AI Article Synopsis

  • * Researchers tested 39 isolates (18 A. baumannii and 21 P. aeruginosa) taken from hospitalized patients in southern Iran, finding that all tested strains of A. baumannii were resistant to imipenem and ceftazidime, while both types of bacteria were susceptible to colistin.
  • * Results showed that colistin had strong in vitro activity, with encouraging minimum inhibitory concentrations, suggesting it could be a useful treatment option for drug-resistant infections; however, more extensive studies are needed for confirmation.

Article Abstract

Objective: The present study aimed to determine in vitro activity of colistin and other agents against drug-resistant isolates of Pseudomonas aeruginosa and Acinetobacter baumannii.

Results: This in vitro study performed on a collection of non-fermenting Gram-negative bacilli (NFB) consist of 18 A. baumannii and 21 P. aeruginosa isolates. Non-duplicated isolates (one per patient) were isolated from blood, endotracheal tube and sputum samples of hospitalized patients in the south of Iran. The minimum inhibitory concentrations (MICs) of each isolate was determined using Epsilometer (E)-test strips containing colistin, imipenem, and ceftazidime. In overall, all A. baumannii isolates were non-susceptible to imipenem and ceftazidime. In contrast, all isolates were susceptible to colistin with MIC50 and MIC90 of 0.75/1.5 µg/mL, respectively. Antibiotic susceptibility results showed that 81% and 23.8% of P. aeruginosa isolates were susceptible to ceftazidime and imipenem, respectively. While, all of the P. aeruginosa isolates were susceptible to colistin with MIC50 and MIC90 of 0.5/1 µg/mL, respectively. In summary, colistin showed the promising in vitro activity against drug-resistant strains of two clinically important NFB in our region. However, investigation on a larger collection of drug-resistant strains demands to support these observations in the near future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540545PMC
http://dx.doi.org/10.1186/s13104-019-4344-7DOI Listing

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