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首页> 外文期刊>Journal of the International Aids Society >Low isoniazid and rifampicin concentrations in TB/HIV co-infected patients in Uganda
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Low isoniazid and rifampicin concentrations in TB/HIV co-infected patients in Uganda

机译:乌干达的TB / HIV共感染患者的低异窦和利福平浓度

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IntroductionThere is limited data available on exposure to anti-tuberculosis (TB) drugs in this region. Peloquin has described reference ranges [1] however some studies have demonstrated that patients actually achieve concentrations below these ranges [2]. There is limited data about exposure to anti-TB drugs in the HIV/TB co-infected population in Sub-Saharan Africa. Our objective is to describe the concentration of anti-TB drug levels in a well characterized prospective cohort of adult patients starting treatment for pulmonary TB.MethodsThis study is an ongoing study carried out in the TB/HIV integrated clinic at the Infectious Diseases Institute in Kampala, Uganda. Sputum culture and microscopy was done for all patients. We performed pharmacokinetic blood sampling of anti-TB drugs for 1 hour, 2 hours and 4 hours post dose at 2 weeks, 8 weeks and 24 weeks after initiation of anti-TB treatment using ultraviolet high-performance liquid chromatography (UV-HPLC). We described the maximum concentration (Cmax) of isoniazid (H), rifampicin (R), ethambutol (E) and pyrazinamide (Z) and compare them with the values observed by Peloquin et al. referenced in other studies.ResultsWe started 113 HIV infected adults on a fixed dose combination of HREZ. The median age of our population was 33 years, of which 52% were male with a median BMI of 19 kg/m2 and a median CD4 cell count of 142 cells/μL. In 90% of the participants, the diagnosis of TB was based on microscopy and or cultures. The boxplot graph shows the median Cmax and IQR of H and R.Levels of H were found to be below the reference ranges (3–6 μg/mL) in 54/77(70.1%), 38/59(64.4%) and 15/24(62.5%) participants at weeks 2, 8 and 24. Rif levels were also found to be below the reference ranges (8–24 μg/mL) in 41/66(62.1%), 26/48(54.2%) and 8/10(8%) participants at weeks 2, 8 and 24, respectively. The mean Cmax of E and Z were within the reference range at week 2 and 8; mean Cmax of 3.2±SD2.1 μg/mL and 4.0±SD3.1 μg/mL for E and 41.6±SD13.1 μg/mL and 42.6±SD16.4 μg/mL for Z.ConclusionWe observed lower concentrations of isoniazid and rifampicin in our study population of HIV/TB co-infected patients. The implications of these findings are not yet clear. We therefore need to correlate our findings with the response to TB treatment.
机译:介绍是在该地区暴露于抗结核(TB)药物的有限数据。 Peloquin描述了参考范围[1]然而,一些研究表明,患者实际上达到这些范围以下的浓度[2]。有关在撒哈拉以南非洲的艾滋病毒/结核病共感染人群中暴露于抗结核药物的数据有限。我们的目标是描述肺结核治疗的良好表征前瞻性患者的抗结核药物水平的浓度。方法是在Kampala的传染病学院的TB / HIV综合诊所中进行的正在进行的研究,乌干达。对所有患者进行了痰培养和显微镜。我们在使用紫外线高性能液相色谱(UV-HPLC)开始后,在2周,8周和24周后给药的药代动力学血液取样1小时,2小时和4小时。我们描述了异烟肼(H),利福平(R),乙胺醇(E)和吡嗪酰胺(Z)的最大浓度(Cmax),并将它们与Peloquin等人观察的值进行比较。在其他研究中引用。培训期开始于113名HIV感染的成年人在Hrez的固定剂量组合上。我们人口的中位年龄为33岁,其中52%是男性,中位BMI为19公斤/平方米和142个细胞/μl的中值CD4细胞计数。在90%的参与者中,TB的诊断基于显微镜和培养物。 Boxplot图显示H和H的中值Cmax和IQR,H的HLEVELS在54/77(70.1%),38/59(64.4%)和38/59(64.4%)和38/59(64.4%)和下方的参考范围(3-6μg/ ml)以下。 15/24(62.5%)参与者在第2周,8和24周的参与者。还发现RIF水平低于参考范围(8-24μg/ ml),41/66(62.1%),26/48(54.2%) 8/10(8%)分别为期2,8和24周的参与者。 E和Z的平均cmax在第2周和第8周的参考范围内;平均CMAX为3.2±SD2.1μg/ mL,E和41.6±Sd13.1μg/ ml和42.6±Sd16.4μg/ ml的Z.ConclusionWE观察到较低浓度的异烟肼和42.6±Sd16.4μg/ ml。利福平在我们的研究人群的HIV / TB COR感染患者中。这些研究结果的含义尚不清楚。因此,我们需要将我们的结果与TB治疗的反应相关联。

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