5182.0 Standards and Interoperability in Health IT: Part II

Wednesday, November 2, 2011: 12:30 PM
Oral
Data collection, at its most efficient, requires standard nomenclature and protocols. This session seeks to explain the value of data standardization, and its impact on interoperability.
Session Objectives: At the end of this session, participants should be able to: 1. evaluate the possibility of standardizing data collection methods used to collect health information about newborns; 2. to determine whether the names and diagnostic codes for certain disease conditions can be standardized to facilitate data collection.
Organizer:
Diane L. Adams, MD, MPH, CHS-III
Moderator:
Sara Copeland, MD

12:30 PM
Developing standard case definitions of newborn screening disorders for epidemiological surveillance
Deboshree Sarkar, MPH and Sara Copeland, MD
     
12:50 PM
Developing standard names and codes for lysosomal storage disorders detectable by newborn screening
Rebecca M. Goodwin, JD, Michael Watson, PhD, FACMG, Dietrich Matern, MD, FACMG, J. Gilbert Hill, MD, PHD, Carla Cuthbert, PhD, FCCMG, FACMG, Swapna Abhyankar, MD, Sara Copeland, MD, Tiina Urv, PhD, Deboshree Sarkar, MPH and Clement McDonald, MD
     
  
1:10 PM
Harmonization of Diagnostic Criteria for Hemoglobinopathies among State NBS Programs
Ellen Werner, PhD and Kathryn Hassell, MD
     

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

Organized by: Health Informatics Information Technology
Endorsed by: International Health

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
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