{"id":1043,"date":"2014-10-08T11:45:21","date_gmt":"2014-10-08T15:45:21","guid":{"rendered":"http:\/\/allphasepharma.com\/dir\/?p=1043"},"modified":"2014-10-08T11:45:21","modified_gmt":"2014-10-08T15:45:21","slug":"cre-surveillance-data-from-france","status":"publish","type":"post","link":"https:\/\/allphasepharma.com\/dir\/2014\/10\/08\/1043\/cre-surveillance-data-from-france\/","title":{"rendered":"CRE Surveillance Data from France"},"content":{"rendered":"<p>Despite all the\u00a0concern about the emergence of CRE pathogens worldwide, it is quite difficult to obtain hard quantitative, prospectively collected incidence figures.<\/p>\n<figure id=\"attachment_1044\" aria-describedby=\"caption-attachment-1044\" style=\"width: 858px\" class=\"wp-caption alignright\"><a href=\"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2014\/10\/CarbapenemMICs.jpg?ssl=1\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" class=\"wp-image-1044 size-full\" src=\"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2014\/10\/CarbapenemMICs.jpg?resize=530%2C239&#038;ssl=1\" alt=\"CarbapenemMICs\" width=\"530\" height=\"239\" \/><\/a><figcaption id=\"caption-attachment-1044\" class=\"wp-caption-text\">R. CANTON &#8211; ISAR 2014<\/figcaption><\/figure>\n<p>A recent article by Robert\u00a0<a href=\"#_ftn1\" name=\"_ftnref1\">[1]<\/a> and colleagues provides useful data from France.\u00a0 Using a practical definition of carbapenem-non-susceptibility (ertapenem &gt; 0.5, imipenem, meropenem &gt; 2, doripenem &gt; 1), they analyzed the antibiograms of &gt; 133,000 isolates of enterobacteriaceae from 71 French laboratories between Nov. 2011 \u2013 April 2012.\u00a0\u00a0<!--more--><\/p>\n<p>The main results were as follows:\u00a0\u00a0 0.6% of all isolates met above CRE definitions, with Enterobacter cloacae being the predominant pathogen (58%).\u00a0 Expressed differently, 8.2% of all Enterobacter cloacae isolates tested were resistant to at least 1 carbapenem.\u00a0\u00a0 There were 5.6% ESBL producers overall, and 2\/3 of all CRE were ESBL producers.<\/p>\n<p>Of note, resistance to carbapenem antibiotics is multifactorial and only approx. 10% of these isolates produced carbapenemase by genomic testing.\u00a0 Most were from the OXA-48 group, only 2 were NDM isolates.<\/p>\n<p>The authors note that their incidence figure of 0.6% for France is lower than what has been reported for Belgium (3.5%) but this may be due to methodological differences.<\/p>\n<p>Of course, definition for what constitutes &#8220;CRE resistance&#8221; is key here as it can affects incidence figures drastically.\u00a0 Remember, break points for carbapenem antibiotics have changed significantly in the past 2 years.\u00a0 CLSI and FDA are supposed to be in sync but are not always, and EUCAST also has definitions that are ever so slightly different from EMA.<\/p>\n<p>Vive la difference? \u00a0Not to worry:\u00a0 ID clinicians can handle small difference in breakpoints and live with the existing wobble of 1-2 dilution steps.\u00a0 It is actually quite amazing that the differences are so small.<\/p>\n<p>So let\u2019s not fuss too much over lack of harmonization: by the time harmonization occurs, the resistance situation will have changed anyway.\u00a0 Call it the microbe\u2019s revenge or the \u201cICH uncertainty principle&#8217;\u00a0\u00e0 la Heisenberg.<\/p>\n<p><strong>Reference:<\/strong><\/p>\n<p><a href=\"#_ftnref1\" name=\"_ftn1\">[1]<\/a> Robert.\u00a0 J Antimicrob Chemother 2014; 69: 2706<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Despite all the\u00a0concern about the emergence of CRE pathogens worldwide, it is quite difficult to obtain hard quantitative, prospectively collected incidence figures. A recent article by Robert\u00a0[1] and colleagues provides useful data from France.