In vitro antimicrobial activity of ceftazidime- avibactam tested against carbapenem resistant enterobacteriaceae and pseudomonas aeruginosa clinical isolates / Amany Mahmoud Ahmed Mohamed ; Supervised Mona Mohieeden Abdelhaleem , Amal Mohamed Sayed , Doaa Mohammad Ghaith
Material type:
- اختبار النشاط المضاد للميكروبات لعقار سيفتازديم افيبكتام داخل المعمل ضد البكتيريا المعوية المقاومة للكاربابينيم وسودوموناس اريوجونوزا للعزلات المرضية [Added title page title]
- Issued also as CD
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2021.Am.I (Browse shelf(Opens below)) | Not for loan | 01010110085107000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2021.Am.I (Browse shelf(Opens below)) | 85107.CD | Not for loan | 01020110085107000 |
Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
Backgroung: The global spread of Carbapenem resistance organisms (CRO) has become a major public health concern especially regarding limited treatment options. Ceftazidime-avibactam (CZA) is a promising therapy for CRO causing infections Aim of work: we aimed to determine the prevalence of carbapenem resistant Enterobacteriaceae and Pseudomonas aeruginosa among clinical isolates and to investigate the in vitro antimicrobial susceptibility of CZA. Methods: Our study was conducted at Cairo university specialized pediatric hospital over one year. A total of 320 isolates were included. CZA.susceptibility testing was done disk diffusion method.The presence of carbapenemases was detected in 170 isolates by modified carbapenem inactivation method (mCIM) and multiplex PCR tests. Results: Prevalence of the prevalence of carbapenem resistant Enterobacteriaceae and Pseudomonas aeruginosa clinical isolates was 72.6%. Among our isolates, 78.8% were Klebsiella pneumoniae. The most frequently detected carbapenemase genes were blaNDM in 70.0% isolates, followed by blaOXA-48 in 67.6% and blaKPC in 16.5% isolates. CZA active against 30.0% of isolates Conclusion: multiplex PCR is sensitive and specific method for carbapenamase detection. CZA exhibited a fairly susceptible rate among our CRO
Issued also as CD
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