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抗真菌药物耐药性的体外评估。

In vitro assessment of antifungal drug resistance.

作者信息

Holmberg K

出版信息

Acta Derm Venereol Suppl (Stockh). 1986;121:131-8.

PMID:3459340
Abstract

Several studies have documented the variability in the susceptibility pattern of fungi to antifungal drugs, and fungi possess resistance determinants to negate the effects of antifungal agents. In vitro assessment of both resistance and susceptibility are measured by suitable concentration endpoints of the antifungal drug, the minimal inhibitory concentration (MIC). MICs serve as the main parameter to define the fungistatic action on fungi growing in culture. For the antifungals used for treatment of local mycoses, the limit between a MIC value indicating susceptibility and one indicating resistance is usually determined empirically on the basis of the correlation between MIC values, and either positive or negative response to chemotherapy. The principles of susceptibility testing of fungi are essentially the same as those for bacteria. However, testing with fungi must deal with the fact that interpretation of the results is complicated by inherent differences in fungal morphology, growth rate, and optimal culture conditions. Several factors could adversely affect the test results and must be considered in the design of susceptibility testing of fungi. It is obvious when the present data on fungal susceptibility testing are reviewed that much more work on standardization of techniques and interpretation of results is necessary. This presentation will focus on the in vitro susceptibility testing for determining primary and secondary drug resistance of griseofulvin and azole antifungal agents, and the correlation between the activities of these antifungals in vitro and in vivo.

摘要

多项研究记录了真菌对抗真菌药物敏感性模式的变异性,并且真菌拥有抗性决定因素以抵消抗真菌剂的作用。抗真菌药物的抗性和敏感性的体外评估通过抗真菌药物的合适浓度终点——最小抑菌浓度(MIC)来测定。MIC作为定义对培养中生长的真菌的抑菌作用的主要参数。对于用于治疗局部真菌病的抗真菌药物,表明敏感性的MIC值与表明抗性的MIC值之间的界限通常根据MIC值之间的相关性以及化疗的阳性或阴性反应凭经验确定。真菌药敏试验的原则与细菌的基本相同。然而,真菌检测必须考虑到这样一个事实,即真菌形态、生长速率和最佳培养条件的固有差异会使结果的解释变得复杂。几个因素可能会对检测结果产生不利影响,在设计真菌药敏试验时必须予以考虑。当回顾目前关于真菌药敏试验的数据时,很明显在技术标准化和结果解释方面需要做更多的工作。本报告将重点关注用于确定灰黄霉素和唑类抗真菌剂的原发性和继发性耐药性的体外药敏试验,以及这些抗真菌剂在体外和体内活性之间的相关性。

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