\u00a0 Using a practical definition of carbapenem-non-susceptibility (ertapenem &gt; 0.5, imipenem, meropenem &gt; 2, doripenem &gt; 1), <a class=\"more-link\" href=\"https:\/\/allphasepharma.com\/dir\/2014\/10\/08\/1043\/cre-surveillance-data-from-france\/\">Continue reading <span class=\"screen-reader-text\">  CRE Surveillance Data from France<\/span><span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":1047,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[227,18],"tags":[403,633,44,628,41,363,629,432,625,630,441,350,626,5,632,631,627,346],"class_list":["post-1043","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-recent_literature","category-the_viewpoint","tag-antibiotic-blog","tag-belgium","tag-carbapenem","tag-carbapenemase","tag-clsi","tag-cre","tag-cre-incidence","tag-doripenem","tag-ema","tag-enterobacter","tag-ertapenem","tag-esbl","tag-eucast","tag-fda","tag-france","tag-ich","tag-imipenem","tag-meropenem"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2014\/10\/CLSI-EUCAST-slider-copy.jpg?fit=640%2C200&ssl=1","jetpack_shortlink":"https:\/\/wp.me\/p4KWFr-gP","jetpack_sharing_enabled":true,"jetpack-related-posts":[{"id":3100,"url":"https:\/\/allphasepharma.com\/dir\/2017\/01\/24\/3100\/kill-mocking-bug-cre-crab-variety\/","url_meta":{"origin":1043,"position":0},"title":"To Kill A Mocking Bug &#8211; of the CRKP or CRAB Variety","author":"Harald","date":"January 24, 2017","format":false,"excerpt":"Meropenem stands out as an antibiotic to be used first in ESBL and MDR infections, given its efficacy profile and safety record (see earlier blog). It also would seem to be appropriate to use relatively high doses or prolonged infusion times \u2013 or both - to improve T>MIC for the\u2026","rel":"","context":"In &quot;Recent Literature&quot;","block_context":{"text":"Recent Literature","link":"https:\/\/allphasepharma.com\/dir\/category\/recent_literature\/"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2017\/01\/Mero-slider.jpg?resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2017\/01\/Mero-slider.jpg?resize=350%2C200 1x, https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2017\/01\/Mero-slider.jpg?resize=525%2C300 1.5x"},"classes":[]},{"id":1887,"url":"https:\/\/allphasepharma.com\/dir\/2015\/08\/26\/1887\/avicaz-approval-and-labeling-restrictions\/","url_meta":{"origin":1043,"position":1},"title":"Avycaz Approval and Labeling Restrictions","author":"Harald","date":"August 26, 2015","format":false,"excerpt":"On Feb 25, 2015 the combination of ceftazidime\/avibactam (Avycaz) was approved by FDA for cUTI and cIAI infections in\u00a0patients \u2018who have limited or no alternative treatment options\u2019.\u00a0 As a QIDP drug, Avycaz\u00a0received priority review.\u00a0 Its label states that it is indicated for infections caused by pathogens proven or \u2018suspected to\u2026","rel":"","context":"In &quot;Did you know...?&quot;","block_context":{"text":"Did you know...?","link":"https:\/\/allphasepharma.com\/dir\/category\/interesting_facts\/"},"img":{"alt_text":"Avycaz - slider","src":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/08\/Avycaz-slider.jpg?resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/08\/Avycaz-slider.jpg?resize=350%2C200 1x, https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/08\/Avycaz-slider.jpg?resize=525%2C300 1.5x"},"classes":[]},{"id":1216,"url":"https:\/\/allphasepharma.com\/dir\/2015\/01\/06\/1216\/meropenem-dosing-for-vap-high-prolonged-beats-conventional-dosing\/","url_meta":{"origin":1043,"position":2},"title":"Meropenem Dosing for VAP: High + Prolonged Beats Conventional Dosing","author":"Harald","date":"January 6, 2015","format":false,"excerpt":"Sometimes an article pops up addressing a question we have been mulling over for quite some time.