5170.0: Wednesday, November 19, 2003: 2:30 PM-4:00 PM | |||
Oral | |||
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Purpose to provide information about data sources and survey results that can be used to improve the organization and delivery of health care to children and youth with special health care needs and their families | |||
Learning Objectives: Identify data sources relevant to CSHCN systems development Describe methods for using existing data to identify systems gaps and opportunity for change | |||
See individual abstracts for presenting author's disclosure statement and author's information. | |||
Deborah Allen, ScD John Reiss, PhD | |||
John Reiss, PhD | |||
Introductory Remarks | |||
Monitoring the Maternal and Child Health Bureau's Core Outcomes for CSHCN Gloria Weissman, Merle G. McPherson, Bonnie B. Strickland, PhD, Peter van Dyck, MD, Stephen Blumberg, PhD, Paul Newacheck, DrPH | |||
A national profile of children with special health care needs Michael D Kogan, PhD, Paul Newacheck, DrPH, Merle G. McPherson, Peter van Dyck, MD | |||
Potential of Medicaid and SCHIP expansions to increase insurance coverage for children with special health care needs * Amy J. Davidoff, PhD, Alshadye Yemane, BA | |||
What can the Behavioral Risk Factor Surveillance System do for children with special health care needs? * Jacqueline L. Stock, MPH, Shervin Churchill, MPH, Stacey DeFries, MSW | |||
Reaching the Children: The Relationship between Title V and Part C Programs Treeby Williamson Brown, MA, Meg Booth, MPH, Peggy Frances Bailey, MPA | |||
Concluding Remarks | |||
Organized by: | Maternal and Child Health | ||
Endorsed by: | School Health Education and Services; Statistics | ||
CE Credits: | CME, Health Education (CHES), Nursing, Pharmacy |