Data were extracted from a review of computerized administrative claims for 15,507 Medicaid youth in an effort to assess differences in rates of mental health treatment for enrollees in one of 3 categories of aid. The study population consisted of individuals aged 0-19 years residing in a suburban county in a mid-Atlantic state during 1996 and enrolled in the fee-for-service Medicaid program. Mental health services were analyzed and compared for youth in foster care, receiving Supplemental Security Income (SSI), and all other forms of assistance such as Aid to Families with Dependent Children (AFDC). The dataset includes demographic information, type of mental health services provided, mental disorder diagnoses (in 15 subcategories), as well as psychotropic and certain nonpsychotropic medications prescribed.
This dataset represents a comparison of polypharmacy among youth with serious emotional and behavioral disorders enrolled in coordinated care services (CCS) versus those receiving traditional mental health services. Data were extracted from Medicaid administrative claims (demographic, diagnosis by ICD-9 code, procedure codes, and psychotropic medication), child welfare administrative records, and juvenile justice records. The final analytic sample included a total of 814 CCS youths and 993 in the traditional care cohort.
This qualitative inquiry investigated caregivers’ experiences with care management services for their child diagnosed with both cognitive and mental health needs. Study eligibility requirements included caring for a child 26 years of age or younger at enrollment, with an intellectual or cognitive developmental disability, and who also had a mental health condition. A total of 37 caregivers participated, 6 of whom were selected for in-depth interviews with the remaining 31 distributed among 5 focus groups. All sessions were recorded and subsequently transcribed verbatim. Data includes family demographics, child characteristics (e.g. school grade level, diagnoses, treatment, behavioral problems, etc.), and the factors promoting family engagement in care management
The Medical Expenditure Panel Survey (MEPS) is a set of large-scale surveys of families and individuals, their medical providers (doctors, hospitals, pharmacies, etc.), and employers across the United States. MEPS collects data on the specific health services that Americans use, how frequently they use them, the cost of these services, and how they are paid for, as well as data on the cost, scope, and breadth of health insurance held by and available to U.S. workers. The two major components of MEPS are the Household Component and the Insurance Component.
Characteristics associated with low availability of treatment facilities and high rates of opioid overdose mortality were analyzed using a cross-sectional analysis design that combined county-level data from January 1, 2017, to December 31, 2021. Data for 3,130 counties in 50 states and Washington D.C. from several sources were accessed through PolicyMap, including American Community Survey (ACS), the Centers for Disease Control and Prevention (CDC), the United States Bureau of Labor Statistics (BLS), and the Substance Abuse and Mental Health Services Administration (SAMSHA).