Rifampicin/imipenem combination in the treatment of carbapenem-resistant Acinetobacter baumannii infections.

J Antimicrob Chemother

Infectious Disease Service, Hospital de Bellvitge, University of Barcelona C/Feixa Llarga s/n 08907, L'Hospitalet de Llobregat, Barcelona, Spain.

Published: September 2006

AI Article Synopsis

  • A significant rise in carbapenem-resistant Acinetobacter baumannii infections has complicated treatment, with colistin being the primary antibiotic used, though its clinical use is limited.
  • A pilot study was conducted on ten patients with serious carbapenem-resistant infections, utilizing a combination of rifampicin and imipenem, which resulted in mixed outcomes and highlighted high resistance development to rifampicin in many cases.
  • The findings indicate that the rifampicin/imipenem combination is not effective for these infections, suggesting the need for further research into alternative antibiotic combinations.

Article Abstract

Background: In the setting of a large endemic of Acinetobacter baumannii infections, treatment of those due to carbapenem-resistant strains, susceptible only to colistin, has become a major problem in our hospital during the past years. Successful results have been reported using colistin, but clinical experience with this antibiotic is limited. In our experimental studies using these strains in a mouse pneumonia model, the best results were observed with a combination of rifampicin and imipenem.

Methods: From July 2000 to September 2001, we performed a pilot study with patients suffering from serious infections due to carbapenem-resistant A. baumannii. Patients were treated with a rifampicin/imipenem combination and followed up prospectively. Cultures were repeated during and after treatment, and in vitro activity of rifampicin was monitored. Genotyping of these strains was performed by means of PFGE.

Results: Ten patients were selected: four with ventilator-associated pneumonia, and six with other infections (one catheter-related bacteraemia, five surgical infections). Three patients died, two of whom were considered therapeutic failures. In five of the seven patients who were cured, other procedures were also performed such as surgical drainage or catheter removal. In vitro development of high resistance to rifampicin was shown in seven (70%). PFGE demonstrated that initial isolates and high-resistant strains belonged to the same clones.

Conclusions: The results of our study argue against the use of a rifampicin/imipenem combination for the treatment of carbapenem-resistant A. baumannii infections. However, combinations of rifampicin with other antibiotics merit further studies.

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Source
http://dx.doi.org/10.1093/jac/dkl274DOI Listing

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