NosoVeille – Bulletin de veille Août 2012
5 / 40
ertapenem and that of total carbapenems (ertapenem, imipenem, and meropenem) increased significantly
from 6.13 to 13.38 defined daily doses per 1000 patient-days for ertapenem and from 20.43 to 34.25 defined
daily doses per 1000 patient-days for total carbapenems. The most common species were Escherichia coli
(n=1095), Klebsiella spp. (n=663), and Enterobacter spp. (n=202). The susceptibility of all isolates to
ertapenem and to imipenem varied during the study period. For ertapenem, the rates of nonsusceptibility
ranged from 3.5% to 10.3% and those for imipenem ranged from 3.5% to 10.7%. Although the use of
carbapenems increased during the study period, there was no marked increase in resistance to
carbapenems. Continuous monitoring of resistance trends is necessary so that antimicrobial prescription
policies can be adjusted and infection control intervention programs can be implemented.
NosoBase n° 34596
Antibiorésistance des entérobactéries, incluant la caractérisation moléculaire des espèces
productrices de bêta-lactamases à spectre étendu dans des isolats urinaires provenant de patients
hospilalisés en Amérique du Nord et en Europe : résultats de l'étude SMART 2009-2010
Hoban DJ; Lascols C; Nicolle LE; Badal R; Bouchillon S; Hackel M; et al. Antimicrobial susceptibility of
enterobacteriaceae, including molecular characterization of extended-spectrum beta-lactamase-producing
species, in urinary tract isolates from hospitalized patients in North America and Europe: results from the
SMART study 2009-2010. Diagnostic microbiology and infectious disease 2012; in press: 6 pages.
Mots-clés : ENTEROBACTERIE; ANTIBIORESISTANCE; INFECTION URINAIRE; BETA-LACTAMASE A
SPECTRE ELARGI; ESCHERICHIA COLI; KLEBSIELLA PNEUMONIAE; CARBAPENEME; IMIPENEME;
BIOLOGIE MOLECULAIRE; AMERIQUE DU NORD; EUROPE; SURVEILLANCE
In 2009-2010, 3646 urinary tract isolates of Enterobacteriaceae spp. were isolated from hospitalized patients
in North America and Europe. Extended-spectrum beta-lactamase (ESBL) production was detected in 8.5%
and 8.8% of Escherichia coli and Klebsiella pneumoniae, respectively, in North America and in 17.6% and
38.9% for Europe, respectively. The carbapenems (ertapenem and imipenem) were the most active agents in
vitro, with ampicillin-sulbactam the least active. Molecular characterization of about 50% of ESBL-positive
isolates identified the presence of bla(CTX-M) genes in over 90% of Escherichia coli from both continents.
bla(KPC) was more common in North American isolates of K. pneumoniae than in European isolates (21.4%
versus 6.9%). bla(TEM) and AmpC genes were infrequent. Enterobacteriaceae spp. isolated from
hospitalized patients with urinary tract infections in both North America and Europe are often resistant to
commonly used antimicrobials with bla(CTX-M) genes common in both Escherichia coli and K. pneumoniae.
NosoBase n° 34646
Benchmarking (comparaison de performance) des traitements antibiotiques empiriques inappropriés
Kariv G; Paul M; Shani V; Muchtar E; Leibovici L. Benchmarking inappropriate empirical antibiotic treatment.
Clinical microbiology and infection 2012; in press: 13 pages.
Mots-clés : ANTIBIOTIQUE; TRAITEMENT; ANTIBIORESISTANCE; MORTALITE; TAUX; ETUDE
PROSPECTIVE; COHORTE; PRESCRIPTION; BIBLIOGRAPHIE
Inappropriate empirical antibiotic treatment for severe infections is associated with increased mortality.
Superfluous treatment is associated with resistance induction. We aimed to define acceptable rates of
inappropriate empirical antibiotic treatment. We included all prospective cohort studies published between
1975 and 2009 reporting the proportion of appropriate and inappropriate empirical antibiotic treatment of
microbiologically documented infections. Studies were identified in PubMed and in reference lists of included
studies. Funnel plots were drawn using the proportion of inappropriate empirical treatment as the effect size.
A pooled estimate of inappropriate empirical antibiotic treatment was calculated using a ß-binomial model.
Control limits were calculated with the overdispersion factor technique and 20% winsorized data.
Heterogeneity was assessed through subgroup analysis for categorical moderators and meta-regression for
continuous variables. Eighty-seven studies, comprising 92 study groups, with 27 628 patients met inclusion
criteria. The pooled rate of inappropriate empirical antibiotic treatment was 28.6% (95% CI 25.4-31.8). Funnel
plot analysis yielded a dispersed graph with only 37 (40%) studies falling within the control limits. Using the
overdispersion factor technique with 20% winsorizing, 79 (86%) studies fell within the control limits. None of
the clinical or methodological factors could explain the large heterogeneity observed. The funnel plot
presented can be used to benchmark rates of inappropriate empirical antibiotic treatment. Based on the
control limits found, at least 500 patients should be evaluated before establishing a local rate. Lower and
higher than expected rates might indicate overly aggressive treatment or poor performance, respectively.