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Inadequate Lopinavir Concentrations With Modified 8-Hourly Lopinavir/Ritonavir 4:1 Dosing During Rifampicin-based Tuberculosis Treatment in Children Living With HIV

Authors :
Chabala, C.
Turkova, A.
Kapasa, M.
LeBeau, K.
Tembo, C.H.
Zimba, K.
Weisner, L.
Zyambo, K.
Choo, L.
Chungu, C.
Lungu, J.
Mulenga, V.
Crook, A.
Aarnoutse, R.E.
Gibb, D.
McIlleron, H.
Chabala, C.
Turkova, A.
Kapasa, M.
LeBeau, K.
Tembo, C.H.
Zimba, K.
Weisner, L.
Zyambo, K.
Choo, L.
Chungu, C.
Lungu, J.
Mulenga, V.
Crook, A.
Aarnoutse, R.E.
Gibb, D.
McIlleron, H.
Source :
Pediatric Infectious Disease Journal; 899; 904; 0891-3668; 10; 42; ~Pediatric Infectious Disease Journal~899~904~~~0891-3668~10~42~~
Publication Year :
2023

Abstract

Item does not contain fulltext<br />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. METHODS: Children with HIV/tuberculosis coinfection weighing 3.0 to 19.9 kg, 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, 1-7 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 curve 0-24 55.32 mg/h/L [0.30-398.7 mg/h/L]; C max 3.04 mg/L [0.03-18.6 mg/L]; C 8hr 0.90 mg/L [0.01-13.7 mg/L]) were lower than on standard dosing without rifampicin (n = 12; area under the curve 24 121.63 mg/h/L [2.56-487.3 mg/h/L]; C max 9.45 mg/L [0.39-26.4 mg/L]; C 12hr 3.03 mg/L [0.01-17.7 mg/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 ≥1mg/L. 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

Details

Database :
OAIster
Journal :
Pediatric Infectious Disease Journal; 899; 904; 0891-3668; 10; 42; ~Pediatric Infectious Disease Journal~899~904~~~0891-3668~10~42~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1402100072
Document Type :
Electronic Resource