Back to Search
Start Over
Risk factors contributing to a low darunavir plasma concentration.
- Source :
-
British journal of clinical pharmacology [Br J Clin Pharmacol] 2018 Mar; Vol. 84 (3), pp. 456-461. Date of Electronic Publication: 2017 Dec 07. - Publication Year :
- 2018
-
Abstract
- Darunavir is an efficacious drug; however, pharmacokinetic variability has been reported. The objective of this study was to find predisposing factors for low darunavir plasma concentrations in patients starting the once- or twice-daily dosage. Darunavir plasma concentrations from January 2010 till December 2014 of human immunodeficiency virus-infected individuals treated in the outpatient clinic of the University Medical Center Groningen were retrospectively reviewed. The first darunavir plasma concentration of patients within 8 weeks after initiation of darunavir therapy was selected. A dichotomous logistic regression analysis was conducted to select the set of variables best predicting a darunavir concentration below median population pharmacokinetic curve. In total 113 patients were included. The variables best predicting a darunavir concentration besides food intake included age together with estimated glomerular filtration rate (Hosmer-Lemeshow test P = 0.945, Nagelkerke R <superscript>2</superscript>  = 0.284). Systematic evaluation of therapeutic drug monitoring results may help to identify patients at risk for low drug exposure.<br /> (© 2017 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.)
- Subjects :
- Adult
Aged
Darunavir pharmacokinetics
Female
Food-Drug Interactions
Glomerular Filtration Rate physiology
HIV Protease Inhibitors pharmacokinetics
Humans
Logistic Models
Male
Middle Aged
Retrospective Studies
Risk Factors
Young Adult
Darunavir administration & dosage
Drug Monitoring methods
HIV Infections drug therapy
HIV Protease Inhibitors administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2125
- Volume :
- 84
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- British journal of clinical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 29077230
- Full Text :
- https://doi.org/10.1111/bcp.13464