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肺结核患者的预剂量样本中利福平的浓度。

Concentrations of rifampicin in pre-dose samples in patients with pulmonary tuberculosis.

机构信息

Universidade Federal do Pará, Faculdade de Farmácia, Laboratório de Toxicologia, Belém, PA, Brazil.

Universidade Federal do Pará, Faculdade de Farmácia, Laboratório de Toxicologia, Belém, PA, Brazil.

出版信息

Braz J Infect Dis. 2019 Mar-Apr;23(2):130-133. doi: 10.1016/j.bjid.2019.05.001. Epub 2019 May 22.

Abstract

Rifampicin is used in both phases of treatment for tuberculosis. In chronic use, the short half-life and the self-induction of metabolism can decrease the levels of the drug below the minimal inhibitory concentration. The aim of the study was to investigate whether plasma concentrations of rifampicin are sustained above 0.5μg/mL in patients with tuberculosis using 600mg/day. Rifampicin was measured in plasma by high-performance liquid chromatography and a sputum smear microscopy was performed in all days of the study. A total of 44 male patients completed the study. On days 31, 61 and 91, the mean plasma concentrations of rifampicin were 0.6 (0.5)μg/mL, 0.55 (0.5)μg/mL and 0.46 (0.4)μg/mL. There was a high variation of rifampicin levels leading to a high percentage of samples with concentrations below 0.5μg/mL. There was no significant association between the frequency of samples with drug levels below 0.5μg/mL with the conversion of the sputum microscopy. These data suggest that pre-doses samples offer limited information on the exposure of M. tuberculosis to rifampicin.

摘要

利福平用于结核病治疗的两个阶段。在慢性使用中,半衰期短和代谢的自我诱导会导致药物水平低于最小抑菌浓度。本研究的目的是研究每天使用 600 毫克是否能使结核病患者的利福平血浆浓度持续维持在 0.5μg/mL 以上。利福平通过高效液相色谱法在血浆中进行测量,并且在研究的所有天数中都进行了痰涂片显微镜检查。共有 44 名男性患者完成了这项研究。在第 31、61 和 91 天,利福平的平均血浆浓度分别为 0.6(0.5)μg/mL、0.55(0.5)μg/mL 和 0.46(0.4)μg/mL。利福平水平的变异很大,导致很大比例的样本浓度低于 0.5μg/mL。药物浓度低于 0.5μg/mL 的样本频率与痰镜检的转化之间没有显著相关性。这些数据表明,预剂量样本提供了对结核分枝杆菌暴露于利福平的有限信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ea/9425676/e96872777067/gr1.jpg

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