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Resistance patterns of Pseudomonas aeruginosa to carbapenems and piperacillin/tazobactam

E M Mokaddas1, S C Sanyal

  • 1Department of Laboratory Medicine, Ibn Sina Hospital, Safat, Kuwait.

Insights

Multiresistant Pseudomonas aeruginosa shows varying resistance to carbapenems and piperacillin/tazobactam. Meropenem demonstrated the lowest resistance, followed by imipenem, indicating potential treatment options for nosocomial infections.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Pseudomonas aeruginosa is a significant nosocomial pathogen, particularly problematic in immunocompromised patients.
  • Multidrug resistance in P. aeruginosa poses a substantial clinical challenge, necessitating evaluation of current therapeutic agents.

Purpose of the Study:

  • To determine the resistance patterns of P. aeruginosa to imipenem, meropenem, and piperacillin/tazobactam.
  • To investigate cross-resistance between carbapenems and piperacillin/tazobactam.
  • To compare the activity of these antipseudomonal drugs against P. aeruginosa isolates.

Main Methods:

  • Prospective study conducted from June 1996 to December 1997.
  • Testing of 357 P. aeruginosa isolates from 188 patients for susceptibility to imipenem, meropenem, and piperacillin/tazobactam.
  • Analysis of cross-resistance patterns among the tested drugs.

Main Results:

  • Resistance rates were 10.4% for imipenem, 5.9% for meropenem, and 14% for piperacillin/tazobactam.
  • Cross-resistance between imipenem and meropenem was observed in 5.9% of isolates; 43% of imipenem-resistant isolates were susceptible to meropenem.
  • Significant cross-resistance was noted between carbapenems and piperacillin/tazobactam.

Conclusions:

  • P. aeruginosa exhibited least resistance to meropenem, followed by imipenem and piperacillin/tazobactam.
  • Cross-resistance exists between carbapenems and between carbapenems and piperacillin/tazobactam.
  • Patients in surgical, cancer, and transplant units are more susceptible to multidrug-resistant P. aeruginosa infections.

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