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Liposomal amphotericin B in critically ill paediatric patients
G Sideri1, M E Falagas, M Grigoriou
1Pediatric Intensive Care Unit, P. & A. Kyriakou Children's Hospital, Athens, Greece.
Insights
Liposomal amphotericin B shows promise for treating fungal infections in critically ill children. This study found it effective in a small case series, with manageable side effects in vulnerable pediatric patients.
Area of Science:
- Pediatric Intensive Care
- Mycology
- Pharmacology
Background:
- Limited data exists on liposomal amphotericin B for critically ill pediatric patients beyond infancy.
- Fungal infections pose a significant threat to immunocompromised and critically ill children.
Purpose of the Study:
- To evaluate the use and outcomes of liposomal amphotericin B in critically ill pediatric patients.
- To assess the efficacy and safety of liposomal amphotericin B in a tertiary care setting.
Main Methods:
- Prospective identification of pediatric patients receiving liposomal amphotericin B in the ICU over 3 years.
- Data collection through medical record evaluation.
Main Results:
- Twenty-three critically ill children (mean age 26.4 months) received liposomal amphotericin B.
- Treatment was for confirmed fungal infections (16/23) or pre-emptive (7/23).
- High rates of cure or improvement were observed (11/16 cured, 5/16 improved for infections; 6/7 improved for pre-emptive use).
Conclusions:
- Liposomal amphotericin B appears effective for fungal infections in critically ill pediatric patients.
- Adverse events like hepatotoxicity and nephrotoxicity were observed but manageable.
- Further research is warranted for this vulnerable population.
What Is Known And Objective:
Literature provides much evidence regarding liposomal amphotericin B treatment for fungal infections in neonates and infants. Relevant data regarding critically ill paediatric patients of older age are scarce. We aimed to present our experience regarding liposomal amphotericin B use in critically ill paediatric patients from a tertiary-care paediatric hospital in Athens, Greece.
Methods:
We prospectively identified all paediatric patients who received treatment with liposomal amphotericin B in the intensive care unit of a tertiary-care paediatric hospital during a 3-year period (2005-2008). Data were retrieved from the evaluation of the available medical records.
Results And Discussion:
Twenty-three (nine females, mean age: 26·4 months, range: 5-39 months) critically ill paediatric patients were included; 12 had malignancy. In 16 of the 23 included children, liposomal amphotericin B was administered for the treatment of confirmed fungal infections (all but one were invasive), whereas in seven patients, it was used as pre-emptive treatment. One patient received voriconazole concomitantly. Eleven of the 16 children with documented infections were cured; five improved. Six of the seven children who received pre-emptive treatment also showed clinical improvement. Nine deaths were noted, all attributed to underlying diseases. Two cases of hepatotoxicity and one case of nephrotoxicity (all leading to drug-discontinuation) occurred. Seven and five cases of mild reversible hypokalaemia and hyponatraemia, respectively, were also noted.
What Is New And Conclusion:
According to the findings of our small case series, liposomal amphotericin B may provide a useful treatment option for fungal infections of vulnerable critically ill paediatric patients with considerable comorbidity.
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