reported25–50%, and two countries reported above 50%(Figure 4.22, Table 4.7).• Trends for the period 2008–2011 were calculated for23 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for three countries (Austria, France andPortugal). For France and Portugal, the trends werenot significant when consider<strong>in</strong>g only data fromlaboratories report<strong>in</strong>g consistently for all four years(Figure 4.28).Figure 4.20: Pseudomonas aerug<strong>in</strong>osa: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to ceftazid<strong>in</strong>e, by country,EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta36


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011• Significantly decreas<strong>in</strong>g trends were observed forfour countries (Czech Republic, Greece, Hungary, andItaly). For Italy, the trend was not significant whenconsider<strong>in</strong>g only data from laboratories report<strong>in</strong>g consistentlyfor all four years (Figure 4.28).Carbapenems• For 2011, 29 countries reported 9 734 isolates, ofwhich 1 807 (18.6%) were resistant to carbapenems.The number of isolates with relevant AST <strong>in</strong>formationreported per country ranged from 9 to 1 622. Onecountry (Romania) reported fewer than 10 isolates andis thus not <strong>in</strong>cluded <strong>in</strong> Figure 4.23.• The percentages of resistant isolates reported bythe countries ranged from 3.5% (the Netherlands)to 66.7% (Romania). Two countries reported <strong>resistance</strong>percentages of 1–5%, eight countries reported5–10%, 14 countries reported 10–25%, three countriesreported 25–50%, and two countries reportedabove 50% (Figure 4.23 and Table 4.7).• Trends for the period 2008–2011 were calculated for22 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for five countries (Austria, Cyprus, Denmark,Greece and France). For Greece, the trend was not significantwhen consider<strong>in</strong>g only data from laboratoriesreport<strong>in</strong>g consistently for all four years (Figure 4.29).• Significantly decreas<strong>in</strong>g trends were observed for fourcountries (Hungary, Italy, the Czech Republic, and theNetherlands). For Hungary, Italy and the Netherlands,the trends were not significant when consider<strong>in</strong>g onlydata from laboratories report<strong>in</strong>g consistently for allfour years (Figure 4.29).Comb<strong>in</strong>ed <strong>resistance</strong> (piperacill<strong>in</strong>±tazobactam, ceftazidime,fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides andcarbapenems)• For 2011, 29 countries reported 9 774 isolates testedfor susceptibility to at least three antimicrobialclasses among piperacill<strong>in</strong>±tazobactam, ceftazidime,fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides and carbapenems.The number of isolates with relevant AST <strong>in</strong>formationreported per country ranged from 9 to 1 621 (Table4.7).• In 2011, 34.7% of the isolates were resistant to oneor more of the five considered antimicrobial classes,while 15.3% were resistant to three or more. The mostcommon pattern was <strong>resistance</strong> to all five antimicrobialclasses (4.6%) (Table 4.8).• The percentages of isolates with comb<strong>in</strong>ed <strong>resistance</strong>,i.e. resistant (R) to at least three of the five consideredantimicrobial classes, were below 1% <strong>in</strong> one country,1–5% <strong>in</strong> six countries, 5–10% <strong>in</strong> four countries,10–25% <strong>in</strong> 13 countries, 25–50% <strong>in</strong> four countries andabove 50% <strong>in</strong> one country (Figure 4.24, Table 4.7).• Trends for the period 2008–2011 were calculated for22 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends of comb<strong>in</strong>ed<strong>resistance</strong> were observed for three countries(Austria, Denmark and France). For France, the trendFigure 4.21: Pseudomonas aerug<strong>in</strong>osa: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to fluoroqu<strong>in</strong>olones, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta37


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTwas not significant when <strong>in</strong>clud<strong>in</strong>g only data fromlaboratories consistently report<strong>in</strong>g for all four years(Figure 4.30).• Significantly decreas<strong>in</strong>g trends of comb<strong>in</strong>ed <strong>resistance</strong>were observed for four countries (the CzechRepublic, Greece, Hungary, and Italy). For Italy, thetrend was not significant when <strong>in</strong>clud<strong>in</strong>g only datafrom laboratories consistently report<strong>in</strong>g for all fouryears (Figure 4.30).4.3.4 Discussion and conclusionsIn 2011, high percentages of <strong>resistance</strong> <strong>in</strong> P. aerug<strong>in</strong>osaisolates were reported, especially by countries <strong>in</strong>southern and eastern <strong>Europe</strong>. Comb<strong>in</strong>ed <strong>resistance</strong> wascommon; 15.3% of the isolates were resistant to at leastthree antimicrobial classes and 4.6% of the isolateswere resistant to all five antimicrobial classes under<strong>surveillance</strong>. Pseudomonas aerug<strong>in</strong>osa carries <strong>in</strong>tr<strong>in</strong>sic<strong>resistance</strong> to a number of antimicrobial classes and anyadditional acquired <strong>resistance</strong> severely limits the therapeuticoptions for treatment of serious <strong>in</strong>fections.Pseudomonas aerug<strong>in</strong>osa is recognised as a major causeof healthcare-associated <strong>in</strong>fection, and <strong>in</strong> data reportedfrom HAI-Net ICU <strong>surveillance</strong>, this pathogen was one ofthe most commonly isolated bacteria <strong>in</strong> pneumonia andbloodstream <strong>in</strong>fections <strong>in</strong> <strong>Europe</strong>an ICUs <strong>in</strong> 2009 25 .Although EARS-Net reports high percentages of <strong>resistance</strong><strong>in</strong> P. aerug<strong>in</strong>osa isolates for 2011, the situationappears generally stable <strong>in</strong> <strong>Europe</strong> with few countriesreport<strong>in</strong>g significantly <strong>in</strong>creas<strong>in</strong>g or decreas<strong>in</strong>g trendsof <strong>resistance</strong> to the antimicrobial agents under <strong>surveillance</strong>.However, due to its ubiquitous nature andpotential virulence, P. aerug<strong>in</strong>osa is a challeng<strong>in</strong>gpathogen to control <strong>in</strong> healthcare sett<strong>in</strong>gs. Prudent antimicrobialuse and high standards of <strong>in</strong>fection control areessential to prevent the situation from deteriorat<strong>in</strong>g.Table 4.8: Pseudomonas aerug<strong>in</strong>osa: overall <strong>resistance</strong> and <strong>resistance</strong> comb<strong>in</strong>ations among <strong>in</strong>vasive isolatestested aga<strong>in</strong>st at least three antimicrobial classes among piperacill<strong>in</strong>±tazobactam, ceftazidime, fluoroqu<strong>in</strong>olones,am<strong>in</strong>oglycosides and carbapenems (n=9 774), EU/EEA countries, 2011Resistance pattern Number of isolates % of totalFully susceptible (to tested antimicrobials) 6 379 65.3S<strong>in</strong>gle <strong>resistance</strong> (to <strong>in</strong>dicated drug classes)Total (all s<strong>in</strong>gle <strong>resistance</strong> types) 1 208 12.4Fluoroqu<strong>in</strong>olones 430 4.4Carbapenems 436 4.5Am<strong>in</strong>oglycosides 162 1.7Ceftazidime 78 0.8Piperacill<strong>in</strong>(±tazobactam) 102 1Resistance to two classes of antimicrobialsTotal (all two classes comb<strong>in</strong>ations) 696 7.1Fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides 211 2.2Piperacill<strong>in</strong> (±tazobactam) + ceftazidime 199 2Fluoroqu<strong>in</strong>olones + carbapenems 103 1.1Piperacill<strong>in</strong> (±tazobactam) +fluoroqu<strong>in</strong>olones 33 0.3Piperacill<strong>in</strong> (±tazobactam) + carbapenems 38 0.4Piperacill<strong>in</strong> (±tazobactam) + am<strong>in</strong>oglycosides 33 0.3Am<strong>in</strong>oglycosides +carbapenems 33 0.3Ceftazidime + carbapenems 17 0.2Fluoroqu<strong>in</strong>olones + ceftazidime 20 0.2Ceftazidime + am<strong>in</strong>oglycosides 9 0.1Resistance to three classes of antimicrobialsTotal (all three classes comb<strong>in</strong>ations) 520 5.3Fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides + carbapenems 181 1.9Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones +am<strong>in</strong>oglycosides 112 1.1Piperacill<strong>in</strong> (±tazobactam) + ceftazidime + carbapenems 66 0.7Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + ceftazidime 51 0.5Fluoroqu<strong>in</strong>olones + ceftazidime + carbapenems 18 0.2Fluoroqu<strong>in</strong>olones +ceftazidime +am<strong>in</strong>oglycosides 29 0.3Piperacill<strong>in</strong> (±tazobactam) + am<strong>in</strong>oglycosides + carbapenems 14 0.1Piperacill<strong>in</strong> (±tazobactam) + ceftazidime +am<strong>in</strong>oglycosides 15 0.2Ceftazidime + am<strong>in</strong>oglycosides + carbapenems 10 0.1Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + carbapenems 24 0.2Resistance to four classes of antimicrobialsTotal (all four classes comb<strong>in</strong>ations) 522 5.3Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + am<strong>in</strong>oglycosides + carbapenems 146 1.5Fluoroqu<strong>in</strong>olones + ceftazidime + am<strong>in</strong>oglycosides + carbapenems 130 1.3Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + ceftazidime + am<strong>in</strong>oglycosides 123 1.3Piperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + ceftazidime + carbapenems 94 1Piperacill<strong>in</strong> (±tazobactam) + ceftazidime + am<strong>in</strong>oglycosides + carbapenems 29 0.3Resistance to five classes of antimicrobialsPiperacill<strong>in</strong> (±tazobactam) + fluoroqu<strong>in</strong>olones + ceftazidime + am<strong>in</strong>oglycosides + carbapenems 449 4.638


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.22: Pseudomonas aerug<strong>in</strong>osa: proportion (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to am<strong>in</strong>oglycosides, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMaltaFigure 4.23: Pseudomonas aerug<strong>in</strong>osa: percentage (%) of <strong>in</strong>vasive isolates with <strong>resistance</strong> to carbapenems, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta39


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.24: Pseudomonas aerug<strong>in</strong>osa: percentage (%) of <strong>in</strong>vasive isolates with comb<strong>in</strong>ed <strong>resistance</strong> (<strong>resistance</strong> tothree or more antimicrobial classes among piperacill<strong>in</strong> (±tazobactam), ceftazidime, fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosidesand carbapenems), by country, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta40


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.25: Pseudomonas aerug<strong>in</strong>osa: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to piperacill<strong>in</strong>±tazobactam, bycountry, EU/EEA countries, 2008–2011IESE (>)UK (>)NO2008200920102011DK (>)ESNLHU ()Country codeFI (>*)DELUPTCYITMT ()BG ( and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. The asterisks <strong>in</strong>dicatesignificant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.41


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.26: Pseudomonas aerug<strong>in</strong>osa: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to ceftazidime, by country, EU/EEAcountries, 2008–2011NOIENLUK2008200920102011DKSESIFIESDELUCountry codeAT (>)HUMT ()ITCZ ( and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively.42


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.28: Pseudomonas aerug<strong>in</strong>osa: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to am<strong>in</strong>oglycosides, by country, EU/EEA countries, 2008–2011NOSEDKUK2008200920102011FIIENLSIDEAT (>)LT (*)LUCYHU (


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.29: Pseudomonas aerug<strong>in</strong>osa: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to carbapenems, by country, EU/EEAcountries, 2008–2011NL ()2008200920102011UKIESEDEFICZ ()Country codeESPTFR (>)LTIT (*)0 10 20 30 40 50 60% carbapenem <strong>resistance</strong>Countries not report<strong>in</strong>g data for all four years (Belgium and Slovakia) and countries report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Estonia, Iceland,Latvia, Luxembourg and Romania) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. Theasterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.** For Czech Republic there is a decreas<strong>in</strong>g trend, but the drop <strong>in</strong> 2010 was caused by the adoption of the new EUCAST breakpo<strong>in</strong>ts.45


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.30: Pseudomonas aerug<strong>in</strong>osa: trends of <strong>in</strong>vasive isolates with comb<strong>in</strong>ed <strong>resistance</strong> (resistant to three or moreantibiotic classes among piperacill<strong>in</strong>±tazobactam, ceftazidime, fluoroqu<strong>in</strong>olones, am<strong>in</strong>oglycosides and carbapenems),by country, EU/EEA countries, 2008–2011NOSEUK2008200920102011NLDK (>)IEFIDELTSICountry codeAT (>)HU (


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114.4 Streptococcus pneumoniae4.4.1 Cl<strong>in</strong>ical and epidemiological importanceStreptococcus pneumoniae is a common cause of disease,especially among young children, elderly peopleand patients with compromised immune functions. Thecl<strong>in</strong>ical spectrum ranges from upper airway <strong>in</strong>fections,such as s<strong>in</strong>usitis, and otitis media to pneumonia and<strong>in</strong>vasive bloodstream <strong>in</strong>fections and men<strong>in</strong>gitis. S<strong>in</strong>ceS. pneumoniae is the most common cause of pneumoniaworldwide, morbidity and mortality are high and annuallyapproximately 3 million people are estimated to dieof pneumococcal <strong>in</strong>fections.Pneumococci carry a variety of virulence factors thatfacilitate adherence and transcytosis of epithelial cells.The cell wall of pneumococci is coated with a viscouspolysaccharide slime layer termed the capsule. This isthe most important virulence factor because it protectsthe bacteria from the adhesion of opsonis<strong>in</strong>g antibodiesand the destruction by leucocytes. Capsular polysaccharidesare highly diverse and play an important role<strong>in</strong> immune evasion. To date, 93 different serotypes havebeen described. The serotype distribution varies withage, disease and geographical region. Interest<strong>in</strong>gly,serotypes most frequently <strong>in</strong>volved <strong>in</strong> pneumococcal diseaseor colonisation <strong>in</strong> <strong>in</strong>fants are also most frequentlyassociated with AMR. However, serotype replacementdue to <strong>in</strong>creased use of the pneumococcal conjugatevacc<strong>in</strong>e (PCV) might change this over time.4.4.2 Resistance mechanismsBeta-lactam antimicrobials b<strong>in</strong>d to cell wall synthesis<strong>in</strong>genzymes, so-called penicill<strong>in</strong>-b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong>s (PBPs),and <strong>in</strong>terfere with the biosynthesis and remodell<strong>in</strong>g ofthe bacterial cell wall dur<strong>in</strong>g cell growth and division.The mechanism of penicill<strong>in</strong> <strong>resistance</strong> <strong>in</strong> S. pneumoniaeconsists of alterations <strong>in</strong> PBPs, which result <strong>in</strong> reducedaff<strong>in</strong>ity to this class of antimicrobial. Alterations <strong>in</strong>PBPs are due to a cont<strong>in</strong>uous mutation process thatcauses different degrees of <strong>resistance</strong> proceed<strong>in</strong>g fromreduced susceptibility through low-level cl<strong>in</strong>ical <strong>resistance</strong>– conventionally termed <strong>in</strong>termediate i (I) – to fullcl<strong>in</strong>ical <strong>resistance</strong> (R). Intermediately resistant stra<strong>in</strong>sare clearly less susceptible than susceptible stra<strong>in</strong>s.However, <strong>in</strong> the absence of men<strong>in</strong>gitis, <strong>in</strong>fections with<strong>in</strong>termediately resistant stra<strong>in</strong>s are often successfullytreated with high doses of benzyl-penicill<strong>in</strong> oram<strong>in</strong>openicill<strong>in</strong>s.Macrolide, l<strong>in</strong>cosamide and streptogram<strong>in</strong> (MLS) antimicrobialsare chemically dist<strong>in</strong>ct, but all b<strong>in</strong>d to aribosomal subunit <strong>in</strong>hibit<strong>in</strong>g the <strong>in</strong>itiation of mRNA b<strong>in</strong>d<strong>in</strong>gand thus act as prote<strong>in</strong> synthesis <strong>in</strong>hibitors. Thereare two predom<strong>in</strong>ant <strong>resistance</strong> mechanisms aga<strong>in</strong>stMLS antimicrobials <strong>in</strong> S. pneumoniae:iMicroorganisms are def<strong>in</strong>ed as <strong>in</strong>termediate by a level ofantimicrobial activity with uncerta<strong>in</strong> cl<strong>in</strong>ical effect. Occasionally, thiscan be overcome if antibiotics can be adm<strong>in</strong>istered at a higher doseand/or are concentrated at the <strong>in</strong>fected body site.Table 4.9: Streptococcus pneumoniae: number of <strong>in</strong>vasive isolates tested for penicill<strong>in</strong> and macrolides susceptibility,percentage (%) be<strong>in</strong>g penicill<strong>in</strong>-non-susceptible (PNSP), penicill<strong>in</strong>-resistant (PRSP), macrolide-non-susceptible(MNSP), s<strong>in</strong>gle penicill<strong>in</strong>-resistant (PENR), s<strong>in</strong>gle macrolide-resistant (MACR) and non-susceptible to penicill<strong>in</strong> andmacrolides, <strong>in</strong>clud<strong>in</strong>g 95% confidence <strong>in</strong>tervals, by country, EU/EEA countries, 2011CountryNumber of isolatestested for (PEN/MACR/both)%PNSP(95%CI)%PRSP(95%CI)%MNSP(95%CI)%s<strong>in</strong>gle PEN(95%CI)%s<strong>in</strong>gle MACR(95%CI)%DUAL(95%CI)Austria 405/373/355 3.0 (2-5) 1.7 (1-4) 11.5 (8-15) 0.8 (0-2) 9.6 (7-13) 2.3 (1-4)Belgium 1829/1829/1829 0.8 (0-1) 0.8 (0-1) 26.0 (24-28) 0.2 (0-1) 25.4 (23-27) 0.6 (0-1)Bulgaria 33/30/30 21.2 (9-39) 21.2 (9-39) 13.3 (4-31) 10.0 (2-27) 0.0 (0-12) 13.3 (4-31)Cyprus 12/12/12 25.0 (5-57) 25.0 (5-57) 25.0 (5-57) 8.3 (0-38) 8.3 (0-38) 16.7 (2-48)Czech Republic 316/316/316 3.8 (2-7) 0.0 (0-1) 3.5 (2-6) 1.9 (1-4) 1.6 (1-4) 1.9 (1-4)Denmark 896/896/896 4.8 (3-6) 0.2 (0-1) 5.1 (4-7) 1.8 (1-3) 2.1 (1-3) 3.0 (2-4)Estonia 51/45/42 2.0 (0-10) 2.0 (0-10) 2.2 (0-12) 2.4 (0-13) 2.4 (0-13) 0.0 (0-8)France 1413/1413/1413 23.8 (22-26) 0.1 (0-1) 26.0 (24-28) 5.1 (4-6) 7.3 (6-9) 18.8 (17-21)Germany 347/353/343 1.7 (1-4) 0.3 (0-2) 7.9 (5-11) 1.2 (0-3) 8.2 (5-12) 0.0 (0-1)Hungary 139/129/129 11.5 (7-18) 5.8 (3-11) 14.7 (9-22) 3.9 (1-9) 6.2 (3-12) 8.5 (4-15)Iceland 32/32/32 9.4 (2-25) 6.3 (1-21) 21.9 (9-40) 0.0 (0-11) 12.5 (4-29) 9.4 (2-25)Ireland 324/310/310 19.4 (15-24) 6.2 (4-9) 18.4 (14-23) 5.5 (3-9) 4.8 (3-8) 13.5 (10-18)Italy 174/266/162 6.9 (4-12) 6.3 (3-11) 27.4 (22-33) 2.5 (1-6) 24.7 (18-32) 4.3 (2-9)Latvia 40/46/38 12.5 (4-27) 10.0 (3-24) 0.0 (0-8) 13.2 (4-28) 0.0 (0-9) 0.0 (0-9)Lithuania 48/41/41 18.8 (9-33) 2.1 (0-11) 26.8 (14-43) 4.9 (1-17) 9.8 (3-23) 17.1 (7-32)Luxembourg 50/52/50 8.0 (2-19) 2.0 (0-11) 15.4 (7-28) 2.0 (0-11) 10.0 (3-22) 6.0 (1-17)Malta 8/10/8 50.0 (25-73) 10.0 (2-71) 12.5 (0-53) 0.0 (0-71) 0.0 (0-71) 12.5 (0-53)Netherlands 1067/1200/978 1.1 (1-2) 0.3 (0-1) 4.5 (3-6) 0.7 (0-1) 4.2 (3-6) 0.3 (0-1)Norway 619/570/567 3.4 (2-5) 0.0 (0-1) 4.2 (3-6) 1.9 (1-3) 2.6 (1-4) 1.4 (1-3)Poland 165/135/134 18.2 (13-25) 4.2 (2-9) 26.7 (19-35) 3.7 (1-8) 11.9 (7-19) 14.9 (9-22)Portugal 439/417/402 10.5 (8-14) 8.4 (6-11) 14.9 (12-19) 5.5 (3-8) 9.2 (7-12) 5.2 (3-8)Romania 36/18/18 61.1 (43-77) 61.1 (43-77) 44.4 (22-69) 16.7 (4-41) 0.0 (0-19) 44.4 (22-69)Slovak Republic 26/25/25 7.7 (1-25) 3.8 (0-20) 12.0 (3-31) 4.0 (0-20) 8.0 (1-26) 4.0 (0-20)Slovenia 252/251/251 12.3 (9-17) 0.8 (0-3) 24.3 (19-30) 6.4 (4-10) 18.3 (14-24) 6.0 (3-10)Spa<strong>in</strong> 736/746/720 30.2 (27-34) 9.8 (8-12) 24.8 (22-28) 13.2 (11-16) 8.3 (6-11) 16.9 (14-20)Sweden 1013/963/963 3.5 (2-5) 3.2 (2-4) 5.2 (4-7) 1.7 (1-3) 3.2 (2-5) 2.0 (1-3)United K<strong>in</strong>gdom 1324/1263/1126 5.4 (4-7) 0.8 (0-1) 5.9 (5-7) 2.7 (2-4) 2.5 (2-4) 3.6 (3-5)47


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT• The acquisition of an erythromyc<strong>in</strong> ribosomal methylationgene (erm) results <strong>in</strong> a post-transcriptionalmodification of the 23S subunit of ribosomal RNA,which blocks the b<strong>in</strong>d<strong>in</strong>g of the macrolide to theribosome. Once expression of the gene is <strong>in</strong>duced,this often results <strong>in</strong> high-level <strong>resistance</strong> (MICs > 128mg/L) to macrolides, l<strong>in</strong>cosamide and streptogram<strong>in</strong>B, termed MLS B <strong>resistance</strong>.• The acquisition of a macrolide efflux system gene(mef(E)) results <strong>in</strong> the excretion of the antimicrobial,and effectively reduces <strong>in</strong>tracellular erythromyc<strong>in</strong>,azithromyc<strong>in</strong> and clarithromyc<strong>in</strong> to sub<strong>in</strong>hibitory concentrations.In contrast to beta-lactam <strong>resistance</strong>,macrolide <strong>resistance</strong> via these mechanisms (particularlyfor MLS B ) provides very high MICs, and cannot beovercome by <strong>in</strong>creas<strong>in</strong>g the dosages of antimicrobials.The two fluoroqu<strong>in</strong>olones with acknowledged cl<strong>in</strong>icalactivity aga<strong>in</strong>st pneumococci are levofloxac<strong>in</strong> and moxifloxac<strong>in</strong>.Resistance to fluoroqu<strong>in</strong>olones is mediatedby the mutations <strong>in</strong> ParC (subunit of topoisomerase IV)and/or GyrA (subunit of DNA gyrase/topoisomerase IV).Additionally, <strong>resistance</strong> may be conferred by efflux.S<strong>in</strong>ce S. pneumoniae is the most frequent cause ofcommunity-acquired pneumonia and cannot cl<strong>in</strong>icallybe easily dist<strong>in</strong>guished from lower airway <strong>in</strong>fectionscaused by other pathogens, empirical treatment ofcommunity-acquired lower respiratory <strong>in</strong>fections needsto be active aga<strong>in</strong>st pneumococci and should take thelocal prevalence of AMR <strong>in</strong>to account. Prescription ofnon-beta-lactam compounds is therefore typical <strong>in</strong>countries where penicill<strong>in</strong> non-susceptibility has beenfrequently reported. Such prescrib<strong>in</strong>g patterns <strong>in</strong>creasethe selection pressure for alternative antimicrobialssuch as macrolides and fluoroqu<strong>in</strong>olones. It is thereforeno surprise to see a dynamic AMR picture emerge<strong>in</strong> different <strong>Europe</strong>an countries. At the same time, theexistence of frequent dual beta-lactam/macrolide <strong>resistance</strong>,particularly among serotypes commonly found <strong>in</strong>children, means that <strong>in</strong> practice the use of agents fromeither of these classes will result <strong>in</strong> <strong>in</strong>creas<strong>in</strong>g percentagesof <strong>resistance</strong> to the other class and frequent use ofmacrolides has been considered as a major driver for the<strong>in</strong>crease <strong>in</strong> beta-lactam <strong>resistance</strong>.Even though a certa<strong>in</strong> small decrease <strong>in</strong> penicill<strong>in</strong> <strong>resistance</strong>had been detected <strong>in</strong> some countries before the<strong>in</strong>troduction of the PCV, the widespread use of this vacc<strong>in</strong>eis an important factor that may have <strong>in</strong>fluenced thedecrease <strong>in</strong> AMR levels, elim<strong>in</strong>at<strong>in</strong>g the <strong>in</strong>fections (andmore importantly, the children’s carriage) of frequent‘classic’ resistant serotypes – 14, 6B, 19F and 23F – allof them covered by the PCV.Figure 4.31: Streptococcus pneumoniae: percentage (%) of <strong>in</strong>vasive isolates non-susceptible to penicill<strong>in</strong> (PNSP), bycountry, EU/EEA countries 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta48


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114.4.3 ResultsPenicill<strong>in</strong>• For 2011, 27 countries reported 11 788 isolates, ofwhich 1 039 (8.8%) were non-susceptible to penicill<strong>in</strong>and 268 of these non-susceptible isolates were identifiedas resistant. Greece and F<strong>in</strong>land did not reportdata for 2011 and Malta reported fewer than 10 isolates(accord<strong>in</strong>gly no data from these countries aredisplayed <strong>in</strong> Figure 4.31).• For 2011, the number of reported S. pneumoniae isolateswith relevant AST <strong>in</strong>formation for penicill<strong>in</strong>(penicill<strong>in</strong>s or oxacill<strong>in</strong>) ranged between 8 (Malta) and1 829 (Belgium) (Table 4.9).• The percentage of isolates reported as non-susceptiblewas below 1% <strong>in</strong> one country, 1–5% <strong>in</strong> eightcountries, 5–10% <strong>in</strong> five countries, 10–25% <strong>in</strong> n<strong>in</strong>ecountries, 25–50% <strong>in</strong> three countries and above 50%<strong>in</strong> one country (Figure 4.31 and Table 4.9).• Trends for the period 2008–2011 were calculatedfor 22 countries. Four countries (Denmark, Estonia,Lithuania and Sweden) had significantly <strong>in</strong>creas<strong>in</strong>gtrends (Figure 4.35).• Significantly decreas<strong>in</strong>g trends were observed for fourcountries (Belgium* i , Portugal, Hungary, and France).For France and Portugal, the trends did not rema<strong>in</strong> significantwhen consider<strong>in</strong>g only data from laboratoriesreport<strong>in</strong>g consistently for all four years (Figure 4.35).Macrolides• For 2011, 27 countries reported 11 739 isolates, ofwhich 1 713 (14.6%) were non-susceptible to macrolidesand 1 658 of these non-susceptible isolateswere identified as resistant (14.1% of total isolates).• The number of reported S. pneumoniae isolates withrelevant AST <strong>in</strong>formation for macrolides (erythromyc<strong>in</strong>,clarithromyc<strong>in</strong> or azitromyc<strong>in</strong>) ranged between 10(Malta) and 1 829 (Belgium) (Table 4.9).• The percentage of isolates reported as non-susceptibleranged from zero (Latvia) to 44.4% (Romania), andwas reported below 5% <strong>in</strong> five countries, 5–10% <strong>in</strong>four countries, 10–25% <strong>in</strong> 11 countries, and 25–50% <strong>in</strong>seven countries (Figure 4.32, Table 4.9).iThe percentage of Streptococcus pneumoniae non-susceptible topenicill<strong>in</strong> reported by Belgium dropped from 8% <strong>in</strong> 2008 to < 1% <strong>in</strong>2009. This is largely due to the fact that the cl<strong>in</strong>ical breakpo<strong>in</strong>ts(CLSI) used to determ<strong>in</strong>e SIR have changed. These new CLSIguidel<strong>in</strong>es started to be used <strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g of 2009.Figure 4.32: Streptococcus pneumoniae: percentage (%) of <strong>in</strong>vasive isolates non-susceptible to macrolides by country,EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta49


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT• Trends for the period 2008–2011 were calculated for21 countries. Significantly <strong>in</strong>creas<strong>in</strong>g trends wereobserved for Lithuania, Slovenia and Spa<strong>in</strong>. For Spa<strong>in</strong>,the trend did not rema<strong>in</strong> significant when consider<strong>in</strong>gonly data from laboratories report<strong>in</strong>g consistentlythroughout the period (Figure 4.36).• Significantly decreas<strong>in</strong>g trends were observed forthree countries (Hungary, Norway and Portugal)(Figure 4.36).Non-susceptibility to penicill<strong>in</strong>s and macrolides• For 2011, 27 countries reported 11 184 isolates testedfor both penicill<strong>in</strong> and macrolides, of which 652 (5.8%)isolates were non-susceptible to both antimicrobialclasses. One country (Malta) reported fewer than 10isolates and is therefore not <strong>in</strong>cluded <strong>in</strong> Figure 4.33.• The number of reported S. pneumoniae isolates withrelevant AST <strong>in</strong>formation for both penicill<strong>in</strong>s and macrolidesranged between 8 (Malta) and 1 829 (Belgium)(Table 4.9).• Percentages of non-susceptibility to penicill<strong>in</strong> andmacrolides ranged from zero (Estonia, Germany andLatvia) to 44.4% (Romania), and were reported below1% <strong>in</strong> five countries, 1–5% <strong>in</strong> eight countries, 5–10% <strong>in</strong>five countries 10–25% <strong>in</strong> eight countries, and 25–50%<strong>in</strong> one country (Figure 4.33 and Table 4.9).• Trends for 2008–2011 were calculated for 21 countries.A significant <strong>in</strong>crease was observed for four countries(Denmark, Lithuania, Spa<strong>in</strong> and Sweden) (Figure 4.37).• Significantly decreas<strong>in</strong>g trends were observed for fivecountries (Belgium, Germany, Hungary, France andPortugal) (Figure 4.37).Fluoroqu<strong>in</strong>olones• For 2011, 24 countries reported susceptibility data forfluoroqu<strong>in</strong>olones <strong>in</strong> 7 275 isolates (58% of all reportedS. pneumoniae isolates). Among them, 4.8% wereresistant to fluoroqu<strong>in</strong>olones. Forty fluoroqu<strong>in</strong>oloneresistantisolates were also penicill<strong>in</strong>-non-susceptible.Serogroups• Fifteen countries reported 3 855 S. pneumoniae isolateswith identification of the serotype/serogroup.Cyprus, Germany, Poland, Romania and Slovakiareported fewer than 30 isolates with serotype/serogroup<strong>in</strong>formation and are hence not <strong>in</strong>cluded <strong>in</strong> theanalysis.• In 2011, serogroups 1 and 19 were the most prevalentserogroups (account<strong>in</strong>g for 14% and 13% of the isolates,respectively), followed by serogroup 7 (12%)and serogroup 3 (9%). This serogroup distribution issimilar to the one reported by EARS-Net <strong>in</strong> 2010.Figure 4.33: Streptococcus pneumoniae: percentage (%) of <strong>in</strong>vasive isolates non-susceptible to penicill<strong>in</strong>s andmacrolides by country, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta50


