4.6 Article

Research-grade data in the real world: challenges and opportunities in data quality from a pragmatic trial in community-based practices

期刊

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jamia/ocz062

关键词

real world data; health information technology; data quality; immigrants; pragmatic trials; health equity

资金

  1. Centers for Disease Control and Prevention (CDC), Prevention Research Centers (PRC) Program [U48DP005008]
  2. National Institutes of Health (NIH) National Institute on Minority Health and Health Disparities (NIMHD) [P60MD000538, U54MD000538]
  3. NIH National Center for the Advancement of Translational Science (NCATS) [UL1TR001445]
  4. NIH National Institute of Diabetes and Digestive Kidney Diseases (NIDDK) [R01DK110048]

向作者/读者索取更多资源

Randomized controlled trials face cost, logistic, and generalizability limitations, including difficulty engaging racial/ethnic minorities. Real-world data (RWD) from pragmatic trials, including electronic health record (EHR) data, may produce intervention evaluation findings generalizable to diverse populations. This case study of Project IMPACT describes unique barriers and facilitators of optimizing RWD to improve health outcomes and advance health equity in small immigrant-serving community-based practices. Project IMPACT tested the effect of an EHR-based health information technology intervention on hypertension control among small urban practices serving South Asian patients. Challenges in acquiring accurate RWD included EHR field availability and registry capabilities, cross-sector communication, and financial, personnel, and space resources. Although using RWD from community-based practices can inform health equity initiatives, it requires multidisciplinary collaborations, clinic support, procedures for data input (including social determinants), and standardized field logic/rules across EHR platforms.

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