مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

1,349
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

EMERGENCE OF IMIPENEM RESISTANCE AND PRESENCE OF METALLO-β-LACTAMASES ENZYMES IN MULTI DRUG RESISTANT GRAM NEGATIVE BACILLI ISOLATED FROM CLINICAL SAMPLES IN KERMAN, 2007-2008

Pages

  208-214

Abstract

 Background & Aims: IMIPENEM is a member of Carbapenem with stability against most b-lactamases .It is of particular use in the treatment of infections associated with drug resistant gram negative bacteria harboring ESBL and AmpC genes. The aim of this study was to determine the IMIPENEM resistance in gram negative bacteria causing nosocomial infections and the presence of metallo-b-lactamases (MBLS) in resistant isolates.Methods: Minimum inhibitory concentration (MIC) of IMIPENEM was determined for 276 multiple drug resistant gram negative bacteria by agar dilution method. Escherichia coli ATCC 25922, Klebsiella pneumoniae ATCC 700603 and Pseudomonas aeruginosa ATCC 27853 were used as standard strains. Disk diffusion method with disks containing IMIPENEM and IMIPENEM+10ml EDTA (0.5 M) was used for determination of the presence of metallo- b-lactamases. Zone diameter ³7mm of IMIPENEM tested in combination with EDTA versus IMIPENEM alone was considered as MBL positive.Results: From a total of 276 b-lactamase producing isolates including K. pneumoniae (n=38), E. coli (n=169) and P.aeruginosa (n=69), 3 isolates with MIC=32mg/ml were found to be resistant to IMIPENEM. From these isolates, one strain of K. pneumoniae and one strain of P.aeruginosa isolates were determined to be MBL producers by phenotypic method. Conclusion: According to the presence of metallo b-lactamases in bacterial strain in the region, resistance to this valuable therapeutic agent is not unexpected.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    KALANTAR, D., MANSOURI, SHAHLA, & RAZAVI, MOZHDEH. (2010). EMERGENCE OF IMIPENEM RESISTANCE AND PRESENCE OF METALLO-β-LACTAMASES ENZYMES IN MULTI DRUG RESISTANT GRAM NEGATIVE BACILLI ISOLATED FROM CLINICAL SAMPLES IN KERMAN, 2007-2008. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, 17(3), 208-214. SID. https://sid.ir/paper/350/en

    Vancouver: Copy

    KALANTAR D., MANSOURI SHAHLA, RAZAVI MOZHDEH. EMERGENCE OF IMIPENEM RESISTANCE AND PRESENCE OF METALLO-β-LACTAMASES ENZYMES IN MULTI DRUG RESISTANT GRAM NEGATIVE BACILLI ISOLATED FROM CLINICAL SAMPLES IN KERMAN, 2007-2008. JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2010;17(3):208-214. Available from: https://sid.ir/paper/350/en

    IEEE: Copy

    D. KALANTAR, SHAHLA MANSOURI, and MOZHDEH RAZAVI, “EMERGENCE OF IMIPENEM RESISTANCE AND PRESENCE OF METALLO-β-LACTAMASES ENZYMES IN MULTI DRUG RESISTANT GRAM NEGATIVE BACILLI ISOLATED FROM CLINICAL SAMPLES IN KERMAN, 2007-2008,” JOURNAL OF KERMAN UNIVERSITY OF MEDICAL SCIENCES, vol. 17, no. 3, pp. 208–214, 2010, [Online]. Available: https://sid.ir/paper/350/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button