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The Data Resource Center for Child and Adolescent Health www.childhealthdata.org. Debra Read, MPH CAHMI – Child & Adolescent Health Measurement Initiative HRTW National Resource Center Topical Call Feb 1, 2008. 2005/06 NS-CSHCN.
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The Data Resource Center for Child and Adolescent Healthwww.childhealthdata.org Debra Read, MPH CAHMI – Child & Adolescent Health Measurement Initiative HRTW National Resource Center Topical Call Feb 1, 2008
2005/06 NS-CSHCN • Asked detailed questionnaire for children with special health care needs • Target = 750 CSHCN Interviews per state • Calling and screening of households continued until met the target in all states • One CSHCN randomly selected from households with multiple CSHCN • Data collected from April 5, 2005 until February 5, 2007
2005/06 NS-CSHCN • 364,841 children screened for special health care needs • Minimum: 5,605 in Delaware • Maximum: 11,275 in California • More than 7,000 in each of 25 states • 40,840 completed interviews for CSHCN • Minimum: 741 in Alaska • Maximum: 939 in California • More than 800 in each of 22 states
CSHCN Interview • Health and functional status • Access to care, utilization, unmet need • Care coordination • Family Centered Care • Transition to Adulthood • Ease of Use & Satisfaction with care • Health insurance and adequacy • Impact on the family
Improved Content for 2005-06 • Functional difficulties list (see resource materials for call) • Health conditions list (see resource materials for call) • Revised/improved care coordination question section • Revised/improved transition to adulthood section (see resource materials for call) • 2005/06: Asked for full sample of 12-17 yrs old CSHCN • Includes new age-appropriate self mgmt question education question for CSHCN ages 5 – 17 yrs old
Click on column heading text to sort Outcome #6:CSHCN ages 12-17 who receive services needed for transition to adult health care, work and independence
Section 6B: Transition Issues 8 questions
Coming March 2008! Outcome #6: CSHCN ages 12-17 who receive services needed for transition to adult health care, work and independence • Component A: Receives anticipatory guidance in the transition to adulthood Part A_1: Drs discuss shift to adult providers, if necessary Part A_2: Drs discuss future health care needs, if necessary Part A_3: Drs discuss maintaining health insurance coverage • Component B: Receives age-appropriate self mgmt education and encouragement from providers
Coming March 2008! • Independent national Referent sample of children • 6,113 household interviews completed • One child randomly selected from household • 4,955 did not have special health care needs • Parent or guardian asked every question from the detailed CSHCN interview • NEW STATE PROFILE REPORT OPTION: Comparing 2005/06 Non-CSHCN estimates from national Referent sample with CSHCN estimates in each state
What features are available? • Learnabout the surveys • Search and comparenational, state, and regional survey results for subgroups of children (age, race, sex, income, insurance and health status, etc.) • Get resources and ideas on how to report your findings in a valid and effective manner • Get expert help– by e-mailing us your questions, plus get links to other data sets and resources
Thinking about ways data could be used • Identifying/documenting needs and performance • Building partnerships • Educating Policymakers • Advocacy • Grant Writing
Visit soon! www.childhealthdata.org • National Survey of Children with Special Health Care Needs www.cshcndata.org • National Survey of Children’s Health www.nschdata.org