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1.
Soc Secur Bull ; 71(1): 1-15, 2011.
Article in English | MEDLINE | ID: mdl-21466031

ABSTRACT

Using a rich dataset that links the Census Bureau's Survey of Income and Program Participation calendar-year 2004 file with Social Security benefit records, this article provides a portrait of the sociodemographic and economic characteristics of Social Security child beneficiaries. We find that the incidence ofbenefit receipt in the child population differs substantially across individual and family-level characteristics. Average benefit amounts also vary across subgroups and benefit types. The findings provide a better understanding of the importance of Social Security to families with beneficiary children. Social Security is a major source of family income for many child beneficiaries, particularly among those with low income or family heads with lower education and labor earnings.


Subject(s)
Aid to Families with Dependent Children/statistics & numerical data , Family Characteristics , Insurance Benefits/statistics & numerical data , Adolescent , Aid to Families with Dependent Children/economics , Aid to Families with Dependent Children/standards , Child , Child, Preschool , Female , Humans , Income/classification , Income/statistics & numerical data , Insurance Benefits/economics , Insurance Benefits/standards , Logistic Models , Male , Socioeconomic Factors , United States
3.
Am J Public Health ; 92(9): 1446-52, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12197971

ABSTRACT

OBJECTIVES: This study evaluated the relationships between health insurance and welfare status and the health and medical care of children with asthma. METHODS: Parents of children with asthma aged 2 to 12 years were interviewed at 6 urban clinical sites and 2 welfare offices. RESULTS: Children whose families had applied for but were denied welfare had more asthma symptoms than did children whose families had had no contact with the welfare system. Poorer mental health in parents was associated with more asthma symptoms and higher rates of health care use in their children. Parents of uninsured and transiently insured children identified more barriers to health care than did parents whose children were insured. CONCLUSIONS: Children whose families have applied for welfare and children who are uninsured are at high risk medically and may require additional services to improve health outcomes.


Subject(s)
Aid to Families with Dependent Children/standards , Asthma/economics , Asthma/therapy , Child Health Services/standards , Insurance Coverage/statistics & numerical data , Medicaid/standards , Medically Uninsured/statistics & numerical data , Quality of Health Care , Adult , Aid to Families with Dependent Children/legislation & jurisprudence , Asthma/physiopathology , Child , Child Health Services/economics , Child, Preschool , Chronic Disease/economics , Cross-Sectional Studies , Female , Health Care Surveys , Health Services Accessibility , Humans , Interviews as Topic , Medicaid/legislation & jurisprudence , Mental Health , Mothers/psychology , Severity of Illness Index , Surveys and Questionnaires
4.
Am J Manag Care ; 5(4): 413-26, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10387381

ABSTRACT

OBJECTIVE: To describe Medicaid recipients' experiences with the outcomes of access, quality, and satisfaction in a mandatory managed care (MC) program. STUDY DESIGN: A qualitative case study design with content analysis of narrative focus group (FG) data, which was part of a comprehensive program evaluation that also involved pre- and postsurveys and analyses of cost and utilization data. PATIENTS AND METHODS: Six FG interviews were conducted in the autumn of 1997 with 31 women on the Aid to Families with Dependent Children program. Participants were recruited from a randomly ordered list of women who had responded to a 1996 premanaged care survey regarding their or their child's healthcare experiences under traditional Medicaid. RESULTS: There was general consensus across all focus groups on a range of issues, including improvements in access to primary care and continuity of care. Overall, few participants expressed discontent with restriction of choice of provider and on MC policies regarding use of the emergency room. There was no consensus on what factors influenced choice of MC plan, although convenience of location was named most frequently. An unanticipated outcome was the recurrent theme across all focus groups of disrespectful treatment by healthcare personnel, especially under traditional Medicaid, which had declined somewhat under managed care. CONCLUSIONS: These contextual accounts identify specific features of a mandatory Medicaid MC program that are viewed as improvements over traditional Medicaid. Specific features that were dissatisfying can be addressed to improve both enrollee satisfaction and the transition to managed care for Medicaid recipients.


Subject(s)
Managed Care Programs/standards , Medicaid/organization & administration , Patient Satisfaction/statistics & numerical data , Aid to Families with Dependent Children/organization & administration , Aid to Families with Dependent Children/standards , Aid to Families with Dependent Children/statistics & numerical data , Female , Focus Groups , Health Care Surveys , Health Services Accessibility , Humans , Interviews as Topic , Managed Care Programs/economics , Managed Care Programs/statistics & numerical data , Medicaid/standards , Medicaid/statistics & numerical data , North Carolina , Program Evaluation , Quality of Health Care , United States
5.
Med Care ; 37(3 Suppl): MS89-96, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10098563

ABSTRACT

OBJECTIVES: Collecting accurate health data on the growing number of ethnic minorities in the United States has increased in policy relevance in recent years. Today, most general population sample surveys conducted in the United States, including the CAHPS 1.0 Surveys, require translation into Spanish and often other languages as well. This article discusses the process used to translate the CAHPS 1.0 survey instruments into Spanish and the techniques used to evaluate these instruments. METHODS: The CAHPS team used a technique of translation-backtranslation to translate the survey instruments into Spanish and conducted cognitive testing and pretesting of preliminary versions of the 1.0 Survey Instruments in both English and Spanish. RESULTS: The translation-backtranslation method produced Spanish-language versions of the survey instruments that were adequate for more educated respondents but were inadequate for less educated respondents and respondents who seemed to be less acculturated. CONCLUSION: Adept translation of a survey instrument is an integral part of the instrument-development process, but it alone does not ensure that a culturally appropriate survey instrument will result. Producing a survey instrument that is culturally appropriate for Latinos in the United States may require modifying the English versions of instruments as well as subjecting Spanish-language instruments to more rigorous testing that includes cognitive testing, pretesting, and an evaluation of the reading level by a literacy expert.


Subject(s)
Data Collection/methods , Health Care Surveys/methods , Hispanic or Latino/psychology , Translating , Adult , Aid to Families with Dependent Children/standards , Child , Cognition , Consumer Behavior , Correspondence as Topic , Data Collection/standards , Educational Status , Health Care Surveys/standards , Humans , Los Angeles , Medicaid/standards , Oklahoma , Reading , Reproducibility of Results , Surveys and Questionnaires/standards , Telephone , United States
6.
Soc Sci Med ; 35(8): 1055-63, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1411700

ABSTRACT

Despite substantial evidence linking improved pregnancy outcomes with receipt of prenatal care and recent improvements in prenatal care utilization, specific subpopulations continue to receive less than adequate care. The study reported here examined the effects on prenatal care utilization of differences among states in AFDC and Medicaid eligibility policies. The study was based on information obtained from birth certificates and a mailed questionnaire to stratified random samples of all women experiencing live births during specified periods in four states. States were selected to provide comparisons between two states with liberal AFDC and Medicaid eligibility standards--Wisconsin and Colorado--and two states--Maine and Texas--which had more restrictive standards at the time data were collected. Study findings generally indicate that more liberal AFDC/Medicaid eligibility standards improve the adequacy of prenatal care among low income women. They also suggest, however, that the often lengthy eligibility process may actually pose barriers to care.


Subject(s)
Aid to Families with Dependent Children/standards , Eligibility Determination , Health Services Accessibility/standards , Medicaid/standards , Prenatal Care/statistics & numerical data , Birth Certificates , Colorado , Female , Health Services Research , Humans , Maine , Poverty , Surveys and Questionnaires , Texas , United States , Wisconsin
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