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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.
Introduction:
Invasive fungal diseases (IFD) cause significant morbidity and mortality in children, who have unique risk factors like premature birth, genetic conditions, and immunodeficiencies. They also share adult risk factors, such as antineoplastic treatments and intensive care. This narrative review summarizes epidemiology and focus on diagnosis, and treatment of IFD in pediatric patients.
Area Covered:
Diagnosing IFD in children is challenging due to the difficulties in obtaining sufficient blood or CSF for cultures from small patients. Additionally, antigen detection methods often perform poorly, except perhaps beta-glucan in newborns and galactomannan in neutropenic patients or samples from the infection site. Nonspecific imaging findings further complicate diagnosis. Therapeutic complexities arise from age- or disease-dependent pharmacokinetics, limited availability of child-friendly drug formulations, and frequent drug-drug and food-drug interactions, often requiring therapeutic drug monitoring for optimal outcomes.
Expert Opinion:
There is and will be further needed therapeutic drug monitoring for all antifungal drugs in children. Prioritizing pediatric-specific research and developing standardized treatment protocols are crucial. Furthermore, regulatory reforms are essential to expedite access to new diagnostic and treatment strategies for IFD in children.
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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