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1.
Health Serv Res ; 54 Suppl 1: 287-296, 2019 02.
Article in English | MEDLINE | ID: mdl-30628052

ABSTRACT

OBJECTIVES: To investigate whether health care experiences of adult Medicaid beneficiaries differ by race/ethnicity and rural/urban status. DATA SOURCES: A total of 270 243 respondents to the 2014-2015 Nationwide Adult Medicaid Consumer Assessment of Healthcare Providers and Systems Survey. STUDY DESIGN: Linear regression was used to estimate case mix adjusted differences in patient experience between racial/ethnic minority and non-Hispanic white Medicaid beneficiaries, and between beneficiaries residing in small urban areas, small towns, and rural areas vs large urban areas. Dependent measures included getting needed care, getting care quickly, doctor communication, and customer service. PRINCIPAL FINDINGS: Compared with white beneficiaries, American Indian/Alaska Native (AIAN) and Asian/Pacific Islander (API) beneficiaries reported worse experiences, while black beneficiaries reported better experiences. Deficits for AIAN beneficiaries were 6-8 points on a 0-100 scale; deficits for API beneficiaries were 13-22 points (P's < 0.001); advantages for black beneficiaries were 3-5 points (P's < 0.001). Hispanic white differences were mixed. Beneficiaries in small urban areas, small towns, and isolated rural areas reported significantly better experiences (2-3 points) than beneficiaries in large urban areas (P's < 0.05), particularly regarding access to care. Racial/ethnic differences typically did not vary by geography. CONCLUSIONS: Improving experiences for racial/ethnic minorities and individuals living in large urban areas should be high priorities for policy makers exploring approaches to improve the value and delivery of care to Medicaid beneficiaries.


Subject(s)
Consumer Behavior/statistics & numerical data , Ethnicity/statistics & numerical data , Health Services Accessibility/statistics & numerical data , Healthcare Disparities/ethnology , Rural Population/statistics & numerical data , Urban Population/statistics & numerical data , Adult , Black or African American/statistics & numerical data , Aged , Asian , Female , Humans , Indians, North American/statistics & numerical data , Male , Medicaid , Middle Aged , Native Hawaiian or Other Pacific Islander/statistics & numerical data , United States , White People/statistics & numerical data , Young Adult
2.
Vital Health Stat 1 ; (59): 1-256, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28796596

ABSTRACT

Objectives This report presents the development, plan, and operation of the 2011-2012 National Survey of Children's Health, a module of the State and Local Area Integrated Telephone Survey, conducted by the National Center for Health Statistics. Funding was provided by the Maternal and Child Health Bureau, Health Resources and Services Administration. The survey was designed to produce national and state prevalence estimates of the physical and emotional health of children aged 0-17 years, as well as factors that may relate to child well-being including medical homes, family interactions, parental health, school and after-school experiences, and neighborhood characteristics.


Subject(s)
Child Health Services/statistics & numerical data , Child Health/statistics & numerical data , Health Surveys/methods , Research Design , Adolescent , Child , Child, Preschool , Family Relations , Female , Health Status , Health Surveys/statistics & numerical data , Humans , Infant , Infant, Newborn , Male , Mental Health/statistics & numerical data , National Center for Health Statistics, U.S. , Parents , Patient-Centered Care/statistics & numerical data , Residence Characteristics/statistics & numerical data , Schools/statistics & numerical data , United States/epidemiology
3.
Vital Health Stat 1 ; (57): 1-271, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25383698

ABSTRACT

OBJECTIVES: This report presents the development, plan, and operation of the 2009-2010 National Survey of Children with Special Health Care Needs, a module of the State and Local Area Integrated Telephone Survey. The survey is conducted by the Centers for Disease Control and Prevention's National Center for Health Statistics. This survey was designed to produce national and state-specific prevalence estimates of children with special health care needs (CSHCN), to describe the types of services that they need and use, and to assess aspects of the system of care for CSHCN. METHODS: A random-digit-dial sample of households with children under age 18 years was constructed for each of the 50 states and the District of Columbia. The sampling frame consisted of landline phone numbers and cellular(cell) phone numbers of households that reported a cell-phone-only or cell-phone-mainly status. Children in identified households were screened for special health care needs. If CSHCN were identified in the household, a detailed interview was conducted for one randomly selected child with special health care needs. Respondents were parents or guardians who knew about the children's health and health care. RESULTS: A total of 196,159 household screening interviews were completed from July 2009 through March 2011, resulting in 40,242 completed special-needs interviews, including 2,991 from cell-phone interviews. The weighted overall response rate was 43.7% for the landline sample, 15.2% for the cell-phone sample, and 25.5% overall.


Subject(s)
Data Collection/methods , Disabled Children/statistics & numerical data , Health Services Needs and Demand/statistics & numerical data , National Center for Health Statistics, U.S. , Research Design , Adolescent , Attention Deficit Disorder with Hyperactivity/epidemiology , Centers for Disease Control and Prevention, U.S. , Child , Child, Preschool , Confidentiality , Data Collection/standards , Female , Health Services Accessibility , Humans , Infant , Insurance Coverage , Male , Patient Care Management , Prevalence , Socioeconomic Factors , Time Factors , United States
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