首页> 美国卫生研究院文献>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America >Efavirenz Pharmacokinetics and Pharmacodynamics in HIV-Infected Persons Receiving Rifapentine and Isoniazid for Tuberculosis Prevention
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Efavirenz Pharmacokinetics and Pharmacodynamics in HIV-Infected Persons Receiving Rifapentine and Isoniazid for Tuberculosis Prevention

机译:依法韦仑药物动力学和药效学在接受利福喷汀和异烟肼预防艾滋病毒感染的艾滋病毒感染者中

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摘要

>Background. Concomitant use of rifamycins to treat or prevent tuberculosis can result in subtherapeutic concentrations of antiretroviral drugs. We studied the interaction of efavirenz with daily rifapentine and isoniazid in human immunodeficiency virus (HIV)–infected individuals receiving a 4-week regimen to prevent tuberculosis.>Methods. Participants receiving daily rifapentine and isoniazid with efavirenz had pharmacokinetic evaluations at baseline and weeks 2 and 4 of concomitant therapy. Efavirenz apparent oral clearance was estimated and the geometric mean ratio (GMR) of values before and during rifapentine and isoniazid was calculated. HIV type 1 (HIV-1) RNA was measured at baseline and week 8.>Results. Eighty-seven participants were evaluable: 54% were female, and the median age was 35 years (interquartile range [IQR], 29–44 years). Numbers of participants with efavirenz concentrations ≥1 mg/L were 85 (98%) at week 0; 81 (93%) at week 2; 78 (90%) at week 4; and 75 (86%) at weeks 2 and 4. Median efavirenz apparent oral clearance was 9.3 L/hour (IQR, 6.42–13.22 L/hour) at baseline and 9.8 L/hour (IQR, 7.04–15.59 L/hour) during rifapentine/isoniazid treatment (GMR, 1.04 [90% confidence interval, .97–1.13]). Seventy-nine of 85 (93%) participants had undetectable HIV-1 RNA (<40 copies/mL) at entry; 71 of 75 (95%) participants had undetectable HIV-1 RNA at week 8. Two participants with undetectable HIV-1 RNA at study entry were detectable (43 and 47 copies/mL) at week 8.>Conclusions. The proportion of participants with midinterval efavirenz concentrations ≥1 mg/L did not cross below the prespecified threshold of >80%, and virologic suppression was maintained. Four weeks of daily rifapentine plus isoniazid can be coadministered with efavirenz without clinically meaningful reductions in efavirenz mid-dosing concentrations or virologic suppression.>Clinical Trials Registration. .
机译:>背景。同时使用利福霉素治疗或预防结核病可能会导致亚治疗浓度的抗逆转录病毒药物。我们研究了在接受人类免疫缺陷病毒(HIV)感染的个体中接受efavirenz与每日利福喷汀和异烟肼相互作用的个体,该个体接受了为期4周的预防结核病治疗。在基线以及伴随治疗的第2和第4周进行评估。估计依非韦伦的表观口腔清除率,并计算出利福喷汀和异烟肼之前和期间的几何平均值(GMR)值。在基线和第8周测量了HIV 1型(HIV-1)RNA。>结果。有87位参与者是可评估的:54%为女性,中位年龄为35岁(四分位间距[IQR] ],29-44岁)。在第0周,依非韦仑浓度≥1mg / L的参与者人数为85(98%);第二周81(93%);第四周78(90%);在第2周和第4周时为75(86%)。依法韦仑的表观清除率在基线时为9.3 L /小时(IQR,6.42–13.22 L /小时),在基线期间为9.8 L /小时(IQR,7.04–15.59 L /小时)。利福喷汀/异烟肼治疗(GMR,1.04 [90%置信区间,0.97-1.13])。 85名参与者中有79名(93%)进入时检测不到HIV-1 RNA(<40拷贝/ mL); 75名参与者中的71名(95%)在第8周时检测不到HIV-1 RNA。两名在研究进入时具有HIV-1 RNA检测不到的参与者在第8周可检测到(43和47拷贝/ mL)。>结论。 strong>间隔期依非韦伦浓度≥1mg / L的参与者比例未超过预定的> 80%阈值,并保持了病毒学抑制作用。每天服用四周的利福喷汀加异烟肼可以与依非韦伦合用,而不会在临床上降低依非韦伦的中等剂量或病毒学抑制作用。>临床试验注册。

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