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Predictors of sputum culture conversion among patients treated for multidrug-resistant tuberculosis

机译:耐多药结核病患者痰培养转化率的预测指标

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OBJECTIVE: To identify predictors of initial sputum culture conversion, estimate the usefulness of persistent positive cultures at different time points in predicting treatment failure, and evaluate different definitions of culture conversion for predicting failure among patients with multidrug-resistant tuberculosis (MDR-TB) in five countries, 2000-2004. METHODS: Predictors of time to conversion were identified using multivariate Cox proportional hazards regression modeling. Receiver operating characteristic curves were plotted to visualize the effect of using different definitions of 'culture conversion' on the balance between sensitivity and specificity. RESULTS: Overall, 1209/1416 (85%) of patients with baseline positive cultures converted in a median of 3.0 months (interquartile range 2.0-5.0). Independent predictors of less likely conversion included baseline positive smear (hazard ratio [HR] 0.60, 95%CI 0.53-0.68), resistance to pyrazinamide (HR 0.82, 95%CI 0.70-0.96), fluoroquinolones (FQs; HR 0.65, 95%CI 0.51-0.83) or thioamide (HR 0.83, 95%CI 0.71-0.96), previous use of FQs (HR 0.71, 95%CI 0.60-0.83), poor outcome of previous anti-tuberculosis treatment (HR 0.69, 95%CI 0.54-0.88) and alcoholism (HR 0.74, 95%CI 0.63-0.87). The maximum combined sensitivity (84%) and specificity (94%) in predicting treatment failure was based on lack of culture conversion at month 9 of treatment, assuming conversion is defined as five consecutive negative cultures. CONCLUSION: Patients with identified risk factors were less likely to achieve sputum culture conversion during MDR-TB treatment.
机译:目的:确定痰培养初始转化的预测因素,估算不同时间点持续性阳性培养在预测治疗失败中的作用,并评估不同文化定义对预测耐多药结核病(MDR-TB)患者失败的影响五个国家,2000-2004年。方法:使用多元Cox比例风险回归模型确定转化时间的预测指标。绘制受体工作特征曲线以可视化使用“培养转化”的不同定义对敏感性和特异性之间的平衡的影响。结果:总体而言,基线培养阳性的1209/1416(85%)患者的中位转化时间为3.0个月(四分位间距为2.0-5.0)。转化可能性较小的独立预测因素包括基线阳性涂片(危险比[HR] 0.60,95%CI 0.53-0.68),对吡嗪酰胺的耐药性(HR 0.82,95%CI 0.70-0.96),氟喹诺酮类药物(FQ; HR 0.65,95%) CI 0.51-0.83)或硫代酰胺(HR 0.83,95%CI 0.71-0.96),先前使用过FQs(HR 0.71,95%CI 0.60-0.83),先前抗结核治疗的预后不良(HR 0.69,95%CI 0.54-0.88)和酗酒(HR 0.74,95%CI 0.63-0.87)。预测治疗失败的最大综合敏感性(84%)和特异性(94%)基于治疗第9个月缺乏培养转化的情况,假设转化被定义为连续5次阴性培养。结论:已确定危险因素的患者在耐多药结核病治疗期间实现痰培养转化的可能性较小。

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