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Peak plasma rifampicin level in tuberculosis patients with slow culture conversion.

机译:缓慢培养转化的结核病患者血浆利福平峰值水平。

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摘要

The clinical utility of therapeutic drug monitoring in tuberculosis has not been adequately evaluated by controlled clinical trials. To examine the relationship between slow culture conversion and peak plasma rifampicin level (Cmax-rfm) in a case-control study, patients with persistence of positive sputum smear despite at least 8 weeks of directly observed treatment with standard pyrazinamide-containing regimens were enrolled prospectively in government chest clinics from 16 December 2005 to 15 November 2006. Patients with multidrug-resistant tuberculosis, human immunodeficiency virus infection, or poor treatment adherence were excluded. Cases referred to patients with persistence of positive culture whereas controls had negative culture despite positive smear. Blood was checked at 2 and 4 hours post-dosing to capture Cmax-rfm. A cohort of 88 patients was identified. After excluding 16 patients, there were 36 controls and 36 cases. None had symptoms of malabsorption. Cmax-rfm was below 6 mg/l among 47%of controls and 44% of cases. Univariate and multiple logistic regression analyses showed no significant association between slow culture conversion and Cmax-rfm after logarithmic transformation. Thus, there is probably no association between Cmax-rfm and slow culture conversion.
机译:对照临床试验尚未充分评估结核病中治疗药物监测的临床效用。为了在病例对照研究中检查慢培养转化率与血浆利福平峰值水平(Cmax-rfm)之间的关系,前瞻性纳入了尽管至少接受了8周含标准吡嗪酰胺治疗的患者直接观察到痰涂片阳性持续存在的患者于2005年12月16日至2006年11月15日在政府胸腔门诊就诊。排除了耐多药结核病,人类免疫缺陷病毒感染或依从性差的患者。病例指的是持续培养阳性的患者,而对照组尽管涂片阳性但培养阴性。给药后2和4小时检查血液以捕获Cmax-rfm。确定了88例患者。排除16例患者后,有36例对照和36例。没有人有吸收不良的症状。 47%的对照组和44%的病例中Cmax-rfm低于6 mg / l。单变量和多逻辑回归分析显示对数转化后慢培养转化率与Cmax-rfm之间无显着关联。因此,Cmax-rfm和缓慢的培养物转化之间可能没有关联。

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