1 research outputs found
Inadequate Lopinavir Concentrations With Modified 8-hourly Lopinavir/Ritonavir 4:1 Dosing During Rifampicin-based Tuberculosis Treatment in Children Living With HIV
Background: Lopinavir/ritonavir plasma concentrations are profoundly
reduced when co-administered with rifampicin. Super-boosting of lopinavir/ritonavir is limited by nonavailability of single-entity ritonavir, while
double-dosing of co-formulated lopinavir/ritonavir given twice-daily produces suboptimal lopinavir concentrations in young children. We evaluated
whether increased daily dosing with modified 8-hourly lopinavir/ritonavir
4:1 would maintain therapeutic plasma concentrations of lopinavir in children living with HIV receiving rifampicin-based antituberculosis treatment.
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Methods: Children with HIV/tuberculosis coinfection weighing 3.0 to
19.9kg, on rifampicin-based antituberculosis treatment were commenced
or switched to 8-hourly liquid lopinavir/ritonavir 4:1 with increased daily
dosing using weight-band dosing approach. A standard twice-daily dosing
of lopinavir/ritonavir was resumed 2 weeks after completing antituberculosis treatment. Plasma sampling was conducted during and 4 weeks after
completing antituberculosis treatment. //
Results: Of 20 children enrolled; 15, 1β7 years old, had pharmacokinetics sampling available for analysis. Lopinavir concentrations (median
[range]) on 8-hourly lopinavir/ritonavir co-administered with rifampicin
(n = 15; area under the curve0β24 55.32mg/h/L [0.30β398.7mg/h/L]; Cmax
3.04mg/L [0.03β18.6mg/L]; C8hr 0.90mg/L [0.01β13.7mg/L]) were lower
than on standard dosing without rifampicin (n = 12; area under the curve24
121.63mg/h/L [2.56β487.3mg/h/L]; Cmax 9.45mg/L [0.39β26.4mg/L];
C12hr 3.03mg/L [0.01β17.7mg/L]). During and after rifampicin cotreatment,
only 7 of 15 (44.7%) and 8 of 12 (66.7%) children, respectively, achieved
targeted pre-dose lopinavir concentrations β₯1mg/L.
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Conclusions: Modified 8-hourly dosing of lopinavir/ritonavir failed to
achieve adequate lopinavir concentrations with concurrent antituberculosis
treatment. The subtherapeutic lopinavir exposures on standard dosing after
antituberculosis treatment are of concern and requires further evaluation