Wexler H M, Lavin P T, Molitoris E, Finegold S M
Medical Service, VA Wadsworth Medical Center, Los Angeles, California.
Antimicrob Agents Chemother. 1990 Nov;34(11):2246-9. doi: 10.1128/AAC.34.11.2246.
A pilot study was designed to estimate the variance components in the determination of the MIC of cefoxitin for isolates of the Bacteroides fragilis group. Twenty different organisms were tested, and replicate, trial, and reader variabilities were examined. When the total-variance component was used, if the true MIC was 16 micrograms/ml, then the chance that the observed MIC was between 8 and 32 micrograms/ml, inclusive, was 95%. For all analyses, the isolate (P = 0.0001) and reader (P less than 0.03) effects were significant. The probability of specific MIC observations for various true MICs (over the range of 16 to 32 micrograms/ml at 4-micrograms/ml increments) was calculated. For true MICs of 20, 24, and 28 micrograms/ml, the probabilities of observing an MIC of 16 or 32 micrograms/ml (inclusive) were 86, 75, and 62%, respectively. An upward bias was shown to exist in addition to sources of sizeable variation. The recommendation stemming from recognition of this inherent variability is that ranges of percent susceptibility at various concentrations be included in reports of in vitro susceptibility studies.
设计了一项初步研究来估计脆弱拟杆菌群分离株中头孢西丁最低抑菌浓度(MIC)测定中的方差成分。对20种不同的微生物进行了测试,并检查了重复、试验和读取器的变异性。当使用总方差成分时,如果真实的MIC为16微克/毫升,那么观察到的MIC在8至32微克/毫升(含)之间的概率为95%。对于所有分析,分离株(P = 0.0001)和读取器(P小于0.03)的影响是显著的。计算了各种真实MIC(在16至32微克/毫升范围内,以4微克/毫升为增量)下特定MIC观察值的概率。对于真实MIC为20、24和28微克/毫升的情况,观察到MIC为16或32微克/毫升(含)的概率分别为86%、75%和62%。除了存在相当大的变异来源外,还显示存在向上偏差。认识到这种固有变异性后得出的建议是,体外药敏研究报告应包括不同浓度下的药敏百分比范围。