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Colonization and infection with extended spectrum beta-lactamase producing Enterobacteriaceae in high-risk patients - Review of the literature from a clinical perspective

Journal

CRITICAL REVIEWS IN MICROBIOLOGY
Volume 42, Issue 1, Pages 1-16

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/1040841X.2013.875515

Keywords

Bloodstream infection; colonization; ESBL; ICU; malignancy; neutropenia

Categories

Funding

  1. German Federal Ministry of Research and Education (BMBF) [01KN1106]
  2. 3M
  3. Actelion
  4. Astellas
  5. Basilea
  6. Bayer
  7. Celgene
  8. Cubist
  9. F2G
  10. Genzyme
  11. Gilead
  12. GSK
  13. Merck/MSD
  14. Miltenyi
  15. Optimer
  16. Pfizer
  17. Quintiles
  18. Sanofi Pasteur
  19. Viropharma

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Background: The prevalence of extended-spectrum -lactamase producing Enterobacteriaceae (ESBL-E) is increasing worldwide. ESBL-E are known to colonize different body sites and cause bloodstream infections (BSI), pneumonia, intra-abdominal infections and urinary tract infections. Even though ESBL-E-related morbidity and mortality in high-risk patients - patients receiving immunosuppressants or chemotherapy, as well as those treated in an ICU - is considerable, the management of ESBL-E in these populations has not been systematically reviewed. Methods: For the purpose of this review, ICU patients, patients in hematology and oncology wards and transplant recipients were considered high-risk. An English-language Medline search was conducted to identify literature on epidemiology, risk factors, clinical impact and measures of infection control regarding ESBL-E in high-risk patients published between June 2002 and May 2013. Results: Using the above described methodology, 43 relevant articles regarding high-risk patients and - for areas where literature on exclusively high-risk patients is scarce - 17 articles in standard risk settings were identified. The evidence on epidemiology, associated risk factors, treatment and hygiene measures were summarized. Discussion: This review gives a complete overview on the management of ESBL-E in the high-risk setting.

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