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011• Among the most commonly reported serogroups,dual non-susceptibility to both penicill<strong>in</strong> and macrolideswas ma<strong>in</strong>ly observed <strong>in</strong> serogroups 19, 14, 6,15 and 9 (by order of decreas<strong>in</strong>g percentage). S<strong>in</strong>glenon-susceptibility to penicill<strong>in</strong> was most common <strong>in</strong>serogroups 19, 14, 9 and 23, and s<strong>in</strong>gle non-susceptibilityto macrolides was most common <strong>in</strong> serogroups19, 1, 14 and 6 (Figure 4.34).4.4.4 Discussion and conclusionsAlthough large <strong>in</strong>ter-country variations can be noted,the overall percentages of S. pneumoniae with nonsusceptibilityto commonly used antimicrobials reportedto EARS-Net have rema<strong>in</strong>ed relatively stable <strong>in</strong> <strong>Europe</strong>dur<strong>in</strong>g recent years. The lowest percentages of S. pneumoniaewith non-susceptibility to penicill<strong>in</strong> and/ormacrolides were reported by countries <strong>in</strong> central andnorthern <strong>Europe</strong>. Geographical differences <strong>in</strong> reportedpercentages of resistant S. pneumoniae have beenshown, <strong>in</strong> several studies, to be associated with differences<strong>in</strong> antimicrobial consumption, both on <strong>in</strong>dividualand population levels 26 . A previous ecological studyl<strong>in</strong>k<strong>in</strong>g data collected by the former EARSS with nationaldata on antimicrobial consumption, supported thisassumption 27 . In addition, differences <strong>in</strong> serotype distributionsand local dom<strong>in</strong>ance of specific clones may also<strong>in</strong>fluence national estimates 25 .It is important to note that the differences and changes<strong>in</strong> cl<strong>in</strong>ical breakpo<strong>in</strong>ts used for determ<strong>in</strong><strong>in</strong>g penicill<strong>in</strong>susceptibility <strong>in</strong> S. pneumoniae might <strong>in</strong>troduce biaswhen compar<strong>in</strong>g national data reported to EARS-Net, butalso when <strong>in</strong>terpret<strong>in</strong>g trends <strong>in</strong> countries that changedcl<strong>in</strong>ical breakpo<strong>in</strong>ts dur<strong>in</strong>g the observation period.Similar <strong>surveillance</strong> artefacts have been reported fromthe United States when S. pneumoniae data were analysedwith new breakpo<strong>in</strong>ts 28 .Although the number of countries report<strong>in</strong>g data onserotype distribution to EARS-Net is <strong>in</strong>creas<strong>in</strong>g, datarema<strong>in</strong> <strong>in</strong>complete. However, data reported for 2011support previous observations that most penicill<strong>in</strong> nonsusceptibleisolates belong to a few serogroups. MostEU/EEA Member States have, <strong>in</strong> recent years, implementedrout<strong>in</strong>e immunisation for children with themultivalent PCV 29 . As a limited number of S. pneumoniaeserotypes are responsible for a considerable percentageof serious pneumococcal <strong>in</strong>fections <strong>in</strong> both adultsand children, <strong>in</strong>troduction of PCV is likely to change theepidemiology of <strong>in</strong>vasive pneumococcal disease <strong>in</strong> many<strong>Europe</strong>an countries.Figure 4.34: Distribution of serogroups and associated <strong>resistance</strong> profiles per serogroup, 2011Serogroups119731262214952381543310111820OtherFully susceptible*S<strong>in</strong>gle penicill<strong>in</strong> non-susceptibleS<strong>in</strong>gle macrolides non-susceptibleDual non-susceptibility**0 2 4 6 8 10 12 14 16Proportion (%)Only countries that reported serogroup <strong>in</strong>formation for more than 30 isolates were <strong>in</strong>cluded <strong>in</strong> the figure.* Susceptible to at least penicill<strong>in</strong> and macrolides.** Non-susceptible to penicill<strong>in</strong> and macrolides.51


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.35: Streptococcus pneumoniae: trends of <strong>in</strong>vasive isolates with non-susceptibility to penicill<strong>in</strong>, by country,EU/EEA countries, 2008–2011BE**NLDE2008200920102011EEATNOSE (>)CZDK (>)UKCountry codeITLUISPT ( and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively. The asterisks<strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.** The percentage of Streptococcus pneumoniae non-susceptible to penicill<strong>in</strong> reported by Belgium dropped from 8% <strong>in</strong> 2008 to < 1% <strong>in</strong> 2009. This is largely due to thefact that the cl<strong>in</strong>ical breakpo<strong>in</strong>ts (CLSI) used to determ<strong>in</strong>e SIR have changed. These new CLSI guidel<strong>in</strong>es began to be used <strong>in</strong> the beg<strong>in</strong>n<strong>in</strong>g of 2009.52


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.36: Streptococcus pneumoniae: trends of <strong>in</strong>vasive isolates with non-susceptibility to macrolides, by country,EU/EEA countries, 2008–2011EECZNO ()IT0 5 10 15 20 25 30 35% macrolide non-susceptibilityCountries not report<strong>in</strong>g data for all four years (F<strong>in</strong>land, Greece and Slovakia) and countries only report<strong>in</strong>g relevant AST data for 19 isolates or fewer per year (Cyprus,Latvia, Malta, Poland and Romania) were excluded from the analysis. The symbols > and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively.The asterisks <strong>in</strong>dicate significant trends <strong>in</strong> the overall data that were not supported by data from laboratories consistently report<strong>in</strong>g for all four years.53


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.37: Streptococcus pneumoniae: trends of <strong>in</strong>vasive isolates with non-susceptibility to penicill<strong>in</strong>s andmacrolides, by country, EU/EEA countries, 2008–2011EEDE ()UKCountry codeITPT ()FR ( and < <strong>in</strong>dicate significant <strong>in</strong>creas<strong>in</strong>g and decreas<strong>in</strong>g trends, respectively.54


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114.5 Staphylococcus aureus4.5.1 Cl<strong>in</strong>ical and epidemiological importanceStaphylococcus aureus is a gram-positive organismthat colonises the sk<strong>in</strong> of about 30% of healthyhumans. Although ma<strong>in</strong>ly a harmless coloniser, S.aureus can cause severe <strong>in</strong>fection. Its oxacill<strong>in</strong>-resistantform (meticill<strong>in</strong>-resistant S. aureus, MRSA) has beenthe most important cause of antimicrobial-resistanthealthcare-associated <strong>in</strong>fections worldwide. S<strong>in</strong>cehealthcare-associated MRSA <strong>in</strong>fections add to the numberof <strong>in</strong>fections caused by meticill<strong>in</strong>-susceptible S.aureus, a high <strong>in</strong>cidence of MRSA adds to the overallburden of <strong>in</strong>fections caused by S. aureus <strong>in</strong> hospitals.Moreover, <strong>in</strong>fections with MRSA may result <strong>in</strong> prolongedhospital stay and <strong>in</strong> higher mortality, ow<strong>in</strong>g ma<strong>in</strong>ly to the<strong>in</strong>ferior effectiveness of alternative treatment regimens.MRSA is still the most commonly identified antimicrobial-resistantpathogen <strong>in</strong> hospitals <strong>in</strong> many parts of theworld, <strong>in</strong>clud<strong>in</strong>g <strong>Europe</strong>, the Americas, North Africa andthe Middle- and Far East.4.5.2 Resistance mechanismsStaphylococcus aureus acquires <strong>resistance</strong> to meticill<strong>in</strong>and all other beta-lactam antimicrobials throughexpression of exogenous mecA gene that code for a variantpenicill<strong>in</strong>-b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong> PBP2’ (PBP2a) with lowaff<strong>in</strong>ity for beta-lactams, thus prevent<strong>in</strong>g the <strong>in</strong>hibitionby beta-lactams of cell wall synthesis. A new mec genehas been discovered, mecC (formerly called mecA lga251 ).The level of meticill<strong>in</strong> <strong>resistance</strong>, as def<strong>in</strong>ed by the MICdepends on the amount of PBP2’ production, which is<strong>in</strong>fluenced by various genetic factors. Resistance levelsof mec-positive stra<strong>in</strong>s can thus range from phenotypicallysusceptible to highly resistant. Upon challenge withbeta-lactam antimicrobials, a population of a heterogeneouslyresistant MRSA stra<strong>in</strong> may quickly be outgrownby a sub-population of highly resistant variants.For rifampic<strong>in</strong>, the mechanism of <strong>resistance</strong> is mutation<strong>in</strong> the rpoB-gene, lead<strong>in</strong>g to production of RNA polymerasewith low aff<strong>in</strong>ity for rifampic<strong>in</strong> and other rifamyc<strong>in</strong>s.Such <strong>resistance</strong> easily occurs with rifampic<strong>in</strong> monotherapy,for which reason the drug should only be used <strong>in</strong>comb<strong>in</strong>ation therapy.Resistance to fluoroqu<strong>in</strong>olones is mediated by the mutations<strong>in</strong> ParC or ParE (subunits of topoisomerase IV)and/or GyrA (subunit of DNA gyrase/topoisomerase IV).Additionally, <strong>resistance</strong> may be conferred by efflux.The most common mechanism of l<strong>in</strong>ezolid <strong>resistance</strong>is mutation <strong>in</strong> the 23S rRNA target site. A more recentmechanism is nonmutational and <strong>in</strong>volves acquisition ofa natural <strong>resistance</strong> gene, cfr (chloramphenicol–florfenicol<strong>resistance</strong>). The cfr gene has been found primarily <strong>in</strong>plasmids that can be spread horizontally. The product ofthe cfr gene is a methyltransferase that catalyses methylationof the 23S rRNA gene.Table 4.10: Staphylococcus aureus: number and percentage (%) of <strong>in</strong>vasive isolates resistant to meticill<strong>in</strong> (MRSA) andrifampic<strong>in</strong>, <strong>in</strong>clud<strong>in</strong>g 95% confidence <strong>in</strong>tervals, by country, EU/EEA countries, 2011CountryMeticill<strong>in</strong>Rifampic<strong>in</strong>Number of isolates tested % MRSA (95%CI) Number of isolates tested % rifampic<strong>in</strong>-resistant (95%CI)Austria 1 966 7.4 (6-9) 1 850 0.3 (0-1)Belgium 1 744 17.4 (16-19) 1 014 0.6 (0-1)Bulgaria 214 22.4 (17-29) 162 14.2 (9-21)Cyprus 113 41.6 (32-51) 113 0.0 (0-3)Czech Republic 1 555 14.5 (13-16) 782 1.8 (1-3)Denmark 1 452 1.2 (1-2) 1 452 0.1 (0-0)Estonia 116 1.7 (0-6) 3 0.0 (0-71)France 4 716 20.1 (19-21) 4 278 1.0 (1-1)Germany 2 388 16.1 (15-18) 1 656 0.7 (0-1)Greece 784 39.2 (36-43) 0 .Hungary 1 156 26.2 (24-29) 570 0.4 (0-1)Iceland 71 2.8 (0-10) 3 0.0 (0-71)Ireland 1 057 23.7 (21-26) 835 1.0 (0-2)Italy 1 261 38.2 (36-41) 970 4.3 (3-6)Latvia 192 9.9 (6-15) 186 0.5 (0-3)Lithuania 278 5.4 (3-9) 158 0.6 (0-2)Luxembourg 127 20.5 (14-29) 90 0.0 (0-4)Malta 130 49.2 (41-59) 130 0.8 (0-4)Netherlands 1 801 1.4 (1-2) 1 581 0.4 (0-1)Norway 1 223 0.3 (0-1) 446 0.0 (0-1)Poland 860 24.3 (21-27) 135 27.4 (20-36)Portugal 1 307 54.6 (52-57) 1 092 1.7 (1-3)Romania 107 50.5 (41-60) 101 7.9 (3-15)Slovakia 560 25.9 (22-30) 478 1.3 (0-3)Slovenia 464 7.1 (5-10) 443 0.5 (0-2)Spa<strong>in</strong> 1 950 22.5 (21-24) 1 826 0.5 (0-1)Sweden 3 099 0.8 (1-1) 2 456 0.2 (0-1)United K<strong>in</strong>gdom 3 408 13.6 (13-15) 1777 0.6 (0-1)55


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.39: Staphylococcus aureus: trends of <strong>in</strong>vasive isolates resistant to meticill<strong>in</strong> (MRSA), by country, EU/EEAcountries, 2008–2011NOSEDKNL2008200920102011EEISLTSIATLVUK (


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 20114.6 Enterococci4.6.1 Cl<strong>in</strong>ical and epidemiological importanceEnterococci belong to the normal bacterial flora of thegastro<strong>in</strong>test<strong>in</strong>al tract of humans, other mammals, birdsand reptiles. Enterococci are regarded harmless commensals,and are even believed to have positive effectson a number of gastro<strong>in</strong>test<strong>in</strong>al and systemic conditions.However, when the commensal relationship withthe host is disrupted, enterococci can cause <strong>in</strong>vasivediseases. Recently, the recognition of high-risk clonessuggests that some particular stra<strong>in</strong>s can act as truepathogens, and not only as opportunistic commensals.Enterococci can cause a variety of <strong>in</strong>fections, <strong>in</strong>clud<strong>in</strong>gendocarditis, bloodstream <strong>in</strong>fections, and ur<strong>in</strong>ary tract<strong>in</strong>fections, and are associated with peritonitis and <strong>in</strong>traabdom<strong>in</strong>alabscesses. In the United States, three to fournosocomial bloodstream <strong>in</strong>fections per 10 000 hospitaldischarges are caused by enterococci, and contribute topatient mortality as well as additional hospital stay.The vast majority of cl<strong>in</strong>ical enterococcal <strong>in</strong>fections <strong>in</strong>humans are caused by Enterococcus faecalis and E. faecium.Epidemiological data collected over the last twodecades have documented the emergence of enterococcias important nosocomial pathogens, exemplifiedby the expansion of a major hospital-adapted polyclonalsubcluster CC17 <strong>in</strong> E. faecium, and by CC2 and CC9 <strong>in</strong> E.faecalis. The latter clones have even been isolated fromfarm animals. The emergence of particular clones andclonal complexes of E. faecalis and E. faecium was paralleledby <strong>in</strong>creases <strong>in</strong> <strong>resistance</strong> to glycopeptides andhigh-level <strong>resistance</strong> to am<strong>in</strong>oglycosides. These twoantimicrobial classes represent the few rema<strong>in</strong><strong>in</strong>g therapeuticoptions for treatment of human <strong>in</strong>fections causedby E. faecium when <strong>resistance</strong> has emerged aga<strong>in</strong>stpenicill<strong>in</strong>s. Besides the fact that <strong>in</strong>fections caused byresistant stra<strong>in</strong>s are difficult to treat, enterococci arehighly tenacious and thus easily dissem<strong>in</strong>ate <strong>in</strong> the hospitalsett<strong>in</strong>g.4.6.2 Resistance mechanismsEnterococci are <strong>in</strong>tr<strong>in</strong>sically resistant to a broad rangeof antimicrobials <strong>in</strong>clud<strong>in</strong>g cephalospor<strong>in</strong>s, sulphonamidesand low concentrations of am<strong>in</strong>oglycosides.Patient safety <strong>in</strong> hospitals is challenged by the ability ofenterococci to acquire additional <strong>resistance</strong> through thetransfer of plasmids and transposons and recomb<strong>in</strong>ationor mutation.Beta-lactam antimicrobialsBy nature, enterococci have low susceptibility to manybeta-lactam antimicrobials as a consequence of theirlow-aff<strong>in</strong>ity PBPs. Two possible mechanisms of <strong>resistance</strong>of enterococci to beta-lactams have been reported:the production of beta-lactamase, which is an extremelyrare f<strong>in</strong>d<strong>in</strong>g, and the overproduction and modificationof PBPs, particularly PBP5, that causes high-levelpenicill<strong>in</strong> <strong>resistance</strong> <strong>in</strong> E. faecium. Resistance to am<strong>in</strong>openicill<strong>in</strong>is currently rare <strong>in</strong> E. faecalis. Therefore, theTable 4.11: Total number of <strong>in</strong>vasive isolates and percentages (%) of high-level am<strong>in</strong>glycoside-resistant E. faecalis andvancomyc<strong>in</strong>-resistant E. faecium, <strong>in</strong>clud<strong>in</strong>g 95% confidence <strong>in</strong>tervals, by country, EU/EEA countries, 2011CountryHigh-level am<strong>in</strong>oglycoside resistant E. faecalisVancomyc<strong>in</strong>-resistant E. faeciumNumber of isolates % R (95% CI) Number of isolates % R (95% CI)Austria 327 30.9 (26-36) 354 4.5 (3-7)Belgium 335 18.2 (14-23) 215 7.0 (4-11)Bulgaria 62 30.6 (20-44) 39 0.0 (0-9)Cyprus 54 18.5 (9-31) 17 0.0 (0-20)Czech Republic 556 46.2 (42-50) 211 7.6 (4-12)Denmark 45 31.1 (18-47) 615 1.3 (1-3)Estonia 32 19.1 (6-43) 15 0.0 (0-25)F<strong>in</strong>land 0 . 169 1.2 (0-4)France 955 20.0 (18-23) 569 1.4 (1-3)Germany 578 41.0 (37-45) 535 11.4 (9-14)Greece 653 37.4 (34-41) 424 23.1 (19-27)Hungary 461 48.6 (44-53) 120 0.8 (0-5)Iceland 19 0.0 (0-18) 13 0.0 (0-25)Ireland 244 29.9 (24-36) 347 34.9 (30-40)Italy 330 50.0 (44-56) 236 4.2 (2-8)Latvia 34 26.5 (13-44) 22 9.1 (1-29)Lithuania 48 43.8 (29-59) 26 7.7 (1-25)Luxembourg 27 44.4 (25-65) 24 4.2 (0-21)Malta 0 . 14 0.0 (0-23)Netherlands 363 33.3 (28-38) 481 1.0 (0-2)Norway 115 21.7 (15-30) 165 1.8 (0-5)Poland 190 48.4 (41-56) 202 8.4 (5-13)Portugal 403 29.8 (25-35) 208 20.2 (15-26)Romania 0 . 12 0.0 (0-26)Slovakia 188 49.5 (42-57) 101 4.0 (1-10)Slovenia 125 36.0 (28-45) 83 0.0 (0-4)Spa<strong>in</strong> 917 39.3 (36-43) 542 1.5 (1-3)Sweden 707 19.2 (16-22) 353 0.0 (0-1)United K<strong>in</strong>gdom 75 16.0 (9-26) 302 8.9 (6-13)59


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTfirst choice for treatment of <strong>in</strong>fections caused by thismicroorganism is still an am<strong>in</strong>openicill<strong>in</strong> such as ampicill<strong>in</strong>.In E. faecium, ampicill<strong>in</strong>-<strong>resistance</strong> has <strong>in</strong>creasedsignificantly <strong>in</strong> recent years not the least due to the widedissem<strong>in</strong>ation of ampicill<strong>in</strong>-resistant stra<strong>in</strong>s belong<strong>in</strong>gto the polyclonal subcluster CC17.Am<strong>in</strong>oglycosidesIn addition to the <strong>in</strong>tr<strong>in</strong>sic mechanism of low-level <strong>resistance</strong>to am<strong>in</strong>oglycosides, which causes a low uptake ofthe drug, enterococci have acquired genes conferr<strong>in</strong>ghigh-level <strong>resistance</strong> to am<strong>in</strong>oglycosides. High-level<strong>resistance</strong> to streptomyc<strong>in</strong> can be mediated by s<strong>in</strong>glemutations with<strong>in</strong> a prote<strong>in</strong> of the 30S ribosomal subunit,the target of am<strong>in</strong>oglycoside activity. In addition,different am<strong>in</strong>oglycoside-modify<strong>in</strong>g enzymes have beenidentified, target<strong>in</strong>g eight different am<strong>in</strong>oglycosides. Thebi-functional APH(2’’)/AAC(6’) enzyme confers high-level<strong>resistance</strong> to all am<strong>in</strong>oglycosides except streptomyc<strong>in</strong>and is now widespread across <strong>Europe</strong>. With high-level<strong>resistance</strong>, any synergistic effect between beta-lactamsand glycopeptides is lost.GlycopeptidesVancomyc<strong>in</strong> <strong>resistance</strong> <strong>in</strong> enterococci was first reported<strong>in</strong> France and England, but showed the most dramatic<strong>in</strong>crease <strong>in</strong> the United States and was attributed to thewidespread use of vancomyc<strong>in</strong> <strong>in</strong> US hospitals. Whilevancomyc<strong>in</strong> consumption was lower <strong>in</strong> <strong>Europe</strong>, a closelyrelated glycopeptide, avoparc<strong>in</strong>, had been widelyused as a growth promoter <strong>in</strong> animal husbandry s<strong>in</strong>cethe late 1970s until it was banned <strong>in</strong> the EU by 1998.Glycopeptide-<strong>resistance</strong> is due to the synthesis of modifiedcell wall precursors that show a decreased aff<strong>in</strong>ityfor glycopeptides. Six phenotypes have been identifiedof which two have cl<strong>in</strong>ical relevance: VanA, with highlevel<strong>resistance</strong> to vancomyc<strong>in</strong> and a variable level of<strong>resistance</strong> to teicoplan<strong>in</strong>; and VanB, with a variablelevel of <strong>resistance</strong> <strong>in</strong> most cases to vancomyc<strong>in</strong> only.The VanA and VanB phenotypes, mostly found among E.faecalis and E. faecium, may be transferred by plasmidsand through conjugative transposition.4.6.3 Results4.6.3.2 E. faecalisHigh-level am<strong>in</strong>oglycoside-<strong>resistance</strong>• For 2011, 26 countries reported 7 843 isolates, ofwhich 2 642 (33.7%) had high-level <strong>resistance</strong> to gentamic<strong>in</strong>.The number of isolates reported per countryranged from 19 to 955 (Table 4.11).• The percentages of high-level am<strong>in</strong>oglycoside-<strong>resistance</strong>reported by the countries ranged from zero(Iceland) to 50.0% (Italy). One country reported <strong>resistance</strong>percentages below 1%, seven countries reported10–25%, and eighteen reported 25–50%. No countryreported a percentage above 50% (Figure 4.40 andTable 4.11).Figure 4.40: Enterococcus faecalis: percentage (%) of <strong>in</strong>vasive isolates with high-level <strong>resistance</strong> to am<strong>in</strong>oglycosides, bycountry, EU/EEA countries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta60


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011• Twenty countries have reported more than 20 isolatesper year s<strong>in</strong>ce 2008 and were thus <strong>in</strong>cluded <strong>in</strong> thetrend analysis for the period 2008–2011. Significantly<strong>in</strong>creas<strong>in</strong>g trends were observed for two countries(Austria and Luxembourg) (Figure 4.42).• Five countries (Belgium, Cyprus, Greece, Portugal, andthe United K<strong>in</strong>gdom) have had significantly decreas<strong>in</strong>gtrends of high-level am<strong>in</strong>oglycoside-<strong>resistance</strong> forthe past four years (Figure 4.42).4.6.3.3 E. faeciumVancomyc<strong>in</strong>• For 2011, 29 countries reported 6 414 isolates, ofwhich 467 (7.3%) were resistant to vancomyc<strong>in</strong>. Thenumber of isolates with relevant AST <strong>in</strong>formationreported per country ranged from 12 to 481. Only onecountry (Estonia) reported fewer than 10 isolates andis thus not shown <strong>in</strong> Figure 4.41).• The percentages of vancomyc<strong>in</strong>-resistant isolatesreported by the countries ranged from zero (Bulgaria,Cyprus, Estonia, Iceland, Malta, Romania, Slovenia,and Sweden) to 34.9% (Ireland). N<strong>in</strong>e countriesreported <strong>resistance</strong> percentages below 1%, ten countriesreported 1-5%, six countries reported 5-10%,three countries reported 10-25%, and one countryreported above 25% (Figure 4.41 and Table 4.11).• Twenty countries have reported more than 20 isolatesper year s<strong>in</strong>ce 2008 and were thus <strong>in</strong>cluded <strong>in</strong> thetrend analysis for the period 2008–2011. Significantly<strong>in</strong>creas<strong>in</strong>g trends were observed only for Germany;however, this trend was not significant when consider<strong>in</strong>gonly data from laboratories report<strong>in</strong>g consistentlyfor all four years (Figure 4.43).• Significantly decreas<strong>in</strong>g trends of vancomyc<strong>in</strong> <strong>resistance</strong>were observed for four countries (Greece,Sweden, Slovenia and the United K<strong>in</strong>gdom). ForGreece and United K<strong>in</strong>gdom the trend did not rema<strong>in</strong>significant when consider<strong>in</strong>g only data from laboratoriesreport<strong>in</strong>g consistently for all four years (Figure4.43).4.6.4 Discussion and conclusionsHigh-level am<strong>in</strong>oglycoside-<strong>resistance</strong> <strong>in</strong> E. faecalisseems stable <strong>in</strong> <strong>Europe</strong>, but at a generally high levelwith the majority of countries report<strong>in</strong>g percentages ofresistant isolates between 25% and 50%. Several countries(Belgium, Cyprus, Greece, Portugal, and UnitedK<strong>in</strong>gdom), which previously reported relatively high levelsof <strong>resistance</strong> now have decreas<strong>in</strong>g trends. Likewise,the occurrence of vancomyc<strong>in</strong>-<strong>resistance</strong> <strong>in</strong> E. faecium isstabilis<strong>in</strong>g or decreas<strong>in</strong>g throughout <strong>Europe</strong>.Despite these stable trends, high levels of antimicrobialresistant enterococci rema<strong>in</strong> a major <strong>in</strong>fection controlchallenge <strong>in</strong> <strong>Europe</strong>.Figure 4.41: Enterococcus faecium: percentage (%) of <strong>in</strong>vasive isolates resistant to vancomyc<strong>in</strong>, by country, EU/EEAcountries, 2011< 1%1% to < 5%5% to < 10%10% to < 25%25% to < 50%≥ 50%No data reported or less than 10 isolatesNot <strong>in</strong>cludedNon-visible countriesLiechtenste<strong>in</strong>LuxembourgMalta61


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure 4.42: Enterococcus faecalis: trends of <strong>in</strong>vasive isolates with high-level <strong>resistance</strong> to am<strong>in</strong>oglycosides, bycountry, EU/EEA countries, 2008–2011UK (


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 4.43: Enterococcus faecium: trends of <strong>in</strong>vasive isolates with <strong>resistance</strong> to vancomyc<strong>in</strong>, by country, EU/EEAcountries, 2008–2011BGSE (


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SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011References1. Ho J, Tambyah PA, Paterson DL. Multiresistant Gram-negative <strong>in</strong>fections:a global perspective. Curr Op<strong>in</strong> Infect Dis 2010;23(6):546-53.2. Giske CG, Monnet DL, Cars O, Carmeli Y; ReAct-Action on AntibioticResistance. Cl<strong>in</strong>ical and economic impact of common multidrugresistantgram-negative bacilli. Antimicrob Agents Chemother2008;52(3):813-21.3. Roberts RR, Hota B, Ahmad I, Scott RD 2nd, Foster SD, Abbasi F, etal. Hospital and societal costs of antimicrobial-resistant <strong>in</strong>fections<strong>in</strong> a Chicago teach<strong>in</strong>g hospital: implications for antibiotic stewardship.Cl<strong>in</strong> Infect Dis 2009;49(8):1175-84.4. Marchaim D, Gottesman T, Schwartz O, Korem M, Maor Y, RahavG, et al. 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Euro Surveill 2008;13(46). pii: 19035.32. de Kraker ME, Davey PG, Grundmann H; BURDEN study group.Mortality and hospital stay associated with resistant Staphylococcusaureus and Escherichia coli bacteremia: estimat<strong>in</strong>g the burden ofantibiotic <strong>resistance</strong> <strong>in</strong> <strong>Europe</strong>. PLoS Med 2011;8(10):e1001104.33. Rampl<strong>in</strong>g A, Wiseman S, Davis L, Hyett AP, Walbridge AN, PayneGC, et al. Evidence that hospital hygiene is important <strong>in</strong> the controlof methicill<strong>in</strong>-resistant Staphylococcus aureus. J Hosp Infect2001;49(2):109-16.34. Thompson DS, Workman R, Strutt M. Decl<strong>in</strong>e <strong>in</strong> the rates of methiicill<strong>in</strong>-resistantStaphlococcus aureus acquisition and bacteraemia<strong>in</strong> a general <strong>in</strong>tensive care unit between 1996 and 2008. J HospInfect 2009;71(4):314-9.35. 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<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT68