\u00a0 It so happened with a recent publication which shed new light on penem dosing for ICU patients[1]. Conducted at a single Belgian centre (sic!), a standard dose of meropenem (1 g IV q8h\u2026","rel":"","context":"In &quot;Recent Literature&quot;","block_context":{"text":"Recent Literature","link":"https:\/\/allphasepharma.com\/dir\/category\/recent_literature\/"},"img":{"alt_text":"3 arrows - slider","src":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/01\/3-arrows-slider.jpg?resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/01\/3-arrows-slider.jpg?resize=350%2C200 1x, https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2015\/01\/3-arrows-slider.jpg?resize=525%2C300 1.5x"},"classes":[]},{"id":1201,"url":"https:\/\/allphasepharma.com\/dir\/2014\/12\/24\/1201\/why-did-pkpd-modeling-fail-doripenem-in-vap\/","url_meta":{"origin":1043,"position":3},"title":"Why Did PK\/PD Modeling Fail Doripenem in VAP?","author":"Harald","date":"December 24, 2014","format":false,"excerpt":"When imipenem is dosed at 1 g q8h for serious infections, it is infused over 40-60 min. Its label states that it is indicated for \u201clower RTI\u201d, an old-fashioned term from the days when bronchitis and pneumonias were still lumped together, CAP was not differentiated from HAP, and HAP and\u2026","rel":"","context":"In &quot;The Viewpoint&quot;","block_context":{"text":"The Viewpoint","link":"https:\/\/allphasepharma.com\/dir\/category\/the_viewpoint\/"},"img":{"alt_text":"see reference Von Wart et al.","src":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2014\/12\/PKPD-1-copy.jpg?resize=350%2C200","width":350,"height":200},"classes":[]},{"id":653,"url":"https:\/\/allphasepharma.com\/dir\/2014\/07\/21\/653\/what-is-the-niche-for-ceftolozane-tazobactam\/","url_meta":{"origin":1043,"position":4},"title":"What is the \u201cNiche\u201d for Ceftolozane \/ Tazobactam?","author":"Harald","date":"July 21, 2014","format":false,"excerpt":"There are currently a total of 6 beta-lactam + beta-lactamase inhibitor combinations in clinical trials. It will be a steep learning curve for the pharma reps (and physicians) to understand the resistance classifications, the confusing ESBL definitions, the CRE nomenclature, and how this all matters in clinical practice, on the\u2026","rel":"","context":"In &quot;QIDP Antibiotics&quot;","block_context":{"text":"QIDP Antibiotics","link":"https:\/\/allphasepharma.com\/dir\/category\/qidp_antibiotic\/"},"img":{"alt_text":"Tazobactam","src":"http:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/8\/84\/Tazobactam.svg\/220px-Tazobactam.svg.png","width":350,"height":200},"classes":[]},{"id":2313,"url":"https:\/\/allphasepharma.com\/dir\/2016\/03\/03\/2313\/iv-fosfomycin-to-the-rescue-and-to-a-place-near-you\/","url_meta":{"origin":1043,"position":5},"title":"IV Fosfomycin To The Rescue \u2013 And To a Place Near You","author":"Harald","date":"March 3, 2016","format":false,"excerpt":"A recent letter to the Editor by Simkins et al. is worth reviewing [1]. The authors describe the complicated course of a patient who suffered graft rejection after liver transplantation, received broad-spectrum antibiotics during prolonged hospitalization and eventually had a bloodstream infection with carbapenem-resistant Klebsiella pneumoniae (CRKP) which was resistant\u2026","rel":"","context":"In &quot;Recent Literature&quot;","block_context":{"text":"Recent Literature","link":"https:\/\/allphasepharma.com\/dir\/category\/recent_literature\/"},"img":{"alt_text":"Fosfomycin - slider copy","src":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2016\/02\/Fosfomycin-slider-copy.jpg?resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2016\/02\/Fosfomycin-slider-copy.jpg?resize=350%2C200 1x, https:\/\/i0.wp.com\/allphasepharma.com\/dir\/wp-content\/uploads\/2016\/02\/Fosfomycin-slider-copy.jpg?resize=525%2C300 1.5x"},"classes":[]}],"jetpack_likes_enabled":true,"_links":{"self":[{"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/posts\/1043","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/comments?post=1043"}],"version-history":[{"count":3,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/posts\/1043\/revisions"}],"predecessor-version":[{"id":1048,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/posts\/1043\/revisions\/1048"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/media\/1047"}],"wp:attachment":[{"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/media?parent=1043"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/categories?post=1043"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/allphasepharma.com\/dir\/wp-json\/wp\/v2\/tags?post=1043"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}