Favorable Effects of Voriconazole Trough Concentrations Exceeding 1 μg/mL on Treatment Success and All-Cause Mortality: A Systematic Review and Meta-Analysis.

meta-analysis mortality therapeutic drug monitoring trough concentration voriconazole

Journal

Journal of fungi (Basel, Switzerland)
ISSN: 2309-608X
Titre abrégé: J Fungi (Basel)
Pays: Switzerland
ID NLM: 101671827

Informations de publication

Date de publication:
16 Apr 2021
Historique:
received: 23 03 2021
revised: 14 04 2021
accepted: 15 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

This systematic review and meta-analysis examined the optimal trough concentration of voriconazole for adult patients with invasive fungal infections. We used stepwise cutoffs of 0.5-2.0 μg/mL for efficacy and 3.0-6.0 μg/mL for safety. Studies were included if they reported the rates of all-cause mortality and/or treatment success, hepatotoxicity, and nephrotoxicity according to the trough concentration. Twenty-five studies involving 2554 patients were included. The probability of mortality was significantly decreased using a cutoff of ≥1.0 μg/mL (odds ratio (OR) = 0.34, 95% confidence interval (CI) = 0.15-0.80). Cutoffs of 0.5 (OR = 3.48, 95% CI = 1.45-8.34) and 1.0 μg/mL (OR = 3.35, 95% CI = 1.52-7.38) also increased the treatment success rate. Concerning safety, significantly higher risks of hepatotoxicity and neurotoxicity were demonstrated at higher concentrations for all cutoffs, and the highest ORs were recorded at 4.0 μg/mL (OR = 7.39, 95% CI = 3.81-14.36; OR = 5.76, 95% CI 3.14-10.57, respectively). Although further high-quality trials are needed, our findings suggest that the proper trough concentration for increasing clinical success while minimizing toxicity is 1.0-4.0 μg/mL for adult patients receiving voriconazole therapy.

Identifiants

pubmed: 33923727
pii: jof7040306
doi: 10.3390/jof7040306
pmc: PMC8072959
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Yuki Hanai (Y)

Department of Pharmacy, Toho University Omori Medical Center, Tokyo 143-8541, Japan.

Yukihiro Hamada (Y)

Department of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo 162-8666, Japan.

Toshimi Kimura (T)

Department of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo 162-8666, Japan.

Kazuaki Matsumoto (K)

Division of Pharmacodynamics, Keio University Faculty of Pharmacy, Tokyo 105-8512, Japan.

Yoshiko Takahashi (Y)

Department of Pharmacy, Hyogo College of Medicine, Hyogo 663-8501, Japan.

Satoshi Fujii (S)

Department of Hospital Pharmacy, Sapporo Medical University Hospital, Hokkaido 060-8543, Japan.

Kenji Nishizawa (K)

Department of Pharmacy, Toho University Omori Medical Center, Tokyo 143-8541, Japan.

Yoshitsugu Miyazaki (Y)

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.

Yoshio Takesue (Y)

Department of Infection Control and Prevention, Hyogo College of Medicine, Hyogo 663-8501, Japan.

Classifications MeSH