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Annex 1 External quality assessment (EQA)2011IntroductionS<strong>in</strong>ce 2000, EARSS/EARS-Net have organised annualexternal quality assessments (EQA) for antimicrobialsusceptibility test<strong>in</strong>g <strong>in</strong> collaboration with UK NEQAS(United K<strong>in</strong>gdom National External Quality AssessmentService). UK NEQAS is based at the Health ProtectionAgency <strong>in</strong> London, and is a non-profit organisation withmore than 35 years of experience <strong>in</strong> external qualityassessment <strong>in</strong> different countries (www.ukneqasmicro.org.uk).The purposes of the EARS-Net EQA are:• to assess the ability of participat<strong>in</strong>g laboratories toidentify antimicrobial <strong>resistance</strong> of cl<strong>in</strong>ical and publichealth importance;• to determ<strong>in</strong>e the accuracy of susceptibility test resultsreported by <strong>in</strong>dividual laboratories;• to estimate the overall comparability of rout<strong>in</strong>ely collectedtest results between laboratories and countriesacross <strong>Europe</strong>.The stra<strong>in</strong>s used for the 2011 EQA were compatiblewith species under <strong>surveillance</strong> at ECDC, namelyStreptococcus pneumoniae, Staphylococcus aureus,Escherichia coli, Klebsiella pneumoniae, Pseudomonasaerug<strong>in</strong>osa and Enterococcus faecium. The referenceMICs of stra<strong>in</strong>s were each tested <strong>in</strong> two of three laboratories:Addenbrookes Hospital, Cambridge (UK),University Hospital of Wales, Cardiff (UK) and CityHospital, Birm<strong>in</strong>gham (UK). Reference laboratories confirmedMICs and results were <strong>in</strong>terpreted accord<strong>in</strong>g tothe most frequently used breakpo<strong>in</strong>t criteria (EUCASTand CLSI), as <strong>in</strong>dicated <strong>in</strong> the summary for each speciesoutl<strong>in</strong>ed below.ResultsSix stra<strong>in</strong>s were distributed to 908 laboratories connectedto EARS-Net. The laboratories were asked toreport the identification of each organism and cl<strong>in</strong>icalsusceptibility characterisation – susceptible, <strong>in</strong>termediateor resistant (S, I, R) – accord<strong>in</strong>g to the guidel<strong>in</strong>eused. The return rate was similar to that <strong>in</strong> previousyears; 817 laboratories (90%) returned reports. FigureA1.1 shows the number of participat<strong>in</strong>g laboratories andthe number return<strong>in</strong>g results per country. Participants’results were analysed and considered ‘concordant’ if thereported categorisation agreed with the <strong>in</strong>terpretationof the MICs determ<strong>in</strong>ed <strong>in</strong> the reference laboratories.Figure A1.1: Number of participat<strong>in</strong>g laboratories return<strong>in</strong>g EQA reports 2011, per countryCountryAustriaBelgiumBosnia & Herzegov<strong>in</strong>aBulgariaCroatiaCyprusCzech RepublicDenmarkEstoniaF<strong>in</strong>landFranceGermanyGreeceHungaryIcelandIrelandItalyLatviaLithuaniaLuxembourgMaltaNetherlandsNorwayPolandPortugalRomaniaSloveniaSpa<strong>in</strong>SwedenTurkeyUnited K<strong>in</strong>gdomResultsNo results0 20 40 60 80 100 120Number of laboratoriesThe external quality assessment exercise was open to all countries participat<strong>in</strong>g <strong>in</strong> EARSS <strong>in</strong> 2011.69


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFor the determ<strong>in</strong>ation of AST results, laboratories usedautomated methods (42%), disc diffusion tests (34%), ora comb<strong>in</strong>ation of methods (16%). For species identification,56% used automated and 44% used conventionalmethods. Increased use of conventional methods was toa large extent associated with identification of S. pneumoniaeand E. faecium.Forty-seven percent of laboratories used CLSI guidel<strong>in</strong>es;this represented a significant reduction from theprevious year when 66% used CLSI guidel<strong>in</strong>es. Nationalguidel<strong>in</strong>es are commonly followed <strong>in</strong> some countries,e.g. SFM (France), BSAC (UK), SRGA (Sweden), CRG(Netherlands) and DIN (Germany). EUCAST guidel<strong>in</strong>eswere reported to be used by 281 (35%) laboratories,an <strong>in</strong>crease of 174 laboratories s<strong>in</strong>ce the previous year(n=107). However, the BSAC, SRGA, CRG, DIN, SFM andNWGA have been implement<strong>in</strong>g EUCAST breakpo<strong>in</strong>ts<strong>in</strong> their national MIC breakpo<strong>in</strong>t recommendations asharmonised breakpo<strong>in</strong>ts have been agreed, and haveFigure A1.2: Guidel<strong>in</strong>es reported to be used by laboratories: number of laboratories per country, 2011CountryAustriaBelgiumBosnia & Herzegov<strong>in</strong>aBulgariaCroatiaCyprusCzech RepublicDenmarkEstoniaF<strong>in</strong>landFranceGermanyGreeceHungaryIcelandIrelandItalyLatviaLithuaniaLuxembourgMaltaNetherlandsNorwayPolandPortugalRomaniaSloveniaSpa<strong>in</strong>SwedenTurkeyUnited K<strong>in</strong>gdomBSACCOMBCRGDINEUCASTCLSINWGAOtherSFMSRGA0 20 40 60 80 100Number of laboratoriesBSAC: British Society for <strong>Antimicrobial</strong> Chemotherapy; CRG: (Dutch) Commissie Richtlijnen Gevoeligheidsbepal<strong>in</strong>gen; DIN: Deutsche Industrie Norm; EUCAST:<strong>Europe</strong>an Committee on <strong>Antimicrobial</strong> Susceptibility Test<strong>in</strong>g; CLSI: Cl<strong>in</strong>ical and Laboratory Standards <strong>in</strong>stitute; NWGA: Norwegian Work<strong>in</strong>g Group on <strong>Antimicrobial</strong>s;SFM: Société Française de Microbiologie; SRGA: Swedish Reference Group for <strong>Antimicrobial</strong>s. Laboratories specify<strong>in</strong>g ‘other’ <strong>in</strong>dicates did they did not use any ofthe specified guidel<strong>in</strong>es above. Where more than one guidel<strong>in</strong>e was used to cover certa<strong>in</strong> antimicrobial/organism comb<strong>in</strong>ations laboratories could select comb<strong>in</strong>ed(COMB) as the guidel<strong>in</strong>e.Table A1.1: Escherichia coli (0270): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reported by thereference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)Amikac<strong>in</strong> 4 8 S 69Amoxicill<strong>in</strong> NT* R 99Ampicill<strong>in</strong> ≥128 ≥128 R 100Cefotaxime ≥128 ≥128 R 100Ceftazidime 16 64 R 95Ceftriaxone ≥128 ≥128 R 100Ciprofloxac<strong>in</strong> 64 ≥128 R 100Gentamic<strong>in</strong> 32 ≥128 R 100Imipenem 0.06 0.12 S 99Meropenem 0.016 0.03 S 100Piperacill<strong>in</strong>* R 99Piperacill<strong>in</strong>–tazobactam 8 16 S/I 56Tobramyc<strong>in</strong> 32 64 R 100ESBL** Positive 100* Not tested, reference MICs were participants’ results.** ESBL: Extended-spectrum beta-lactamaseS: susceptible; R: resistant; I: <strong>in</strong>termediate.70


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011adjusted the <strong>in</strong>terpretation of their disc diffusion methodsaccord<strong>in</strong>gly. Therefore, a comb<strong>in</strong>ed total of some48% of laboratories used EUCAST breakpo<strong>in</strong>ts. FigureA1.2 shows the adherence to (<strong>in</strong>ter)national guidel<strong>in</strong>esby number of laboratories per country.Specimen 0270 Escherichia coliThis specimen consisted of an Escherichia coli witha CTX-M-15 ESBL. There were no problems detect<strong>in</strong>g<strong>resistance</strong> to cephalospor<strong>in</strong>s or <strong>in</strong> identify<strong>in</strong>g that theorganism was an ESBL-producer.Reference MICs of piperacill<strong>in</strong>–tazobactam were 8–16mg/L (fixed concentration of 4 mg/L tazobactam), sosusceptibility was borderl<strong>in</strong>e and <strong>in</strong>terpreted as susceptibleor <strong>in</strong>termediate by EUCAST breakpo<strong>in</strong>ts andsusceptible by CLSI breakpo<strong>in</strong>ts. Results of participantswere also variable, with 32.7% report<strong>in</strong>g piperacill<strong>in</strong>–tazobactam-susceptible,23.7% <strong>in</strong>termediate and ahigher than expected rate (43.6%) report<strong>in</strong>g resistant.The percentage of participants report<strong>in</strong>g susceptible or<strong>in</strong>termediate was similar for those us<strong>in</strong>g EUCAST-basedbreakpo<strong>in</strong>ts (57% of 356 laboratories) and those us<strong>in</strong>gCLSI breakpo<strong>in</strong>ts (59.2% of 341 laboratories). Thoseus<strong>in</strong>g automated methods were more likely to report<strong>resistance</strong> (63.1% of 225 participants) than those us<strong>in</strong>gMIC methods (55.3% of 103), multiple methods (44.6%of 94) or disc diffusion methods (24.5% of 310). Currentguidel<strong>in</strong>es from both EUCAST and CLSI recommendreport<strong>in</strong>g β-lactamase <strong>in</strong>hibitor comb<strong>in</strong>ations ‘as found’<strong>in</strong> rout<strong>in</strong>e tests. Despite this, for participants where dataare available, some laboratories edited susceptible testresults to <strong>in</strong>termediate or resistant, or edited <strong>in</strong>termediatetest results to resistant (<strong>in</strong> total around 34% ofparticipants us<strong>in</strong>g disc diffusion methods, 24% us<strong>in</strong>gMIC methods and 9% us<strong>in</strong>g automated methods).Reference MICs of amikac<strong>in</strong> were 4–8 mg/L, which isslightly raised compared with typical susceptible isolates,but <strong>in</strong>terpreted as susceptible by both EUCASTand CLSI breakpo<strong>in</strong>ts. The isolate was reportedsusceptible by 61.8% participants, <strong>in</strong>termediate by31.6% and resistant by 6.6% (Table A1.1).Specimen 0271 Klebsiella pneumoniaeThis specimen consisted of a Klebsiella pneumoniaewhich produces both a KPC carbapenemase and an SHV-12 ESBL.Although the organism is a carbapenemase producer,reference carbapenem MICs by the ISO broth microdilutionmethod were low, 0.5–1 mg/L for imipenem, whichwould be reported susceptible by both EUCAST and CLSI,and 4 mg/L for meropenem, which would be reported<strong>in</strong>termediate by EUCAST breakpo<strong>in</strong>ts and resistant byCLSI breakpo<strong>in</strong>ts. Most participants, however, reportedreduced susceptibility to imipenem (6.3% susceptible,19.3% <strong>in</strong>termediate and 74.4% resistant) and to meropenem(6.4% susceptible, 9.5% <strong>in</strong>termediate and 84.1%resistant). MICs reported by participants were very variable,from 0.12 to 256 mg/L with a mode of 8 mg/L forimipenem and 0.5–128 mg/L with a mode of 2 mg/L formeropenem. The reason for the highly variable carbapenemMICs is unclear, but repeat MICs by the ISO brothmicrodilution method <strong>in</strong> one of the reference laboratoriesafter the distribution were 16 mg/L for imipenemand 32 mg/L for meropenem, suggest<strong>in</strong>g that there mayhave been variation <strong>in</strong> the stra<strong>in</strong>, which would <strong>in</strong>evitablyresult <strong>in</strong> variable report<strong>in</strong>g.Detection of ESBLs may be required for epidemiologicalpurposes and the presence of a carbapenemase <strong>in</strong>addition to an ESBL <strong>in</strong> this isolate makes detection ofthe SHV-12 ESBL problematic. With this isolate, clavulanicacid synergy tests were difficult to <strong>in</strong>terpretas there was only slight reduction <strong>in</strong> third- generationcephalospor<strong>in</strong> MICs, depend<strong>in</strong>g on the cephalospor<strong>in</strong>tested, and <strong>resistance</strong> mediated by carbapenemasescan also be marg<strong>in</strong>ally affected by clavulanate. Amongparticipants, 54.2% reported the presence of an ESBL.Report<strong>in</strong>g of susceptibility to β-lactam agents other thancarbapenems was not an issue as reference MICs wereuniformly high.Table A1.2: Klebsiella pneumoniae (0271): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reported bythe reference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)Amikac<strong>in</strong> 16 16 S/I/R 100Amoxicill<strong>in</strong> ≥128 I/R 100Ampicill<strong>in</strong> ≥128 ≥128 R 100Cefotaxime ≥128 ≥128 R 100Ceftazidime ≥128 ≥128 R 100Ceftriaxone ≥128 ≥128 R 100Ciprofloxac<strong>in</strong> ≥128 ≥128 R 100Gentamic<strong>in</strong> 1 1 S 87Imipenem 1 1 S 10Meropenem 4 4 I/R 94Piperacill<strong>in</strong>* R 100Piperacill<strong>in</strong>–tazobactam ≥128 ≥128 R 100Tobramyc<strong>in</strong> ≥128 ≥128 R 99ESBL** Positive 57* Not tested, reference MICs were participants’ results.** ESBL: Extended-spectrum beta-lactamaseS: susceptible; R: resistant; I: <strong>in</strong>termediate.71


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTAm<strong>in</strong>oglycoside susceptibility was typical of an organismproduc<strong>in</strong>g AAC(6’)I <strong>in</strong> that it was resistant totobramyc<strong>in</strong> (MIC ≥128 mg/L), susceptible to gentamic<strong>in</strong>(MIC 1 mg/L) and borderl<strong>in</strong>e to amikac<strong>in</strong> (MIC 16 mg/L;<strong>in</strong>termediate by EUCAST breakpo<strong>in</strong>ts and susceptibleby CLSI breakpo<strong>in</strong>ts). EUCAST expert rules note thatacquired AAC(6’)I may not confer phenotypic <strong>resistance</strong>to amikac<strong>in</strong> despite modification of amikac<strong>in</strong>, and thatsuch organisms should be reported <strong>in</strong>termediate evenif they appear susceptible. There were no significantproblems with tobramyc<strong>in</strong> and only 1.2% of participantsreported the organism susceptible to amikac<strong>in</strong>, themajority (89.8%) report<strong>in</strong>g <strong>resistance</strong>. For gentamic<strong>in</strong>,88.7% of participants reported the isolate as susceptible,8.1% as <strong>in</strong>termediate and 3.2% as resistant (TableA1.2).Specimen 0272 Streptococcus pneumoniaeThis specimen consisted of a Streptococcus pneumoniaewith reduced susceptibility to penicill<strong>in</strong> (MIC 0.5 mg/L).For S. pneumoniae with no mechanism of <strong>resistance</strong> topenicill<strong>in</strong>, MICs are ≤0.06 mg/L. However, the <strong>in</strong>terpretationof susceptibility to penicill<strong>in</strong> depends on whetherthe isolate is from a patient with pneumonia, men<strong>in</strong>gitisor other <strong>in</strong>fections. Stra<strong>in</strong>s with <strong>in</strong>termediate susceptibility(EUCAST MIC 0.06–2 mg/L, CLSI MIC 0.06–4 mg/L)are treatable with the high doses of penicill<strong>in</strong>, ampicill<strong>in</strong>or amoxicill<strong>in</strong> rout<strong>in</strong>ely used to treat pneumonia. Hencesuch stra<strong>in</strong>s may be reported susceptible <strong>in</strong> this situation.Patients with men<strong>in</strong>gitis caused by stra<strong>in</strong>s with<strong>in</strong>termediate susceptibility to penicill<strong>in</strong> are unlikely torespond to therapy, and hence such stra<strong>in</strong>s should bereported as resistant <strong>in</strong> this situation. Participants wereasked to give the <strong>in</strong>terpretations that would be reportedif the isolate was from a case of pneumonia and if theisolate was from a case of men<strong>in</strong>gitis.Overall, 90.8% participants reported <strong>resistance</strong> <strong>in</strong> theoxacill<strong>in</strong> screen<strong>in</strong>g test for penicill<strong>in</strong> <strong>resistance</strong>. An additional4.6% reported oxacill<strong>in</strong> <strong>in</strong>termediate althoughthere is no <strong>in</strong>termediate category for the oxacill<strong>in</strong>screen<strong>in</strong>g test. There were no problems <strong>in</strong> detect<strong>in</strong>greduced susceptibility to oxacill<strong>in</strong> <strong>in</strong> reference tests bythe EUCAST and CLSI methods.The participants’ results for penicill<strong>in</strong> without a siteof <strong>in</strong>fection cannot be <strong>in</strong>terpreted because guidel<strong>in</strong>ebreakpo<strong>in</strong>ts relate to the site of <strong>in</strong>fection. However, forpenicill<strong>in</strong> without a site of <strong>in</strong>fection 69.8% designatedthe isolate as be<strong>in</strong>g of <strong>in</strong>termediate susceptibility topenicill<strong>in</strong>, with a further 6.7% report<strong>in</strong>g the isolateresistant and 23.5% susceptible. Susceptibility reportedto cl<strong>in</strong>icians <strong>in</strong>dicates variable practice <strong>in</strong> that some participantsdo not <strong>in</strong>terpret test results to suit the cl<strong>in</strong>icalsituation, as only 86.4% reported the isolate resistant ifthe isolate was from a case of men<strong>in</strong>gitis and only 76.1%Table A1.3: Streptococcus pneumoniae (0272): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reportedby the reference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)CefotaximeMen<strong>in</strong>gitis S -Pneumonia 0.25 0.25S/- 95Other S/- 99Non-men<strong>in</strong>gitis - -Ceftriaxone99Men<strong>in</strong>gitis S -Pneumonia 0.25 0.25S/- 96Other S/- 99Non-men<strong>in</strong>gitis -/S -Ciprofloxac<strong>in</strong> 0.5 1 I/no <strong>in</strong>terpretation 35Cl<strong>in</strong>damyc<strong>in</strong> 0.12 0.12 S 98Erythromyc<strong>in</strong> 32 > 128 R 96Penicill<strong>in</strong>Men<strong>in</strong>gitis R -Pneumonia 0.5 0.5S/- 86Other I/- 73Non-men<strong>in</strong>gitis -/S -S: susceptible; R: resistant; I: <strong>in</strong>termediate.Table A1.4: Enterococcus faecium (0273): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reported by thereference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)Amoxicill<strong>in</strong> NT* R 89Ampicill<strong>in</strong> 16 32 R 98High-level gentamic<strong>in</strong> 4 4 S (not high-level <strong>resistance</strong>) 74Teicoplan<strong>in</strong> 0.5 1 S 98Vancomyc<strong>in</strong> 8 16 R/I 79* Not tested, result <strong>in</strong>ferred from ampicill<strong>in</strong> result.S: susceptible; R: resistant; I: <strong>in</strong>termediate.72


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011reported susceptible if the isolate was from a case ofpneumonia. Significant numbers of participants <strong>in</strong>terpretedthe isolate as <strong>in</strong>termediate <strong>in</strong> susceptibility topenicill<strong>in</strong> irrespective of whether the isolate was frommen<strong>in</strong>gitis (8.1% reported <strong>in</strong>termediate) or from pneumonia(20.8% reported <strong>in</strong>termediate). These differenceswill partly relate to national differences <strong>in</strong> report<strong>in</strong>gpractices.Resistance to cefotaxime and ceftriaxone is rare <strong>in</strong>S. pneumoniae and a high percentage of participantsreported the isolate susceptible to these agents whateverthe source of the <strong>in</strong>fection.Ciprofloxac<strong>in</strong> is not the fluoroqu<strong>in</strong>olone of choice fortreatment of <strong>in</strong>fections with S. pneumoniae. EUCAST categorisewild-type isolates as <strong>in</strong>termediate and CLSI donot <strong>in</strong>clude breakpo<strong>in</strong>ts <strong>in</strong> current tables. Only aroundhalf the participants tested this organism aga<strong>in</strong>st ciprofloxac<strong>in</strong>and, contrary to guidel<strong>in</strong>es, 55.4% of thosetest<strong>in</strong>g ciprofloxac<strong>in</strong> reported the isolate susceptible(Table A1.3).Specimen 0273 Enterococcus faeciumThis specimen consisted of an Enterococcus faecium withvanB-mediated <strong>resistance</strong> to vancomyc<strong>in</strong>.Vancomyc<strong>in</strong> MICs can be low for VanB stra<strong>in</strong>s, as <strong>in</strong>this case (MICs 8–16 mg/L), and the isolate would be<strong>in</strong>terpreted as resistant by EUCAST breakpo<strong>in</strong>ts but<strong>in</strong>termediate by CLSI breakpo<strong>in</strong>ts. The borderl<strong>in</strong>e susceptibilitymakes detection of reduced susceptibilitymore difficult, particularly with disc diffusion methodswhere the difference <strong>in</strong> zone diameter between susceptibleand resistant isolates may be small and <strong>resistance</strong>may be seen only as small colonies <strong>in</strong>side zone edges,or ‘fuzzy’ zone edges after 24 hours <strong>in</strong>cubation, <strong>in</strong> contrastwith the sharp zone edges seen with susceptibleisolates. Reduced susceptibility to vancomyc<strong>in</strong> wasdetected by only 92% of participants (8.6% <strong>in</strong>termediate,83.4% resistant).Gentamic<strong>in</strong> mono-therapy is <strong>in</strong>effective aga<strong>in</strong>st enterococci.There is, however, synergism between gentamic<strong>in</strong>and β-lactam agents aga<strong>in</strong>st enterococci without mechanismsconferr<strong>in</strong>g high-level gentamic<strong>in</strong> <strong>resistance</strong>(usually production of the bi-functional enzyme APH(2’’)/AAC(6’)). Overall, 24.7% of participants <strong>in</strong>correctlyreported this isolate as high-level gentamic<strong>in</strong>-resistant.Previously, similar errors have been related to theerroneous use of lower content gentamic<strong>in</strong> discs thanspecified <strong>in</strong> disc diffusion method guidel<strong>in</strong>es; this mayalso expla<strong>in</strong> the <strong>in</strong>correct results for 2011.This organism is resistant to ampicill<strong>in</strong> and amoxicill<strong>in</strong>with EUCAST breakpo<strong>in</strong>ts. CLSI specifies that susceptibilityof enterococci to amoxicill<strong>in</strong> should be <strong>in</strong>ferredfrom the ampicill<strong>in</strong> susceptibility, so the organismTable A1.5: Pseudomonas aerug<strong>in</strong>osa (0274): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reported bythe reference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)Amikac<strong>in</strong> 1 4 S 94Ceftazidime 1 2 S 98Ciprofloxac<strong>in</strong> 0.12 0.5 S 99Gentamic<strong>in</strong> 16 ≥128 R* 99Imipenem 1 2 S 99Meropenem 0,5 2 S 98Piperacill<strong>in</strong>–tazobactam 4 8 S 83Tobramyc<strong>in</strong> 0.5 1 S 99* Reference MICs covered the range of susceptible to resistant by both EUCAST and CLSI.S: susceptible; R: resistant; I: <strong>in</strong>termediate.Table A1.6: Staphylococcus aureus (0275): M<strong>in</strong>imum <strong>in</strong>hibitory concentration (MIC) and <strong>in</strong>tended results reported bythe reference laboratories and the overall concordance of the participat<strong>in</strong>g laboratoriesAntibiotic agentMIC range (mg/L) ref. lab.Intended <strong>in</strong>terpretationfrom to EUCAST/CLSI Overall concordance (%)Cefoxit<strong>in</strong> 8 16 R 95Ciprofloxac<strong>in</strong> 0.5 0.5 S 98Cl<strong>in</strong>damyc<strong>in</strong> 0.12 0.12 dissociated <strong>resistance</strong> 75Erythromyc<strong>in</strong> 8 64 R 92Fusidic acid 0.06 0.12 S 99Gentamic<strong>in</strong> 0.25 0.5 S/no <strong>in</strong>terpretation 98Meticill<strong>in</strong> NT* R 99Oxacill<strong>in</strong> 8 32 R 96Penicill<strong>in</strong> 1 4 R 100Rifampic<strong>in</strong> 0.004 0.008 S 100Teicoplan<strong>in</strong> 1 1 S 100Tetracycl<strong>in</strong>e 64 64 R 98Vancomyc<strong>in</strong> 1 2 S 99* Not tested, result <strong>in</strong>ferred from oxacill<strong>in</strong> and cefoxit<strong>in</strong> results.S: susceptible; R: resistant; I: <strong>in</strong>termediate.73


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTshould also be reported resistant to ampicill<strong>in</strong> andamoxicill<strong>in</strong> by CLSI guidel<strong>in</strong>es. Overall, 98.8% of participantsreported <strong>resistance</strong> to ampicill<strong>in</strong>. Only one thirdof participants reported susceptibility results for amoxicill<strong>in</strong>and of these only 84.2% reported <strong>resistance</strong>, with7.9% report<strong>in</strong>g <strong>in</strong>termediate and another 7.9% report<strong>in</strong>gsusceptible (Table A1.4).Specimen 0274 Pseudomonas aerug<strong>in</strong>osaThis specimen consisted of a Pseudomonas aerug<strong>in</strong>osaresistant to gentamic<strong>in</strong> and susceptible to other referenceagents tested.Some laboratories experienced problems with piperacill<strong>in</strong>–tazobactamtest<strong>in</strong>g <strong>in</strong> that overall 6.2% ofparticipants reported the isolate <strong>in</strong>termediate and 5.7%resistant. The reason for the problems is not obvious asthe isolate was clearly susceptible <strong>in</strong> reference tests byboth MIC and disc diffusion methods (Table A1.5).Specimen 0275 Staphylococcus aureusThis specimen consisted of a meticill<strong>in</strong>-resistantStaphylococcus aureus with dissociated <strong>resistance</strong> tocl<strong>in</strong>damyc<strong>in</strong>.Test<strong>in</strong>g for meticill<strong>in</strong> <strong>resistance</strong> still causes problems <strong>in</strong>some laboratories as only 95.2% reported <strong>resistance</strong> tocefoxit<strong>in</strong> and 95% to oxacill<strong>in</strong>.As seen with previous distributions of organisms withdissociated <strong>resistance</strong>, there were significant discrepancies<strong>in</strong> report<strong>in</strong>g susceptibility to cl<strong>in</strong>damyc<strong>in</strong>,with 74.2% report<strong>in</strong>g resistant, 1.8% <strong>in</strong>termediate and24.0% susceptible. In staphylococci, most <strong>resistance</strong>to macrolide, l<strong>in</strong>cosamide and streptogram<strong>in</strong> type B(MLS B ) antimicrobials is mediated by the erm genes andis <strong>in</strong>duced by erythromyc<strong>in</strong>, clarithromyc<strong>in</strong> and azithromyc<strong>in</strong>,but not by cl<strong>in</strong>damyc<strong>in</strong> (dissociated <strong>resistance</strong>or MLS B -<strong>in</strong>ducible <strong>resistance</strong>). Hence <strong>in</strong>ducible stra<strong>in</strong>sare resistant to erythromyc<strong>in</strong> but not to cl<strong>in</strong>damyc<strong>in</strong><strong>in</strong> susceptibility tests. Stra<strong>in</strong>s with MLS B -constitutive<strong>resistance</strong> are resistant to both agents.There has been debate about whether staphylococciwith <strong>in</strong>ducible <strong>resistance</strong> (erythromyc<strong>in</strong>-resistant,cl<strong>in</strong>damyc<strong>in</strong>-susceptible) should be reported resistantas <strong>in</strong>ducible stra<strong>in</strong>s segregate cl<strong>in</strong>damyc<strong>in</strong>-resistantmutants, which may be selected dur<strong>in</strong>g therapy. EUCASTexpert rules <strong>in</strong>dicate that such stra<strong>in</strong>s should either bereported as resistant to cl<strong>in</strong>damyc<strong>in</strong> or reported as susceptiblewith a warn<strong>in</strong>g of possible cl<strong>in</strong>ical failure dur<strong>in</strong>gtreatment with cl<strong>in</strong>damyc<strong>in</strong> due to selection of constitutivelyresistant mutants. EUCAST also states that theuse of cl<strong>in</strong>damyc<strong>in</strong> is best avoided for severe <strong>in</strong>fectionscaused by isolates with dissociated <strong>resistance</strong>. CLSIsuggest that such stra<strong>in</strong>s should be reported resistantbut that a comment may be added that cl<strong>in</strong>damyc<strong>in</strong> maystill be effective <strong>in</strong> some patients. Inducible cl<strong>in</strong>damyc<strong>in</strong><strong>resistance</strong> is detected <strong>in</strong> disc diffusion tests witha cl<strong>in</strong>damyc<strong>in</strong> disc placed adjacent to an erythromyc<strong>in</strong>disc; stra<strong>in</strong>s with <strong>in</strong>ducible <strong>resistance</strong> show flatten<strong>in</strong>g ofthe cl<strong>in</strong>damyc<strong>in</strong> zone adjacent to the erythromyc<strong>in</strong> disc(Table A1.6).ConclusionsThe response to the 2011 EARS-Net EQA was very goodwith a high return rate and very few late responders.Performance was generally very good and consistentwith that seen <strong>in</strong> previous EQA. Problems, where experienced,were related to borderl<strong>in</strong>e susceptibility andwhen guidel<strong>in</strong>es revealed rema<strong>in</strong><strong>in</strong>g discrepancies <strong>in</strong>rout<strong>in</strong>e susceptibility test<strong>in</strong>g.ECDC would like to thank UK NEQAS, the reference laboratories,the members of the EARS-Net Coord<strong>in</strong>ationGroup and the country coord<strong>in</strong>ators for the swift distributionof the stra<strong>in</strong>s, and all the participat<strong>in</strong>g laboratoriesfor their efforts and timely response to the assessment.74


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Annex 2 EARS-Net laboratory/hospitaldenom<strong>in</strong>ator data 2011IntroductionFor correct <strong>in</strong>terpretation of the EARS-Net data on antimicrobial<strong>resistance</strong>, accurate background <strong>in</strong>formationis important. Therefore, laboratory and hospital denom<strong>in</strong>atordata are collected and presented <strong>in</strong> this Annex.MethodsQuestionnaires (Microsoft Excel files) were sent to theEARS-Net contact po<strong>in</strong>ts <strong>in</strong> May 2012. The contact po<strong>in</strong>tsdistributed the questionnaires to the participat<strong>in</strong>g laboratoriesand hospitals <strong>in</strong> their country. Information wascollected on the total number of blood culture sets processed<strong>in</strong> the laboratories, and the number of hospitalbeds for each participat<strong>in</strong>g hospital, the type of hospital,the bed occupancy and the number of admissions. Thenational data managers received the completed questionnaires,compiled them and produced the f<strong>in</strong>al formatsuitable for upload<strong>in</strong>g to The <strong>Europe</strong>an SurveillanceSystem (TESSy). Laboratories were def<strong>in</strong>ed as report<strong>in</strong>gdenom<strong>in</strong>ator data if they provided the number ofblood culture sets performed for one or more hospitals.Hospitals were def<strong>in</strong>ed as report<strong>in</strong>g denom<strong>in</strong>ator data ifthey provided the number of beds.Organisation of health care systems and affiliationbetween laboratories and hospitals differsconsiderably between countries, which might <strong>in</strong>fluencedata comparability. For countries submitt<strong>in</strong>g denom<strong>in</strong>atordata for a small percentage of hospitals and/orlaboratories contribut<strong>in</strong>g data to EARS-Net, the reportedfigures might not be representative for the overall countryprofile.ParticipationSixteen of the 29 countries report<strong>in</strong>g AMR data alsoreturned hospital and laboratory denom<strong>in</strong>ator datareferr<strong>in</strong>g to 2011, while for eight countries, hospitaland laboratory denom<strong>in</strong>ator data referr<strong>in</strong>g to 2010 wereavailable and <strong>in</strong>cluded <strong>in</strong> the analysis. In total, 1 012(70 %) of the 1 445 hospitals and 477 (61 %) of the 784laboratories report<strong>in</strong>g AST results for the 24 countries,also provided denom<strong>in</strong>ator data (Figures A2.1, A2.2 andTables A2.1–A2.3). Some denom<strong>in</strong>ator data for laboratoriesand hospitals not report<strong>in</strong>g AMR data, or report<strong>in</strong>gzero cases, have been <strong>in</strong>cluded <strong>in</strong> Figure A2.1, but werenot <strong>in</strong>cluded <strong>in</strong> other parts of the analysis.Population coverageData on population coverage for AMR data at countrylevel are not reported because of the <strong>in</strong>herentlimitations of these data. Not all laboratories/hospitalsreport<strong>in</strong>g AST data also provide denom<strong>in</strong>ator data, andthis would <strong>in</strong>troduce bias <strong>in</strong>to the calculation of countrypopulation coverage s<strong>in</strong>ce only laboratories/hospitalsTable A2.1: Hospital denom<strong>in</strong>ator data for 2010 or 2011 (us<strong>in</strong>g latest available data)CountryHospitals report<strong>in</strong>g(denom<strong>in</strong>ator/AMRdata)Total number of bedsProportion of ICUbeds (%)Annual occupancyrate (%)Median length ofstay (days)IQR length of stay(days)Austria* (140/142) 54 743 5 67 4.7 4.1-5.4Bulgaria (21/22) 9 474 8 76 6.1 5.4-6.6Cyprus (5/5) 1 316 10 77 5.3 5.1-5.4Czech Republic (68/76) 38 911 11 70 7.2 6.1-8.3Denmark (5/69) 3 254 82 3.2 2.8-3.6Estonia* (10/11) 4 472 4 76 6.3 5.1-7.1France (260/264) 156 586 5 81 7.4 6.2-8.8Germany (46/189) 18 296 7 76 6.9 6.5-7.9Hungary (66/73) 51 240 2 74 8.5 7.1-9.4Ireland (53/59) 12 265 3 87 5.5 4.6-6.8Italy* (31/35) 10 249 83 .-.Latvia* (11/12) 5 135 3 71 6.1 4.1-6.8Lithuania (21/25) 10 734 4 74 7.1 6.0-8.8Malta (3/3) 1 157 6 87 5.3 4.8-45.0Netherlands* (37/55) 14 886 67 5.2 4.9-5.6Norway* (14/49) 4 347 5 84 4.4 4.0-4.7Poland (41/58) 20 432 2 71 5.0 4.0-6.0Portugal (21/21) 9 680 6 79 7.1 5.7-7.9Romania (5/5) 2 964 6 85 6.2 5.7-6.4Slovakia (21/21) 11 354 9 70 6.9 6.2-7.9Slovenia* (15/15) 7 265 6 71 5.8 4.8-6.5Spa<strong>in</strong>* (39/49) 24 571 4 79 .-.Sweden (46/66) 15 882 4 91 4.7 4.1-5.2United K<strong>in</strong>gdom (33/121) 11 561 2 79 4.4 2.9-7.7* Data from 2010.75


