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Published Online First: 5 February 2008. doi:10.1136/adc.2007.118844
Archives of Disease in Childhood 2008;93:578-581
Copyright © 2008 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.

Original articles

Voriconazole plasma monitoring

A C Pasqualotto1,2, M Shah3, R Wynn4, D W Denning1,2,5

1 School of Medicine, University of Manchester, UK
2 Wythenshawe Hospital, Manchester, UK
3 Burn Unit, Booth Hall Children’s Hospital, Manchester, UK
4 Department of Haematology, Royal Manchester Children’s Hospital, Manchester, UK
5 Regional Mycology Laboratory, Manchester, UK

Alessandro Pasqualotto, Education and Research Centre, Wythenshawe Hospital, Southmoor Road, Manchester, M23 9LT, UK; acpasqualotto{at}hotmail.com

Aims: Very little information is available regarding the use of voriconazole drug monitoring in children with invasive fungal infections. The purpose of this study was to report the cases of five paediatric patients treated with voriconazole, in which plasma levels were used to monitor therapy.

Methods: Five children treated with voriconazole were included in this case series. Voriconazole plasma levels were determined using either a bioassay or liquid chromatography–tandem mass spectrometry.

Results: The patients’ ages ranged from 2 to 10 years old (mean 6.2 years). Three patients had acute leukaemia and two had suffered severe burn injuries. Doses administered varied from 3.4 mg/kg every 12 h to 8.1 mg/kg every 8 h. Plasma voriconazole concentrations were unpredictable for these paediatric patients. Subtherapeutic levels were frequently observed, despite progressive increments in dosage. For others, voriconazole levels markedly increased after a small increment in dosage. Phenobarbitone caused important drug interactions with voriconazole for two of the patients.

Conclusions: The dose administered did not correlate with exposure as measured by plasma levels of voriconazole. While the optimal dosage for voriconazole in children is still unknown, drug monitoring seems warranted to ensure adequate exposure, and after dose increments to prevent excessive exposure. Drug interactions significantly altered exposure.


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This article has been cited by other articles:

  • Andes, D., Pascual, A., Marchetti, O. (2009). Antifungal Therapeutic Drug Monitoring: Established and Emerging Indications. Antimicrob. Agents Chemother. 53: 24-34 [Full Text]  
  • Hafner, V., Albermann, N., Haefeli, W. E., Ebinger, F. (2008). Inhibition of Voriconazole Metabolism by Chloramphenicol in an Adolescent with Central Nervous System Aspergillosis. Antimicrob. Agents Chemother. 52: 4172-4174 [Abstract] [Full Text]  

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