Department of Clinical Microbiology, Central Hospital, Växjö, Sweden.
EUCAST Development Laboratory, Växjö, Sweden.
J Antimicrob Chemother. 2023 Dec 1;78(12):2926-2932. doi: 10.1093/jac/dkad332.
Antimicrobial resistance rates are continuously increasing, driving the need for rapid antimicrobial susceptibility testing (RAST) results, especially in the treatment of bloodstream infections. The EUCAST RAST method performed directly from positive blood cultures with incubation times from 4 to 8 h was developed in 2018 and is now used in many laboratories. To increase the practicality of the method, an extended incubation time of 16 and 20 h was evaluated in this study.
Blood culture bottles were spiked with clinical isolates (n = 325) of the seven most important sepsis pathogens. The EUCAST RAST method was performed, extending the incubation time to 16 and 20 h. Broth microdilution (BMD) was used as a reference, except for screening tests where standard disc diffusion or presence of resistance genes was used.
Inhibition zones were possible to read for all species-agent combinations. For 16 and 20 h, the MIC zone diameter correlations were sufficiently similar to allow establishment of common breakpoints for the time interval of 16-20 h. The proportion of isolates in the area of technical uncertainty was, on average, 6% for all species and the number of errors were low, with <1% false-resistant and <0.5% false-susceptible results.
This study shows that, for EUCAST RAST, prolonging the recommended incubation to 16-20 h is possible and can be used as a complement when the intended shorter incubation is not possible to achieve. The introduction of the prolonged incubation will increase the usefulness of the EUCAST RAST method in clinical laboratories with limited opening hours.
抗菌药物耐药率不断上升,迫切需要快速进行抗菌药物敏感性检测(RAST),尤其是在治疗血流感染时。2018 年开发了一种从阳性血培养物直接进行的 EUCAST RAST 方法,孵育时间为 4 至 8 小时,目前许多实验室都在使用该方法。为了提高该方法的实用性,本研究评估了延长孵育时间至 16 小时和 20 小时的效果。
用七种最重要的脓毒症病原体的临床分离株(n=325)对血培养瓶进行了加标。采用 EUCAST RAST 方法,延长孵育时间至 16 小时和 20 小时。除了筛选试验(使用标准纸片扩散或耐药基因存在作为替代)外,肉汤微量稀释(BMD)被用作参考。
所有种属-药物组合的抑菌圈均可以进行判读。对于 16 小时和 20 小时,MIC 区带直径的相关性非常相似,足以确定 16-20 小时时间间隔的共同断点。在技术不确定区域的分离株比例平均为所有种属的 6%,错误数量较少,假耐药率<1%,假敏感率<0.5%。
本研究表明,对于 EUCAST RAST,延长推荐的孵育时间至 16-20 小时是可行的,当无法实现预期的较短孵育时间时,可以作为补充。引入延长孵育时间将提高 EUCAST RAST 方法在营业时间有限的临床实验室中的实用性。