Abstract

BackgroundThe secondary use of electronic health records (EHRs) promises to facilitate medical research. We reviewed general data requirements in observational studies and analyzed the feasibility of conducting observational studies with structured EHR data, in particular diagnosis and procedure codes.MethodsAfter reviewing published observational studies from the University Hospital of Erlangen for general data requirements, we identified three different study populations for the feasibility analysis with eligibility criteria from three exemplary observational studies. For each study population, we evaluated the availability of relevant patient characteristics in our EHR, including outcome and exposure variables. To assess data quality, we computed distributions of relevant patient characteristics from the available structured EHR data and compared them to those of the original studies. We implemented computed phenotypes for patient characteristics where necessary. In random samples, we evaluated how well structured patient characteristics agreed with a gold standard from manually interpreted free texts. We categorized our findings using the four data quality dimensions “completeness”, “correctness”, “currency” and “granularity”.ResultsReviewing general data requirements, we found that some investigators supplement routine data with questionnaires, interviews and follow-up examinations. We included 847 subjects in the feasibility analysis (Study 1 n = 411, Study 2 n = 423, Study 3 n = 13). All eligibility criteria from two studies were available in structured data, while one study required computed phenotypes in eligibility criteria. In one study, we found that all necessary patient characteristics were documented at least once in either structured or unstructured data. In another study, all exposure and outcome variables were available in structured data, while in the other one unstructured data had to be consulted. The comparison of patient characteristics distributions, as computed from structured data, with those from the original study yielded similar distributions as well as indications of underreporting. We observed violations in all four data quality dimensions.ConclusionsWhile we found relevant patient characteristics available in structured EHR data, data quality problems may entail that it remains a case-by-case decision whether diagnosis and procedure codes are sufficient to underpin observational studies. Free-text data or subsequently supplementary study data may be important to complement a comprehensive patient history.

Highlights

  • The secondary use of electronic health records (EHRs) promises to facilitate medical research

  • We initially report on general data requirements in observational studies, and cover the feasibility analysis of conducting observational studies with structured EHR data

  • Feasibility analysis Data availability assessment The university hospital in Erlangen has yet to incorporate all its information systems into the EHR; our assessment of data availability was limited to the current state of the EHR at the time of our analysis

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Summary

Introduction

The secondary use of electronic health records (EHRs) promises to facilitate medical research. Medical research provides evidence to support clinical decisions through experimental and observational studies [1, 2]. The investigator determines who is exposed to interventions such as novel treatment options, whereas in observational studies the investigator can only observe the effect of an intervention and does not exert influence on patient exposures. Both of these study types, examine potential associations as indicators of causal relationships between exposures and outcomes. The initiation and completion of experimental studies is complex and expensive, and still may not be appropriate to all research questions due to practical and ethical issues, such as those found in the context of testing medications for embryotoxicity during pregnancy or in surgical studies

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