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:

994
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:

1

Information Journal Paper

Title

ANTIMICROBIAL SUSCEPTIBILITY PATTERNS AND MOLECULAR EPIDEMIOLOGY OF PSEUDOMONAS AERUGINOSA ISOLATED FROM BURN PATIENTS

Pages

  694-706

Keywords

METALLO-Β-LACTAMASE (MBL) ENZYMEQ2
PULSED-FIELD GEL ELECTROPHORESIS (PFGE)Q2

Abstract

 Background & aim: Because of emerging multi-drug resistance (MDR) PSEUDOMONAS AERUGINOSA strains, treatment of BURN PATIENTS infected by this bacterium is difficult. The aim of this study was to detect antimicrobial profile and molecular epidemiology of metallo-beta-lactamase (MBL) producer strains.Methods: In this cross-sectional investigation 270 PSEUDOMONAS AERUGINOSA isolates were collected from the BURN PATIENTS. Carbapenem sresistance strains were detected by phenotypic Etest method. Susceptibility profiles of metallo-b-lactamase (MβL) enzyme producing isolates of this bacterium to 11 antimicrobial drugs were determined by disc diffusion method according Clinical and Laboratory Standards Institute (CLSI) guidelines. The genetic correlations between isolates were determined by Pulsed-Field Gel Electrophoresis (PFGE) method.Results: Among 270 P. aeruginosa isolates, 60 (22.2%) strains showed resistant to meropenem (MEM) and imipenem (IMI) and were considered as metallo-b-lactamase positive. All metallo-β- lactamase positive isolates were resistant to five tested antimcrobial while their sensitivities to the three best effective antibiotics including ciprofloxacin, amikacin and ceftazidime were 1.7%, 6.7 % and 23.3%, respectively. Majority of the isolates (71.6%) showed more than 80% similarity based on the drawn dendrogram.Conclusion: Our results showed, the tested antimicrobials are not safe to prescribe for BURN PATIENTS. According PFGE pulsotypes, a limited number of P.aeruginosa types are common in the hospital burn units which infect the patients hospitalized in this ward.

Cites

References

  • No record.
  • Cite

    APA: Copy

    ANVARINEJAD, M., JAPONI, A., RAFAATPOUR, N., ALIPOUR, E., ABBASI, P., SHAHIDI, M.A., & MARDANEH, J.. (2014). ANTIMICROBIAL SUSCEPTIBILITY PATTERNS AND MOLECULAR EPIDEMIOLOGY OF PSEUDOMONAS AERUGINOSA ISOLATED FROM BURN PATIENTS. ARMAGHAN DANESH, 19(8 (91)), 694-706. SID. https://sid.ir/paper/78040/en

    Vancouver: Copy

    ANVARINEJAD M., JAPONI A., RAFAATPOUR N., ALIPOUR E., ABBASI P., SHAHIDI M.A., MARDANEH J.. ANTIMICROBIAL SUSCEPTIBILITY PATTERNS AND MOLECULAR EPIDEMIOLOGY OF PSEUDOMONAS AERUGINOSA ISOLATED FROM BURN PATIENTS. ARMAGHAN DANESH[Internet]. 2014;19(8 (91)):694-706. Available from: https://sid.ir/paper/78040/en

    IEEE: Copy

    M. ANVARINEJAD, A. JAPONI, N. RAFAATPOUR, E. ALIPOUR, P. ABBASI, M.A. SHAHIDI, and J. MARDANEH, “ANTIMICROBIAL SUSCEPTIBILITY PATTERNS AND MOLECULAR EPIDEMIOLOGY OF PSEUDOMONAS AERUGINOSA ISOLATED FROM BURN PATIENTS,” ARMAGHAN DANESH, vol. 19, no. 8 (91), pp. 694–706, 2014, [Online]. Available: https://sid.ir/paper/78040/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