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J Am Med Inform Assoc. 2017 Nov 1;24(6):1134-1141. doi: 10.1093/jamia/ocx071.

Biases introduced by filtering electronic health records for patients with "complete data".

Author information

1
Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
2
Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
3
Department of Pediatrics, Boston Medical Center, Boston, MA, USA.
4
Department of Internal Medicine, McGovern Medical School, School of Biomedical Informatics, The University of Texas Health Science Center, Houston, TX, USA.
5
Computational Health Informatics Program, Boston Children's Hospital, Boston, MA, USA.
6
Department of Analytics and Behavior Change, Aetna, Hartford, CT, USA.
7
Department of Pediatrics, Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
8
Scientific Information Management, Merck, Boston, MA, USA.
9
Division of Endocrinology, Brigham and Women's Hospital, Boston, MA, USA.
10
Department of Radiology, Wake Forest University School of Medicine, Winston Salem, NC, USA.
11
Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.

Abstract

Objective:

One promise of nationwide adoption of electronic health records (EHRs) is the availability of data for large-scale clinical research studies. However, because the same patient could be treated at multiple health care institutions, data from only a single site might not contain the complete medical history for that patient, meaning that critical events could be missing. In this study, we evaluate how simple heuristic checks for data "completeness" affect the number of patients in the resulting cohort and introduce potential biases.

Materials and Methods:

We began with a set of 16 filters that check for the presence of demographics, laboratory tests, and other types of data, and then systematically applied all 216 possible combinations of these filters to the EHR data for 12 million patients at 7 health care systems and a separate payor claims database of 7 million members.

Results:

EHR data showed considerable variability in data completeness across sites and high correlation between data types. For example, the fraction of patients with diagnoses increased from 35.0% in all patients to 90.9% in those with at least 1 medication. An unrelated claims dataset independently showed that most filters select members who are older and more likely female and can eliminate large portions of the population whose data are actually complete.

Discussion and Conclusion:

As investigators design studies, they need to balance their confidence in the completeness of the data with the effects of placing requirements on the data on the resulting patient cohort.

KEYWORDS:

claims data; data accuracy; electronic health records; information storage and retrieval; selection bias

PMID:
29016972
PMCID:
PMC6080680
DOI:
10.1093/jamia/ocx071
[Indexed for MEDLINE]
Free PMC Article

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