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使用预测性检测板开发用于头孢哌酮-舒巴坦扩散试验的新型试纸条。

Use of a predictor panel for development of a new disk for diffusion tests with cefoperazone-sulbactam.

作者信息

Bradford P A, Sanders C C

机构信息

Department of Medical Microbiology, Creighton University, Omaha, Nebraska 68178.

出版信息

Antimicrob Agents Chemother. 1992 Feb;36(2):394-400. doi: 10.1128/AAC.36.2.394.

Abstract

The proper disk mass for diffusion susceptibility tests with cefoperazone-sulbactam was determined by using a predictor panel of clinical isolates that included staphylococci and gram-negative bacteria intrinsically susceptible, intrinsically resistant, and of various susceptibilities because of the production of different types and amounts of beta-lactamase. A primary panel of 24 isolates was used to screen various disk masses of cefoperazone and sulbactam in disk diffusion susceptibility tests. Regression analyses were performed for each combination by comparing MICs to zone diameters. Analysis of each component demonstrated that decreasing the disk mass of cefoperazone shifted the regression line to the left while decreasing the disk mass of sulbactam diminished the slope of the line. Ten candidate disks that adequately separated susceptible and resistant strains among the primary panel were identified, and these 10 disks, along with the previously proposed 75/30-micrograms disk, were then tested against an expanded panel of 265 isolates. Results indicated that a 30/20-micrograms cefoperazone-sulbactam disk provided the best separation between susceptible and resistant strains when interpretive criteria of less than or equal to 15 mm for resistance, 16 to 19 mm for moderate susceptibility, and greater than or equal to 20 mm for susceptibility were used. They also identified discrepancies between agar and broth microdilution MICs of sufficient size to warrant separate interpretive criteria for the two methods. Overall, the use of a predictor panel to develop interpretive criteria for susceptibility tests appeared to be a very useful approach, especially when antibiotics designed to be used against drug-resistant organisms are involved.

摘要

通过使用一组临床分离菌株预测板来确定头孢哌酮-舒巴坦扩散药敏试验的合适纸片含量,该预测板包括葡萄球菌和革兰氏阴性菌,这些细菌具有内在敏感性、内在耐药性,以及由于产生不同类型和数量的β-内酰胺酶而具有不同的敏感性。在纸片扩散药敏试验中,使用一个由24株分离菌组成的初步菌组来筛选头孢哌酮和舒巴坦的各种纸片含量。通过将最低抑菌浓度(MIC)与抑菌圈直径进行比较,对每种组合进行回归分析。对每个成分的分析表明,降低头孢哌酮的纸片含量会使回归线向左移动,而降低舒巴坦的纸片含量会减小回归线的斜率。确定了10个能在初步菌组中充分区分敏感菌和耐药菌的候选纸片,然后将这10个纸片与先前提出的75/30微克纸片一起,针对一个由265株分离菌组成的扩展菌组进行测试。结果表明,当采用耐药性小于或等于15毫米、中度敏感性为16至19毫米、敏感性大于或等于20毫米的解释标准时,30/20微克的头孢哌酮-舒巴坦纸片能在敏感菌和耐药菌之间提供最佳区分。他们还发现琼脂稀释法和肉汤稀释法的MIC之间存在足够大的差异,需要为这两种方法制定单独的解释标准。总体而言,使用预测菌组来制定药敏试验的解释标准似乎是一种非常有用的方法,尤其是在涉及针对耐药菌设计的抗生素时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efd4/188447/e424e49c7219/aac00036-0182-a.jpg

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