Patient information, such as date of birth, sex, race, hispanic ethnicity, etc.
Encounter type, date, provider, location, discharge disposition, etc.
Diagnosis code(s) associated with each encounter.
Procedure code(s) associated with each encounter.
Rx order information such as order date, start date, end date, RxNorm CUI, refills, quantity, etc.
Vital Signs and Smoking Info
Measure date, weight, height, blood pressure, smoking/tobacco status, etc.
Death Date and Cause
Death date and associated cause of death diagnosis.
Result date, result value, units, normal range, LOINC, etc.
Problems list and medical history diagnoses. Report date, onset date, resolved date, etc.
Medication dispensing records for publicly and privately insured patients. Dispense date, NDC, amount, etc.
Community Vital Signs
Community indicators at the census track, ZCTA and/or county levels such as census indicators. These indicators have been linked to current and historical patient addresses.
Patient Reported Outcomes
Screening tool scores such as PHQ, DAST, SBIRT, AUDIT, etc.
The ADVANCE Data Warehouse is the nation’s most comprehensive database on health care and outcomes of safety net patients.
By Ludmilla Paul, MPH - Research Program Coordinator at Health Choice Network Cervical cancer is a disease of major public health importance. Although screening and immunization against human papilloma virus (HPV), which causes cervical cancer, provide highly...read more
Written by The EVERYWOMAN Study Team: Jee Oakley Anna Templeton, Erika Cottrell, Brigit Hatch, and Megan Hoopes EVERYWOMAN (Reproductive Care in the Safety-Net: Women’s Health Care after Affordable Care Act Implementation) is a reproductive health study currently...read more
Happy December, everyone! I, for one, am enjoying the winter holiday season and am looking forward to ringing in the New Year. Here are a few updates from ADVANCE: Earlier this month, University of Washington’s School of Public Health graciously hosted Drs. Rebecca...read more
Jon Puro, MPA, HA
ADVANCE is one of 13 CDRNs participating in the Patient Centered Outcomes Research Institute’s (PCORI) distributed research network, called PCORnet. The goal of PCORnet is to create a national network of representative data for conducting comparative effectiveness and clinical outcomes research.