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. 2016 Sep;111(9):551–558. doi: 10.1590/0074-02760160116

TABLE IV. Mechanisms of carbapenem resistance and antimicrobial resistance among clinical Pseudomonas aeruginosa isolates from infection.

Mechanisms of resistance: efflux system, AmpC, oprD mutation* (number of isolates) Antimicrobial resistance profile** (number of isolates) MIC*** (μg/mL)

IPM MER
+,+,+ (3) IPM MEM FEP CIP CAZ TZP TOB GEN (1) 32 32
IPM MEM (1) 24 12
IPM (1) 12 4
+,-,+ (3) IPM MEM AMK FEP CIP CAZ TZP TOB GEN (1) 24 > 32
IPM MEM FEP CIP CAZ TZP TOB GEN (1) 16 > 32
IPM (1) 6 1.5
-,+,+ (3) IPM MEM FEP CIP CAZ TZP TOB GEN (2) 24 > 32
  32 > 32
IPM (1) 16 2
-,-,+ (1) IPM MEM FEP CIP CAZ TZP TOB GEN (1) 4 6
+,+,-(1) Susceptible (1) 1.5 0.38
-,+,- (3) Susceptible (3) 1.5-0.75 0.19-0.38
-,-,- (21) AMK FEP CIP CAZ TZP TOB GEN (2) 0.75-1.5 0.094-2
  AMK FEP CIP CAZ TOB GEN (2) 0.75 1
  AMK FEP CAZ PIP (1) 0.75 0.19
  TOB, GEN (1) 1 0.25
  Susceptible (15) 0.5-1 0.064-0.5

*: assessed by comparison of carbapenem minimum inhibitory concentration (MIC) and in combination with PAβN or cloxacillin and sequencing of oprD. Antimicrobial susceptibility was determined by disc diffusion (**) or E-test (***); + or - : presence or absence of mechanism of resistance, respectively; AMK: amikacin; CAZ: ceftazidime; CIP: ciprofloxacin; FEP: cefepime; GEN: gentamicin; IPM: imipenem; MEM: meropenem; TZP: piperacillin-tazobactam; TOB: tobramycin; IMP and MER MIC interpretation: ≤ 2, susceptible; 4, intermediate; ≥ 8, resistant.