[在体外测试霉菌机会性制剂对抗真菌药物的敏感性]。

M Otcenásek, V Buchta
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引用次数: 0

摘要

作者试图规范抗真菌药物的最低抑菌浓度(MIC)的评估方法,以评估真菌病的机会致病菌的敏感性。他们注意到导致试验可重复性恶化和导致实验室内部和实验室间结果变异性的因素。与此同时,作者提请注意对这些测试在临床实践中的应用缺乏统一的看法。作者认为,关于体外和体内结果不适当的相关性的保留意见并不怀疑实验室敏感性评估的权宜性。测试具有低药物治疗指数和相对较高的继发耐药频率的全身抗真菌药物是特别合理的。在这些情况下,MIC值的评估是监测充分抗真菌化疗的重要组成部分,特别是当对免疫改变的患者长期施用抗真菌药物时。
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[Testing the sensitivity of opportunistic agents of mycoses to antimycotic drugs in vitro].

The authors tried to standardize the method of assessment of the minimal inhibitory concentration (MIC) of antimycotics for the evaluation of the sensitivity of opportunistic causal agents of mycoses. They paid attention to factors which cause deterioration of the reproducibility of tests and lead to intra- and interlaboratory variability of results. In conjunction with this the authors drew attention to the lack of uniformity of views on the application of these tests in clinical practice. In the author's view the reservation pertaining in particular to an inadequate correlation of results in vitro and in vivo do not cast doubts on the expedience of laboratory assessment of sensitivity. Testing of systemic antimycotics with a low pharmacotherapeutic index and a relatively high frequency of secondary resistance is particularly justified. In those instances assessment of MIC values is a significant component of monitoring of adequate antifungal chemotherapy, in particular when antimycotics are administered for prolonged periods to patients with altered immunity.

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