Magdalena Skoworonska, Annika Blank, Irene Centeno, Caroline Hammer, Aurel Perren, Inti Zlobec, Tilman T Rau
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With this preanalytical study, we outlined real-life data in a variety of organs with specific differences in WIT, CIT, and FIT values. Furthermore, our FIT data indicate the potential to adapt the SPREC fixation toward concrete paraffin-embedding time points and to extend its categories beyond 72 h due to weekend delays. Additionally, we identified dependencies of preanalytical variables from workload, daytime, and clinics that were actionable with LEAN process management. Thus, streamlined biobanking workflows during the day were significantly resilient to workload peaks, diminishing the turnaround times of native tissue processing (i.e. CIT) from 74.6 to 46.1 min under heavily stressed conditions. In conclusion, there are surgery-specific preanalytics that are surgico-pathologically limited even under process optimization, which might affect biomarker transfer from one entity to another. 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引用次数: 0
摘要
标准化分析前代码(SPREC)以精确的格式汇总了热缺血(WIT)、冷缺血(CIT)和固定时间(FIT)。尽管欧洲体外诊断法规或美国国立卫生研究院(National Institutes of Health)广泛的前分析项目支持了其日益增长的重要性,但人们对其在生物银行外科标本中的实际发生情况知之甚少。通过几个步骤,伯尔尼组织库获得了包含10,555个CIT值、4,740个WIT值和3,121个FIT值的全面信息的SPREC代码。在根据精益六西格玛原则进行工艺优化期间,我们确定了SPREC代码作为样本特征和可追溯工艺参数的双重作用。在这项分析前研究中,我们概述了各种器官中具有WIT、CIT和FIT值特定差异的真实数据。此外,我们的FIT数据表明,SPREC固定适用于混凝土石蜡包埋时间点,并且由于周末延迟而将其类别延长至72小时以上。此外,我们从工作量、白天和诊所中确定了可通过精益流程管理操作的分析前变量的依赖关系。因此,白天简化的生物银行工作流程对工作量高峰具有显著的弹性,在高压力条件下将原生组织处理(即CIT)的周转时间从74.6分钟减少到46.1分钟。总之,即使在工艺优化的情况下,也存在手术特异性预分析在手术病理学上的局限性,这可能会影响生物标志物从一个实体到另一个实体的转移。除了样本特征外,SPREC编码对组织库和病理研究所跟踪WIT、CIT和FIT非常有益,可用于过程优化和监测测量。
Real-life data from standardized preanalytical coding (SPREC) in tissue biobanking and its dual use for sample characterization and process optimization
The standardized preanalytical code (SPREC) aggregates warm ischemia (WIT), cold ischemia (CIT), and fixation times (FIT) in a precise format. Despite its growing importance underpinned by the European in vitro diagnostics regulation or broad preanalytical programs by the National Institutes of Health, little is known about its empirical occurrence in biobanked surgical specimen. In several steps, the Tissue Bank Bern achieved a fully informative SPREC code with insights from 10,555 CIT, 4,740 WIT, and 3,121 FIT values. During process optimization according to LEAN six sigma principles, we identified a dual role of the SPREC code as a sample characteristic and a traceable process parameter. With this preanalytical study, we outlined real-life data in a variety of organs with specific differences in WIT, CIT, and FIT values. Furthermore, our FIT data indicate the potential to adapt the SPREC fixation toward concrete paraffin-embedding time points and to extend its categories beyond 72 h due to weekend delays. Additionally, we identified dependencies of preanalytical variables from workload, daytime, and clinics that were actionable with LEAN process management. Thus, streamlined biobanking workflows during the day were significantly resilient to workload peaks, diminishing the turnaround times of native tissue processing (i.e. CIT) from 74.6 to 46.1 min under heavily stressed conditions. In conclusion, there are surgery-specific preanalytics that are surgico-pathologically limited even under process optimization, which might affect biomarker transfer from one entity to another. Beyond sample characteristics, SPREC coding is highly beneficial for tissue banks and Institutes of Pathology to track WIT, CIT, and FIT for process optimization and monitoring measurements.
期刊介绍:
The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies.
The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.