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFigure A2.1: Number of hospitals (A) and laboratories (B) report<strong>in</strong>g AMR and/or denom<strong>in</strong>ator data <strong>in</strong> 2010 or 2011(us<strong>in</strong>g latest available data)A)CountryAustria*BulgariaCyprusCzech RepublicDenmarkEstonia*FranceGermanyHungaryIrelandItaly*Latvia*LithuaniaMaltaNetherlands*Norway*PolandPortugalRomaniaSlovakiaSlovenia*Spa<strong>in</strong>*SwedenUnited K<strong>in</strong>gdomAMR and denom<strong>in</strong>ator <strong>in</strong>formationAMR <strong>in</strong>formation onlyDenom<strong>in</strong>ator <strong>in</strong>formation only0 50 100 150 200 250 300Number of hospitalsB)CountryAustria*BulgariaCyprusCzech RepublicDenmarkEstonia*FranceGermanyHungaryIrelandItaly*Latvia*LithuaniaMaltaNetherlands*Norway*PolandPortugalRomaniaSlovakiaSlovenia*Spa<strong>in</strong>*SwedenUnited K<strong>in</strong>gdomAMR and denom<strong>in</strong>ator <strong>in</strong>formationAMR <strong>in</strong>formation onlyDenom<strong>in</strong>ator <strong>in</strong>formation only0 50 100 150 200 250 300Number of laboratories* Denom<strong>in</strong>ator data from 2010.76


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011report<strong>in</strong>g denom<strong>in</strong>ator data can be <strong>in</strong>cluded. Secondly,laboratories and hospitals cluster <strong>in</strong> big cities and, forthis reason, some of the catchment areas overlap. Thiscould lead to double counts, which would artificially<strong>in</strong>crease the estimated coverage.Hospital denom<strong>in</strong>ator<strong>in</strong>formationThe total number of hospital beds for hospitals report<strong>in</strong>gboth AMR and denom<strong>in</strong>ator data <strong>in</strong> differentcountries ranged from 1 157 <strong>in</strong> Malta to 156 586 <strong>in</strong> France,reflect<strong>in</strong>g the size of the country as well as the rate ofparticipation to EARS-Net and the rate of response to thequestionnaires.The percentage of ICU beds over total hospital bedsshows wide variation by country, rang<strong>in</strong>g from 2 % <strong>in</strong>Hungary, Poland and the United K<strong>in</strong>gdom to 11 % <strong>in</strong> theCzech Republic. The overall median length of stay <strong>in</strong> hospitalwas 5.9 days with the lowest median <strong>in</strong> Denmark(3.2 days) and the highest <strong>in</strong> Hungary (8.5 days). Theannual occupancy rate was 75 % or higher <strong>in</strong> 15 out of 24countries (Table A2.1).Hospital characteristicsBoth the size of a hospital and the level of specialisationmay <strong>in</strong>fluence the occurrence of antimicrobial <strong>resistance</strong><strong>in</strong> the hospital. As can be seen from Table A2.2 and FigureA2.2, the distribution of size and specialisation level ofhospitals varied considerably between the report<strong>in</strong>gcountries. This does not necessarily reflect differentdistributions of the orig<strong>in</strong> of EARS-Net blood culturesper country, as not all hospitals contribute evenly to theEARS-Net database. On the other hand, this diversitycan <strong>in</strong>dicate differences <strong>in</strong> case-mix, which may confoundcomparison of AMR results between countries.The type of hospital and the size of hospital are notalways l<strong>in</strong>ked and it is not rare, especially <strong>in</strong> smallercountries, that university hospitals have fewer than 500beds.Laboratory denom<strong>in</strong>ator<strong>in</strong>formationIn 2010/2011 (latest available data), the number of bloodculture sets processed <strong>in</strong> the EARS-Net laboratoriesrespond<strong>in</strong>g to the questionnaire was 3 278 850. Themedian cultur<strong>in</strong>g frequency was 28.3 blood culture setsper 1 000 patient days. The highest rate was reportedby Italy (91.3) and the lowest by Lithuania (5.5). Forthe majority of the report<strong>in</strong>g countries, there are onlym<strong>in</strong>or changes <strong>in</strong> the number of blood culture sets takenper 1 000 patient days (Table A2.3) when compar<strong>in</strong>g2009/2010 (latest available data) data with 2010/2011(latest available data). The highest total number ofblood culture sets was reported by France (881 270) followedby Sweden (352 450).Figure A2.2: Percentage of small, medium and large hospitals per country, based on the number of beds, for allhospitals report<strong>in</strong>g both antimicrobial <strong>resistance</strong> data and denom<strong>in</strong>ator data <strong>in</strong> 2010 or 2011 (us<strong>in</strong>g latest availabledata)CountryAustria* (140/142)Bulgaria (21/22)Cyprus (5/5)Czech Republic (68/76)Denmark (5/69)Estonia* (10/11)France (260/264)Germany (46/189)Hungary (66/73)Ireland (53/59)Italy* (31/35)Latvia* (11/12)Lithuania (21/25)Malta (3/3)Netherlands* (37/55)Norway* (14/49)Poland (41/58)Portugal (21/21)Romania (5/5)Slovakia (21/21)Slovenia* (15/15)Spa<strong>in</strong>* (39/49)Sweden (46/66)United K<strong>in</strong>gdom (33/121)Large hospitals(> 500 beds)Medium-sized hospitals(201–500 beds)Small hospitals(≤ 200 beds)0 20 40 60 80 100* Denom<strong>in</strong>ator data from 2010.Percentage hospital type77


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTTable A2.2: Hospital characteristics for 2010 or 2011 (us<strong>in</strong>g latest available data)CountryHospitals report<strong>in</strong>g(denom<strong>in</strong>ator/AMR data)Proportion of hospitals by level of care (%)Tertiary level Secondary level Primary level Other UnknownAustria* (140/142) 8 24 39 29 0Bulgaria (21/22) 52 33 5 10 0Cyprus (5/5) 20 20 40 20 0Czech Republic (68/76) 34 34 29 3 0Denmark (5/69) 40 40 0 0 20Estonia* (10/11) 0 50 20 30 0France (260/264) 22 77 0 0 1Germany (46/189) 33 30 28 7 0Hungary (66/73) 50 26 14 11 0Ireland (53/59) 17 55 11 17 0Italy* (31/35) 16 16 0 0 0Latvia* (11/12) 45 18 9 27 0Lithuania (21/25) 48 38 10 5 0Malta (3/3) 33 33 0 33 0Netherlands* (37/55) 8 73 19 0 0Norway* (14/49) 36 36 29 0 0Poland (41/58) 29 66 0 5 0Portugal (21/21) 57 33 5 5 0Romania (5/5) 80 20 0 0 0Slovakia (21/21) 67 0 5 29 0Slovenia* (15/15) 13 47 20 13 7Spa<strong>in</strong>* (39/49) 56 38 5 0 0Sweden (46/66) 17 39 43 0 0United K<strong>in</strong>gdom (33/121) 27 27 24 6 9* Data from 2010.Primary level or district hospital = has few specialties, limited laboratory services; bed capacity ranges from 30 to 200 beds. Secondary level, or prov<strong>in</strong>cial hospital= highly differentiated by function with five to 10 cl<strong>in</strong>ical specialties; bed capacity rang<strong>in</strong>g from 200 to 800 beds. Tertiary level or central/regional hospital = highlyspecialised staff and technical equipment; cl<strong>in</strong>ical services are highly differentiated by function; may have teach<strong>in</strong>g activities; bed capacity ranges from 300 to 1500beds. Other = hospitals for a specific patient population, like a military hospital, or hospitals with any s<strong>in</strong>gle specialty, like a burns unit.Unknown = not available.Table A2.3: Laboratory denom<strong>in</strong>ator <strong>in</strong>formation for 2010 or 2011 (us<strong>in</strong>g latest available data)CountryLaboratories report<strong>in</strong>g(denom<strong>in</strong>ator/AMR data)Number of hospitals Total number of blood culture setsNumber of blood culture sets per1000 patient daysAustria* (36/39) 127 178 672 14.1Bulgaria (20/20) 21 19 642 7.5Cyprus (5/5) 5 13 513 36.5Czech Republic (44/46) 68 144 615 14.5Denmark (4/13) 4 79 269 81Estonia* (10/11) 11 20 593 16.6France (52/263) 52 881 270 61Germany (11/19) 37 69 259 16.5Hungary (24/31) 54 87 980 7.8Ireland (38/40) 53 180 995 46.7Italy* (30/35) 30 209 974 91.3Latvia* (11/11) 11 12 726 9.6Lithuania (10/10) 21 15 920 5.5Malta (1/1) 3 8 796 24Netherlands* (13/22) 28 99 034 38.3Norway* (9/15) 14 62 532 46.7Poland (41/45) 41 125 330 23.4Portugal (18/18) 21 122 744 43.8Romania (5/5) 5 27 252 29.5Slovakia (11/11) 21 60 922 20.9Slovenia* (10/10) 14 50 480 27Spa<strong>in</strong>* (39/41) 39 308 872 43.4Sweden (18/18) 46 352 450 67.1United K<strong>in</strong>gdom (17/55) 26 146 763 48.1* Data from 2010.78


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Discussion and conclusionsIn summary, the situation for most countries as assessedfrom denom<strong>in</strong>ator data reported to EARS-Net <strong>in</strong> 2011appears stable and similar to 2010. This <strong>in</strong>dicates thatbased on EARS-Net data the comparison of <strong>resistance</strong>percentages over time rema<strong>in</strong>s valid.The BSIs ascerta<strong>in</strong>ment is strongly l<strong>in</strong>ked to the bloodculture rate. Therefore, the wide range <strong>in</strong> blood culturerates observed <strong>in</strong> the countries provid<strong>in</strong>g denom<strong>in</strong>atordata has implications for <strong>in</strong>ter-country comparisonsof both the <strong>in</strong>cidence rate of <strong>in</strong>fections, which couldbe underestimated <strong>in</strong> some countries, and of the percentageof <strong>resistance</strong>. In particular, the percentage of<strong>resistance</strong> could be overestimated if blood cultures arenot systematically performed before start<strong>in</strong>g empirictherapy and if blood cultures are more likely to be performed<strong>in</strong> patients not respond<strong>in</strong>g to <strong>in</strong>itial empirictreatment.For future improvement of the denom<strong>in</strong>ator data collectionand analysis, a further <strong>in</strong>crease <strong>in</strong> the numberof countries report<strong>in</strong>g denom<strong>in</strong>ator data, as well asan <strong>in</strong>creased number of hospital and laboratoriesparticipat<strong>in</strong>g with<strong>in</strong> countries, would be desirable.Furthermore, an improved estimation of the coverageof the EARS-Net <strong>surveillance</strong>, e.g. by us<strong>in</strong>g estimationsdone at the national level based on knowledge of thecountry-specific situation, would also be desirable.79


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SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Country summary sheets81


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORT82


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Explanation to the countrysummary sheetsGeneral <strong>in</strong>formation about EARS-Netparticipat<strong>in</strong>g laboratories and hospitalsTable 1 gives the number of laboratories and isolatesreported by year and by pathogen under EARSS/EARS-Net <strong>surveillance</strong> for the period 2003–2011.Antibiotic <strong>resistance</strong> 2003–2011Table 2 provides <strong>in</strong>formation on the proportion of <strong>in</strong>vasivebacterial isolates non-susceptible (I+R) or resistant(R) to the antibiotics or antibiotic classes mentioned <strong>in</strong>the EARSS/EARS-Net protocols. When <strong>in</strong>terpret<strong>in</strong>g theresults <strong>in</strong> Table 2, always check the number of isolatesprovided <strong>in</strong> Table 1.PNSP at laboratory level/MRSA, FREC and3GCRKP at hospital levelFigures 1, 2, 3 and 4 show the local variation <strong>in</strong> the percentageof PNSP by laboratory and of MRSA, FREC and3GCRKP by hospital. These figures are based on datafrom 2010 and 2011, only <strong>in</strong>clud<strong>in</strong>g the laboratories andhospitals that reported at least five isolates <strong>in</strong> these twoyears. The total number of laboratories or hospitals, them<strong>in</strong>imum, maximum, median, first and third quartile ofthe proportion of <strong>resistance</strong> is displayed <strong>in</strong> a box <strong>in</strong> thefigures.Demographic characteristicsTable 3 gives the proportional distribution of the isolatesreported by source, gender, age, and hospitaldepartment, and the percentage of <strong>resistance</strong> with<strong>in</strong> thedifferent groups, for the period 2010–2011.The abbreviations used <strong>in</strong> this table stand for:PNSP = penicill<strong>in</strong>-non-susceptible S. pneumoniae;MRSA = meticill<strong>in</strong>-resistant S. aureus;FREC = fluoroqu<strong>in</strong>olone-resistant E. coli;VRE = vancomyc<strong>in</strong>-resistant E. faecalis or E. faecium;3GCRKP = third-generation cephalospor<strong>in</strong>-resistantK. pneumoniae; andCRPA = carbapenem-resistant P. aerug<strong>in</strong>osa.If the number of isolates <strong>in</strong> a certa<strong>in</strong> category accountsfor less than 0.5% of the total number of isolates, the %total is set at


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTAustriaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 20 163 20 871 21 985 19 327 - - - -2004 28 257 30 1 453 31 1 862 28 604 - - - -2005 31 298 32 1 481 33 2 058 30 568 7 89 8 772006 32 293 33 1 640 33 2 483 33 699 30 434 31 4052007 35 322 34 1 577 34 2 545 33 688 33 445 33 4112008 38 380 38 1 899 38 2 985 38 864 38 583 38 5102009 38 379 38 1 794 38 2 625 36 825 37 622 36 5252010 35 375 39 1 840 39 2 937 39 944 39 722 39 5042011 39 438 40 1 982 40 3 174 40 894 40 799 40 544Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 1 1


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 97 3 100 7 100 22 100 1 100 4 100 13 100 14CSF 3 4 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTAustriaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesAT016 (0/12)AT022 (0/10)AT038 (0/7)AT019 (0/25)AT015 (0/18)AT009 (0/8)AT033 (0/11)AT042 (0/6)AT021 (0/17)AT030 (0/35)AT018 (0/26)AT023 (0/16)AT003 (0/14)AT032 (0/5)AT002 (0/37)AT034 (0/9)AT031 (0/17)AT036 (0/9)AT037 (0/35)AT014 (0/6)AT026 (0/29)AT005 (1/64)AT001 (1/37)AT007 (1/35)AT006 (2/48)AT012 (1/22)AT028 (2/37)AT024 (1/14)AT010 (2/27)AT027 (3/33)AT017 (1/10)AT025 (4/34)AT020 (1/8)AT041 (2/12)AT043 (3/7)N laboratories 35M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 5.4Maximum 42.90 25 50 75 100Hospital codesAT30UE (0/13)AT030G (0/21)AT022R (0/8)AT006N (0/32)AT036B (0/9)AT022Z (0/6)AT042B (0/35)AT007E (0/8)AT001B (0/31)AT015M (0/11)AT008S (0/7)N hospitals 111M<strong>in</strong>imum 0First quartile 0Median 3.7Third quartile 11.1Maximum 37.5AT036D (0/5)AT022B (0/29)AT043H (0/8)AT010R (0/9)AT030F (0/29)AT015S (0/24)AT005J (0/6)AT009S (0/13)AT030V (0/7)AT009R (0/21)AT007V (0/6)AT019L (0/7)AT008B (0/7)AT011P (0/7)AT007W (0/21)AT009W (0/16)AT022S (0/7)AT036U (0/8)AT016G (0/16)AT032R (0/11)AT009K (0/17)AT006M (0/9)AT030W (0/17)AT043G (0/13)AT040A (0/19)AT010L (0/11)AT006O (0/9)AT010F (0/60)AT030L (0/5)AT030H (0/9)AT022A (0/5)AT043W (0/14)AT015A (0/29)AT003M (0/16)AT005S (0/13)AT022K (0/17)AT037P (1/98)AT014R (1/75)AT001E (1/63)AT016W (2/104)AT007K (3/136)AT005L (1/33)AT012T (1/33)AT005Z (1/28)AT019P (4/107)AT011W (2/49)AT021S (1/23)AT005I (4/93)AT017K (2/45)AT026S (3/66)AT012W (2/39)AT022L (1/19)AT005R (1/18)AT020N (1/17)AT010H (1/17)AT003G (2/34)AT028R (6/96)AT005H (1/16)AT001S (3/48)AT023S (5/77)AT010B (1/15)AT026Z (1/15)AT035H (4/57)AT024V (6/79)AT023K (2/26)AT005K (2/23)AT036H (1/11)AT021V (6/65)AT024G (2/21)AT029O (2/20)AT025K (14/139)AT033D (6/57)AT032V (2/18)AT006B (1/9)AT033F (3/26)AT019T (3/26)AT038M (4/34)AT041E (4/33)AT006S (13/105)AT023F (1/8)AT002A (25/195)AT015W (1/7)AT023E (1/7)AT032J (1/7)AT020W (16/108)AT017T (4/27)AT018M (14/92)AT031W (12/78)AT007F (2/13)AT012D (3/19)AT018S (1/6)AT012H (1/6)AT032E (1/6)AT027L (30/166)AT043J (2/11)AT024B (6/30)AT034E (12/59)AT038B (11/37)AT005N (2/6)AT032D (3/8)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA86


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesAT008K (0/5)AT001W (0/8)AT008A (0/5)AT032H (0/6)AT009S (1/26)AT008S (1/21)AT024G (3/53)AT007W (1/16)AT007F (1/16)AT006O (1/16)AT003G (2/30)AT010L (2/27)N hospitals 117M<strong>in</strong>imum 0First quartile 13.2Median 20Third quartile 28.6Maximum 60AT30UE (2/27)AT032D (1/13)AT015S (3/38)AT010R (2/22)AT032V (2/22)AT005L (6/65)AT012T (4/40)AT032R (1/10)AT023K (6/57)AT023S (12/112)AT010B (8/74)AT021V (7/64)AT022S (1/9)AT036B (1/9)AT024V (10/85)AT034E (11/90)AT021S (2/16)AT006B (5/38)AT007V (6/43)AT010H (6/42)AT036D (1/7)AT009K (2/14)AT019L (2/14)AT026S (15/104)AT017T (6/41)AT028R (30/204)AT005K (8/53)AT015A (10/63)AT005Z (8/49)AT043J (2/12)AT005R (3/18)AT024B (9/54)AT026Z (4/24)AT030N (1/6)AT016G (6/34)AT011W (13/73)AT033F (7/39)AT022B (5/28)AT043H (2/11)AT007K (30/162)AT042B (14/72)AT041E (20/102)AT019T (9/46)AT040A (6/30)AT036H (5/25)AT038B (13/65)AT007E (2/10)AT030L (1/5)AT010F (19/94)AT016W (30/142)AT025K (54/256)AT006S (39/184)AT012W (11/52)AT033D (28/130)AT020N (8/37)AT030V (5/23)AT001E (23/105)AT001B (8/36)AT022A (2/9)AT015M (3/13)AT005S (7/30)AT001S (29/123)AT017K (15/63)AT003M (5/21)AT030W (7/29)AT018M (29/118)AT027L (67/270)AT009W (2/8)AT005H (10/40)AT020W (29/113)AT030F (21/81)AT015W (4/15)AT014R (26/96)AT012D (7/25)AT038M (19/67)AT032P (2/7)AT035H (29/101)AT002A (72/250)AT019P (37/127)AT043G (7/24)AT030G (12/41)AT005J (5/17)AT037P (46/155)AT030Z (4/13)AT029O (7/22)AT023F (3/9)AT006N (3/9)AT022L (18/52)AT023E (9/26)AT031W (35/101)AT005I (69/198)AT009R (8/23)AT011P (9/24)AT012H (6/16)AT018S (3/8)AT022K (8/20)AT043W (8/20)AT006M (10/24)AT030H (7/16)AT005C (5/11)AT022R (6/12)AT023G (3/6)AT003L (3/6)AT005N (5/9)AT015U (3/5)0 25 50 75 100Hospital codesAT010R (0/5)AT016G (0/13)AT005H (0/6)AT005S (0/5)AT022K (0/5)AT042B (0/19)AT006N (0/8)AT022A (0/5)N hospitals 75M<strong>in</strong>imum 0First quartile 0Median 10Third quartile 20Maximum 60AT020N (0/13)AT023K (0/10)AT023E (0/5)AT029O (0/5)AT006B (0/7)AT022L (0/14)AT009R (0/11)AT021S (0/6)AT032P (0/5)AT043J (0/7)AT007V (0/9)AT032V (0/9)AT032R (0/8)AT007E (0/5)AT033F (0/10)AT001S (1/36)AT025K (2/69)AT041E (1/20)AT031W (2/40)AT010F (1/16)AT026S (1/15)AT024V (1/14)AT005Z (1/13)AT006S (5/64)AT007K (3/38)AT015A (1/12)AT027L (7/82)AT016W (4/42)AT023S (2/21)AT005L (1/10)AT001B (1/10)AT010B (1/10)AT017K (2/19)AT028R (7/66)AT022B (1/9)AT001E (4/36)AT020W (5/44)AT018M (3/26)AT011W (4/34)AT005R (1/8)AT021V (2/15)AT037P (4/28)AT014R (2/13)AT034E (2/12)AT017T (1/6)AT002A (14/78)AT012T (2/11)AT015M (1/5)AT003M (1/5)AT043W (1/5)AT033D (9/39)AT038B (2/8)AT005K (2/8)AT024G (2/8)AT038M (4/15)AT035H (7/26)AT005I (20/73)AT011P (3/10)AT030F (2/6)AT003G (4/11)AT019T (4/11)AT019P (20/53)AT005C (2/5)AT001W (2/5)AT009K (4/9)AT009W (3/6)AT040A (3/5)0 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>87


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTBelgiumGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 107 1488 47 1 133 24 1 326 16 146 - - - -2004 95 1 443 49 1 227 25 1 601 18 228 - - - -2005 97 1 539 41 1 048 25 1 592 19 223 - - - -2006 98 1 427 33 858 21 1 632 22 267 - - - -2007 105 1 511 34 855 17 1 460 20 245 - - - -2008 101 1 647 38 906 16 1 430 19 236 - - - -2009 101 1 885 34 949 18 1 610 14 227 8 142 8 1362010 97 1 797 40 1 088 23 1 966 22 323 14 145 15 1302011 91 1 829 50 1 771 43 4 039 46 754 44 676 43 460Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 96 0 100 19 100 22 100 0 100 6 100 13 99 9CSF 4 15 - - 0 0 - - - - 0 0 1 20GenderMale 55 1 59 19 47 26 63 0 58 6 58 13 62 9Female 44 1 40 18 53 18 37 0 42 5 42 14 38 9Unknown 1 2


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTBelgiumFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesBE114 (0/24)BE047 (0/25)BE166 (0/18)BE109 (0/5)BE090 (0/17)BE030 (0/50)BE072 (0/24)BE107 (0/29)BE033 (0/24)BE001 (0/50)N laboratories 94M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 0Maximum 5.6BE130 (0/38)BE024 (0/70)BE061 (0/49)BE022 (0/46)BE081 (0/9)BE164 (0/29)BE011 (0/10)BE093 (0/20)BE054 (0/46)BE170 (0/7)BE003 (0/35)BE065 (0/9)BE097 (0/78)BE102 (0/25)BE043 (0/74)BE060 (0/23)BE077 (0/68)BE139 (0/58)BE026 (0/22)BE032 (0/36)BE046 (0/59)BE108 (0/156)BE129 (0/13)BE063 (0/40)BE092 (0/90)BE029 (0/17)BE057 (0/16)BE100 (0/17)BE023 (0/35)BE084 (0/32)BE007 (0/16)BE049 (0/49)BE051 (0/36)BE161 (0/33)BE073 (0/9)BE091 (0/86)BE141 (0/13)BE031 (0/17)BE083 (0/17)BE103 (0/33)BE002 (0/22)BE146 (0/44)BE113 (0/74)BE018 (0/15)BE160 (0/18)BE101 (0/27)BE159 (0/16)BE004 (0/54)BE037 (0/31)BE110 (0/39)BE152 (0/16)BE116 (0/40)BE104 (0/45)BE137 (0/28)BE087 (0/30)BE064 (0/8)BE056 (0/109)BE125 (0/10)BE112 (0/96)BE071 (0/20)BE105 (0/39)BE098 (0/26)BE035 (0/23)BE014 (0/29)BE008 (1/88)BE111 (1/82)BE016 (1/78)BE075 (1/67)BE115 (1/55)BE143 (1/52)BE021 (1/52)BE045 (1/53)BE070 (2/94)BE044 (1/45)BE095 (1/42)BE074 (1/40)BE019 (1/38)BE006 (1/35)BE118 (1/30)BE048 (1/22)BE017 (1/21)BE154 (1/21)BE069 (1/20)BE012 (1/18)0 25 50 75 100Hospital codesBE0071 (0/11)BE0751 (1/30)BE0771 (3/86)BE0031 (3/43)BE1581 (2/25)BE0601 (6/63)BE1151 (10/100)BE0721 (1/10)BE1141 (1/10)BE0921 (11/108)BE0911 (5/46)BE0611 (16/132)BE0451 (8/64)BE1301 (7/55)BE0301 (2/15)BE1121 (10/73)BE1611 (1/7)BE1111 (9/62)BE0631 (13/87)BE0371 (3/20)BE0191 (2/13)BE0741 (13/84)BE0081 (19/122)BE1391 (12/75)BE0561 (17/103)BE0841 (3/18)BE0011 (7/42)BE0161 (21/125)BE0241 (14/78)BE0481 (2/11)BE0121 (7/38)BE0971 (25/134)BE0021 (9/47)BE1431 (11/56)BE1641 (6/29)BE0061 (9/43)BE0541 (12/57)BE0571 (6/26)BE1091 (7/30)BE1571 (3/12)BE0221 (15/58)BE1521 (2/7)BE0701 (35/120)BE0842 (13/42)BE0321 (24/77)BE1701 (11/35)BE1601 (6/18)BE1291 (19/54)BE1021 (11/31)BE0171 (8/22)BE0511 (8/22)BE1361 (8/22)BE0331 (16/43)BE1251 (4/9)BE1161 (6/13)BE0291 (8/17)BE0401 (8/17)N hospitals 57M<strong>in</strong>imum 0First quartile 13.3Median 17.9Third quartile 29.2Maximum 47.10 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA90


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesBE0011 (9/121)BE0321 (29/240)BE1391 (27/173)BE0541 (15/94)BE1121 (38/231)BE0031 (13/78)BE0751 (10/57)BE1291 (24/131)BE0221 (29/157)BE0061 (18/95)BE0511 (16/80)BE0601 (24/120)BE0331 (13/63)BE0971 (64/309)BE0611 (44/213)BE1141 (5/24)BE0721 (14/67)BE1111 (38/181)BE0291 (13/62)BE0371 (12/57)BE1571 (8/38)BE0301 (4/19)BE0071 (19/88)BE0921 (36/167)BE0451 (35/161)BE0631 (56/253)BE0842 (25/113)BE1161 (15/66)BE1251 (9/38)BE0701 (54/220)BE0081 (82/327)BE1361 (25/98)BE0771 (36/140)BE0161 (76/296)BE0441 (43/166)BE0121 (26/97)BE1601 (12/44)BE1091 (21/76)BE0911 (45/163)BE0841 (9/32)BE1641 (23/74)BE1581 (34/102)N hospitals 42M<strong>in</strong>imum 7.4First quartile 20Median 21.1Third quartile 25.5Maximum 33.30 25 50 75 100Hospital codesBE0371 (0/9)BE0011 (0/11)BE0061 (0/12)BE1251 (0/5)BE0751 (0/10)BE1121 (0/11)BE1641 (0/5)BE0842 (0/17)BE0841 (0/5)BE0221 (0/9)BE1601 (0/10)BE0561 (1/35)BE0611 (1/30)BE1111 (1/26)BE1391 (1/25)BE0241 (1/17)BE0451 (2/29)BE0911 (3/42)BE0171 (1/13)BE0321 (1/12)BE0161 (1/11)BE1161 (1/9)BE0331 (1/8)BE0721 (1/8)BE0541 (2/16)BE0971 (5/37)BE1361 (1/7)BE1291 (5/34)BE1581 (5/33)BE0441 (4/26)BE0631 (3/19)BE0031 (3/19)BE0601 (3/18)BE0081 (8/48)BE0701 (4/21)BE1091 (2/10)BE0511 (3/12)BE1021 (2/7)BE0771 (6/19)BE0921 (11/34)BE1151 (19/53)BE1571 (2/5)BE0291 (4/10)N hospitals 43M<strong>in</strong>imum 0First quartile 0Median 11.1Third quartile 16.7Maximum 400 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>91


