4.7 Article

Summary of Ceftaroline Activity against Pathogens in the United States, 2010: Report from the Assessing Worldwide Antimicrobial Resistance Evaluation (AWARE) Surveillance Program

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ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 56, 期 6, 页码 2933-2940

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.00330-12

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资金

  1. Cerexa, Inc. (Oakland, CA), a wholly owned subsidiary of Forest Laboratories, Inc. (New York, NY)
  2. Achaogen
  3. Aires
  4. American Proficiency Institute (API)
  5. Anacor
  6. Astellas
  7. AstraZeneca
  8. Bayer
  9. bioMerieux
  10. Cempra
  11. Cerexa
  12. Cosmo Technologies
  13. Contrafect
  14. Cubist
  15. Daiichi
  16. Dipexium
  17. Enanta
  18. Furiex
  19. GlaxoSmithKline
  20. Johnson & Johnson (Ortho McNeil)
  21. LegoChem Biosciences Inc.
  22. Meiji Seika Kaisha
  23. Merck
  24. Nabriva
  25. Novartis
  26. Paratek
  27. Pfizer (Wyeth)
  28. PPD Therapeutics
  29. Premier Research Group
  30. Rempex
  31. Rib-X Pharmaceuticals
  32. Seachaid
  33. Shionogi
  34. Shionogi USA
  35. The Medicines Co.
  36. Theravance
  37. ThermoFisher
  38. Trek Diagnostics
  39. Vertex Pharmaceuticals

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The Assessing Worldwide Antimicrobial Resistance Evaluation (AWARE) surveillance program is a sentinel resistance monitoring system designed to track the activity of ceftaroline and comparator agents. In the United States, a total of 8,434 isolates were collected during the 2010 surveillance program from 65 medical centers distributed across the nine census regions (5 to 10 medical centers per region). All organisms were isolated from documented infections, including 3,055 (36.2%) bloodstream infections, 2,282 (27.1%) respiratory tract infections, 1,965 (23.3%) acute bacterial skin and skin structure infections, 665 (7.9%) urinary tract infections, and 467 (5.5%) miscellaneous other infection sites. Ceftaroline was the most potent beta-lactam agent tested against staphylococci. The MIC90 values were 1 mu g/ml for methicillin-resistant Staphylococcus aureus (MRSA; 98.4% susceptible) and 0.5 mu g/ml for methicillin-resistant coagulase-negative staphylococci (CoNS). Ceftaroline was 16- to 32-fold more potent than ceftriaxone against methicillin-susceptible staphylococcal strains. All staphylococcus isolates (S. aureus and CoNS) were inhibited at ceftaroline MIC values of <= 2 mu g/ml. Ceftaroline also displayed potent activity against streptococci (MIC90, 0.015 mu g/ml for beta-hemolytic streptococci; MIC90, 0.25 mu g/ml for penicillin-resistant Streptococcus pneumoniae). Potent activity was also shown against Gram-negative pathogens (Haemophilus influenzae, Haemophilus parainfluenzae, and Moraxella catarrhalis). Furthermore, wild-type strains of Enterobacteriaceae (non-extended-spectrum beta-lactamase [ESBL]-producing strains and non-AmpC-hyperproducing strains) were often susceptible to ceftaroline. Continued monitoring through surveillance networks will allow for the assessment of the evolution of resistance as this new cephalosporin is used more broadly to provide clinicians with up-to-date information to assist in antibiotic stewardship and therapeutic decision making.

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