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Antimicrobial activity of Cefepime-Tazobactam combination against extended Spectrum Beta- Lactamase and/or AampC Beta-Lactamase- producing gram-negative bacilli / Noha Refaat Mahmoud ; Supervised Azza Essam Eldin Badr , Hala Elsayed Badawi , Basma Ahmed Elawady

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Noha Refaat Mahmoud , 2016Description: 113 P. : charts , facsimils ; 25cmOther title:
  • تأثير مركب السيفيبيم- تازوباكتم ضد العصويات سالبة التصبغ المنتجة لإنزيمات البيتا لاكتميز ممتدة المفعول أوالأم-بي-سي [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Microbiology and Immunology Summary: Introduction: The purpose of this study was to evaluate the sensitivity of cefepime /tazobactam combination against ESBL- and/or AmpC-producing Gram-negative bacilli. Materials and method: The study was conducted on 100 Gram-negative bacilli. ESBL production was screened by using the disc diffusion test and was confirmed by the combined disc confirmatory test, screening of AmpC production was done by cefoxitin disc test and confirmation was done by AmpC disc test. Isolates confirmed positive for ESBL and/ or AmpC production were investigated for their susceptibility to the following antibiotics: cefepime, imipenem, ertapenem, meropenem, piperacillin/tazobactam, cefoperazone/sulbactam and cefepime/tazobactam. Results: Among 100 Gram-negative bacilli, 56 isolates screened positive for ESBL production by the disc diffusion test and 44 were confirmed as ESBL producers by the combined disc confirmatory test. Thirty-two isolates were screened positive for AmpC production by cefoxitin disc test and 9 isolates were confirmed as AmpC producers by AmpC disc test. Using MAST D68C set, 32 isolates were ESBL producers, 3 were AmpC producers, and 4 isolates were both ESBL and AmpC producers. Forty-three isolates were sensitive to cefepime/tazobactam combination, 10 isolates were sensitive to cefoperazone/sulbactam, 13 isolates were sensitive to piperacillin/tazobactam, 37 isolates were sensitive to meropenem, 32 isolates were sensitive to ertapenem, 37 isolates were sensitive to imipenem and 8 isolates were sensitive to cefepime. Conclusion: Cefepime/tazobactam revealed excellent activity against ESBL and/or AmpC-producing Gram-negative bacilli and may be considered as a therapeutic alternative to carbapenems in infections caused by these organisms
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.19.M.Sc.2016.No.A (Browse shelf(Opens below)) Not for loan 01010110071893000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.19.M.Sc.2016.No.A (Browse shelf(Opens below)) 71893.CD Not for loan 01020110071893000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Microbiology and Immunology

Introduction: The purpose of this study was to evaluate the sensitivity of cefepime /tazobactam combination against ESBL- and/or AmpC-producing Gram-negative bacilli. Materials and method: The study was conducted on 100 Gram-negative bacilli. ESBL production was screened by using the disc diffusion test and was confirmed by the combined disc confirmatory test, screening of AmpC production was done by cefoxitin disc test and confirmation was done by AmpC disc test. Isolates confirmed positive for ESBL and/ or AmpC production were investigated for their susceptibility to the following antibiotics: cefepime, imipenem, ertapenem, meropenem, piperacillin/tazobactam, cefoperazone/sulbactam and cefepime/tazobactam. Results: Among 100 Gram-negative bacilli, 56 isolates screened positive for ESBL production by the disc diffusion test and 44 were confirmed as ESBL producers by the combined disc confirmatory test. Thirty-two isolates were screened positive for AmpC production by cefoxitin disc test and 9 isolates were confirmed as AmpC producers by AmpC disc test. Using MAST D68C set, 32 isolates were ESBL producers, 3 were AmpC producers, and 4 isolates were both ESBL and AmpC producers. Forty-three isolates were sensitive to cefepime/tazobactam combination, 10 isolates were sensitive to cefoperazone/sulbactam, 13 isolates were sensitive to piperacillin/tazobactam, 37 isolates were sensitive to meropenem, 32 isolates were sensitive to ertapenem, 37 isolates were sensitive to imipenem and 8 isolates were sensitive to cefepime. Conclusion: Cefepime/tazobactam revealed excellent activity against ESBL and/or AmpC-producing Gram-negative bacilli and may be considered as a therapeutic alternative to carbapenems in infections caused by these organisms

Issued also as CD

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