Abstract

We designed an algorithm to identify abdominal aortic aneurysm cases and controls from electronic health records to be shared and executed within the "electronic Medical Records and Genomics" (eMERGE) Network. Structured Query Language, was used to script the algorithm utilizing "Current Procedural Terminology" and "International Classification of Diseases" codes, with demographic and encounter data to classify individuals as case, control, or excluded. The algorithm was validated using blinded manual chart review at three eMERGE Network sites and one non-eMERGE Network site. Validation comprised evaluation of an equal number of predicted cases and controls selected at random from the algorithm predictions. After validation at the three eMERGE Network sites, the remaining eMERGE Network sites performed verification only. Finally, the algorithm was implemented as a workflow in the Konstanz Information Miner, which represented the logic graphically while retaining intermediate data for inspection at each node. The algorithm was configured to be independent of specific access to data and was exportable (without data) to other sites. The algorithm demonstrated positive predictive values (PPV) of 92.8% (CI: 86.8-96.7) and 100% (CI: 97.0-100) for cases and controls, respectively. It performed well also outside the eMERGE Network. Implementation of the transportable executable algorithm as a Konstanz Information Miner workflow required much less effort than implementation from pseudo code, and ensured that the logic was as intended. This ePhenotyping algorithm identifies abdominal aortic aneurysm cases and controls from the electronic health record with high case and control PPV necessary for research purposes, can be disseminated easily, and applied to high-throughput genetic and other studies.

Highlights

  • Electronic health records (EHRs) capture a large volume of clinical and physiologic data, and present a valuable resource for research

  • The “electronic Medical Records and Genomics” Network was organized by the National Human Genome Research Institute (NHGRI) in 2007 to develop, disseminate, and apply approaches to combine DNA biorepositories with electronic medical record (EMR) systems for large-scale, high-throughput genetic research with the ultimate goal of returning genomic testing results to patients in a clinical care setting [1]

  • Developed by one or more primary sites, validated at secondary sites and verified at all other sites that implement them. The results of this rigorous development effort are accurate, robust algorithms that may be used at other sites outside the Electronic Medical Records and Genomics (eMERGE) Network

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Summary

Introduction

Electronic health records (EHRs) capture a large volume of clinical and physiologic data, and present a valuable resource for research. The “electronic Medical Records and Genomics” (eMERGE) Network was organized by the National Human Genome Research Institute (NHGRI) in 2007 to develop, disseminate, and apply approaches to combine DNA biorepositories with electronic medical record (EMR) systems for large-scale, high-throughput genetic research with the ultimate goal of returning genomic testing results to patients in a clinical care setting [1]. To accomplish these goals in the eMERGE Network an important first step is to develop robust algorithms, so called “ePhenotyping”. We designed an algorithm to identify abdominal aortic aneurysm cases and controls from electronic health records to be shared and executed within the “electronic Medical Records and Genomics” (eMERGE) Network

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