Literature DB >> 27910211

Comparison of serum concentrations between different dosing strategies of posaconazole delayed-release tablet at a large academic medical centre.

Sarah Welch1, Andrea Pallotta1, Catherine Weber1, Caitlin Siebenaller1, Eric Cober2, Elizabeth Neuner1.   

Abstract

It is unclear if the prophylaxis dose of 300 mg/day is sufficient for achieving serum concentrations targeting the treatment of invasive fungal infections. To evaluate differences between PCZ serum concentrations in patients receiving the DRT vs the OS and in patients receiving higher doses than 300 mg/day of the DRT, a retrospective review was conducted on inpatients who received PCZ for either treatment or prophylaxis. Baseline demographics including comorbid conditions, indication and dose of therapy were collected. Serum trough concentrations were collected at steady state. Fifty-seven patients received PCZ during the study period. A total of 35 levels were collected (DRT n = 18, OS n = 17). Patients receiving the DRT had levels >0.7 mcg/mL 100% of the time compared to 58.8% in those receiving the OS. No significant difference was seen in serum concentrations at 300 mg/day (n = 14) vs 400 mg/day (n = 8) of the DRT (1.55 mcg/mL (1.08-2.50) vs 2.5 mcg/mL (1.85-2.70), P = .19). The DRT leads to more consistent levels in the therapeutic range than the OS. Standard dosing of 300 mg/day with DRT achieves adequate concentrations for prophylaxis and treatment of IFIs, although further data are needed to determine optimal serum concentrations for treatment.
© 2016 Blackwell Verlag GmbH.

Entities:  

Keywords:  azole antifungals; invasive fungal infections; posaconazole; therapeutic drug monitoring

Mesh:

Substances:

Year:  2016        PMID: 27910211     DOI: 10.1111/myc.12587

Source DB:  PubMed          Journal:  Mycoses        ISSN: 0933-7407            Impact factor:   4.377


  4 in total

1.  Antifungal Prophylaxis with Posaconazole Delayed-Release Tablet and Oral Suspension in a Real-Life Setting: Plasma Levels, Efficacy, and Tolerability.

Authors:  Martin Hoenigl; Robert Krause; David Lenczuk; Wilma Zinke-Cerwenka; Hildegard Greinix; Albert Wölfler; Jürgen Prattes; Ines Zollner-Schwetz; Thomas Valentin; Timothy C Lin; Andreas Meinitzer
Journal:  Antimicrob Agents Chemother       Date:  2018-05-25       Impact factor: 5.191

2.  Comparison of the Efficacy of Posaconazole Delayed Release Tablets and Suspension in Pediatric Hematology/Oncology Patients.

Authors:  Erika N Wass; Elvin A Hernandez; Caroline M Sierra
Journal:  J Pediatr Pharmacol Ther       Date:  2020 Jan-Feb

3.  Using State Transition Models to Explore How the Prevalence of Subtherapeutic Posaconazole Exposures Impacts the Clinical Utility of Therapeutic Drug Monitoring for Posaconazole Tablets and Oral Suspension.

Authors:  Russell E Lewis; Dimitrios P Kontoyiannis; Pierluigi Viale; Eric M Sarpong
Journal:  Antimicrob Agents Chemother       Date:  2019-09-16       Impact factor: 5.191

4.  Clinical Pharmacokinetics and Dose Recommendations for Posaconazole in Infants and Children.

Authors:  Sophida Boonsathorn; Iek Cheng; Frank Kloprogge; Carlos Alonso; Charmion Lee; Bilyana Doncheva; John Booth; Robert Chiesa; Adam Irwin; Joseph F Standing
Journal:  Clin Pharmacokinet       Date:  2019-01       Impact factor: 6.447

  4 in total

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