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ESCMID* guideline for the diagnosis and management of Candida diseases 2012: prevention and management of invasive infections in neonates and children caused by Candida spp.

Journal

CLINICAL MICROBIOLOGY AND INFECTION
Volume 18, Issue -, Pages 38-52

Publisher

ELSEVIER SCI LTD
DOI: 10.1111/1469-0691.12040

Keywords

Antifungal agents; candida disease; children; Europe; neonates

Funding

  1. National Institute of Health Research (NIHR)
  2. Medical Research Council
  3. National Institute for the Replacement, Refinement and Reduction, of Animals in Research
  4. Pfizer
  5. Gilead
  6. Schering-Plough
  7. Merck
  8. Astellas
  9. Enzon
  10. Schering
  11. Astellas Pharma
  12. Gilead Sciences
  13. Merck Sharp and Dohme
  14. MSD
  15. German Federal Ministry of Research and Education (BMBF) [01KN1106]
  16. bioMerieux
  17. Soria Melguizo SA
  18. Ferrer International
  19. European Union
  20. ALBAN program
  21. Spanish Agency for International Cooperation
  22. Spanish Ministry of Culture and Education
  23. Spanish Health Research Fund
  24. Instituto de Salud Carlos III
  25. Ramon Areces Foundation
  26. Mutua Madrilena Foundation
  27. Bio-Merieux
  28. Cephalon
  29. Merck Sharp
  30. Dohme
  31. Astra Zeneca
  32. Novartis
  33. GSK
  34. ESCMID
  35. Abbott
  36. BMS
  37. Nadirex Internation (Pavia, Italy)
  38. Jansen
  39. MSD (Schering-Plough)
  40. National Institute for Health Research [CS/08/08/10] Funding Source: researchfish

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Clin Microbiol Infect 2012; 18 (Suppl. 7): 3852 Abstract Invasive candidiasis (IC) is a relatively common syndrome in neonates and children and is associated with significant morbidity and mortality. These guidelines provide recommendations for the prevention and treatment of IC in neonates and children. Appropriate agents for the prevention of IC in neonates at high risk include fluconazole (A-I), nystatin (B-II) or lactoferrin +/- Lactobacillus (B-II). The treatment of IC in neonates is complicated by the high likelihood of disseminated disease, including the possibility of infection within the central nervous system. Amphotericin B deoxycholate (B-II), liposomal amphotericin B (B-II), amphotericin B lipid complex (ABLC) (C-II), fluconazole (B-II), micafungin (B-II) and caspofungin (C-II) can all be potentially used. Recommendations for the prevention of IC in children are largely extrapolated from studies performed in adults with concomitant pharmacokinetic data and models in children. For allogeneic HSCT recipients, fluconazole (A-I), voriconazole (A-I), micafungin (A-I), itraconazole (B-II) and posaconazole (B-II) can all be used. Similar recommendations are made for the prevention of IC in children in other risk groups. With several exceptions, recommendations for the treatment of IC in children are extrapolated from adult studies, with concomitant pharmacokinetic studies. Amphotericin B deoxycholate (C-I), liposomal amphotericin B (A-I), ABLC (B-II), micafungin (A-I), caspofungin (A-I), anidulafungin (B-II), fluconazole (B-I) and voriconazole (B-I) can all be used.

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