*Joint first authors.
Therapeutic drug monitoring of lopinavir/ritonavir in pregnancy
Article first published online: 18 AUG 2010
© 2010 British HIV Association
Volume 12, Issue 3, pages 166–173, March 2011
How to Cite
Lambert, J., Else, L., Jackson, V., Breiden, J., Gibbons, S., Dickinson, L., Back, D., Brennan, M., Connor, E., Boyle, N., Fleming, C., Coulter-Smith, S. and Khoo, S. (2011), Therapeutic drug monitoring of lopinavir/ritonavir in pregnancy. HIV Medicine, 12: 166–173. doi: 10.1111/j.1468-1293.2010.00865.x
- Issue published online: 6 FEB 2011
- Article first published online: 18 AUG 2010
- Accepted 18 May 2010
- therapeutic drug monitoring;
- protein binding
The aim of the study was to determine total and unbound lopinavir (LPV) plasma concentrations in HIV-infected pregnant women receiving lopinavir/ritonavir (LPV/r tablet) undergoing therapeutic drug monitoring (TDM) during pregnancy and postpartum.
Women were enrolled in the study who were receiving the LPV/r tablet as part of their routine prenatal care. Demographic and clinical data were collected and LPV plasma (total) and ultrafiltrate (unbound) concentrations were determined in the first, second and third trimesters using high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS). Postpartum sampling was performed where applicable. Antepartum and postpartum trough concentrations (Ctrough) were compared independently [using analysis of variance (anova)] and on a longitudinal basis (using a paired t-test).
Forty-six women were enrolled in the study (38 Black African). Forty women initiated LPV/r treatment in pregnancy. Median (range) gestation at initiation was 25 (15–36) weeks and median (range) baseline CD4 count and viral load were 346 (14–836) cells/μL and 8724 (<50–267408) HIV-1 RNA copies/mL, respectively. Forty women (87%) had LPV concentrations above the accepted minimum effective concentration for wild-type virus (MEC; 1000 ng/mL). Geometric mean (95% confidence interval [CI]) total LPV concentrations in the first/second [3525 (2823–4227) ng/mL; n=16] and third [3346 (2813–3880) ng/mL; n=43] trimesters were significantly lower relative to postpartum [5136 (3693–6579) ng/mL; n=12] (P=0.006). In a paired analysis (n=12), LPV concentrations were reduced in the third trimester [3657 (2851–4463) ng/mL] vs. postpartum (P=0.021). No significant differences were observed in the LPV fraction unbound (fu%).
Conclusions The above target concentrations achieved in the majority of women and similarities in the fu% suggest standard dosing of the LPV/r tablet is appropriate during pregnancy. However, reduced LPV concentrations in the second/third trimesters and potentially compromised adherence highlight the need for TDM-guided dose adjustment in certain cases.