Journals / Haydarpaşa Numune Medical Journal / 2020 / Cilt: 60 - Sayı: 4

Detection of the Presence of Extended-Spectrum Beta-Lactamase Enzyme in Gram-negative Bacteria According to CLSI and EUCAST Criteria

Pages
352–356
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

For both standards, the use of cefpodoxime,cefotaxime or ceftriaxone disks in screening and; cefotaxime and cefotaxime- clavulanate disks in confirmation tests will provide more accurate results.

📌 3 Key Takeaways

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Objective & Hypothesis:Introduction: Expanded spectrum beta-lactamase is a critical source that is limiting the using areas of beta-lactam antibi- otics by hydrolysing them.
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Key Findings & Data:The method to be used for accurate detection of ESBL production is significant.
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Conclusion & Impact:For both standards, the use of cefpodoxime,cefotaxime or ceftriaxone disks in screening and; cefotaxime and cefotaxime- clavulanate disks in confirmation tests will provide more accurate results.
🔬Design:Research Article
📍Scope:2014 Verileri
⚙️Variables:Domain Parameters

Özet

Introduction: Expanded spectrum beta-lactamase is a critical source that is limiting the using areas of beta-lactam antibi- otics by hydrolysing them. The method to be used for accurate detection of ESBL production is significant. CLSI and EUCAST are the two most commonly used standards for the determination of antibiotic susceptibility. This study aimed to investigate the sensitivity and specificity of these standards for ESBL detection. Methods: This study includes 76 ESBL producers and 74 ESBL negative strains, which were isolated from urine specimens that sent to the Medical Microbiology Laboratory of Haydarpasa Numune Training and Research Hospital from April to July 2014. For screening tests, ceftazidime (10μg and 30μg), cefotaxime (5μg and 30μg), ceftriaxone (30μg), cefpodoxime (10μg), cefepime (30μg) ve aztreonam (30μg) disks; for confirmation tests double-disk synergy and combination disk method were used. For molecular confirmation tests, CTX-M, TEM and SHV resistance genes were investigated by polymerase chain reaction. Results: ESBL producing isolates were found at 86.8% as CTX-M, 47.4% as TEM and 9.2% as SHV. More than one resistance gene was detected in some isolates. Beta-lactam susceptibilities of ESBL producers with CLSI and EUCAST breakpoints were 29.2% and 19.7% for ceftazidime, 14.5% and 15.8% for cefepime, 2.6% and 13.2% for aztreonam, respectively. Among the screening disks, cefpodoxime (interpreted by EUCAST criteria), showed the highest sensitivity and specificity. This was followed by cefpodoxime (CLSI), cefotaxime and ceftriaxone with similar sensitivity and specificity for both standards. Discussion and Conclusion: There was no significant difference between CLSI and EUCAST in determining ESBL production. The suggestion of EUCAST that using different disks for screening and confirmation tests increases the sensitivity of detecting ESBL, especially in ceftazidime; however, it may cause practical difficulties. For both standards, the use of cefpodoxime,cefotaxime or ceftriaxone disks in screening and; cefotaxime and cefotaxime- clavulanate disks in confirmation tests will provide more accurate results.

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Cite This Article

TOPTAN, H., BALKÖSE, G., DOĞAN, Ö., ADALETİ, R., AKSARAY, S. (2020). Detection of the Presence of Extended-Spectrum Beta-Lactamase Enzyme in Gram-negative Bacteria According to CLSI and EUCAST Criteria. Haydarpaşa Numune Medical Journal, Cilt: 60 - Sayı: 4, 352–356. https://ajindex.com/articles/160166

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References (11)

  1. Rawat D, Nair D. Extended-spectrum β-lactamases in Gram Negative Bacteria. J Glob Infect Dis 2010;2:263–74
  2. Dhillon RH, Clark J. ESBLs: A Clear and Present Danger? Crit Care Res Pract 2012;2012:625170
  3. Taşova Y. Gram negatif enterik bakteri enfeksiyonlarının yöne- timi, ANKEM Derg 2011;25:34–44. 4. de Kraker ME, Wolkewitz M, Davey PG, Koller W, Berger J, Na- gler J, et al. Burden of antimicrobial resistance in European hospitals: excess mortality and length of hospital stay associated with bloodstream infections due to Escherichia coli resistant to third-generation cephalosporins. J Antimicrob Chemother 2011;66:398–407
  4. CLSI. M100 Performance Standards for Antimicrobial Susceptibility Testing. 27th ed. Wayne, PA: Clinical and Laboratory Standards Institute; 2017
  5. EUCAST. Breakpoint Tables for Interpretation of MICs and Zone Diameters, Version 7.1, 2017. Available at: http://www.eucast.org/ast_of_bacteria/previous_versions_of_docu- ments/. Accessed 20 Nov, 2018
  6. Blandino G, Mastrojeni S, Inturri R, Sciacca A, Nicoletti G. An- timicrobial susceptibility of strains of Enterobactericeae iso- lated from bloodstream infections using current CLSI and EUCAST breakpoints. Health 2014;6:153–7
  7. Rodríguez-Baño J, Picón E, Navarro MD, López-Cerero L, Pascual A; ESBL-REIPI Group. Impact of changes in CLSI and EUCAST breakpoints for susceptibility in bloodstream infections due to extended-spectrum β-lactamase-producing Escherichia coli. Clin Microbiol Infect 2012;18:894–900
  8. Hombach M, Mouttet B, Bloemberg GV. Consequences of revised CLSI and EUCAST guidelines for antibiotic susceptibility patterns of ESBL- and AmpC β-lactamase-producing clinical Enterobacteriaceae isolates. J Antimicrob Chemother 2013;68:2092–8
  9. Polsfuss S, Bloemberg GV, Giger J, Meyer V, Hombach M. Com- parison of European Committee on Antimicrobial Susceptibility Testing (EUCAST) and CLSI screening parameters for the detection of extended-spectrum β-lactamase production in clinical Enterobacteriaceae isolates. J Antimicrob Chemother 2012;67:159–66
  10. Coque TM, Baquero F, Canton R. Increasing prevalence of ESBL-producing Enterobacteriaceae in Europe. Euro Surveill 2008;13:19044
  11. Görgeç S, Kuzucu Ç, Otlu B, Yetkin F, Ersoy Y. Genişlemiş spek- trumlu beta-laktamaz üreten nozokomiyal Escherichia coli izolatlarında beta-laktamaz gen oranları ve klonal ilişkinin araştırılması [Investigation of beta-lactamase genes and clonal relationship among the extended-spectrum beta- la