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTBulgariaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 13 22 20 157 20 158 16 49 - - - -2004 13 32 22 170 20 167 16 75 - - - -2005 16 43 26 160 23 203 21 95 15 34 9 342006 11 29 23 159 20 196 19 98 15 55 13 312007 10 32 14 121 15 127 13 65 9 29 6 142008 13 29 21 160 22 147 18 70 11 49 10 232009 10 27 20 221 17 194 16 92 12 95 11 362010 13 22 20 200 21 153 16 108 15 127 11 422011 16 33 19 214 19 179 16 117 15 121 12 48Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 9 22 30 7 9 21 22 18 21Penicill<strong>in</strong> RI 14 22 33 7 16 21 37 18 21Macrolides RI 11 17 8 15 17 4 27 25 13Staphylococcus aureusOxacill<strong>in</strong>/Meticill<strong>in</strong> R 31 23 29 28 13 25 16 19 22Escherichia coliAm<strong>in</strong>openicil<strong>in</strong>s R 54 64 69 64 70 65 66 72 61Am<strong>in</strong>oglycosides R 22 20 24 28 20 31 18 16 17Fluoroqu<strong>in</strong>olones R 19 24 29 26 35 32 28 33 30Third-gen. cephalospor<strong>in</strong>s R 18 22 28 29 23 29 19 25 23Carbapenems R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 64 20 100 21 98 32 100 0 100 0 98 79 97 30CSF 36 20 - - 2 17 - - - - 2 50 3 33GenderMale 56 23 64 22 54 34 63 0 61 0 65 78 60 31Female 44 17 35 17 46 28 37 0 39 0 35 78 40 28Unknown - - 1 67 0 0 - - - - - - - -Age (years)0–4 15 38 3 42 2 20 3 0 5 0 9 91 8 295–19 11 33 4 24 2 14 1 0 3 0 2 100 1 020–64 42 17 42 21 35 32 45 0 48 0 32 85 40 3365 and over 24 15 30 22 42 33 35 0 26 0 23 68 30 7Unknown 9 0 21 14 19 30 16 0 18 0 34 74 21 58Hospital departmentICU 18 10 19 34 17 44 22 0 32 0 19 79 34 52Internal med. 24 15 38 11 47 25 31 0 16 0 21 51 17 7Surgery - - 11 35 10 42 13 0 19 0 13 94 9 0Other 58 25 32 20 26 31 33 0 32 0 46 86 40 28Unknown - - 0 0 - - 1 0 - - 1 67 - -PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.93


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTBulgariaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 4M<strong>in</strong>imum 14.3First quartile 21.4Median 28.6Third quartile 28.6Maximum 28.6BG014A (0/5)BG002A (0/10)N hospitals 19M<strong>in</strong>imum 0First quartile 5.6Median 17.8Third quartile 33.3Maximum 64.1BG016 (1/7)BG013A (1/22)BG017A (4/71)BG011A (1/18)BG003A (2/20)BG007A (5/35)BG013 (2/7)BG001A (4/26)Laboratory codesHospital codesBG018A (3/18)BG005A (8/45)BG029A (1/5)BG003 (2/7)BG021A (8/32)BG022A (4/15)BG004A (4/12)BG009A (2/6)BG026A (5/14)BG017 (2/7)BG027A (4/11)BG008A (3/5)BG006A (25/39)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA94


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)BG029A (0/7)BG013A (1/19)N hospitals 15M<strong>in</strong>imum 0First quartile 14.3Median 26.3Third quartile 36.8Maximum 58.3BG013A (2/8)N hospitals 10M<strong>in</strong>imum 25First quartile 66.7Median 82.1Third quartile 86.7Maximum 95.7BG026A (2/18)BG018A (8/16)BG014A (1/7)BG009A (4/6)BG018A (6/31)BG022A (1/5)BG021A (51/67)BG021A (6/27)BG017A (42/52)Hospital codesBG001A (5/19)BG027A (4/14)Hospital codesBG007A (10/12)BG007A (10/31)BG026A (5/6)BG005A (7/20)BG003A (7/19)BG011A (13/15)BG017A (24/54)BG006A (22/25)BG006A (15/27)BG011A (7/12)BG001A (22/23)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>95


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 83 25 100 37 100 45 100 2 100 0 98 38 98 36CSF 17 75 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTCyprusFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 2M<strong>in</strong>imum 28.6First quartile 28.6Median 28.6Third quartile 28.6Maximum 28.6CY004A (2/7)N hospitals 5M<strong>in</strong>imum 28.6First quartile 33.3Median 35.8Third quartile 38.3Maximum 50CY001 (4/14)CY003A (8/24)Laboratory codesHospital codesCY002A (19/53)CY001A (46/120)CY002 (2/7)CY005A (4/8)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA98


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTCzech RepublicGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 32 204 45 1 387 43 1 766 44 630 - - - -2004 37 162 45 1444 44 1 966 41 660 - - - -2005 39 195 47 1 553 47 2 234 45 758 37 478 36 2572006 39 172 47 1 527 47 2 176 45 697 45 1 130 43 4902007 41 205 47 1 653 48 2 407 47 816 48 1 230 41 5172008 40 244 47 1 715 46 2 738 44 883 45 1 493 42 5682009 41 297 46 1 695 45 2 759 44 835 45 1 415 45 5752010 41 288 44 1 593 43 2 484 41 759 44 1 264 41 5112011 42 316 46 1 555 45 2 696 44 767 44 1 287 42 448Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 86 4 100 14 100 23 100 0 100 6 99 48 100 15CSF 14 5 - - 0 0 - - - - 1 41 0 0GenderMale 60 3 62 14 43 27 65 1 64 6 60 50 62 15Female 40 6 38 15 57 20 35 0 36 7 40 46 38 14Unknown - - - - - - - - - - - - - -Age (years)0–4 5 3 5 1 2 9 4 2 2 0 1 39 1 175–19 5 0 2 1 1 20 1 0 2 14 1 60 2 1620–64 47 5 41 13 29 21 39 0 48 10 42 51 42 1865 and over 42 5 52 17 68 25 56 1 49 2 56 46 54 13Hospital departmentICU 25 5 26 17 19 26 46 0 38 1 42 56 49 19Internal med. 37 4 43 14 50 22 26 1 18 5 31 40 23 7Surgery 1 0 8 14 5 23 6 0 7 8 7 39 5 13Other 32 5 23 10 26 23 22 0 37 12 20 47 23 15Unknown 5 6 0 21 0 0 0 0 - - 0 75 - -PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.101


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTCzech RepublicFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesCZ004 (0/7)CZ030 (0/13)CZ003 (0/11)CZ032 (0/15)CZ019 (0/9)CZ037 (0/11)CZ011 (0/9)CZ026 (0/5)CZ041 (0/8)CZ024 (0/19)CZ036 (0/10)CZ051 (0/5)CZ023 (0/15)CZ044 (1/34)CZ016 (2/54)CZ017 (1/27)CZ009 (1/26)CZ027 (1/24)CZ018 (1/23)CZ049 (1/21)CZ013 (1/20)CZ031 (1/20)CZ006 (3/57)CZ042 (1/19)CZ015 (1/16)CZ029 (1/16)CZ033 (2/30)CZ007 (1/14)CZ002 (1/10)CZ047 (1/9)CZ005 (1/5)CZ014 (2/7)N laboratories 32M<strong>in</strong>imum 0First quartile 0Median 3.8Third quartile 5.8Maximum 28.60 25 50 75 100Hospital codesCZ031J (0/18)CZ029A (0/32)CZ036A (0/35)CZ034B (0/5)CZ021A (2/86)CZ030A (2/53)CZ011A (1/25)CZ026A (3/72)CZ038A (1/20)CZ044A (3/52)CZ009B (1/17)CZ048A (1/17)CZ028A (4/57)CZ013A (4/52)CZ002A (7/86)CZ047A (1/12)CZ009A (11/133)CZ034A (5/58)CZ017A (8/87)CZ004A (6/59)CZ022A (4/37)CZ020A (10/92)CZ032A (8/73)CZ024A (16/140)CZ031A (6/52)CZ016A (10/86)CZ007A (10/82)CZ015A (16/125)CZ019A (6/46)CZ006A (30/216)CZ035A (7/50)CZ047B (1/7)CZ044C (3/20)CZ033A (11/66)CZ037A (5/30)CZ027A (22/128)CZ018A (31/171)CZ039A (2/11)CZ040A (3/16)CZ051A (4/21)CZ003A (15/78)CZ012B (2/10)CZ041A (7/34)CZ014A (11/51)CZ050A (5/23)CZ012C (2/9)CZ008A (8/35)CZ005A (26/113)CZ017B (7/30)CZ039B (4/17)CZ023A (8/33)CZ049A (9/37)CZ037D (6/24)CZ012A (8/32)CZ037C (2/7)CZ025A (14/48)CZ007D (3/10)CZ042A (9/29)CZ031P (3/9)CZ015B (2/6)CZ031C (3/8)CZ034C (6/15)CZ007B (5/12)CZ031F (5/8)N hospitals 64M<strong>in</strong>imum 0First quartile 8.3Median 14.6Third quartile 23.2Maximum 62.50 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA102


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesCZ015B (0/6)CZ030A (9/164)CZ031V (1/10)CZ040A (1/10)CZ047A (4/37)CZ012A (4/33)CZ020A (10/81)CZ032A (20/159)CZ038A (8/60)CZ011A (5/36)CZ031P (5/35)CZ037A (8/56)CZ031F (3/20)CZ015A (33/209)CZ014A (12/75)CZ003A (20/123)CZ017A (19/112)CZ051A (5/29)CZ019A (17/98)CZ047B (4/23)CZ037D (8/44)CZ007A (20/109)CZ029A (15/82)CZ016A (40/214)CZ033A (16/85)CZ017B (14/73)CZ022A (12/61)CZ039A (8/40)CZ028A (16/80)CZ031Y (1/5)CZ050A (5/24)CZ026A (18/86)CZ048A (3/14)CZ013A (21/94)CZ004A (20/89)CZ044A (14/62)CZ006A (100/443)CZ037C (6/25)CZ041A (15/62)CZ007D (5/20)CZ036A (16/63)CZ023A (14/54)CZ009A (36/136)CZ049A (20/74)CZ031A (23/85)CZ012B (6/22)CZ024A (63/225)CZ018A (63/216)CZ021A (42/143)CZ035A (15/50)CZ039B (9/30)CZ005A (47/152)CZ042A (27/87)CZ034A (10/32)CZ027A (65/201)CZ002A (67/205)CZ008A (30/89)CZ031J (14/40)CZ031C (5/13)CZ034B (3/7)CZ031K (4/9)CZ007B (11/24)CZ025A (28/61)CZ049B (5/9)CZ007E (4/7)CZ012C (11/18)N hospitals 67M<strong>in</strong>imum 0First quartile 17Median 22.3Third quartile 30Maximum 63.6CZ034C (7/11)0 25 50 75 100Hospital codesCZ032A (2/29)CZ037D (1/8)CZ015A (7/41)CZ014A (7/39)CZ037A (3/14)CZ019A (7/32)CZ048A (2/9)CZ030A (7/29)CZ020A (15/59)CZ029A (10/33)CZ008A (9/29)CZ007A (11/35)CZ031P (4/12)CZ044A (8/24)CZ031F (4/12)CZ005A (33/89)CZ034B (3/8)CZ051A (4/10)CZ044C (6/15)CZ039B (2/5)CZ031A (25/62)CZ018A (66/159)CZ016A (25/60)CZ012B (3/7)CZ049A (13/30)CZ006A (77/178)CZ035A (32/73)CZ021A (8/18)CZ028A (22/46)CZ034A (17/35)CZ024A (63/127)CZ039A (4/8)CZ012A (6/12)CZ017A (36/71)CZ017B (24/47)CZ041A (10/19)CZ033A (44/81)CZ031K (6/11)CZ004A (22/40)CZ027A (72/131)CZ025A (25/45)CZ003A (40/72)CZ022A (18/32)CZ002A (25/43)CZ009B (10/17)CZ009A (106/175)CZ036A (22/36)CZ031C (8/13)CZ049B (8/13)CZ013A (20/32)CZ043C (5/8)CZ047A (12/19)CZ042A (23/35)CZ034C (4/6)CZ026A (50/71)CZ007B (18/25)CZ038A (19/26)CZ023A (28/38)CZ050A (16/20)CZ011A (12/15)CZ031J (14/17)CZ012C (15/17)N hospitals 62M<strong>in</strong>imum 6.9First quartile 37.1Median 49.8Third quartile 61.1Maximum 88.20 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>103


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTDenmarkGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 5 606 5 671 - - - - - - - -2004 15 1 188 15 1 436 - - - - - - - -2005 14 1 081 15 1 350 5 1 283 - - - - - -2006 15 872 15 1 279 11 2 723 11 711 11 607 - -2007 15 1 030 14 1 315 12 3 021 13 927 13 784 13 4172008 15 934 15 1 295 14 3 283 14 1 005 14 793 14 4202009 15 996 15 1 395 14 3 532 14 1 100 14 822 14 4292010 15 954 15 1 362 14 3 418 14 1 112 14 799 14 3762011 13 896 13 1 452 12 3 642 12 1 197 12 910 12 407Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 93 4 100 1 100 14 100 0 100 2 100 11 99 4CSF 7 4 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTDenmarkFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesDK005 (0/8)DK012 (1/101)DK015 (1/70)DK016 (4/183)DK011 (2/71)DK013 (2/63)DK009 (6/189)DK002 (11/275)DK006 (9/224)DK014 (12/242)DK001 (3/47)DK003 (11/172)DK010 (2/30)DK007 (4/57)DK004 (9/118)N laboratories 15M<strong>in</strong>imum 0First quartile 2.2Median 4Third quartile 6.4Maximum 7.60 25 50 75 100Hospital codesDK016X (0/9)DK014A (0/26)DK016F (0/8)DK014X (0/14)DK007B (0/82)DK016P (0/5)DK016Q (0/9)DK007X (0/6)DK014B (0/44)DK014D (0/78)DK011X (0/5)DK012F (0/52)DK011A (0/96)DK012E (0/42)DK002E (0/20)DK013A (0/50)DK008A (0/19)DK015X (0/39)DK013B (0/65)DK015C (0/31)DK009X (0/12)DK009A (0/41)DK004X (0/23)DK016D (0/8)DK012D (0/46)DK012B (0/35)DK016C (0/13)DK014Y (0/38)DK003B (0/30)DK005A (0/63)DK014E (0/5)DK011D (0/5)DK016A (1/153)DK009B (2/260)DK004A (1/98)DK002A (1/86)DK014N (1/80)DK016B (1/61)DK006A (1/60)DK015A (1/57)DK003A (1/56)DK014C (1/56)DK001A (4/208)DK006B (1/52)DK005B (1/43)DK002X (2/86)DK003C (4/164)DK002F (1/36)DK002B (4/112)DK006X (1/25)DK007A (2/42)DK004B (1/15)DK004C (1/12)N hospitals 53M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 1.8Maximum 8.30 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA106


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesDK014I (0/7)DK006C (0/11)DK016C (3/65)DK007B (4/69)DK016D (4/62)DK016F (3/44)DK008A (5/71)DK016B (13/178)DK014D (19/256)DK012B (7/84)DK011D (2/23)DK012E (12/134)DK003B (15/154)DK013B (15/153)DK007A (8/78)DK006A (15/141)DK015G (5/45)DK012F (17/151)DK015C (5/42)DK012D (18/151)DK006B (16/129)DK009A (27/216)DK014B (24/188)DK004A (29/224)DK011A (31/236)DK002E (16/120)DK015A (23/172)DK003A (20/147)DK004C (17/121)DK009B (55/391)DK002A (48/319)DK002B (54/352)DK003C (95/580)DK016A (61/368)DK016G (4/24)DK015B (1/6)DK014C (32/190)DK002F (25/146)DK013A (18/103)DK005B (25/141)DK014A (14/78)DK005A (26/133)DK004B (15/69)DK014N (23/101)DK001A (68/259)N hospitals 45M<strong>in</strong>imum 0First quartile 9Median 12.8Third quartile 16.6Maximum 26.30 25 50 75 100Hospital codesDK015G (0/8)DK016C (0/9)DK008A (0/14)DK002E (0/21)DK016F (0/8)DK016D (0/11)DK003B (0/9)DK016G (0/6)DK015C (0/5)DK012E (0/22)DK012F (1/24)DK009A (2/48)DK009B (6/119)DK002A (4/73)DK012B (1/17)DK016A (5/81)DK016B (2/30)DK004B (1/15)DK015A (3/42)DK004A (3/40)DK011A (4/52)DK014A (2/23)DK014C (6/52)DK011D (1/8)DK002B (12/87)DK014D (9/51)DK014B (8/45)DK001A (29/143)DK002F (8/38)DK012D (7/31)DK004C (5/22)DK014N (9/32)DK014Y (2/5)N hospitals 33M<strong>in</strong>imum 0First quartile 0Median 6.7Third quartile 13.8Maximum 400 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>107


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTEstoniaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 8 26 9 98 9 98 6 27 - - - -2004 6 40 9 104 10 167 5 63 - - - -2005 7 53 8 141 10 156 7 66 7 38 5 382006 8 52 9 154 9 215 8 85 6 47 6 432007 8 64 10 206 11 219 8 66 9 63 8 482008 10 66 11 185 11 267 11 86 10 72 8 412009 8 82 11 213 11 320 8 72 7 60 6 432010 10 64 9 152 11 317 8 66 9 82 8 432011 9 54 11 121 11 315 8 77 6 91 6 17Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 97 2 100 1 100 9 100 0 100 0 100 25 98 19CSF 3 0 - - 0 0 - - - - - - 2 0GenderMale 57 3 57 1 38 13 70 0 56 0 50 21 52 25Female 43 0 43 2 62 7 30 0 44 0 50 29 48 12Unknown - - - - 0 0 - - - - - - - -Age (years)0–4 7 0 6 0 3 6 13 0 - - 5 0 2 05–19 3 25 2 0 2 0 4 0 - - 2 0 4 020–64 65 1 49 0 41 11 39 0 52 0 48 31 43 1365 and over 24 0 43 3 53 9 41 0 48 0 46 23 52 25Unknown - - 0 0 - - 2 0 - - - - - -Hospital departmentICU 30 3 20 6 15 12 26 0 41 0 35 33 33 22Internal med. 36 2 37 0 46 5 20 0 15 0 28 26 28 20Surgery 1 0 5 0 6 11 9 0 7 0 7 22 2 100Other 34 0 38 0 33 13 43 0 37 0 30 16 37 10Unknown - - - - 0 100 2 0 - - - - - -PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.109


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTEstoniaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)EE002 (0/12)N laboratories 7M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 9.1Maximum 12.5EE005X (0/29)N hospitals 9M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 0Maximum 5.7EE010X (0/9)EE011 (0/11)EE011X (0/9)EE001 (0/19)EE003X (0/7)Laboratory codesEE006 (0/11)Hospital codesEE002X (0/5)EE009X (0/28)EE004 (0/34)EE004X (0/60)EE009 (1/11)EE001X (1/76)EE005 (1/8)EE006X (2/35)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA110


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)EE011X (1/28)N hospitals 10M<strong>in</strong>imum 3.6First quartile 5.5Median 10.4Third quartile 11.8Maximum 27.8EE005X (0/5)N hospitals 6M<strong>in</strong>imum 0First quartile 11.4Median 33.8Third quartile 50Maximum 50EE001X (8/150)EE005X (3/55)EE002X (5/44)EE008X (2/27)EE001X (7/26)EE010X (1/10)Hospital codesEE002X (8/74)Hospital codesEE004X (11/27)EE004X (12/103)EE006X (10/85)EE009X (3/6)EE009X (3/21)EE006X (5/10)EE003X (5/18)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>111


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTF<strong>in</strong>landGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 16 517 16 727 15 1 450 15 266 - - - -2004 17 548 17 883 17 1 749 17 336 - - - -2005 17 543 17 790 17 1 924 17 340 14 175 13 1082006 15 501 15 894 15 1 875 15 348 14 228 14 1622007 16 547 16 814 16 1 949 16 400 15 273 14 1832008 15 643 15 923 15 2 111 15 381 12 288 12 1752009 20 688 20 978 20 2 224 20 506 20 375 18 2332010 20 622 20 1 094 20 2 551 20 521 20 401 20 2812011 - - - - 17 2 470 16 375 17 319 16 221Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 2


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae* S. aureus* E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 97 14 100 2 100 10 100 0 100 0 100 4 99 10CSF 3 10 - - 0 0 - - - - 0 0 1 29GenderMale 55 15 63 2 38 14 69 0 62 0 54 5 62 12Female 45 13 37 3 62 8 31 0 38 1 46 2 38 7Age (years)0–4 16 25 4 0 2 6 7 0 2 0 1 25 1 05–19 3 11 4 0 1 8 1 0 1 0 1 0 2 3620–64 44 11 39 2 27 9 24 0 32 0 26 4 29 1565 and over 37 14 53 3 70 10 68 0 65 1 72 3 67 7Hospital departmentICU 0 0 2 0 0 9 0 0 2 0 1 17 2 27Internal med. 6 3 6 1 5 8 3 0 6 0 4 4 5 15Surgery 2 5 1 7 2 0 4 0 2 6 2 18Other 21 8 17 2 16 11 11 0 7 0 16 4 11 2Unknown 73 17 73 2 77 10 84 0 81 1 78 4 80 10* Data only for 2010.PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.113


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTF<strong>in</strong>landFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)No data reported for 2011 No data reported for 2011114


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)FI021X (11/205)FI008X (6/108)N hospitals 20M<strong>in</strong>imum 5.4First quartile 6.3Median 9.4Third quartile 11.9Maximum 14.7FI00CX (0/49)FI008X (0/13)N hospitals 19M<strong>in</strong>imum 0First quartile 0Median 3.7Third quartile 6.3Maximum 12.1FI017X (11/195)FI00AX (0/9)FI010X (5/87)FI021X (0/35)FI018X (4/68)FI010X (0/15)FI00EX (16/236)FI017X (0/23)FI012X (10/143)FI009X (0/12)FI014X (12/169)FI002X (5/185)FI00CX (24/320)FI003X (1/35)Hospital codesFI003X (25/267)FI00LX (7/74)Hospital codesFI020X (3/82)FI019X (1/24)FI020X (55/525)FI011X (1/23)FI015X (12/106)FI009X (9/79)FI014X (1/21)FI002X (157/1330)FI00HX (3/61)FI005X (28/234)FI012X (1/16)FI00AX (7/58)FI015X (1/16)FI011X (20/164)FI00LX (1/13)FI00HX (57/459)FI00EX (5/47)FI019X (21/143)FI005X (4/33)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>115


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFranceGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 403 1 389 21 1 710 21 2 266 20 468 - - - -2004 403 515 50 3 355 50 5 678 46 871 - - - -2005 195 632 50 3 484 50 6 056 47 1 023 49 838 48 9932006 97 371 50 3 824 50 6 718 50 1 152 50 963 47 1 0062007 168 663 57 4 265 57 8 093 56 1 545 56 1 187 56 1 3052008 127 557 56 4 380 56 7 993 54 1 555 54 1 138 54 1 2252009 225 826 54 4 727 54 8 451 54 1 969 52 1 378 32 1 2212010 181 1 127 56 4 883 56 9 028 54 1 970 56 1 542 36 1 1912011 255 1 413 52 4 740 52 8 790 46 2 163 52 1 691 52 1 634Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R - - 5 4 4 7 6


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates from the report<strong>in</strong>g period 2009 and 2010CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 68 24 100 21 100 18 100 0 100 1 100 22 100 19CSF 32 28 - - - - - - - - - - - -GenderMale 55 26 63 21 48 20 67 0 64 1 61 23 65 18Female 45 25 35 21 51 16 32 0 35 2 37 20 34 20Unknown - - 2 10 2 15 1 0 1 0 2 13 1 19Age (years)0–4 21 28 4 9 2 7 5 0 2 30 2 19 2 45–19 9 13 3 3 1 9 1 0 1 0 1 38 2 1220–64 36 23 40 14 34 18 36 0 45 1 47 24 49 2365 and over 34 30 52 28 63 18 58 0 51 1 50 19 47 16Unknown - - 0 0


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTFranceFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesFR257 (0/5)FR144 (0/6)FR201 (0/5)FR129 (0/5)FR460 (0/7)FR050 (0/9)FR069 (0/6)FR521 (0/9)FR054 (0/7)FR125 (0/15)FR188 (0/5)FR146 (0/6)FR133 (0/5)FR450 (0/12)N laboratories 140M<strong>in</strong>imum 0First quartile 14.3Median 23.1Third quartile 33.3Maximum 80FR306 (0/5)FR492 (0/5)FR473 (0/10)FR528 (1/11)FR170 (1/11)FR098 (1/10)FR004 (1/10)FR465 (1/10)FR160 (1/10)FR043 (1/9)FR022 (1/9)FR066 (1/8)FR239 (1/8)FR162 (2/16)FR232 (2/15)FR100 (1/7)FR015 (1/7)FR020 (2/14)FR024 (1/7)FR217 (1/7)FR434 (1/7)FR235 (1/7)FR052 (5/34)FR142 (2/13)FR507 (2/13)FR224 (3/19)FR249 (4/24)FR488 (1/6)FR418 (1/6)FR062 (1/6)FR148 (1/6)FR116 (5/29)FR175 (3/17)FR076 (9/51)FR479 (10/56)FR260 (5/28)FR198 (2/11)FR277 (2/11)FR241 (2/11)FR040 (7/37)FR172 (2/10)FR105 (1/5)FR506 (1/5)FR271 (3/15)FR218 (1/5)FR270 (1/5)FR524 (1/5)FR254 (2/10)FR112 (1/5)FR462 (1/5)FR107 (1/5)FR514 (3/14)FR208 (3/14)FR167 (5/23)FR079 (2/9)FR131 (3/13)FR234 (3/13)FR164 (7/30)FR009 (5/21)FR149 (3/12)FR999 (2/8)FR251 (3/12)FR498 (4/16)FR174 (2/8)FR269 (15/59)FR010 (13/50)FR467 (12/45)FR126 (3/11)FR094 (21/76)FR064 (5/18)FR263 (26/92)FR137 (13/46)FR038 (4/14)FR194 (6/21)FR403 (2/7)FR063 (2/7)FR032 (2/7)FR071 (9/31)FR153 (5/17)FR250 (5/17)FR505 (3/10)FR518 (3/10)FR196 (3/10)FR470 (4/13)FR109 (15/48)FR213 (10/32)FR246 (17/54)FR496 (6/19)FR028 (3/9)FR121 (2/6)FR214 (14/42)FR274 (4/12)FR219 (2/6)FR400 (2/6)FR051 (3/9)FR414 (2/6)FR476 (19/57)FR108 (18/53)FR266 (8/23)FR067 (6/17)FR228 (5/14)FR279 (5/14)FR490 (5/14)FR186 (7/19)FR230 (3/8)FR238 (3/8)FR138 (3/8)FR127 (20/50)FR037 (2/5)FR135 (2/5)FR120 (8/19)FR130 (11/26)FR036 (6/14)FR248 (3/7)FR493 (3/7)FR502 (3/7)FR068 (4/8)FR252 (3/6)FR096 (3/6)FR115 (3/6)FR240 (8/15)FR006 (10/18)FR140 (4/7)FR276 (4/7)FR077 (3/5)FR072 (4/5)0 25 50 75 100Hospital codesFR164A (39/380)FR145A (3/27)FR095A (6/52)FR193A (5/41)FR076A (45/304)FR134A (15/99)FR249A (29/188)FR226A (83/533)FR248A (29/183)FR208A (4/25)FR010A (48/295)FR084A (6/36)FR109A (46/276)FR403A (9/54)FR202A (5/28)FR072A (7/38)FR052A (36/193)FR055A (3/16)FR362A (10/53)FR434A (17/90)FR179A (12/63)FR138A (74/376)FR401A (11/55)FR126A (16/80)FR214A (56/275)FR040A (49/239)FR165A (57/272)FR006A (128/607)FR130A (81/381)FR094A (77/359)FR263A (147/679)FR250A (46/209)FR238A (66/298)FR224A (15/66)FR121A (42/182)FR194A (23/99)FR135A (10/43)FR105A (31/131)FR213A (27/113)FR037A (11/46)FR246A (88/361)FR400A (11/45)FR067A (33/135)FR015A (4/16)FR276A (31/122)FR008A (15/58)FR259A (45/167)FR120A (24/89)FR237A (32/115)FR009A (39/139)FR479A (113/398)FR260A (36/125)FR064A (56/192)FR098A (22/70)FR046A (12/36)FR531A (14/23)N hospitals 56M<strong>in</strong>imum 10.3First quartile 17.3Median 21.2Third quartile 24.4Maximum 60.90 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA118


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesFR276A (23/268)FR434A (21/236)FR250A (41/446)FR145A (7/72)FR531A (4/41)FR208A (8/81)FR037A (8/79)FR130A (63/614)FR194A (24/232)FR238A (59/568)FR126A (15/143)FR072A (10/94)FR362A (15/135)FR009A (35/307)FR224A (20/167)FR008A (22/183)FR249A (36/298)FR202A (17/136)FR134A (26/206)FR067A (34/266)FR400A (20/142)FR010A (65/460)FR226A (111/776)FR179A (23/159)FR120A (32/219)FR213A (51/332)FR135A (18/115)FR193A (16/99)FR040A (67/406)FR109A (87/527)FR094A (96/555)FR260A (47/271)FR084A (13/71)FR052A (84/454)FR246A (127/643)FR164A (121/612)FR138A (148/746)FR098A (33/161)FR076A (106/507)FR263A (192/901)FR121A (55/257)FR214A (119/550)FR403A (29/134)FR259A (52/234)FR401A (25/112)FR015A (16/70)FR064A (101/432)FR006A (253/1071)FR095A (17/71)FR105A (79/324)FR165A (140/561)FR248A (80/316)FR237A (52/200)FR479A (141/542)FR055A (15/55)FR046A (19/44)N hospitals 56M<strong>in</strong>imum 8.6First quartile 11.7Median 16.3Third quartile 21.6Maximum 43.20 25 50 75 100Hospital codesFR276A (0/10)FR008A (0/18)FR055A (0/7)FR434A (0/20)FR400A (0/19)FR072A (0/6)FR202A (0/8)FR224A (0/16)FR246A (1/95)FR164A (2/59)FR362A (1/23)FR194A (2/35)FR052A (4/70)FR120A (2/26)FR076A (9/111)FR010A (2/24)FR237A (2/23)FR260A (2/22)FR067A (3/33)FR084A (2/20)FR006A (19/181)FR259A (7/61)FR249A (3/26)FR098A (1/8)FR214A (17/131)FR130A (8/59)FR064A (11/81)FR250A (5/35)FR208A (1/7)FR109A (13/88)FR238A (11/70)FR094A (17/107)FR105A (18/97)FR531A (2/10)FR126A (5/24)FR193A (4/19)FR401A (9/42)FR479A (24/104)FR248A (28/118)FR135A (5/19)FR095A (5/18)FR179A (11/39)FR165A (50/166)FR121A (19/63)FR145A (4/13)FR403A (14/45)FR009A (10/32)FR213A (17/52)FR138A (70/203)FR040A (23/66)FR015A (5/14)FR134A (7/19)FR263A (101/253)FR046A (4/10)FR226A (103/245)FR037A (11/26)N hospitals 56M<strong>in</strong>imum 0First quartile 7.9Median 14.3Third quartile 29.2Maximum 42.30 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>119


