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A patient and family data domain collection framework for identifying disparities in pediatrics: results from the pediatric health equity collaborative.

Aswita Tan-McGroryCaroline Bennett-AbuAyyashStephanie GeeKirk DabneyJohn D CowdenLaura WilliamsSarah RaftonArie NettlesSonia PaguraLaurens HolmesJane GolemanLaVone CaldwellJames PagePatricia OceanicErika J McMullenAdriana LoperaSarah BeiterLenny López
Published in: BMC pediatrics (2018)
There is no single approach that will work for all organizations when collecting race, ethnicity, language and other social determinants of health data. Each organization will need to tailor their data collection based on the population they serve, the financial resources available, and the capacity of the electronic health record.
Keyphrases
  • electronic health record
  • clinical decision support
  • healthcare
  • public health
  • mental health
  • big data
  • adverse drug
  • health information
  • case report
  • health promotion
  • quality improvement
  • young adults
  • affordable care act