Evidence map›Paper›PMID 40036551›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2025

Assessment of health conditions from patient electronic health record portals vs self-reported questionnaires: an analysis of the INSPIRE study.

Rohan Khera, Mitsuaki Sawano, Frederick Warner, Andreas Coppi, Aline F Pedroso, Erica S Spatz, Huihui Yu, Michael Gottlieb, Sharon Saydah, Kari A Stephens and 9 more

Abstract readComparative Study
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Observational
  3. Review
  4. Article
  5. 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

19 authors.

Rohan KheraSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.ORCID 0000-0001-9467-6199
Mitsuaki SawanoSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.
Frederick WarnerSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.
Andreas CoppiSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.
Aline F PedrosoSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.ORCID 0000-0002-1876-8304
Erica S SpatzSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.
Huihui YuSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, United States.
Michael GottliebDepartment of Emergency Medicine, Rush University Medical Center, Chicago, IL 60612, United States.ORCID 0000-0003-3276-8375
Sharon SaydahNational Center for Immunizations and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30329, United States.ORCID 0000-0002-6350-5300
Kari A StephensDepartment of Biomedical Informatics and Medical Education, University of Washington, Seattle, WA 98195, United States.ORCID 0000-0002-2520-5526
Kristin L RisingDepartment of Emergency Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA 19107, United States.
Joann G ElmoreDivision of General Internal Medicine and Health Services Research, David Geffen School of Medicine, University of California, Los Angeles (UCLA), Los Angeles, CA 90024, United States.
Mandy J HillDepartment of Emergency Medicine, UTHealth Houston, Houston, TX 77030, United States.ORCID 0000-0001-9778-358X
Ahamed H IdrisDepartment of Emergency Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.
Juan Carlos C MontoyDepartment of Emergency Medicine, University of California, San Francisco, San Francisco, CA 94143, United States.
Kelli N O'LaughlinDepartment of Emergency Medicine, University of Washington, Seattle, WA 98195, United States.
Robert A WeinsteinDivision of Infectious Diseases, Department of Internal Medicine, Rush University Medical Center, Chicago, IL 60612, United States.ORCID 0000-0002-3390-858X
Arjun VenkateshCenter for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT 06510, United States.ORCID 0000-0002-8248-0567
INSPIRE Group

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Achieving HIV viral suppression in refugee settlements in Uganda with Head StART: a cluster randomized trial evaluating the effectiveness of community ART delivery for people newly diagnosed with HIVR01MH130216 · NIMH · UNIVERSITY OF WASHINGTON · PI Kelli Nicole O'Laughlin · 2023 to 2026
$2.5M
Deep learning enhanced detection and personalized monitoring of aortic stenosis - The DETECT-AS StudyR01AG089981 · NIA · YALE UNIVERSITY · PI Rohan Khera · 2024 to 2026
$2.4M
Translating Personalized Inference from Randomized Clinical Trials to Real-World Cardiovascular CareR01HL167858 · NHLBI · YALE UNIVERSITY · PI Rohan Khera · 2024 to 2026
$2.3M
PROmotion of COVid-19 VA(X)ccination in the Emergency Department - PROCOVAXEDR01AI166967 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RODRIGUEZ, ROBERT · 2021 to 2023
$1.9M
Evaluating and Improving Utilization of Evidence-Based Medical Therapy in Patients with Heart Failure using Automated Tools in the Electronic Health RecordK23HL153775 · NHLBI · YALE UNIVERSITY · PI KHERA, ROHAN · 2021 to 2025
$918k
Abbott DiagnosticsCDC HHSCDC HHS U01CK00048DermTechDoris Duke Charitable Foundation 2022060Institute of Translational Health SciencesMeMedNational Institute of Aging R01AG089981NCATS NIH HHS UL1 TR002319NHLBI NIH HHS K23 HL153775NHLBI NIH HHS R01HL167858NIAID NIH HHS 1R01AI166967NIAID NIH HHS R01 AI166967NIAID NIH HHS R01AI166967NIA NIH HHS R01 AG089981NIH HHSNIH HHS UL1TR002319NIMH NIH HHS R01 MH130216NIMH NIH HHS R01MH130216PrenosisSiemens Healthcare DiagnosticsUniversity of Washington
6 · The paper itself

Abstract

objectivesDirect electronic access to multiple electronic health record (EHR) systems through patient portals offers a novel avenue for decentralized research. Given the critical value of patient characterization, we sought to compare computable evaluation of health conditions from patient-portal EHR against the traditional self-report. MATERIALS AND

methodsIn the nationwide Innovative Support for Patients with SARS-CoV-2 Infections Registry (INSPIRE) study, which linked self-reported questionnaires with multiplatform patient-portal EHR data, we compared self-reported health conditions across different clinical domains against computable definitions based on diagnosis codes, medications, vital signs, and laboratory testing. We assessed their concordance using Cohen's Kappa and the prognostic significance of differentially captured features as predictors of 1-year all-cause hospitalization risk.

resultsAmong 1683 participants (mean age 41 ± 15 years, 67% female, 63% non-Hispanic Whites), the prevalence of conditions varied substantially between EHR and self-report (-13.2% to +11.6% across definitions). Compared with comprehensive EHR phenotypes, self-report under-captured all conditions, including hypertension (27.9% vs 16.2%), diabetes (10.1% vs 6.2%), and heart disease (8.5% vs 4.3%). However, diagnosis codes alone were insufficient. The risk for 1-year hospitalization was better defined by the same features from patient-portal EHR (area under the receiver operating curve [AUROC] 0.79) than from self-report (AUROC 0.68). DISCUSSION: EHR-derived computable phenotypes identified a higher prevalence of comorbidities than self-report, with prognostic value of additionally identified features. However, definitions based solely on diagnosis codes often undercaptured self-reported conditions, suggesting a role of broader EHR elements.

conclusionIn this nationwide study, patient-portal-derived EHR data enabled extensive capture of patient characteristics across multiple EHR platforms, allowing better disease phenotyping compared with self-report.

Indexed as

COVID-19Electronic Health RecordsPatient PortalsSelf ReportAdultFemaleHospitalizationHumansMaleMiddle AgedRegistriesSARS-CoV-2Surveys and Questionnairesdecentralizedmulticenterpatient portalpragmatic studies

Identifiers

PMID40036551
PMCPMC12012333

What OpenQuestion holds

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Registered trials

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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.