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Published on: January 17, 2011
[Use of posaconazole in children: Experience in a tertiary pediatric hospital]
María T Rosanova1, Carla Voto2, María S Mussini2
1Servicio de Control Epidemiológico e Infectología, Hospital "Prof. Dr. Juan P. Garrahan", Ciudad Autónoma de Buenos Aires, Argentina. margris2@yahoo.com.ar.
Insights
This study evaluated posaconazole use in pediatric invasive fungal infections. Posaconazole demonstrated clinical utility, with most patients tolerating the antifungal medication well.
Area of Science:
- Pediatric Mycology
- Infectious Diseases
- Clinical Pharmacology
Background:
- Limited data exists on pediatric use of posaconazole.
- Invasive fungal infections (IFIs) pose significant risks in immunocompromised children.
- Posaconazole is a broad-spectrum triazole antifungal agent.
Purpose of the Study:
- To assess the clinical and microbiological characteristics of pediatric patients treated with posaconazole.
- To evaluate the treatment outcomes and adverse effects of posaconazole in children with IFIs.
Main Methods:
- Retrospective, descriptive study design.
- Inclusion of 16 pediatric patients with proven IFIs treated between 2010 and 2017.
- Analysis of patient demographics, underlying conditions, fungal pathogens, posaconazole dosage, treatment duration, and adverse events.
Main Results:
- The median age of patients was 161 months; all had underlying diseases and IFIs.
- Mucor spp. and Aspergillus spp. were the most common fungal isolates.
- The mean posaconazole dose was 600 mg/day, with a median treatment duration of 223 days. Ten patients experienced adverse effects, with only one discontinuation due to electrolyte imbalance.
Conclusions:
- Posaconazole can be a viable treatment option for invasive fungal infections in children.
- The drug was generally well-tolerated in this pediatric cohort, with a low rate of treatment discontinuation due to adverse events.
Abstract:
There is limited information on the use of posaconazole in children. This retrospective and descriptive study was conducted to evaluate the clinical, microbiological characteristics and evolution of patients treated with posaconazole between August 2010 and March 2017. We included 16 children. Median age: 161 months (interquartile range -IQR- 69-173 m). All had underlying disease and a proven invasive fungal infection. The most frequent isolated were Mucor spp. and Aspergillus spp. The mean posaconazole dose was 600 mg/day (400-800 mg/day) and the median duration of treatment was 223 days (IQR 48-632). Ten patients had adverse effects, but only one required suspension of the antifungal treatment due to hydroelectrolytic disorders.
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