Antiretroviral treatment in HIV-infected children who require a rifamycin-containing regimen for tuberculosis

被引:13
作者
Rabie, Helena [1 ,2 ,3 ]
Decloedt, Eric H. [2 ,4 ]
Garcia-Prats, Anthony J. [5 ]
Cotton, Mark F. [1 ,2 ,3 ]
Frigati, Lisa [1 ,2 ,3 ]
Lallemant, Marc [6 ]
Hesseling, Anneke [5 ]
Schaaf, H. Simon [1 ,2 ,5 ]
机构
[1] Stellenbosch Univ, Dept Paediat & Child Hlth, Fac Med & Hlth Sci, POB 241, ZA-8000 Cape Town, South Africa
[2] Tygerberg Hosp, Cape Town, South Africa
[3] Stellenbosch Univ, Childrens Infect Dis Clin Res Unit, Cape Town, South Africa
[4] Stellenbosch Univ, Div Clin Pharmacol, Fac Med & Hlth Sci, Cape Town, South Africa
[5] Stellenbosch Univ, Desmond Tutu TB Ctr, Fac Med & Hlth Sci, Cape Town, South Africa
[6] Drugs Neglected Dis Initiat, Pediat HIV Program, Geneva, Switzerland
基金
新加坡国家研究基金会;
关键词
Children; drug-drug interaction; HIV; rifamycin; tuberculosis; LOPINAVIR-RITONAVIR; RECEIVING RIFAMPICIN; SOUTH-AFRICA; PHARMACOKINETICS; RIFABUTIN; NEVIRAPINE; EFAVIRENZ; THERAPY; DRUG; RALTEGRAVIR;
D O I
10.1080/14656566.2017.1309023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In high prevalence settings, tuberculosis and HIV dual infection and co-treatment is frequent. Rifamycins, especially rifampicin, in combination with isoniazid, ethambutol and pyrazinamide are key components of short-course antituberculosis therapy.Areas covered: We reviewed available data, for which articles were identified by a Pubmed search, on rifamycin-antiretroviral interactions in HIV-infected children. Rifamycins have potent inducing effects on phase I and II drug metabolising enzymes and transporters. Antiretroviral medications are often metabolised by the enzymes induced by rifamycins or may suppress specific enzyme activity leading to drug-drug interactions with rifamycins. These may cause significant alterations in their phamacokinetic and pharmacodynamic properties, and sometimes that of the rifamycin. Recommended strategies to adapt to these interactions include avoidance and dose adjustment.Expert opinion: Despite the importance and frequency of tuberculosis as an opportunistic disease in HIV-infected children, current data on the management of co-treated children is based on few studies. We need new strategies to rapidly assess the use of rifamycins, new anti-tuberculosis drugs and antiretroviral drugs together as information on safety and dosing of individual drugs becomes available.
引用
收藏
页码:589 / 598
页数:10
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