Administration of efavirenz (600 mg/day) with rifampicin results in highly variable levels but excellent clinical outcomes in patients treated for tuberculosis and HIV

被引:88
作者
Friedland, Gerald
Khoo, Saye
Jack, Christopher
Lalloo, Umesh
机构
[1] Yale Univ, Sch Med, AIDS Program, New Haven, CT 06510 USA
[2] Univ Liverpool, Liverpool L69 3BX, Merseyside, England
[3] Univ KwaZulu Natal, Nelson R Mandela Sch Med, Durban, South Africa
基金
英国惠康基金;
关键词
antiretroviral therapy; drug interactions; TB;
D O I
10.1093/jac/dkl399
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Pharmacokinetic interactions between rifampicin and antiretroviral therapy (ART), including efavirenz, are problematic and need to be better defined to determine proper dose and to be correlated with short-term and long-term clinical outcomes. Patients and methods: Consenting patients with smear-positive pulmonary TB and HIV received once daily didanosine + lamivudine + efavirenz (600 mg), with rifampicin-containing TB regimen by directly observed therapy and self-administration at TB therapy completion. Trough efavirenz levels were measured by HPLC at 1, 2, 4 and 6 months while on rifampicin and after discontinuation. HIV and TB outcomes were monitored. Results: Twenty African patients were enrolled [15 female, mean age 31 years, baseline weight 59.4 kg (range 45-97), viral load 5.75 log(10) copies/mL and CD4 230 cells/mm(3)]. Seventy-two efavirenz concentrations were available from 19 patients (58 on, 14 after rifampicin). The geometric mean efavirenz concentration was 1730 ng/mL (range 354-27 179) on and 1377 ng/mL (range 572-3975) off rifampicin (P = 0.55). Inter-subject variability in efavirenz concentrations was greater on rifampicin (CV 157% versus 58% off) with relatively consistent intra-subject variation over time (median CV 24%). Over half of patients had efavirenz concentrations above or below the expected therapeutic range (1000-4000 ng/mL). Efavirenz levels were not predicted by weight or gender and were not associated with HIV clinical outcomes. Overall 80% of patients had non-detectable viral loads at 6 months and 65% at 21 months with a cumulative CD4 cell increase of 196 cells/mm(3). Conclusions: In this longitudinal study, despite wide variability in plasma efavirenz concentrations during rifampicin administration, excellent clinical outcomes were obtained. In African patients treated for HIV and TB, our data support the routine use of efavirenz at 600 mg/day when receiving rifampicin.
引用
收藏
页码:1299 / 1302
页数:4
相关论文
共 10 条
[1]  
ALMOND L, 2005, 6 INT WORKSH CLIN PH, P15
[2]   Intracellular and plasma pharmacokinetics of efavirenz in HIV-infected individuals [J].
Almond, LM ;
Hoggard, PG ;
Edirisinghe, D ;
Khoo, SH ;
Back, DJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (04) :738-744
[3]  
[Anonymous], 2003, AM J RESP CRIT CARE, V167, P603
[4]  
[Anonymous], 2004, INT POL COLL TB HIV
[5]   Pharmacokinetic interactions between efavirenz and rifampicin in the treatment of HIV and tuberculosis: one size does not fit all [J].
Brennan-Benson, P ;
Lyus, R ;
Harrison, T ;
Pakianathan, M ;
Macallan, D .
AIDS, 2005, 19 (14) :1541-1543
[6]  
Haas DW, 2004, AIDS, V18, P2391
[7]   A pilot study of once-daily antiretroviral therapy integrated with tuberculosis directly observed therapy in a resource-limited setting [J].
Jack, C ;
Lalloo, U ;
Karim, QA ;
Karim, SA ;
El-Sadr, W ;
Cassol, S ;
Friedland, G .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2004, 36 (04) :929-934
[8]   Efavirenz levels and 24-week efficacy in HIV-infected patients with tuberculosis receiving highly active antiretroviral therapy and rifampicin [J].
Manosuthi, W ;
Sungkanuparph, S ;
Thakkinstian, A ;
Vibhagool, A ;
Kiertiburanakul, S ;
Rattanasiri, S ;
Prasithsirikul, W ;
Sankote, J ;
Mahanontharit, A ;
Ruxrungtham, K .
AIDS, 2005, 19 (14) :1481-1486
[9]   BHIVA treatment guidelines for tuberculosis (TB)/HIV infection 2005 [J].
Pozniak, AL ;
Miller, RF ;
Lipman, MCI ;
Freedman, AR ;
Ormerod, LP ;
Johnson, MA ;
Collins, S ;
Lucas, SB .
HIV MEDICINE, 2005, 6 :62-83
[10]  
*WHO, 2006, SCAL ANT THER RES LT