Literature DB >> 32885240

Recommendations for improving national clinical datasets for health equity research.

Rebecca G Block1, Jon Puro1, Erika Cottrell1,2, Mitchell R Lunn3, M J Dunne1, Ana R Quiñones1,2, Bowen Chung4, William Pinnock1, Georgia M Reid1,5, John Heintzman1,2.   

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.
© The Author(s) 2020. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  clinical research; data science; data warehousing; electronic health records; health equity; healthcare disparities

Mesh:

Year:  2020        PMID: 32885240      PMCID: PMC7671626          DOI: 10.1093/jamia/ocaa144

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  24 in total

1.  "Community vital signs": incorporating geocoded social determinants into electronic records to promote patient and population health.

Authors:  Andrew W Bazemore; Erika K Cottrell; Rachel Gold; Lauren S Hughes; Robert L Phillips; Heather Angier; Timothy E Burdick; Mark A Carrozza; Jennifer E DeVoe
Journal:  J Am Med Inform Assoc       Date:  2015-07-13       Impact factor: 4.497

2.  Report of the AMIA EHR-2020 Task Force on the status and future direction of EHRs.

Authors:  Thomas H Payne; Sarah Corley; Theresa A Cullen; Tejal K Gandhi; Linda Harrington; Gilad J Kuperman; John E Mattison; David P McCallie; Clement J McDonald; Paul C Tang; William M Tierney; Charlotte Weaver; Charlene R Weir; Michael H Zaroukian
Journal:  J Am Med Inform Assoc       Date:  2015-05-28       Impact factor: 4.497

3.  ONC issues guides for SAFER EHRs.

Authors:  Dean F Sittig; Joan S Ash; Hardeep Singh
Journal:  J AHIMA       Date:  2014-04

4.  Database of patients' experiences (DIPEx): a multi-media approach to sharing experiences and information.

Authors:  A Herxheimer; A McPherson; R Miller; S Shepperd; J Yaphe; S Ziebland
Journal:  Lancet       Date:  2000-04-29       Impact factor: 79.321

Review 5.  Opportunities and challenges in developing risk prediction models with electronic health records data: a systematic review.

Authors:  Benjamin A Goldstein; Ann Marie Navar; Michael J Pencina; John P A Ioannidis
Journal:  J Am Med Inform Assoc       Date:  2016-05-17       Impact factor: 4.497

6.  Avoiding the Unintended Consequences of Screening for Social Determinants of Health.

Authors:  Arvin Garg; Renée Boynton-Jarrett; Paul H Dworkin
Journal:  JAMA       Date:  2016 Aug 23-30       Impact factor: 56.272

Review 7.  Racial and Ethnic Disparities in the Quality of Health Care.

Authors:  Kevin Fiscella; Mechelle R Sanders
Journal:  Annu Rev Public Health       Date:  2016-01-18       Impact factor: 21.981

8.  Using Health Information Technology to Bring Social Determinants of Health into Primary Care: A Conceptual Framework to Guide Research.

Authors:  Erika K Cottrell; Rachel Gold; Sonja Likumahuwa; Heather Angier; Nathalie Huguet; Deborah J Cohen; Khaya D Clark; Laura M Gottlieb; Jennifer E DeVoe
Journal:  J Health Care Poor Underserved       Date:  2018

9.  Are informed policies in place to promote safe and usable EHRs? A cross-industry comparison.

Authors:  Erica L Savage; Rollin J Fairbanks; Raj M Ratwani
Journal:  J Am Med Inform Assoc       Date:  2017-07-01       Impact factor: 4.497

Review 10.  Electronic health records: new opportunities for clinical research.

Authors:  P Coorevits; M Sundgren; G O Klein; A Bahr; B Claerhout; C Daniel; M Dugas; D Dupont; A Schmidt; P Singleton; G De Moor; D Kalra
Journal:  J Intern Med       Date:  2013-10-18       Impact factor: 8.989

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  2 in total

1.  Toward diversity, equity, and inclusion in informatics, health care, and society.

Authors:  Suzanne Bakken
Journal:  J Am Med Inform Assoc       Date:  2020-11-01       Impact factor: 4.497

2.  Commentary: Quantifying the health needs of migrants in vulnerable circumstances registered with a nurse-led primary care service.

Authors:  Ruth De Souza
Journal:  J Res Nurs       Date:  2022-06-14
  2 in total

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