Department of Pathology and Immunology, Washington University School of Medicine, 660 S Euclid Ave, Campus Box 8118, St. Louis, MO, 63130, USA.
Eur J Clin Microbiol Infect Dis. 2019 Jun;38(6):1135-1141. doi: 10.1007/s10096-019-03512-3. Epub 2019 Feb 26.
In order to realize the full potential of total laboratory automation (TLA) in the clinical microbiology laboratory, workflows must be optimized to match each laboratory's capabilities, patient population, and staffing model. Using TLA-based digital photography to monitor urine cultures, we sought to improve culture result turn-around-time (TAT) by changing the time at which a culture is first photographed and thus available for analysis/work-up (Pre1) from 18 h (16,391 cultures) to 16 h (53,113 cultures) (with a total of 24-h culture incubation in both time periods); in both time periods, cultures were set up 24/7, and culture work-up occurred during the day shift only. With this change, we observed a significant decrease in time-to-final-result TAT for positive cultures (18 h-Pre1 median: 71.6 h; 16 h-Pre1 median: 61.0 h). This effect was most pronounced for Gram-negative organisms, with a median reduction in time-to-final-result for Escherichia coli cultures (51.8% of positive urine cultures) of 14.2 h (18 h-Pre1 median: 77.3 h; 16 h-Pre1 median: 63.1 h). This reduction in TAT was accompanied by a decrease in sensitivity at the Pre1 time point (18 h-Pre1 91.01%; 16 h-Pre1 88.06%), which we also found to vary by species: there was a reduction in sensitivity at the first culture reading of 1 to 2% for cultures with Gram-negative microorganisms, but for some Gram-positive microorganisms (e.g., Aerococcus urinae and non-aureus Staphylococcus species), there was a reduction in sensitivity at the Pre1 time-point of 3 to 7%. These results can guide workflow decisions for laboratories seeking to implement and/or optimize TLA systems, demonstrating a tradeoff between TAT and the sensitivity of preliminary urine culture results.
为了充分发挥全实验室自动化(TLA)在临床微生物实验室中的潜力,工作流程必须进行优化,以适应每个实验室的能力、患者人群和人员配备模式。我们使用基于 TLA 的数字摄影来监测尿液培养物,旨在通过改变首次拍摄培养物的时间(Pre1)来提高培养物结果的周转时间(TAT),即将培养物首次拍照并可供分析/处理的时间从 18 小时(16391 个培养物)改为 16 小时(53113 个培养物)(两个时间段的总培养时间为 24 小时);在两个时间段内,培养物均 24/7 设置,仅在白天班进行培养物处理。通过这一改变,我们观察到阳性培养物的最终结果 TAT 显著缩短(18 小时-Pre1 中位数:71.6 小时;16 小时-Pre1 中位数:61.0 小时)。对于革兰氏阴性菌,这种效果最为明显,大肠埃希菌(阳性尿液培养物的 51.8%)的最终结果时间中位数减少了 14.2 小时(18 小时-Pre1 中位数:77.3 小时;16 小时-Pre1 中位数:63.1 小时)。这种 TAT 的缩短伴随着 Pre1 时间点的敏感性降低(18 小时-Pre1 91.01%;16 小时-Pre1 88.06%),我们还发现这种敏感性的降低因物种而异:对于革兰氏阴性微生物的第一次培养物读数,敏感性降低了 1%到 2%,而对于一些革兰氏阳性微生物(如尿肠球菌和非金黄色葡萄球菌),在 Pre1 时间点,敏感性降低了 3%到 7%。这些结果可以为寻求实施和/或优化 TLA 系统的实验室提供工作流程决策指导,展示了 TAT 和初步尿液培养结果敏感性之间的权衡。