Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.
Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Switzerland.
Clin Infect Dis. 2018 Aug 16;67(5):708-716. doi: 10.1093/cid/ciy179.
The relationship between concentrations of antituberculosis drugs, sputum culture conversion, and treatment outcome remains unclear. We sought to determine the association between antituberculosis drug concentrations and sputum conversion among patients coinfected with tuberculosis and human immunodeficiency virus (HIV) and receiving first-line antituberculosis drugs.
We enrolled HIV-infected Ugandans with pulmonary tuberculosis. Estimation of first-line antituberculosis drug concentrations was performed 1, 2, and 4 hours after drug intake at 2, 8, and 24 weeks of tuberculosis treatment. Serial sputum cultures were performed at each visit. Time-to-event analysis was used to determine factors associated with sputum culture conversion.
We enrolled 268 HIV-infected patients. Patients with low isoniazid and rifampicin concentrations were less likely to have sputum culture conversion before the end of tuberculosis treatment (hazard ratio, 0.54; 95% confidence interval, .37-.77; P = .001) or by the end of follow-up (0.61; .44-.85; P = .003). Patients in the highest quartile for area under the rifampicin and isoniazid concentration-time curves for were twice as likely to experience sputum conversion than those in the lowest quartile. Rifampicin and isoniazid concentrations below the thresholds and weight <55 kg were both risk factors for unfavorable tuberculosis treatment outcomes. Only 4.4% of the participants had treatment failure.
Although low antituberculosis drug concentrations did not translate to a high proportion of patients with treatment failure, the association between low concentrations of rifampicin and isoniazid and delayed culture conversion may have implications for tuberculosis transmission. Clinical Trials Registration: NCT01782950.
抗结核药物浓度、痰培养转化与治疗结局之间的关系尚不清楚。我们旨在确定合并结核分枝杆菌与人类免疫缺陷病毒(HIV)感染的患者接受一线抗结核药物治疗时,抗结核药物浓度与痰培养转化之间的相关性。
我们纳入了感染 HIV 的肺结核乌干达患者。在抗结核治疗的第 2、8 和 24 周时,于服药后 1、2 和 4 小时,对一线抗结核药物浓度进行评估。每次就诊时均进行连续痰培养。采用生存分析来确定与痰培养转化相关的因素。
我们共纳入了 268 例 HIV 感染患者。在治疗结束前(风险比,0.54;95%置信区间,0.37-0.77;P =.001)或随访结束时(0.61;0.44-0.85;P =.003)痰培养仍未转化的患者,异烟肼和利福平的药物浓度较低。利福平及异烟肼浓度时间曲线下面积最高四分位数组的患者较最低四分位数组的患者更可能出现痰培养转化。利福平及异烟肼浓度低于阈值且体重 <55kg 均是结核病治疗结局不良的危险因素。仅有 4.4%的患者发生治疗失败。
尽管抗结核药物浓度较低并未导致高比例的患者治疗失败,但利福平及异烟肼浓度较低与痰培养转化延迟之间的相关性可能对结核病传播产生影响。临床试验注册:NCT01782950。