Microbiological and Minimum Inhibitory Concentration Study of Ventilator-associated Pneumonia Agents in Two University-associated Hospital Intensive Care Units in Mazandaran

Message:
Abstract:
Background
Ventilator-associated pneumonia (VAP) is a type of nosocomial pneumonia which develops more than 48 hours after endotracheal intubation. Early recognition and treatment of VAP is important, since timely and appropriate management can be lifesaving..
Objectives
This study aimed to determine the antimicrobial susceptibility pattern of microorganisms causing VAP in the intensive care units (ICU) of two university associated hospitals in the province of Mazandaran in Iran from 2008 to 2010..
Materials And Methods
This study was performed on VAP patients diagnosed with the clinical pulmonary infection score (CPIS) in ICU’s of two university hospitals. For each patient suspected of VAP, quantitative culture of endotracheal aspiration (QEA) was performed and minimum inhibitory concentration (MIC) was determined by a micro dilution test. Data was analyzed by the SPSS 17 software and a P < 0.05 was considered to be statistically significant..
Results
In this study, the type and the frequency of the microbial agents causing VAP was as follows: coagulate negative staphylococci (23.3%), Escherichia coli (E. coli) (21.7%), Staphylococcus aureus (S. aureus) (18.3%), Pseudomonas aeruginosa (P. aeroginosa) (18.3%), Enterobacter spp (11.7%). and Klebsiella pneumoniae (K. pneumonia) (6.7%). 35.71% of coagulate negative staphylococci were sensitive to vancomycin. All of the isolated E. coli was resistant to ceftazidime, but 50% sensitive to gentamicin and meropenem. 54.54% of isolated S. aureus were resistant to vancomycin. All of the isolated P. aeroginosa cases were sensitive to imipenem while 50% were resistant to ceftazidime..
Conclusions
In patients with VAP, carbapenems had good activity against P. aeroginosa. Increasing resistance of S. aureus to vancomycin requires more attention and further studies..
Language:
English
Published:
Archives of Clinical Infectious Diseases, Volume:8 Issue: 1, Jan 2013
Pages:
8 to 13
https://www.magiran.com/p1223226  
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