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Different analytic techniques operate optimally with different types of data. As the use of EHR-based analytics expands to newer tasks, data will have to be transformed into different representations, so the tasks can be optimally solved. We classified representations into broad categories based on their characteristics, and proposed a new knowledge-driven representation for clinical data mining as well as trajectory mining, called Severity Encoding Variables (SEVs). Additionally, we studied which characteristics make representations most suitable for particular clinical analytics tasks including trajectory mining. Our evaluation shows that, for regression, most data representations performed similarly, with SEV achieving a slight (albeit statistically significant) advantage. For patients at high risk of diabetes, it outperformed the competing representation by (relative) 20%. For association mining, SEV achieved the highest performance. Its ability to constrain the search space of patterns through clinical knowledge was key to its success. [ABSTRACT FROM AUTHOR]

Different analytic techniques operate optimally with different types of data. As the use of EHR-based analytics expands to newer tasks, data will have to be transformed into different representations, so the tasks can be optimally solved. We classified representations into broad categories based on their characteristics, and proposed a new knowledge-driven representation for clinical data mining as well as trajectory mining, called Severity Encoding Variables (SEVs). Additionally, we studied which characteristics make representations most suitable for particular clinical analytics tasks including trajectory mining. Our evaluation shows that, for regression, most data representations performed similarly, with SEV achieving a slight (albeit statistically significant) advantage. For patients at high risk of diabetes, it outperformed the competing representation by (relative) 20%. For association mining, SEV achieved the highest performance. Its ability to constrain the search space of patterns through clinical knowledge was key to its success.

The true onset time of a disease, particularly slow-onset diseases like Type 2 diabetes mellitus (T2DM), is rarely observable in electronic health records (EHRs). However, it is critical for analysis of time to events and for studying sequences of diseases. The aim of this study is to demonstrate a method for estimating the onset time of such diseases from intermittently observable laboratory results in the specific context of T2DM. A retrospective observational study design is used. A cohort of 5,874 non-diabetic patients from a large healthcare system in the Upper Midwest United States was constructed with a three-year follow-up period. The HbA1c level of each patient was collected from earliest and the latest follow-up. We modeled the patients' HbA1c trajectories through Bayesian networks to estimate the onset time of diabetes. Due to non-random censoring and interventions unobservable from EHR data (such as lifestyle changes), naïve modeling of HbA1c through linear regression or modeling time-to-event through proportional hazard model leads to a clinically infeasible model with no or limited ability to predict the onset time of diabetes. Our model is consistent with clinical knowledge and estimated the onset of diabetes with less than a six-month error for almost half the patients for whom the onset time could be clinically ascertained. To our knowledge, this is the first study of modeling long-term HbA1c progression in non-diabetic patients and estimating the onset time of diabetes.