Laboratory for Medical Microbiology and Immunology, Elisabeth-TweeSteden Hospital, Hilvarenbeekse weg 60, 5022GC Tilburg, The Netherlands; Department of Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, The Netherlands.
Laboratory for Medical Microbiology and Immunology, Elisabeth-TweeSteden Hospital, Hilvarenbeekse weg 60, 5022GC Tilburg, The Netherlands.
Int J Antimicrob Agents. 2017 May;49(5):631-637. doi: 10.1016/j.ijantimicag.2016.12.019. Epub 2017 Mar 3.
The standard incubation time for antimicrobial susceptibility testing (AST) by disk diffusion is primarily based on laboratory working hours rather than growth and kill characteristics of bacteria. Faster AST results could result in better patient outcomes and reduced costs by initiating earlier appropriate therapy. The earliest possible reading moment for disk diffusion using established disk zone diameter breakpoints for Enterobacteriaceae was determined with a special focus on the accuracy of the results. A total of 88 Enterobacteriaceae challenge isolates, including isolates with specific resistance mechanisms such as extended-spectrum β-lactamase (ESBL), were subjected to disk diffusion with 15 antibiotics. Hourly images were automatically produced by an incubator/camera combination from 1 h to 20 h. Disk zones were plotted over time for all combinations. Essential and categorical agreement rates using the final reading after 20 h of incubation as a reference were calculated for every hour. In total, 1320 antibiotic-micro-organism combinations were tested. Clear growth with readable inhibition zones was visible after 6 h of incubation for the majority (95.8%) of plates and after 7 h for all incubated plates. However, zone sizes changed significantly after those time points for a number of strains. After 10 h of incubation, minor, major and very major error rates were 1.6% (n = 21), 0.2% (n = 1) and 0.7% (n = 4), respectively. The results of this study clearly indicate that early reading of inhibition zones to 10 h after incubation is feasible and accurate and thus may save significantly on turnaround time.
抗菌药物敏感性试验(AST)的标准孵育时间主要基于实验室工作时间,而不是细菌的生长和杀菌特性。更快的 AST 结果可能会通过更早地开始适当的治疗来改善患者的治疗效果并降低成本。使用已建立的肠杆菌科药敏纸片扩散法的临界直径断点,确定了最早可能的读取时间,特别关注结果的准确性。使用 15 种抗生素对 88 株肠杆菌科挑战分离株(包括具有扩展型β-内酰胺酶(ESBL)等特定耐药机制的分离株)进行了药敏纸片扩散试验。孵育器/相机组合自动生成 1 小时至 20 小时的每小时图像。为所有组合绘制了随时间推移的药敏纸片扩散区。计算了以 20 小时孵育后的最终读数为参考的所有时间点的主要和次要符合率。总共测试了 1320 种抗生素-微生物组合。大多数(95.8%)平板在孵育 6 小时后可见清晰的生长和可读的抑菌环,所有平板在孵育 7 小时后可见。然而,对于许多菌株,在这些时间点之后,药敏纸片扩散区的大小发生了显著变化。孵育 10 小时后,次要、主要和非常大的误差率分别为 1.6%(n=21)、0.2%(n=1)和 0.7%(n=4)。本研究的结果清楚地表明,在孵育 10 小时后读取抑菌环是可行且准确的,因此可以显著缩短周转时间。