Abstract
Objectives: We investigated the clinical significance of monitoring the mid-dosing interval atazanavir (ATV) concentration (measured 12 ± 2 h after intake; C12 h) in patients taking this drug once daily in the evening. Methods: We retrospectively selected HIV-infected patients harbouring ATV-susceptible virus who underwent therapeutic drug monitoring (TDM) of ATV C12 h during routine out-patient visits, and we correlated C12 h to the 24-week virological response and toxicity. Results: A total of 115 plasma samples from 86 patients (76.7% with baseline HIV RNA0.23 mg/L showed virological failure in 14.3% of cases (P=0.021). In multivariate analysis, C12 h>0.23 mg/L was an independent predictor of virological response [odds ratio (OR) 4.23, P=0.031]. ATV levels correlated with concomitant unconjugated bilirubin levels (r=0.223, P=0.037), but a concentration cut-off predictive of moderate/severe hyperbilirubinaemia could not be identified. Conclusions: We identified a C12 h efficacy threshold that predicted virological response; this could be useful for morning TDM in selected subjects receiving ATV in the evening. Results must be interpreted with caution given the retrospective design of the study. © 2010 British HIV Association.
Original language | English |
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Pages (from-to) | 326-333 |
Number of pages | 7 |
Journal | HIV Medicine |
Volume | 11 |
Issue number | 5 |
Publication status | Published - May 2010 |
Keywords
- Antiretroviral therapy
- Atazanavir
- HIV-1
- Pharmacokinetic variability
- Therapeutic drug monitoring