3236.0 Development of a Registry as a Quality Improvement Tool for Assessing Access

Monday, October 29, 2012: 12:30 PM - 2:00 PM
Roundtable
Data registries are a compelling tool for tracking disease across populations, from access and diagnosis to improvements in care that lead to better outcomes. Participants in this session will be engaged in a robust discussion about promising examples from across the country regarding the role of health IT in increasing the nation's knowledge base regarding disease progression.
Session Objectives: 1.Describe the development of a disease registry for helping to understand variation in access and longitudinal care; 2.Evaluate the role of a disease registry as a quality improvement tool for optimizing delivery of treatment and outcomes in highly vulnerable patient populations.
Organizer:
Diane L. Adams, MD, MPH, CHS-III
Moderator:
Chinua Lambie, MHA

Table 1
Patient-level record de-duplication for immunization information systems and disease registries: Old problems with new solutions
Frederic Grant, PhD, MPH, PMP and Jennifer Wain, IIS Program Manager
  
Table 2
Development of a Diabetes Registry as a Quality Improvement Tool for Assessing Access, Service Utilization and Health Outcomes in Economically Vulnerable Populations
Camerino I. Salazar, MS, Barbara Turner, MD, MSED, MACP, Lisa Wammack, MSN, RN, Edward Aguilar, Fei Du and Adriana G. Perez
Table 3
Lessons learned in developing a national registry for community-led Patient Centered Outcomes Research
Reesa Laws, BS, Thu Quach, PhD, MPH, Rosy Chang Weir, PhD, Erin Kaleba, MPH, Chris Grasso, MPH, Stephen Van Rompaey, PhD, Jon Puro, MPH-HA, Joe Carroll, MD, PhD and Suzanne Gillespie, MS
  
Table 4
Tackling hospital-acquired infections with systems-based highly-detailed simulations
Jose Jimenez, MS, MEM, PhD/MPH Candidate, Bryan Lewis, MPH, PhD, Brian Kleiner, PhD, MS and Stephen Eubank, PhD
Table 5
Utilizing the Pacific Innovation Collaborative (PIC) data repository and online reporting system to promote meaningful use of centralized community health center data for underserved Asian American, Native Hawaiian, & other Pacific Islander patients
Heather Law, MA, Rosy Chang Weir, PhD and Jeffrey Caballero, MPH
     
Table 6
Reaction of health professionals to chronic disease Clinical Decision Support (CDS)
Mary K. Goldstein, MD, MS, Susana Martins, MD, James Schlosser, MD, Nancy Kim, MD, Wildon Farwell, MD, Tyson Holmes, PhD, Mark Musen, MD, PhD, Samson Tu, MS, Dallas Chambers, BS, Timothy Keng and Brian Hoffman, MD
        

See individual abstracts for presenting author's disclosure statement and author's information.

Organized by: Health Informatics Information Technology
Endorsed by: American Indian, Alaska Native and Native Hawaiian Caucus

CE Credits: Medical (CME), Health Education (CHES), Nursing (CNE), Public Health (CPH) , Masters Certified Health Education Specialist (MCHES)

See more of: Health Informatics Information Technology
<< Previous Session | Next Session >>