Management of Invasive Fungal Disease in Neonates and Children

Laura Ferreras-Antolín1,2, Mike Sharland2, Adilia Warris1,3

  • 1From the MRC Centre for Medical Mycology, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.

Insights

Management of invasive fungal diseases (IFD) in children and neonates presents challenges. A UK survey revealed varied diagnostic and treatment approaches, highlighting the need for clinical trials to optimize care for pediatric IFD.

Area of Science:

  • Pediatric Infectious Diseases
  • Mycology
  • Clinical Pharmacy

Background:

  • Invasive fungal diseases (IFD) significantly contribute to morbidity and mortality in vulnerable pediatric populations, including premature neonates and immunocompromised children.
  • Current diagnostic and therapeutic strategies for IFD in these patients are complex and present ongoing management challenges.

Purpose of the Study:

  • To investigate and understand the current practices in managing IFD among neonates and children across major UK pediatric centers.
  • To identify variations in diagnostic tool utilization, imaging, and antifungal treatment protocols.

Main Methods:

  • A nationwide survey was conducted involving 13 of the largest pediatric tertiary teaching centers in the United Kingdom.
  • Data collected focused on diagnostic methods, imaging modalities, antifungal prophylaxis, empirical treatment, and first-line therapies for common IFDs like candidemia and invasive aspergillosis.

Main Results:

  • Significant variability was observed in the use of fungal diagnostic tools and imaging across surveyed centers.
  • Antifungal prophylaxis was common for extremely low birth weight infants and high-risk hematology-oncology patients, but with diverse drug choices.
  • Empirical treatment was favored for febrile neutropenia, with specific first-line agents identified for candidemia and invasive aspergillosis; combination therapy was often used for disseminated aspergillosis.

Conclusions:

  • The survey underscores the need for standardized approaches and further pediatric clinical trials to address knowledge gaps in IFD management.
  • Optimizing the care of neonates and children with IFD requires focused attention on refining diagnostic and therapeutic strategies based on evidence.

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