Fungal infections in pediatric patients: challenges and considerations in treatment

Elio Castagnola1, Marcelo Mariani1, Erica Ricci1

  • 1Department of Medical-Pediatric Sciences, Infectious Diseases Unit IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Abstract

Insights

Invasive fungal diseases (IFDs) in children are challenging to diagnose and treat. This review highlights the need for improved pediatric-specific research, diagnostic tools, and standardized treatment protocols for better outcomes.

Area of Science:

  • Pediatric Infectious Diseases
  • Mycology
  • Clinical Pharmacology

Background:

  • Invasive fungal diseases (IFDs) pose significant risks in children, stemming from unique factors like prematurity and genetic conditions, alongside shared adult risks such as chemotherapy and intensive care.
  • Pediatric IFD diagnosis is complicated by challenges in sample collection, variable performance of antigen detection, and nonspecific imaging.
  • Treatment of pediatric IFD is complex due to age-dependent pharmacokinetics, limited pediatric formulations, and drug interactions requiring therapeutic drug monitoring.

Purpose of the Study:

  • To provide a narrative review of the epidemiology, diagnosis, and treatment of IFD in pediatric patients.
  • To highlight the challenges and complexities in managing IFD in children.
  • To emphasize the need for improved pediatric-specific strategies.

Main Methods:

  • Narrative review of existing literature on pediatric invasive fungal diseases.
  • Synthesis of information on epidemiological factors, diagnostic modalities, and therapeutic approaches.
  • Analysis of challenges in diagnosis and treatment specific to the pediatric population.

Main Results:

  • IFDs contribute significantly to child morbidity and mortality.
  • Diagnostic difficulties include obtaining adequate samples, limitations of current antigen tests, and nonspecific imaging.
  • Therapeutic challenges involve pharmacokinetics, drug availability, drug interactions, and the necessity for therapeutic drug monitoring.

Conclusions:

  • Therapeutic drug monitoring for antifungal drugs in children is essential and likely to increase.
  • Prioritizing pediatric-specific research and standardized treatment protocols is crucial.
  • Regulatory reforms are needed to accelerate access to novel diagnostic and treatment strategies for pediatric IFD.

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