Evidence map›Paper›PMID 41843603›Full record

ArticlePLOS digital health2026

Evaluating the impact of discordant and missing demographic information on population health assessments using linked electronic health records and Census Bureau microdata.

Derek Ouyang, Aubrey Limburg, David H Rehkopf, Jacob Goldin, Robert L Phillips, Victoria Udalova, Daniel E Ho

Abstract read
In one paragraph

Article in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Derek OuyangStanford Law School, Stanford, California, United States of America.ORCID https://orcid.org/0000-0001-7823-0752
Aubrey LimburgU.S. Census Bureau, Suitland, Maryland, United States of America.
David H RehkopfSchool of Medicine, Stanford University, Stanford, California, United States of America.
Jacob GoldinUniversity of Chicago Law School, Chicago, Illinois, United States of America.
Robert L PhillipsAmerican Board of Family Medicine, Lexington, Kentucky, United States of America.
Victoria UdalovaU.S. Census Bureau, Suitland, Maryland, United States of America.ORCID https://orcid.org/0000-0003-2239-1439
Daniel E HoStanford Law School, Stanford, California, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Administrative records are increasingly being used to study population-level outcomes, despite high rates of missingness and discrepancies (i.e., discordance) in demographic identifiers across different sources of data, which could reduce the quality of such assessments. Few studies have evaluated the relationship between these phenomena in administrative records and downstream impacts on assessments in consequential domains such as healthcare. We characterize patterns of discordance and missingness of race and ethnicity in electronic health records (EHR; 2010-2021) derived from the American Board of Family Medicine's primary care registry, linked at the individual-level to restricted U.S. Census Bureau microdata (2000, 2010, 2020 Census; American Community Survey 2005-2022). Among 5.86 million linked patients, 19.3% were missing race and ethnicity information in EHRs, and 8.0% had race and ethnicity information that was recorded discordantly between the two sources, with the lowest discordance for White, Black, and Asian patients and the highest for American Indian and Alaska Native, Native Hawaiian and Pacific Islander (NHPI), and Multiracial patients. Missingness and discordance impacted estimation of group differences for all 50 health outcomes we consider, particularly for smaller racial/ethnic groups, such as a 24 percent change in NHPI Type 2 diabetes diagnosis rates. Our research has three major implications for the work of government agencies, academics, clinicians, and other stakeholders interested in utilizing EHRs for research purposes. First, we demonstrate how the quality of demographic data in administrative records can be comprehensively assessed, which previously has not been possible due to limitations in data access and linkage. Second, we systematically evaluate the impact of discordant and missing demographic information on our ability to accurately estimate disease prevalence. Third, we underscore the importance of evaluating discordance of demographic information both within and across different administrative domains.

Identifiers

PMID41843603
PMCPMC12994837

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.