Evidence map›Paper›PMID 32885240›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2020

Recommendations for improving national clinical datasets for health equity research.

Rebecca G Block, Jon Puro, Erika Cottrell, Mitchell R Lunn, M J Dunne, Ana R Quiñones, Bowen Chung, William Pinnock, Georgia M Reid, John Heintzman

Abstract read
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. A Scoping Review of Approaches to Improving Quality of Data Relating to Health Inequalities.International journal of environmental research and public health · 2022
    Article
  8. Article
  9. Toward diversity, equity, and inclusion in informatics, health care, and society.Journal of the American Medical Informatics Association : JAMIA · 2020
    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

10 authors.

Rebecca G BlockDepartment of Research, OCHIN, Portland, Oregon, USA.
Jon PuroDepartment of Research, OCHIN, Portland, Oregon, USA.
Erika CottrellDepartment of Research, OCHIN, Portland, Oregon, USA.
Mitchell R LunnDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
M J DunneDepartment of Research, OCHIN, Portland, Oregon, USA.
Ana R QuiñonesDepartment of Research, OCHIN, Portland, Oregon, USA.
Bowen ChungDepartment of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
William PinnockDepartment of Research, OCHIN, Portland, Oregon, USA.
Georgia M ReidDepartment of Research, OCHIN, Portland, Oregon, USA.
John HeintzmanDepartment of Research, OCHIN, Portland, Oregon, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Health and healthcare disparities continue despite clinical, research, and policy efforts. Large clinical datasets may not contain data relevant to healthcare disparities and leveraging these for research may be crucial to improve health equity. The Health Disparities Collaborative Research Group was commissioned by the Patient-Centered Outcomes Research Institute to examine the data science needs for quality and complete data and provide recommendations for improving data science around health disparities. The group convened content experts, researchers, clinicians, and patients to produce these recommendations and suggestions for implementation. Our desire was to produce recommendations to improve the usability of healthcare datasets for health equity research. The recommendations are summarized in 3 primary domains: patient voice, accurate variables, and data linkage. The implementation of these recommendations in national datasets has the potential to accelerate health disparities research and promote efforts to reduce health inequities.

Indexed as

Health EquityBiomedical ResearchDatasets as TopicElectronic Health RecordsHealthcare DisparitiesHumansPatient Participationclinical researchdata sciencedata warehousingelectronic health recordshealthcare disparitieshealth equity

Identifiers

PMID32885240
PMCPMC7671626

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.