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTGermanyGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 17 175 20 920 19 997 17 347 - - - -2004 16 145 22 1 107 22 1 217 22 606 - - 1 12005 15 119 17 827 17 961 17 569 12 105 12 1172006 15 85 18 799 18 850 16 529 14 148 12 1622007 11 75 12 853 12 977 12 648 10 173 11 1972008 11 209 14 1 090 14 1 615 13 451 11 235 11 1672009 16 346 17 1 893 17 2 803 17 952 15 479 16 2872010 16 363 17 1 980 17 3 024 16 1 009 15 478 15 3152011 18 359 19 2 388 19 3 650 17 1 231 17 519 17 389Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 94 3 100 18 100 24 100 0 100 10 99 12 99 11CSF 6 2 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTGermanyFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesDE0907 (0/94)DE0202 (0/6)DE1001 (0/31)DE1101 (0/7)DE1304 (0/23)DE0107 (0/30)DE1303 (0/26)DE0401 (0/22)DE0110 (2/157)DE0911 (3/111)DE0908 (2/51)DE0102 (2/40)DE0402 (1/18)DE1302 (1/13)DE0301 (3/35)DE0111 (5/32)N laboratories 16M<strong>in</strong>imum 0First quartile 0Median 0.6Third quartile 5.3Maximum 15.60 25 50 75 100Hospital codesDE010703 (0/7)DE070102 (0/6)DE091133 (0/8)DE011044 (0/12)DE100127 (0/5)DE090717 (0/5)DE100109 (0/10)DE100110 (0/9)DE100103 (0/8)DE011007 (0/27)DE091106 (0/23)DE030107 (0/8)DE011027 (0/9)DE130404 (0/11)N hospitals 144M<strong>in</strong>imum 0First quartile 9.1Median 16.7Third quartile 25Maximum 83.3DE011062 (1/26)DE040202 (1/25)DE010701 (3/67)DE011028 (1/20)DE070103 (1/20)DE011086 (2/40)DE011018 (1/16)DE100128 (1/16)DE091104 (1/16)DE040204 (1/15)DE011039 (1/14)DE090715 (2/27)DE030103 (2/27)DE0102A (13/172)DE091105 (2/26)DE011066 (2/25)DE0401A (12/145)DE0102B (1/12)DE090832 (1/12)DE091135 (3/36)DE011003 (2/23)DE011041 (1/11)DE0401D (1/11)DE091120 (3/31)DE011081 (1/10)DE030101 (4/37)DE100113 (1/9)DE011022 (4/36)DE011045 (3/26)DE090708 (5/43)DE011020 (6/50)DE110101 (7/58)DE091119 (1/8)DE011019 (1/8)DE091129 (3/24)DE091114 (1/8)DE0401C (1/8)DE011010 (6/47)DE090707 (4/31)DE070101 (16/124)DE011005 (2/15)DE090704 (2/15)DE091132 (6/45)DE091143 (2/15)DE011032 (1/7)DE011026 (4/28)DE100131 (1/7)DE090716 (15/104)DE011068 (3/20)DE091107 (2/13)DE011004 (4/26)DE011021 (10/65)DE090719 (2/13)DE011031 (4/26)DE120301 (20/129)DE091117 (5/32)DE011083 (14/89)DE091146 (3/18)DE011024 (6/36)DE100108 (1/6)DE011029 (2/12)DE030110 (1/6)DE030801 (1/6)DE090706 (6/34)DE2020 (11/62)DE090710 (4/22)DE011087 (2/11)DE011101 (30/165)DE100101 (5/27)DE090819 (3/16)DE091126 (6/32)DE091134 (3/16)DE090718 (9/47)DE090701 (14/70)DE091121 (1/5)DE100136 (5/25)DE030109 (7/34)DE090807 (4/19)DE011012 (8/38)DE011063 (4/19)DE091108 (3/14)DE090713 (6/28)DE090709 (14/65)DE100107 (2/9)DE010702 (2/9)DE011037 (6/27)DE090814 (3/13)DE030108 (8/34)DE030102 (5/21)DE011038 (15/61)DE090705 (21/84)DE100119 (2/8)DE130307 (12/48)DE091116 (3/12)DE011061 (4/16)DE011085 (11/44)DE011016 (2/8)DE090806 (12/47)DE130403 (20/75)DE011042 (7/26)DE130320 (7/26)DE091101 (12/44)DE040201 (10/36)DE091131 (7/25)DE100129 (2/7)DE100120 (2/7)DE011025 (8/27)DE090812 (3/10)DE091145 (3/10)DE091125 (12/39)DE011017 (4/13)DE091122 (11/35)DE090833 (6/19)DE090803 (8/25)DE090905 (3/9)DE090901 (3/9)DE0401B (3/9)DE090906 (3/9)DE090714 (7/21)DE011014 (7/20)DE130201 (51/143)DE090801 (19/52)DE130312 (20/53)DE090804 (13/31)DE100111 (5/11)DE090802 (7/13)DE011088 (4/7)DE011050 (3/5)DE011079 (17/26)DE011058 (5/6)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSANote. Individual laboratories may serve a large number of hospitals over awide geographical area with<strong>in</strong> Germany.122


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesDE090717 (0/6)DE011041 (0/8)DE090814 (0/6)DE011015 (0/12)DE100103 (1/16)DE011088 (1/16)DE100110 (1/16)DE011029 (2/30)DE090803 (2/26)DE090807 (2/25)DE090706 (3/37)DE100102 (1/12)DE011028 (2/23)DE091114 (1/11)DE030107 (1/11)N hospitals 154M<strong>in</strong>imum 0First quartile 16.3Median 22.7Third quartile 29.4Maximum 61.1DE091117 (6/61)DE100138 (2/20)DE011079 (1/9)DE090812 (1/9)DE040204 (4/32)DE130320 (5/39)DE090718 (10/77)DE011039 (5/38)DE100106 (2/15)DE011026 (4/30)DE091145 (2/15)DE090901 (4/30)DE0401B (2/14)DE090704 (4/28)DE100111 (1/7)DE011022 (10/69)DE010701 (22/151)DE011062 (7/48)DE011032 (2/13)DE091116 (2/13)DE091122 (15/97)DE100108 (3/19)DE130307 (4/25)DE040202 (7/43)DE030103 (10/60)DE090804 (3/18)DE091126 (10/60)DE090833 (7/41)DE091131 (6/35)DE091143 (4/23)DE100109 (4/23)DE100136 (7/40)DE090715 (10/57)DE100131 (3/17)DE100119 (2/11)DE011045 (6/33)DE0401A (37/200)DE090806 (11/59)DE011003 (6/32)DE130403 (29/147)DE100107 (2/10)DE011068 (5/25)DE030110 (1/5)DE100132 (1/5)DE011031 (11/54)DE011038 (16/78)DE091133 (8/39)DE091104 (6/29)DE011021 (11/53)DE090906 (5/24)DE090713 (4/19)DE091106 (8/38)DE070103 (4/19)DE011012 (10/47)DE091120 (12/56)DE091129 (12/55)DE090802 (7/32)DE100128 (2/9)DE100129 (2/9)DE011006 (2/9)DE091105 (13/58)DE011018 (5/22)DE091108 (5/22)DE011017 (8/35)DE090719 (6/26)DE040201 (15/64)DE011020 (20/84)DE011087 (5/21)DE090705 (21/88)DE010703 (7/29)DE100101 (14/58)DE090819 (11/45)DE011010 (15/61)DE091121 (3/12)DE090905 (2/8)DE100113 (3/12)DE100120 (5/20)DE011081 (3/12)DE091101 (13/51)DE090801 (23/90)DE091125 (10/39)DE090707 (8/31)DE011024 (25/96)DE091132 (18/69)DE090708 (16/61)DE011083 (44/167)DE011086 (12/45)DE090701 (23/86)DE090709 (30/110)DE030109 (15/55)DE010702 (9/33)DE120301 (42/154)DE011042 (11/40)DE011007 (12/43)DE011004 (9/32)DE091147 (4/14)DE130312 (18/63)DE090716 (49/171)DE070101 (61/212)DE030102 (9/31)DE011061 (10/34)DE130201 (35/119)DE090832 (5/17)DE090710 (8/27)DE091135 (19/64)DE011025 (14/47)DE2020 (15/50)DE030101 (18/60)DE011027 (3/10)DE091146 (9/30)DE0102B (3/10)DE011063 (7/23)DE0102A (96/301)DE011085 (17/52)DE100112 (3/9)DE011066 (16/48)DE011067 (5/15)DE090820 (2/6)DE030108 (13/38)DE011014 (13/38)DE011005 (12/35)DE090714 (9/26)DE110101 (25/68)DE011044 (3/8)DE130404 (5/13)DE011101 (100/257)DE011102 (2/5)DE091138 (2/5)DE011050 (2/5)DE011001 (4/10)DE091112 (5/12)DE011037 (19/45)DE011016 (9/20)DE091134 (5/11)DE091107 (5/11)DE070102 (7/14)DE0401C (3/6)DE091119 (7/13)DE011019 (11/18)0 25 50 75 100Hospital codesDE040202 (0/5)DE100128 (0/5)DE091129 (0/6)DE030109 (0/9)DE011063 (0/6)DE011014 (0/6)DE011012 (0/6)N hospitals 70M<strong>in</strong>imum 0First quartile 0Median 6.5Third quartile 16Maximum 57.1DE090706 (0/6)DE011024 (0/15)DE011007 (0/6)DE011066 (0/6)DE011004 (0/10)DE011038 (0/8)DE091126 (0/7)DE011044 (0/5)DE091105 (0/11)DE090705 (0/7)DE091106 (0/5)DE090804 (0/5)DE090718 (0/7)DE011022 (0/10)DE030108 (0/7)DE030101 (0/15)DE090719 (0/5)DE030103 (0/13)DE090833 (0/5)DE090802 (0/6)DE011042 (0/10)DE090715 (0/9)DE091131 (0/7)DE011025 (0/6)DE090906 (0/7)DE0401A (2/39)DE011083 (1/19)DE0102A (3/51)DE120301 (2/28)DE090801 (1/14)DE090701 (1/13)DE090806 (1/12)DE011031 (1/10)DE130312 (2/20)DE011062 (1/9)DE011021 (1/8)DE130307 (1/8)DE091101 (1/8)DE100101 (1/7)DE110101 (2/14)DE011086 (1/7)DE011017 (1/7)DE090708 (1/7)DE011020 (2/13)DE090716 (3/19)DE070101 (4/25)DE040201 (2/12)DE011005 (1/5)DE2020 (2/10)DE070103 (1/5)DE011010 (2/10)DE091135 (1/5)DE090819 (1/5)DE090709 (4/19)DE130403 (8/35)DE091122 (3/13)DE091132 (2/8)DE130201 (4/16)DE011101 (25/81)DE091134 (2/5)DE091125 (3/6)DE011058 (4/8)DE091133 (4/7)0 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>123


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTGreeceGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 - - 34 682 35 1 076 32 621 - - - -2004 - - 35 610 39 1 131 34 565 - - - -2005 - - 35 682 35 1 140 34 737 33 774 33 6992006 - - 42 828 41 1 253 39 949 38 841 38 8182007 - - 41 819 43 1 234 39 999 38 972 37 8022008 - - 46 907 44 1 462 42 992 41 1 093 42 9202009 - - 48 1 025 49 1 831 47 1 190 47 1 649 47 1 1232010 - - 44 902 45 1 549 43 1 105 40 1 703 42 1 0142011 - - 39 826 37 1 437 36 1 122 38 1 671 35 948Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R - - - - - - - - -Penicill<strong>in</strong> RI - - - - - - - - -Macrolides RI - - - - - - - - -Staphylococcus aureusOxacill<strong>in</strong>/Meticill<strong>in</strong> R 45 44 42 43 48 41 40 39 39Escherichia coliAm<strong>in</strong>openicil<strong>in</strong>s R 44 46 46 46 48 50 51 52 55Am<strong>in</strong>oglycosides R 6 6 7 7 9 15 14 16 17Fluoroqu<strong>in</strong>olones R 12 12 12 14 19 22 23 24 27Third-gen. cephalospor<strong>in</strong>s R 6 6 7 6 8 10 10 14 15Carbapenems R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood - - 100 39 100 25 100 5 100 23 97 75 97 48CSF - - - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTGreeceFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)No data reportedGR009X (0/5)GR052X (1/8)GR043X (3/18)GR018X (3/17)GR062X (4/18)GR027X (12/50)GR050X (8/31)GR026X (7/27)GR047X (33/122)GR031X (20/72)GR035X (15/53)GR030X (29/88)GR010X (4/12)GR038X (3/9)GR005X (10/29)GR051X (7/19)GR037X (29/78)GR001X (20/53)N hospitals 40M<strong>in</strong>imum 0First quartile 28Median 38.9Third quartile 51Maximum 77.8Hospital codesGR028X (20/53)GR024X (25/66)GR055X (4/10)GR015X (20/50)GR075X (25/62)GR040X (81/192)GR042X (7/16)GR068X (17/38)GR070X (9/20)GR039X (35/74)GR013X (9/18)GR049X (15/30)GR014X (27/52)GR041X (25/48)GR007X (33/63)GR048X (7/13)GR033X (27/49)GR012X (18/32)GR071X (4/7)GR032X (11/17)GR004X (6/9)GR059X (7/9)0 25 50 75 100% MRSA126


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesGR026X (0/27)GR010X (1/15)GR027X (13/130)GR051X (2/16)GR052X (3/24)GR038X (4/28)GR009X (1/7)GR050X (14/87)GR068X (6/37)GR004X (1/6)GR064X (1/6)GR048X (4/23)GR071X (4/23)GR018X (8/45)GR042X (7/39)GR032X (6/33)GR011X (8/39)GR012X (11/50)GR047X (71/315)GR001X (28/123)GR024X (35/152)GR062X (4/17)GR028X (20/84)GR035X (35/145)GR041X (33/133)GR033X (21/80)GR030X (38/140)GR070X (6/22)GR015X (26/93)GR043X (14/50)GR060X (4/14)GR075X (37/127)GR031X (30/101)GR014X (32/107)GR037X (28/85)GR040X (89/268)GR005X (26/74)GR013X (9/24)GR055X (6/14)GR049X (9/21)GR059X (3/7)GR039X (34/77)GR007X (17/36)N hospitals 43M<strong>in</strong>imum 0First quartile 16.7Median 23.5Third quartile 29.7Maximum 47.20 25 50 75 100Hospital codesGR011X (3/13)GR051X (2/7)GR052X (2/6)GR055X (7/15)GR018X (10/20)GR038X (7/14)GR047X (93/159)GR033X (48/82)GR049X (18/30)GR027X (102/170)GR062X (8/13)GR028X (51/81)GR070X (14/21)GR035X (75/108)GR001X (63/89)GR048X (25/35)GR012X (43/60)GR005X (49/65)GR039X (154/204)GR031X (100/132)GR075X (92/121)GR026X (32/42)GR030X (183/238)GR014X (157/201)GR010X (31/39)GR007X (44/55)GR068X (81/101)GR024X (94/117)GR013X (9/11)GR041X (118/144)GR050X (55/67)GR040X (380/459)GR043X (54/65)GR032X (13/15)GR015X (79/91)GR037X (211/243)N hospitals 36M<strong>in</strong>imum 23.1First quartile 60Median 75.4Third quartile 80.3Maximum 86.80 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>127


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTHungaryGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 20 134 27 858 27 842 25 279 - - - -2004 26 143 30 1 020 28 967 26 366 - - - -2005 23 133 28 1 083 27 1 046 27 476 21 314 24 5072006 23 151 27 1 127 26 1 135 25 453 24 302 25 5462007 22 146 26 1 199 25 1 179 26 400 23 322 24 5182008 22 166 26 1 181 25 1 057 21 428 23 369 25 5132009 22 143 26 1 068 25 1 057 27 444 24 361 25 5182010 27 140 30 1 224 29 1 385 29 591 29 514 28 6362011 27 139 28 1 156 30 1 227 28 582 27 432 29 606Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 3


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 67 11 100 28 100 34 100 0 100 1 98 49 97 23CSF 33 18 - - - - - - - - 2 57 3 19GenderMale 54 10 57 28 43 36 57 0 56 2 56 54 57 25Female 44 18 41 28 56 33 41 0 42 0 43 42 40 21Unknown 2 0 2 33 1 19 2 0 2 0 1 86 3 16Age (years)0–4 9 20 1 6 3 12 4 0 4 0 7 48 5 185–19 6 18 2 5 1 22 1 0 1 0 1 60 2 1220–64 48 15 45 26 38 33 39 0 46 1 43 50 49 2765 and over 36 8 52 31 58 36 57 0 48 2 48 48 45 20Unknown


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTHungaryFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesHU024 (0/10)HU035 (0/10)HU040 (0/12)HU039 (0/5)HU020 (0/7)HU019 (0/8)HU009 (1/22)HU022 (3/43)HU002 (1/9)HU034 (2/15)HU041 (1/7)HU029 (4/25)HU033 (2/10)HU028 (2/10)HU026 (1/5)HU006 (2/8)HU032 (7/28)HU027 (2/7)HU005 (2/7)HU025 (4/10)N laboratories 20M<strong>in</strong>imum 0First quartile 0Median 13.8Third quartile 22.5Maximum 400 25 50 75 100Hospital codesHU034C (0/11)HU002Y (0/14)HU038X (0/12)HU025A (4/94)HU034A (5/71)HU024A (7/60)HU020L (1/8)HU002M (1/8)HU019A (17/123)HU022Y (1/7)HU027A (3/20)HU002L (1/6)HU022P (8/41)HU037A (2/10)HU041A (15/69)HU006W (2/9)HU002G (7/30)HU035A (18/74)HU009B (9/35)HU028A (38/145)HU006B (5/19)HU038I (4/15)HU022I (39/143)HU026A (24/87)HU012G (13/47)HU040A (34/121)HU001Q (2/7)HU019H (3/10)HU032A (49/162)HU001P (4/13)HU033A (48/135)HU009A (55/154)HU031A (4/11)HU029V (93/250)HU005A (21/56)HU020A (20/53)HU007C (6/14)HU020C (3/7)HU008F (3/7)HU039A (22/49)HU007B (16/34)HU012P (10/19)HU004G (5/9)HU038A (14/25)HU006A (9/16)HU022S (9/14)N hospitals 46M<strong>in</strong>imum 0First quartile 16.7Median 27.4Third quartile 37.5Maximum 64.30 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA130


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesHU002L (0/7)HU001R (0/10)HU009B (1/16)HU034C (1/12)HU022P (2/18)HU004G (1/7)HU038X (1/6)HU032X (1/6)HU038A (3/18)HU002G (5/28)HU037A (1/5)HU012P (4/19)HU019A (25/114)HU024A (20/91)HU020L (4/18)HU027A (12/48)HU006B (2/8)HU020C (2/8)HU038I (3/12)HU026A (13/47)HU022I (84/298)HU002M (4/14)HU006A (9/31)HU012G (9/31)HU029V (78/265)HU040A (28/95)HU034A (28/89)HU019H (2/6)HU002D (2/6)HU031A (3/9)HU007C (2/6)HU001P (2/6)HU033A (43/128)HU039A (23/66)HU025A (52/149)HU020A (17/46)HU041A (29/77)HU006W (2/5)HU016D (2/5)HU032A (59/146)HU035A (32/75)HU007B (20/41)HU005A (22/45)HU028A (102/208)HU027L (3/6)HU009A (96/174)HU022S (8/14)HU006R (3/5)N hospitals 48M<strong>in</strong>imum 0First quartile 21.5Median 29.2Third quartile 37.3Maximum 600 25 50 75 100Hospital codesHU024A (0/10)HU019A (0/18)HU034A (1/14)HU040A (3/22)HU022I (2/11)HU002G (2/9)HU026A (3/13)HU041A (7/27)HU007B (5/18)HU027A (2/7)HU033A (19/42)HU009A (19/42)HU039A (10/21)HU025A (32/64)HU031A (4/8)HU029V (63/126)HU006A (8/15)HU032A (68/127)HU001P (14/26)HU020A (6/11)HU004G (5/9)HU035A (20/34)HU032X (3/5)HU001R (3/5)HU005A (11/18)HU028A (99/154)HU012G (6/9)HU012P (35/40)N hospitals 28M<strong>in</strong>imum 0First quartile 24.5Median 50Third quartile 57.2Maximum 87.50 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>131


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTIcelandGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 2 35 2 64 2 100 2 22 - - - -2004 2 54 2 55 2 119 1 27 - - - -2005 2 37 2 78 2 130 2 31 2 22 1 132006 2 52 2 57 2 130 2 40 2 13 1 92007 2 42 2 65 2 105 1 29 2 27 1 112008 2 46 2 63 2 123 2 17 1 24 2 72009 2 35 2 59 2 111 2 51 2 27 2 162010 2 37 2 65 2 104 2 31 2 27 2 122011 2 32 2 71 2 130 2 32 2 26 2 17Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 90 5 100 2 100 13 100 0 100 3 100 6 100 3CSF 10 29 - - - - - - - - - - - -GenderMale 65 7 63 2 45 15 50 0 66 5 57 7 72 5Female 35 8 38 2 55 10 50 0 34 0 43 4 28 0Age (years)0–4 12 38 5 0 2 0 3 0 3 0 - - 3 05–19 3 0 4 0 1 0 - - 3 0 - -20–64 43 3 44 3 37 14 35 0 48 0 51 4 52 065 and over 42 3 46 2 60 12 62 0 45 8 49 8 45 8Hospital departmentICU 6 0 3 0


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTIcelandFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 2M<strong>in</strong>imum 6.6First quartile 6.6Median 9.5Third quartile 12.5Maximum 12.5N hospitals 2M<strong>in</strong>imum 0First quartile 0Median 1.4Third quartile 2.8Maximum 2.8IS001 (4/61)IS003A (0/21)Laboratory codesHospital codesIS003 (1/8)IS001A (3/109)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA134


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)N hospitals 4M<strong>in</strong>imum 0First quartile 0Median 6.5Third quartile 20.8Maximum 28.6N hospitals 2M<strong>in</strong>imum 0First quartile 0Median 3.3Third quartile 6.7Maximum 6.7IS001G (0/5)IS003A (0/5)IS001B (0/10)Hospital codesHospital codesIS001A (24/185)IS001A (3/45)IS001C (2/7)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>135


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTIrelandGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 24 363 26 1 108 26 978 21 348 - - - -2004 28 399 38 1 286 37 1 235 29 418 - - - -2005 31 397 38 1 360 39 1 424 33 502 15 42 11 292006 32 406 38 1 347 39 1 638 32 550 28 211 23 1282007 33 435 41 1 332 42 1 750 37 598 31 237 29 1722008 35 442 38 1 242 41 1 875 37 685 33 307 29 1912009 34 356 41 1 261 41 2 012 38 671 37 316 30 2362010 32 310 39 1 207 40 2 121 38 670 34 318 30 2192011 32 324 39 1 057 38 2 167 36 608 34 304 28 181Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 3 3 3 3 6 6 6 5 6Penicill<strong>in</strong> RI 12 10 11 16 17 23 20 18 19Macrolides RI 12 14 12 16 17 17 17 16 18Staphylococcus aureusOxacill<strong>in</strong>/Meticill<strong>in</strong> R 42 41 42 42 38 33 27 24 24Escherichia coliAm<strong>in</strong>openicil<strong>in</strong>s R 61 65 67 69 65 67 66 67 70Am<strong>in</strong>oglycosides R 4 5 7 7 10 9 9 10 10Fluoroqu<strong>in</strong>olones R 10 12 17 21 21 23 22 23 23Third-gen. cephalospor<strong>in</strong>s R 2 2 4 4 5 6 6 8 9Carbapenems R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 97 19 100 24 100 23 100 2 100 37 100 8 99 6CSF 3 13 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTIrelandFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)IE-60 (0/17)IE-18 (0/6)IE-15 (2/34)N laboratories 27M<strong>in</strong>imum 0First quartile 12.7Median 16.7Third quartile 30.8Maximum 44.4IE-49 (0/21)IE-65 (0/11)IE-37 (0/8)IE-21 (0/17)IE-63 (0/5)IE-77 (0/15)N hospitals 50M<strong>in</strong>imum 0First quartile 17.3Median 24.4Third quartile 31.3Maximum 57.1IE-32 (2/24)IE-59 (1/35)IE-48 (2/20)IE-43 (1/19)IE-46 (6/56)IE-49 (1/8)IE-71 (1/8)IE-57 (2/15)IE-10 (9/71)IE-64 (1/7)IE-60 (9/52)IE-46 (2/15)IE-11 (9/51)IE-4 (19/103)IE-61 (1/7)IE-48 (14/74)IE-15 (29/153)IE-2 (6/41)IE-76 (2/10)IE-79 (2/10)IE-1 (6/40)IE-12 (7/31)IE-31 (2/13)IE-6 (12/53)IE-18 (5/22)Laboratory codesIE-50 (7/45)IE-65 (1/6)IE-34 (11/55)Hospital codesIE-36 (4/17)IE-50 (35/145)IE-44 (9/37)IE-34 (30/123)IE-20 (34/139)IE-35 (2/8)IE-30 (4/19)IE-2 (48/192)IE-1 (39/152)IE-44 (3/14)IE-33 (7/27)IE-31 (11/41)IE-6 (4/15)IE-73 (5/17)IE-4 (9/33)IE-29 (38/128)IE-32 (11/37)IE-25 (10/34)IE-10 (28/91)IE-61 (5/16)IE-58 (4/13)IE-80 (5/16)IE-30 (11/35)IE-62 (5/16)IE-52 (6/19)IE-70 (9/28)IE-20 (10/30)IE-62 (5/15)IE-74 (12/36)IE-43 (2/6)IE-47 (13/37)IE-47 (6/16)IE-38 (4/11)IE-58 (16/41)IE-70 (5/12)IE-13 (10/25)IE-51 (4/8)IE-74 (4/9)0 25 50 75 100IE-26 (8/14)IE-81 (4/7)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA138


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesIE-57 (0/24)IE-77 (0/23)IE-37 (0/8)IE-59 (0/23)IE-51 (3/35)IE-65 (3/25)IE-72 (1/8)IE-73 (6/47)IE-46 (4/31)IE-11 (13/98)IE-80 (4/29)IE-2 (46/330)IE-68 (1/7)IE-18 (5/31)IE-13 (14/86)IE-67 (2/12)IE-10 (28/167)IE-30 (13/76)IE-49 (3/17)IE-60 (23/119)IE-48 (30/154)IE-50 (37/188)IE-44 (15/74)IE-70 (13/64)IE-21 (7/34)IE-38 (6/29)IE-81 (4/19)IE-76 (4/19)IE-47 (23/107)IE-33 (11/51)IE-74 (22/99)IE-61 (10/44)IE-35 (6/26)IE-63 (4/17)IE-34 (43/182)IE-12 (18/75)IE-31 (25/102)IE-1 (69/277)IE-64 (2/8)IE-32 (29/116)IE-15 (62/244)IE-52 (11/42)IE-26 (9/34)IE-43 (14/51)IE-20 (70/251)IE-6 (26/89)IE-4 (48/157)IE-62 (17/54)IE-36 (14/43)IE-53 (4/12)IE-40 (2/6)IE-27 (2/6)IE-29 (79/218)IE-79 (7/19)IE-58 (41/101)IE-71 (13/30)IE-23 (3/6)N hospitals 57M<strong>in</strong>imum 0First quartile 16.3Median 21.5Third quartile 26.5Maximum 500 25 50 75 100Hospital codesIE-32 (0/11)IE-47 (0/14)IE-80 (0/7)IE-30 (0/11)IE-48 (0/16)IE-31 (0/9)IE-33 (0/5)IE-6 (0/10)IE-50 (0/20)IE-13 (0/8)IE-73 (0/7)IE-12 (0/10)IE-21 (0/11)IE-29 (1/31)IE-1 (3/57)IE-74 (1/16)IE-60 (1/14)IE-10 (2/20)IE-44 (1/10)IE-34 (4/38)IE-11 (1/9)IE-2 (6/53)IE-15 (6/50)IE-58 (2/15)IE-20 (7/51)IE-18 (2/12)IE-4 (5/28)IE-71 (1/5)IE-46 (2/7)IE-81 (3/5)N hospitals 30M<strong>in</strong>imum 0First quartile 0Median 5.8Third quartile 12Maximum 600 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>139


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTItalyGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 44 293 46 1 480 17 923 44 634 - - - -2004 37 271 42 1 225 14 645 40 576 - - - -2005 38 331 41 1 479 16 1 195 40 714 38 344 - -2006 34 269 38 1 164 13 910 35 650 32 321 12 1832007 34 298 38 1 167 14 1 052 36 656 37 391 10 1852008 27 194 30 939 14 957 31 580 27 331 11 1682009 21 216 23 987 9 863 22 509 22 313 10 1952010 33 323 35 1 886 23 2 623 35 1 106 34 739 23 5172011 29 294 31 1 372 21 2 098 31 841 30 688 21 355Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 5 5 5


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 88 8 100 37 100 40 100 2 100 4 98 46 98 21CSF 12 8 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTItalyFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)IT024 (0/15)IT028 (0/6)N laboratories 18M<strong>in</strong>imum 0First quartile 0Median 6.5Third quartile 7.7Maximum 50IT0071 (1/25)IT0001 (6/44)IT0024 (7/46)IT0019 (24/125)N hospitals 42M<strong>in</strong>imum 4First quartile 26.3Median 35.7Third quartile 43.4Maximum 64.9IT0059 (29/147)IT086 (0/5)IT0088 (8/39)IT0064 (16/76)IT037 (0/52)IT0077 (10/47)IT0025 (11/49)IT0015 (5/22)IT090 (0/24)IT0067 (49/186)IT0028 (9/33)IT064 (1/23)IT0045 (14/50)IT0092 (23/74)IT091 (2/34)IT0072 (39/125)IT004E (12/37)IT0061 (71/217)IT019 (1/16)IT0047 (9/26)IT004B (7/20)Laboratory codesIT004 (2/31)IT061 (2/31)Hospital codesIT0049 (17/48)IT0042 (16/45)IT0022 (43/120)IT004D (9/25)IT004A (11/30)IT022 (1/15)IT004F (14/38)IT0023 (30/81)IT072 (2/30)IT0090 (22/59)IT0031 (19/49)IT089 (2/28)IT0060 (22/55)IT0070 (29/71)IT004G (34/81)IT060 (2/26)IT0085 (33/76)IT0074 (32/73)IT085 (3/12)IT0091 (78/158)IT0052 (26/52)IT042 (2/8)IT004C (6/12)IT0037 (65/130)IT0034 (40/70)IT077 (2/6)IT0086 (39/65)IT0040 (46/74)IT034 (7/14)IT0035 (59/93)IT0089 (87/134)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA142


