<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Huang, Te-Din</dc:creator>
  <dc:creator>Poirel, Laurent</dc:creator>
  <dc:creator>Bogaerts, Pierre</dc:creator>
  <dc:creator>Berhin, Catherine</dc:creator>
  <dc:creator>Nordmann, Patrice</dc:creator>
  <dc:creator>Glupczynski, Youri</dc:creator>
  <dc:date>2013-09-20</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">&lt;strong&gt;Objectives&lt;/strong&gt; To assess the performance of the agar disc diffusion method for the detection of carbapenemase-producing Enterobacteriaceae (CPE) referred to the national reference laboratories (NRLs) in Belgium and France.&lt;strong&gt;Methods&lt;/strong&gt; All Enterobacteriaceae isolates referred to the NRLs for the confirmation of CPE in 2012 were included. The inhibition zone diameters of meropenem, piperacillin/tazobactam and temocillin using CLSI disc diffusion methodology were recorded. Phenotypic and molecular detection of carbapenemases was performed on all isolates.&lt;strong&gt;Results&lt;/strong&gt; A total of 1354 Enterobacteriaceae isolates, including 435 (32.1%) confirmed CPE isolates [OXA-48 (&lt;em&gt;n&lt;/em&gt; = 323), KPC (&lt;em&gt;n&lt;/em&gt; = 60), VIM (&lt;em&gt;n&lt;/em&gt; = 32) and NDM (&lt;em&gt;n&lt;/em&gt; = 20)] and 919 carbapenemase-negative isolates, were tested. Using recommended interpretative criteria, non-susceptibility to meropenem had poor sensitivity (52.0% by CLSI susceptibility breakpoint and 80.0% by EUCAST screening breakpoints), while non-susceptibility to piperacillin/tazobactam (according to CLSI breakpoint) or to temocillin (according to Fuchs, Barry, Thornsberry &lt;em&gt;et al. Eur J Clin Microbiol&lt;/em&gt; 1985; &lt;strong&gt;4&lt;/strong&gt;: 30–3) was highly sensitive (99.8% and 98.2%, respectively) but poorly specific (29.4% and 42.9%, respectively) for the detection of CPE. Temocillin diameters &lt;12 mm alone had high specificity (90.0%) and the combination of temocillin diameters ≥12 mm with piperacillin/tazobactam diameters ≥16 mm observed in 40% of all referred isolates displayed excellent negative predictive value (99.2%).&lt;strong&gt;Conclusions&lt;/strong&gt; In geographical areas with a high prevalence of OXA-48 producers, recommended meropenem susceptibility or screening breakpoints failed to detect CPE in a large proportion of isolates. The combination of modified zone diameter cut-offs for piperacillin/tazobactam (≥16 mm) and temocillin (≥12 mm) can be used to rule out the presence of carbapenemase and avoid unnecessary additional testing for confirmation of CPE.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/303541</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/303541/files/dkt367.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/303541/files/nor_tpt_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/jac/dkt367</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of Antimicrobial Chemotherapy. - 2014, vol. 69, no. 2, p. 445-450</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Temocillin and piperacillin/tazobactam resistance by disc diffusion as antimicrobial surrogate markers for the detection of carbapenemase-producing Enterobacteriaceae in geographical areas with a high prevalence of OXA-48 producers</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
