Wiltshire Christine Sekaggya, Lamorde Mohammed, Scherrer Alexandra, Musaazi Joseph, Corti Natascia, Allan Buzibye, Nakijoba Rita, Nalwanga Damalie, Henning Lars, Von Braun Amrei, Okware Solome, Castelnuovo Barbara, Kambugu Andrew, Fehr Jan
Infectious Diseases Institute, Research, Kampala, Uganda.
Infectious Disease and Hospital Epidemiology, University Hospital of Zurich, Zurich, Switzerland.
J Int AIDS Soc. 2014 Nov 2;17(4 Suppl 3):19585. doi: 10.7448/IAS.17.4.19585. eCollection 2014.
There 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.
This 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.
We 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/m(2) 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.
We 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.
该地区关于抗结核药物暴露的数据有限。佩洛喹已描述了参考范围[1],然而一些研究表明患者实际达到的浓度低于这些范围[2]。关于撒哈拉以南非洲艾滋病毒/结核病合并感染人群中抗结核药物暴露的数据有限。我们的目的是描述在一组特征明确的开始接受肺结核治疗的成年患者前瞻性队列中抗结核药物水平的浓度。
本研究是在乌干达坎帕拉传染病研究所的结核病/艾滋病毒综合诊所进行的一项正在进行的研究。对所有患者进行痰培养和显微镜检查。在开始抗结核治疗后2周、8周和24周,使用紫外高效液相色谱法(UV-HPLC)在给药后1小时、2小时和4小时对抗结核药物进行药代动力学血样采集。我们描述了异烟肼(H)、利福平(R)、乙胺丁醇(E)和吡嗪酰胺(Z)的最大浓度(Cmax),并将其与其他研究中引用的佩洛喹等人观察到的值进行比较。
我们让113名感染艾滋病毒的成年人开始使用固定剂量组合的HREZ。我们研究人群的中位年龄为33岁,其中52%为男性,中位体重指数为19 kg/m²,中位CD4细胞计数为142个/微升。在90%的参与者中,结核病诊断基于显微镜检查和/或培养。箱线图显示了H和R的中位Cmax和四分位间距。
在我们的艾滋病毒/结核病合并感染患者研究人群中,我们观察到异烟肼和利福平的浓度较低。这些发现的影响尚不清楚。因此,我们需要将我们的发现与结核病治疗反应相关联。