Clonal Spread of Imipenem-ResistantPseudomonas aeruginosain the Intensive Care Unit of a Turkish Hospital
- 1 January 2001
- journal article
- Published by Taylor & Francis in Journal of Chemotherapy
- Vol. 13 (5) , 546-554
- https://doi.org/10.1179/joc.2001.13.5.546
Abstract
Pseudomonas aeruginosa may cause life-threatening infections, especially in nosocomial settings. Although carbapenems are considered as one of the most effective alternatives in antipseudomonal therapy, resistance to the carbapenem group of antibacterials is a growing problem. In the first 6 months of 1997, P. aeruginosa isolates that were resistant to almost all antipseudomonal agents including imipenem were recovered from various specimens from intensive, care unit (ICU) patients. Isolates with the same antibiogram profile caused a small outbreak in May 1997. A retrospective case-control study revealed that the major risk factors for infection/colonization with multiresistant P. aeruginosa were prolonged stay in the ICU (p<0.001), previous and lengthy imipenem usage (p<0.001 and p<0.0001, respectively), and mechanical ventilation (p<0.001). Analytical isoelectric focusing of the sonicates prepared from the isolates showed that each isolate produced 1-5 beta-lactamases, enzymes with isoelectric points (pIs) of 5.1, 6.4, 8.5-8.7 being the most prevalent. DNA macrorestriction patterns of imipenem-resistant isolates were distinct from those of the imipenem-sensitive isolates recovered from ICU patients during the same interval and from the environmental isolates (controls). Thus, our results indicate that colonized patients appear to be the major source for cross-contamination of other patients and if imipenem is selected for empirical therapy, emergence of resistant strains should be anticipated and appropriate precautions taken.Keywords
This publication has 22 references indexed in Scilit:
- Epidemiology and Clinical Outcomes of Patients with Multiresistant Pseudomonas aeruginosaClinical Infectious Diseases, 1999
- Resistance Mechanisms inPseudomonas aeruginosaand Other Nonfermentative Gram‐Negative BacteriaClinical Infectious Diseases, 1998
- OXA-14, another extended-spectrum variant of OXA-10 (PSE-2) beta-lactamase from Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1995
- β-Lactum resistance in aerobic commensal faecal floraInternational Journal of Antimicrobial Agents, 1994
- Assessment of Bacterial Cross-Transmission as a Cause of Infections in Patients in Intensive Care UnitsClinical Infectious Diseases, 1994
- Imipenem resistance among gram-negative bacilliEuropean Journal of Clinical Microbiology & Infectious Diseases, 1994
- Characterization of a novel extended-spectrum beta-lactamase from Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1993
- ARI 1: β-lactamase-mediated imipenem resistance in Acinetobacter baumanniiInternational Journal of Antimicrobial Agents, 1993
- Imipenem-induced resistance to antipseudomonal beta-lactams in Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1985
- The Use of Analytical Isoelectric Focusing for Detection and Identification of -LactamasesJournal of General Microbiology, 1975