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Comparative In Vitro Activity of Carbapenems Against Clinical Isolates of Acinetobacter Baumannii Publisher Pubmed



Douraghi M1, 2 ; Ghalavand Z3 ; Nateghi Rostami M4 ; Zeraati H5 ; Aliramezani A1 ; Rahbar M6 ; Mohammadzadeh M7 ; Ghourchian S1 ; Boroumand MA8 ; Abdollahi A9
Authors
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Authors Affiliations
  1. 1. Division of Microbiology, Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Food Microbiology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Microbiology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. Center for Research and Training in Skin Diseases and Leprosy, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Epidemiology and Biostatistics, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Microbiology, Reference Health Laboratories, Ministry of Health, Tehran, Iran
  7. 7. Pediatrics Infectious Diseases Research Center, Department of Infectious Diseases, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Pathology, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Department of Pathology, Imam Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Applied Microbiology Published:2016


Abstract

Aims: The aim of this multi-hospital study was to assess the in vitro activity of doripenem and its comparators, imipenem and meropenem, using the new CLSI breakpoints against a large population of a frequently isolated nosocomial pathogen, Acinetobacter baumannii. Methods and Results: During a 2-year period, four referral or tertiary hospitals submitted 400 isolates of Ac. baumannii for susceptibility testing using imipenem, meropenem and doripenem via disc diffusion and E-test methods. A subset of 390 isolates was resistant to all three tested carbapenems. Doripenem and meropenem (MIC50, 32 μg ml−1) had comparable activity, albeit doripenem's activity was greater than imipenem (MIC50, >32 μg ml−1). A significantly higher proportion of the isolates were inhibited by doripenem than by imipenem at MIC values of 12, 16, 24 and 32 μg ml−1 (P < 0·05). The cumulative percentage of imipenem MICs was lower compared to its comparators. The comparison of resistance rate to imipenem and meropenem based on old and new breakpoints showed <1% difference. The overall agreement between the two susceptibility testing methods was ≥95%. Conclusion: Doripenem has a slightly greater in vitro activity than imipenem in terms of zone breakpoints and MIC values, but its activity is comparable to meropenem. Significance and Impact of the Study: Doripenem should be considered as a therapeutic option for monotherapy or combination therapy, particularly when the therapeutic options are limited. © 2016 The Society for Applied Microbiology
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