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133. Considerations for building federal data capacity for patient-centered outcomes research related to intellectual and developmental disabilities

Author(s):
Dhopeshwarkar, Rina, author
Heaney-Huls, Krysta, author
Hovey, Lauren, author
Leaphart, Desirae, author
Dullabh, Prashila, author
Publication:
Washington, D.C. : Department of Health and Human Services, Office of the Assistant Secretary for Planning and Evaluation, September 22, 2021
Subject(s):
Data Collection
Developmental Disabilities
Intellectual Disability
Patient-Centered Care
Research Design
United States
United States. Department of Health and Human Services.

137. Collection and availability of data on race, ethnicity and immigrant groups in federal surveys that measure health insurance coverage and access to care

Author(s):
Bernard, Sydney, author
Au-Yeung, Carrie, author
Publication:
Minneapolis, Minnesota : State Health Access Data Assistance Center, September 2021
Subject(s):
Data Collection
Emigrants and Immigrants
Ethnicity
Health Services Accessibility
Insurance Coverage
Racial Groups
Surveys and Questionnaires
Federal Government
United States

138. An overview of new CMS data on the number of adults enrolled in the ACA Medicaid expansion

Author(s):
Snyder, Laura, author
Artiga, Samantha, author
Rudowitz, Robin, author
Stephens, Jessica, author
Publication:
Menlo Park, CA : Henry J. Kaiser Family Foundation, February 2015
Subject(s):
Data Collection
Eligibility Determination -- statistics & numerical data
Medicaid -- statistics & numerical data
Medicaid -- trends
United States
United States.
Centers for Medicare & Medicaid Services (U.S.)