4.5 Article

Molds and More: Rare Fungal Infections in Preterm Infants <24 Weeks of Gestation

Journal

PEDIATRIC INFECTIOUS DISEASE JOURNAL
Volume 41, Issue 4, Pages 352-357

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/INF.0000000000003407

Keywords

Mycoses; preterm infants; Aspergillus; fungal infection; cutaneous aspergillosis

Funding

  1. German Federal Ministry of Research and Education - Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [EXC 2030 - 390661388]
  2. Actelion
  3. Allecra Therapeutics
  4. Al-Jazeera Pharmaceuticals
  5. Amplyx
  6. Astellas
  7. Basilea
  8. Biosys
  9. Cidara
  10. Da Volterra
  11. Entasis
  12. F2G
  13. Gilead
  14. Grupo Biotoscana
  15. Immunic
  16. IQVIA
  17. Janssen
  18. Matinas
  19. Medicines Company
  20. MedPace
  21. Melinta Therapeutics
  22. Menarini
  23. Merck/MSD
  24. Mylan
  25. Nabriva
  26. Noxxon
  27. Octapharma
  28. Paratek
  29. Pfizer
  30. PSI
  31. Roche Diagnostics
  32. Scynexis
  33. Shionogi
  34. German Research Foundation (DFG)
  35. German Centre for Infection Research (DZIF)
  36. Federal Ministry of Education and Research, Accelerate, and Entasis

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Extremely immature preterm infants are at increased risk of rare fungal infections, particularly cutaneous Aspergillosis, which may cause severe disease. Treatment with Voriconazole has a high rate of liver toxicity and is difficult to achieve target levels in extremely immature infants.
Background: Extreme immature infants are at an increased risk of fungal infection due to immaturity of the skin barrier and the immune system. Besides Candida infections, in particular, Aspergillus may cause life-threatening diseases in preterm infants. Frequently, Aspergillus primarily affects the skin and may cause extensive damage. Methods: We searched our hospital database for fungal infections other than Candida in preterm infants treated between 2015 and 2020 at our level III neonatal intensive care unit of the University Hospital of Cologne. Results: In total, 13 preterm infants were identified. Of these, 11 had cutaneous Aspergillosis, one infant had severe enterocolitis caused by Aspergillus and Rhizopus and one had invasive intraabdominal Trichosporon mucoides infection. All infants were born <24 weeks of gestation, were delivered due to premature labor or chorioamnionitis, and had received prenatal steroids and/or hydrocortisone. Voriconazole and liposomal Amphotericin B were first-line treatments and the length of treatment varied between 3 and 148 days. Two infants died associated with severe infection. Liver toxicity was observed in six infants treated with Voriconazole. Therapeutic drug management for Voriconazole was performed in four infants. Target levels were not achieved by the doses that are recommended. Conclusions: Rare fungal infections, predominantly cutaneous Aspergillosis affects the most immature preterm infants and may cause severe disease. Treatment with Voriconazole has a high rate of liver toxicity and target levels are difficult to achieve in extremely immature infants.

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