Abstract
Extracting patient phenotypes from routinely collected health data (such as Electronic Health Records) requires translating clinically-sound phenotype definitions into queries/computations executable on the underlying data sources by clinical researchers. This requires significant knowledge and skills to deal with heterogeneous and often imperfect data. Translations are time-consuming, error-prone and, most importantly, hard to share and reproduce across different settings. This paper proposes a knowledge driven framework that (1) decouples the specification of phenotype semantics from underlying data sources; (2) can automatically populate and conduct phenotype computations on heterogeneous data spaces. We report preliminary results of deploying this framework on five Scottish health datasets.
Original language | English |
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Pages (from-to) | 1327-1328 |
Number of pages | 2 |
Journal | Studies in Health Technology and Informatics |
Volume | 270 |
DOIs | |
Publication status | Published - 16 Jun 2020 |
Keywords
- Electronic Health Records
- Information Storage and Retrieval
- Semantics