Evidence map›Paper›PMID 40720880›Full record

ArticleJMIR formative research2025

Concordance Between Survey and Electronic Health Record Data in the COVID-19 Citizen Science Study: Retrospective Cohort Analysis.

Elizabeth Crull, Emily C O'Brien, Pavel Antiperovitch, Kirubel Asfaw, Alexis L Beatty, Djeneba Audrey Djibo, Alan F Kaul, John Kornak, Gregory M Marcus, Madelaine Faulkner Modrow and 6 more

Abstract read
In one paragraph

Article in JMIR formative research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Elizabeth CrullDepartment of Health Services Research, Louisiana Public Health Institute, 400 Poydras Street, Suite 1250, New Orleans, LA, 70130, United States, 1 5044954903.ORCID 0000-0003-3658-8355
Emily C O'BrienDuke Clinical Research Institute, School of Medicine, Duke University, Durham, NC, United States.ORCID 0000-0002-8257-7561
Pavel AntiperovitchDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0002-8814-9015
Kirubel AsfawDuke Clinical Research Institute, School of Medicine, Duke University, Durham, NC, United States.ORCID 0009-0007-1129-6969
Alexis L BeattyDivision of Cardiology, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0001-8405-7386
Djeneba Audrey DjiboSafety, Surveillance, and Collaboration, CVS Health, Blue Bell, PA, United States.ORCID 0000-0003-3378-0691
Alan F KaulMedical Outcomes Management, Inc., Sharon, MA, United States.ORCID 0000-0002-2501-6346
John KornakDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0002-0089-0619
Gregory M MarcusDivision of Cardiology, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0001-5197-7696
Madelaine Faulkner ModrowDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0001-7153-2731
Jeffrey E OlginDivision of Cardiology, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0003-1684-9327
Jaime OrozcoDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0009-0008-0813-1175
Soo ParkDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0009-0009-3866-2919
Noah PeyserDivision of Cardiology, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0003-4529-8325
Mark J PletcherDepartment of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.ORCID 0000-0002-6966-1312
Thomas W CartonDepartment of Health Services Research, Louisiana Public Health Institute, 400 Poydras Street, Suite 1250, New Orleans, LA, 70130, United States, 1 5044954903.ORCID 0000-0003-0059-1990

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Real-world data reported by patients and extracted from electronic health records (EHRs) are increasingly leveraged for research, policy, and clinical decision-making. However, it is not always obvious the extent to which these 2 data sources agree with each other. Objective: This study aimed to evaluate the concordance of variables reported by participants enrolled in an electronic cohort study and data available in their EHRs. Methods: Survey data from COVID-19 Citizen Science, an electronic cohort study, were linked to EHR data from 7 health systems, comprising 34,908 participants. Concordance was evaluated for demographics, chronic conditions, and COVID-19 characteristics. Overall agreement, sensitivity, specificity, positive predictive value, negative predictive value, and κ statistics with 95% CIs were calculated. Results: Of 34,017 participants with complete information, 62.3% (21,176/34,017) reported being female, and 62.4% (21,217/34,017) were female according to EHR data. The median age was 57 (IQR 42-68) years. Out of 34,017 participants, 81.6% (27,744/34,017) of participants reported being White, and 79.5% (27,054/34,017) were White according to EHR data. In addition, 9.2% (3,124/34,017) of participants reported being Hispanic, and 6.6% (2,249/34,017) were Hispanic according to EHR data. Statistically significant discordance between data sources was detected for all demographic characteristics (P<.05) except the female category (P=.57) and the American Indian and Alaska Native (P=.21) and "other" race categories (P=.33). Statistically significant discordance was detected for the 2 COVID-19 traits and all baseline medical conditions except diabetes (P=.17). The starkest absolute difference between data sources was for COVID-19 vaccination, which was 48.4% according to the EHR and 97.4% according to participant report. Overall agreement was high for all demographic characteristics, although chance-corrected agreement (κ) and sensitivity were lower for the "other" race category (κ=0.31, sensitivity =26.6%), Hispanic ethnicity (κ=0.82, sensitivity=74%), and current smoker status (κ=0.54, sensitivity=49.4%). Specificity and negative predictive value (NPV) were higher than corresponding specificity and positive predictive value (PPV) for all baseline medical conditions. Sleep apnea had the highest sensitivity of all medical conditions (83.5%), and anemia had the lowest (32.8%). Chance-corrected agreement (κ) was highly variable for baseline medical conditions, ranging from 0.26 for anemia to 0.71 for diabetes. Overall and chance-corrected agreement between data sources for COVID-19 traits such as infection (84.6%, κ=0.34) and vaccination (51.0%, κ=0.05) was relatively lower than all other evaluated traits. The sensitivity for COVID-19 infection was 32.2%, and the sensitivity for COVID-19 vaccination was 49.7%. Although PPV for COVID-19 vaccination was 99.9%, the NPV was 5%. Conclusions: Results suggest the need for improvements to point-of-care capture of patient demographic traits and COVID-19 infection and vaccination history, patient education about their medical conditions, and linkage to external data sources in EHR-only pragmatic research. Further, these results indicate that additional work is required to integrate and prioritize participant-reported data in pragmatic research.

Indexed as

Citizen ScienceCOVID-19Electronic Health RecordsAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesSARS-CoV-2Surveys and Questionnairescohortcohort analysisconcordanceCOVID-19data accuracydata validationEHRelectronic health recordsinternet-basedparticipantportalreal-world datareportreportedself-report

Identifiers

PMID40720880
PMCPMC12303549

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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.