- ACA Implementation & State Health Reform
- Coverage and Access
- Federal/State Issues
- Medicaid and CHIP
- Population and Public Health
- Providers and Services
- Acute Care
- Assisted Living
- Behavioral Health
- Case Management
- Child Development Services
- Chronic Care Management
- Community Health Centers
- Developmental Screening
- Early Childhood Services
- Emergency Care
- EPSDT
- Family Planning
- Federally Qualified Health Centers
- Home & Community Based Services
- Hospitals
- Long Term Services & Supports
- Medical Homes & Health Homes
- Mental Health
- Nursing Homes
- Oral Health
- Preventive Care
- Primary Care
- Safety Net Providers
- Quality, Cost, and Health System Performance
- ACOs
- Adverse Event Reporting
- Care Transitions
- Comparative Effectiveness
- Cost Sharing
- Delivery System Reform
- Fraud and Abuse
- Health Care Workforce
- Health Information Technology
- Managed Care
- Medical Homes & Health Homes
- Medical Malpractice
- Patient Safety
- Payment Reform
- Performance Measurement
- Provider Payment Policy
- Quality Oversight
- Specific Populations
- Adolescents
- Childless Adults
- Children
- Children with Special Health Care Needs
- Dual Eligibles
- Elders
- Families
- Low Income People
- Parents
- People with Chronic Conditions
- People with Developmental Disabilities
- Transitional Youth
- Vulnerable Populations
- Young Adults
- Youth
- Youth in Foster Care System
- Youth in Juvenile Justice System
The State of Utah initiated its patient safety program through the use of two administrative rules.
R380-200, entitled the Patient Safety Sentinel Event Report, requires all licensed hospitals and ambulatory surgical centers to report the occurrence of sentinel events and the findings and action plans of the root cause analyses that follow. R380-210, entitled the Health Care Facility Patient Safety Program, requires all licensed hospitals and ambulatory surgical centers to report on an annual basis through the UB92 HCFA administrative billing structure ICD9 coded adverse drug events. Additionally this rule requires a once every three year independent audit of each facility's adverse drug event reduction program. Both of these administrative rules are authorized under Title 26-1-30(a), (b), (d), (e), and (g) and Section 26-3-8.
