Publication

Posaconazole trough concentrations are not influenced by inflammation: a prospective study

Märtson, A-G., Veringa, A., Bakker, M., van den Heuvel, E. R., Touw, D., van der Werf, T. S., Span, L. F. R. & Alffenaar, J-W. C., Mar-2019, In : International journal of antimicrobial agents. 53, 3, p. 325-329 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

BACKGROUND: During inflammation several cytochrome P450 enzymes are down-regulated. Recently it was shown that voriconazole metabolism is reduced during inflammation. Posaconazole, another triazole with broad-spectrum antifungal activity, is only to a limited extent metabolized by cytochrome P450 enzymes and to a wider extent by phase 2 enzyme systems. The aim of this study was to investigate posaconazole concentrations during inflammation.

MATERIALS/METHODS: In a prospective observational study, we enrolled patients (aged ≥18 years) receiving posaconazole prophylaxis or treatment for fungal infections. Samples for posaconazole and C-reactive protein (CRP) concentrations were collected routinely for each patient. A longitudinal data analysis was performed to analyse the correlation between posaconazole serum trough concentrations and CRP values, corrected for potential factors that could influence the posaconazole concentration.

RESULTS: Between August 2015 and June 2017 64 patients were recruited to this study. Data of 54 patients (511 posaconazole samples) were included in the final analysis. The overall median posaconazole concentration was 1.8 mg/L (IQR 1-2.9 mg/L, range 0.1-7.94 mg/L) and the the overall median CRP concentration was 23.5 mg/L (IQR 5-75 mg/L, range 0-457 mg/L). The longitudinal data analysis showed that only the posaconazole daily dose (in mg/kg body weight) had a significant influence on posaconazole concentration after correction for other factors (p<0.0001). Posaconazole concentrations were not influenced by CRP concentrations (p=0.77).

CONCLUSIONS: Posaconazole concentrations are not influenced by inflammation, reflected by CRP concentration. Therefore, more frequent TDM of posaconazole during inflammation or after an infection subsides is not necessary.

Original languageEnglish
Pages (from-to)325-329
Number of pages5
JournalInternational journal of antimicrobial agents
Volume53
Issue number3
Early online date10-Jan-2019
Publication statusPublished - Mar-2019

    Keywords

  • EXPOSURE, PHARMACOKINETICS, VORICONAZOLE

View graph of relations

Download statistics

No data available

ID: 74429373