Author/Authors :
Moniri Rezvan نويسنده , Sehat Mojtaba نويسنده Department of Epidemiology and Biostatistics, School of Public Health, And Oncopathology Research Centre, Tehran , Khaltabadi Farahani Reza نويسنده Department of Microbiology and Immunology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, IR Iran Khaltabadi Farahani Reza , Dastehgoli Kamran نويسنده Anatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, IR Iran Dastehgoli Kamran , Firoozeh Farzaneh نويسنده Department of Microbiology and Immunology, School of Medicine, Kashan University of Medical Sciences, Kashan, IR Iran , Bagheri Josheghani Sareh نويسنده Department of Microbiology and Immunology, Faculty of Medicine,Kashan University of Medical Sciences, Kashan, IranKashan University of Medical Sciences Bagheri Josheghani Sareh , Koosha Hasan نويسنده Shahid Beheshti Hospital, Kashan University of Medical
Sciences, Kashan, IR Iran
Abstract :
Background Emergence of multidrug-resistant (MDR)
Acinetobacter baumannii infections is becoming a
worldwide threat to hospitalized patients, particularly in intensive
care units. Objectives The aim of this study was to investigate the
antimicrobial susceptibility patterns and prevalence of
blaOXA-type carbapenemases of
A. baumannii isolates in a teaching hospital in Iran.
Patients and Methods The study included a total of 40 isolates of
carbapenem-resistant A. baumannii, obtained from 103
tracheal tubes in hospitalized ICU patients. Antimicrobial
susceptibility testing was performed according to CLSI guidelines. The
blaOXA-51,
blaOXA-23,
blaOXA-24,
blaOXA-58, and
ISAba1 genes were detected by PCR. Results All of the
A. baumannii isolates were resistant to imipenem and
meropenem, and 100% of the isolates were MDR. The
blaOXA-51 and
ISAba1 genes were detected in 100% of the isolates.
blaOXA-23 and
blaOXA-24 were detected in 90%
and 40% of the isolates, respectively, but
blaOXA-58 was absent in the
A. baumannii isolates. In addition, 32.5% of
carbapenem-resistant strains contained at least three genes encoding
blaOXA-type carbapenemase.
Colistin and polymyxin B were the most effective antibiotics. The sole
risk factor for infection of hospitalized patients with
carbapenem-resistant Acinetobacter strains was age over 40 years (P =
0.042). The mortality rate was 27.5%. Conclusions These findings signify
the alarming spread of OXA genes in A. baumannii
strains in our intensive care unit. The spread of carbapenem-resistant
Acinetobacter strains has serious health implications
and requires the application of strict infection-control measures.