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Therapeutic drug monitoring of voriconazole in Japanese patients: analysis based on clinical practice data

机译:日本患者伏立康唑的治疗药物监测:基于临床实践数据的分析

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摘要

The aim of this study was to investigate whether routine therapeutic drug monitoring (TDM) of voriconazole (VRCZ) reduced discontinuation due to hepatotoxicity. Hepatotoxicity was observed in 15 (51.7%) out of 29 patients. The percentages of patients who developed hepatotoxicity within 4 days and 1 week were 26.7 and 46.7%, respectively. The drug trough concentrations in patients with and without hepatotoxicity were 5.55 +/- 2.73 and 2.36 +/- 1.67 mu g/ml (P<0.01, the two-sided Student's t-test), respectively. Trough concentrations reached the target of 1-5 mu g/ml in patients with gradual dose reductions based on TDM, and, consequently, liver enzyme levels returned to the original levels before the VRCZ treatment. All patients eventually continued effective VRCZ therapy despite its hepatotoxicity. Thus, dose adjustments by TDM to achieve the target trough concentrations is useful in order to avoid hepatotoxicity and enable continued effective VRCZ therapy for Japanese patients with invasive fungal infections.
机译:这项研究的目的是调查伏立康唑(VRCZ)的常规治疗药物监测(TDM)是否减少了因肝毒性引起的停药。 29名患者中有15名(51.7%)观察到肝毒性。在4天和1周内发生肝毒性的患者百分比分别为26.7和46.7%。有和无肝毒性患者的药物谷浓度分别为5.55 +/- 2.73和2.36 +/- 1.67μg / ml(P <0.01,双向学生t检验)。在根据TDM逐渐降低剂量的患者中,谷浓度达到1-5μg / ml的目标,因此,肝酶水平恢复至VRCZ治疗前的原始水平。尽管有肝毒性,所有患者最终仍继续有效的VRCZ治疗。因此,通过TDM调整剂量以达到目标谷浓度对于避免肝毒性和使侵袭性真菌感染的日本患者能够继续有效进行VRCZ治疗很有用。

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