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)IT0047 (9/44)IT0001 (16/56)IT0061 (71/248)N hospitals 32M<strong>in</strong>imum 20.5First quartile 36Median 39.8Third quartile 47.3Maximum 62.6IT0061 (3/84)IT004G (2/21)IT004C (1/8)IT0059 (6/45)N hospitals 42M<strong>in</strong>imum 3.6First quartile 27.8Median 48.1Third quartile 63.5Maximum 80.3IT004G (58/192)IT0023 (6/29)IT0037 (100/294)IT0070 (54/157)IT0024 (2/9)IT0072 (6/26)IT0070 (4/17)IT0035 (55/154)IT004E (6/25)IT0059 (105/292)IT0072 (59/164)IT0086 (7/26)IT004F (5/18)IT0028 (2/7)IT004C (15/41)IT0035 (14/44)IT004D (26/68)IT0090 (51/133)IT0025 (12/34)IT0090 (5/14)IT0088 (16/44)IT0023 (58/151)IT0085 (12/30)Hospital codesIT0019 (107/275)IT0086 (44/112)IT004F (33/83)IT0089 (105/264)IT004B (27/67)IT0092 (61/145)Hospital codesIT0031 (10/22)IT0042 (10/22)IT0034 (16/34)IT0091 (41/87)IT0019 (26/53)IT0089 (21/42)IT0074 (3/6)IT0047 (9/18)IT0091 (101/238)IT0067 (72/169)IT004E (70/156)IT0034 (63/140)IT0085 (61/129)IT0015 (9/19)IT0042 (35/71)IT0049 (35/69)IT004A (35/68)IT0025 (73/140)IT0040 (33/59)IT0075 (17/30)IT0088 (67/107)0 25 50 75 100IT004A (5/10)IT0037 (34/66)IT0067 (22/41)IT0022 (15/25)IT004B (12/20)IT0015 (14/23)IT0040 (40/63)IT0064 (21/33)IT004D (13/20)IT0001 (18/27)IT0060 (6/9)IT0077 (24/35)IT0049 (30/42)IT0052 (18/25)IT0075 (27/36)IT0071 (13/17)IT0092 (57/71)0 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>143


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLatviaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2004–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2004 4 17 7 87 - - - - - - - -2005 5 36 7 127 - - - - - - - -2006 7 37 11 172 10 62 10 56 6 28 9 162007 6 31 12 169 9 76 8 57 7 27 6 162008 3 18 12 164 10 90 9 51 11 40 6 112009 7 30 12 188 9 86 8 48 10 44 7 182010 4 38 10 155 8 98 8 61 8 64 6 212011 5 51 11 197 9 132 8 59 9 65 4 12Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R -


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 73 5 100 12 100 16 100 0 100 11 98 46 97 13CSF 27 19 - - 0 0 - - - - 2 100 3 0GenderMale 55 2 53 13 32 21 51 0 51 9 53 43 39 15Female 45 17 47 10 68 14 49 0 49 14 47 50 61 10Age (years)0–4 13 40 8 4 8 6 8 0 2 0 16 33 9 05–19 1 100 4 7 2 0 1 0 - - 2 100 - -20–64 58 2 47 14 41 15 43 0 49 14 49 52 42 2965 and over 27 5 40 9 49 19 47 0 47 10 33 43 48 0Unknown - - 1 100 0 0 - - 2 0 1 0 - -Hospital departmentICU 57 5 23 19 25 28 38 0 67 13 43 61 48 19Internal med. 9 29 41 11 27 15 24 0 16 14 19 40 33 9Surgery - - 8 15 4 44 8 0 9 0 4 40 6 0Other 19 13 20 9 27 7 19 0 7 0 18 35 9 0Unknown 14 9 8 0 17 8 11 0 2 0 16 30 3 0PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.145


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLatviaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 4M<strong>in</strong>imum 0First quartile 1.2Median 3.7Third quartile 30.3Maximum 55.6LV009A (0/5)N hospitals 11M<strong>in</strong>imum 0First quartile 0Median 5.9Third quartile 14.4Maximum 16.7LV001 (0/7)LV006A (0/5)LV005A (0/18)LV008A (0/6)LV004 (1/41)LV002A (1/25)Laboratory codesHospital codesLV003A (2/34)LV012A (2/23)LV003 (1/20)LV013A (1/7)LV004A (14/97)LV002 (5/9)LV001A (19/117)LV011A (1/6)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA146


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)LV005A (0/7)N hospitals 6M<strong>in</strong>imum 0First quartile 0Median 8Third quartile 18.2Maximum 34.7LV003A (1/7)N hospitals 5M<strong>in</strong>imum 14.3First quartile 36.1Median 40Third quartile 44.4Maximum 63.3LV002A (0/14)LV004A (13/36)LV003A (2/58)Hospital codesHospital codesLV012A (4/10)LV012A (2/16)LV002A (8/18)LV004A (14/77)LV001A (17/49)LV001A (31/49)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>147


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLithuaniaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2006–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2006 9 35 13 167 11 171 8 30 8 35 7 142007 10 67 12 240 13 235 10 56 10 41 7 212008 11 48 12 278 12 304 10 67 11 54 7 212009 10 46 13 258 13 297 11 57 12 68 8 212010 9 40 11 257 10 333 10 59 9 81 8 312011 8 48 10 279 10 385 9 74 10 137 6 30Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R - - -


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 92 18 100 10 100 13 100 0 100 8 99 56 100 23CSF 8 0 - - - - - - - - 1 100 - -GenderMale 70 11 54 9 37 16 65 0 54 15 60 60 67 20Female 30 27 45 11 62 12 35 0 46 0 40 52 33 30Unknown - - 1 0 0 0 - - - - - - - -Age (years)0–4 26 26 4 5 4 15 10 0 8 0 6 85 2 05–19 5 25 6 0 2 7 1 0 6 33 1 100 2 020–64 51 14 44 8 38 18 35 0 32 13 39 52 45 3065 and over 18 6 45 13 56 10 54 0 54 4 54 56 52 19Unknown - - 1 0 0 0 - - - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLithuaniaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)LT004 (0/7)N laboratories 6M<strong>in</strong>imum 0First quartile 0Median 8Third quartile 26.7Maximum 37.5LT002A (0/14)N hospitals 13M<strong>in</strong>imum 0First quartile 3.8Median 7.7Third quartile 16.7Maximum 50LT009F (0/8)LT013B (0/17)LT005 (0/5)LT011A (1/26)LT012A (1/21)LT007 (1/13)LT007A (4/82)Laboratory codesHospital codesLT001A (11/142)LT013 (2/24)LT013A (4/33)LT005A (10/69)LT001 (4/15)LT004A (11/66)LT003A (4/19)LT013D (2/6)LT011 (6/16)LT001B (3/6)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA150


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)LT013C (0/9)N hospitals 14M<strong>in</strong>imum 0First quartile 6.5Median 12.9Third quartile 18.2Maximum 23.5LT013A (6/19)N hospitals 9M<strong>in</strong>imum 31.6First quartile 47.6Median 56.8Third quartile 57.9Maximum 100LT005A (4/106)LT012A (1/16)LT007A (8/20)LT009F (2/31)LT005A (10/21)LT007A (7/99)LT013B (1/13)LT009F (3/6)Hospital codesLT013A (11/101)LT002A (3/20)Hospital codesLT001A (25/44)LT004A (8/51)LT003A (12/21)LT002F (1/6)LT012A (11/19)LT001B (2/11)LT003A (6/31)LT004A (32/39)LT011A (4/19)LT011A (12/12)LT001A (42/179)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>151


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLuxembourgGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 7 54 8 95 8 227 7 41 - - - -2004 6 36 7 96 7 216 5 28 - - - -2005 5 47 5 83 5 188 5 31 - - 1 12006 5 31 5 77 5 167 4 42 4 21 4 232007 6 48 6 117 6 275 5 37 6 52 5 362008 6 59 5 117 6 303 5 61 6 52 4 332009 6 67 6 113 6 301 5 54 3 28 6 352010 6 50 6 134 6 354 6 70 6 59 6 322011 5 52 5 127 5 354 5 76 4 48 5 32Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 87 10 100 18 100 25 100 4 100 17 98 18 97 13CSF 13 8 - - - - - - - - 2 50 3 0GenderMale 54 9 63 15 42 25 72 4 65 23 58 21 55 17Female 46 11 37 24 58 25 28 4 33 0 42 16 45 7Unknown - - - - - - - - 2 100 - - - -Age (years)0–4 3 0 2 0 1 11 4 0 2 0 6 50 2 05–19 3 33 4 20 1 0 1 0 2 0 - - 2 020–64 45 11 37 15 26 22 30 7 30 29 27 38 19 865 and over 49 8 57 21 72 27 65 3 65 13 67 8 78 14Hospital departmentICU 12 25 12 32 6 24 16 0 20 0 12 23 17 9Internal med. 8 13 8 23 8 28 8 0 2 0 7 0 5 0Surgery 4 0 6 25 11 26 8 0 9 25 15 25 5 33Other 36 14 40 11 35 25 38 0 46 29 37 25 38 13Unknown 40 3 33 20 40 24 30 13 24 9 28 10 36 13PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.153


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTLuxembourgFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)LU007 (0/9)N laboratories 5M<strong>in</strong>imum 0First quartile 6.3Median 6.3Third quartile 7.7Maximum 20.7LU003C (1/13)N hospitals 7M<strong>in</strong>imum 7.7First quartile 10Median 16.7Third quartile 22.5Maximum 22.5LU001A (4/40)LU001 (2/32)LU003B (1/6)Laboratory codesLU006 (1/16)Hospital codesLU004A (3/18)LU007A (7/36)LU004 (1/13)LU006A (9/40)LU003 (6/29)LU003A (23/102)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA154


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)LU003D (0/10)N hospitals 9M<strong>in</strong>imum 0First quartile 21.4Median 25.5Third quartile 26.1Maximum 38.1LU007A (1/14)N hospitals 5M<strong>in</strong>imum 7.1First quartile 10Median 14.3Third quartile 23.4Maximum 60LU003B (1/8)LU006A (28/131)LU001A (2/20)LU004A (22/88)Hospital codesLU001A (26/102)Hospital codesLU006A (2/14)LU007A (22/85)LU003A (11/47)LU003A (63/241)LU004B (5/14)LU003B (3/5)LU003C (8/21)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>155


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTMaltaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 1 9 1 121 1 91 1 26 - - - -2004 1 18 1 94 1 91 1 41 - - - -2005 1 13 1 77 1 85 1 38 1 18 1 452006 1 31 1 90 1 94 1 53 1 32 1 512007 1 13 1 105 1 117 1 37 1 28 1 362008 1 17 1 108 1 128 1 32 1 36 1 312009 1 8 1 85 1 158 1 36 1 38 1 582010 1 11 1 108 1 192 1 37 1 57 1 422011 1 11 1 130 1 220 1 53 1 52 1 42Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTMaltaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 1M<strong>in</strong>imum 16.7First quartile 16.7Median 16.7Third quartile 16.7Maximum 16.7N hospitals 3M<strong>in</strong>imum 42.9First quartile 42.9Median 48.6Third quartile 60Maximum 60MT001E (3/7)Laboratory codesMT001 (2/12)Hospital codesMT001A (107/220)MT001F (6/10)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA158


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)N hospitals 3M<strong>in</strong>imum 27.8First quartile 27.8Median 32.5Third quartile 50Maximum 50N hospitals 3M<strong>in</strong>imum 0First quartile 0Median 12.5Third quartile 16.7Maximum 16.7MT001E (10/36)MT001E (0/6)Hospital codesMT001A (114/351)Hospital codesMT001A (12/96)MT001F (12/24)MT001F (1/6)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>159


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTNetherlandsGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 24 891 23 1 422 23 2 133 23 480 - - - -2004 22 758 22 1 339 21 2 111 22 444 - - - -2005 23 815 23 1 407 23 2 201 23 563 16 301 16 2102006 22 1 006 23 1 636 22 2 905 23 776 18 458 19 3302007 21 940 21 1 471 21 2 801 21 827 19 497 19 3382008 17 723 16 1 191 16 2 283 17 632 15 463 15 3452009 17 746 16 1 035 16 2 398 16 522 15 408 15 2352010 22 971 21 1 565 21 3 422 20 834 20 647 21 3762011 25 1 289 23 1 815 23 4 436 23 1 108 23 729 23 434Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 94 1 100 1 100 14 100 0 100 1 99 8 99 3CSF 6 3 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTNetherlandsFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesNL005 (0/23)NL112 (0/70)NL139 (0/48)NL119 (0/68)NL132 (0/77)NL131 (0/121)NL030 (0/76)NL125 (0/72)NL111 (1/98)NL134 (1/94)NL141 (1/78)NL007 (1/71)NL031 (2/123)NL026 (1/60)NL113 (3/164)NL145 (2/107)NL002 (3/149)NL126 (2/87)NL101 (2/84)NL023 (2/77)NL104 (1/19)NL014 (5/47)N laboratories 22M<strong>in</strong>imum 0First quartile 0Median 1.3Third quartile 2Maximum 10.60 25 50 75 100Hospital codesNL125B (0/21)NL014X (0/6)NL030C (0/19)NL030A (0/27)NL023B (0/25)NL026C (0/16)NL131E (0/5)N hospitals 63M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 2Maximum 12.5NL113A (0/105)NL125C (0/27)NL030D (0/53)NL113B (0/27)NL007B (0/11)NL118A (0/48)NL139B (0/43)NL118C (0/70)NL139D (0/13)NL134B (0/13)NL007C (0/21)NL112X (0/48)NL014G (0/41)NL113E (0/9)NL101B (0/14)NL132A (0/106)NL030B (0/15)NL113C (0/28)NL030F (0/28)NL030G (0/35)NL030I (0/24)NL139C (0/6)NL145B (0/29)NL111C (0/36)NL111D (0/30)NL125A (0/20)NL119A (1/135)NL145A (1/127)NL002A (1/116)NL112A (1/98)NL101A (1/96)NL131A (1/89)NL131B (1/88)NL007A (1/83)NL030E (1/78)NL126A (1/74)NL031A (1/68)NL030H (1/66)NL026A (1/66)NL104A (2/101)NL126B (3/148)NL111B (1/48)NL134A (3/143)NL141A (4/182)NL002B (2/83)NL031B (2/75)NL005A (1/37)NL023A (2/74)NL026B (2/62)NL113D (1/31)NL007X (3/80)NL118B (1/25)NL111A (1/23)NL014V (1/19)NL131X (1/10)NL131F (1/8)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA162


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesNL007B (0/18)NL026C (1/18)NL030A (5/73)NL118B (9/128)NL014V (4/53)NL111A (4/51)NL113E (4/49)N hospitals 64M<strong>in</strong>imum 0First quartile 10.4Median 13.7Third quartile 17.1Maximum 28.6NL014G (11/133)NL111D (6/70)NL104A (17/191)NL031A (13/141)NL002B (18/195)NL113C (10/102)NL118C (20/199)NL145A (28/272)NL030D (13/126)NL002A (25/240)NL007C (2/19)NL030G (12/105)NL134A (26/222)NL126B (35/296)NL134X (1/8)NL113B (12/95)NL030H (24/187)NL139C (4/31)NL131A (24/186)NL131X (5/38)NL118A (17/129)NL023B (12/91)NL113A (37/278)NL112A (25/187)NL031B (28/206)NL113D (20/145)NL111C (18/129)NL023A (22/155)NL119A (42/287)NL126A (15/102)NL005A (20/130)NL134B (4/26)NL112X (23/149)NL125C (14/89)NL101A (34/216)NL139D (9/54)NL131E (1/6)NL145B (13/77)NL132A (51/301)NL111B (22/129)NL125B (7/41)NL007A (18/105)NL139B (16/93)NL131B (37/214)NL125A (8/45)NL030C (13/72)NL030F (16/88)NL030E (40/210)NL007X (24/125)NL026A (21/109)NL141A (56/278)NL131F (6/29)NL030I (17/75)NL030B (15/65)NL014X (4/17)NL026B (28/99)NL101B (8/28)0 25 50 75 100Hospital codesNL145B (0/8)NL030E (0/31)NL030D (0/22)NL131X (0/7)NL125B (0/10)NL030F (0/11)NL031A (0/26)NL113D (0/28)NL030G (0/17)NL030A (0/12)NL126B (0/43)NL118B (0/17)NL014V (0/8)NL113E (0/6)NL030C (0/6)NL026A (0/26)NL005A (0/9)NL007B (0/6)NL023B (0/7)NL014G (0/19)NL134B (0/5)NL125A (0/5)NL113B (0/12)NL139B (0/14)NL030B (0/12)NL101A (0/43)NL023A (1/36)NL113A (1/32)NL145A (2/44)NL118A (1/21)NL113C (1/14)NL131B (3/40)NL031B (3/39)NL126A (1/13)NL026B (2/24)NL112A (3/35)NL125C (2/21)NL141A (5/52)NL118C (3/30)NL002B (3/30)NL112X (3/29)NL002A (6/56)NL030H (3/28)NL111A (1/9)NL134A (7/62)NL119A (6/53)NL007A (4/34)NL030I (1/8)NL007X (3/23)NL111C (3/22)NL111B (4/29)NL007C (1/7)NL104A (5/31)NL111D (2/12)NL139D (1/6)NL131A (9/40)NL132A (12/53)N hospitals 57M<strong>in</strong>imum 0First quartile 0Median 4.5Third quartile 10.7Maximum 22.60 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>163


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTNorwayGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 11 512 11 506 11 1 179 11 192 4 46 4 252004 11 600 11 516 11 1 212 11 235 4 51 4 272005 11 606 11 553 11 1 331 11 304 11 193 11 972006 12 601 12 734 12 1 574 12 349 12 263 12 962007 13 616 13 794 13 1 713 13 416 13 320 13 1052008 13 576 13 837 13 1 799 13 403 13 349 13 1482009 12 554 12 909 12 1 846 12 478 12 396 12 1662010 15 576 15 1 050 15 2 277 15 563 15 479 15 1682011 17 622 17 1 223 17 2 620 17 588 17 450 17 148Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 96 4 100 0 100 9 100 0 100 2 100 2 99 2CSF 4 2 - - 0 0 - - - - 0 0 1 50GenderMale 51 4 64 0 46 12 74 0 61 2 58 2 67 2Female 49 3 36 0 54 6 26 0 39 0 42 3 33 3Unknown - - 0 0


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTNorwayFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)NO402 (0/29)NO401 (0/9)N laboratories 17M<strong>in</strong>imum 0First quartile 1.1Median 2.4Third quartile 5.9Maximum 6.8NO206O (0/74)NO502K (0/19)NO304J (0/35)NO501B (0/12)NO203D (0/15)N hospitals 47M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 0Maximum 6.7NO103X (0/9)NO404 (0/26)NO404F (0/23)NO502L (0/16)NO106V (0/38)NO105 (0/49)NO501E (0/20)NO403E (0/23)NO402B (0/37)NO203 (1/89)NO206Q (0/8)NO106T (0/25)NO501 (1/56)NO106S (0/46)NO502D (0/15)NO105K (0/82)NO104 (2/93)NO106U (0/13)NO204E (0/126)NO203C (0/85)Laboratory codesNO403 (2/84)NO101 (3/123)NO204 (4/161)Hospital codesNO101D (0/59)NO304M (0/6)NO102B (0/82)NO401A (0/15)NO204M (0/11)NO502I (0/20)NO103E (0/125)NO203K (0/21)NO102 (1/27)NO203X (0/10)NO206P (0/49)NO501F (0/6)NO301 (3/61)NO404G (0/16)NO304K (0/7)NO501G (0/16)NO502 (3/51)NO104J (0/184)NO106P (0/54)NO304 (2/34)NO401C (0/14)NO501C (0/16)NO106Q (0/57)NO106 (9/137)NO101A (1/219)NO301A (1/102)NO502H (1/99)NO206 (6/91)NO204I (1/87)NO501A (1/55)NO403D (3/148)NO103 (5/74)NO101C (1/48)NO402H (1/15)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA166


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesNO501F (0/16)NO204L (0/17)NO103X (0/20)NO501E (0/34)NO204N (0/7)NO501G (0/36)NO203X (0/10)NO501A (2/122)NO106Q (3/136)NO304J (3/90)NO106S (2/59)NO502I (2/57)NO204I (5/131)NO106U (1/26)NO101C (6/131)NO501C (2/38)NO106T (4/64)NO403E (6/90)NO104J (29/409)NO101D (7/96)NO501B (3/40)NO404F (4/51)NO204M (3/37)NO401C (2/24)NO103E (29/342)NO106V (10/117)NO403D (28/323)NO206O (11/121)NO203K (5/55)NO404G (1/11)NO401A (3/32)NO502L (3/31)NO502H (14/133)NO106P (12/108)NO105K (22/195)NO204E (31/270)NO502K (3/26)NO101A (32/269)NO203C (24/193)NO304M (2/16)NO206P (12/96)NO402H (8/62)NO206Q (3/23)NO304K (2/15)NO301A (33/243)NO203D (3/22)NO402B (15/103)NO102B (27/184)NO502D (5/34)N hospitals 49M<strong>in</strong>imum 0First quartile 3.8Median 8.5Third quartile 11.5Maximum 14.70 25 50 75 100Hospital codesNO106S (0/11)NO101D (0/12)NO403E (0/15)NO206P (0/19)NO106P (0/15)NO304K (0/6)NO106T (0/9)NO106V (0/12)NO206O (0/39)NO301A (0/45)NO502I (0/6)NO106Q (0/15)NO105K (0/26)NO304J (0/12)NO501B (0/6)NO204I (0/35)NO204M (0/5)NO501G (0/6)NO204E (0/56)NO402H (0/19)NO206Q (0/7)NO204L (0/5)NO403D (0/57)NO501E (0/6)NO102B (1/40)NO103E (2/76)NO502H (1/36)NO203C (1/34)NO104J (2/59)NO501A (1/26)NO101C (1/25)NO402B (2/24)NO501C (1/11)NO101A (8/69)NO203K (1/7)NO502K (1/6)N hospitals 36M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 2.9Maximum 16.70 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>167


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTPolandGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 11 16 24 166 25 124 16 64 - - - -2004 11 16 30 262 29 192 23 52 - - - -2005 6 6 30 198 30 176 21 54 17 53 14 262006 4 9 24 174 26 206 21 68 15 42 16 372007 10 22 24 185 27 256 20 71 18 32 23 672008 34 84 15 99 14 84 11 26 11 19 8 222009 21 71 30 551 29 625 28 267 25 151 27 1532010 26 76 35 527 35 771 32 286 33 246 29 1692011 41 166 45 868 45 1 188 44 484 45 391 35 199Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 19


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 83 21 100 20 100 27 100 0 100 8 99 50 98 24CSF 17 18 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTPolandFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)PL138 (0/6)PL107 (0/8)N laboratories 20M<strong>in</strong>imum 0First quartile 15.6Median 21.1Third quartile 28.6Maximum 50PL0120 (0/10)PL0118 (0/33)PL0143 (0/30)PL0122 (0/7)PL0141 (0/16)N hospitals 44M<strong>in</strong>imum 0First quartile 7.6Median 15.7Third quartile 25Maximum 92.6PL150 (1/14)PL0136 (0/10)PL0148 (1/40)PL148 (1/13)PL0109 (2/61)PL0123 (2/46)PL110 (3/22)PL0108 (1/15)PL0121 (2/28)PL123 (3/17)PL0138 (6/74)PL0131 (1/12)PL0103 (2/20)PL143 (3/15)PL0139 (2/19)PL0107 (6/55)PL119 (1/5)PL0105 (6/52)PL0132 (1/8)PL126 (2/10)PL0149 (1/8)PL0137 (4/31)Laboratory codesPL134 (1/5)PL118 (2/9)PL116 (4/16)Hospital codesPL0150 (3/23)PL0124 (5/33)PL0106 (6/37)PL00 (1/6)PL0134 (1/6)PL0127 (3/18)PL0115 (6/34)PL121 (2/8)PL0130 (9/50)PL0101 (12/66)PL147 (2/7)PL0112 (12/58)PL0113 (4/19)PL117 (2/7)PL0104 (2/9)PL0110 (9/36)PL105 (2/7)PL0117 (3/12)PL0116 (17/68)PL0102 (6/21)PL102 (2/5)PL0119 (7/23)PL0114 (29/77)PL127 (3/7)PL0129 (2/5)PL0147 (32/79)PL106 (3/6)PL0135 (9/20)PL0133 (6/13)PL101 (3/6)PL0126 (32/67)PL0142 (25/27)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA170


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)PL0132 (0/7)PL0133 (0/7)PL0139 (2/25)PL0108 (3/21)N hospitals 41M<strong>in</strong>imum 0First quartile 17.6Median 22.8Third quartile 34.3Maximum 63.6PL0121 (0/6)PL0127 (0/6)PL0138 (0/11)N hospitals 31M<strong>in</strong>imum 0First quartile 25Median 46.2Third quartile 58.3Maximum 87.9PL0149 (2/13)PL0149 (1/14)PL0101 (8/50)PL0118 (7/43)PL0123 (7/43)PL0142 (1/8)PL0106 (1/6)PL0143 (16/94)PL0143 (3/16)PL0124 (5/29)PL0109 (13/74)PL0148 (14/79)PL0123 (2/8)PL0110 (2/7)PL0141 (4/22)PL0133 (2/6)PL0113 (9/47)PL0107 (21/107)PL0134 (4/19)PL0124 (2/6)PL0103 (4/10)PL0129 (4/19)PL0117 (2/5)Hospital codesPL0119 (3/14)PL0136 (4/18)PL0102 (8/36)PL0110 (26/114)PL0127 (11/48)PL0117 (4/16)PL0137 (12/48)Hospital codesPL0115 (15/36)PL0137 (5/11)PL0114 (6/13)PL0107 (15/32)PL0126 (10/20)PL0150 (6/23)PL0141 (4/8)PL0121 (16/61)PL0105 (11/40)PL0114 (13/47)PL0131 (10/20)PL0130 (32/59)PL0116 (25/90)PL0116 (13/23)PL0103 (10/33)PL0112 (24/70)PL0138 (23/65)PL0101 (11/19)PL0113 (7/12)PL0147 (21/58)PL0109 (11/18)PL0115 (24/66)PL0130 (31/73)PL0126 (37/85)PL0118 (4/6)PL0120 (4/6)PL0135 (8/18)PL0119 (9/11)PL0106 (18/39)PL0135 (5/6)PL0131 (13/27)PL0120 (7/12)PL0105 (7/8)PL0142 (14/22)PL0112 (51/58)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>171


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTPortugalGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 12 95 22 1 033 21 792 18 398 - - - -2004 14 166 23 1 063 19 761 19 410 - - - -2005 13 202 19 1 153 19 1 171 17 405 1 1 - -2006 15 183 17 1 306 18 1 331 17 464 13 315 11 2662007 12 202 20 1 383 20 1 432 19 518 18 370 16 3402008 14 260 20 1 557 21 1 625 20 588 21 543 19 4672009 17 237 20 1 824 20 2 040 19 675 20 564 18 5362010 12 156 18 1 633 19 1 980 19 621 19 596 19 5482011 17 455 18 1 507 18 1 963 18 684 18 619 18 526Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 96 11 100 54 100 27 100 3 100 22 99 32 99 18CSF 4 24 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTPortugalFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)PT005 (0/10)PT026 (0/9)N laboratories 19M<strong>in</strong>imum 0First quartile 0Median 10.3Third quartile 16.7Maximum 36.4PT021A (0/32)PT031A (11/54)N hospitals 22M<strong>in</strong>imum 0First quartile 41.1Median 53.5Third quartile 61.9Maximum 67.7PT029A (8/28)PT022 (0/9)PT011A (71/210)PT016 (0/12)PT030A (18/44)PT021 (0/5)PT026A (23/56)PT002 (0/11)PT003A (102/223)PT003 (1/61)PT024A (11/23)PT031 (3/91)PT001A (87/176)Laboratory codesPT024 (4/49)PT029 (3/29)PT012 (1/9)Hospital codesPT027A (27/53)PT031B (120/231)PT031D (72/131)PT023A (90/160)PT001 (8/58)PT019A (162/286)PT018 (1/7)PT016A (83/141)PT007 (4/26)PT012A (102/169)PT027 (1/6)PT022A (13/21)PT011 (15/85)PT019 (16/80)PT007A (291/456)PT031C (29/45)PT002A (53/82)PT008 (8/27)PT005A (107/164)PT030 (4/11)PT008A (105/155)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA174


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)PT031A (3/19)PT021A (13/81)N hospitals 22M<strong>in</strong>imum 15.8First quartile 23.3Median 26.8Third quartile 33Maximum 37.3PT021A (1/17)PT023A (3/49)N hospitals 21M<strong>in</strong>imum 5.9First quartile 15.3Median 27.8Third quartile 34.6Maximum 66.7PT030A (15/78)PT008A (3/25)PT024A (39/190)PT016A (5/39)PT011A (66/294)PT011A (14/99)PT019A (65/279)PT003A (19/124)PT026A (12/50)PT031C (3/15)PT003A (123/508)PT029A (8/34)PT023A (62/255)PT022A (4/15)Hospital codesPT016A (27/108)PT022A (12/47)PT007A (160/569)PT001A (45/151)Hospital codesPT031B (25/93)PT031A (5/18)PT024A (14/47)PT031B (79/253)PT031D (75/239)PT005A (9/30)PT019A (32/101)PT031C (8/25)PT026A (4/12)PT029A (37/112)PT031D (44/127)PT002A (46/137)PT030A (7/17)PT027A (21/62)PT001A (31/59)PT008A (31/87)PT012A (18/34)PT012A (62/174)PT007A (126/229)PT005A (44/118)PT027A (6/9)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>175


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTRomaniaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 5 26 9 85 9 50 5 12 - - - -2004 4 9 15 95 12 48 4 9 - - - -2005 5 18 13 93 13 84 7 14 1 3 2 232006 8 29 11 83 9 41 9 28 5 32 2 32007 5 27 9 42 9 63 5 14 6 30 2 42008 4 14 5 39 4 58 4 16 3 6 3 82009 3 17 6 48 7 90 5 27 4 27 4 242010 2 13 5 47 5 35 2 19 3 17 5 102011 3 36 4 107 3 91 3 31 4 25 3 9Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 21 11 22 10 22 54 24 31 61Penicill<strong>in</strong> RI 33 11 39 28 33 69 29 31 61Macrolides RI 29


