Cited by 887Antifungal resistance and susceptibilityAntibiotics Pharmacokinetics and EfficacyPharmacogenetics and Drug Metabolism

Voriconazole therapeutic drug monitoring in patients with invasive mycoses improves efficacy and safety outcomes

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Pascual, A., Calandra, T., Bolay, S., Buclin, T., Bille, J., Marchetti, O.·2008·Clinical Infectious Diseases

Abstract

Background. Voriconazole is the therapy of choice for aspergillosis and a new treatment option for candidiasis. Liver disease, age, genetic polymorphism of the cytochrome CYP2C19, and comedications influence voriconazole metabolism. Large variations in voriconazole pharmacokinetics may be associated with decreased efficacy or with toxicity. Methods. This study was conducted to assess the utility of measuring voriconazole blood levels with individualized dose adjustments. Results. A total of 181 measurements with high-pressure liquid chromatography were performed during 2388 treatment days in 52 patients. A large variability in voriconazole trough blood levels was observed, ranging from ⩽1 mg/L (the minimum inhibitory concentration at which, for most fungal pathogens, 90% of isolates are susceptible) in 25% of cases to >5.5 mg/L (a level possibly associated with toxicity) in 31% of cases. Lack of response to therapy was more frequent in patients with voriconazole levels ⩽1 mg/L (6 [46%] of 13 patients, including 5 patients with aspergillosis, 4 of whom were treated orally with a median dosage of 6 mg/kg per day) than in those with voriconazole levels >1 mg/L (15 [12%] of 39 patients; P=.02). Blood levels >1 mg/L were reached after increasing the voriconazole dosage, with complete resolution of infection in all 6 cases. Among 16 patients with voriconazole trough blood levels >5.5 mg/L, 5 patients (31%) presented with an encephalopathy, including 4 patients who were treated intravenously with a median voriconazole dosage of 8 mg/kg per day, whereas none of the patients with levels ⩽5.5 mg/L presented with neurological toxicity (P=.002). Comedication with omeprazole possibly contributed to voriconazole accumulation in 4 patients. In all cases, discontinuation of therapy resulted in prompt and complete neurological recovery. Conclusions. Voriconazole therapeutic drug monitoring improves the efficacy and safety of therapy in severely ill patients with invasive mycoses.

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  • Treatment success in retrospective analyses has been associated with voriconazole serum trough concentrations of 1 to 2 mg/mL.

    “Treatment success in these retrospective analyses has been associated with serum trough concentrations of 1 to 2 mg/mL.”

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  1. [15]15. Smith J, Safdar N, Knasinski V, et al. Voriconazole therapeutic drug monitoring. Antimicrob Agents Chemother 2006 ; 50:1570-2.
  2. [34]34. Trifilio S, Singhal S, Winter J, et al. ASH Annual Meeting 2006, Orlando, FL [abstract 2849]. Blood 2006 ; 108:806a-807a.

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Authors
Pascual, A., Calandra, T., Bolay, S., Buclin, T., Bille, J., & Marchetti, O.
Affiliations
Centre Hospitalier Universitaire Vaudois (CH)
Corresponding author
Marchetti, O.
Venue
Clinical Infectious Diseases
Published
2008-01-15
Volume
46
Issue
2
Pages
201-211
ISSN
  • 1058-4838 (ISSN-L)
  • 1537-6591
OpenAlex
W2162857158
Cited by
887
References
36
Citations by year
2026: 19 · 2025: 27 · 2024: 26 · 2023: 34 · 2022: 30 · 2021: 37 · 2020: 45 · 2019: 42 · 2018: 36 · 2017: 42 · 2016: 63 · 2015: 61 · 2014: 58 · 2013: 57 · 2012: 66
FWCI
35.86
Type
journal article
Language
en
Open access
Locations
  • Clinical Infectious Diseases (publishedVersion)
  • PubMed (publishedVersion)
  • SERVAL (Université de Lausanne) (publishedVersion, other-oa)
  • reroDoc Digital Library (submittedVersion)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Health Sciences › Medicine › Pharmacology › Antibiotics Pharmacokinetics and Efficacy
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
Keywords
voriconazole, therapeutic drug monitoring, invasive fungal infections, aspergillosis, candidiasis, pharmacokinetics, dose adjustment, CYP2C19 polymorphism, encephalopathy, antifungal toxicity, treatment efficacy
MeSH terms
Adult, Aged, Antifungal Agents, Aspergillosis, Candidiasis, Chromatography, High Pressure Liquid, Female, Humans, Male, Middle Aged, Mycoses, Pyrimidines, Retrospective Studies, Triazoles, Drug Monitoring, Voriconazole

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