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Published on: February 14, 2018
Antifungal agents in neonates: issues and recommendations
Benito Almirante1, Dolors Rodríguez
1Infectious Diseases Department, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain. balmirante@vhebron.net
Abstract:
Fungal infections are responsible for considerable morbidity and mortality in the neonatal period, particularly among premature neonates. Four classes of antifungal agents are commonly used in the treatment of fungal infections in pediatric patients: polyene macrolides, fluorinated pyrimidines, triazoles, and echinocandins. Due to the paucity of pediatric data, many recommendations for the use of antifungal agents in this population are derived from the experience in adults. The purpose of this article was to review the published data on fungal infections and antifungal agents, with a focus on neonatal patients, and to provide an overview of the differences in antifungal pharmacology in neonates compared with adults. Pharmacokinetic data suggest dosing differences in children versus adult patients with some antifungals, but not all agents have been fully evaluated. The available pharmacokinetic data on the amphotericin B deoxycholate formulation in neonates exhibit considerable variability; nevertheless, the dosage regimen suggested in the neonatal population is similar to that used in adults. More pharmacokinetic information is available on the liposomal and lipid complex preparations of amphotericin B and fluconazole, and it supports their use in neonates; however, the optimal dosage and duration of therapy is difficult to establish. All amphotericin-B formulations, frequently used in combination with flucytosine, are useful for treating disseminated fungal infections and Candida meningitis in neonates. Fluconazole, with potent in vitro activity against Cryptococcus neoformans and almost all Candida spp., has been used in neonates with invasive candidiasis at dosages of 6 mg/kg/day, and for antifungal prophylaxis in high-risk neonates. There are limited data on itraconazole, voriconazole, and posaconazole use in neonates. Caspofungin, which is active against Candida spp. and Aspergillus spp., requires higher doses in children relative to adults, and dosing is best accomplished based on body surface area. Micafungin shows a clear trend toward lower levels in the smallest patients. There are no data on the use of other new antifungal drugs (ravuconazole and anidulafungin) in neonates. In summary, the initial data suggest dosage differences in neonates for some antifungal agents, although the newer agents have not been fully tested for optimal administration in these patients.
Insights
Neonatal fungal infections require careful antifungal treatment. Pharmacokinetic data reveal potential dosing differences in neonates compared to adults for certain antifungal agents, necessitating further research for optimal use.
Area of Science:
- Neonatal pharmacology
- Infectious diseases
- Pediatric medicine
Background:
- Fungal infections cause significant mortality and morbidity in neonates, especially premature infants.
- Current antifungal treatment guidelines for pediatric patients often rely on adult data due to limited pediatric-specific research.
- Understanding antifungal pharmacokinetics in neonates is crucial for effective treatment and prophylaxis.
Purpose of the Study:
- To review existing data on fungal infections and antifungal agents in neonatal patients.
- To highlight differences in antifungal pharmacology between neonates and adults.
- To inform optimal antifungal dosing and usage in the neonatal population.
Main Methods:
- Systematic review of published literature on neonatal fungal infections and antifungal agents.
- Analysis of pharmacokinetic data for various antifungal classes in neonates versus adults.
- Evaluation of clinical data on the efficacy and safety of antifungals in neonatal populations.
Main Results:
- Pharmacokinetic data suggest potential dosing variations for some antifungals in neonates compared to adults, though not all agents are fully evaluated.
- Amphotericin B deoxycholate shows variable pharmacokinetics in neonates, but recommended doses are similar to adults.
- Fluconazole and newer amphotericin B formulations (liposomal, lipid complex) have supporting pharmacokinetic data for neonatal use, but optimal dosing remains challenging.
- Echinocandins like caspofungin require higher doses in children based on body surface area, while micafungin levels may be lower in smaller infants.
- Limited data exist for newer azoles (itraconazole, voriconazole, posaconazole) in neonates, and no data are available for ravuconazole and anidulafungin.
Conclusions:
- Pharmacological differences necessitate distinct dosing strategies for certain antifungal agents in neonates.
- Further research and pharmacokinetic studies are essential to establish optimal dosing and duration for newer antifungal agents in neonatal care.
- Current evidence supports the use of amphotericin B formulations and fluconazole, with ongoing evaluation for other agents to improve outcomes for neonatal fungal infections.
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