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates from the report<strong>in</strong>g period 2009 and 2010CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 57 46 100 47 99 27 100 0 100 0 100 55 100 68CSF 43 62 - - 1 100 - - - - - - - -GenderMale 57 50 69 45 54 42 75 0 73 0 60 56 74 79Female 41 55 29 53 46 11 25 0 27 0 38 56 26 40Unknown 2 100 2 33 - - - - - - 2 0 - -Age (years)0–4 12 50 5 63 1 0 11 0 64 0 26 91 32 505–19 12 50 5 13 4 33 - - 5 0 7 67 11 10020–64 10 0 54 45 51 25 36 0 14 0 10 25 21 5065 and over 22 64 10 44 35 29 18 0 - - 10 50 21 75Unknown 43 62 25 56 9 43 36 0 18 0 48 40 16 100Hospital departmentICU - - 1 100 - - - - - - - - 16 100Internal med. - - 5 57 6 0 - - - - 5 0 11 0Surgery - - 1 0 - - - - 5 0 5 100 11 100Other 57 46 58 42 53 33 64 0 77 0 40 71 47 56Unknown 43 62 35 56 41 25 36 0 18 0 50 43 16 100PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.177


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTRomaniaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 2M<strong>in</strong>imum 40.9First quartile 40.9Median 49.6Third quartile 58.3Maximum 58.3RO001D (2/5)N hospitals 5M<strong>in</strong>imum 40First quartile 40.5Median 52Third quartile 53.7Maximum 62.5RO01A (9/22)RO001A (30/74)Laboratory codesHospital codesRO002A (13/25)RO001E (22/41)RO01E (14/24)RO001B (5/8)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA178


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)N hospitals 4M<strong>in</strong>imum 24.3First quartile 25.9Median 28.8Third quartile 36.4Maximum 42.9N hospitals 3M<strong>in</strong>imum 33.3First quartile 33.3Median 40Third quartile 91.7Maximum 91.7RO002A (8/33)RO001D (2/6)RO001A (8/29)Hospital codesHospital codesRO001E (8/20)RO001D (3/10)RO001B (11/12)RO001E (3/7)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>179


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSlovakiaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 14 27 16 269 16 239 10 75 - - - -2004 9 17 15 289 15 310 12 82 - - - -2005 4 8 12 147 13 134 8 46 - - - -2006 - - - - - - - - - - - -2007 - - - - - - - - - - - -2008 - - - - - - - - - - - -2009 - - - - - - - - - - - -2010 - - - - - - - - - - - -2011 7 26 11 565 11 738 11 302 11 463 11 265Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 4 24


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 65 6 100 26 99 42 100 0 100 4 97 68 98 30CSF 35 11 - - 1 57 - - - - 3 83 2 50GenderMale 50 0 61 25 47 52 63 0 61 5 62 75 57 31Female 50 15 39 27 53 33 37 0 39 3 38 57 43 30Age (years)0–4 15 0 8 9 6 9 8 0 4 0 9 74 12 175–19 4 0 3 14 3 47 2 0 3 42 4 3020–64 50 0 47 25 37 45 44 0 59 3 43 71 53 3565 and over 31 25 42 32 54 43 47 0 37 5 45 65 31 29Hospital departmentICU 31 13 14 30 12 37 28 0 29 0 22 79 28 51Internal med. 27 0 52 26 40 44 34 0 30 0 31 61 22 13Surgery - - 10 36 10 45 12 0 9 11 10 65 8 35Other 42 9 21 19 35 41 26 0 32 9 36 67 40 27Unknown - - 3 28 3 36 2 0 1 0 2 75 2 0PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.181


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSlovakiaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)N laboratories 2M<strong>in</strong>imum 0First quartile 0Median 7.1Third quartile 14.3Maximum 14.3SKSK15F (0/9)SKSK15G (0/7)N hospitals 20M<strong>in</strong>imum 0First quartile 16.7Median 25Third quartile 29.8Maximum 54.2SKSK16A (4/36)SKSK15I (4/25)SKSK10A (3/18)SK005 (0/6)SKSK10B (2/12)SKSK15H (1/5)SKSK09A (11/51)SKSK15E (3/13)Laboratory codesHospital codesSKSK08A (15/63)SKSK07A (16/61)SKSK04A (7/26)SKSK15C (10/37)SKSK12A (3/11)SKSK15B (19/69)SK008 (1/7)SKSK11A (9/28)SKSK15A (4/11)SKSK06A (13/34)SKSK10C (8/18)SKSK05A (13/24)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA182


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)SKSK10B (4/22)SKSK11A (13/49)N hospitals 18M<strong>in</strong>imum 18.2First quartile 31.4Median 38.4Third quartile 49Maximum 56.9SKSK15E (2/5)SKSK12A (7/16)N hospitals 17M<strong>in</strong>imum 40First quartile 53.7Median 64.5Third quartile 70Maximum 89.7SKSK05A (9/32)SKSK08A (11/24)SKSK15E (2/7)SKSK10B (7/15)SKSK16A (16/51)SKSK15I (22/41)SKSK08A (16/45)SKSK16A (12/20)SKSK15A (4/11)SKSK10A (10/16)SKSK15G (3/8)SKSK15F (5/8)Hospital codesSKSK15I (24/64)SKSK07A (35/89)Hospital codesSKSK07A (40/62)SKSK04A (16/24)SKSK15F (2/5)SKSK15G (4/6)SKSK10A (11/27)SKSK05A (21/30)SKSK12A (9/22)SKSK04A (25/51)SKSK15C (14/20)SKSK09A (29/57)SKSK15B (32/43)SKSK15B (40/74)SKSK09A (32/40)SKSK15C (31/57)SKSK06A (37/43)SKSK06A (33/58)SKSK11A (35/39)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>183


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSloveniaGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 11 172 11 299 11 401 10 76 - - - -2004 10 166 11 347 11 573 9 91 - - - -2005 11 208 11 349 11 657 11 119 10 78 8 382006 11 167 11 365 11 717 10 145 10 145 10 722007 10 195 10 422 10 851 9 183 10 170 9 882008 10 209 10 418 10 874 10 196 9 157 10 952009 10 253 10 471 10 893 10 198 10 189 10 1072010 10 232 10 476 10 952 10 196 10 196 10 952011 10 253 10 464 10 1 002 10 208 10 232 10 118Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 2 2 2 5 4 3 1


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 94 14 100 10 100 20 100 0 100 1 98 26 98 22CSF 6 11 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSloveniaFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)SI011 (0/23)N laboratories 10M<strong>in</strong>imum 0First quartile 10.5Median 11.5Third quartile 17.4Maximum 30.8SI002A (0/38)SI003B (0/20)N hospitals 15M<strong>in</strong>imum 0First quartile 2.5Median 11.1Third quartile 13.3Maximum 18.2SI005 (2/20)SI010A (0/21)SI008 (4/38)SI003A (3/119)SI004A (3/85)SI010 (3/28)SI011A (2/40)Laboratory codesSI004 (10/90)SI007 (2/17)Hospital codesSI001B (1/13)SI004C (1/9)SI005A (6/49)SI001 (24/165)SI001A (44/354)SI001C (3/23)SI002 (4/23)SI009A (6/45)SI003 (10/55)SI008A (12/72)SI007A (7/41)SI009 (8/26)SI004B (2/11)0 25 50 75 1000 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA186


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)SI004C (1/18)SI010A (7/59)N hospitals 15M<strong>in</strong>imum 5.6First quartile 15.8Median 19.6Third quartile 23.4Maximum 30.7SI011A (0/9)N hospitals 11M<strong>in</strong>imum 0First quartile 8.7Median 14.3Third quartile 36.8Maximum 54.5SI009A (2/24)SI011A (16/116)SI004B (6/38)SI008A (2/23)SI002A (21/133)SI002A (2/16)SI001C (8/48)SI004A (6/44)SI004A (36/199)Hospital codesSI003A (55/280)Hospital codesSI001B (3/21)SI003B (8/39)SI007A (2/12)SI008A (23/109)SI001A (31/137)SI001A (118/558)SI005A (18/77)SI001C (7/19)SI001B (10/42)SI003A (50/100)SI009A (41/163)SI007A (23/75)SI005A (6/11)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>187


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSpa<strong>in</strong>General <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 35 656 36 1 391 29 2 650 36 608 - - - -2004 36 684 36 1 527 36 3 471 36 710 - - - -2005 34 740 34 1 337 34 2 997 35 623 14 56 13 702006 35 625 35 1 483 35 3 364 34 755 33 564 32 4052007 35 862 35 1 645 35 3 678 35 885 33 618 35 4482008 31 695 32 1 505 32 3 626 32 1 002 30 639 32 5482009 32 708 33 1 715 33 3 821 33 1 093 32 628 33 5442010 41 862 41 1 986 41 5 696 41 1 467 41 1 161 41 7492011 40 763 40 1 965 40 5 605 39 1 478 40 1 145 40 839Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 7 9 9 8 8 7 8 10 10Penicill<strong>in</strong> RI 32 29 25 27 22 23 22 30 30Macrolides RI 27 27 23 22 18 22 19 27 25Staphylococcus aureusOxacill<strong>in</strong>/Meticill<strong>in</strong> R 24 26 27 25 25 27 26 25 22Escherichia coliAm<strong>in</strong>openicil<strong>in</strong>s R 58 60 62 64 62 63 65 65 66Am<strong>in</strong>oglycosides R 7 7 10 9 10 11 13 14 15Fluoroqu<strong>in</strong>olones R 21 25 28 28 30 33 31 33 34Third-gen. cephalospor<strong>in</strong>s R 4 7 8 7 7 9 11 12 12Carbapenems R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 92 30 100 24 100 34 100 0 100 1 99 12 98 17CSF 8 32 - -


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSpa<strong>in</strong>Figure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesES047 (1/15)ES062 (6/64)ES005 (7/61)ES016 (1/8)ES010 (5/35)ES057 (2/13)ES059 (7/31)ES043 (5/22)ES042 (18/79)ES011 (13/54)ES044 (11/43)ES054 (28/108)ES032 (6/23)ES021 (16/61)ES026 (4/15)ES058 (18/67)ES064 (20/73)ES012 (8/27)ES048 (18/60)ES049 (3/10)ES065 (7/23)ES019 (12/39)ES046 (12/38)ES041 (6/19)ES060 (8/24)ES018 (5/15)ES031 (26/78)ES029 (8/23)ES038 (24/68)ES020 (10/28)ES004 (13/34)ES056 (18/45)ES015 (4/10)ES017 (5/12)ES053 (23/55)ES051 (3/7)ES002 (13/29)ES061 (51/113)ES063 (18/38)ES003 (15/27)N laboratories 40M<strong>in</strong>imum 6.7First quartile 24.8Median 30.2Third quartile 37Maximum 55.60 25 50 75 100Hospital codesES0043 (1/29)ES0046 (1/26)ES020A (1/13)ES048A (3/35)ES046A (3/32)ES0042 (5/47)ES015A (1/8)ES0061 (14/101)ES0044 (7/46)N hospitals 82M<strong>in</strong>imum 3.4First quartile 18Median 23.5Third quartile 30.6Maximum 66.7ES0063 (7/46)ES021A (13/85)ES032A (2/13)ES0020 (2/13)ES0048 (6/38)ES0049 (6/37)ES043A (5/30)ES0018 (6/36)ES0051 (2/12)ES0038 (11/63)ES058A (12/68)ES0041 (11/61)ES0053 (22/122)ES0032 (4/22)ES0060 (10/54)ES005A (5/27)ES061A (24/128)ES010A (7/37)ES005 (4/21)ES0021 (15/78)ES060A (17/86)ES051A (3/15)ES031A (22/110)ES0062 (19/92)ES053A (13/62)ES054A (17/80)ES047A (5/23)ES0026 (17/77)ES0010 (8/36)ES042A (12/53)ES0019 (19/83)ES0064 (11/48)ES0058 (14/58)ES004 (21/86)ES019A (28/114)ES0056 (17/67)ES013A (11/42)ES044A (10/38)ES038A (14/53)ES064A (9/34)ES0054 (20/75)ES018A (8/30)ES002 (11/40)ES063A (11/40)ES011A (12/43)ES0057 (7/25)ES004A (18/63)ES0015 (2/7)ES0059 (7/24)ES003 (5/17)ES016A (9/30)ES012A (15/50)ES062A (19/62)ES003A (5/16)ES0031 (24/76)ES056A (18/57)ES041A (20/63)ES0011 (14/44)ES0013 (15/46)ES026A (28/84)ES0012 (15/45)ES057A (6/18)ES017A (13/37)ES0029 (11/31)ES0017 (10/27)ES065A (28/73)ES002A (15/39)ES0065 (33/84)ES0047 (2/5)ES029A (15/36)ES049A (13/31)ES059A (11/24)ES032B (4/6)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA190


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesES021B (0/6)ES0026 (17/96)ES026A (23/118)ES020A (1/5)ES064A (29/134)ES0011 (40/181)ES065A (34/151)ES0015 (5/22)ES0064 (33/143)ES013A (16/65)ES060A (33/134)ES058A (41/165)ES062A (51/204)ES011A (44/167)ES0010 (35/131)ES038A (49/182)ES0021 (68/239)ES029A (20/69)ES032A (25/86)ES048A (33/113)ES019A (94/317)ES0065 (35/118)ES0013 (18/60)ES0018 (42/139)ES041A (35/115)ES0012 (43/140)ES0062 (59/192)ES010A (38/123)ES015A (9/29)ES054A (111/354)ES018A (39/124)ES0053 (74/235)ES0046 (24/76)ES0032 (26/80)ES061A (93/280)ES0048 (47/141)ES0043 (43/128)ES043A (43/128)ES005 (39/116)ES0019 (109/324)ES005A (47/138)ES057A (29/85)ES042A (86/251)ES0060 (40/116)ES002 (48/139)ES021A (86/249)N hospitals 83M<strong>in</strong>imum 0First quartile 29.7Median 34.1Third quartile 39.2Maximum 75ES0061 (109/314)ES0058 (60/171)ES046A (19/54)ES016A (36/102)ES003A (30/85)ES063A (27/76)ES0041 (46/129)ES053A (57/159)ES031A (84/232)ES0049 (22/60)ES0042 (106/289)ES004 (61/164)ES002A (63/169)ES0038 (68/180)ES0059 (40/104)ES0044 (58/149)ES0063 (47/120)ES059A (40/102)ES0054 (132/335)ES003 (30/76)ES047A (17/43)ES044A (65/162)ES004A (72/177)ES0031 (82/200)ES032B (7/17)ES012A (56/135)ES0057 (30/72)ES0017 (31/74)ES0029 (24/57)ES0051 (13/29)ES017A (26/58)ES051A (18/39)ES049A (25/53)ES056A (114/241)ES0056 (104/212)ES0047 (7/14)ES051E (12/16)0 25 50 75 100Hospital codesES0011 (0/22)ES046A (0/22)ES0048 (0/30)ES015A (0/7)ES005 (0/20)ES0032 (0/12)ES051E (0/6)ES064A (0/16)N hospitals 78M<strong>in</strong>imum 0First quartile 3.8Median 6.7Third quartile 15.2Maximum 40ES051A (0/8)ES0051 (0/10)ES032A (0/16)ES029A (0/8)ES057A (0/10)ES017A (0/7)ES0064 (0/22)ES0057 (0/6)ES0053 (1/41)ES063A (1/31)ES0021 (1/27)ES0018 (1/26)ES048A (1/25)ES0058 (2/47)ES011A (1/22)ES0012 (1/21)ES012A (1/21)ES019A (1/20)ES004A (1/20)ES0041 (1/19)ES002 (1/18)ES0010 (1/18)ES041A (2/35)ES0026 (2/34)ES053A (2/34)ES0013 (1/16)ES0049 (1/15)ES0063 (3/45)ES010A (1/15)ES0059 (1/15)ES002A (2/30)ES061A (8/119)ES059A (1/14)ES049A (1/14)ES005A (2/26)ES058A (3/34)ES0065 (2/22)ES042A (5/53)ES065A (2/19)ES0054 (6/56)ES062A (8/73)ES026A (3/27)ES0015 (1/9)ES0017 (1/9)ES021A (3/26)ES0061 (16/134)ES054A (8/64)ES0019 (1/8)ES038A (6/40)ES056A (7/46)ES0044 (7/46)ES0062 (11/72)ES013A (3/19)ES044A (7/42)ES0043 (5/29)ES003A (3/17)ES060A (8/43)ES031A (14/72)ES016A (2/10)ES018A (4/19)ES0046 (4/18)ES003 (3/13)ES043A (7/29)ES0056 (11/45)ES0042 (11/40)ES0060 (7/25)ES004 (10/33)ES0031 (15/46)ES0038 (22/59)ES0029 (2/5)0 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>191


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSwedenGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 21 919 21 1 855 21 3 350 21 850 - - - -2004 21 955 21 1 906 21 3 372 21 856 - - - -2005 21 1025 21 1 774 21 3 241 21 821 18 282 17 1492006 21 996 21 1 968 20 3 539 21 884 20 621 18 3002007 21 1 032 21 2 163 20 3 749 21 932 20 649 20 3432008 21 1 219 21 2 410 20 4 032 21 1 059 20 826 20 3152009 19 1 063 19 2 460 18 4 247 19 967 18 706 18 3382010 19 1 008 19 2 867 18 4 846 18 1 038 18 878 18 3772011 18 1 015 18 3 113 17 5 253 18 1 239 17 966 17 412Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 98 4 100 1 100 9 100 0 100 0 100 2 100 6CSF 2 5 - - 0 0 - - - - - - - -GenderMale 53 4 63 1 50 12 73 0 61 0 60 3 69 6Female 47 3 37 1 50 6 27 0 39 0 40 1 31 6Age (years)0–4 3 5 4 0 1 8 3 0 2 0 1 0 2 145–19 2 3 3 1 1 12 1 0 2 0 1 8 3 820–64 40 3 30 1 23 12 23 0 29 0 25 3 25 765 and over 54 4 63 1 73 8 72 0 65 0 72 2 69 6Unknown 1 5 1 0 2 8 1 0 1 0 1 0 1 13Hospital departmentICU 6 3 4 1 3 8 6 0 12 0 4 6 5 15Internal med. 36 3 34 0 32 7 28 0 24 0 27 2 32 5Surgery 3 7 12 0 15 10 20 0 26 0 21 0 13 3Other 49 4 44 1 39 10 40 0 34 0 39 3 44 6Unknown 6 3 7 1 11 7 7 0 4 0 9 2 6 12PNSP: penicill<strong>in</strong>-non-susceptible S. pneumoniae; MRSA: meticill<strong>in</strong>-resistant S. aureus; FREC: fluoroqu<strong>in</strong>olone-resistant E. coli; VRE: vancomyc<strong>in</strong>-resistantEnterococcus; 3GCRKP: third-generation cephalospor<strong>in</strong>-resistant K. pneumoniae; CRPA: carbapenem-resistant P. aerug<strong>in</strong>osa.193


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTSwedenFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesSE540 (0/15)SE230 (0/48)SE600 (1/92)SE450 (1/79)SE240 (1/71)SE110 (1/64)SE250 (1/56)SE320 (2/92)SE730 (2/87)SE440 (3/122)SE610 (2/79)SE350 (3/102)SE620 (3/91)SE120 (9/263)SE400 (5/125)SE200 (6/134)SE310 (5/76)SE430 (4/58)SE100 (22/319)N laboratories 19M<strong>in</strong>imum 0First quartile 1.4Median 2.5Third quartile 4Maximum 6.90 25 50 75 100Hospital codesSE440B (0/54)SE350B (0/73)SE610B (0/51)SE100E (0/251)SE400B (0/117)SE730E (0/44)SE250B (0/73)SE220B (0/72)SE310A (0/70)SE230B (0/12)SE400X (0/37)SE600C (0/34)SE610A (0/194)SE730C (0/28)SE620A (0/163)SE450C (0/23)SE730F (0/91)SE610C (0/97)SE350C (0/113)SE200C (0/47)SE220C (0/22)SE100C (0/52)SE450D (0/38)SE730B (0/30)SE730D (0/17)SE620B (0/18)SE100G (0/16)SE110B (0/38)SE400C (0/28)SE110A (0/86)SE240C (0/40)SE440C (0/33)SE120B (0/40)SE100I (0/11)SE220A (0/126)SE620D (0/12)SE620C (0/61)SE200B (0/166)SE450B (0/11)SE200D (0/7)SE600A (1/282)SE120A (1/282)SE320A (1/194)SE430A (1/193)SE440A (1/174)SE200A (2/255)SE230A (1/116)SE310B (2/211)SE100B (2/199)SE450A (2/161)SE250A (2/150)SE100D (3/223)SE350A (2/147)SE400A (2/129)SE100A (6/368)SE240A (3/136)SE320B (1/42)SE100F (1/38)SE540A (2/62)SE430D (2/55)SE240B (1/25)N hospitals 61M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 0.8Maximum 40 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA194


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)Hospital codesSE100D (0/10)SE620B (0/41)SE240C (1/47)SE610B (1/39)SE730B (1/38)SE440B (3/102)SE450C (1/33)SE730C (2/50)SE320A (6/125)SE100C (1/20)SE450A (15/287)SE730D (2/37)SE450B (2/35)SE220B (1/17)SE240B (1/17)SE440C (4/67)SE610C (5/83)SE240A (7/112)SE200C (4/60)SE350C (5/75)SE230B (1/15)SE610A (9/135)SE620C (6/88)SE730E (5/69)SE310B (19/255)SE730F (12/159)SE200B (19/243)SE440A (22/279)SE110A (14/176)SE540A (7/88)SE400B (18/224)SE400C (8/95)SE620A (19/224)SE320B (3/35)SE120A (5/55)SE350A (11/120)SE430D (8/85)SE350B (7/69)SE450D (7/65)SE230A (5/44)SE430A (39/338)SE110B (8/68)SE400A (33/279)SE100B (14/115)SE200A (41/318)SE200D (2/15)SE310A (5/35)SE220A (34/201)SE220C (9/53)SE620D (3/17)SE100E (2/11)SE100A (27/137)SE120B (3/10)N hospitals 53M<strong>in</strong>imum 0First quartile 5.9Median 7.8Third quartile 11.4Maximum 300 25 50 75 100Hospital codesSE620A (0/44)SE450B (0/11)SE220A (0/46)SE240C (0/19)SE440B (0/12)SE450D (0/17)SE310B (0/57)SE450C (0/8)SE430D (0/12)SE400C (0/9)SE250A (0/44)SE730E (0/11)SE350B (0/17)SE320B (0/21)SE620B (0/5)SE230A (0/32)SE100E (0/6)SE610A (0/47)SE610C (0/20)SE730C (0/10)SE440C (0/19)SE110B (0/9)SE100A (0/38)SE440A (0/53)SE220C (0/11)SE350A (0/45)SE200C (0/10)SE220B (0/7)SE100D (0/7)SE250B (0/29)SE730F (0/36)SE310A (0/25)SE610B (0/8)SE200A (2/97)SE350C (1/34)SE200B (2/60)SE320A (2/60)SE430A (2/59)SE540A (1/24)SE400B (2/45)SE400X (1/21)SE240A (2/40)SE450A (4/73)SE100B (1/18)SE400A (4/70)SE110A (2/35)SE620C (1/16)SE120A (1/13)SE730D (1/6)N hospitals 49M<strong>in</strong>imum 0First quartile 0Median 0Third quartile 3.3Maximum 16.70 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>195


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTUnited K<strong>in</strong>gdomGeneral <strong>in</strong>formation about EARS-Net participat<strong>in</strong>g laboratoriesTable 1: Annual number of report<strong>in</strong>g laboratories and number of reported isolates, 2003–2011YearS. pneumoniae S. aureus E. coli Enterecocci K. pneumoniae P. aerug<strong>in</strong>osaLabs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates Labs Isolates2003 50 1 334 51 3 548 19 2 253 - - - - - -2004 54 1 059 54 3 562 20 2 091 - - - - - -2005 53 1 375 58 3 971 23 2 359 27 591 23 420 25 4382006 51 1 514 55 4 132 26 2 438 22 547 22 404 24 3532007 50 1 785 55 4 865 20 2 374 18 435 18 382 19 3702008 51 1 223 55 3 355 15 2 456 14 274 15 350 14 3452009 59 1 396 69 2 977 28 4 712 26 712 27 725 26 6392010 50 1 459 55 2 730 29 5 389 28 651 28 840 28 5882011 53 1 513 53 3 430 29 5 971 28 723 28 1 007 28 599Antibiotic <strong>resistance</strong> from 2003 to 2011Table 2: Annual percentage (%) of antimicrobial non-susceptible and resistant isolates, 2003–2011Pathogens by antimicrobial classes 2003 2004 2005 2006 2007 2008 2009 2010 2011Streptococcus pneumoniaePenicill<strong>in</strong> R 1


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Demographic characteristicsTable 3: Selected details on <strong>in</strong>vasive isolates reported for 2010 and 2011CharacteristicS. pneumoniae S. aureus E. coli E. faecalis E. faecium K. pneumoniae P. aerug<strong>in</strong>osa% total % PNSP % total % MRSA % total % FREC % total % VRE % total % VRE % total % 3GCRKP % total % CRPAIsolate sourceBlood 99 4 100 17 100 17 100 2 100 10 100 7 100 6CSF 1 7 - - - - - - - - - - - -GenderMale 51 4 61 18 48 20 65 0 63 8 59 8 61 6Female 48 4 39 16 52 15 35 3 37 12 41 6 39 6Unknown 1 0


<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011SURVEILLANCE REPORTUnited K<strong>in</strong>gdomFigure 1: S. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with penicill<strong>in</strong> non-susceptibility by laboratory(2010–2011)Figure 2: S. aureus: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to meticill<strong>in</strong> (MRSA) by hospital(2010–2011)Laboratory codesUK059 (0/56)UK096 (0/51)UK054 (0/27)UK023 (0/38)UK091 (0/101)UK102 (0/11)UK033 (0/20)UK046 (0/24)UK011 (0/28)UK026 (0/27)UK097 (0/48)UK042 (0/25)UK027 (0/22)UK101 (1/105)UK093 (1/85)UK051 (1/77)UK094 (1/56)UK015 (2/107)UK017 (1/53)UK008 (1/53)UK099 (3/143)UK004 (1/45)UK092 (2/84)UK069 (1/42)UK052 (1/34)UK007 (4/129)UK100 (1/25)UK020 (2/49)UK049 (1/24)UK047 (5/91)UK001 (1/18)UK012 (4/72)UK043 (4/68)UK053 (2/34)UK064 (4/65)UK066 (2/32)UK057 (2/31)UK055 (1/15)UK098 (4/59)UK090 (2/28)UK045 (7/93)UK078 (6/75)UK050 (4/50)UK056 (1/12)UK010 (1/12)UK068 (11/119)UK063 (3/24)UK032 (7/56)UK076 (5/38)UK048 (4/25)UK084 (6/35)UK075 (2/10)N laboratories 52M<strong>in</strong>imum 0First quartile 0.5Median 3.6Third quartile 7Maximum 200 25 50 75 100Hospital codesUK027X (0/33)UK017X (0/74)UK053X (0/13)UK032X (0/75)UK072A (0/19)UK015X (0/168)UK008X (0/32)UK047B (0/5)UK090X (0/41)N hospitals 92M<strong>in</strong>imum 0First quartile 9Median 15.9Third quartile 26.5Maximum 100UK020X (0/26)UK052A (1/34)UK055A (1/32)UK045X (3/91)UK001X (1/30)UK066A (2/41)UK026X (7/128)UK050A (5/81)UK092X (9/138)UK096X (7/94)UK049A (3/40)UK102X (9/103)UK054A (7/80)UK033X (9/102)UK052X (1/11)UK053D (6/63)UK064A (13/135)UK091X (20/205)UK078C (2/20)UK044B (1/9)UK004X (13/116)UK097X (10/82)UK045A (26/209)UK098X (16/126)UK012X (10/76)UK055X (2/15)UK066X (2/15)UK100X (9/67)UK059A (17/125)UK003X (3/22)UK084B (1/7)UK072X (1/7)UK059X (10/65)UK049X (4/26)UK093X (28/180)UK051A (19/122)UK046X (5/32)UK101X (45/279)UK048X (3/18)UK099X (39/224)UK068B (52/295)UK050X (5/28)UK047X (21/116)UK063A (8/44)UK069X (11/58)UK051X (11/57)UK068X (32/164)UK044D (3/15)UK064X (15/75)UK056X (2/10)UK075A (11/54)UK048A (11/53)UK047A (57/273)UK063X (4/19)UK044C (2/9)UK056A (24/107)UK054X (9/36)UK083A (23/91)UK084A (27/104)UK044A (24/91)UK076D (4/15)UK057A (11/41)UK069A (23/82)UK076A (14/47)UK057X (4/13)UK078A (42/130)UK079A (3/9)UK078B (2/6)UK046A (10/28)UK077A (14/37)UK081A (5/13)UK080A (17/41)UK011A (9/10)UK043X (16/17)UK094X (24/25)UK023A (5/5)UK017B (24/24)UK023B (6/6)UK008A (12/12)UK032A (8/8)UK007A (13/13)UK015A (7/7)UK007B (12/12)0 25 50 75 100% penicill<strong>in</strong> non-susceptible % MRSA100% meticill<strong>in</strong> <strong>resistance</strong> rates for isolates of S. aureus reflect report<strong>in</strong>g ofMRSA only.198


SURVEILLANCE REPORT<strong>Antimicrobial</strong> <strong>resistance</strong> <strong>surveillance</strong> <strong>in</strong> <strong>Europe</strong> 2011Figure 3: E. coli: percentage (%) of <strong>in</strong>vasive isolateswith <strong>resistance</strong> to fluoroqu<strong>in</strong>olones by hospital(2010–2011)Figure 4: K. pneumoniae: percentage (%) of <strong>in</strong>vasiveisolates with <strong>resistance</strong> to third-generationcephalospor<strong>in</strong>s by hospital (2010–2011)UK023X (42/429)UK004X (17/169)UK090X (25/246)N hospitals 29M<strong>in</strong>imum 9.8First quartile 13.3Median 17.2Third quartile 21.2Maximum 49UK023X (0/52)UK003X (0/12)UK017X (1/86)N hospitals 25M<strong>in</strong>imum 0First quartile 2.8Median 6.6Third quartile 9.4Maximum 83.3UK001X (13/124)UK093X (46/434)UK033X (1/47)UK017X (47/423)UK008X (1/37)UK098X (61/499)UK032X (3/109)UK032X (88/664)UK004X (1/36)UK008X (31/231)UK020X (1/29)UK033X (36/266)UK027X (1/25)UK097X (43/290)UK026X (70/451)UK092X (2/40)UK100X (29/183)UK096X (2/35)Hospital codesUK020X (32/195)UK092X (68/396)UK011X (49/275)Hospital codesUK098X (5/78)UK015X (12/182)UK101X (11/157)UK015X (201/1102)UK102X (44/233)UK091X (104/545)UK012X (83/405)UK003X (31/147)UK012X (3/42)UK026X (8/110)UK093X (6/81)UK042X (4/49)UK101X (164/775)UK097X (3/32)UK042X (58/273)UK096X (59/270)UK099X (190/826)UK007X (19/78)UK027X (42/155)UK094X (66/191)UK043X (51/104)UK102X (5/49)UK091X (18/174)UK099X (12/116)UK011X (8/46)UK100X (7/39)UK094X (5/6)0 25 50 75 1000 25 50 75 100% fluoroqu<strong>in</strong>olone <strong>resistance</strong> % third-generation cephalospor<strong>in</strong> <strong>resistance</strong>199

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