4.7 Article

Wild-Type MIC Distributions and Epidemiological Cutoff Values for Amphotericin B, Flucytosine, and Itraconazole and Candida spp. as Determined by CLSI Broth Microdilution

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JOURNAL OF CLINICAL MICROBIOLOGY
卷 50, 期 6, 页码 2040-2046

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/JCM.00248-12

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资金

  1. Achaogen
  2. Aires
  3. American Proficiency Institute (API)
  4. Anacor
  5. Astellas
  6. AstraZeneca
  7. Bayer
  8. bioMerieux
  9. Cempra
  10. Cerexa
  11. Cosmo Technologies
  12. Contrafect
  13. Cubist
  14. Daiichi
  15. Dipexium
  16. Enanta
  17. Furiex
  18. GlaxoSmithKline
  19. Johnson Johnson (JJ)
  20. LegoChem Biosciences Inc.
  21. Meiji Seika Kaisha
  22. Merck
  23. Nabriva
  24. Novartis
  25. Paratek
  26. Pfizer (Wyeth)
  27. PPD Therapeutics
  28. Premier Research Group
  29. Rempex
  30. Rib-X Pharmaceuticals
  31. Seachaid
  32. Shionogi
  33. Shionogi USA
  34. Medicines Co.
  35. Theravance
  36. ThermoFisher
  37. TREK Diagnostics
  38. Vertex Pharmaceuticals
  39. Astellas Pharma
  40. Gilead Sciences
  41. Merck Sharp and Dohme
  42. Pfizer
  43. Schering Plough
  44. Soria Melguizo SA
  45. Ferrer International
  46. European Union
  47. ALBAN
  48. Spanish Agency for International Cooperation
  49. Spanish Ministry of Culture and Education
  50. Spanish Health Research Fund
  51. Instituto de Salud Carlos III
  52. Ramon Areces Foundation
  53. Mutua Madrile a Foundation
  54. Merck, Astellas
  55. Innovative Biosensors
  56. PurThread Technologies

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Clinical breakpoints (CBPs) and epidemiological cutoff values (ECVs) have been established for several Candida spp. and the newer triazoles and echinocandins but are not yet available for older antifungal agents, such as amphotericin B, flucytosine, or itraconazole. We determined species-specific ECVs for amphotericin B (AMB), flucytosine (FC) and itraconazole (ITR) for eight Candida spp. (30,221 strains) using isolates from 16 different laboratories in Brazil, Canada, Europe, and the United States, all tested by the CLSI reference microdilution method. The calculated 24- and 48-h ECVs expressed in mu g/ml (and the percentages of isolates that had MICs less than or equal to the ECV) for AMB, FC, and ITR, respectively, were 2 (99.8)/2 (99.2), 0.5 (94.2)/1 (91.4), and 0.12 (95.0)/0.12 (92.9) for C. albicans; 2 (99.6)/2 (98.7), 0.5 (98.0)/0.5 (97.5), and 2 (95.2)/4 (93.5) for C. glabrata; 2 (99.7)/2 (97.3), 0.5 (98.7)/0.5 (97.8), and 05. (99.7)/0.5 (98.5) for C. parapsilosis; 2 (99.8)/2 (99.2), 0.5 (93.0)/1 (90.5), and 0.5 (97.8)/0.5 (93.9) for C. tropicalis; 2 (99.3)/4 (100.0), 32 (99.4)/32 (99.3), and 1 (99.0)/2 (100.0) for C. krusei; 2 (100.0)/4 (100.0), 0.5 (95.3)/1 (92.9), and 0.5 (95.8)/0.5 (98.1) for C. lusitaniae; -/2 (100.0), 0.5 (98.8)/0.5 (97.7), and 0.25 (97.6)/0.25 (96.9) for C. dubliniensis; and 2 (100.0)/2 (100.0), 1 (92.7)/-, and 1 (100.0)/2 (100.0) for C. guilliermondii. In the absence of species-specific CBP values, these wild-type (WT) MIC distributions and ECVs will be useful for monitoring the emergence of reduced susceptibility to these well-established antifungal agents.

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