Skip to main content
. 2020 Jun 28;3(2):178–184. doi: 10.1093/jamiaopen/ooaa019

Table 1.

Summary of approach to health disparity through demographic data collection, stratification quality measures, and registry-based infrastructure

Population health informatics approach Quality measurement Informatics workflows and registry infrastructure
Standardized demographic data collection
  • Complete documentation of race, ethnicity, and language

  • Complete documentation of sexual orientation and gender identity

Structured standardized fields for data collection of REAL and SOGI
  • Mandatory completion of REAL by all registration staff

  • Patient portal enabled completion of REAL SO/GI

  • Clinical back office and nurse entered SO/GI detail for all primary care patient face to face visits

  • Clinical REAL SO/GI navigator section for clinicians

Stratification of quality measures by race, ethnicity, language, sexual orientation, and gender identity
  • Controlling blood pressure [National Quality Forum (NQF) 0018]

  • Ischemic vascular disease [NQF 0068]

  • Prevention of quality overall composite [Agency for Healthcare Research and Quality Indicator (PQI )#90]

  • Alcohol and drug misuse [Stewards: Alameda Health System, San Francisco Health Network, University of California Irvine]

  • Screening for depression and follow-up [NQF 0418]

  • Tobacco assessment and counseling [NQF 0028e]

  • Colorectal cancer screening [NQF 0034]

  • Hemoglobin A1C poor control [NQF 0059]

  • Analytics enabled stratification of quality measures by demographic strata showing measure performance and percentage of total population

    • Performance by race

    • Performance by ethnicity

    • Performance by language

    • Performance by sexual orientation

  • Performance by gender identity

Electronic health record-based registries to support population health informatics infrastructure
  • Hypertension registry for improved opportunities to identify patients with poor blood pressure control

  • Ischemic vascular disease and hemorrhage registries to identify patients appropriate for antiplatelet therapy

  • Diabetes, chronic obstructive lung disease, heart failure registries to support improved chronic disease management reducing acute utilization as measured by the prevention of quality overall composite

  • No current registry for alcohol and drug misuse

  • Depression registry to support appropriate level of screening for depression and follow-up

  • Tobacco registry to support assessment and counseling

Registry-based rule driven patient engagement, clinical decision support tools for providers, and care gap outreach
  • System level rules set at a patient level for health maintenance

  • Patient portal engagement through display of current care gaps and receipt of registry driven outreach

  • Nurse tee-up of orders based on registry-based care gaps

  • Provider-based decision support for care gap completion, summary of chronic disease control, navigator banner alert, and dynamic rule-based links to medication, laboratory testing, and referrals

  • Collaborative care team outreach based on registry driven metrics identifying need for follow-up

  • Pharmacist outreach by registry cohort

  • Nurse and patient navigator outreach by registry