Poole Sarah, Schroeder Lee Frederick, Shah Nigam
Center for Biomedical Informatics Research, Stanford University, Stanford, CA, United States.
Department of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
J Biomed Inform. 2016 Feb;59:276-84. doi: 10.1016/j.jbi.2015.12.010. Epub 2015 Dec 19.
Reference intervals are critical for the interpretation of laboratory results. The development of reference intervals using traditional methods is time consuming and costly. An alternative approach, known as an a posteriori method, requires an expert to enumerate diagnoses and procedures that can affect the measurement of interest. We develop a method, LIMIT, to use laboratory test results from a clinical database to identify ICD9 codes that are associated with extreme laboratory results, thus automating the a posteriori method. LIMIT was developed using sodium serum levels, and validated using potassium serum levels, both tests for which harmonized reference intervals already exist. To test LIMIT, reference intervals for total hemoglobin in whole blood were learned, and were compared with the hemoglobin reference intervals found using an existing a posteriori approach. In addition, prescription of iron supplements were used to identify individuals whose hemoglobin levels were low enough for a clinician to choose to take action. This prescription data indicating clinical action was then used to estimate the validity of the hemoglobin reference interval sets. Results show that LIMIT produces usable reference intervals for sodium, potassium and hemoglobin laboratory tests. The hemoglobin intervals produced using the data driven approaches consistently had higher positive predictive value and specificity in predicting an iron supplement prescription than the existing intervals. LIMIT represents a fast and inexpensive solution for calculating reference intervals, and shows that it is possible to use laboratory results and coded diagnoses to learn laboratory test reference intervals from clinical data warehouses.
参考区间对于实验室结果的解读至关重要。使用传统方法制定参考区间既耗时又昂贵。一种被称为后验方法的替代方法,需要专家列举可能影响相关测量的诊断和程序。我们开发了一种名为LIMIT的方法,利用临床数据库中的实验室检测结果来识别与极端实验室结果相关的ICD9编码,从而实现后验方法的自动化。LIMIT是利用血清钠水平开发的,并使用血清钾水平进行了验证,这两种检测都已有统一的参考区间。为了测试LIMIT,我们学习了全血中总血红蛋白的参考区间,并将其与使用现有后验方法得出的血红蛋白参考区间进行比较。此外,通过铁补充剂的处方来识别血红蛋白水平低到足以让临床医生选择采取行动的个体。然后,利用这些表明临床行动的处方数据来评估血红蛋白参考区间集的有效性。结果表明,LIMIT可为钠、钾和血红蛋白实验室检测生成可用的参考区间。与现有区间相比,使用数据驱动方法得出的血红蛋白区间在预测铁补充剂处方方面始终具有更高的阳性预测值和特异性。LIMIT为计算参考区间提供了一种快速且经济的解决方案,并表明利用实验室结果和编码诊断从临床数据仓库中学习实验室检测参考区间是可行的。