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Gliklich RE, Dreyer NA, Leavy MB, editors. Registries for Evaluating Patient Outcomes: A User's Guide [Internet]. 3rd edition. Rockville (MD): Agency for Healthcare Research and Quality (US); 2014 Apr.

Cover of Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes: A User's Guide [Internet]. 3rd edition.

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Table 4–2Examples of possible baseline data elements

Enrollee contact information
  • Enrollee contact information for registries with direct-to-enrollee contact
  • Another individual who can be reached for followup (address, telephone, email)
Enrollment data elements
  • Patient identifiers (e.g., name [last, first, middle initial], date of birth, place of birth, Social Security number)
  • Permission/consent
  • Source of enrollment (e.g., provider, institution, phone number, address, contact information)
  • Enrollment criteria
  • Sociodemographic characteristics, including race, gender, and age or date of birth
  • Education and/or economic status, insurance, etc.
  • Preferred language
  • Place of birth
  • Location of residence at enrollment
  • Source of information
  • Country, State, city, county, ZIP Code of residence

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