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

被引:0
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作者
Chabala, Chishala [1 ,2 ,3 ,6 ]
Turkova, Anna [4 ]
Kapasa, Monica [3 ]
Lebeau, Kristen [4 ]
Tembo, Chimuka H. [3 ]
Zimba, Kevin [3 ]
Weisner, Lubbe [2 ]
Zyambo, Khozya [3 ]
Choo, Louise [4 ]
Chungu, Chalilwe [3 ]
Lungu, Joyce [3 ]
Mulenga, Veronica [3 ]
Crook, Angela
Gibb, Diana [4 ]
Mcilleron, Helen [2 ,5 ]
机构
[1] Univ Zambia, Sch Med, Dept Paediat, Lusaka, Zambia
[2] Univ Cape Town, Fac Hlth Sci, Dept Med, Div Clin Pharmacol, Cape Town, South Africa
[3] Univ Teaching Hosp, Childrens Hosp, Lusaka, Zambia
[4] Univ Coll London UCL, Inst Clin Trials & Methodol, Med Res Council, Clin Trials Unit, London, England
[5] Univ Cape Town, Inst Infect Dis & Mol Med, Wellcome Ctr Infect Dis Res Africa CIDRI Africa, Cape Town, South Africa
[6] Univ Zambia, Sch Med, Dept Paediat & Child Hlth, POB 50110,Ridgeway, Lusaka, Zambia
基金
英国医学研究理事会; 英国惠康基金;
关键词
HIV; lopinavir/ritonavir; pharmacokinetics; rifampicin; tuberculosis; INFECTED CHILDREN; POPULATION PHARMACOKINETICS; ACCEPTABILITY; MALNUTRITION; RITONAVIR; TABLETS; SYRUPS;
D O I
10.1097/INF.0000000000004047
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 curve0-24 55.32 mg/h/L [0.30-398.7 mg/h/L]; Cmax 3.04 mg/L [0.03-18.6 mg/L]; C8hr 0.90 mg/L [0.01-13.7 mg/L]) were lower than on standard dosing without rifampicin (n = 12; area under the curve24 121.63 mg/h/L [2.56-487.3 mg/h/L]; Cmax 9.45 mg/L [0.39-26.4 mg/L]; C12hr 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 & GE;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 treatment are of concern and requires further evaluation.
引用
收藏
页码:899 / 904
页数:6
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